US20140178866A1 - Genetic loci associated with soybean cyst nematode resistance and methods of use - Google Patents

Genetic loci associated with soybean cyst nematode resistance and methods of use Download PDF

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US20140178866A1
US20140178866A1 US13/781,963 US201313781963A US2014178866A1 US 20140178866 A1 US20140178866 A1 US 20140178866A1 US 201313781963 A US201313781963 A US 201313781963A US 2014178866 A1 US2014178866 A1 US 2014178866A1
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soybean
marker
resistance
germplasm
nucleic acid
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Joshua M. Shendelman
John B. Woodward
Meizhu Yang
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Pioneer Hi Bred International Inc
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Priority to BR112015015057-8A priority patent/BR112015015057B1/en
Priority to CA2893975A priority patent/CA2893975C/en
Priority to PCT/US2013/076218 priority patent/WO2014100229A1/en
Priority to ARP130104971A priority patent/AR094234A1/en
Assigned to PIONEER HI-BRED INTERNATIONAL, INC reassignment PIONEER HI-BRED INTERNATIONAL, INC ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: WOODWARD, JOHN B, SHENDELMAN, JOSHUA M, YANG, MEIZHU
Publication of US20140178866A1 publication Critical patent/US20140178866A1/en
Priority to ZA2015/03068A priority patent/ZA201503068B/en
Priority to US15/001,290 priority patent/US9994920B2/en
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    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6876—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
    • C12Q1/6888—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for detection or identification of organisms
    • C12Q1/6895—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for detection or identification of organisms for plants, fungi or algae
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q2600/00—Oligonucleotides characterized by their use
    • C12Q2600/13—Plant traits
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q2600/00—Oligonucleotides characterized by their use
    • C12Q2600/156—Polymorphic or mutational markers
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q2600/00—Oligonucleotides characterized by their use
    • C12Q2600/158—Expression markers
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q2600/00—Oligonucleotides characterized by their use
    • C12Q2600/172—Haplotypes

Definitions

  • This invention relates to methods of identifying and/or selecting soybean plants or germplasm that display resistance or improved resistance to Soybean Cyst Nematode.
  • sequence listing is submitted concurrently with the specification as a text file via EFS-Web, in compliance with the American Standard Code for Information Interchange (ASCII), with a file name of 430267seqlist.txt, a creation date of Feb. 21, 2013 and a size of 229 KB.
  • ASCII American Standard Code for Information Interchange
  • the sequence listing filed via EFS-Web is part of the specification and is hereby incorporated in its entirety by reference herein.
  • Soybeans Glycine max L. Merr.
  • Soybean oil is one of the most widely used edible oils, and soybeans are used worldwide both in animal feed and in human food production. Additionally, soybean utilization is expanding to industrial, manufacturing, and pharmaceutical applications.
  • Soybean Cyst Nematode is a parasitic pest which has threatened soybean production in the U.S. for more than fifty years. Soybean cyst nematode resistance is an economically important trait as infection can substantially reduce yields. Molecular characterization of soybean cyst nematode resistance would have important implications for soybean cultivar improvement.
  • the method comprises detecting at least one marker locus that is associated with resistance to soybean cyst nematode. In other embodiments, the method further comprises detecting at least one marker profile or haplotype associated with resistance to soybean cyst nematode. In further embodiments, the method comprises crossing a selected soybean plant with a second soybean plant. Further provided are markers, primers, probes and kits useful for identifying and/or selecting soybean plants or soybean germplasm with resistance or improved resistance to soybean cyst nematode.
  • FIG. 1 A-D provides a genetic map for loci on linkage group A2.
  • kits comprising one pair of oligonucleotide primers may have two or more pairs of oligonucleotide primers.
  • the term “comprising” is intended to include examples encompassed by the terms “consisting essentially of” and “consisting of.” Similarly, the term “consisting essentially of” is intended to include examples encompassed by the term “consisting of.”
  • Agronomics refers to the traits (and underlying genetic elements) of a given plant variety that contribute to yield over the course of a growing season.
  • Individual agronomic traits include emergence vigor, vegetative vigor, stress tolerance, disease resistance or tolerance, insect resistance or tolerance, herbicide resistance, branching, flowering, seed set, seed size, seed density, standability, threshability, and the like.
  • Allele means any of one or more alternative forms of a genetic sequence. In a diploid cell or organism, the two alleles of a given sequence typically occupy corresponding loci on a pair of homologous chromosomes. With regard to a SNP marker, allele refers to the specific nucleotide base present at that SNP locus in that individual plant.
  • amplifying in the context of nucleic acid amplification is any process whereby additional copies of a selected nucleic acid (or a transcribed form thereof) are produced.
  • An “amplicon” is an amplified nucleic acid, e.g., a nucleic acid that is produced by amplifying a template nucleic acid by any available amplification method.
  • An “ancestral line” is a parent line used as a source of genes, e.g., for the development of elite lines.
  • An “ancestral population” is a group of ancestors that have contributed the bulk of the genetic variation that was used to develop elite lines.
  • Backcrossing is a process in which a breeder crosses a progeny variety back to one of the parental genotypes one or more times.
  • chromosome segment designates a contiguous linear span of genomic DNA that resides in planta on a single chromosome.
  • Chrosome interval refers to a chromosome segment defined by specific flanking marker loci.
  • Crop and “variety” are used synonymously and mean a group of plants within a species (e.g., Glycine max ) that share certain genetic traits that separate them from other possible varieties within that species. Soybean cultivars are inbred lines produced after several generations of self-pollinations. Individuals within a soybean cultivar are homogeneous, nearly genetically identical, with most loci in the homozygous state.
  • An “elite line” is an agronomically superior line that has resulted from many cycles of breeding and selection for superior agronomic performance. Numerous elite lines are available and known to those of skill in the art of soybean breeding.
  • An “elite population” is an assortment of elite individuals or lines that can be used to represent the state of the art in terms of agronomically superior genotypes of a given crop species, such as soybean.
  • an “exotic soybean strain” or an “exotic soybean germplasm” is a strain or germplasm derived from a soybean not belonging to an available elite soybean line or strain of germplasm.
  • an exotic germplasm is not closely related by descent to the elite germplasm with which it is crossed. Most commonly, the exotic germplasm is not derived from any known elite line of soybean, but rather is selected to introduce novel genetic elements (typically novel alleles) into a breeding program.
  • a “genetic map” is a description of genetic association or linkage relationships among loci on one or more chromosomes (or linkage groups) within a given species, generally depicted in a diagrammatic or tabular form.
  • Gene is a description of the allelic state at one or more loci.
  • Germplasm means the genetic material that comprises the physical foundation of the hereditary qualities of an organism. As used herein, germplasm includes seeds and living tissue from which new plants may be grown; or, another plant part, such as leaf, stem, pollen, or cells, that may be cultured into a whole plant. Germplasm resources provide sources of genetic traits used by plant breeders to improve commercial cultivars.
  • An individual is “homozygous” if the individual has only one type of allele at a given locus (e.g., a diploid individual has a copy of the same allele at a locus for each of two homologous chromosomes).
  • An individual is “heterozygous” if more than one allele type is present at a given locus (e.g., a diploid individual with one copy each of two different alleles).
  • the term “homogeneity” indicates that members of a group have the same genotype at one or more specific loci. In contrast, the term “heterogeneity” is used to indicate that individuals within the group differ in genotype at one or more specific loci.
  • “Introgression” means the entry or introduction of a gene, QTL, haplotype, marker profile, trait, or trait locus from the genome of one plant into the genome of another plant.
  • label or “detectable label” refer to a molecule capable of detection.
  • a detectable label can also include a combination of a reporter and a quencher, such as are employed in FRET probes or TaqManTM probes.
  • reporter refers to a substance or a portion thereof which is capable of exhibiting a detectable signal, which signal can be suppressed by a quencher.
  • the detectable signal of the reporter is, e.g., fluorescence in the detectable range.
  • quencher refers to a substance or portion thereof which is capable of suppressing, reducing, inhibiting, etc., the detectable signal produced by the reporter.
  • quenching and “fluorescence energy transfer” refer to the process whereby, when a reporter and a quencher are in close proximity, and the reporter is excited by an energy source, a substantial portion of the energy of the excited state non-radiatively transfers to the quencher where it either dissipates non-radiatively or is emitted at a different emission wavelength than that of the reporter.
  • a “line” or “strain” is a group of individuals of identical parentage that are generally inbred to some degree and that are generally homozygous and homogeneous at most loci (isogenic or near isogenic).
  • a “subline” refers to an inbred subset of descendants that are genetically distinct from other similarly inbred subsets descended from the same progenitor. Traditionally, a subline has been derived by inbreeding the seed from an individual soybean plant selected at the F3 to F5 generation until the residual segregating loci are “fixed” or homozygous across most or all loci.
  • soybean varieties are typically produced by aggregating (“bulking”) the self-pollinated progeny of a single F3 to F5 plant from a controlled cross between 2 genetically different parents. While the variety typically appears uniform, the self-pollinating variety derived from the selected plant eventually (e.g., F8) becomes a mixture of homozygous plants that can vary in genotype at any locus that was heterozygous in the originally selected F3 to F5 plant.
  • Marker-based sublines that differ from each other based on qualitative polymorphism at the DNA level at one or more specific marker loci are derived by genotyping a sample of seed derived from individual self-pollinated progeny derived from a selected F3-F5 plant.
  • the seed sample can be genotyped directly as seed, or as plant tissue grown from such a seed sample.
  • seed sharing a common genotype at the specified locus (or loci) are bulked providing a subline that is genetically homogenous at identified loci important for a trait of interest (e.g., yield, tolerance, etc.).
  • Linkage refers to the tendency for alleles to segregate together more often than expected by chance if their transmission was independent. Typically, linkage refers to alleles on the same chromosome. Genetic recombination occurs with an assumed random frequency over the entire genome. Genetic maps are constructed by measuring the frequency of recombination between pairs of traits or markers, the lower the frequency of recombination, and the greater the degree of linkage. “Linkage disequilibrium” is a non-random association of alleles at two or more loci and can occur between unlinked markers. It is based on allele frequencies within a population and is influenced by but not dependent on linkage.
  • Linkage group refers to traits or markers that generally co-segregate.
  • a linkage group generally corresponds to a chromosomal region containing genetic material that encodes the traits or markers.
  • “Locus” is a defined segment of DNA.
  • a “map location” or “map position” is an assigned location on a genetic map relative to linked genetic markers where a specified marker can be found within a given species. Map positions are generally provided in centimorgans (cM), unless otherwise indicated, genetic positions provided are based on the Glycine max consensus map v 4.0 as provided by Hyten et al. (2010) Crop Sci 50:960-968.
  • a “physical position” or “physical location” or “physical map location” is the position, typically in nucleotides bases, of a particular nucleotide, such as a SNP nucleotide, on a chromosome. Unless otherwise indicated, the physical position within the soybean genome provided is based on the Glyma 1.0 genome sequence described in Schmutz et al. (2010) Nature 463:178-183, available from the Phytozome website (phytozome-dot-net/soybean).
  • Mapping is the process of defining the association and relationships of loci through the use of genetic markers, populations segregating for the markers, and standard genetic principles of recombination frequency.
  • Marker or “molecular marker” or “marker locus” is a term used to denote a nucleic acid or amino acid sequence that is sufficiently unique to characterize a specific locus on the genome. Any detectable polymorphic trait can be used as a marker so long as it is inherited differentially and exhibits linkage disequilibrium with a phenotypic trait of interest.
  • Marker assisted selection refers to the process of selecting a desired trait or traits in a plant or plants by detecting one or more nucleic acids from the plant, where the nucleic acid is linked to the desired trait, and then selecting the plant or germplasm possessing those one or more nucleic acids.
  • Haplotype refers to a combination of particular alleles present within a particular plant's genome at two or more linked marker loci, for instance at two or more loci on a particular linkage group. For instance, in one example, two specific marker loci on LG-A2 are used to define a haplotype for a particular plant. In still further examples, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, or more linked marker loci are used to define a haplotype for a particular plant.
  • a “marker profile” means a combination of particular alleles present within a particular plant's genome at two or more marker loci which are not linked, for instance two or more loci on two or more different linkage groups or two or more chromosomes.
  • a particular combination of marker loci or a particular combination of haplotypes define the marker profile of a particular plant.
  • plant includes reference to an immature or mature whole plant, including a plant from which seed or grain or anthers have been removed. Seed or embryo that will produce the plant is also considered to be the plant.
  • Plant parts means any portion or piece of a plant, including leaves, stems, buds, roots, root tips, anthers, seed, grain, embryo, pollen, ovules, flowers, cotyledons, hypocotyls, pods, flowers, shoots, stalks, tissues, tissue cultures, cells and the like.
  • Polymorphism means a change or difference between two related nucleic acids.
  • a “nucleotide polymorphism” refers to a nucleotide that is different in one sequence when compared to a related sequence when the two nucleic acids are aligned for maximal correspondence.
  • Polynucleotide “polynucleotide sequence,” “nucleic acid,” “nucleic acid molecule,” “nucleic acid sequence,” “nucleic acid fragment,” and “oligonucleotide” are used interchangeably herein to indicate a polymer of nucleotides that is single- or multi-stranded, that optionally contains synthetic, non-natural, or altered RNA or DNA nucleotide bases.
  • a DNA polynucleotide may be comprised of one or more strands of cDNA, genomic DNA, synthetic DNA, or mixtures thereof.
  • Primer refers to an oligonucleotide which is capable of acting as a point of initiation of nucleic acid synthesis or replication along a complementary strand when placed under conditions in which synthesis of a complementary strand is catalyzed by a polymerase.
  • primers are about 10 to 30 nucleotides in length, but longer or shorter sequences can be employed.
  • Primers may be provided in double-stranded form, though the single-stranded form is more typically used.
  • a primer can further contain a detectable label, for example a 5′ end label.
  • Probe refers to an oligonucleotide that is complementary (though not necessarily fully complementary) to a polynucleotide of interest and forms a duplexed structure by hybridization with at least one strand of the polynucleotide of interest.
  • probes are oligonucleotides from 10 to 50 nucleotides in length, but longer or shorter sequences can be employed.
  • a probe can further contain a detectable label.
  • Quantitative trait loci or “QTL” refer to the genetic elements controlling a quantitative trait.
  • Recombination frequency is the frequency of a crossing over event (recombination) between two genetic loci. Recombination frequency can be observed by following the segregation of markers and/or traits during meiosis.
  • Resistance and “improved resistance” are used interchangeably herein and refer to any type of increase in resistance or tolerance to, or any type of decrease in susceptibility.
  • a “resistant plant” or “resistant plant variety” need not possess absolute or complete resistance. Instead, a “resistant plant,” “resistant plant variety,” or a plant or plant variety with “improved resistance” will have a level of resistance or tolerance which is higher than that of a comparable susceptible plant or variety.
  • Self-crossing or “self-pollination” or “selfing” is a process through which a breeder crosses a plant with itself; for example, a second generation hybrid F2 with itself to yield progeny designated F2:3.
  • SNP single nucleotide polymorphism
  • yield refers to the productivity per unit area of a particular plant product of commercial value. For example, yield of soybean is commonly measured in bushels of seed per acre or metric tons of seed per hectare per season. Yield is affected by both genetic and environmental factors.
  • an “isolated” or “purified” polynucleotide or polypeptide, or biologically active portion thereof is substantially or essentially free from components that normally accompany or interact with the polynucleotide or polypeptide as found in its naturally occurring environment.
  • an “isolated” polynucleotide is free of sequences (optimally protein encoding sequences) that naturally flank the polynucleotide (i.e., sequences located at the 5′ and 3′ ends of the polynucleotide) in the genomic DNA of the organism from which the polynucleotide is derived.
  • the isolated polynucleotide can contain less than about 5 kb, 4 kb, 3 kb, 2 kb, 1 kb, 0.5 kb, or 0.1 kb of nucleotide sequence that naturally flank the polynucleotide in genomic DNA of the cell from which the polynucleotide is derived.
  • a polypeptide that is substantially free of cellular material includes preparations of polypeptides having less than about 30%, 20%, 10%, 5%, or 1% (by dry weight) of contaminating protein, culture media or other chemical components.
  • Standard recombinant DNA and molecular cloning techniques used herein are well known in the art and are described more fully in Sambrook, J., Fritsch, E. F. and Maniatis, T. Molecular Cloning: A Laboratory Manual; Cold Spring Harbor Laboratory Press: Cold Spring Harbor, 1989 (hereinafter “Sambrook”).
  • Methods are provided for identifying and/or selecting a soybean plant or soybean germplasm that displays resistance or improved resistance to soybean cyst nematode.
  • the method comprises detecting in the soybean plant or germplasm, or a part thereof, at least one marker locus associated with resistance to soybean cyst nematode.
  • marker loci associated with soybean cyst nematode resistance have been identified and mapped to the rhg4 (resistance to Heterodera glycines 4) locus on linkage group A2 on chromosome 8.
  • Examples of soybean lines known to comprise the rhg4 resistance locus include, for example, Peking and PI437654.
  • Marker loci, haplotypes and marker profiles associated with resistance to soybean cyst nematode are provided. Further provided are genomic loci that are associated with soybean resistance to soybean cyst nematode.
  • soybean plants or germplasm are identified that have at least one favorable allele, marker locus, haplotype or marker profile that positively correlates with resistance or improved resistance to soybean cyst nematode.
  • it is useful for exclusionary purposes during breeding to identify alleles, marker loci, haplotypes, or marker profiles that negatively correlate with resistance for example, to eliminate such plants or germplasm from subsequent rounds of breeding.
  • marker loci useful for identifying a first soybean plant or first soybean germplasm that displays resistance or improved resistance to soybean cyst nematode are associated with the rhg4 locus on linkage group A2 on chromosome 8.
  • the marker locus comprises: (a) S07160-1 or a closely linked marker on linkage group A2; or (b) Gm08:8300131, Gm08:8257778, Gm08:8257785, Gm08:8258163, Gm08:8258688, Gm08:8258742, Gm08:8259928, Gm08:8260451, Gm08:8260590, Gm08:8261480, Gm08:8261684, Gm08:8262165, Gm08:8263213, Gm08:8263250, Gm08:8263611, Gm08:8264149, Gm08:8265227, Gm08:8265364, Gm08:8265614, Gm08:8266183,
  • multiple marker loci that collectively make up a soybean cyst nematode resistance haplotype of interest are investigated.
  • 2, 3, 4, 5, 6, 7, 8, 9, 10, or more of the various marker loci provided herein can comprise a soybean cyst nematode resistance haplotype.
  • the haplotype comprises: (a) two or more marker loci associated with the Rhg4 locus on linkage group A2; or (b) two or more marker loci comprising S07160-1, Gm08:8300131, Gm08:8257778, Gm08:8257785, Gm08:8258163, Gm08:8258688, Gm08:8258742, Gm08:8259928, Gm08:8260451, Gm08:8260590, Gm08:8261480, Gm08:8261684, Gm08:8262165, Gm08:8263213, Gm08:8263250, Gm08:8263611, Gm08:8264149, Gm08:8265227, Gm08:8265364, Gm08:8265614, Gm08:8266183, Gm08:8266185, Gm08:8266263, Gm08:8266350, Gm08:8266386, Gm08:8266473,
  • the method of identifying a first soybean plant or a first soybean germplasm that displays resistance or improved resistance to soybean cyst nematode comprises detecting in the genome of the first soybean plant or in the genome of the first soybean germplasm at least one haplotype that is associated with the resistance, wherein the at least one haplotype comprises at least two of the various marker loci provided herein.
  • two or more marker loci or haplotypes can collectively make up a marker profile.
  • the marker profile can comprise any two or more marker loci comprising: (a) marker loci comprising S07160-1 on linkage group A2, or a closely linked marker; (b) marker loci comprising Gm08:8300131, Gm08:8257778, Gm08:8257785, Gm08:8258163, Gm08:8258688, Gm08:8258742, Gm08:8259928, Gm08:8260451, Gm08:8260590, Gm08:8261480, Gm08:8261684, Gm08:8262165, Gm08:8263213, Gm08:8263250, Gm08:8263611, Gm08:8264149, Gm08:8265227, Gm08:8265364, Gm08:8265614, Gm08:8266183, Gm08:8266185, Gm08:8266263, Gm
  • the marker profile can comprise 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, or more marker loci or haplotypes associated with resistance to soybean cyst nematode.
  • a method of identifying a first soybean plant or a first soybean germplasm that displays resistance or improved resistance to soybean cyst nematode comprises detecting in the genome of the first soybean plant or in the genome of the first soybean germplasm at least one marker profile that is associated with the resistance, wherein the at least one marker profile comprises the marker locus provided herein.
  • soybean markers In addition to the markers discussed herein, information regarding useful soybean markers can be found, for example, on the USDA's Soybase website, available at www.soybase.org.
  • identification of favorable marker alleles may be germplasm-specific. The determination of which marker alleles correlate with resistance (or susceptibility) is determined for the particular germplasm under study.
  • methods for identifying the favorable alleles are routine and well known in the art, and furthermore, that the identification and use of such favorable alleles is well within the scope of the invention.
  • the method of identifying comprises detecting at least one marker locus associated with resistance to soybean cyst nematode.
  • the term “associated with” in connection with a relationship between a marker locus and a phenotype refers to a statistically significant dependence of marker frequency with respect to a quantitative scale or qualitative gradation of the phenotype.
  • an allele of a marker is associated with a trait of interest when the allele of the marker locus and the trait phenotypes are found together in the progeny of an organism more often than if the marker genotypes and trait phenotypes segregated separately.
  • Any combination of the marker loci provided herein can be used in the methods to identify a soybean plant or soybean germplasm that displays resistance or improved resistance to soybean cyst nematode. Any one marker locus or any combination of the markers set forth herein, or any closely linked marker can be used to aid in identifying and selecting soybean plants or soybean germplasm with resistance or improved resistance to soybean cyst nematode.
  • a method of identifying a first soybean plant or a first soybean germplasm that displays resistance or improved resistance to soybean cyst nematode comprises detecting in the genome of the first soybean plant or first soybean germplasm at least one marker locus that is associated with resistance.
  • the at least one marker locus can comprise the marker locus S07160-1 on linkage group A2, or a closely linked marker; (b) can comprise the marker loci Gm08:8300131, Gm08:8257778, Gm08:8257785, Gm08:8258163, Gm08:8258688, Gm08:8258742, Gm08:8259928, Gm08:8260451, Gm08:8260590, Gm08:8261480, Gm08:8261684, Gm08:8262165, Gm08:8263213, Gm08:8263250, Gm08:8263611, Gm08:8264149, Gm08:8265227, Gm08:8265364, Gm08:8265614, Gm08:8266183, Gm08:8266185, Gm08:8266263, Gm08:8266350, Gm08:8266386, Gm08:8266473, Gm08
  • two or more marker loci are detected in the method.
  • the germplasm is a soybean variety.
  • the method further comprises crossing the selected first soybean plant or first soybean germplasm with a second soybean plant or second soybean germplasm.
  • the second soybean plant or second soybean germplasm comprises an exotic soybean strain or an elite soybean strain.
  • the first soybean plant or first soybean germplasm comprises a soybean variety. Any soybean line known to the art or disclosed herein may be used. Non-limiting examples of soybean varieties and their associated soybean cyst nematode resistance alleles encompassed by the methods provided herein include, for example, Peking and PI437654.
  • the detection method comprises amplifying at least one marker locus and detecting the resulting amplified marker amplicon.
  • amplifying comprises (a) admixing an amplification primer or amplification primer pair for each marker locus being amplified with a nucleic acid isolated from the first soybean plant or the first soybean germplasm such that the primer or primer pair is complementary or partially complementary to a variant or fragment of the genomic locus comprising the marker locus and is capable of initiating DNA polymerization by a DNA polymerase using the soybean nucleic acid as a template; and (b) extending the primer or primer pair in a DNA polymerization reaction comprising a DNA polymerase and a template nucleic acid to generate at least one amplicon.
  • the primer or primer pair can comprise a variant or fragment of one or more of the genomic loci provided herein.
  • the method involves amplifying a variant or fragment of one or more polynucleotides comprising SEQ ID NOS: 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, 100, 101, 102, 103, 104, 105, 106, 107, 108, 109, 110, 111, 11
  • the primer or primer pair can comprise a variant or fragment of one or more polynucleotides comprising SEQ ID NOS: 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, 100, 101, 102, 103, 104, 105, 106, 107, 108, 109, 110, 111,
  • the primer or primer pair comprises a nucleic acid sequence comprising SEQ ID NOS: 1, 2, 3, 4, 5, 6, 7, 8 or variants or fragments thereof.
  • the primer pair comprises SEQ ID NO:1 and SEQ ID NO:2.
  • the method further comprises providing one or more labeled nucleic acid probes suitable for detection of each marker locus being amplified.
  • the labeled nucleic acid probe can comprise a sequence comprising a variant or fragment of one or more of the genomic loci provided herein.
  • the labeled nucleic acid probe can comprise a sequence comprising a variant or fragment of one or more polynucleotides comprising SEQ ID NOS: 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, 100, 101, 102, 103, 104, 105, 106, 107, 108
  • the labeled nucleic acid probe comprises a nucleic acid sequence comprising SEQ ID NOS: 9, 10 or variants or fragments thereof.
  • Non-limiting examples of primers, probes, genomic loci and amplicons that can be used in the methods and compositions provided herein are summarized in Tables 1, 2, 3A, 3B and 4, respectively.
  • Probe Sequences Linkage Marker Group Marker Probe 1* Probe 2** Position (ch) Name Name Probe 1 Sequence Name Probe 2 Sequence 8300131 A2 S07160-1 102389 ATTCCTAAAGATAGT 102390 CTAAAGATACATGCA (Gm08) CCAAT (SEQ IDNO: 9) AGTC (SEQ ID NO: 10) *Probe 1 detects the susceptible allele. **Probe 2 detects the resistant allele.
  • Genomic Loci Comprising the Various Marker Loci Provided Herein.
  • Genomic Loci Comprising the Various Marker Loci Provided herein.
  • SEQ SEQ SNP ID ID ID Consensus Reference Sequence Marker SNP SNP NO NO r 2 with r 2 with (200 by flanking SNP) Name Position [S/R] [S] [R] 8357600 8356824 [S/R] 8356824 [C/G] 15 198 0.857 GCCGGGCAACCGCTACTACGGCGGCAATGAATA CATCGACCAGATCGAAAACCTCTGCCGCTCACGC Gm08:85 GCCCTCCAAGCCTTCCACCTCGACGCCCAATCCT 6824 GGGGCGTCAACGTCCAGCCCTACTCCGGCTCCCC (Rhg4 GGCCAACTTCGCCGCCTACACCGCCGTCCTCAAC mutation CCCCACGACCGCATCATGGGGCTAGATCTCC +C/G from Liu +CTCCGGCGGCCACCTCACCCACGGCTACTACAC et al
  • the method of detecting comprises DNA sequencing of at least one of the marker loci provided herein.
  • sequencing refers to sequencing methods for determining the order of nucleotides in a molecule of DNA. Any DNA sequencing method known in the art can be used in the methods provided herein. Non-limiting examples of DNA sequencing methods useful in the methods provided herein include Next Generation Sequencing (NGS) technologies, for example, as described in Egan, A. N, et al. (2012) American Journal of Botany 99(2):175-185; genotyping by sequencing (GBS) methods, for example, as described in Elshire, R. J., et al.
  • NGS Next Generation Sequencing
  • An active variant of any one of SEQ ID NOS: 1-380 can comprise a polynucleotide having at least 75%, 80% 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% sequence identity to SEQ ID NOS: 1-380 as long as it is capable of amplifying and/or detecting the marker locus of interest.
  • fragment is intended a portion of the polynucleotide.
  • a fragment or portion can comprise at least 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 25, 30, 40, 50, 75, 100, 150, 200, 250, 300, 350, 400 contiguous nucleotides of SEQ ID NOS: 1-380 as long as it is capable of amplifying and/or detecting the marker locus of interest.
  • sequence identity/similarity values provided herein refer to the value obtained using GAP Version 10 using the following parameters: % identity and % similarity for a nucleotide sequence using GAP Weight of 50 and Length Weight of 3, and the nwsgapdna.cmp scoring matrix; or any equivalent program thereof.
  • equivalent program is intended any sequence comparison program that, for any two sequences in question, generates an alignment having identical nucleotide residue matches and an identical percent sequence identity when compared to the corresponding alignment generated by GAP Version 10.
  • Traits or markers are considered to be linked if they co-segregate.
  • a 1/100 probability of recombination per generation is defined as a map distance of 1.0 centiMorgan (1.0 cM).
  • Genetic elements or genes located on a single chromosome segment are physically linked. Two loci can be located in close proximity such that recombination between homologous chromosome pairs does not occur between the two loci during meiosis with high frequency, e.g., such that linked loci co-segregate at least about 90% of the time, e.g., 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, 99.5%, 99.75%, or more of the time.
  • Genetic elements located within a chromosome segment are also genetically linked, typically within a genetic recombination distance of less than or equal to 50 centimorgans (cM), e.g., about 49, 40, 30, 20, 10, 5, 4, 3, 2, 1, 0.75, 0.5, or 0.25 cM or less. That is, two genetic elements within a single chromosome segment undergo recombination during meiosis with each other at a frequency of less than or equal to about 50%, e.g., about 49%, 40%, 30%, 20%, 10%, 5%, 4%, 3%, 2%, 1%, 0.75%, 0.5%, or 0.25% or less.
  • cM centimorgans
  • Closely linked markers display a cross over frequency with a given marker of about 10% or less (the given marker is within about 10 cM of a closely linked marker).
  • a closely linked marker is within 10 cM, 9 cM, 8 cM, 7 cM, 6 cM, 5 cM, 4 cM, 3 cM, 2 cM or 1 cM of any given marker disclosed herein.
  • a marker associated with one of the markers disclosed herein can be within 75 Kb, 60 Kb, 50 Kb, 40 Kb, 30 Kb, 20 K, 10 Kb, 5 Kb or less of the disclosed marker.
  • closely linked markers can be separated, for example, by about 1 megabase (Mb; 1 million nucleotides), about 500 kilobases (Kb; 1000 nucleotides), about 400 Kb, about 300 Kb, about 200 Kb, about 100 Kb, about 50 Kb, about 25 Kb, about 10 Kb, about 5 Kb, about 2 Kb, about 1 Kb, about 500 nucleotides, about 250 nucleotides, or less.
  • Mb megabase
  • Kb 500 kilobases
  • “coupling” phase linkage indicates the state where the “favorable” allele at the resistance locus is physically associated on the same chromosome strand as the “favorable” allele of the respective linked marker locus.
  • both favorable alleles are inherited together by progeny that inherit that chromosome strand.
  • the “favorable” allele at the locus of interest e.g., a QTL for resistance
  • the two “favorable” alleles are not inherited together (i.e., the two loci are “out of phase” with each other).
  • Markers are used to define a specific locus on the soybean genome. Each marker is therefore an indicator of a specific segment of DNA, having a unique nucleotide sequence. Map positions provide a measure of the relative positions of particular markers with respect to one another. When a trait is stated to be linked to a given marker it will be understood that the actual DNA segment whose sequence affects the trait generally co-segregates with the marker. More precise and definite localization of a trait can be obtained if markers are identified on both sides of the trait.
  • Favorable genotypes associated with at least trait of interest may be identified by one or more methodologies.
  • one or more markers are used, including but not limited to AFLPs, RFLPs, ASH, SSRs, SNPs, indels, padlock probes, molecular inversion probes, microarrays, sequencing, and the like.
  • a target nucleic acid is amplified prior to hybridization with a probe. In other cases, the target nucleic acid is not amplified prior to hybridization, such as methods using molecular inversion probes (see, for example Hardenbol et al. (2003) Nat Biotech 21:673-678).
  • the genotype related to a specific trait is monitored, while in other examples, a genome-wide evaluation including but not limited to one or more of marker panels, library screens, association studies, microarrays, gene chips, expression studies, or sequencing such as whole-genome resequencing and genotyping-by-sequencing (GBS) may be used.
  • a genome-wide evaluation including but not limited to one or more of marker panels, library screens, association studies, microarrays, gene chips, expression studies, or sequencing such as whole-genome resequencing and genotyping-by-sequencing (GBS) may be used.
  • GGS genotyping-by-sequencing
  • no target-specific probe is needed, for example by using sequencing technologies, including but not limited to next-generation sequencing methods (see, for example, Metzker (2010) Nat Rev Genet 11:31-46; and, Egan et al.
  • Each of these may be coupled with one or more enrichment strategies for organellar or nuclear genomes in order to reduce the complexity of the genome under investigation via PCR, hybridization, restriction enzyme (see, e.g., Elshire et al. (2011) PLoS ONE 6:e19379), and expression methods.
  • no reference genome sequence is needed in order to complete the analysis.
  • MAS marker assisted selection
  • soybean plants or germplasm can be selected for markers or marker alleles that positively correlate with soybean cyst nematode resistance, without actually raising soybean and measuring for resistance (or, contrawise, soybean plants can be selected against if they possess markers that negatively correlate with resistance).
  • MAS is a powerful tool to select for desired phenotypes and for introgressing desired traits into cultivars of soybean (e.g., introgressing desired traits into elite lines).
  • MAS is easily adapted to high throughput molecular analysis methods that can quickly screen large numbers of plant or germplasm genetic material for the markers of interest and is much more cost effective than raising and observing plants for visible traits.
  • the molecular markers or marker loci are detected using a suitable amplification-based detection method.
  • nucleic acid primers are typically hybridized to the conserved regions flanking the polymorphic marker region.
  • nucleic acid probes that bind to the amplified region are also employed.
  • synthetic methods for making oligonucleotides, including primers and probes are well known in the art.
  • oligonucleotides can be synthesized chemically according to the solid phase phosphoramidite triester method described by Beaucage and Caruthers (1981) Tetrahedron Letts 22:1859-1862, e.g., using a commercially available automated synthesizer, e.g., as described in Needham-VanDevanter, et al. (1984) Nucleic Acids Res. 12:6159-6168.
  • Oligonucleotides, including modified oligonucleotides can also be ordered from a variety of commercial sources known to persons of skill in the art.
  • primers and probes to be used can be designed using any suitable method. It is not intended that the invention be limited to any particular primer, primer pair or probe.
  • primers can be designed using any suitable software program, such as LASERGENE® or Primer3.
  • primers be limited to generating an amplicon of any particular size.
  • the primers used to amplify the marker loci and alleles herein are not limited to amplifying the entire region of the relevant locus.
  • marker amplification produces an amplicon at least 20 nucleotides in length, or alternatively, at least 50 nucleotides in length, or alternatively, at least 100 nucleotides in length, or alternatively, at least 200 nucleotides in length.
  • Non-limiting examples of polynucleotide primers useful for detecting the marker loci provided herein are provided in Table 1 and include, for example, SEQ ID NOS: 1, 2, 3, 4, 5, 6, 7, 8 or variants or fragments thereof.
  • PCR, RT-PCR, and LCR are in particularly broad use as amplification and amplification-detection methods for amplifying nucleic acids of interest (e.g., those comprising marker loci), facilitating detection of the markers.
  • nucleic acids of interest e.g., those comprising marker loci
  • Details regarding the use of these and other amplification methods are well known in the art and can be found in any of a variety of standard texts. Details for these techniques can also be found in numerous journal and patent references, such as Mullis, et al. (1987) U.S. Pat. No. 4,683,202; Arnheim & Levinson (Oct. 1, 1990) C&EN 36-47; Kwoh, et al. (1989) Proc. Natl. Acad. Sci.
  • nucleic acid amplification techniques can be applied to amplify and/or detect nucleic acids of interest, such as nucleic acids comprising marker loci.
  • Amplification primers for amplifying useful marker loci and suitable probes to detect useful marker loci or to genotype SNP alleles are provided.
  • exemplary primers and probes are provided in SEQ ID NOS: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10 and in Tables 1 and 2, and the genomic loci comprising the various marker loci provided herein are provided in SEQ ID NOS: 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, 100, 101, 102,
  • primers to either side of the given primers can be used in place of the given primers, so long as the primers can amplify a region that includes the allele to be detected, as can primers and probes directed to other SNP marker loci.
  • the precise probe to be used for detection can vary, e.g., any probe that can identify the region of a marker amplicon to be detected can be substituted for those examples provided herein.
  • the configuration of the amplification primers and detection probes can, of course, vary. Thus, the compositions and methods are not limited to the primers and probes specifically recited herein.
  • probes will possess a detectable label. Any suitable label can be used with a probe.
  • Detectable labels suitable for use with nucleic acid probes include, for example, any composition detectable by spectroscopic, radioisotopic, photochemical, biochemical, immunochemical, electrical, optical, or chemical means.
  • Useful labels include biotin for staining with labeled streptavidin conjugate, magnetic beads, fluorescent dyes, radiolabels, enzymes, and colorimetric labels.
  • Other labels include ligands, which bind to antibodies labeled with fluorophores, chemiluminescent agents, and enzymes.
  • a probe can also constitute radiolabelled PCR primers that are used to generate a radiolabelled amplicon.
  • Labeling strategies for labeling nucleic acids and corresponding detection strategies can be found, e.g., in Haugland (1996) Handbook of Fluorescent Probes and Research Chemicals Sixth Edition by Molecular Probes, Inc. (Eugene O R); or Haugland (2001) Handbook of Fluorescent Probes and Research Chemicals Eighth Edition by Molecular Probes, Inc. (Eugene O R).
  • Detectable labels may also include reporter-quencher pairs, such as are employed in Molecular Beacon and TaqManTM probes.
  • the reporter may be a fluorescent organic dye modified with a suitable linking group for attachment to the oligonucleotide, such as to the terminal 3′ carbon or terminal 5′ carbon.
  • the quencher may also be an organic dye, which may or may not be fluorescent, depending on the embodiment. Generally, whether the quencher is fluorescent or simply releases the transferred energy from the reporter by non-radiative decay, the absorption band of the quencher should at least substantially overlap the fluorescent emission band of the reporter to optimize the quenching.
  • Non-fluorescent quenchers or dark quenchers typically function by absorbing energy from excited reporters, but do not release the energy radiatively.
  • reporter-quencher pairs for particular probes may be undertaken in accordance with known techniques. Fluorescent and dark quenchers and their relevant optical properties from which exemplary reporter-quencher pairs may be selected are listed and described, for example, in Berlman, Handbook of Fluorescence Spectra of Aromatic Molecules , 2nd ed., Academic Press, New York, 1971, the content of which is incorporated herein by reference.
  • modifying reporters and quenchers for covalent attachment via common reactive groups that can be added to an oligonucleotide in the present invention may be found, for example, in Haugland, Handbook of Fluorescent Probes and Research Chemicals , Molecular Probes of Eugene, Oreg., 1992, the content of which is incorporated herein by reference.
  • reporter-quencher pairs are selected from xanthene dyes including fluoresceins and rhodamine dyes. Many suitable forms of these compounds are available commercially with substituents on the phenyl groups, which can be used as the site for bonding or as the bonding functionality for attachment to an oligonucleotide. Another useful group of fluorescent compounds for use as reporters are the naphthylamines, having an amino group in the alpha or beta position.
  • naphthylamino compounds include 1-dimethylaminonaphthyl-5 sulfonate, 1-anilino-8-naphthalene sulfonate and 2-p-touidinyl-6-naphthalene sulfonate.
  • Other dyes include 3-phenyl-7-isocyanatocoumarin; acridines such as 9-isothiocyanatoacridine; N-(p-(2-benzoxazolyl)phenyl)maleimide; benzoxadiazoles; stilbenes; pyrenes and the like.
  • the reporters and quenchers are selected from fluorescein and rhodamine dyes.
  • Suitable examples of reporters may be selected from dyes such as SYBR green, 5-carboxyfluorescein (5-FAMTM available from Applied Biosystems of Foster City, Calif.), 6-carboxyfluorescein (6-FAM), tetrachloro-6-carboxyfluorescein (TET), 2,7-dimethoxy-4,5-dichloro-6-carboxyfluorescein, hexachloro-6-carboxyfluorescein (HEX), 6-carboxy-2′,4,7,7′-tetrachlorofluorescein (6-TETTM available from Applied Biosystems), carboxy-X-rhodamine (ROX), 6-carboxy-4′,5′-dichloro-2′,7′-dimethoxyfluorescein (6-JOETM available from Applied Biosystems), VICTM dye products available from Molecular Probes, Inc., NEDTM dye products available from Applied Biosystems, and the like.
  • dyes such as SYBR green
  • Suitable examples of quenchers may be selected from 6-carboxy-tetramethyl-rhodamine, 4-(4-dimethylaminophenylazo) benzoic acid (DABYL), tetramethylrhodamine (TAMRA), BHQ-0TM, BHQ-1TM, BHQ-2TM, and BHQ-3TM, each of which are available from Biosearch Technologies, Inc. of Novato, Calif., QSY-7TM, QSY-9TM, QSY-21TM and QSY-35TM, each of which are available from Molecular Probes, Inc., and the like.
  • DABYL 4-(4-dimethylaminophenylazo) benzoic acid
  • TAMRA tetramethylrhodamine
  • a molecular beacon is an oligonucleotide which, under appropriate hybridization conditions, self-hybridizes to form a stem and loop structure.
  • the MB has a label and a quencher at the termini of the oligonucleotide; thus, under conditions that permit intra-molecular hybridization, the label is typically quenched (or at least altered in its fluorescence) by the quencher.
  • the MB label is unquenched. Details regarding standard methods of making and using MBs are well established in the literature and MBs are available from a number of commercial reagent sources. See also, e.g., Leone, et al., (1995) Molecular beacon probes combined with amplification by NASBA enable homogenous real-time detection of RNA, Nucleic Acids Res.
  • TaqManTM assay Another real-time detection method is the 5′-exonuclease detection method, also called the TaqManTM assay, as set forth in U.S. Pat. Nos. 5,804,375; 5,538,848; 5,487,972; and 5,210,015, each of which is hereby incorporated by reference in its entirety.
  • a modified probe typically 10-25 nucleic acids in length, is employed during PCR which binds intermediate to or between the two members of the amplification primer pair.
  • the modified probe possesses a reporter and a quencher and is designed to generate a detectable signal to indicate that it has hybridized with the target nucleic acid sequence during PCR.
  • the quencher stops the reporter from emitting a detectable signal.
  • the polymerase extends the primer during amplification, the intrinsic 5′ to 3′ nuclease activity of the polymerase degrades the probe, separating the reporter from the quencher, and enabling the detectable signal to be emitted.
  • the amount of detectable signal generated during the amplification cycle is proportional to the amount of product generated in each cycle.
  • the efficiency of quenching is a strong function of the proximity of the reporter and the quencher, i.e., as the two molecules get closer, the quenching efficiency increases.
  • the reporter and the quencher are preferably attached to the probe within a few nucleotides of one another, usually within 30 nucleotides of one another, more preferably with a separation of from about 6 to 16 nucleotides. Typically, this separation is achieved by attaching one member of a reporter-quencher pair to the 5′ end of the probe and the other member to a nucleotide about 6 to 16 nucleotides away, in some cases at the 3′ end of the probe.
  • Separate detection probes can also be omitted in amplification/detection methods, e.g., by performing a real time amplification reaction that detects product formation by modification of the relevant amplification primer upon incorporation into a product, incorporation of labeled nucleotides into an amplicon, or by monitoring changes in molecular rotation properties of amplicons as compared to unamplified precursors (e.g., by fluorescence polarization).
  • amplification is not a requirement for marker detection—for example, one can directly detect unamplified genomic DNA simply by performing a Southern blot on a sample of genomic DNA.
  • Procedures for performing Southern blotting, amplification e.g., (PCR, LCR, or the like), and many other nucleic acid detection methods are well established and are taught, e.g., in Sambrook, et al., Molecular Cloning—A Laboratory Manual (3d ed.), Vol. 1-3, Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y., 2000 (“Sambrook”); Current Protocols in Molecular Biology , F. M.
  • ASH allele specific hybridization
  • ASH technology is based on the stable annealing of a short, single-stranded, oligonucleotide probe to a completely complementary single-stranded target nucleic acid. Detection is via an isotopic or non-isotopic label attached to the probe.
  • two or more different ASH probes are designed to have identical DNA sequences except at the polymorphic nucleotides. Each probe will have exact homology with one allele sequence so that the range of probes can distinguish all the known alternative allele sequences.
  • Each probe is hybridized to the target DNA. With appropriate probe design and hybridization conditions, a single-base mismatch between the probe and target DNA will prevent hybridization.
  • Real-time amplification assays including MB or TaqManTM based assays, are especially useful for detecting SNP alleles.
  • probes are typically designed to bind to the amplicon region that includes the SNP locus, with one allele-specific probe being designed for each possible SNP allele. For instance, if there are two known SNP alleles for a particular SNP locus, “A” or “C,” then one probe is designed with an “A” at the SNP position, while a separate probe is designed with a “C” at the SNP position. While the probes are typically identical to one another other than at the SNP position, they need not be.
  • the two allele-specific probes could be shifted upstream or downstream relative to one another by one or more bases.
  • the probes are not otherwise identical, they should be designed such that they bind with approximately equal efficiencies, which can be accomplished by designing under a strict set of parameters that restrict the chemical properties of the probes.
  • a different detectable label for instance a different reporter-quencher pair, is typically employed on each different allele-specific probe to permit differential detection of each probe.
  • each allele-specific probe for a certain SNP locus is 11-20 nucleotides in length, dual-labeled with a florescence quencher at the 3′ end and either the 6-FAM (6-carboxyfluorescein) or VIC (4,7,2′-trichloro-7′-phenyl-6-carboxyfluorescein) fluorophore at the 5′ end.
  • a real-time PCR reaction can be performed using primers that amplify the region including the SNP locus, for instance the sequences listed in Tables 3A and 3B, the reaction being performed in the presence of all allele-specific probes for the given SNP locus.
  • detecting signal for each detectable label employed and determining which detectable label(s) demonstrated an increased signal a determination can be made of which allele-specific probe(s) bound to the amplicon and, thus, which SNP allele(s) the amplicon possessed.
  • 6-FAM- and VIC-labeled probes the distinct emission wavelengths of 6-FAM (518 nm) and VIC (554 nm) can be captured.
  • a sample that is homozygous for one allele will have fluorescence from only the respective 6-FAM or VIC fluorophore, while a sample that is heterozygous at the analyzed locus will have both 6-FAM and VIC fluorescence.
  • KASPar® and Illumina® Detection Systems are additional examples of commercially-available marker detection systems.
  • KASPar® is a homogeneous fluorescent genotyping system which utilizes allele specific hybridization and a unique form of allele specific PCR (primer extension) in order to identify genetic markers (e.g. a particular SNP locus associated with soybean cyst nematode resistance).
  • Illumina® detection systems utilize similar technology in a fixed platform format. The fixed platform utilizes a physical plate that can be created with up to 384 markers. The Illumina® system is created with a single set of markers that cannot be changed and utilizes dyes to indicate marker detection.
  • Introgression of soybean cyst nematode resistance into non-resistant or less-resistant soybean germplasm is provided. Any method for introgressing one or more marker loci into soybean plants known to one of skill in the art can be used. Typically, a first soybean germplasm that contains soybean cyst nematode resistance derived from a particular marker locus, haplotype or marker profile and a second soybean germplasm that lacks such resistance derived from the marker locus, haplotype or marker profile are provided. The first soybean germplasm may be crossed with the second soybean germplasm to provide progeny soybean germplasm.
  • progeny germplasm are screened to determine the presence of soybean cyst nematode resistance derived from the marker locus, haplotype or marker profile, and progeny that tests positive for the presence of resistance derived from the marker locus, haplotype or marker profile are selected as being soybean germplasm into which the marker locus, haplotype or marker profile has been introgressed. Methods for performing such screening are well known in the art and any suitable method can be used.
  • MAS One application of MAS is to use the resistance markers, haplotypes or marker profiles to increase the efficiency of an introgression or backcrossing effort aimed at introducing a resistance trait into a desired (typically high yielding) background.
  • marker assisted backcrossing of specific markers from a donor source e.g., to an elite genetic background
  • markers and methods can be utilized to guide marker assisted selection or breeding of soybean varieties with the desired complement (set) of allelic forms of chromosome segments associated with superior agronomic performance (resistance, along with any other available markers for yield, disease tolerance, etc.).
  • Any of the disclosed marker loci, marker alleles, haplotypes, or marker profiles can be introduced into a soybean line via introgression, by traditional breeding (or introduced via transformation, or both) to yield a soybean plant with superior agronomic performance.
  • the number of alleles associated with resistance that can be introduced or be present in a soybean plant ranges from 1 to the number of alleles disclosed herein, each integer of which is incorporated herein as if explicitly recited.
  • any of the marker loci provided herein can be introduced into a soybean line having one or more of the soybean cyst nematode resistance loci rhg1, rhg2, rhg3 or rhg5.
  • any one or more of the marker loci provided herein can be stacked with the rhg1 locus.
  • any one or more of the marker loci provided herein can be stacked with the rhg2 locus.
  • any one or more of the marker loci provided herein can be stacked with the rhg1 and rhg2 loci.
  • This also provides a method of making a progeny soybean plant and these progeny soybean plants, per se.
  • the method comprises crossing a first parent soybean plant with a second soybean plant and growing the female soybean plant under plant growth conditions to yield soybean plant progeny. Methods of crossing and growing soybean plants are well within the ability of those of ordinary skill in the art.
  • Such soybean plant progeny can be assayed for alleles associated with resistance and, thereby, the desired progeny selected.
  • Such progeny plants or seed can be sold commercially for soybean production, used for food, processed to obtain a desired constituent of the soybean, or further utilized in subsequent rounds of breeding.
  • At least one of the first or second soybean plants is a soybean plant in that it comprises at least one of the marker loci or marker profiles, such that the progeny are capable of inheriting the marker locus or marker profile.
  • a method is applied to at least one related soybean plant such as from progenitor or descendant lines in the subject soybean plants pedigree such that inheritance of the desired resistance can be traced.
  • the number of generations separating the soybean plants being subject to the methods provided herein will generally be from 1 to 20, commonly 1 to 5, and typically 1, 2, or 3 generations of separation, and quite often a direct descendant or parent of the soybean plant will be subject to the method (i.e., 1 generation of separation).
  • MAS provides an indication of which genomic regions and which favorable alleles from the original ancestors have been selected for and conserved over time, facilitating efforts to incorporate favorable variation from exotic germplasm sources (parents that are unrelated to the elite gene pool) in the hopes of finding favorable alleles that do not currently exist in the elite gene pool.
  • markers, haplotypes, primers, probes, and marker profiles can be used for MAS in crosses involving elite x exotic soybean lines by subjecting the segregating progeny to MAS to maintain major yield alleles, along with the resistance marker alleles herein.
  • transgenic approaches can also be used to create transgenic plants with the desired traits.
  • exogenous nucleic acids that encode a desired marker loci, marker profile or haplotype are introduced into target plants or germplasm.
  • a nucleic acid that codes for a resistance trait is cloned, e.g., via positional cloning, and introduced into a target plant or germplasm.
  • plant breeders can recognize resistant soybean plants in the field, and can select the resistant individuals or populations for breeding purposes or for propagation.
  • the plant breeder recognizes “resistant” and “non-resistant” or “susceptible” soybean plants.
  • plant resistance is a phenotypic spectrum consisting of extremes in resistance and susceptibility, as well as a continuum of intermediate resistance phenotypes. Evaluation of these intermediate phenotypes using reproducible assays are of value to scientists who seek to identify genetic loci that impart resistance, to conduct marker assisted selection for resistant populations, and to use introgression techniques to breed a resistance trait into an elite soybean line, for example.
  • improved resistance is intended that the plants show a decrease in the disease symptoms that are the outcome of plant exposure to soybean cyst nematode. That is, the damage caused by soybean cyst nematode is prevented, or alternatively, the disease symptoms caused by soybean cyst nematode is minimized or lessened.
  • improved resistance to soybean cyst nematode can result in reduction of the disease symptoms by at least about 2% to at least about 6%, at least about 5% to about 50%, at least about 10% to about 60%, at least about 30% to about 70%, at least about 40% to about 80%, or at least about 50% to about 90% or greater.
  • the methods provided herein can be utilized to protect plants from soybean cyst nematode.
  • soybean cyst nematode resistance can be determined by visual observations after plant exposure to a particular race of soybean cyst nematode, such as race 1, 2, 3, 5 or 14. Scores range from 1 to 9 and indicate visual observations of resistance as compared to other genotypes in the test. A score of 1 indicates soybean cyst nematode are able to infect the plant and cause yield loss, while a score of 9 indicates soybean cyst nematode resistance. Preliminary scores are reported as double digits, for example, ‘55’ indicates a preliminary score of 5 on the scale of 1 to 9.
  • Non-limiting examples of soybean cyst nematode resistance phenotypic screening are described in detail below.
  • E2 Eggs or second stage juveniles (J2) are used to inoculate host plants to increase their population. Soybean cyst nematode infestation requires a minimum 35 days before the cysts reach maturity and can be used to inoculate soybean experiments. Cyst eggs/J2 inoculant is harvested through a series of washings, grindings, and screenings. Screens are used progressing from larger to smaller sizes, ending with a #500 (25 ⁇ m) screen.
  • Soybean plants are grown in cones.
  • Cones are long containers approximately 12 inches long and 1.5 inches in diameter at the top (e.g., Ray Leach Cone-tainersTM).
  • the cone is designed to easily remove the root mass.
  • an inoculum channel is made in the cone containing the experimental line by poking a 4 inch hole with a 10 ml pipette tip.
  • One ml of inoculum is dispensed into the channel.
  • the plants are watered manually for the duration of the test, with watering being moderately light during the first 3-5 days until J2 infects the roots.
  • Plants are scored approximately 28-35 days following inoculation when cyst reproduction on susceptible checks is sufficiently high. Plants are removed from their cones and the soil is removed from the roots by gently dipping the roots into a bucket of water. The plants are screened to identify native resistance to one or more of the five races of soybean cyst nematode inoculated using a combination of three methods (1) visual 9-6-1 score; (2) visual full count; and/or (3) microscope count score depending on the stage of the line when screened. In general, lines earlier in the development cycle (R1-R2) are screened by the visual 9-6-1 method, and lines that have progressed to later development phases (R3-R5) are screened by the visual full count and/or microscope count method(s).
  • One typical phenotyping method is a visual evaluation of the roots. Susceptible checks are first evaluated for the development of cysts on the root system. These counts are recorded and averaged across the experiment to determine the susceptible (SUS) check average. Roots from the test plants are then scored based on a comparison with the average of the susceptible checks as follows:
  • roots from the susceptible check controls are examined for yellow cysts to assess whether to begin the process of evaluating the test.
  • Experimental lines are compared with known standard checks. Once adequate levels of cysts are detected on the check varieties, plants from the test lines are removed from cones one at a time. Soil is removed from roots by gently dipping the roots into a bucket of water. The root tissue is placed on a 850 micron (#20) pore sieve stacked over a 250 micron (#60) pore sieve and sprayed with a jet of water to dislodge cysts from the roots. Collected cysts are rinsed from the #60 sieve into a clean labeled cup using no more than 30 mls of additional water.
  • each sample is counted using a gridded counting dish under a stereo microscope. The number of cysts counted are recorded for each sample. Cyst counts on the test plants are converted to the 1-9 scoring scale based on the female index (FI) described above.
  • soybean cyst nematode checks provided in Table 5, can be planted and used to monitor cyst development:
  • kit refers to a set of reagents for the purpose of performing the various methods of detecting or identifying herein, more particularly, the identification and/or the detection of a soybean plant or germplasm having improved resistance to soybean cyst nematode.
  • a kit for detecting or selecting at least one soybean plant or soybean germplasm with resistance or improved resistance to soybean cyst nematode comprises (a) primers or probes for detecting one or more marker loci associated with resistance to soybean cyst nematode, wherein at least one of the primers and probes in the kit are capable of detecting a marker locus, wherein the marker locus is associated with the rhg4 locus on linkage group A2; and (b) instructions for using the primers or probes for detecting the one or more marker loci and correlating the detected marker loci with predicted resistance to soybean cyst nematode.
  • the primers and probes of the kit are capable of detecting a marker locus comprising: (a) S07160-1 or a marker closely linked thereto on linkage group A2; or (ii) a marker locus comprising Gm08:8300131, Gm08:8257778, Gm08:8257785, Gm08:8258163, Gm08:8258688, Gm08:8258742, Gm08:8259928, Gm08:8260451, Gm08:8260590, Gm08:8261480, Gm08:8261684, Gm08:8262165, Gm08:8263213, Gm08:8263250, Gm08:8263611, Gm08:8264149, Gm08:8265227, Gm08:8265364, Gm08:8265614, Gm08:8266183, Gm08:8266185, Gm08:8266263, Gm08:8266350, Gm08:8266
  • a typical kit or system can include a set of marker probes or primers configured to detect at least one favorable allele of one or more marker loci associated with resistance to soybean cyst nematode, for instance a favorable marker locus, haplotype or marker profile.
  • These probes or primers can be configured, for example, to detect the marker loci noted in the tables and examples herein, e.g., using any available allele detection format, such as solid or liquid phase array based detection, microfluidic-based sample detection, etc.
  • the systems and kits can further include packaging materials for packaging the probes, primers, or instructions, controls such as control amplification reactions that include probes, primers or template nucleic acids for amplifications, molecular size markers, or the like.
  • a typical system can also include a detector that is configured to detect one or more signal outputs from the set of marker probes or primers, or amplicon thereof, thereby identifying the presence or absence of the allele.
  • a detector that is configured to detect one or more signal outputs from the set of marker probes or primers, or amplicon thereof, thereby identifying the presence or absence of the allele.
  • signal detection apparatus including photo multiplier tubes, spectrophotometers, CCD arrays, scanning detectors, phototubes and photodiodes, microscope stations, galvo-scans, microfluidic nucleic acid amplification detection appliances and the like.
  • the precise configuration of the detector will depend, in part, on the type of label used to detect the marker allele, as well as the instrumentation that is most conveniently obtained for the user.
  • Detectors that detect fluorescence, phosphorescence, radioactivity, pH, charge, absorbance, luminescence, temperature, magnetism or the like can be used.
  • Typical detector examples include light (e.g., fluorescence) detectors or radioactivity detectors.
  • detection of a light emission (e.g., a fluorescence emission) or other probe label is indicative of the presence or absence of a marker allele.
  • Fluorescent detection is generally used for detection of amplified nucleic acids (however, upstream and/or downstream operations can also be performed on amplicons, which can involve other detection methods).
  • the detector detects one or more label (e.g., light) emission from a probe label, which is indicative of the presence or absence of a marker allele.
  • the detector(s) optionally monitors one or a plurality of signals from an amplification reaction. For example, the detector can monitor optical signals which correspond to “real time” amplification assay results.
  • the system instructions include at least one look-up table that includes a correlation between the presence or absence of the favorable alleles and predicted resistance.
  • the instructions also typically include instructions providing a user interface with the system, e.g., to permit a user to view results of a sample analysis and to input parameters into the system.
  • the isolated polynucleotide comprises a polynucleotide capable of detecting a marker locus of the soybean genome comprising: (a) S07160-1, or a marker closely linked thereto on linkage group A2; or (b) Gm08:8300131, Gm08:8257778, Gm08:8257785, Gm08:8258163, Gm08:8258688, Gm08:8258742, Gm08:8259928, Gm08:8260451, Gm08:8260590, Gm08:8261480, Gm08:8261684, Gm08:8262165, Gm08:8263213, Gm08:8263250, Gm08:8263611, Gm08:8264149, Gm08:8265227, Gm08:8265364, Gm08:82
  • the isolated polynucleotide comprises: (a) a polynucleotide comprising SEQ ID NOS: 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10; (c) a polynucleotide having at least 90% sequence identity to SEQ ID NOs: 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10; or (d) a polynucleotide comprising at least 10 contiguous nucleotides of SEQ ID NOs: 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10.
  • the isolated nucleic acids are capable of hybridizing under stringent conditions to nucleic acids of a soybean cultivar resistant to soybean cyst nematode, for instance to particular SNPs that comprise a marker locus, haplotype or marker profile.
  • a substantially identical or complementary sequence is a polynucleotide that will specifically hybridize to the complement of the nucleic acid molecule to which it is being compared under high stringency conditions.
  • a polynucleotide is said to be the “complement” of another polynucleotide if they exhibit complementarity.
  • molecules are said to exhibit “complete complementarity” when every nucleotide of one of the polynucleotide molecules is complementary to a nucleotide of the other.
  • Two molecules are said to be “minimally complementary” if they can hybridize to one another with sufficient stability to permit them to remain annealed to one another under at least conventional “low-stringency” conditions.
  • the molecules are said to be “complementary” if they can hybridize to one another with sufficient stability to permit them to remain annealed to one another under conventional “high-stringency” conditions.
  • Appropriate stringency conditions which promote DNA hybridization for example, 6 ⁇ sodium chloride/sodium citrate (SSC) at about 45° C., followed by a wash of 2 ⁇ SSC at 50° C., are known to those skilled in the art or can be found in Current Protocols in Molecular Biology , John Wiley & Sons, N.Y. (1989), 6.3.1-6.3.6.
  • stringent conditions for hybridization and detection will be those in which the salt concentration is less than about 1.5 M Na ion, typically about 0.01 to 1.0 M Na ion concentration (or other salts) at pH 7.0 to 8.3 and the temperature is at least about 30° C. for short probes (e.g., 10 to 50 nucleotides) and at least about 60° C.
  • Stringent conditions may also be achieved with the addition of destabilizing agents such as formamide.
  • Exemplary moderate stringency conditions include hybridization in 40 to 45% formamide, 1.0 M NaCl, 1% SDS at 37° C., and a wash in 0.5 ⁇ to 1 ⁇ SSC at 55 to 60° C.
  • Exemplary high stringency conditions include hybridization in 50% formamide, 1 M NaCl, 1% SDS at 37° C., and a wash in 0.1 ⁇ SSC at 60 to 65° C.
  • wash buffers may comprise about 0.1% to about 1% SDS.
  • Duration of hybridization is generally less than about 24 hours, usually about 4 to about 12 hours. The duration of the wash time will be at least a length of time sufficient to reach equilibrium.
  • a method of identifying a first soybean plant or a first soybean germplasm that displays resistance or improved resistance to soybean cyst nematode comprising detecting in the genome of said first soybean plant or in the genome of said first soybean germplasm at least one marker locus that is associated with the resistance, wherein the at least one marker locus comprises (a) S07160-1 or a marker closely linked thereto on linkage group A2; or (b) Gm08:8300131, Gm08:8257778, Gm08:8257785, Gm08:8258163, Gm08:8258688, Gm08:8258742, Gm08:8259928, Gm08:8260451, Gm08:8260590, Gm08:8261480, Gm08:8261684, Gm08:8262165, Gm08:8263213, Gm08:8263250, Gm08:8263611, Gm08:8264149, Gm08:8265227, Gm08:8265364, Gm
  • the detecting comprises amplifying at least one of said marker loci and detecting the resulting amplified marker amplicon.
  • the amplifying comprises: (a) admixing an amplification primer or amplification primer pair for each marker locus being amplified with a nucleic acid isolated from the first soybean plant or the first soybean germplasm, wherein the primer or primer pair is complementary or partially complementary to a variant or fragment of the genomic locus comprising the marker locus, and is capable of initiating DNA polymerization by a DNA polymerase using the soybean nucleic acid as a template; and (b) extending the primer or primer pair in a DNA polymerization reaction comprising a DNA polymerase and a template nucleic acid to generate at least one amplicon.
  • said primer or primer pair comprises a variant or fragment of one or more polynucleotides comprising SEQ ID NOs: 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, 100, 101, 102, 103, 104, 105, 106, 107, 108, 109, 110,
  • said primer or primer pair comprises a nucleic acid sequence comprising SEQ ID NOs: 1, 2, 3, 4, 5, 6, 7, 8 or variants or fragments thereof. 14. The method of embodiment 13, wherein said primer pair comprises SEQ ID NO: 1 and SEQ ID NO: 2. 15. The method of embodiment 10, wherein the method further comprises providing one or more labeled nucleic acid probes suitable for detection of each marker locus being amplified. 16.
  • said labeled nucleic acid probe comprises a nucleic acid sequence comprising a variant or fragment of one or more polynucleotides comprising SEQ ID NOs: 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, 100, 101, 102, 103, 104, 105, 106
  • the labeled nucleic acid probe comprises a nucleic acid sequence comprising SEQ ID NOs: 9 or 10.
  • An isolated polynucleotide capable of detecting a marker locus of the soybean genome comprising (a) S07160-1 or a marker closely linked thereto on linkage group A2; or (b) Gm08:8300131, Gm08:8257778, Gm08:8257785, Gm08:8258163, Gm08:8258688, Gm08:8258742, Gm08:8259928, Gm08:8260451, Gm08:8260590, Gm08:8261480, Gm08:8261684, Gm08:8262165, Gm08:8263213, Gm08:8263250, Gm08:8263611, Gm08:8264149, Gm08:8265227, Gm08:8265364, Gm08:8265614, Gm08:8266183, Gm08:82:82
  • polynucleotide comprises: (a) a polynucleotide comprising SEQ ID NOs: 1, 2, 3, 4, 5, 6, 7, or 8; (b) a polynucleotide comprising SEQ ID NOs: 9 or 10; (c) a polynucleotide having at least 90% sequence identity to the polynucleotides set forth in parts (a) or (b); or (d) a polynucleotide comprising at least 10 contiguous nucleotides of the polynucleotides set forth in parts (a) or (b). 20.
  • a kit for detecting or selecting at least one soybean plant or soybean germplasm with resistance or improved resistance to soybean cyst nematode comprising: a) primers or probes for detecting one or more marker loci associated with resistance to soybean cyst nematode, wherein the primers or probes are capable of detecting a marker locus comprising (i) S07160-1 or a marker closely linked thereto; or (ii) Gm08:8300131, Gm08:8257778, Gm08:8257785, Gm08:8258163, Gm08:8258688, Gm08:8258742, Gm08:8259928, Gm08:8260451, Gm08:8260590, Gm08:8261480, Gm08:8261684, Gm08:8262165, Gm08:8263213, Gm08:8263250, Gm08:8263611, Gm08:8264149, Gm08:8265227, Gm08:8265364, Gm08
  • Rhg4 locus Soybean Cyst Nematode Resistance
  • Linkage Group A2 was developed for use in high throughput genotype screening, this marker, as well as markers genetically associated to this marker, are provided. Markers from this region are relevant to elite breeding populations and facilitate selection of soybean plants with resistance to SCN at the Rhg4 locus tracing back to PI437654 and Peking as well as stacks with other marker assisted traits, including yield genes.
  • S07160-1-Q1 was developed and optimized for high throughput PCR-based methods, such as TaqmanTM assays. Optimization involved evaluation of amplification, Res, Sus, and heterozygous clustering, primer length, primer composition and the like.
  • the marker distinguishes between the resistant allele from P1437654 or Peking (C) and a susceptible allele from BSR101 (A). Primers and probes useful for detecting the polymorphism are summarized below in Tables 6 and 7, respectively.
  • the marker was validated against a panel of 31 public or proprietary soybean lines comprising 2 resistant check lines, 27 susceptible lines, and 2 other lines.
  • a summary of the rhg4 marker is provided below in Table 8.
  • Exemplary Amplification Mix H20 4.28 ul Hot Tub buffer 0.5 ul Rox Dye (50X) 0.075 ul DNTPs(24 mM each) 0.039 ul Primer(100 uM) 0.0375 ul Primer(100 uM) 0.0375 ul FAM Probe(100 uM 0.005 ul VIC Probe(100 uM 0.005 ul Hot Tub enzyme 0.025 ul Total volume 5.005 ul
  • Rhg4 locus which conditions resistance to soybean cyst nematode, has been cloned and found to encode a serine hydroxymethyltransferase (Liu et al. (2012). A soybean cyst nematode resistance gene points to a new mechanism of plant resistance to pathogens. Nature 492, 256-260). Two non-synonymous base substitutions that tightly correlate with SCN resistance were identified in the Rhg4 allele from the resistant source Forrest (Liu et al. Nature, 2012). Using SNP genotype data obtained from re-sequencing 385 Pioneer proprietary elite lines, 181 SNPs were identified that are in high linkage disequilibrium with the described mutations. These SNPs can be used for a variety of plant breeding efforts, including marker assisted selection of the Rhg4 locus.

Abstract

Various methods and compositions are provided for identifying and/or selecting soybean plants or soybean germplasm with resistance or improved resistance to soybean cyst nematode. In certain embodiments, the method comprises detecting at least one marker locus that is associated with resistance to soybean cyst nematode. In other embodiments, the method further comprises detecting at least one marker profile or haplotype associated with resistance to soybean cyst nematode. In further embodiments, the method comprises crossing a selected soybean plant with a second soybean plant. Further provided are markers, primers, probes and kits useful for identifying and/or selecting soybean plants or soybean germplasm with resistance or improved resistance to soybean cyst nematode.

Description

    CROSS-REFERENCE TO RELATED APPLICATIONS
  • This application claims the benefit of U.S. Provisional Application No. 61/740,567, filed Dec. 21, 2012, which is hereby incorporated herein in its entirety by reference.
    • FIELD OF THE INVENTION
  • This invention relates to methods of identifying and/or selecting soybean plants or germplasm that display resistance or improved resistance to Soybean Cyst Nematode.
    • REFERENCE TO A SEQUENCE LISTING SUBMITTED AS A TEXT FILE VIA EFS-WEB
  • The official copy of the sequence listing is submitted concurrently with the specification as a text file via EFS-Web, in compliance with the American Standard Code for Information Interchange (ASCII), with a file name of 430267seqlist.txt, a creation date of Feb. 21, 2013 and a size of 229 KB. The sequence listing filed via EFS-Web is part of the specification and is hereby incorporated in its entirety by reference herein.
    • BACKGROUND
  • Soybeans (Glycine max L. Merr.) are a major cash crop and investment commodity in North America and elsewhere. Soybean oil is one of the most widely used edible oils, and soybeans are used worldwide both in animal feed and in human food production. Additionally, soybean utilization is expanding to industrial, manufacturing, and pharmaceutical applications.
  • Soybean Cyst Nematode (SCN) is a parasitic pest which has threatened soybean production in the U.S. for more than fifty years. Soybean cyst nematode resistance is an economically important trait as infection can substantially reduce yields. Molecular characterization of soybean cyst nematode resistance would have important implications for soybean cultivar improvement.
  • There remains a need for soybean plants with improved resistance to soybean cyst nematode and methods for identifying and selecting such plants.
    • SUMMARY
  • Various methods and compositions are provided for identifying and/or selecting soybean plants or soybean germplasm with resistance or improved resistance to soybean cyst nematode. In certain embodiments, the method comprises detecting at least one marker locus that is associated with resistance to soybean cyst nematode. In other embodiments, the method further comprises detecting at least one marker profile or haplotype associated with resistance to soybean cyst nematode. In further embodiments, the method comprises crossing a selected soybean plant with a second soybean plant. Further provided are markers, primers, probes and kits useful for identifying and/or selecting soybean plants or soybean germplasm with resistance or improved resistance to soybean cyst nematode.
    • BRIEF DESCRIPTION OF THE FIGURES
  • FIG. 1 A-D provides a genetic map for loci on linkage group A2.
    •  DETAILED DESCRIPTION
  • Before describing the present invention in detail, it is to be understood that this invention is not limited to particular embodiments, which can, of course, vary. It is also to be understood that the terminology used herein is for the purpose of describing particular embodiments only, and is not intended to be limiting.
  • Certain definitions used in the specification and claims are provided below. In order to provide a clear and consistent understanding of the specification and claims, including the scope to be given such terms, the following definitions are provided:
  • As used in this specification and the appended claims, terms in the singular and the singular forms “a,” “an,” and “the,” for example, include plural referents unless the content clearly dictates otherwise. Thus, for example, reference to “plant,” “the plant,” or “a plant” also includes a plurality of plants; also, depending on the context, use of the term “plant” can also include genetically similar or identical progeny of that plant; use of the term “a nucleic acid” optionally includes, as a practical matter, many copies of that nucleic acid molecule; similarly, the term “probe” optionally (and typically) encompasses many similar or identical probe molecules.
  • Additionally, as used herein, “comprising” is to be interpreted as specifying the presence of the stated features, integers, steps, or components as referred to, but does not preclude the presence or addition of one or more features, integers, steps, or components, or groups thereof. Thus, for example, a kit comprising one pair of oligonucleotide primers may have two or more pairs of oligonucleotide primers. Additionally, the term “comprising” is intended to include examples encompassed by the terms “consisting essentially of” and “consisting of.” Similarly, the term “consisting essentially of” is intended to include examples encompassed by the term “consisting of.”
  • “Agronomics,” “agronomic traits,” and “agronomic performance” refer to the traits (and underlying genetic elements) of a given plant variety that contribute to yield over the course of a growing season. Individual agronomic traits include emergence vigor, vegetative vigor, stress tolerance, disease resistance or tolerance, insect resistance or tolerance, herbicide resistance, branching, flowering, seed set, seed size, seed density, standability, threshability, and the like.
  • “Allele” means any of one or more alternative forms of a genetic sequence. In a diploid cell or organism, the two alleles of a given sequence typically occupy corresponding loci on a pair of homologous chromosomes. With regard to a SNP marker, allele refers to the specific nucleotide base present at that SNP locus in that individual plant.
  • The term “amplifying” in the context of nucleic acid amplification is any process whereby additional copies of a selected nucleic acid (or a transcribed form thereof) are produced. An “amplicon” is an amplified nucleic acid, e.g., a nucleic acid that is produced by amplifying a template nucleic acid by any available amplification method.
  • An “ancestral line” is a parent line used as a source of genes, e.g., for the development of elite lines.
  • An “ancestral population” is a group of ancestors that have contributed the bulk of the genetic variation that was used to develop elite lines.
  • “Backcrossing” is a process in which a breeder crosses a progeny variety back to one of the parental genotypes one or more times.
  • The term “chromosome segment” designates a contiguous linear span of genomic DNA that resides in planta on a single chromosome. “Chromosome interval” refers to a chromosome segment defined by specific flanking marker loci.
  • “Cultivar” and “variety” are used synonymously and mean a group of plants within a species (e.g., Glycine max) that share certain genetic traits that separate them from other possible varieties within that species. Soybean cultivars are inbred lines produced after several generations of self-pollinations. Individuals within a soybean cultivar are homogeneous, nearly genetically identical, with most loci in the homozygous state.
  • An “elite line” is an agronomically superior line that has resulted from many cycles of breeding and selection for superior agronomic performance. Numerous elite lines are available and known to those of skill in the art of soybean breeding.
  • An “elite population” is an assortment of elite individuals or lines that can be used to represent the state of the art in terms of agronomically superior genotypes of a given crop species, such as soybean.
  • An “exotic soybean strain” or an “exotic soybean germplasm” is a strain or germplasm derived from a soybean not belonging to an available elite soybean line or strain of germplasm. In the context of a cross between two soybean plants or strains of germplasm, an exotic germplasm is not closely related by descent to the elite germplasm with which it is crossed. Most commonly, the exotic germplasm is not derived from any known elite line of soybean, but rather is selected to introduce novel genetic elements (typically novel alleles) into a breeding program.
  • A “genetic map” is a description of genetic association or linkage relationships among loci on one or more chromosomes (or linkage groups) within a given species, generally depicted in a diagrammatic or tabular form.
  • “Genotype” is a description of the allelic state at one or more loci.
  • “Germplasm” means the genetic material that comprises the physical foundation of the hereditary qualities of an organism. As used herein, germplasm includes seeds and living tissue from which new plants may be grown; or, another plant part, such as leaf, stem, pollen, or cells, that may be cultured into a whole plant. Germplasm resources provide sources of genetic traits used by plant breeders to improve commercial cultivars.
  • An individual is “homozygous” if the individual has only one type of allele at a given locus (e.g., a diploid individual has a copy of the same allele at a locus for each of two homologous chromosomes). An individual is “heterozygous” if more than one allele type is present at a given locus (e.g., a diploid individual with one copy each of two different alleles). The term “homogeneity” indicates that members of a group have the same genotype at one or more specific loci. In contrast, the term “heterogeneity” is used to indicate that individuals within the group differ in genotype at one or more specific loci.
  • “Introgression” means the entry or introduction of a gene, QTL, haplotype, marker profile, trait, or trait locus from the genome of one plant into the genome of another plant.
  • The terms “label” or “detectable label” refer to a molecule capable of detection. A detectable label can also include a combination of a reporter and a quencher, such as are employed in FRET probes or TaqMan™ probes. The term “reporter” refers to a substance or a portion thereof which is capable of exhibiting a detectable signal, which signal can be suppressed by a quencher. The detectable signal of the reporter is, e.g., fluorescence in the detectable range. The term “quencher” refers to a substance or portion thereof which is capable of suppressing, reducing, inhibiting, etc., the detectable signal produced by the reporter. As used herein, the terms “quenching” and “fluorescence energy transfer” refer to the process whereby, when a reporter and a quencher are in close proximity, and the reporter is excited by an energy source, a substantial portion of the energy of the excited state non-radiatively transfers to the quencher where it either dissipates non-radiatively or is emitted at a different emission wavelength than that of the reporter.
  • A “line” or “strain” is a group of individuals of identical parentage that are generally inbred to some degree and that are generally homozygous and homogeneous at most loci (isogenic or near isogenic). A “subline” refers to an inbred subset of descendants that are genetically distinct from other similarly inbred subsets descended from the same progenitor. Traditionally, a subline has been derived by inbreeding the seed from an individual soybean plant selected at the F3 to F5 generation until the residual segregating loci are “fixed” or homozygous across most or all loci. Commercial soybean varieties (or lines) are typically produced by aggregating (“bulking”) the self-pollinated progeny of a single F3 to F5 plant from a controlled cross between 2 genetically different parents. While the variety typically appears uniform, the self-pollinating variety derived from the selected plant eventually (e.g., F8) becomes a mixture of homozygous plants that can vary in genotype at any locus that was heterozygous in the originally selected F3 to F5 plant. Marker-based sublines that differ from each other based on qualitative polymorphism at the DNA level at one or more specific marker loci are derived by genotyping a sample of seed derived from individual self-pollinated progeny derived from a selected F3-F5 plant. The seed sample can be genotyped directly as seed, or as plant tissue grown from such a seed sample. Optionally, seed sharing a common genotype at the specified locus (or loci) are bulked providing a subline that is genetically homogenous at identified loci important for a trait of interest (e.g., yield, tolerance, etc.).
  • “Linkage” refers to the tendency for alleles to segregate together more often than expected by chance if their transmission was independent. Typically, linkage refers to alleles on the same chromosome. Genetic recombination occurs with an assumed random frequency over the entire genome. Genetic maps are constructed by measuring the frequency of recombination between pairs of traits or markers, the lower the frequency of recombination, and the greater the degree of linkage. “Linkage disequilibrium” is a non-random association of alleles at two or more loci and can occur between unlinked markers. It is based on allele frequencies within a population and is influenced by but not dependent on linkage.
  • “Linkage group” (LG) refers to traits or markers that generally co-segregate. A linkage group generally corresponds to a chromosomal region containing genetic material that encodes the traits or markers.
  • “Locus” is a defined segment of DNA.
  • A “map location” or “map position” is an assigned location on a genetic map relative to linked genetic markers where a specified marker can be found within a given species. Map positions are generally provided in centimorgans (cM), unless otherwise indicated, genetic positions provided are based on the Glycine max consensus map v 4.0 as provided by Hyten et al. (2010) Crop Sci 50:960-968. A “physical position” or “physical location” or “physical map location” is the position, typically in nucleotides bases, of a particular nucleotide, such as a SNP nucleotide, on a chromosome. Unless otherwise indicated, the physical position within the soybean genome provided is based on the Glyma 1.0 genome sequence described in Schmutz et al. (2010) Nature 463:178-183, available from the Phytozome website (phytozome-dot-net/soybean).
  • “Mapping” is the process of defining the association and relationships of loci through the use of genetic markers, populations segregating for the markers, and standard genetic principles of recombination frequency.
  • “Marker” or “molecular marker” or “marker locus” is a term used to denote a nucleic acid or amino acid sequence that is sufficiently unique to characterize a specific locus on the genome. Any detectable polymorphic trait can be used as a marker so long as it is inherited differentially and exhibits linkage disequilibrium with a phenotypic trait of interest.
  • “Marker assisted selection” refers to the process of selecting a desired trait or traits in a plant or plants by detecting one or more nucleic acids from the plant, where the nucleic acid is linked to the desired trait, and then selecting the plant or germplasm possessing those one or more nucleic acids.
  • “Haplotype” refers to a combination of particular alleles present within a particular plant's genome at two or more linked marker loci, for instance at two or more loci on a particular linkage group. For instance, in one example, two specific marker loci on LG-A2 are used to define a haplotype for a particular plant. In still further examples, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, or more linked marker loci are used to define a haplotype for a particular plant.
  • As used herein, a “marker profile” means a combination of particular alleles present within a particular plant's genome at two or more marker loci which are not linked, for instance two or more loci on two or more different linkage groups or two or more chromosomes. For instance, in one example, a particular combination of marker loci or a particular combination of haplotypes define the marker profile of a particular plant.
  • The term “plant” includes reference to an immature or mature whole plant, including a plant from which seed or grain or anthers have been removed. Seed or embryo that will produce the plant is also considered to be the plant.
  • “Plant parts” means any portion or piece of a plant, including leaves, stems, buds, roots, root tips, anthers, seed, grain, embryo, pollen, ovules, flowers, cotyledons, hypocotyls, pods, flowers, shoots, stalks, tissues, tissue cultures, cells and the like.
  • “Polymorphism” means a change or difference between two related nucleic acids. A “nucleotide polymorphism” refers to a nucleotide that is different in one sequence when compared to a related sequence when the two nucleic acids are aligned for maximal correspondence.
  • “Polynucleotide,” “polynucleotide sequence,” “nucleic acid,” “nucleic acid molecule,” “nucleic acid sequence,” “nucleic acid fragment,” and “oligonucleotide” are used interchangeably herein to indicate a polymer of nucleotides that is single- or multi-stranded, that optionally contains synthetic, non-natural, or altered RNA or DNA nucleotide bases. A DNA polynucleotide may be comprised of one or more strands of cDNA, genomic DNA, synthetic DNA, or mixtures thereof.
  • “Primer” refers to an oligonucleotide which is capable of acting as a point of initiation of nucleic acid synthesis or replication along a complementary strand when placed under conditions in which synthesis of a complementary strand is catalyzed by a polymerase. Typically, primers are about 10 to 30 nucleotides in length, but longer or shorter sequences can be employed. Primers may be provided in double-stranded form, though the single-stranded form is more typically used. A primer can further contain a detectable label, for example a 5′ end label.
  • “Probe” refers to an oligonucleotide that is complementary (though not necessarily fully complementary) to a polynucleotide of interest and forms a duplexed structure by hybridization with at least one strand of the polynucleotide of interest. Typically, probes are oligonucleotides from 10 to 50 nucleotides in length, but longer or shorter sequences can be employed. A probe can further contain a detectable label.
  • “Quantitative trait loci” or “QTL” refer to the genetic elements controlling a quantitative trait.
  • “Recombination frequency” is the frequency of a crossing over event (recombination) between two genetic loci. Recombination frequency can be observed by following the segregation of markers and/or traits during meiosis.
  • “Resistance and “improved resistance” are used interchangeably herein and refer to any type of increase in resistance or tolerance to, or any type of decrease in susceptibility. A “resistant plant” or “resistant plant variety” need not possess absolute or complete resistance. Instead, a “resistant plant,” “resistant plant variety,” or a plant or plant variety with “improved resistance” will have a level of resistance or tolerance which is higher than that of a comparable susceptible plant or variety.
  • “Self-crossing” or “self-pollination” or “selfing” is a process through which a breeder crosses a plant with itself; for example, a second generation hybrid F2 with itself to yield progeny designated F2:3.
  • “SNP” or “single nucleotide polymorphism” means a sequence variation that occurs when a single nucleotide (A, T, C, or G) in the genome sequence is altered or variable. “SNP markers” exist when SNPs are mapped to sites on the soybean genome.
  • The term “yield” refers to the productivity per unit area of a particular plant product of commercial value. For example, yield of soybean is commonly measured in bushels of seed per acre or metric tons of seed per hectare per season. Yield is affected by both genetic and environmental factors.
  • As used herein, an “isolated” or “purified” polynucleotide or polypeptide, or biologically active portion thereof, is substantially or essentially free from components that normally accompany or interact with the polynucleotide or polypeptide as found in its naturally occurring environment. Typically, an “isolated” polynucleotide is free of sequences (optimally protein encoding sequences) that naturally flank the polynucleotide (i.e., sequences located at the 5′ and 3′ ends of the polynucleotide) in the genomic DNA of the organism from which the polynucleotide is derived. For example, the isolated polynucleotide can contain less than about 5 kb, 4 kb, 3 kb, 2 kb, 1 kb, 0.5 kb, or 0.1 kb of nucleotide sequence that naturally flank the polynucleotide in genomic DNA of the cell from which the polynucleotide is derived. A polypeptide that is substantially free of cellular material includes preparations of polypeptides having less than about 30%, 20%, 10%, 5%, or 1% (by dry weight) of contaminating protein, culture media or other chemical components.
  • Standard recombinant DNA and molecular cloning techniques used herein are well known in the art and are described more fully in Sambrook, J., Fritsch, E. F. and Maniatis, T. Molecular Cloning: A Laboratory Manual; Cold Spring Harbor Laboratory Press: Cold Spring Harbor, 1989 (hereinafter “Sambrook”).
  • Methods are provided for identifying and/or selecting a soybean plant or soybean germplasm that displays resistance or improved resistance to soybean cyst nematode. The method comprises detecting in the soybean plant or germplasm, or a part thereof, at least one marker locus associated with resistance to soybean cyst nematode. Also provided are isolated polynucleotides and kits for use in identifying and/or detecting a soybean plant or soybean germplasm that displays resistance or improved resistance to soybean cyst nematode, and soybean plants, cells, and/or seeds comprising at least one marker locus conferring improved resistance to soybean cyst nematode.
  • Provided herein, marker loci associated with soybean cyst nematode resistance have been identified and mapped to the rhg4 (resistance to Heterodera glycines 4) locus on linkage group A2 on chromosome 8. Examples of soybean lines known to comprise the rhg4 resistance locus include, for example, Peking and PI437654.
  • These findings have important implications for soybean production, as identifying markers that can be used for selection of soybean cyst nematode resistance will greatly expedite the development of soybean cyst nematode resistance into elite cultivars.
  • Marker loci, haplotypes and marker profiles associated with resistance to soybean cyst nematode, are provided. Further provided are genomic loci that are associated with soybean resistance to soybean cyst nematode.
  • In certain embodiments, soybean plants or germplasm are identified that have at least one favorable allele, marker locus, haplotype or marker profile that positively correlates with resistance or improved resistance to soybean cyst nematode. However, in other embodiments, it is useful for exclusionary purposes during breeding to identify alleles, marker loci, haplotypes, or marker profiles that negatively correlate with resistance, for example, to eliminate such plants or germplasm from subsequent rounds of breeding.
  • In one embodiment, marker loci useful for identifying a first soybean plant or first soybean germplasm that displays resistance or improved resistance to soybean cyst nematode are associated with the rhg4 locus on linkage group A2 on chromosome 8. In another embodiment, the marker locus comprises: (a) S07160-1 or a closely linked marker on linkage group A2; or (b) Gm08:8300131, Gm08:8257778, Gm08:8257785, Gm08:8258163, Gm08:8258688, Gm08:8258742, Gm08:8259928, Gm08:8260451, Gm08:8260590, Gm08:8261480, Gm08:8261684, Gm08:8262165, Gm08:8263213, Gm08:8263250, Gm08:8263611, Gm08:8264149, Gm08:8265227, Gm08:8265364, Gm08:8265614, Gm08:8266183, Gm08:8266185, Gm08:8266263, Gm08:8266350, Gm08:8266386, Gm08:8266473, Gm08:8266888, Gm08:8267085, Gm08:8267166, Gm08:8267721, Gm08:8267826, Gm08:8268336, Gm08:8268861, Gm08:8269148, Gm08:8269785, Gm08:8270037, Gm08:8270562, Gm08:8270652, Gm08:8271540, Gm08:8271591, Gm08:8271649, Gm08:8271672, Gm08:8271955, Gm08:8273257, Gm08:8273355, Gm08:8273979, Gm08:8275766, Gm08:8275780, Gm08:8275959, Gm08:8276701, Gm08:8276849, Gm08:8276913, Gm08:8277162, Gm08:8277227, Gm08:8277248, Gm08:8277381, Gm08:8277383, Gm08:8277542, Gm08:8277625, Gm08:8277643, Gm08:8277876, Gm08:8277880, Gm08:8277969, Gm08:8278001, Gm08:8278167, Gm08:8278274, Gm08:8278434, Gm08:8279165, Gm08:8279230, Gm08:8279854, Gm08:8280901, Gm08:8280937, Gm08:8281564, Gm08:8282902, Gm08:8284027, Gm08:8286864, Gm08:8287265, Gm08:8287278, Gm08:8287453, Gm08:8287459, Gm08:8288039, Gm08:8288141, Gm08:8288200, Gm08:8288470, Gm08:8288831, Gm08:8289392, Gm08:8290740, Gm08:8291682, Gm08:8292207, Gm08:8297064, Gm08:8299433, Gm08:8299672, Gm08:8301839, Gm08:8302134, Gm08:8303450, Gm08:8305237, Gm08:8305348, Gm08:8305905, Gm08:8306090, Gm08:8306141, Gm08:8306210, Gm08:8306492, Gm08:8306627, Gm08:8307172, Gm08:8307665, Gm08:8308019, Gm08:8308891, Gm08:8308917, Gm08:8309316, Gm08:8309423, Gm08:8309837, Gm08:8310383, Gm08:8310464, Gm08:8310503, Gm08:8310663, Gm08:8311631, Gm08:8311906, Gm08:8312536, Gm08:8312819, Gm08:8313273, Gm08:8313923, Gm08:8314010, Gm08:8314025, Gm08:8314208, Gm08:8314292, Gm08:8314295, Gm08:8314513, Gm08:8314736, Gm08:8314791, Gm08:8314860, Gm08:8315543, Gm08:8315644, Gm08:8316113, Gm08:8316689, Gm08:8316899, Gm08:8317852, Gm08:8317861, Gm08:8318033, Gm08:8319087, Gm08:8319642, Gm08:8319647, Gm08:8320068, Gm08:8321253, Gm08:8321649, Gm08:8323937, Gm08:8324341, Gm08:8325127, Gm08:8325214, Gm08:8326696, Gm08:8326877, Gm08:8328633, Gm08:8330929, Gm08:8331132, Gm08:8331181, Gm08:8331408, Gm08:8331827, Gm08:8332651, Gm08:8332685, Gm08:8332957, Gm08:8343167, Gm08:8345187, Gm08:8345720, Gm08:8346030, Gm08:8346050, Gm08:8346352, Gm08:8346726, Gm08:8347799, Gm08:8348022, Gm08:8348028, Gm08:8349925, Gm08:8350122, Gm08:8350277, Gm08:8351061, Gm08:8351503, Gm08:8352313, Gm08:8352743, Gm08:8353341, Gm08:8355175, Gm08:8360133, Gm08:8363193, Gm08:8363888, Gm08:8364195 or a marker closely linked thereto.
  • In certain embodiments, multiple marker loci that collectively make up a soybean cyst nematode resistance haplotype of interest are investigated. For example, 2, 3, 4, 5, 6, 7, 8, 9, 10, or more of the various marker loci provided herein can comprise a soybean cyst nematode resistance haplotype. In some embodiments, the haplotype comprises: (a) two or more marker loci associated with the Rhg4 locus on linkage group A2; or (b) two or more marker loci comprising S07160-1, Gm08:8300131, Gm08:8257778, Gm08:8257785, Gm08:8258163, Gm08:8258688, Gm08:8258742, Gm08:8259928, Gm08:8260451, Gm08:8260590, Gm08:8261480, Gm08:8261684, Gm08:8262165, Gm08:8263213, Gm08:8263250, Gm08:8263611, Gm08:8264149, Gm08:8265227, Gm08:8265364, Gm08:8265614, Gm08:8266183, Gm08:8266185, Gm08:8266263, Gm08:8266350, Gm08:8266386, Gm08:8266473, Gm08:8266888, Gm08:8267085, Gm08:8267166, Gm08:8267721, Gm08:8267826, Gm08:8268336, Gm08:8268861, Gm08:8269148, Gm08:8269785, Gm08:8270037, Gm08:8270562, Gm08:8270652, Gm08:8271540, Gm08:8271591, Gm08:8271649, Gm08:8271672, Gm08:8271955, Gm08:8273257, Gm08:8273355, Gm08:8273979, Gm08:8275766, Gm08:8275780, Gm08:8275959, Gm08:8276701, Gm08:8276849, Gm08:8276913, Gm08:8277162, Gm08:8277227, Gm08:8277248, Gm08:8277381, Gm08:8277383, Gm08:8277542, Gm08:8277625, Gm08:8277643, Gm08:8277876, Gm08:8277880, Gm08:8277969, Gm08:8278001, Gm08:8278167, Gm08:8278274, Gm08:8278434, Gm08:8279165, Gm08:8279230, Gm08:8279854, Gm08:8280901, Gm08:8280937, Gm08:8281564, Gm08:8282902, Gm08:8284027, Gm08:8286864, Gm08:8287265, Gm08:8287278, Gm08:8287453, Gm08:8287459, Gm08:8288039, Gm08:8288141, Gm08:8288200, Gm08:8288470, Gm08:8288831, Gm08:8289392, Gm08:8290740, Gm08:8291682, Gm08:8292207, Gm08:8297064, Gm08:8299433, Gm08:8299672, Gm08:8301839, Gm08:8302134, Gm08:8303450, Gm08:8305237, Gm08:8305348, Gm08:8305905, Gm08:8306090, Gm08:8306141, Gm08:8306210, Gm08:8306492, Gm08:8306627, Gm08:8307172, Gm08:8307665, Gm08:8308019, Gm08:8308891, Gm08:8308917, Gm08:8309316, Gm08:8309423, Gm08:8309837, Gm08:8310383, Gm08:8310464, Gm08:8310503, Gm08:8310663, Gm08:8311631, Gm08:8311906, Gm08:8312536, Gm08:8312819, Gm08:8313273, Gm08:8313923, Gm08:8314010, Gm08:8314025, Gm08:8314208, Gm08:8314292, Gm08:8314295, Gm08:8314513, Gm08:8314736, Gm08:8314791, Gm08:8314860, Gm08:8315543, Gm08:8315644, Gm08:8316113, Gm08:8316689, Gm08:8316899, Gm08:8317852, Gm08:8317861, Gm08:8318033, Gm08:8319087, Gm08:8319642, Gm08:8319647, Gm08:8320068, Gm08:8321253, Gm08:8321649, Gm08:8323937, Gm08:8324341, Gm08:8325127, Gm08:8325214, Gm08:8326696, Gm08:8326877, Gm08:8328633, Gm08:8330929, Gm08:8331132, Gm08:8331181, Gm08:8331408, Gm08:8331827, Gm08:8332651, Gm08:8332685, Gm08:8332957, Gm08:8343167, Gm08:8345187, Gm08:8345720, Gm08:8346030, Gm08:8346050, Gm08:8346352, Gm08:8346726, Gm08:8347799, Gm08:8348022, Gm08:8348028, Gm08:8349925, Gm08:8350122, Gm08:8350277, Gm08:8351061, Gm08:8351503, Gm08:8352313, Gm08:8352743, Gm08:8353341, Gm08:8355175, Gm08:8360133, Gm08:8363193, Gm08:8363888, Gm08:8364195 or a marker closely linked thereto.
  • In one embodiment, the method of identifying a first soybean plant or a first soybean germplasm that displays resistance or improved resistance to soybean cyst nematode comprises detecting in the genome of the first soybean plant or in the genome of the first soybean germplasm at least one haplotype that is associated with the resistance, wherein the at least one haplotype comprises at least two of the various marker loci provided herein.
  • In certain embodiments, two or more marker loci or haplotypes can collectively make up a marker profile. The marker profile can comprise any two or more marker loci comprising: (a) marker loci comprising S07160-1 on linkage group A2, or a closely linked marker; (b) marker loci comprising Gm08:8300131, Gm08:8257778, Gm08:8257785, Gm08:8258163, Gm08:8258688, Gm08:8258742, Gm08:8259928, Gm08:8260451, Gm08:8260590, Gm08:8261480, Gm08:8261684, Gm08:8262165, Gm08:8263213, Gm08:8263250, Gm08:8263611, Gm08:8264149, Gm08:8265227, Gm08:8265364, Gm08:8265614, Gm08:8266183, Gm08:8266185, Gm08:8266263, Gm08:8266350, Gm08:8266386, Gm08:8266473, Gm08:8266888, Gm08:8267085, Gm08:8267166, Gm08:8267721, Gm08:8267826, Gm08:8268336, Gm08:8268861, Gm08:8269148, Gm08:8269785, Gm08:8270037, Gm08:8270562, Gm08:8270652, Gm08:8271540, Gm08:8271591, Gm08:8271649, Gm08:8271672, Gm08:8271955, Gm08:8273257, Gm08:8273355, Gm08:8273979, Gm08:8275766, Gm08:8275780, Gm08:8275959, Gm08:8276701, Gm08:8276849, Gm08:8276913, Gm08:8277162, Gm08:8277227, Gm08:8277248, Gm08:8277381, Gm08:8277383, Gm08:8277542, Gm08:8277625, Gm08:8277643, Gm08:8277876, Gm08:8277880, Gm08:8277969, Gm08:8278001, Gm08:8278167, Gm08:8278274, Gm08:8278434, Gm08:8279165, Gm08:8279230, Gm08:8279854, Gm08:8280901, Gm08:8280937, Gm08:8281564, Gm08:8282902, Gm08:8284027, Gm08:8286864, Gm08:8287265, Gm08:8287278, Gm08:8287453, Gm08:8287459, Gm08:8288039, Gm08:8288141, Gm08:8288200, Gm08:8288470, Gm08:8288831, Gm08:8289392, Gm08:8290740, Gm08:8291682, Gm08:8292207, Gm08:8297064, Gm08:8299433, Gm08:8299672, Gm08:8301839, Gm08:8302134, Gm08:8303450, Gm08:8305237, Gm08:8305348, Gm08:8305905, Gm08:8306090, Gm08:8306141, Gm08:8306210, Gm08:8306492, Gm08:8306627, Gm08:8307172, Gm08:8307665, Gm08:8308019, Gm08:8308891, Gm08:8308917, Gm08:8309316, Gm08:8309423, Gm08:8309837, Gm08:8310383, Gm08:8310464, Gm08:8310503, Gm08:8310663, Gm08:8311631, Gm08:8311906, Gm08:8312536, Gm08:8312819, Gm08:8313273, Gm08:8313923, Gm08:8314010, Gm08:8314025, Gm08:8314208, Gm08:8314292, Gm08:8314295, Gm08:8314513, Gm08:8314736, Gm08:8314791, Gm08:8314860, Gm08:8315543, Gm08:8315644, Gm08:8316113, Gm08:8316689, Gm08:8316899, Gm08:8317852, Gm08:8317861, Gm08:8318033, Gm08:8319087, Gm08:8319642, Gm08:8319647, Gm08:8320068, Gm08:8321253, Gm08:8321649, Gm08:8323937, Gm08:8324341, Gm08:8325127, Gm08:8325214, Gm08:8326696, Gm08:8326877, Gm08:8328633, Gm08:8330929, Gm08:8331132, Gm08:8331181, Gm08:8331408, Gm08:8331827, Gm08:8332651, Gm08:8332685, Gm08:8332957, Gm08:8343167, Gm08:8345187, Gm08:8345720, Gm08:8346030, Gm08:8346050, Gm08:8346352, Gm08:8346726, Gm08:8347799, Gm08:8348022, Gm08:8348028, Gm08:8349925, Gm08:8350122, Gm08:8350277, Gm08:8351061, Gm08:8351503, Gm08:8352313, Gm08:8352743, Gm08:8353341, Gm08:8355175, Gm08:8360133, Gm08:8363193, Gm08:8363888, Gm08:8364195 or a marker closely linked thereto; (c) any marker loci associated with the rhg4 locus on linkage group A2; (d) any marker loci associated with the rhg1 locus on linkage group G, or a closely linked marker; (e) any marker loci associated with the rhg2 locus on linkage group M; and/or (f) any marker loci associated with resistance to soybean cyst nematode.
  • Any of the marker loci in any of the genomic loci disclosed herein can be combined in the marker profile. For example, the marker profile can comprise 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, or more marker loci or haplotypes associated with resistance to soybean cyst nematode.
  • In one embodiment, a method of identifying a first soybean plant or a first soybean germplasm that displays resistance or improved resistance to soybean cyst nematode comprises detecting in the genome of the first soybean plant or in the genome of the first soybean germplasm at least one marker profile that is associated with the resistance, wherein the at least one marker profile comprises the marker locus provided herein.
  • Not only can one detect the various markers provided herein, it is recognized that one could detect any markers that are closely linked to the various markers discussed herein. Non-limiting examples of closely linked markers on linkage group A2 are provided in FIG. 1 A-D.
  • In addition to the markers discussed herein, information regarding useful soybean markers can be found, for example, on the USDA's Soybase website, available at www.soybase.org. One of skill in the art will recognize that the identification of favorable marker alleles may be germplasm-specific. The determination of which marker alleles correlate with resistance (or susceptibility) is determined for the particular germplasm under study. One of skill will also recognize that methods for identifying the favorable alleles are routine and well known in the art, and furthermore, that the identification and use of such favorable alleles is well within the scope of the invention.
  • Various methods are provided to identify soybean plants and/or germplasm with resistance or improved resistance to soybean cyst nematode. In one embodiment, the method of identifying comprises detecting at least one marker locus associated with resistance to soybean cyst nematode. The term “associated with” in connection with a relationship between a marker locus and a phenotype refers to a statistically significant dependence of marker frequency with respect to a quantitative scale or qualitative gradation of the phenotype. Thus, an allele of a marker is associated with a trait of interest when the allele of the marker locus and the trait phenotypes are found together in the progeny of an organism more often than if the marker genotypes and trait phenotypes segregated separately.
  • Any combination of the marker loci provided herein can be used in the methods to identify a soybean plant or soybean germplasm that displays resistance or improved resistance to soybean cyst nematode. Any one marker locus or any combination of the markers set forth herein, or any closely linked marker can be used to aid in identifying and selecting soybean plants or soybean germplasm with resistance or improved resistance to soybean cyst nematode.
  • In one embodiment, a method of identifying a first soybean plant or a first soybean germplasm that displays resistance or improved resistance to soybean cyst nematode is provided. The method comprises detecting in the genome of the first soybean plant or first soybean germplasm at least one marker locus that is associated with resistance. In such a method, the at least one marker locus: (a) can comprise the marker locus S07160-1 on linkage group A2, or a closely linked marker; (b) can comprise the marker loci Gm08:8300131, Gm08:8257778, Gm08:8257785, Gm08:8258163, Gm08:8258688, Gm08:8258742, Gm08:8259928, Gm08:8260451, Gm08:8260590, Gm08:8261480, Gm08:8261684, Gm08:8262165, Gm08:8263213, Gm08:8263250, Gm08:8263611, Gm08:8264149, Gm08:8265227, Gm08:8265364, Gm08:8265614, Gm08:8266183, Gm08:8266185, Gm08:8266263, Gm08:8266350, Gm08:8266386, Gm08:8266473, Gm08:8266888, Gm08:8267085, Gm08:8267166, Gm08:8267721, Gm08:8267826, Gm08:8268336, Gm08:8268861, Gm08:8269148, Gm08:8269785, Gm08:8270037, Gm08:8270562, Gm08:8270652, Gm08:8271540, Gm08:8271591, Gm08:8271649, Gm08:8271672, Gm08:8271955, Gm08:8273257, Gm08:8273355, Gm08:8273979, Gm08:8275766, Gm08:8275780, Gm08:8275959, Gm08:8276701, Gm08:8276849, Gm08:8276913, Gm08:8277162, Gm08:8277227, Gm08:8277248, Gm08:8277381, Gm08:8277383, Gm08:8277542, Gm08:8277625, Gm08:8277643, Gm08:8277876, Gm08:8277880, Gm08:8277969, Gm08:8278001, Gm08:8278167, Gm08:8278274, Gm08:8278434, Gm08:8279165, Gm08:8279230, Gm08:8279854, Gm08:8280901, Gm08:8280937, Gm08:8281564, Gm08:8282902, Gm08:8284027, Gm08:8286864, Gm08:8287265, Gm08:8287278, Gm08:8287453, Gm08:8287459, Gm08:8288039, Gm08:8288141, Gm08:8288200, Gm08:8288470, Gm08:8288831, Gm08:8289392, Gm08:8290740, Gm08:8291682, Gm08:8292207, Gm08:8297064, Gm08:8299433, Gm08:8299672, Gm08:8301839, Gm08:8302134, Gm08:8303450, Gm08:8305237, Gm08:8305348, Gm08:8305905, Gm08:8306090, Gm08:8306141, Gm08:8306210, Gm08:8306492, Gm08:8306627, Gm08:8307172, Gm08:8307665, Gm08:8308019, Gm08:8308891, Gm08:8308917, Gm08:8309316, Gm08:8309423, Gm08:8309837, Gm08:8310383, Gm08:8310464, Gm08:8310503, Gm08:8310663, Gm08:8311631, Gm08:8311906, Gm08:8312536, Gm08:8312819, Gm08:8313273, Gm08:8313923, Gm08:8314010, Gm08:8314025, Gm08:8314208, Gm08:8314292, Gm08:8314295, Gm08:8314513, Gm08:8314736, Gm08:8314791, Gm08:8314860, Gm08:8315543, Gm08:8315644, Gm08:8316113, Gm08:8316689, Gm08:8316899, Gm08:8317852, Gm08:8317861, Gm08:8318033, Gm08:8319087, Gm08:8319642, Gm08:8319647, Gm08:8320068, Gm08:8321253, Gm08:8321649, Gm08:8323937, Gm08:8324341, Gm08:8325127, Gm08:8325214, Gm08:8326696, Gm08:8326877, Gm08:8328633, Gm08:8330929, Gm08:8331132, Gm08:8331181, Gm08:8331408, Gm08:8331827, Gm08:8332651, Gm08:8332685, Gm08:8332957, Gm08:8343167, Gm08:8345187, Gm08:8345720, Gm08:8346030, Gm08:8346050, Gm08:8346352, Gm08:8346726, Gm08:8347799, Gm08:8348022, Gm08:8348028, Gm08:8349925, Gm08:8350122, Gm08:8350277, Gm08:8351061, Gm08:8351503, Gm08:8352313, Gm08:8352743, Gm08:8353341, Gm08:8355175, Gm08:8360133, Gm08:8363193, Gm08:8363888, Gm08:8364195 or a marker closely linked thereto; or (c) can be any marker associated with the rhg4 locus on linkage group A2.
  • In other embodiments, two or more marker loci are detected in the method. In a specific embodiment, the germplasm is a soybean variety.
  • In other embodiments, the method further comprises crossing the selected first soybean plant or first soybean germplasm with a second soybean plant or second soybean germplasm. In a further embodiment of the method, the second soybean plant or second soybean germplasm comprises an exotic soybean strain or an elite soybean strain.
  • In specific embodiments, the first soybean plant or first soybean germplasm comprises a soybean variety. Any soybean line known to the art or disclosed herein may be used. Non-limiting examples of soybean varieties and their associated soybean cyst nematode resistance alleles encompassed by the methods provided herein include, for example, Peking and PI437654.
  • In another embodiment, the detection method comprises amplifying at least one marker locus and detecting the resulting amplified marker amplicon. In such a method, amplifying comprises (a) admixing an amplification primer or amplification primer pair for each marker locus being amplified with a nucleic acid isolated from the first soybean plant or the first soybean germplasm such that the primer or primer pair is complementary or partially complementary to a variant or fragment of the genomic locus comprising the marker locus and is capable of initiating DNA polymerization by a DNA polymerase using the soybean nucleic acid as a template; and (b) extending the primer or primer pair in a DNA polymerization reaction comprising a DNA polymerase and a template nucleic acid to generate at least one amplicon. In such a method, the primer or primer pair can comprise a variant or fragment of one or more of the genomic loci provided herein.
  • In one embodiment, the method involves amplifying a variant or fragment of one or more polynucleotides comprising SEQ ID NOS: 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, 100, 101, 102, 103, 104, 105, 106, 107, 108, 109, 110, 111, 112, 113, 114, 115, 116, 117, 118, 119, 120, 121, 122, 123, 124, 125, 126, 127, 128, 129, 130, 131, 132, 133, 134, 135, 136, 137, 138, 139, 140, 141, 142, 143, 144, 145, 146, 147, 148, 149, 150, 151, 152, 153, 154, 155, 156, 157, 158, 159, 160, 161, 162, 163, 164, 165, 166, 167, 168, 169, 170, 171, 172, 173, 174, 175, 176, 177, 178, 179, 180, 181, 182, 183, 184, 185, 186, 187, 188, 189, 190, 191, 192, 193, 194, 195, 196, 197, 198, 199, 200, 201, 202, 203, 204, 205, 206, 207, 208, 209, 210, 211, 212, 213, 214, 215, 216, 217, 218, 219, 220, 221, 222, 223, 224, 225, 226, 227, 228, 229, 230, 231, 232, 233, 234, 235, 236, 237, 238, 239, 240, 241, 242, 243, 244, 245, 246, 247, 248, 249, 250, 251, 252, 253, 254, 255, 256, 257, 258, 259, 260, 261, 262, 263, 264, 265, 266, 267, 268, 269, 270, 271, 272, 273, 274, 275, 276, 277, 278, 279, 280, 281, 282, 283, 284, 285, 286, 287, 288, 289, 290, 291, 292, 293, 294, 295, 296, 297, 298, 299, 300, 301, 302, 303, 304, 305, 306, 307, 308, 309, 310, 311, 312, 313, 314, 315, 316, 317, 318, 319, 320, 321, 322, 323, 324, 325, 326, 327, 328, 329, 330, 331, 332, 333, 334, 335, 336, 337, 338, 339, 340, 341, 342, 343, 344, 345, 346, 347, 348, 349, 350, 351, 352, 353, 354, 355, 356, 357, 358, 359, 360, 361, 362, 363, 364, 365, 366, 367, 368, 369, 370, 371, 372, 373, 374, 375, 376, 377, 378, 379, 380 or variants or fragments thereof.
  • In one embodiment, the primer or primer pair can comprise a variant or fragment of one or more polynucleotides comprising SEQ ID NOS: 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, 100, 101, 102, 103, 104, 105, 106, 107, 108, 109, 110, 111, 112, 113, 114, 115, 116, 117, 118, 119, 120, 121, 122, 123, 124, 125, 126, 127, 128, 129, 130, 131, 132, 133, 134, 135, 136, 137, 138, 139, 140, 141, 142, 143, 144, 145, 146, 147, 148, 149, 150, 151, 152, 153, 154, 155, 156, 157, 158, 159, 160, 161, 162, 163, 164, 165, 166, 167, 168, 169, 170, 171, 172, 173, 174, 175, 176, 177, 178, 179, 180, 181, 182, 183, 184, 185, 186, 187, 188, 189, 190, 191, 192, 193, 194, 195, 196, 197, 198, 199, 200, 201, 202, 203, 204, 205, 206, 207, 208, 209, 210, 211, 212, 213, 214, 215, 216, 217, 218, 219, 220, 221, 222, 223, 224, 225, 226, 227, 228, 229, 230, 231, 232, 233, 234, 235, 236, 237, 238, 239, 240, 241, 242, 243, 244, 245, 246, 247, 248, 249, 250, 251, 252, 253, 254, 255, 256, 257, 258, 259, 260, 261, 262, 263, 264, 265, 266, 267, 268, 269, 270, 271, 272, 273, 274, 275, 276, 277, 278, 279, 280, 281, 282, 283, 284, 285, 286, 287, 288, 289, 290, 291, 292, 293, 294, 295, 296, 297, 298, 299, 300, 301, 302, 303, 304, 305, 306, 307, 308, 309, 310, 311, 312, 313, 314, 315, 316, 317, 318, 319, 320, 321, 322, 323, 324, 325, 326, 327, 328, 329, 330, 331, 332, 333, 334, 335, 336, 337, 338, 339, 340, 341, 342, 343, 344, 345, 346, 347, 348, 349, 350, 351, 352, 353, 354, 355, 356, 357, 358, 359, 360, 361, 362, 363, 364, 365, 366, 367, 368, 369, 370, 371, 372, 373, 374, 375, 376, 377, 378, 379, 380 or complements thereof.
  • In specific embodiments, the primer or primer pair comprises a nucleic acid sequence comprising SEQ ID NOS: 1, 2, 3, 4, 5, 6, 7, 8 or variants or fragments thereof.
  • In a specific embodiment, the primer pair comprises SEQ ID NO:1 and SEQ ID NO:2.
  • In another embodiment, the method further comprises providing one or more labeled nucleic acid probes suitable for detection of each marker locus being amplified. In such a method, the labeled nucleic acid probe can comprise a sequence comprising a variant or fragment of one or more of the genomic loci provided herein. In one embodiment, the labeled nucleic acid probe can comprise a sequence comprising a variant or fragment of one or more polynucleotides comprising SEQ ID NOS: 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, 100, 101, 102, 103, 104, 105, 106, 107, 108, 109, 110, 111, 112, 113, 114, 115, 116, 117, 118, 119, 120, 121, 122, 123, 124, 125, 126, 127, 128, 129, 130, 131, 132, 133, 134, 135, 136, 137, 138, 139, 140, 141, 142, 143, 144, 145, 146, 147, 148, 149, 150, 151, 152, 153, 154, 155, 156, 157, 158, 159, 160, 161, 162, 163, 164, 165, 166, 167, 168, 169, 170, 171, 172, 173, 174, 175, 176, 177, 178, 179, 180, 181, 182, 183, 184, 185, 186, 187, 188, 189, 190, 191, 192, 193, 194, 195, 196, 197, 198, 199, 200, 201, 202, 203, 204, 205, 206, 207, 208, 209, 210, 211, 212, 213, 214, 215, 216, 217, 218, 219, 220, 221, 222, 223, 224, 225, 226, 227, 228, 229, 230, 231, 232, 233, 234, 235, 236, 237, 238, 239, 240, 241, 242, 243, 244, 245, 246, 247, 248, 249, 250, 251, 252, 253, 254, 255, 256, 257, 258, 259, 260, 261, 262, 263, 264, 265, 266, 267, 268, 269, 270, 271, 272, 273, 274, 275, 276, 277, 278, 279, 280, 281, 282, 283, 284, 285, 286, 287, 288, 289, 290, 291, 292, 293, 294, 295, 296, 297, 298, 299, 300, 301, 302, 303, 304, 305, 306, 307, 308, 309, 310, 311, 312, 313, 314, 315, 316, 317, 318, 319, 320, 321, 322, 323, 324, 325, 326, 327, 328, 329, 330, 331, 332, 333, 334, 335, 336, 337, 338, 339, 340, 341, 342, 343, 344, 345, 346, 347, 348, 349, 350, 351, 352, 353, 354, 355, 356, 357, 358, 359, 360, 361, 362, 363, 364, 365, 366, 367, 368, 369, 370, 371, 372, 373, 374, 375, 376, 377, 378, 379, 380 or complements thereof.
  • In specific embodiments, the labeled nucleic acid probe comprises a nucleic acid sequence comprising SEQ ID NOS: 9, 10 or variants or fragments thereof.
  • Non-limiting examples of primers, probes, genomic loci and amplicons that can be used in the methods and compositions provided herein are summarized in Tables 1, 2, 3A, 3B and 4, respectively.
  • TABLE 1 
    Non-Limiting Examples of Primer Sequences.
    Linkage SEQ
    Marker Group Marker Primer ID Allele
    position (ch) Name Name NO Primer Sequence (R/S)
    8300131 A2 S07160-1 136868 1 TGTGTTGTGTTTGACTGCCATA C/A
      (Gm08)
    8300131 A2 S07160-1 136869 2 CATTTCCCAAGCCTCTTGAT C/A
    (Gm08)
    8300131 A2 S07160-1 100532 3 TCTAGCTCTGACATATTGATGA C/A
    (Gm08) TTCTTTTGTGTTGT
    8300131 A2 S07160-1 80588  4 AAGCCTCTTGATAAGACAGTGT C/A
    (Gm08) CTTCCAAATC
    8300131 A2 S07160-1 136870 5 TCTTTTGTGTTGTGTTTGACTGC C/A
    (Gm08)
    8300131 A2 S07160-1 136871 6 TGAGGCTTTCCAGCATCTAAC C/A
    (Gm08)
    8300131 A2 S07160-1 136872 7 GGACTGGATCATGAGAATTGG C/A
    (Gm08)
    8300131 A2 S07160-1 136873 8 AAGCAGAAGGAGCATTGAGG C/A
    (Gm08)
    R=Resistant; S=Susceptible
  • TABLE 2 
    Non-Limiting Examples of Probe Sequences.
    Linkage
    Marker Group Marker Probe 1* Probe 2**
    Position (ch) Name Name Probe 1 Sequence Name Probe 2 Sequence
    8300131 A2 S07160-1 102389 ATTCCTAAAGATAGT 102390 CTAAAGATACATGCA
    (Gm08) CCAAT (SEQ IDNO: 9) AGTC (SEQ ID NO: 10)
    *Probe 1 detects the susceptible allele.
    **Probe 2 detects the resistant allele.
  • TABLE 3A 
    Non-Limiting Examples of Genomic Loci Comprising the Various Marker
    Loci Provided Herein.
    Resistant
    Marker (R) or
    Marker SEQ Susceptible
    Position Name NO ID (S) Allele Reference Sequence
    8300131 S07160-1 13 R TGGAATCTGAGAAGAGACTTGAGAAATGGTACTCTTTGAATCCATGTAAGG
    TAATCATTGCCACTGGATTCATTGCAAGCACACCTCAAAACATTCCTACCAC
    ACTGAAGAGAGATGGAAGTGACTTCTCGGCAGCAATTATGGGTGCTCTATT
    TAAGGCTCGTCAGGTCACAATTTGGACAGATGTTGATGGTGTGTATAGTGC
    AGATCCTAGAAAAGGTTTGTTATGCTTCGTACTCTGTCTCTGAGTTAAACAA
    TGAGTGGACTGGATCATGAGAATTGGTTTTTAGTAACCAGAGGGAGTTCTA
    GCTCTGACATATTGATGATTCTTTTGTGTTGTGTTTGACTGCCATAACATGA
    TGTTTGGATTAAATATAAACAATAATATCCTATGCAGTTAGTGAGGCTGTG
    ATTTGGAAGACACTGTCTTATCAAGAGGCTTGGGAAATGGTGAGTTAGATG
    CTGGAAAGCCTCAATGCTCCTTCTGCTTGTAAAATTAAGGAGATTAACTTGC
    AAATTGTCTGTTGTACAGTCTTATTTGGGTGCCAATGTCTTGCATCCCCGCA
    CAATTATTCCTGTGATGCGATATGGCATACCCATTATGATAAGGAACATTCC
    CA
    8300131 S07160-1 14 S TGGAATCTGAGAAGAGACTTGAGAAATGGTACTCTTTGAATCCATGTAAGG
    TAATCATTGCCACTGGATTCATTGCAAGCACACCTCAAAACATTCCTACCAC
    ACTGAAGAGAGATGGAAGTGACTTCTCGGCAGCAATTATGGGTGCTCTATT
    TAAGGCTCGTCAGGTCACAATTTGGACAGATGTTGATGGTGTGTATAGTGC
    AGATCCTAGAAAAGGTTTGTTATGCTTCGTACTCTGTCTCTGAGTTAAACAA
    TGAGTGGACTGGATCATGAGAATTGGTTTTTAGTAACCAGAGGGAGTTCTA
    GCTCTGACATATTGATGATTCTTTTGTGTTGTGTTTGACTGCCATAACATGA
    TGTTTGGATTAAATATAAACAATAATATCATATGCAGTTAGTGAGGCTGTG
    ATTTGGAAGACACTGTCTTATCAAGAGGCTTGGGAAATGGTGAGTTAGATG
    CTGGAAAGCCTCAATGCTCCTTCTGCTTGTAAAATTAAGGAGATTAACTTGC
    AAATTGTCTGTTGTACAGTCTTATTTGGGTGCCAATGTCTTGCATCCCCGCA
    CAATTATTCCTGTGATGCGATATGGCATACCCATTATGATAAGGAACATTCC
    CA
  • TABLE 3B 
    Non-Limiting Examples of Genomic Loci Comprising the Various Marker
    Loci Provided Herein.
    SEQ SEQ
    SNP ID ID Consensus Reference Sequence
    Marker SNP SNP NO NO r2 with r2 with (200 by flanking SNP)
    Name Position [S/R] [S] [R] 8357600 8356824 [S/R]
    8356824 [C/G] 15 198 0.857 GCCGGGCAACCGCTACTACGGCGGCAATGAATA
    CATCGACCAGATCGAAAACCTCTGCCGCTCACGC
    Gm08:85 GCCCTCCAAGCCTTCCACCTCGACGCCCAATCCT
    6824 GGGGCGTCAACGTCCAGCCCTACTCCGGCTCCCC
    (Rhg4 GGCCAACTTCGCCGCCTACACCGCCGTCCTCAAC
    mutation   CCCCACGACCGCATCATGGGGCTAGATCTCC +C/G
    from Liu +CTCCGGCGGCCACCTCACCCACGGCTACTACAC
    et al CTCCGGCGGAAAGAAGATCTCCGCCACCTCCATT
    Nature TACTTCGAGAG TCTCCCTTACAAGGTAAACTCCA
    2012*) CCACCGGCTACATCGACTAYGACCGCTTGGAAGA
    AAAAGCCCTAGACTTCAGGCCAAAACTCATAATC
    TGCGGTGGCAGCGCGTACCCTCGCGA TTGGG
    CCGTTGCGCTTGGAAAATACTTGATGGGGAAAGG
    GTACAGCCTTGTCACTGGCGGAACGGAGAACCAT
    G08:835 CTTGTTTTGTGGGATCTGAGACCTCTTGGATTGAC
    7600 TGGTAATATATATAGGATTGGATCTCTACCTTCT
    (Rhg4 8357600 [A/T] 16 199 0.857 GGTTTTGATTTGTTACAAATGTCTATAAATCTGAC
    mutation TTGTTCGTTGTGTGATTGTTTTGCAGGG+AfI+ATA
    from Liu AGGTGGAGAAACTCTGTGATCTCTGTAACATTAC
    et al. TGTTAACAAGAACGCTGTTTTTGGTGATAGCAGT
    Nature GCCTTGGCCCCTGGTGGAGTGCGAATTGGTAACG
    2012) ATCTTACTTCTCTTTTATATGCTACAATACAAATC
    TTGCTTTACTAACTCAATTGGAAACAAGATCTCA
    TTTATAAGATTATAAAAATGATTTCC
    CATATCGCATCACAGGAATAATTGTGCGGGGATG
    CAAGACATTGGCACCAAAATAAGACTGTACAAC
    AGACAATTTGCAAGTTAATCTCCTTAATTTTACA
    AGCAGAAGGAGCATTGAGGCTTTCCAGCATCTAA
    Gm08:830 CTCACCATTTCCCAAGCCTCTTGATAAGACAGTG
    0131 8300131 [A/C] 17 200 0.818 0.738 TCTTCAAAATCACAGCCTCACTAACTGCATA[A/C]
    (S07160- GATATTATTGTTTATATTTAATCAAAACATCATGT
    1) TATGGCAGTCAAACACAACACAAAAGAATCATC
    AATATGTCAGAGCTAGAACTCCCTCTGGTTACTA
    AAAACCAATTCTCATGATCCAGTCCACTCATTGT
    TTAACTCAGAGACAGAGTACGAAGCATAACAAA
    CCTTTTCTAGGATCTGCACTATACACACCAT
    TAGGATGTTTTTCAAATACACTCTTTTCTCGCTGT
    TTAAAAAAAAAAATACACTCTCTTCTAATAATTA
    AAAGTTATTAAAAATCATAAATTTGAATGGATCT
    CATTTTTCATTGAGTAACTCTCTCTCGTGATTTTA
    TATTATCTCTGTGCTTTTTATTTTTTATTTTTAAAA
    Gm08:825 8257778 [A/T] 18 201 0.857 0.679 AATATGTAAAAACCAAGAAACATAAT[A/T]AATG
    7778 TGSTTCATCTTAATAAAACACTTCTTTCATCCTTA
    AATATAAGACTTTTATAATTAATTCACACTTATTA
    ATAAAATTACAAAGACTTTTATAATTAATTCACA
    CTTATTAATAAAATTGCTCGATTTAGTTAGTAATT
    AACATTATATTTGTTTGTAATTTTAATATTTTTTA
    AGATTATCTTTAAAATTATTCA
    TTTTTCAAATACACTCTTTTCTCGCTGTTTAAAAA
    AAAAAATACACTCTCTTCTAATAATTAAAAGTTA
    TTAAAAATCATAAATTTGAATGGATCTCATTTTTC
    ATTGAGTAACTCTCTCTCGTGATTTTATATTATCT
    CTGTGCTTTTTATTTTTTATTTTTAAAAAATATGT
    AAAAACCAAGAAACATAATWAATGTG[C/G]TTCA
    Gm08:825 8257785 [C/G] 19 202 0.848 0.68
    7785 TCTTAATAAAACACTTCTTTCATCCTTAAATATAA
    GACTTTTATAATTAATTCACACTTATTAATAAAAT
    TACAAAGACTTTTATAATTAATTCACACTTATTA
    ATAAAATTGCTCGATTTAGTTAGTAATTAACATT
    ATATTTGTTTGTAATTTTAATATTTTTTAAGATTA
    TCTTTAAAATTATTCAGACTAAA
    TCTTTAAAATTATTCAGACTAAATATATATTTTTT
    TCATTTAATTATTTTCTACCCAAACAATTAACATA
    TGAAAAGAGAATAATAGTAGTCGAGTTTTAATTT
    TAAAATTAAATCCTTCAATTCTCCAATCCTCCCAC
    GAAAGAGAAAATGACAATTCATAGCAATTRTTAT
    Gm08:825 TTATAGACTACAACAACTAGGGGTATT[A/C]TAGT
     8163 8258163 [C/A] 20 203 0.843 0.681
    AAAAAGAAAAACAAGTAATGCAAGAAAGAAGTC
    TTATACAAAAGAACAAAGAATTTTTTAAATAATG
    TCTTATATTCATAGACGAAAGAAACAATTGATCC
    TTTATCATTTTTATTAAACAATAAATGCATAGAT
    GTAAATAAATTAAAGATTAGAAAAAAGTAAGAA
    CATAATTGGCAAAAAAATAATTAATGTC
    TAAAAAAAGAAAACGTGGGAGAGTGCAATTAGG
    ATAAAGGGATTGGATTACTTGAAGAAAAAAARA
    ATAAAGGGGTTAGAAAAAGACCCTCTAGAAGTA
    TACGACAGCCTAAATTGAAATTGGGATACATAGT
    TTGGACTGTAATAGAATTGTGGATCTGTTTGCTC
    Gm08:825 GTTTTATTTCAAAATAAAACAAAATAAAGAACT+
    8688 8258688 [C/G] 21 204 0.895 0.688
    C/G+ CTAGCATRACAACAAAAAGTACTAATTTTTA
    ATCTCAAKGATC RGAAC TTTGC RTTTC TTTC CC GT
    ATCTTGTCGAATTTTYATTGTAAGAAATATTCTTT
    GTGGGTTCAGTTATTCACCATTATTATTTCAGAG
    GGAGCGATGGGWGGAATTATAATACTTCTTCATC
    AGATTCAATTTTGATAAAGAAAATCATTCAA
    AAGAAAAAAARAATAAAGGGGTTAGAAAAAGAC
    CC TCTAGAAGTATAC GACAGCC TAAATTGAAATT
    GGGATACATAGTTTGGACTGTAATAGAATTGTGG
    ATCTGTTTGCTCGTTTTATTTCAAAATAAAACAA
    AATAAAGAACTSCTAGCATRACAACAAAAAGTA
    Gm08:825 8258742 [G/A] 22 205 1 0.587 CTAATTTTTAATCTCAAKGATCRGAACTTTGC +A/
    8742 G+ TTTCTTTCCCGTATCTTGTCGAATTTTYATTGTA
    AGAAATATTCTTTGTGGGTTCAGTTATTCACCATT
    ATTATTTCAGAGGGAGCGATGGGWGGAATTATA
    ATACTTCTTCATCAGATTCAATTTTGATAAAGAA
    AATCATTCAAATAAGAGACTTTATTATCTTCAAA
    AAGCTAAGTACGGAAGATGCCAAAAAGAAA
    TTGGATCATTTAATTTATGAGGTGTGTGATTTTGT
    TTCCTAGTTTTTAATTTTGCAAATTGGATCATTTA
    AGTATTACAGGAATCCAATTTACTCAATTGAATT
    CTGAAAGATCAAAATTAAATAAATGCAATACCTA
    AGAGACAAAAAATAATTAATCTATTTTTTTAAAG
    Gm08:825 8259928 [C/T] 23 206 0.896 0.688 AAAATACTACTATCAGATATGGAAGCAC [C/T]AA
    9928 CAAAACCAGTCCAGGAGAGACATCAGCACCTAC
    CTACGCACCCCAAAATCAGATACAACTTTAAGCT
    TACAACATCACCTATAGTAACCTAATATTGCTCA
    AAATGGAAGCAACCATTCCACAACCAATACAAC
    AAACAAAATCAATAAATTTACTACAAACTAGTCG
    AAC CGTAC CTC GTTAATGCCATAAACC TAG
    AC TAAGC TACACAAAC TGAATCAC GTC TAAGAC G
    CTCTAAAAACAAAATCAGGAGGCAGGTTCCGCA
    AAATAGGACTGGATAATGATGTTGAAGCAGTAA
    TTTCTATCAAAATTAACAGGAAAAACTCTAAAAA
    AATCAGC CC CRGGAGAAATTTATATATATTTTTT
    Gm08:826 8260451 [C/T] 24 207 0.818 0.622 GTAGATAAAAATTTAAATTAGGGGAAGACACG+C
    0451 /T+ CTTCTTGTAAAACTACAAGAAAAATTAACAAC
    ATCAGCATTATAAAATTTATACATCGCATAACAA
    TATGCAAAATCCAAAAATCAATAAACCTAAATTA
    TTGCTGGTATAACTATTTGACTAAATGTGCCATT
    GTTGS CCAGAGAATATTAAAATGTAATGAAATAA
    AGTATTTTAAATTAATTGACTAAGAATTGGCA
    GC CC CRGGAGAAATTTATATATATTTTTTGTAGA
    TAAAAATTTAAATTAGGGGAAGACAC GYCTTC TT
    GTAAAACTACAAGAAAAATTAACAACATCAGCA
    TTATAAAATTTATACATCGCATAACAATATGCAA
    AATCCAAAAATCAATAAACCTAAATTATTGCTGG
    Gm08:826 8260590 [G/C] 25 208 0.918 0.772 TATAACTATTTGACTAAATGTGCCATTGTTG[C/G]
    0590 CCAGAGAATATTAAAATGTAATGAAATAAAGTA
    TTTTAAATTAATTGACTAAGAATTGGCATGGC TA
    TGAGAAATCATGCACTAATTGAGCAAAGATATG
    ATATATTTTTTATACTTGTCCTAACAATGTACTCC
    CACTAATTAAGTTACTAATTGAGCACTCCATAAT
    TTTTTTTGGAAGATGTTCTTTGGACACTGTG
    TCATGTCTACCAAGTCCGACTAACTTWTCCGTCC
    ATCAACCATTTTTTAACTGAGAATTGGTATGATA
    TCAAGAGTTAAGAGTTGTGACTGTATTTGGAAAA
    ATATTTCTTAAAATAAAATGATATTCAAAAAATA
    TATTTTTAATAGTTTTTTCTGCTGATTTTCAGTCT
    Gm08:826 8261480 26 209 1 0.856 ATAATTAAACGAATTTAGATACTCTATAT[G/T]AA
    1480 AAAAGAGAAAATCATTTTTTCAATAACAGTCCCA
    AAACTTTTAAATTAAAAAAAATAAAGTAAAATTT
    ATCTTTTATTTTGAATTAAATCAAGACATACTACT
    ATACCTGATCAGTCCTGGATCGAATTCTCCCAAC
    CAAATCAACTCGCCATAAATACCCTCTTATATCC
    AGTTAATTAATGGTCCATCTCGTTTTG
    AAAGAGAAAATCATTTTTTCAATAACAGTCCCAA
    AACTTTTAAATTAAAAAAAATAAAGTAAAATTTA
    TCTTTTATTTTGAATTAAATCAAGACATACTACTA
    TACCTGATCAGTCCTGGATCGAATTCTCCCAACC
    AAATCAACTCGCCATAAATACCCTCTTATATCCA
    Gm08:826 8261684 [A/T] 27 210 1 0.791 GTTAATTAATGGTCCATCTCGTTTTGAAA[A/T]TT
    1684 TTTTAACCATGAAGTTTTTTTTTAGTTACATGAGG
    AAAAGAAAGACAAGGGACAACCAAAAAAACTAC
    ACGTACTACTAAATTAAGGCAGATCACACTGCCA
    CTCCCTCTGCACAAAAACTGGTGGCCTCTGCCAG
    ACCACAGCATCAGAACTCAGAAGCATTGGTTGCA
    TCAGAGTTTTGTTATGGTGTATTTAGAA
    CCAATCCCGACACAACCAGCTCGAAATTTTCCGC
    ACCGCAGAATGTCGTGATTCTTGTGGCAACCAGA
    GTTGTTGTTCTTGCTAGCTCTATATTCTTCTCCTG
    TGTGGCAGTATTGCATCAATGCTACCATGCAGTG
    TCTAACAAGACTATATCATATATTTATGATAGTC
    Gm08:826 8262165 28 211 0.919 0.918 TCTAATCAATTTTTGAAAAAATTAGAGTC[A/T]TA
    2165 ATATTTATACATCTCATTTTCTTATAATTCACTTG
    CATCTTATTTCATTTTTTCCCCTATCATATAACAT
    ATCATATTTATTACATTCTCTCTATTTTTATTTTTA
    TTTCTCTCTCCATCTCTCTTCTCTTTTCACCCTAAA
    ATGGGGGTGAACACTCAACATGTTTTGAAAAATT
    ATTATTAGATTAATATGTATTG
    GGGTCATCCTTTCACTTGTTTGGTCTACACCACAC
    TCTTGTCTTGGGTCGCTGAGGTGGCGCGTGAGTT
    TCACCTCCCAACAGCGATGCTGTGGACTCAACCA
    GCTACGATACTCGACATCTTCTATTACTACTTTCA
    CGAACACGGTGAATACATCAAAGACAAAATCAA
    Gm08:826 8263213 [G/C] 29 212 0.913 0.09 AGACCCCTCGTGTTTCATTGAATTACCAG[C/G]AT
    3213 TGCCATTGTTGCTTGCACCACGGGACCTACCCTC
    YTTTTTATTGGGTTCAAACCCTACTATTGACTCTT
    TCATTGTCCCAATGTTTGAAAAGATGTTTTATGAT
    CTTGACGTGGAGACAAAGCCCAGAATACTTGTCA
    ACACCTTCGAAGCCTTGGAAGCGGAGGCTCTCAG
    AGCCGTTGATAAGTTCAACATGATCC
    TTGTCTTGGGTCGCTGAGGTGGCGCGTGAGTTTC
    ACCTCCCAACAGCGATGCTGTGGACTCAACCAGC
    TACGATACTCGACATCTTCTATTACTACTTTCACG
    AACACGGTGAATACATCAAAGACAAAATCAAAG
    ACCCCTCGTGTTTCATTGAATTACCAGSATTGCCA
    Gm08:826 8263250 30 213 1 0.678 TTGTTGCTTGCACCACGGGACCTACCCTC[C/T]TT
    3250 TTTATTGGGTTCAAACCCTACTATTGACTCTTTCA
    TTGTCCCAATGTTTGAAAAGATGTTTTATGATCTT
    GACGTGGAGACAAAGCCCAGAATACTTGTCAAC
    ACCTTCGAAGCCTTGGAAGCGGAGGCTCTCAGAG
    CCGTTGATAAGTTCAACATGATCCCAATCGGGCC
    GTTGATTCCCTCGGCTTTCTTGGATGG
    TCC CAATC GGGC CGTTGATTC CC TCGGCTTTC TTG
    GATGGGAAAGATMCTAATGATACTTCATTTGGCG
    GTGACATCTTC C GC CTC TCTAATGGTTGCAGC GA
    ATGGTTGGACTCGAAGCCAGAGATGTCGGTGGTT
    TATGTCTCGTTTGGTAGCCTTTGCGTGTTGCCTAA
    Gm08:826 8263611 [C/T] 31 214 0.924 0.682 GAC GCAAATGGAGGAAC TTGCACGTGC G[C/T] TA
    3611 TTAGATTGTGGAAGTCCTTTCCTGTGGGTCATTA
    AAGAAAAAGAAAATAAGTCACAAGTGGAAGGAA
    AAGAGGAGCTGAGCTGCATAGAGGAATTGGAAC
    AGAAGGGGAAGATAGTAAACTGGTGTTCTCAAG
    TGGAGGTTCTTTCACATGGTTCTGTGGGTTGTTTT
    GTTACACACTGTGGTTGGAATTCAACCATG
    AAATGAAGAAATTAGGCGGTGTTTGGAAGAGGT
    GATGGGGAGTGGAGAGAAAGGACAAGAATTGAG
    AAACAATGCAGAAAAGTGGAGGGGACTGGCCAG
    GGAAGCTGTCAAGGAAGGTGGCTCTTCGGATAA
    GAATCTAAGGGCTTTTTTAGATGATGTTGAAGTT
    Gm08:826 TGACCATATGGCTGTCACATCAGCTTTTCCGTTT+
    4149 8264149 [C/T] 32 215 0.933 0.702 C/T+TGAATTTTCCTGTCCGTTTCATTTTTCTTTTCT
    ATTATTGCATTTGCATGACTGAGAATCAAGTGAA
    ATTTCTTCTATATTAGTTTGAAATTTAAAAATATC
    TAAATGAGCCATGACTCCATGAGTAGTAATTTTG
    TGTTATAATTGATATATATATTTTCTCTTAAGTAG
    TGGCCAAAAATTTAATCTTTATGTAGATG
    ATGCATC TGGATCTGGTTTC CC TATTCATATTTC C
    AAAGCTTGCATGCTTTCTGGTTTCCTTGCCAATCA
    CTGCATGGAACAATCTTACCATCATAGGGCATGC
    TTCTTTTTTTAAGCTCGCTTGTGGTCTTCTTTTGGT
    ACATATGC TC CC CTCC CCCC TTTTTGTTTATTTTT
    Gm08:826 8265227 [C/T] 33 216 0.933 0.736 GTTTTATGGTTCATAATAGAGTTTA[C/T] TGATGA
    5227 AATAGCCAAATCATAGAATTAGTAAAATATCATG
    TACAAGGTCAAAATAGTATTTTTAGTAACCATCT
    TTTTTTTCTCGTACCTTACATAGAAGCTGACTCAA
    TGATAAAGGAAACCTAAAAATTAGTTTWAAAAA
    AACCTTTTGGCCTTTTTGACATMATATATGATATT
    TTTGTCAAAATATGAGACTTTTT
    GGTACATATGC TCC CC TCCCC CCTTTTTGTTTATT
    TTTGTTTTATGGTTCATAATAGAGTTTAYTGATGA
    AATAGCCAAATCATAGAATTAGTAAAATATCATG
    TACAAGGTCAAAATAGTATTTTTAGTAACCATCT
    TTTTTTTCTCGTACCTTACATAGAAGCTGACTCAA
    Gm08:826 8265364 [A/T] 34 217 1 0.824 TGATAAAGGAAACCTAAAAATTAGTTT[A/T]AAA
    5364 AAAACCTTTTGGCCTTTTTGACATMATATATGAT
    ATTTTTGTCAAAATATGAGACTTTTTTTTTATAAA
    AAC TAATAAAAAAATATTTTTTATTGGTAAAC CT
    AGAAC TTAAATTTTAGTTATTTTATTCTTAGAS AA
    AC CTTACC TAACAAATAATTTAATTCAAATATTT
    GC CTTTCATTC TATTTTATTTCAC C
    ATATGAGACTTTTTTTTTATAAAAACTAATAAAA
    AAATATTTTTTATTGGTAAACCTAGAACTTAAAT
    TTTAGTTATTTTATTCTTAGASAAACCTTACCTAA
    CAAATAATTTAATTCAAATATTTGCCTTTCATTCT
    ATTTTATTTCACCTTAACAACTTCCCTGGCCACAA
    Gm08:826 8265614 [G/A] 35 218 0.838 0.8 CATGTTGGATCTCAGTAAAAATTGATG[A/G]TGTA
    5614 AGATCATTCCATTAC GAAGAGATGCATGGCC TAT
    TATTCTTTCTCCATCCAAGAAAAAAATACATTTA
    TTCTTGCTTCCTGTTAAAACATAAAAAGACGTTTT
    AC CTTAGTATGATAACC TTCATAAATAGTTAAAT
    ATAGCATTGTCTTGAACTTTGAAATAAATTATGT
    TTAATTAGAACTTATAACTATAAGT
    ATATGTCAAGTATTATAATAAATATTTAATTATA
    TAAATAAATAATTTTATTCTTAAATATAAACATTT
    ACAAAGTTAAAGTAACAAAAAAGTAAGTTTTTA
    ATTCTCTTAATAATGTCATATCCTAATTTCGTACT
    AGGACTATCATTCGTCAACGTTTTGATTCTCCATT
    Gm08:826 8266183 36 219 0.924 0.773 GTCAAATTGAATTGTTCGACACCAGTTG[C/T] TRT
    6183 GTAAGACGGAAGATTATTCGACATTTCAGTAAAG
    AATGCAAAAAATGCCCAAATGGAAGGACAAAAG
    GATCATTTTRAGGC TTTTTCAGACCC CTGACTC GC
    TCAGGC TAGTC TCTGGC TCAC CTAGGC CC CTAAA
    TAGTTTAGGGGTGAAGTAACTAGCTCGYCTGGAC
    GAGCAAGGTTACTTCAGGTTGAAGCAA
    ATGTCAAGTATTATAATAAATATTTAATTATATA
    AATAAATAATTTTATTCTTAAATATAAACATTTA
    CAAAGTTAAAGTAACAAAAAAGTAAGTTTTTAAT
    TCTCTTAATAATGTCATATCCTAATTTCGTACTAG
    GACTATCATTCGTCAACGTTTTGATTCTCCATTGT
    Gm08:826 CAAATTGAATTGTTC GACACCAGTTGYT [A/G] TGT
    6185 8266185 [G/A] 37 220 0.924 0.773 AAGACGGAAGATTATTCGACATTTCAGTAAAGA
    ATGCAAAAAATGCCCAAATGGAAGGACAAAAGG
    ATCATTTTRAGGCTTTTTCAGACCCCTGACTCGCT
    CAGGCTAGTCTC TGGC TCAC CTAGGCC CC TAAAT
    AGTTTAGGGGTGAAGTAACTAGCTCGYCTGGACG
    AGCAAGGTTACTTCAGGTTGAAGCAACA
    GTAACAAAAAAGTAAGTTTTTAATTCTCTTAATA
    ATGTCATATCCTAATTTCGTACTAGGACTATCATT
    CGTCAACGTTTTGATTCTCCATTGTCAAATTGAAT
    TGTTCGACACCAGTTGYTRTGTAAGACGGAAGAT
    TATTCGACATTTCAGTAAAGAATGCAAAAAATGC
    Gm08:826 8266263 [A/G] 38 221 0.904 0.816 CCAAATGGAAGGACAAAAGGATCATTTT [A/G] AG
    6263 GC TTTTTCAGACC CC TGAC TC GC TCAGGC TAGTC T
    CTGGC TCACC TAGGCC CC TAAATAGTTTAGGGGT
    GAAGTAACTAGCTCGYCTGGACGAGCAAGGTTA
    CTTCAGGTTGAAGCAACARCTC GC TTGGGTGAGC
    TCCAGATCAAC TAAGTC CC CTCATTTCC TATAAA
    TAGGCATGAGGGGCTGAAAGAAAGGGTT
    CCATTGTCAAATTGAATTGTTCGACACCAGTTGY
    TRTGTAAGACGGAAGATTATTCGACATTTCAGTA
    AAGAATGCAAAAAATGCCCAAATGGAAGGACAA
    AAGGATCATTTTRAGGC TTTTTCAGAC CC CTGAC
    TCGC TCAGGC TAGTC TCTGGC TCACC TAGGC CC C
    Gm08:826 8266350 39 222 1 0.895 TAAATAGTTTAGGGGTGAAGTAACTAGCTCG+C/T
    6350 +CTGGACGAGCAAGGTTACTTCAGGTTGAAGCAA
    CARCTCGCTTGGGTGAGCTCCAGATCAACTAAGT
    CCCCTCATTTCCTATAAATAGGCATGAGGGGCTG
    AAAGAAAGGGTTCARCCTTCARATATTGAAAGG
    ATTTAGTGAAATTTGAAGAAAAGAAGAARAAAT
    AAAGGAAAAACAAGGTCGAGGTGCTACCGAATC
    TGTAAGACGGAAGATTATTCGACATTTCAGTAAA
    GAATGCAAAAAATGCCCAAATGGAAGGACAAAA
    GGATCATTTTRAGGC TTTTTCAGAC CC CTGACTC G
    CTCAGGC TAGTC TC TGGCTCACC TAGGC CC CTAA
    ATAGTTTAGGGGTGAAGTAACTAGCTCGYCTGGA
    Gm08:826 8266386 [A/G] 40 223 1 0.824 CGAGCAAGGTTACTTCAGGTTGAAGCAACA[A/G]
    6386 CTC GC TTGGGTGAGC TCCAGATCAAC TAAGTC CC
    CTCATTTCCTATAAATAGGCATGAGGGGCTGAAA
    GAAAGGGTTCARCCTTCARATATTGAAAGGATTT
    AGTGAAATTTGAAGAAAAGAAGAARAAATAAAG
    GAAAAACAAGGTCGAGGTGCTACCGAATCACGA
    TCGTAATCGATTTTCACATCGTTCTTCGTTCG
    CAGACCCCTGACTCGCTCAGGCTAGTCTCTGGCT
    CACCTAGGCCCCTAAATAGTTTAGGGGTGAAGTA
    ACTAGCTCGYCTGGACGAGCAAGGTTACTTCAGG
    TTGAAGCAACARCTCGCTTGGGTGAGCTCCAGAT
    CAACTAAGTCCCCTCATTTCCTATAAATAGGCAT
    Gm08:826 8266473 [G/A] 41 224 0.918 08 GAGGGGCTGAAAGAAAGGGTTCARCCTTCA[A/G]
    6473 ATATTGAAAGGATTTAGTGAAATTTGAAGAAAA
    GAAGAARAAATAAAGGAAAAACAAGGTCGAGGT
    GCTACCGAATCACGATCGTAATCGATTTTCACAT
    CGTTCTTCGTTCGTCATCCGGTTAGTATTTATTTT
    AAGTATTTCAATTCAATCTATGCACCCATAAGGG
    TCTTCTTTGTCGATTCATGCATCTTCATCTC
    TGTAATCTATTTTCTTTTGGTAAAGTGAGTTTTGA
    CCGGTCATTTACGTCACCAAACATCTTTTAATTA
    GTTTGAAGTTTAATAAGTGAAATCAAGTTAAAAT
    CAACATGTAACCGAGCTTTTTATCCGCAAAATTC
    ACTTAAATCCGTTCAAGGTCCAAGGCCTTAATGG
    Gm08:826 TCTCTTTTATTTTTGTTGGTTCGAATGAA[C/T]TTT
    6888 8266888 42 225 0.924 0.08 TCAAAAGTTTAAAATCAACTCGACACGCAATTTT
    CTTGTTTTAAGAACTATGTAGGTCTGAGTTTCTCA
    TCGCAMTTGAGGATACGTAGGAGCAAGGGCAAC
    GCCTTTGTCGACCCGAAAAAATAAAGAAGCATA
    AAAAGGGAAAATAAGTAATATTGAAGTCACGTT
    TTTGCACATTCGATTAAAGGTTGTCRTCC
    GAAYTTTTCAAAAGTTTAAAATCAACTCGACACG
    CAATTTTCTTGTTTTAAGAACTATGTAGGTCTGAG
    TTTCTCATCGCAMTTGAGGATACGTAGGAGCAAG
    GGCAACGCCTTTGTCGACCCGAAAAAATAAAGA
    AGCATAAAAAGGGAAAATAAGTAATATTGAAGT
    Gm08:826 8267085 [A/G] 43 226 0.912 0.808 CACGTTTTTGCACATTCGATTAAAGGTTGTC[A/G]
    7085 TCCCCTGTGACGAAYACGTGGGGTGTTAATACCT
    TTTTCGCTCGTAAATAACTCCCGTACCCTTATTTT
    CAAAATTCGCAKATCCCCCTTTTTGGTTTTTCTAA
    CGTTTTCCTCGAATAAACGTTGGTGGCGACTCCC
    GCGTGTTTTTCTTTTTGGAAGACGCATCCTTGAGT
    CTCGCCTCACCCCTCCCGTCGAAGGGT
    MTTGAGGATACGTAGGAGCAAGGGCAACGCCTT
    TGTCGACCCGAAAAAATAAAGAAGCATAAAAAG
    GGAAAATAAGTAATATTGAAGTCACGTTTTTGCA
    CATTCGATTAAAGGTTGTCRTCCCCTGTGACGAA
    YACGTGGGGTGTTAATACCTTTTTCGCTCGTAAA
    Gm08:826 8267166 44 227 1 0.836 TAACTCCCGTACCCTTATTTTCAAAATTCGCA+G/T
    7166 +ATCCCCCTTTTTGGTTTTTCTAACGTTTTCCTCGA
    ATAAACGTTGGTGGCGACTCCCGCGTGTTTTTCTT
    TTTGGAAGACGCATCCTTGAGTCTCGCCTCACCC
    CTCCCGTCGAAGGGTAGGTTGCAACAGATAATAA
    TAAAAAAATTCAACCATGATATTCGCAACAATAA
    ATTAAATGCACACATACATATATATAGT
    GAATTAGTGTGAGTCTCAGATTCTTCAAATGGTC
    TATGAGTTCATATTCATGCAGTAAYGTCTCACTG
    CTTTTCTTATCATATATGAAAGTATTCAAAATCTC
    TTCTTCATCCTAGATGGAGGTATCTATAACTTCAT
    CTCCATCCCAAATGAAGGTGTCTCGTACATATTC
    Gm08:826 8267721 [C/T] 45 228 0.817 0.772 AATTCTCAAAATAAAACATAAATTGTCA[C/T]TAC
    7721 TTCCTAAAGGATGATAACCAATTCACACATATTT
    ATAAAATATCATTTCAAATAACTATCAAATAAAT
    ACTTTAATTCCATATACACTAATTAATAACTTGSA
    AGGTCATACCTTAGTTATAGCATCACGTAAGTCA
    ATTTATAATTAACTATGAAATAAAACATACACAC
    AAATTAAAATATATTTTAGTTGCTAT
    CTTCATCCTAGATGGAGGTATCTATAACTTCATCT
    CCATCCCAAATGAAGGTGTCTCGTACATATTCAA
    TTCTCAAAATAAAACATAAATTGTCAYTACTTCC
    TAAAGGATGATAACCAATTCACACATATTTATAA
    AATATCATTTCAAATAAC TATCAAATAAATAC TT
    Gm08:826 8267826 [G/C] 46 229 0.831 0.824 TAATTC CATATACAC TAATTAATAAC TTG[C/G]AA
    7826 GGTCATACCTTAGTTATAGCATCACGTAAGTCAA
    TTTATAATTAACTATGAAATAAAACATACACACA
    AATTAAAATATATTTTAGTTGCTATATATGATAG
    CTAAACACAAAATCCAAACAAGCTGATTGATGA
    ATTTTCAAATAAATTTTAAGATTGAATATGCAAC
    TAGTGAATATTTGTACATTGTAATACCTT
    ATCTAGTTTCTATCGTGCATATTTGTTGAAGTTAA
    ACACAAGATCCAAGYAAGCACATATGATGCATT
    ATAATTGCAC TAAAATTTGAATATAGTTTC TATA
    TATCGTGCATGTTTGTTGGCTCTCCTTGACAAGCA
    TATCTATTTAATTTATACAAGTAGTAAATAAAAT
    Gm08:826 GATAAGACTAAATGATGAGTTCACATATA[C/T] TT
    8336 8268336 [C/T] 47 230 0.829 0.561 TATTTGTACTCWTATATATATATATATATATAATT
    CTTGGATGGAAAGGAC CC CGAAGATAC TTC CTTG
    GGTGGTGACTTGTTACCGGTTTCAAATGGTTACG
    TTGAGTGGCTTGACTCAAAGGAAGACAAGTCCGT
    GGTTTACATTTCATTTGGGAGCTACTTTGTGTTGT
    CTAAGAGACAAACGGAGGAAATTGCA
    CAGGTGGAGGTTCAGTGGGTTGTTTTGTGACGCA
    CTGTGGTTGGAATTCGACCATGGAGAGCTAGGTT
    TCGGGGGTGCCCATGGTGGTGTTTCCTCAGTGGT
    CGTACCAAAAGACAAATGCTAAACTGATAGAAA
    ATGTGTGGAAGATAGGGGTGAGGGTGGATCATG
    Gm08:826 8268861 [A/C] 48 231 1 0.722 AGGATGGGAAAGTAGAAGGAGAAAGAGATTAA+
    8861 A/C+ AAGTGTTC GGAAGAGGTGATGGGGAGTGGA
    GAGTTGAGAATGAATGTAAAGAAATGGAAGGGT
    TTGGCCAGGGAGGCAGC CAAGGAAGGTGGTC CT
    TCAGATTTCTTGATGCCATGACGTTGCAGAATCG
    ATAATCAATGCACGTGTTTGCCAAATAATTGACT
    TGGATTCCCGTGTTCTCAGTTCTTCCATGCTAAAT
    T
    AGGTGGTC CTTCAGATTTC TTGATGCCATGAC GT
    TGCAGAATCGATAATCAATGCACGTGTTTGCCAA
    ATAATTGACTTGGATTCCCGTGTTCTCAGTTCTTC
    CATGC TAAATTATTC TTTTTC TGCTTC TWTTTC TT
    TTTCCAATCAATTGATTCTATGTTTAAGATTTTTA
    Gm08:826 8269148 49 232 0.842 0.627 TTATTTAGAACAATTAAATTATTATTG[C/T]TTTA
    9148 AGAGATAGTATTATTTTAAGTTTAAATGTATATTT
    TTTATTCATAATTATATCTCTATTTAATCTGGTAT
    AC TCC TTAAAATTAC TTTTATTTAATTATGTTTTT
    TTTTAAAATAATCAAATTATTCAATCTTATTGATA
    AGTGGTTTGTATCAAATGCTCACCTAAAAAAGAT
    AAATAGACTCCCAAATATTAGA
    AGATAATTAATTTCTTTTAAATGGATGTAGGAAG
    AGACTAAATTATTACTAATCTTATTGCTTTATATT
    TTTTATAGTTATCTTTCCACTCCTACAGTACGAAA
    CACATGTAATAAATCAGTGCCATTAACATACAAC
    TCGACCTAATTGTAATTTGTAGTAACTTAGATAG
    Gm08:826 TTTAGATTTTTTTTTTGTTATGGTATTA[C/T] GTAT
    9785 8269785 [T/C] 50 233 0.912 0.808
    TTCATAAAAATTTATATTAATTTTCTTTTGAAAAA
    TATTATACWTCATATTGTCTTCTTGCCTTTGTAAA
    ATAAAAGTGTTAAAATATCAATACTYATGTTTAT
    TTGAACAAGTGAGATGCATGTAATC RC TATCATT
    ATTTAGGAATGYTAATGAACCTACTTGTTGCACT
    AATTAAGCYTGTTTCAACCTGTAA
    TATTGTCTTCTTGCCTTTGTAAAATAAAAGTGTTA
    AAATATCAATACTYATGTTTATTTGAACAAGTGA
    GATGCATGTAATC RC TATCATTATTTAGGAATGY
    TAATGAACCTACTTGTTGCACTAATTAAGCYTGT
    TTCAACCTGTAAAAAAAAGTCTGTTTCAAAATTA
    Gm08:827 8270037 [G/T] 51 234 0.924 0.823 TTTTTTATGCATTTTACTTAAAAAAATTA[G/T] AC
    0037 CTAATGAATTTTGAATATTGATTTGATTTTTTTAA
    GAGAATATATTTTTGAGTTATATATATATATATTA
    GTAGTCCTACCTCGTTCTAATATTTTATATTTTTT
    TAATAAAATATACAAATTTTTAAACAATTTTGTA
    TTAAGGAAAAATTAATCATTTTATTMTTATAATT
    ATACAAAATTTAGCTTTGAATGACC
    AATGAAAGTTTGAATATAAAAGGTTACTTTGTTT
    AAACTTAAAAAAAAATTCTAAAAAATATTTTTTA
    AGAAGTAAATATGATTTATTTATTAACAAGACAT
    TTTTCTATTTTTAAGAAAAAAATACATAAAAAAT
    AATTATTTTATTAAAAAATGATC CAAAC CC TTCA
    Gm08:827 8270562 [C/A] 52 235 1 0.704 TCATTAATGTTAATGATTAATCTATTAATT [A/C] A
    0562 TGTTTAATTTATTATATTATAATTATAATAGATTA
    TACAAAAAGCAATTATACGATTTAATGTTTTATA
    TATTTAATTTTATATTTAARATGTGGAAGATGC GT
    TAGCAAGTATTAAGATATTGACTAAAAAAGAAA
    ATTAAAAAATATATAATTAAAACTAAAGCATTTT
    CTATAAATAAAAAATATAAGACTTTTTT
    TTAACAAGACATTTTTCTATTTTTAAGAAAAAAA
    TACATAAAAAATAATTATTTTATTAAAAAATGAT
    CCAAACCCTTCATCATTAATGTTAATGATTAATCT
    ATTAATTMATGTTTAATTTATTATATTATAATTAT
    AATAGATTATACAAAAAGCAATTATACGATTTAA
    Gm08:827 8270652 [A/G] 53 236 1 1 TGTTTTATATATTTAATTTTATATTTAA[A/G]ATGT
    0652 GGAAGATGCGTTAGCAAGTATTAAGATATTGACT
    AAAAAAGAAAATTAAAAAATATATAATTAAAAC
    TAAAGCATTTTCTATAAATAAAAAATATAAGACT
    TTTTTTTTACATGACATATAAAACTTACTCTATTC
    AATATTAAAATTGTTAAAGATTTAACTGGTATAT
    AC TAATAGTGTAAATATATTTTACAC
    TCAMATATTGATTCATCATGTAGTGAAAAACTAA
    TCWCTTTTACTCAACCTAAS CTGTATCGATGYTA
    ATCATTGCTCTTAGTACATTGATTATAAAAAAAA
    TACTAGAAAGATAAAGTTTTTGTTAGAAATCATT
    TGCGAGTATATTTTAAAATAATTGAAGAATACAT
    Gm08:827 8271540 54 237 1 0.419 TTTTATGCATTATATAGTTAAAGTGTTTTT [G/T] TT
    1540 TTCCTTTTTTCACTTCCTCTATTTTAACCACTATTT
    TCTTTCTACACAMAAAAAAAAATCCATCATTTTT
    CTTTTATCCTTTTAACAAATTTTGGTTTTGGACAG
    TRAACACACACAAAATATATATTTYTCTTCTAAT
    ATGATTTGTTTTATTTTTGATGCCAATATGTTATG
    ATTGTTTGATAATGTAAAAAATAT
    AAS CTGTATCGATGYTAATCATTGCTCTTAGTAC
    ATTGATTATAAAAAAAATACTAGAAAGATAAAG
    TTTTTGTTAGAAATCATTTGCGAGTATATTTTAAA
    ATAATTGAAGAATACATTTTTATGCATTATATAG
    TTAAAGTGTTTTTKTTTTCCTTTTTTCACTTCCTCT
    Gm08:827 8271591 [C/A] 55 238 0.919 0.625 ATTTTAACCACTATTTTCTTTCTACACA[A/C]AAA
    1591 AAAAAATCCATCATTTTTCTTTTATCCTTTTAACA
    AATTTTGGTTTTGGACAGTRAACACACACAAAAT
    ATATATTTYTCTTCTAATATGATTTGTTTTATTTTT
    GATGCCAATATGTTATGATTGTTTGATAATGTAA
    AAAATATTAS AC TAATAATGC GTAGTAC TAGYAA
    TTAACCTCATTTTTWAAATAGTTA
    AAGATAAAGTTTTTGTTAGAAATCATTTGCGAGT
    ATATTTTAAAATAATTGAAGAATACATTTTTATG
    CATTATATAGTTAAAGTGTTTTTKTTTTCCTTTTTT
    CACTTCCTCTATTTTAACCACTATTTTCTTTCTAC
    ACAMAAAAAAAAATCCATCATTTTTCTTTTATCC
    Gm08:827 8271649 [A/G] 56 239 1 0.895 TTTTAACAAATTTTGGTTTTGGACAGT[A/G]AACA
    1649 CACACAAAATATATATTTYTCTTCTAATATGATTT
    GTTTTATTTTTGATGCCAATATGTTATGATTGTTT
    GATAATGTAAAAAATATTASACTAATAATGCGTA
    GTACTAGYAATTAACCTCATTTTTWAAATAGTTA
    AAAGAACTTGCTCATTCATTATTAATTTTTCATTA
    AAAATATTGTACCGGCCACTTTA
    CATTTGCGAGTATATTTTAAAATAATTGAAGAAT
    ACATTTTTATGCATTATATAGTTAAAGTGTTTTTK
    TTTTCCTTTTTTCACTTCCTCTATTTTAACCACTAT
    TTTCTTTCTACACAMAAAAAAAAATCCATCATTT
    TTCTTTTATCCTTTTAACAAATTTTGGTTTTGGAC
    Gm08:827 8271672 57 240 1 0.824 AGTRAACACACACAAAATATATATTT[C/T]TCTTC
    1672 TAATATGATTTGTTTTATTTTTGATGCCAATATGT
    TATGATTGTTTGATAATGTAAAAAATATTASACT
    AATAATGCGTAGTACTAGYAATTAACCTCATTTT
    TWAAATAGTTAAAAGAACTTGCTCATTCATTATT
    AATTTTTCATTAAAAATATTGTACCGGCCACTTTA
    ATTTATTTTCAAATGCTATTAAA
    GTAGTACTAGYAATTAACCTCATTTTTWAAATAG
    TTAAAAGAACTTGCTCATTCATTATTAATTTTTCA
    TTAAAAATATTGTACCGGCCACTTTAATTTATTTT
    CAAATGCTATTAAAATAAAGCAATGAGTTAATGA
    CATTAATTAAGAAATGCATTTAAAATTTTATTAA
    Gm08:827 8271955 58 241 0.09 0.847 TATTAAGGATCTTGTTAATTAATGTTTT[C/T]CCCC
    1955 CACAAGTCTTCTCTTTCAAAGGCCTAATGTACAT
    TAGGACACTAAATGTCACCCCTTTAAATGAATAT
    TCAAACATTGATTCATCACTTAGTGAAAARTTAA
    TCTCTTCCACTTGACTCAACCGGTGCTGATGTTAA
    CCATTGCTCTTAATATTGGTTATAAAAAATAATA
    AAAAGATAAAGTTTTTGTTAGAAAT
    ACCCAACGGTGCTTGTGAACACCTTTGAAGCTTT
    GGAAGAAGAAGCGTTGAGGGCCATTGATAAGAT
    CAACATGATCCCCATCGGGCCGTTGATTCCTTCT
    GCGTTCTTGGACGGGAATGACCCAACTGATACTT
    CGTTTGGTGGGGACATTTTTCAAGTCTCAAATGA
    Gm08:827 8273257 [G/A] 59 242 0.933 0.721 TTACGTTGAATGGCTTGACTCAAAGGAAGAG+A/G
    3257 +ATTCGGTGGTTTACGTTTCATTTGGTAGCTACTT
    TGAGCTTTCTAAGAGACAAATGGAGGAAATTGC
    ACGTGGGTTATTAGATTGTGGACGTCCATTYTTG
    TGGGTCGTTAGAGAAAAGGTAATTAATGGAAAA
    AAAGAAGAGGAGGAGGAGCTTTGTTGTTTCAGA
    GAGGAATTGGAGAAGTGGGGGAAGATAGTGACA
    TCTGCGTTCTTGGACGGGAATGACCCAACTGATA
    CTTCGTTTGGTGGGGACATTTTTCAAGTCTCAAAT
    GATTACGTTGAATGGCTTGACTCAAAGGAAGAGR
    ATTCGGTGGTTTACGTTTCATTTGGTAGCTACTTT
    GAGCTTTCTAAGAGACAAATGGAGGAAATTGCA
    Gm08:827 8273355 60 243 0.854 0.825 CGTGGGTTATTAGATTGTGGACGTCCATT[C/T]TT
    3355 GTGGGTCGTTAGAGAAAAGGTAATTAATGGAAA
    AAAAGAAGAGGAGGAGGAGCTTTGTTGTTTCAG
    AGAGGAATTGGAGAAGTGGGGGAAGATAGTGAC
    ATGGTGTTCTCAGGTGGAGGTTCTTTCGCATTCTT
    CTGTGGGTTGTTTTTTAACACACTGTGGGTGGAA
    TTCGACCATGGAAAGCCTTGTTTCTGGGGT
    GCGAAAGAAGGTGGCTCTTCAGAGAAGAATCTG
    AGGGCATTTGTGGATGATGTTAGACAAAAATTTA
    TGCATACACATGTGGGTGAATATTAATTAAGTTC
    GTCTCTAACTAGCTAGTAGTAAGCTGTAATGTGT
    TATTGTATGCTTATGATGCATGGCTTCAAACATT
    Gm08:827 8273979 [A/C] 61 244 0.87 0.734 GAAAGATGAACTGAAAAAATTAAGAAATTAT+A/
    3979 C+AGTCAGTTAATAAAAATGTGCGAAAATGGAAT
    ATCTTCAATAATAACATGTGCGTRTTGCTAAAAA
    ATGAGTTGTTGTCACGTTAGATGGTGGATGCCAT
    ATAACTGTCCAATATGTTGCCCAATTCGTCAGGA
    AAAGATAAATATTTTGATAAAGATTATTATTACA
    TTGTTGCTTTATACTCCCTTCCTTTCTTTTTA
    TGAAATGTCAATCAAAATATACAACAGTATGTGC
    ATGGATTCTTGATGACAATAATTCCAAAACCACA
    AATATGTATTTATAATCATCTTAAAAGCTCTAGT
    GAGACACTTAGCKGTACAAATTAAATTTTTTAAA
    TCGTTGGGCAAAGAATCATCAGCAAATGTAGTTT
    Gm08:827 8275766 62 245 0.928 0.903 TTTTTTTTTTTTGAGAAATCACCCAATGTA[G/T]TC
    5766 AATTGCGGAAGSAGGAGCTTGTCATTCCAGTAGT
    CCAATTTTTCAGTTATACTTTTGATTTTTATAGGG
    TAAGTACTAAGTAACCTAGCTAGTTTCTTAATCT
    CATGATCTCTTGGCTTATYTTTTTTTTTTTTWAAT
    TTGTGCTTGAGTCACTATACATATTTACTTGGTTG
    TCGAACAAAATTAAAATYTCTTCGT
    AAATATACAACAGTATGTGCATGGATTCTTGATG
    ACAATAATTCCAAAACCACAAATATGTATTTATA
    ATCATCTTAAAAGCTCTAGTGAGACACTTAGCKG
    TACAAATTAAATTTTTTAAATCGTTGGGCAAAGA
    ATCATCAGCAAATGTAGTTTTTTTTTTTTTTTGAG
    Gm08:827 8275780 [C/G] 63 246 0.924 0.823 AAATCACCCAATGTAKTCAATTGCGGAAG[C/G]A
    5780 GGAGCTTGTCATTCCAGTAGTCCAATTTTTCAGTT
    ATACTTTTGATTTTTATAGGGTAAGTACTAAGTA
    ACCTAGCTAGTTTCTTAATCTCATGATCTCTTGGC
    TTATYTTTTTTTTTTTTWAATTTGTGCTTGAGTCA
    CTATACATATTTACTTGGTTGTCGAACAAAATTA
    AAATYTCTTCGTACCTAAACAAAACC
    CAATGTAKTCAATTGCGGAAGSAGGAGCTTGTCA
    TTCCAGTAGTCCAATTTTTCAGTTATACTTTTGAT
    TTTTATAGGGTAAGTACTAAGTAACCTAGCTAGT
    TTCTTAATCTCATGATCTCTTGGCTTATYTTTTTTT
    TTTTTWAATTTGTGCTTGAGTCACTATACATATTT
    Gm08:827 8275959 64 247 0.929 0.837 ACTTGGTTGTCGAACAAAATTAAAAT[C/T]TCTTC
    5959 GTACCTAAACAAAACCTAACTTAAAGTCCCAGAC
    TAATTCAACAATAATCAACTCAATTTTTTTTTTTT
    TGCATGTTACATTTCATACATTAACTGTTGAGCTA
    CTTTATGGGTTCCCTCCCGTGTAGGGTTTGTTTAA
    TGATATTAGCTTGAAGTTTTCACTCTTTTGATCTT
    CAAGAAGAGTTAAAGGTGGAC
    GCAACTTGAGGCTGAACTCGGTCGTGCGGTCAAG
    CAAGACATTTCTGTGTACGTAGCTGTACAATAAT
    ATACAATGAATTAGAATAATAACAGATTATGTGG
    CATTAATTATTACAGCAGCAACTCATTCCTTGATT
    CTGGGAATTAGCAATTTCTTCCAGCTTATATATAT
    Gm08:827 8276701 65 248 0.874 0.923 ACCAGCATCTCAATCCTTGATTGTACGA[C/T]ATA
    6701 ATTTTGCAATTTGATCCAAATTTATTACAGCTAGT
    TAGGATACTACTCGTCTTACAATTTTTGACAAGG
    TTTTGTCAGCAATGTTGAGGATGTTTAAGCTGAA
    CACCGTCCGAGAAGTAAAATACTATTAAAGGAG
    GCTAAAGGRATATATTGGATTAGAATTTTAAAAG
    ATTATTTTAATATAAAAGGTTATATGA
    Gm08:827 8276849 [A/G] 66 249 0.904 0.79
    6849
    Gm08:827 8276913 67 250 0.684 0.827
    6913
    Gm08:827 8277162 [A/G] 68 251 0.904 0.655
    7162
    Gm08:827 8277227 69 252 0.918 0.743
    7227
    Gm08:827 8277248 [A/G] 70 253 1 0.824
    7248
    GTTATGGAATGCAATAATAAATATATACTAAAAA
    AGAGTAATAAGAGTGTGAAATTGGTAY[A/G]ASA
    71 254 1 0.756
    GTTATTAAGTCATGTGGATAATGAAATTAAGAGT
    AACATTTATGAAAATATTATATTGAGCAAGTTAT
    AAACATAATCAMTAAAACTCATCATAAGAAAAA
    AAACATGATTAGTCTTGACACATAAGATAAACAT
    TAATTTAATTTAAAAAACAAAGRAAAAAGTGTA
    GAGGGGAGACATATATTTGACATTTTTTA
    ATTCTCCTATATTAACCTTTCATGCAATAATATCT
    TCTCATTCTYACTTTTGAATTTGAACAATARATTT
    AAAATTATACATTGATTTTCTGATTTTTTTAATTA
    GTCTAATTATTTCATAATAAATATAATGACATGT
    TATGGAATGCAATAATAAATATATACTAAAAAA
    GAGTAATAAGAGTGTGAAATTGGTAYRA[C/G]AG
    72 255 1 0.755
    TTATTAAGTCATGTGGATAATGAAATTAAGAGTA
    ACATTTATGAAAATATTATATTGAGCAAGTTATA
    AACATAATCAMTAAAACTCATCATAAGAAAAAA
    AACATGATTAGTCTTGACACATAAGATAAACATT
    AATTTAATTTAAAAAACAAAGRAAAAAGTGTAG
    AGGGGAGACATATATTTGACATTTTTTATT
    ATATACTAAAAAAGAGTAATAAGAGTGTGAAAT
    TGGTAYRASAGTTATTAAGTCATGTGGATAATGA
    AATTAAGAGTAACATTTATGAAAATATTATATTG
    AGCAAGTTATAAACATAATCAMTAAAACTCATC
    ATAAGAAAAAAAACATGATTAGTCTTGACACAT
    AAGATAAACATTAATTTAATTTAAAAAACAAAG+
      73 256 0.862 0.648 A/G+AAAAAGTGTAGAGGGGAGACATATATTTGA
    CATTTTTTATTTCAAAAGAATAAGAGAAATATAT
    ATGGTGCTTGCATCTTGAWGAACATTAAATAGAT
    AARAAGATATGTGTGATAAAAGAAAAAAAAAAG
    TGTGGTAATCAATAGAAAAAAAAAAGAGWAAA
    ATCATTCAAATCATTCAATAGAAAAGTGTGGGGT
    TGT
    TATGAAAATATTATATTGAGCAAGTTATAAACAT
    AATCAMTAAAACTCATCATAAGAAAAAAAACAT
    GATTAGTCTTGACACATAAGATAAACATTAATTT
    AATTTAAAAAACAAAGRAAAAAGTGTAGAGGGG
    AGACATATATTTGACATTTTTTATTTCAAAAGAA
    TAAGAGAAATATATATGGTGCTTGCATCTTGA+A/
    74 257 0.895 0.622
    T+GAACATTAAATAGATAARAAGATATGTGTGAT
    AAAAGAAAAAAAAAAGTGTGGTAATCAATAGAA
    AAAAAAAAGAGWAAAATCATTCAAATCATTCAA
    TAGAAAAGTGTGGGGTTGTTTAATTGATGTTTTA
    TATTAAAAAATTAGATGAAATTCATCCAAATCAT
    TCTTAAAAAATAATGCATCAAAATTTGTATATTT
    AGCAAGTTATAAACATAATCAMTAAAACTCATC
    ATAAGAAAAAAAACATGATTAGTCTTGACACAT
    AAGATAAACATTAATTTAATTTAAAAAACAAAGR
    AAAAAGTGTAGAGGGGAGACATATATTTGACAT
    TTTTTATTTCAAAAGAATAAGAGAAATATATATG
    GTGCTTGCATCTTGAWGAACATTAAATAGATAA+
    75 258 0.87 0.53
    A/G+AAGATATGTGTGATAAAAGAAAAAAAAAAG
    TGTGGTAATCAATAGAAAAAAAAAAGAGWAAA
    ATCATTCAAATCATTCAATAGAAAAGTGTGGGGT
    TGTTTAATTGATGTTTTATATTAAAAAATTAGATG
    AAATTCATCCAAATCATTCTTAAAAAATAATGCA
    TCAAAATTTGTATATTTTTAAATATTAAAAGACTT
    TGGTAATCAATAGAAAAAAAAAAGAGWAAAATC
    ATTCAAATCATTCAATAGAAAAGTGTGGGGTTGT
    TTAATTGATGTTTTATATTAAAAAATTAGATGAA
    ATTCATCCAAATCATTCTTAAAAAATAATGCATC
    AAAATTTGTATATTTTTAAATATTAAAAGACTTTT
    Gm08:827 8277876 [C/T] 76 259 0.836 0.713 TTATAAGTTATAAAAAATTATAATTGAATA[C/T] C
    7876 ACMAAATTTTATTATTTTTCTTAAAAAATCTTAW
    ATGTTTTAATTGAATACCATAAGACTTTTTTATAT
    AAAAAHTATTTTAAAATCTTTTMAAATCTTAATC
    YAATATATCCACTAAGTTATYAAAGGCTAGGAG
    GAAACAAGTGGASCATGAGACAATACATATATA
    GGGGGGAATATATGGAAATTGAAAAAAAAA
    AATCAATAGAAAAAAAAAAGAGWAAAATCATTC
    AAATCATTCAATAGAAAAGTGTGGGGTTGTTTAA
    TTGATGTTTTATATTAAAAAATTAGATGAAATTC
    ATCCAAATCATTCTTAAAAAATAATGCATCAAAA
    TTTGTATATTTTTAAATATTAAAAGACTTTTTTAT
    Gm08:827 AAGTTATAAAAAATTATAATTGAATAYCAC [A/C]
    7880 8277880 [C/A] 77 260 0.809 0.673 AAATTTTATTATTTTTCTTAAAAAATCTTAWATGT
    TTTAATTGAATACCATAAGACTTTTTTATATAAA
    AAHTATTTTAAAATCTTTTMAAATCTTAATCYAA
    TATATC CAC TAAGTTATYAAAGGC TAGGAGGAA
    ACAAGTGGAS CATGAGACAATACATATATAGGG
    GGGAATATATGGAAATTGAAAAAAAAAAGAT
    TAGATGAAATTCATCCAAATCATTCTTAAAAAAT
    AATGCATCAAAATTTGTATATTTTTAAATATTAA
    AAGACTTTTTTATAAGTTATAAAAAATTATAATT
    GAATAYCACMAAATTTTATTATTTTTCTTAAAAA
    ATCTTAWATGTTTTAATTGAATACCATAAGAC TT
    Gm08:827 8277969 [C/A] 78 261 0.87 0.658 TTTTATATAAAAAHTATTTTAAAATCTTTT +A/C +A
    7969 AATCTTAATCYAATATATCCACTAAGTTATYAAA
    GGCTAGGAGGAAACAAGTGGAS CATGAGACAAT
    ACATATATAGGGGGGAATATATGGAAATTGAAA
    AAAAAAAGATGTGAAAAATAATAAATCTCAATA
    GAAAATGAAGGAAGCATAAATGAAATAAAAGTG
    AAATCAGGTGATGAGATAAAAAACAATTGTS TA
    ATAATGCATCAAAATTTGTATATTTTTAAATATTA
    AAAGACTTTTTTATAAGTTATAAAAAATTATAAT
    TGAATAYCACMAAATTTTATTATTTTTCTTAAAA
    AATCTTAWATGTTTTAATTGAATACCATAAGACT
    TTTTTATATAAAAAHTATTTTAAAATCTTTTMAA
    Gm08:827 8278001 79 262 0.884 0.741 ATCTTAATCYAATATATCCACTAAGTTAT[C/T]AA
    8001 AGGCTAGGAGGAAACAAGTGGASCATGAGACAA
    TACATATATAGGGGGGAATATATGGAAATTGAA
    AAAAAAAAGATGTGAAAAATAATAAATCTCAAT
    AGAAAATGAAGGAAGCATAAATGAAATAAAAGT
    GAAATCAGGTGATGAGATAAAAAACAATTGTS TA
    AAAAAATTGACGATAAGTCTATAATAAATAAA
    TTMAAATCTTAATCYAATATATCCACTAAGTTAT
    YAAAGGCTAGGAGGAAACAAGTGGASCATGAGA
    CAATACATATATAGGGGGGAATATATGGAAATT
    GAAAAAAAAAAGATGTGAAAAATAATAAATCTC
    AATAGAAAATGAAGGAAGCATAAATGAAATAAA
    AGTGAAATCAGGTGATGAGATAAAAAACAATTG
    Gm08:827 8278167 [C/G] 80 263 0.861 0.847 T[C/G]TAAAAAAATTGACGATAAGTCTATAATAA
    8167
    ATAAAAAGTGAGGTCATATACATATTCCCGATTT
    CTATAAAAAAAAATGAATATTTGAAAATCAATTC
    ATTTTCAATYTTTAAAAAATAAATAAAAAAGAAT
    TGAAGTTGTATATCAATCTATGGAGAATTAATTC
    AAAAAATGATTTATAGAAGTTAGCAATAGAAAA
    AT
    AAAAGATGTGAAAAATAATAAATCTCAATAGAA
    AATGAAGGAAGCATAAATGAAATAAAAGTGAAA
    TCAGGTGATGAGATAAAAAACAATTGTSTAAAAA
    AATTGACGATAAGTCTATAATAAATAAAAAGTG
    AGGTCATATACATATTC CC GATTTC TATAAAAAA
    Gm08:827 8278274 [C/T] 81 264 0.831 0.628 AAATGAATATTTGAAAATCAATTCATTTTCAAT+C
    8274 /T+ TTTAAAAAATAAATAAAAAAGAATTGAAGTTG
    TATATCAATCTATGGAGAATTAATTCAAAAAATG
    ATTTATAGAAGTTAGCAATAGAAAAATACGTACT
    AACATTATAAGAAAGAGAAAATATTTTAAGAGA
    TAAATAGCAAAATAATATTTATTTAAS TGAATGA
    GTATCTTAAACCATATATCAAAATTTACAACAC
    TAAAAAAAAATGAATATTTGAAAATCAATTCATT
    TTCAATYTTTAAAAAATAAATAAAAAAGAATTGA
    AGTTGTATATCAATCTATGGAGAATTAATTCAAA
    AAATGATTTATAGAAGTTAGCAATAGAAAAATA
    CGTACTAACATTATAAGAAAGAGAAAATATTTTA
    Gm08:827 AGAGATAAATAGCAAAATAATATTTATTTAA+C/G
    8434 8278434 [C/G] 82 265 0.858 0.647 + TGAATGAGTATCTTAAACCATATATCAAAATTTA
    CAACACATTAAAATGAAAAATCTTAAAAAGAAG
    GAACAACAAAACTTTTTATGAAAATTATAACCAA
    AAAAAAATAAAAATTAATATAAAGCTTAACATTT
    CTTTTGTTGAAGTACTAATATAAAGCTTAACATG
    ATAGCTAGGATAAGCACTATCC TATGGC CAC
    TTTTGGTAAACAGATTTAATTTGATGTAAATCAT
    ATTAACATAATTAATATTAGGTATTTTAATAATTT
    TTTATTATTTTATTTGTATTGTTCATTAWTTGTTR
    AATAATATATAAGATAAAAAACATTTTGTCATTT
    ATCTTTATCCTATCTTATTTTTTATCTTGTCTAATA
    Gm08:827 8279165 83 266 0.83 0.759 TCATATTTTTAACAAATCAAATWGGG[G/T] GTAA
    9165 GTGTTTGATAAATTTTTTCAAACAAATTACAAAT
    GTTAATATATTTTATTTTTTCAACAAKTAATATGT
    TAATCTTAATAAACAAATTCACATTTTATTTTTCA
    TTTACCAAAATAGATATATTATTTTTAAATATTGT
    TTGAAATAAATAATTTATAATTAATTWAAAAAA
    ATAAWAATTTCATTTCGTAACATA
    ATTTTTTATTATTTTATTTGTATTGTTCATTAWTT
    GTTRAATAATATATAAGATAAAAAACATTTTGTC
    ATTTATCTTTATCCTATCTTATTTTTTATCTTGTCT
    AATATCATATTTTTAACAAATCAAATWGGGKGTA
    AGTGTTTGATAAATTTTTTCAAACAAATTACAAA
    Gm08:827 8279230 84 267 0.903 0.797 TGTTAATATATTTTATTTTTTCAACAA [G/T] TAATA
    9230 TGTTAATCTTAATAAACAAATTCACATTTTATTTT
    TCATTTACCAAAATAGATATATTATTTTTAAATAT
    TGTTTGAAATAAATAATTTATAATTAATTWAAAA
    AAATAAWAATTTCATTTCGTAACATATTTTTCAC
    ATTGAAATAAACATGTACGACACACATATATACA
    TACATATATATATATATATATAT
    AAAAATAATTCATATTAATATACCAACTTAAGAA
    AGCTGTTAAATATATTAAAAAAAGGAAATATGTT
    ATTATTAAATCAAATTTTCATCAGTTAACAACCA
    ACATTTTAATCTAATTTAGTTGTTTAAACAAAATT
    TGTATGTATTATAAATTTTTAATATTATTTTTATT
    Gm08:827 TTTAAAAATAAAAAACAGTGAAAACAAT [A/C] AA
    9854 8279854 [A/C] 85 268 0.842 0.759
    CC TTGCATTATCATATATAGTCAATTAAAAAAAA
    GGAATGAGTGAAGGGGAAAAAGTGGAGGAAAA
    GGTAATGGATTCAATTCCTTCCATTAATATTTTAA
    ACAAAAATTAATAAATTAACATATTGGTAAAAA
    ATATAATATTAATTTCTTGAAAATTTGTATCCAGT
    AGTACAACATTATAAATTATTTTTTAGGT
    TTCTGCCAATGGAAGGGTATCCAATGCGATTCAT
    CCAGCCACGTGACCAGCATAAGCCTCGCTTCGCA
    KTCCCTCACCGGAACACTCCCCTCGGATCTCAAT
    TCCCTCTCTCAACTCCGCACTCTCTCCCTCCAAGA
    CAATTCCCTCACCGGCACCCTCCCTTCTCTCTCCA
    Gm08:828 8280901 [A/C] 86 269 0.929 0.848 ACCTTTCTTTCCTCCAAACCGTCTAC TT [A/C] AAC
    0901 CGCAACAACTTCTCCTCCGTGTCCCCCACCGCYT
    TCGCCTCCCTAACCTCCCTCCAAACCCTCAGCCTC
    GGCTCCAACCCTGCTCTCCAACCCTGGTCCTTCCC
    CACCGACCTCACTTCCTCCTCTAACCTAATCGAC
    CTCGACCTCGCCACCGTATCCCTCACCGGTCCC TT
    GCCGGACATTTTCGACAAATTCCC
    AGCCACGTGACCAGCATAAGCCTCGCTTCGCAKT
    CCCTCACCGGAACACTCCCCTCGGATCTCAATTC
    CC TCTC TCAACTCCGCAC TCTC TCCCTCCAAGACA
    ATTCCCTCACCGGCACCCTCCCTTCTCTCTCCAAC
    CTTTCTTTCCTCCAAACCGTCTACTTMAACCGCA
    Gm08:828 8280937 87 270 1 0.848 ACAACTTCTCCTCCGTGTCCCCCACCGC [C/T] TTC
    0937 GCCTCCCTAACCTCCCTCCAAACCCTCAGCCTCG
    GC TCCAACCC TGCTC TCCAACCC TGGTCC TTCCCC
    ACCGACCTCACTTCCTCCTCTAACCTAATCGACCT
    CGACCTCGCCACCGTATCCCTCACCGGTCCCTTG
    CCGGACATTTTCGACAAATTCCCTTCCCTTCAAC
    ACCTTCGCCTCTCTTACAACAACCT
    GTTCCCGCTTCATTGACAAGTCTTCCTAGTTTGAA
    GAAAGTTTCTCTGGATAATAATGAGCTTCAGGGG
    CC TGTGCCCGTGTTTGGGAAAGGTGTGAATGTTA
    CTCTCGATGGGATTAATAGTTTTTGTCTTGATACT
    CC TGGGAATTGTGATCCCAGGGTGATGGTTTTGC
    Gm08:828 8281564 [A/G] 88 271 0.924 0.824 TGCAGATTGCCGAGGCATTCGGGTATCC [A/G] ATT
    1564 CGGTYGGCAGAGTCGTGGAAGGGGAATGATCCG
    TGTGATGGTTGGAACTATGTTGTGTGTGCTGCCG
    GAAAGATTATTACTGTCAATTTCGAGAAACAGGG
    TTTGCAGGGTACCATCTCCCCTGCATTTGCCAATT
    TGACTGACTTGAGGACTTTGTTTCTCAATGGCAA
    TAATTTGATCGGTTCTATACCTGATAG
    AAGGTTGCTGATTTTGGGTTGGTTAAAAATGCAC
    CAGATGGGAAGTATTCTGTTGAGACACGGTTGGC
    TGGAACATTTGGATATCTTGCACCTGAGTATGCA
    GGTACAGAAAGCCTTTGATTTTAGTTTTGTACAA
    TTGTGCCTTAATTTTGAAGTTCATATTTTATATGC
    Gm08:828 8282902 89 272 1 0.848 TCGTATTTGGTGGTTATAGCTGTTGGTTA[G/T] TA
    2902 CTTCAATATCATGCTTCGGTGTTCAGCAAATTTA
    AGTAGTTCACCAGAGTAATCGCTCACATACAAAA
    AAAAAGTAGAAAGAGTTGAAGGGAAAATAATTG
    ATACTCAATTCCTAGATACATGGCTACTTCAAAA
    TTCTTTGTGGCTATTTCTTTGCAATGTTATATTTT
    GC TC TTTTCACGTGTTTTGTTGAGTTGG
    GGAGCAATGGAAACCTACTAGCCATGATGAAGA
    AGAGGAAGACGGCTCTGGCGGTGACCTTCATATG
    AGCCTTCCTCAAGCTCTACGAAGGTGGCAAGCCA
    ACGAAGGCACTTCCTCAATATTTAATGACATTTC
    CATCTCACAAACCCAATCAAGCATCTCCTCTAAA
    Gm08:828 8284027 90 273 0.863 0.744 CC TGCAGGGTTTGCAGAC TCC TTTGATTCAA [C/T]
    4027 GGATTGCCGTTAACCGAATTGATAAACGAGACA
    AC TATCCAAGGGCATCTTAGTCCATATGATAGTG
    GAAGGTTTAGTTGAGAATACCCAAGAAAACCAG
    AGGTTGTAAAGCTGTTTTGATCTATTAGCATCGC
    CAATTTCTTTGTAATTATTTATTATTGTTCAAAAT
    GTCATTTTTATGGTGTTCTTAAAATCTCCTC
    CAAGATTTGTAAGAGAAAAC TTC TTGGCTC TATA
    TTTAASAACAAAAAATCTAAGAKRAAATGGGATT
    KAATGGAAATGATCGGTCGCAAGCATATCTAAAT
    TTGACAGGAAATCCATAAATGAC TTGACCAC CAT
    TAACAAGATAAATATTGTGTGAGATCTTTAAAAR
    Gm08:828 8286864 [A/T] 91 274 1 0.687 TGAAGATTTTAC GGGTTTAACAGATTAAAA [A/T] C
    6864 TTTTACAATTTAATATCACATTCTTTTGAACACAT
    GAACACTTATTGATGATAGTTACATTCCATGCTT
    GC TTTCC TTGCAC TTTATTTTTTGTTGGAAATTGA
    TCTAYGGAGAGATC TTTCAAGGAACATTGGC TAT
    AGCTGACATGATGATWGRAGGAAAAATTACAAA
    CAATAATTTATACAAATTTTATGTTTCA
    TAMAATAGAAGAAACCAGTATCTTGACTTCTTGA
    GAAATGAGGACAAGGAGCAAAACTATGCTAAGA
    ATCTTGATGGCTGAACCASCCATTTCAGAAAATG
    TAAATACAAGCTTCGATTCTCGAATTGCATAGCT
    CTTATATGTCGCGTTATTTATAAATGAATTGTTGT
    Gm08:828 AATTTGTAAAACAATATGTTTTACGTTTCG[C/T] G
    7265 8287265 92 275 0.776 0.917 TGAAGAATATCRCATTTATGAATGACTGAATTTT
    TAAGACAATGAAACTGAAGTTAAAGAAACATAA
    ATTACTCTAAAAAAAATTAAATACAGTGAAATTG
    TATAGATTTGATAAATATTTTTTTAATAGTTGATA
    TGATTTTGTTTTGTTAGGAGAAAGCTATCATTTTG
    TTCTCCTATAGTTATS TTTAGYAAGTTA
    AC CAGTATCTTGACTTCTTGAGAAATGAGGACAA
    GGAGCAAAACTATGCTAAGAATCTTGATGGCTGA
    AC CAS C CATTTCAGAAAATGTAAATACAAGCTTC
    GATTCTCGAATTGCATAGCTCTTATATGTCGCGTT
    ATTTATAAATGAATTGTTGTAATTTGTAAAACAA
    Gm08:828 8287278 [A/G] 93 276 0.76 0.91 TATGTTTTACGTTTCGYGTGAAGAATATC [A/G] CA
    7278 TTTATGAATGACTGAATTTTTAAGACAATGAAAC
    TGAAGTTAAAGAAACATAAATTACTCTAAAAAA
    AATTAAATACAGTGAAATTGTATAGATTTGATAA
    ATATTTTTTTAATAGTTGATATGATTTTGTTTTGT
    TAGGAGAAAGCTATCATTTTGTTCTCCTATAGTT
    ATS TTTAGYAAGTTATTTTAATTAAATT
    TTTTACGTTTCGYGTGAAGAATATCRCATTTATG
    AATGACTGAATTTTTAAGACAATGAAACTGAAGT
    TAAAGAAACATAAATTACTCTAAAAAAAATTAA
    ATACAGTGAAATTGTATAGATTTGATAAATATTT
    TTTTAATAGTTGATATGATTTTGTTTTGTTAGGAG
    Gm08:828 8287453 [G/C] 94 277 1 0.738 AAAGCTATCATTTTGTTCTCCTATAGTTAT[C/G]TT
    7453 TAGYAAGTTATTTTAATTAAATTTTTTTATTAATT
    AAAAGATTTATTTGACTATTTGATAAATAATTTTT
    TTAAGTAATTTTTAATGTTTCTCTAGTATYTTTTA
    GTATTTTTTTAAAATATTATTTAAAATAACATTTT
    TTAAACACTAATTTTTAATTTTTAACCTTTTAATT
    TTATTCTCTTTATATCTTAAAAT
    GTTTCGYGTGAAGAATATCRCATTTATGAATGAC
    TGAATTTTTAAGACAATGAAACTGAAGTTAAAGA
    AACATAAATTACTCTAAAAAAAATTAAATACAGT
    GAAATTGTATAGATTTGATAAATATTTTTTTAATA
    GTTGATATGATTTTGTTTTGTTAGGAGAAAGC TA
    Gm08:828 8287459 95 278 1 0.591 TCATTTTGTTCTCCTATAGTTATSTTTAG[C/T]AAG
    7459 TTATTTTAATTAAATTTTTTTATTAATTAAAAGAT
    TTATTTGACTATTTGATAAATAATTTTTTTAAGTA
    ATTTTTAATGTTTCTCTAGTATYTTTTAGTATTTTT
    TTAAAATATTATTTAAAATAACATTTTTTAAACA
    CTAATTTTTAATTTTTAACCTTTTAATTTTATTCTC
    TTTATATCTTAAAATATTTAT
    TAACTTTTCAGTTTACTTTTGCAAATAAYATATTT
    CTTTCCTGGMATATKACAAAGCTAAACAATATTT
    CTTGAGTGTTTAATTGTTTTAAATTGAAATAGGA
    AGTGAGCATTTMCTAATATCTTAGCTCGAAACAT
    CTCTTTCATCTTTGTTGAAGTAAACCTCTGTATGG
    Gm08:828 8288039 [G/C] 96 279 0.884 0.584 TAAAATTAAGAGGAGAAAGAAAAATGAA[C/G]T
    8039 GGAGTAAGGTCTTGTTTGAAATTATTTTTTAATTT
    CAAAACTTGTTTTCAATATAATTTTTAGCTTTGTT
    ATATTTTAAAAATAAAATAAAAAGAAAAAAYAT
    TTGTTAAAATTCAAAAATAGATTTTTTTTAAAAA
    AATGTTCATAAAATATCAGCATYTGTCAATTGCA
    TGTTTATGAGGTAAAAAATTGCTTTATT
    AAGTGAGCATTTMCTAATATCTTAGCTCGAAACA
    TCTCTTTCATCTTTGTTGAAGTAAACCTCTGTATG
    GTAAAATTAAGAGGAGAAAGAAAAATGAAS TGG
    AGTAAGGTCTTGTTTGAAATTATTTTTTAATTTCA
    AAACTTGTTTTCAATATAATTTTTAGCTTTGTTAT
    Gm08:828 ATTTTAAAAATAAAATAAAAAGAAAAAA [C/T] AT
    8141 8288141 97 280 0.823 0.713 TTGTTAAAATTCAAAAATAGATTTTTTTTAAAAA
    AATGTTCATAAAATATCAGCATYTGTCAATTGCA
    TGTTTATGAGGTAAAAAATTGCTTTATTTATGAA
    AATATTTAGGATCCAAAACAAGAGTAGGAAAGT
    AATTTTTAAAAGACATTTTTTTCCAGCACTGCAAT
    TGTAGGAACAAGTTTTAAAATACAAATG
    CC TCTGTATGGTAAAATTAAGAGGAGAAAGAAA
    AATGAAS TGGAGTAAGGTCTTGTTTGAAATTATT
    TTTTAATTTCAAAACTTGTTTTCAATATAATTTTT
    AGCTTTGTTATATTTTAAAAATAAAATAAAAAGA
    AAAAAYATTTGTTAAAATTCAAAAATAGATTTTT
    Gm08:828 8288200 [C/T] 98 281 0.883 0.851 TTTAAAAAAATGTTCATAAAATATCAGCAT[C/T] T
    8200 GTCAATTGCATGTTTATGAGGTAAAAAATTGC TT
    TATTTATGAAAATATTTAGGATCCAAAACAAGAG
    TAGGAAAGTAATTTTTAAAAGACATTTTTTTCCA
    GCACTGCAATTGTAGGAACAAGTTTTAAAATACA
    AATGYCTTGAAAATCTTTCTAATACTTAATGGAA
    AATATTAAATAAAAATAAAAATAAAAATA
    TAGGAAAGTAATTTTTAAAAGACATTTTTTTCCA
    GCACTGCAATTGTAGGAACAAGTTTTAAAATACA
    AATGYCTTGAAAATCTTTCTAATACTTAATGGAA
    AATATTAAATAAAAATAAAAATAAAAATAAAAA
    TATTTAATGTTTTAAAAACTTTAAAAACATTCAA
    Gm08:828 8288470 [A/T] 99 282 0.852 0.652 ATACTTTC TTTATTTAATAAGAGGAGGATGA [A/T]
    8470 GGGATTAGAATTATTCAATTTTTTTATATTAAAAT
    ATAACGAATCCATAACAAATTTACAGTAGTACTT
    TGTTTCATAAAAAAATACTGATTGGATGAAGCAG
    AKAGGAGAGAGGAAGATGTCAGTAAGTCATAAA
    TGTGCCATTAATACATTTAATAACTTTTTTTTTTT
    ACAAAAGGGAGAAAGGCTTACATTTAAAT
    TTTTTTTTTTTACAAAAGGGAGAAAGGCTTACAT
    TTAAATTGCTATTACTTTTTTTAAACGAAAAAGG
    GGTGAAAC GC CCAAAATAAATCATCATAAATAA
    GATAATAAGATAAGGAAGGAGAAAATAAATTTA
    AATATTGATCACAAATAAATTTTGYATAAATACA
    Gm08:828 8288831 100 283 0.852 0.612 AATAAAATATAAGATAATAAATATCGATCAAT+C/
    8831 T+CGTGAAACAATTTGCGGAAGAGCAAAATTTGA
    GAAAAAAAATCGAAGAARCAAAATTCGCGATAT
    TATAAAACTTTAGAGATAAAAAAAAATTCATGAT
    AAATAATACAGTATATTATAATTTTAATCTTTAGT
    TTTTAATACAACTGTAAAAAAAATTCATGATAAA
    TAATATATTATAATTATAATCTTTAGTTTTAA
    AACTTTTTGTTAGTAACAGAAAGTGTAAACTGGT
    TTGGAGAAAATGTGAGAGATGGCAGGATACTAT
    GAGTAACTAGTTGGATTGGAAAATGTTGTATCCA
    GCTGTAAATTACCCATTCCATTATTGGAAGGAAA
    TATTCCGCATGAGCCAAACTATGCGAAAATGACA
    Gm08:828 TGGTGAAAATTGATAAAGGTAAAGAAAAAGT+A/
    9392 8289392 [G/A] 101 284 0.929 0.785 G+GAGCTCAGAAAGGTGTTATTCTTCATCAAGAA
    GAGCTATTTCCAAAGCAACTATRTTACTTGTGCA
    ACTCTTTATTTTTTGTACATATACTACTATTATTA
    TTACTTGTGCTACTCTGATAAATAGAAAGTAGAA
    AACAAAGAAGTGGTATTGATTGATGTTACGTAAG
    TTACATAAAAGTTTGATGCGTATTGATTGAT
    ACAAAGCAATGGATCCAGGACTCATATATGATAT
    CACCACTGAGGATTATGTCCAATTCCTATGTTCC
    ATGGATCACAGTAGTGCATCCATTAGCAAAGTGA
    CTAAGACCACCACAAGTTGTAAGAAAGGAAATC
    ACCAAGCACTGAACCTCAACCTTCCTTCCATATC
    Gm08:829 AGTGCCAAACCTGAAGAGGGCTGCAACAGTA+A/
    0740 8290740 [A/T] 102 285 1 0.912 T+TGAGAACAGTGACAAACGTGGGAAATATTACT
    GCAGTCTRCAAAGCTCTAGTGAAAGTTCCACATG
    GCATAAAAGTTAGAGTTGAACCTCAAACTTTGAG
    TTTCAATTCAGRTGTACGAATCCTTAACTTTAKTG
    TCAGTTTTCTGTCAACTMAAAAATTTCATGGAGA
    TTACAAATTTGGGAGCCTAACATGGACAGAT
    TAATATTTTTTCTTTTTAAAATACAGAWGGAAGT
    ACAAGAATAAAAAGTGGTTCAACTTCCATGAATA
    AAAATGGTCTTTACATGATTTGCACTTAATCTAA
    ATAACCAAGCACAAAATATATCAAAYWTGTGTA
    TATTTTCAGTTTAGTATTAATTATTAATGACTAGC
    Gm08:829 8291682 [G/A] 103 286 0.866 0.715 AATAGAATTTAGATTTATAGAGACAATACA[A/G]
    1682 TTAGTAAATTTTATTTTAGAAATTATTTTAAAATA
    TTCTAATAATTAAATTACTCTTTTGTTTTTACATT
    GCAAGTGCAAGCATCTAYGTGCAAAAGGAGGGT
    ACGATACTCAACAATAGATAAATTTGCACAACAT
    CATCAGTCTTTGTTYTTCTTTTTCTTTTTTACTTTA
    GATACGTAAGGCAGTAACAACATACGA
    GACAAAAGATAAGAGAAACAAGCTTACATTACT
    ACAACGTTATAAGAAGCAAATAACCTACGAAGA
    AAATCAAGATAAATAAATAGATGGTACAAATTT
    GCATGTGTTCGGATATCCATCGACATCATTCATTT
    CGATCAAAATTCACGTTTTGGACATAAAAGCAAT
    Gm08:829 TCTTCGTCGCTTCAGATAATGCGTGTCGTGGA+A/
    2207 8292207 [G/A] 104 287 0.912 0.904 G+CAGAGGATGCAAAACCATACATGCAGAAAATT
    ATGCTTGCAGAATGACACWTACGATGGAGCACC
    AAGATATGAGGCAAGTCGTAAAATATCACTAAA
    TATTCCACCAGCGGTGACTTGAGCACCAGCTCCT
    GGCCCACGAACTATCAGAGGCTGATCCTTATACC
    TTCGTGTTGTAAATGCAATAATGTTATCTGACCC
    CTGTTATTGATTGATSAATCACTTATTACTATCTG
    ATGGAAGATGAGTTTTATATAATAGAGTTACCTT
    GTCCTGCAAGCTTACAATAGAAAMTTCAGCTGYC
    TACAGCTATTAAGACTAACTAAACTTCAGTTAAG
    CCAATATTAATTGTGTTTTACTATTTAAGTCCTAG
    Gm08:829 8297064 [C/T] 105 288 0.929 0.857 TTTACAATTTCTCCTATATTTTTATTTC[C/T]ATTA
    7064 CTTGTTTCGAAAGCAATCATCTGAATTTTCTCTAT
    CTTCTTGTATAATGATAAGAACCTTGGGAGATCT
    ACACCACAAAAACTAGTCATTGTAGTTTGGAGAG
    CCAAGGACCTTATACATCCTAAACTTCAAATGTG
    AGACTCAAGTCTCATACCTTGCAATTGGATCCTA
    ACATTCCATCTTGCTTTGCAGCCAC
    AAATGTAGAATGATAAATCTTCAGTCTGATATCA
    CTAAAGAGAGTCAAGTCTTAACAATTGAACAGA
    AACATGCATTTGGTTTTAGAAGAATTGGATTTAG
    CACC TGAGAAAGAC GC CCATTATC CAAAGCTTGA
    CGAAATC TAGATTGCAATGCC TCAGCAACAGC TT
    Gm08:829 8299433 [A/T] 106 289 0.929 0.787 TTACTTCTTTCTCGGGCACAGCAAAGCATAC [A/T]
    9433 GAATGCTCACTACTAGCCTACATAAATACTGTTA
    ATGATTAATGCCATTTCTTATATATCARCGTGGA
    CAACTAGAAAAATTGAAAAAAGTTATAAGTGCA
    CC TGAGATATCATGATAACATTAGCTC CAACATC
    TTTTACTGCACCAAAAATAGCACTGGCAGTACCT
    GGAACACCAGCCATTCCAGTTCTGCAAAAAA
    TTAATGCCATTTCTTATATATCARCGTGGACAACT
    AGAAAAATTGAAAAAAGTTATAAGTGCACCTGA
    GATATCATGATAACATTAGCTCCAACATCTTTTA
    CTGCACCAAAAATAGCACTGGCAGTACCTGGAA
    CACCAGCCATTCCAGTTCTGCAAAAAAGCATCAA
    Gm08:829 8299672 [A/T] 107 290 0.919 0.702 AGAAAAATTTATTGGAATCTACAACTTGGAC +A/T
    9672 +ATTAATATTGGTTAAAGAAAACCTTAAATTAAA
    TAGAAATC CTC GTGCAGCAAAAAATGC CAAC TAT
    TCATCATGTAACACAACTGCAATTCATGACTCAC
    CCCTCGACGTTTACAAGTGCCAAGTTGTCTATGG
    TTGCAAATCCTTTGACAAAATTTTGCAGGTTCTG
    GC TATC TTCATGATCATTAACAGAAGGATGG
    CTTGTGGATAAGGTCATACATCATATCTGTCACC
    TTTGACATTGCAGAAACAACCACCAATTTCCTCT
    CC GAATCATCC TTAAGAATTATGTC YGCAACATT
    TTTTATTCTC TGAGAGGTTCC CACACAGGTTC CAC
    CAAATTTGTGAACAGACCAAGTTTCTCCTTTGGG
    Gm08:830 8301839 +GIN 108 291 0.937 0.721 TAGTTGTTTTTCCTCCAAGGACACATTCG[A/G] TG
    1839 AAACATCTGCTAGCAAATATAGAAAGGACAAAA
    AAACATAAGTTACTGTATTTGTCTATTAGAGTTCT
    AAGGTTGACTTGATGGTAAAAGGAGAAGGGAGA
    GAGGGAAAGGTCGTGGGTGGGTTCAATTTTCTCC
    GC TAACAAAAAAC TAACAATTAACAAC TAATATT
    TGCTGATAATAAAAAAAACTRTATTCGTC
    GAAGGGAGAGAGGGAAAGGTCGTGGGTGGGTTC
    AATTTTCTCCGCTAACAAAAAACTAACAATTAAC
    AACTAATATTTGCTGATAATAAAAAAAACTRTAT
    TCGTCTATTTCAAAACATAACCATAAGAGTAAGT
    CGTAACCTGTAAATGAAGCACGTACAGATGTACT
    Gm08:830 8302134 [C/A] 109 292 0.924 0.758 CGGTGCC TC TCTTC CC CGTGGTAAAGTAAGA [A/C]
    2134 CC TTCC TGAGACAGAAACCATTGTATC GTC GTGA
    ATCAGTATATAGCAAAACACAAAAATCCAATTA
    ATCTCATGGGGAGAATATCATTTAAACTGCCAAA
    ATTCCGAAAACACTCTAATCTCTGCAAAGGATAA
    ATATACAAAAAGGAAAAAAAAAAGTACAGAATA
    TACTGCTTGTAGAACAACCAATCATCTAAGAG
    TTGAGTTGAAATAATGAAATGAAATGGATCATAA
    TCCATCATCATCTTCCATTATGTTTCATTTCAACT
    TTTACAAATCAAACAATCCAACACCTTTTCCTTCC
    AC TCCATCC TTC TTCATTC CATACTC TACAACCAA
    TCAAAACATATTCGAAGGTTTCCATGTATGTAGA
    Gm08:830 8303450 110 293 0.843 0.582 ATTATAAATAGGTTGAACAAAATTTTA[C/T]TGRG
    3450 TAGGTTGAAMAGAATTATTTGGTAYTATTATTCG
    TACGCC CC TAAC CATGTGTTTGGATGAAGAATTT
    AAAAATTTCTAAGAAATTTAAATTCATAACATTT
    TAATTGCCTTGATTTTAATTCCTTTCCTTTTGTAA
    ATATTTTGTTTGGATGAGGTAATTCAAATTCTTGT
    ATTTTAATTTTCTTS TTTGGACAA
    AATGATAACAAATTGTACATATTATAGACTAAAA
    TGACAATAATTTTAATCTAAACAATTTATTTATAT
    TTTTTTAATTTTATGATGTGTTAAATTGTGACAGT
    GC CC TACAATTTTAAAGAAC GTACAAAATAATTA
    TTTATTCAAAATTTTAAACATAACATTACCTTTCC
    Gm08:830 8305237 [A/G] 111 294 0.817 0.722 CTACAAC GTCC CC CCGATAGTGTCATC [A/G] GTAG
    5237 GAC TC TTGC TTCAGAACAAAAC GC GAGTC CATAT
    AAGGCAACTGCAATTTTTTTAATTAGTCTTCCGTT
    TGTTTCGGGGGCTAATGGGGAATTATAGCAAGTG
    TGAKAATTTTCTATGCTTTTAAACTAAAATCTAC
    ATATTTATAAAAATATAAAAGTAAAAAAAAAAT
    GC CAC GGATAGTTCAGTCAAAGATAA
    AATTTTAAAGAACGTACAAAATAATTATTTATTC
    AAAATTTTAAACATAACATTACCTTTCCCTACAA
    CGTCC CC CCGATAGTGTCATCRGTAGGAC TC TTG
    CTTCAGAACAAAACGCGAGTCCATATAAGGCAA
    CTGCAATTTTTTTAATTAGTCTTCCGTTTGTTTCG
    Gm08:830 8305348 [G/T] 112 295 0.919 0.737 GGGGC TAATGGGGAATTATAGCAAGTGTGA [G/T]
    5348 AATTTTCTATGCTTTTAAACTAAAATCTACATATT
    TATAAAAATATAAAAGTAAAAAAAAAATGCCAC
    GGATAGTTCAGTCAAAGATAATTCGAAATCATAG
    TAAATATTAAATGATTGGATTTTACAACATS TATT
    TGAAAGAGTCATCATAAAACTTAATACCACAYTT
    TAACCMAAAACTTTAAAAGTCAACTTTAT
    CCAATCCTATTATGTTACCCAAGATGYCGTWAGT
    TCTCTAGGTGGTTTTTTCRAAACAAAAAAAAWTT
    ATTTGTAATAAAATAAATAATATTACTTCATTCTC
    ATGTCTTTTTATATTTAAGGTTATTATTAAGAAAT
    ATTTGATGAAAATAAACATTGTTCACCCTCGTAG
    Gm08:830 8305905 113 296 1 0.491 CC TCC GTTATGGC GAGAGTGCC TCTCAT [C/T] TGC
    5905 GTTC CRAACAGC CC TAGC TTRCACCATAATGGGT
    TGTGTCACCCTCGTAGCCTTCCYTGCATTCTCATT
    ATCATAAACGAYGCCGCTTTGGGAGACGCCTTCC
    ATGTC TATRCCAC CC TTCAGAGCATAGGC CC CAC
    CATCTTGAGCTTGTGGGYTGTCGGACTAGGGYCG
    CTCTCTAAAGYCACCACCGCTGTAGC
    GAGAGTGCC TCTCATYTGCGTTC CRAACAGCC CT
    AGC TTRCACCATAATGGGTTGTGTCAC CC TCGTA
    GC CTTCC YTGCATTCTCATTATCATAAAC GAYGC
    CGCTTTGGGAGACGCCTTCCATGTCTATRCCACC
    CTTCAGAGCATAGGC CC CACCATCTTGAGCTTGT
    Gm08:830 8306090 114 297 1 0.494 GGGYTGTC GGACTAGGGYC GC TC TCTAAAG[C/T]
    6090 CACCAC CGCTGTAGC GGTGGC GCTC GC CGC GTTT
    GTGGTGGTTCTTTCCTRGCCTCAGAGCACAAATT
    TGATAGCTAAACGCATATCATTGGGTCAGATAGT
    AC CACCATGTTGAAATTRAGAGGAAAGAAGTTTT
    AAAAAC CC TAATTTGAGGAAGAAGAAGCAAGTG
    AAGAAGAAAATATTTGACAACTTTTTAAAAT
    GTTGTGTCAC CC TCGTAGCC TTC C YTGCATTCTCA
    TTATCATAAAC GAYGCC GC TTTGGGAGAC GC CTT
    CCATGTCTATRC CACC CTTCAGAGCATAGGC CC C
    AC CATC TTGAGC TTGTGGGYTGTC GGAC TAGGGY
    CGCTC TCTAAAGYCAC CACC GC TGTAGC GGTGGC
    Gm08:830 8306141 [G/A] 115 298 0.848 0.737 GC TC GC CGC GTTTGTGGTGGTTC TTTC CT [A/G] GC
    6141 CTCAGAGCACAAATTTGATAGCTAAACGCATATC
    ATTGGGTCAGATAGTACCACCATGTTGAAATTRA
    GAGGAAAGAAGTTTTAAAAACCCTAATTTGAGG
    AAGAAGAAGCAAGTGAAGAAGAAAATATTTGAC
    AACTTTTTAAAATTTGCATCAAAGTCCAGCTTAC
    ATGTCATAATCTAGGACAATTTGWCACGTT
    CCATGTCTATRCCACCCTTCAGAGCATAGGCCCC
    ACCATCTTGAGCTTGTGGGYTGTCGGACTAGGGY
    CGCTCTCTAAAGYCACCACCGCTGTAGCGGTGGC
    GCTCGCCGCGTTTGTGGTGGTTCTTTCCTRGCCTC
    AGAGCACAAATTTGATAGCTAAACGCATATCATT
    Gm08:830 8306210 [A/G] 116 299 0.929 0.772 GGGTCAGATAGTACCACCATGTTGAAATT[A/G]A
    6210 GAGGAAAGAAGTTTTAAAAACCCTAATTTGAGG
    AAGAAGAAGCAAGTGAAGAAGAAAATATTTGAC
    AACTTTTTAAAATTTGCATCAAAGTCCAGCTTAC
    ATGTCATAATCTAGGACAATTTGWCACGTTAGAT
    AATCTATGTGACAYTAAAATTATTAAAAATATAT
    CTCATTAATGGYGTTAYTTTTAAATTTAACG
    TGCATCAAAGTCCAGCTTACATGTCATAATCTAG
    GACAATTTGWCACGTTAGATAATCTATGTGACAY
    TAAAATTATTAAAAATATATCTCATTAATGGYGT
    TAYTTTTAAATTTAACGGCAAAKACTATTTTRTA
    AAATTTATGCAAAAATAGAGACTATTTTTTACAT
    Gm08:830 8306492 [A/G] 117 300 0.853 0.614 TTAAAAAAAGATAAAGACTAATTTGCAAAA[A/G]
    6492 GAATCAAAAGTTAGAAATCAAAATACCTATTTAY
    TTAAWAAAAAAAACATCATGCGTTAGTTATAAC
    CTTAACTTCTAATTTTTTGCTAACGCCCAAAAAA
    ACTAAGAATTCGAATCAGAAGTAGGYAGAATAG
    KCAATTTGGTTCTTAAAAGTGTATGGAAGGAAAA
    AWTTTCCTTTGACTTTTTAAATTGGAACACGT
    AAAATTTATGCAAAAATAGAGACTATTTTTTACA
    TTTAAAAAAAGATAAAGACTAATTTGCAAAARG
    AATCAAAAGTTAGAAATCAAAATACCTATTTAYT
    TAAWAAAAAAAACATCATGCGTTAGTTATAACC
    TTAACTTCTAATTTTTTGCTAACGCCCAAAAAAA
    Gm08:830 8306627 [G/T] 118 301 0.811 0.689 CTAAGAATTCGAATCAGAAGTAGGYAGAATAG+G
    6627 /T+CAATTTGGTTCTTAAAAGTGTATGGAAGGAAA
    AAWTTTCCTTTGACTTTTTAAATTGGAACACGTC
    TTGATTTTTTTCCCTTGTTGCCCAAAAGCAGTCTT
    ATTATTCATCCGTTGGGAATTTTTGTTTTAATTTC
    GCTGATMAAAAAATTGAGAATTTTATGTCTGCTT
    TGTGAATTACCATTTTWTCGGAACCTGCAT
    TAGAAGKAATAATTTTGTTTTGGCTTGTTGAATT
    GGAAAATGTTACAGTCCCGGTCATTCTTTTTATTT
    TTATATGTTTATTTATTTTTGTCCAAATAGCAGGG
    TCATATTCAAAACTTGGGTTTTACTTTCAAGCTTT
    GGAACAATGTTAGTGTAATTTGTGACTTTTGATA
    Gm08:830 8307172 119 302 0.854 0.63 AAGCCAAAGAAGTAACTTTCGTTCTTA[C/T]TTTC
    7172 ATGTGACTTGTAACAAGTTACAAGTCAGTAATAT
    AACCTATAACTTWYTCTTCATCRTCTGCTTCTTCT
    TTTGATCATAATATCTGTTAAGTGATCTTTCATAG
    AGAGAGAGAGAGAGAGATGGAGAGGTGTGACA
    AGGTGATGAACCAACGCAACATGCATGATTGTCC
    TAAAACAGGTCCTGGCTATCCTTCAC
    TCTGAAAAGGCCAATTCAGCTTCATTGGAGGAAT
    AGATAGGCATTAGGCAGAGAGATCAAGATAGGT
    TTCTCAAGTTGTTGTTACAAACATTTTATATGACA
    TGATACTGGGAACAAGTGACATGTAGAAATATCT
    ATCTCTTTCTAGTGCTATGCATGAAGACTTGGTG
    Gm08:830 8307665 [G/T] 120 303 0.924 0.772 CAGCTTAAACAATTTCTGTCAAAACGTGTA[G/T]T
    7665 TTGGTGATTTTATATATATATATTGGTGATGAATA
    TTCAATTCAATGCAGGAACAGGAAGGGATAAGC
    CTGACTTTCTGGCCACAGTGGATGTGGATCCAAG
    CTCTCCAACGTATTCAAAAGTTATCCATAGGTTA
    CCTGTACCTTATTTAGGTGATGAACTGCACCATTT
    TGGGTGGAATTCATGCAGCTCTTGCTAT
    GTGATGAACTGCACCATTTTGGGTGGAATTCATG
    CAGCTCTTGCTATGGAGATCCATCAGCAGTTCGG
    CGATATCTGATTCTACCTTCACTGGTGTAAGATA
    CTAAACAGC CAC TTTGGATTTTACTTGCAC GCAT
    ATGCGCATGCAYACACACACATAACAAACACTG
    Gm08:830 8308019 [A/G] 121 304 1 0.837 ACAAGGTTCAAGAACTTCACTGGTGTAAGAC +A/G
    8019
    GATTTACCATATTTCAGATCAGGCCGCATTTATG
    TGGTTGACACAAGATCAAATCCAAGGTCTCCATC
    TTTGCACAAAGTTGTTGAGCCAGAAGACATCATA
    AGTAAGACTGGATTAGCTTATGCACACACATCTC
    ATTGTCTTGCTTCTGGTGACGTCATGATCT
    CTGGTACCAACCACAGCATAAGACTATGATTAGC
    TCATCATGGGGTGCTCCTGCTGCTTTCACCAAAG
    GTTTTAACTTACAGCATGTCTCTGATGGTCTTTAT
    GGGAGGCATCTACATGTATACAGCTGGCCTGGGG
    GTGAACTGAGACAAACATTGGACCTTGGTGAGTC
    Gm08:830 8308891 122 305 0.936 0.801 AGGGGTTC TACC CTTGGAGGTACATTGC T [C/T] AA
    8891 TAAATAATTCTGGAGTTATTTCCWCCAATTATAA
    GCACTTTATGTTAATGTACTTGTGATTTAATCATA
    AATATGTTTGTCCTTTGCTACATTTTTTCTCTCTA
    GC CTGTACTTGTGAAGTAATATGTTAAAGGTGGC
    ATAATTTGTAAGCAACTTGTCCTAAATGCAGGTA
    AGGTTTCTGCATGATCCTTCTAAAGA
    TGATTAGCTCATCATGGGGTGCTCCTGCTGCTTTC
    AC CAAAGGTTTTAACTTACAGCATGTC TCTGATG
    GTCTTTATGGGAGGCATCTACATGTATACAGCTG
    GC CTGGGGGTGAAC TGAGACAAACATTGGAC CTT
    GGTGAGTCAGGGGTTCTAC CC TTGGAGGTACATT
    Gm08:830 8308917 [A/T] 123 306 0.87 0.865 GC TYAATAAATAATTC TGGAGTTATTTCC [A/T] CC
    8917 AATTATAAGCACTTTATGTTAATGTACTTGTGATT
    TAATCATAAATATGTTTGTCCTTTGCTACATTTTT
    TCTCTCTAGCCTGTACTTGTGAAGTAATATGTTAA
    AGGTGGCATAATTTGTAAGCAACTTGTCCTAAAT
    GCAGGTAAGGTTTCTGCATGATCCTTCTAAAGAT
    ACAGGTTTCGTKGGGTGTGCATTGT
    GTCAAGTAACATGGTAC GGTTTTTCAAGAC C GAG
    GATGAATCATGGAGTCATGAGGTACACAAAAAG
    GATATAGTAAAAAATCAATGCCTAAATTTTAGGA
    GAATCATGACATCTCATTAATCAGAAGGTTTACA
    TTCAGCTATTCTATTTTTATTTCATTCCTATAATTT
    Gm08:830 8309316 124 307 0.924 0.912 TGGGATTCC TGGTTC TTGGAATTTCC TTT [A/T] TA
    9316 ATTTTCTTCACCTTTTCTATATATTGTATCTGTGCT
    CATATGAAATAATAGAGATGATATAATTTTCATA
    CTCTACTCTACTCATAGATATCCATACTCATTTTR
    TATTGTCATCTGGTATGCGTTTGTGCAGCTTCAAC
    CAAGGTATAATGATCAATAATAC TTACACAC TAG
    AC TGAC TTTGCAGGTTGCAATATC
    TGACATCTCATTAATCAGAAGGTTTACATTCAGC
    TATTCTATTTTTATTTCATTCCTATAATTTTGGGA
    TTCC TGGTTCTTGGAATTTC CTTTWTAATTTTC TT
    CACCTTTTCTATATATTGTATCTGTGCTCATATGA
    AATAATAGAGATGATATAATTTTCATAC TC TACT
    Gm08:830 8309423 [G/A] 125 308 0.854 0.824 CTAC TCATAGATATC CATAC TCATTTT [A/G] TATT
    9423 GTCATCTGGTATGCGTTTGTGCAGCTTCAACCAA
    GGTATAATGATCAATAATACTTACACACTAGACT
    GACTTTGCAGGTTGCAATATCAGTGAAACCATTG
    AAAGTGCAAAACTGGATTCTTCCAGAAATGCCTG
    GGCTTATAACTGATTTTCTGATATCTCTTGATGAT
    CGGTTTCTGTACTTTGTGAATTGGC
    TAGACAATATAACATTGAGGAC C CTAAAAATC CT
    GTACTGACTGGCCAAGTATGGGTTGGGGGACTAC
    TTCAGAAAGGAAGCCCTATAGTAGCAATAACCG
    AAGATGGTAATACTTGGCAATCTGATGTTCCAGA
    CATCCAGGTTTGTGCAGTTTAACTTTTGAAATTA
    Gm08:830 GTGATTCTAGTGTCATGCTTGTTGATTTCTC [A/C]
    8309837 [A/C] 126 309 0.924 0.824
    9837 CATGTTTGGAGTTGATTGGTTCTTAGATGTACTA
    GATATAATAGACTTGTGCATTACATTGGTGCCTT
    CAAACTTTTTGTCACTTTTGTATTTTATCTTGTGTT
    ATGCTTAAACGTGGTAAATAATTGCACTTTAAAT
    TTTGAC CC TTTAGTGGTTGAAGGTGAAGAGATCA
    AAATTTTTAATTTCAGGGAAATAAGTTG
    AAAATGGTGGTC TGAAAATTAAC CCTAATTTC TT
    TGTTGAC TTTGGAGC TGAGCC TGGGGGTC CC TGC
    CTTGCCCATGAGATGAGATATCCTGGTGGTGACT
    GCACTTCAGATATATGGATTTAATAGC TATGC TA
    CTTGAGGCCAGGCTACAAGCAATATCCATGTGAA
    Gm08:831 TAAAATCCTTAGTCCTAGAATGAATCGAGG[A/T]
    8310383 [A/T] 127 310 0.918 0.677
    0383 GGGCTAATGTTATAAATAAATAATAGTTGCATAT
    GTATGATGGTTGCATTGTAATAAAGTTATATTGT
    CATGTAGTTTTCMGTACTTTCTCATTTACATCATC
    CTAAACAGTGTTCTCTRTGAAATAAATCTTGCTC
    AC CTACAAAATTTGGGTC TTC TGATTGAGTAAAT
    CTCTATTGGAGTAACATTCTAGATTAATG
    TGAGATATCCTGGTGGTGACTGCACTTCAGATAT
    ATGGATTTAATAGCTATGCTACTTGAGGCCAGGC
    TACAAGCAATATCCATGTGAATAAAATCCTTAGT
    CC TAGAATGAATC GAGGWGGGC TAATGTTATAA
    ATAAATAATAGTTGCATATGTATGATGGTTGCAT
    Gm08:831 8310464 [A/C] 128 311 0.924 0.787 TGTAATAAAGTTATATTGTCATGTAGTTTTC [A/C]
    0464 GTACTTTCTCATTTACATCATCCTAAACAGTGTTC
    TCTRTGAAATAAATCTTGCTCACCTACAAAATTT
    GGGTCTTCTGATTGAGTAAATCTCTATTGGAGTA
    ACATTCTAGATTAATGGCCTTACTTGGGATTCTAT
    GATTTTCATTCACATCATGAATGTGCTGCACCTTC
    TACGTTGCTTGTTCCCATTTGAATGYA
    TTTAATAGCTATGCTACTTGAGGCCAGGCTACAA
    GCAATATCCATGTGAATAAAATCC TTAGTCC TAG
    AATGAATCGAGGWGGGCTAATGTTATAAATAAA
    TAATAGTTGCATATGTATGATGGTTGCATTGTAA
    TAAAGTTATATTGTCATGTAGTTTTCMGTACTTTC
    Gm08:831 TCATTTACATCATC CTAAACAGTGTTC TCT [A/G] T
    8310503 [A/G] 129 312 0.933 0.734
    0503 GAAATAAATCTTGCTCACCTACAAAATTTGGGTC
    TTCTGATTGAGTAAATCTCTATTGGAGTAACATT
    CTAGATTAATGGCCTTACTTGGGATTCTATGATTT
    TCATTCACATCATGAATGTGC TGCAC CTTC TAC GT
    TGCTTGTTCCCATTTGAATGYATTTGAAATCACA
    AC CCAAC CAAATCATTTCAATATGATG
    CMGTACTTTCTCATTTACATCATCCTAAACAGTG
    TTCTCTRTGAAATAAATCTTGCTCACCTACAAAA
    TTTGGGTCTTCTGATTGAGTAAATCTCTATTGGAG
    TAACATTCTAGATTAATGGCCTTACTTGGGATTCT
    ATGATTTTCATTCACATCATGAATGTGC TGCAC CT
    Gm08:831 TCTACGTTGCTTGTTCCCATTTGAATG[C/T]ATTTG
    8310663 130 313 1 0.847
    0663 AAATCACAACCCAACCAAATCATTTCAATATGAT
    GTACTTCTTAACAAATCAATGCACAAATAATTTT
    AATCATAAATTCAGAACTTATGCAGTGAATATTC
    TCGTTGTTAAGTTATAAGGGGC GGGGGGAATC TT
    ATATATGTGATTTTTGGTATATGAACGTTTGGTTT
    GTGAATTGTGATTGTCAGATGGTA
    ACAACAGAGGATGCTCCAGGATATGCAAATGCA
    GAAAATGAAGTCTTCAGTTCGTTCAATGGGAAGA
    ATAAGGAAATCATATACCTATTTTTCATCTTTTAT
    ATTTATGCAGTCGTCTATGATGAATTGATGAGTG
    TTTTCCTGGCCATGTGTGTTGTTTTGGCTTCTGCT
    Gm08:831 TTGTAAACACAAGATAATAATACAGGCAC [A/C] A
    8311631 [A/C] 131 314 0.843 0.772
    1631 TAATAAACTGTATAATGACATGAAGATCAATATC
    TTTCTTTGAAGCTAAGAAAAATTGTTATAGCATG
    TAGCTACTTTTGTTGTCCCACAAATGTGTGGCAT
    GGAGCAATTTTTTAATATATTCAAAATATTTATTT
    TGTGGACTCGACAGTCTACATCTATTTTATGAAG
    TGTAGTGAATCCAACATCAAACCCCTTT
    AC TTTTGTTGTC CCACAAATGTGTGGCATGGAGC
    AATTTTTTAATATATTCAAAATATTTATTTTGTGG
    AC TC GACAGTC TACATC TATTTTATGAAGTGTAG
    TGAATC CAACATCAAACC CC TTTGTCC CACTTTA
    CAAAAACCCTCTGATCATTTGAACCTCCTAAATG
    Gm08:831 AATACAAAC TGTGTCCATAAAAAAAAATT [A/G] T
    8311906 [A/G] 132 315 0.824 0.62
    1906 TGTGTCCTACGTGCTT
    CACTAC CC TATTTTGTTTTTATCATGTTAAATATA
    TGAAAATAAATTATTGCCAAGTCCAAATTGTTTG
    CTACTATTGAAGCCTGCATTTGTCTCGATGTAAA
    ATAGTAGTACTTATCCAAACACAGTATCAGGTTG
    AAGCAAACTAGTTCATATTATTGATGAGA
    CCACCACAACTGTATGTTGAGGTCCATTGTCTGA
    TAGAAGACTGAGAGTTTAGGTGGGGCAACTTCG
    AGGAATATGTACCAAATATTTTAGATGTATGATT
    ATATCAACACACACACCTTTGCCTCTGTTCTCTCC
    TTTTTC TTTTGCCATGATAATAC CC TTCC TATAAT
    Gm08:831 8312536 133 316 0.924 0.824 CC TATTCAC CCAAC GC CACATTTGTTTTC [A/T] TG
    2536 TATACTTAAATGTGTGTTAAGGGTAAGGGCTTCA
    AATAAGAAACTTAGCTAAAACAGTTAAGTAACT
    ATTTACTCCCATCATTTTGCACAAATTTTTATGAA
    CTTAGATTTTACCAAAGGAGGGACAAAACTAAG
    AAC CAAAAAAWTATCATCATATTCAGAWGC CAC
    AACCAACCACATGTTTTCTATACATATTTT
    ATTTTGCACAAATTTTTATGAACTTAGATTTTACC
    AAAGGAGGGACAAAACTAAGAACCAAAAAAWT
    ATCATCATATTCAGAWGCCACAACCAACCACAT
    GTTTTCTATACATATTTTTTCAATATGGGGTACTA
    ACAAAAAAGTCTTATTTGGTATGGAATTTTTAAT
    Gm08:831 TACTCTATATTTATAGTATACAATATACTTG[A/G]
    8312819+ G/A+ 134 317 0.87 0.836
    2819 GACATATTAGAATTTTATCTTCCAAGAGCAACCT
    AATCTCAGTTATC TCATACATATGCAATC GC TTAT
    TAGCAGAGTAAATCAGWAGTCTTCACAGAAAAG
    AGAAAAAAAATCATCTGTAGCACATGGAAAATA
    ACATAATTTCCTTGTTGTCCAAAAGGTTTGGTGA
    AGTGC GC TCTATCAGC TTATCAC TAATGCAA
    GC TTC TTAGTGGAGAGTGGAAGRWAGGGTACAT
    CCAATCCAAGACACAGAACAGAAGAATGGCCTC
    AAAATCATCCACCATYARACTTGTTTGTTTCTGCT
    AC TTCATGC TCTTCAGC TCTATGCATTTCAC CAGC
    TGCACCGTGCTCTCATTGAAAAGTCATGCAAGCA
    Gm08:831 CATGCAATGGTTCCATAGCTGAATGCAATC [A/G]
    8313273 [A/G] 135 318 0.854 09
    3273 AGAAGATGAGCTGTTGATGGAGTCTGAAATAAG
    CC GAAGGTTTC TGGAGCAGAAGAGATCATACATT
    TCCAATGGAGCTTTACAGAGAGACAAACCAGTTT
    GTAATGGTGGTGGCTCTGGTGAAGCTTATAGTAA
    AACTGGAGGGTGTCTTCCTCCCCCCTCAAATCCT
    CAAAGTAGAGGCTGCTCTAAGTATTATCGTT
    AGGAAAGATCTATGATTGTATTAATTATCCGTTT
    CTTGTCATCTCCAATCTTTCTTTGTTCCATTATGC
    TRGATGGAATTTGATTTTTTCTTCTTTTTTTTTTGG
    GTGAAATGTTTTKGTAATGCACATAATGCAAC CA
    TAAGGTATAAATC CTC TTACACATTCTAC CTC GA
    Gm08:831 TATACATATTTAAATAATAAAATATAT [A/G] AAA
    8313923 [A/G] 136 319 0.655 0.806
    3923 ATATAGAATTATATAAAATGAGATTTTATTTTAA
    ACATATAAGAGTTCACRTGGGTAAAGTATTCACA
    TTCAC TTTACTATTAYCAAATAAAATTTGTS AGA
    AACATTTTCGGCTCAACATCATGCAATTAAACCA
    GAAACTTATGTCTCAATGTCAYATTCTATYAGAT
    CATTTTATTCYGACATCCTCCAACATA
    TTCTTCTTTTTTTTTTGGGTGAAATGTTTTKGTAA
    TGCACATAATGCAACCATAAGGTATAAATCCTCT
    TACACATTCTACCTCGATATACATATTTAAATAA
    TAAAATATATRAAAATATAGAATTATATAAAATG
    AGATTTTATTTTAAACATATAAGAGTTCACRTGG
    Gm08:831 GTAAAGTATTCACATTCACTTTACTATTA[C/T] CA
    8314010 137 320 0.842 0.823
    4010 AATAAAATTTGTSAGAAACATTTTCGGCTCAACA
    TCATGCAATTAAACCAGAAACTTATGTCTCAATG
    TCAYATTCTATYAGATCATTTTATTCYGACATC CT
    CCAACATAAGATTTCTTAAAGCAATCCATCTAGT
    CATTTGCTTCCACAAACACAAGGTTCGAGATCAT
    CACAAGATCCAAACACAAACAGCAYAC
    TGGGTGAAATGTTTTKGTAATGCACATAATGCAA
    CCATAAGGTATAAATCCTCTTACACATTCTACCT
    CGATATACATATTTAAATAATAAAATATATRAAA
    ATATAGAATTATATAAAATGAGATTTTATTTTAA
    ACATATAAGAGTTCACRTGGGTAAAGTATTCACA
    Gm08:831 8314025 [C/G] 138 321 0.817 0.808 TTCACTTTACTATTAYCAAATAAAATTTGT[C/G]A
    4025 GAAACATTTTCGGCTCAACATCATGCAATTAAAC
    CAGAAACTTATGTCTCAATGTCAYATTCTATYAG
    ATCATTTTATTCYGACATCCTCCAACATAAGATTT
    CTTAAAGCAATCCATCTAGTCATTTGCTTCCACA
    AACACAAGGTTCGAGATCATCACAAGATCCAAA
    CACAAACAGCAYACARGGAATGAGTTATC
    TAYCAAATAAAATTTGTSAGAAACATTTTCGGCT
    CAACATCATGCAATTAAACCAGAAACTTATGTCT
    CAATGTCAYATTCTATYAGATCATTTTATTCYGA
    CATCC TCCAACATAAGATTTC TTAAAGCAATC CA
    TCTAGTCATTTGCTTCCACAAACACAAGGTTCGA
    Gm08:831 GATCATCACAAGATCCAAACACAAACAGCA[C/T]
    8314208 139 322 0.757 0.829
    4208 ACARGGAATGAGTTATCACATTCCCAACTAATAG
    AGAGAAACGAGACAATATGTAGATATACATATT
    ATATAAATGAAATATARCTYACTYAAACATAGCT
    CACATCATTCCATCACTTATCGTGTAACATCACA
    TCTCAACACTACACATCTCACACATTTTCACATTA
    TTTACGTRCTCAAGGATCGAAACACAATAT
    YAGATCATTTTATTCYGACATCCTCCAACATAAG
    ATTTCTTAAAGCAATCCATCTAGTCATTTGCTTCC
    ACAAACACAAGGTTCGAGATCATCACAAGATCC
    AAACACAAACAGCAYACARGGAATGAGTTATCA
    CATTCCCAACTAATAGAGAGAAACGAGACAATA
    Gm08:831 TGTAGATATACATATTATATAAATGAAATATA+A/
    8314292 [A/G] 140 323 1 0.715
    4292 G+ CTYACTYAAACATAGCTCACATCATTCCATCAC
    TTATCGTGTAACATCACATCTCAACACTACACAT
    CTCACACATTTTCACATTATTTACGTRCTCAAGGA
    TCGAAACACAATATCACTCAACCAATCAATATCG
    AYCAATRCACAAGCGTTATGCAACAAATATACTA
    AGACTTAATCCTATATGTAATGTGGTATCA
    ATCATTTTATTCYGACATCCTCCAACATAAGATTT
    CTTAAAGCAATCCATCTAGTCATTTGCTTCCACA
    AACACAAGGTTCGAGATCATCACAAGATCCAAA
    CACAAACAGCAYACARGGAATGAGTTATCACAT
    TCCCAACTAATAGAGAGAAACGAGACAATATGT
    Gm08:831 AGATATACATATTATATAAATGAAATATARCT+C/
    8314295 [C/T] 141 324 1 0.715
    4295 T+ACTYAAACATAGCTCACATCATTCCATCACTTA
    TCGTGTAACATCACATCTCAACACTACACATCTC
    ACACATTTTCACATTATTTACGTRCTCAAGGATC
    GAAACACAATATCAC TCAAC CAATCAATATC GAY
    CAATRCACAAGCGTTATGCAACAAATATACTAAG
    AC TTAATCC TATATGTAATGTGGTATCATGT
    ATCATTCCATCACTTATCGTGTAACATCACATCTC
    AACACTACACATCTCACACATTTTCACATTATTTA
    CGTRCTCAAGGATCGAAACACAATATCACTCAAC
    CAATCAATATCGAYCAATRCACAAGCGTTATGCA
    ACAAATATACTAAGACTTAATCCTATATGTAATG
    Gm08:831 TGGTATCATGTYAGTGAAAAATCTCATC [A/G] GG
    8314513 [A/G] 142 325 1 0.895
    4513 CGCCTAGAAGTATATGACAAGATAAACCACACA
    CTGGTAAGTCAGGTCACTCTCAYTAGATAAAATC
    ATAAGGAGATTAGTTAGGGTCACTCTRTTTTGCG
    AGAACACTTCAATCATACGAAATCAACATAGGTT
    TCAAGGAACATTCAAACC GAGTATATTTAC CC CT
    AAGGCCTACACTCTAAAGAGTCCGTTAGG
    GATAAACCACACACTGGTAAGTCAGGTCACTCTC
    AYTAGATAAAATCATAAGGAGATTAGTTAGGGT
    CACTC TRTTTTGC GAGAACAC TTCAATCATAC GA
    AATCAACATAGGTTTCAAGGAACATTCAAACCGA
    GTATATTTAC CC CTAAGGCC TACAC TCTAAAGAG
    Gm08:831 8314736 143 326 0.871 0.614 TCCGTTAGGACCTCTCCCTCTTGATTCAGGT[C/T]
    4736 CAACCTAGAAAATATTTTAGCACCYAGACTCTAT
    TTATGAACTGTACAAAACACYCGACTCCTCAATT
    GTTC TCAAAATAATTTTATCTCATCGC GC CTCAA
    AGTGATTAAACTCGTCGAGTTYCCACAATGGTTC
    TCATCACAATAC TC GTCGCACATTAAC TCATC GT
    TCTGAAAGGGTCTTATAGTCGTGTGGTGGT
    ATTAGTTAGGGTCACTCTRTTTTGCGAGAACACT
    TCAATCATACGAAATCAACATAGGTTTCAAGGAA
    CATTCAAACC GAGTATATTTAC C CCTAAGGCC TA
    CACTC TAAAGAGTC C GTTAGGACC TCTC CCTC TT
    GATTCAGGTYCAACCTAGAAAATATTTTAGCACC
    Gm08:831 YAGACTCTATTTATGAACTGTACAAAACAC [C/T] C
    8314791 144 327 0.884 0.688
    4791 GACTCCTCAATTGTTCTCAAAATAATTTTATCTCA
    TCGC GC CTCAAAGTGATTAAAC TCGTC GAGTTYC
    CACAATGGTTCTCATCACAATACTCGTCGCACAT
    TAACTCATCGTTCTGAAAGGGTCTTATAGTCGTG
    TGGTGGTAYGGTACATAACTCAAAACTCCATGCA
    CACAATATTTCAATACACATGTATTTTA
    ATTCAAAC C GAGTATATTTAC CC CTAAGGCC TAC
    AC TC TAAAGAGTC CGTTAGGAC CTC TCC CTC TTG
    ATTCAGGTYCAACCTAGAAAATATTTTAGCACCY
    AGACTCTATTTATGAACTGTACAAAACACYCGAC
    TCCTCAATTGTTCTCAAAATAATTTTATCTCATCG
    Gm08:831 CGCCTCAAAGTGATTAAACTCGTCGAGTT[C/T] CC
    8314860 145 328 0.912 0.715
    4860 ACAATGGTTCTCATCACAATACTCGTCGCACATT
    AACTCATCGTTCTGAAAGGGTCTTATAGTCGTGT
    GGTGGTAYGGTACATAACTCAAAACTCCATGCAC
    ACAATATTTCAATACACATGTATTTTAYAATTCA
    ACAYGCAC TCAATTTATCACATAC GC TCAATC TC
    GTTATAATCTCAATATAACAATTTATCA
    GTTTATTCTAACCTCAATTGCGATAAACTCATCTC
    TTACCTCTAAGYAGGCTCACATGTGTAGTCYGAC
    AACGATAGTGACGTTTCTAGCGATTTCCTAAGAT
    TCTTCAAAATTTTCCTAAGATTTTCTAACRTYAGA
    GAAAAAGAGAAAGGATTATAACCTATATTTCACT
    Gm08:831 GTCTCCGTCTCCRTGCGAGGGACATTTC [A/T] CTA
    8315543 [A/T] 146 329 0.825 0.756
    5543 AC TGAAGACATTGTTTCACAAATCC TAAYAGTGG
    GATTGTGAGAAAATGAGTTTYAAACCTGATTTTT
    AAATTTCACAATGATTCAATGGTTAATGARTCCG
    AGATCATAGTTTTAATGGRACAAGTTTGGATGTA
    TGCAGGAAGAGCATCTTGTGAGGGACATTGTTCT
    CACCACAGACATTATTTAAAAATTCCA
    ATTCTTCAAAATTTTCCTAAGATTTTCTAACRTYA
    GAGAAAAAGAGAAAGGATTATAACCTATATTTC
    AC TGTC TCC GTCTC CRTGCGAGGGACATTTCWCT
    AACTGAAGACATTGTTTCACAAATCCTAAYAGTG
    GGATTGTGAGAAAATGAGTTTYAAACCTGATTTT
    Gm08:831 TAAATTTCACAATGATTCAATGGTTAATGA[A/G]T
    8315644 [G/A] 147 330 0.929 0.786
    5644 CC GAGATCATAGTTTTAATGGRACAAGTTTGGAT
    GTATGCAGGAAGAGCATCTTGTGAGGGACATTGT
    TCTCACCACAGACATTATTTAAAAATTCCAAC GA
    TGGGAATGTGAGAAAATGAGTTTGGAACTTGGTG
    TTCAAATTTCATGATAATTCAATGATTAACGAGT
    ATAGGATCGTAGTTTTACCTGATAGGTTT
    TAGAAATATATTATGTGTAAAATCTGATCTAATA
    TRTCTATTTATAGATATS GTACTCTYAATTTATTA
    TTTACTCTAKCTTTTCTTTATTTTATTATTTTATW
    AAAAAAATTCTATTTTTACTCCCTATCAAATGAA
    TAAATAAAATATTCTTTTTTATTTTCCTTCAAAYT
    Gm08:831 8316113 148 331 1 0.85 ATTATTTTAATTAATAAAATTATTTTT[C/T]CTAAT
    6113 TTATTTAATTATAAAAATCTTATTATTTTTCAAAA
    AC TC TATTTATTTTTAAATAAAATGCTTTTWAATT
    TATTTAAAAAAAGACGAGATGTTACAAATGTTTG
    AAGCACACTTTGCAATGTTATAAATGTTGACCTC
    AGACATCAATTGCAATATACACACCATAAAACA
    ACATATGAAGTACACGTATGAGAT
    GC TC GAATATAATGAATC TAAACATATATGAAAA
    ATCAGTAACTGACCTTTTCGACACAGTCACATGA
    ACAAACTCGCAGCAACAACGCATACACTAGTAA
    CAGCAGTCARCGCACTCTCTTGAGAAAATTTGAT
    GTAAATGTATTTATAACTTTGTGACAAATATTTTT
    Gm08:831 TTTC CC TCATTC CACACAGGAATAAAAAGT [A/G] T
    8316689 [G/A] 149 332 0.896 0.63
    6689 CCAAGTGAGTGAAAGAGATGAGGAATAGATAGA
    CWTCTTTCTCCTTATTTTAAAATCCCAAGAAACT
    AATTACCTAGAACATTTGTAACAAAAACTAGTGT
    TAATTTATTTC CATTTATC CC TTTTC TC TCTGC TTT
    ATTTRTGGGAWGCTATAAAGAACGCTCTTCTCTC
    CTGAAAATTGCTMATTTAAGAAATTATT
    GTGAAAGAGATGAGGAATAGATAGACWTCTTTC
    TCC TTATTTTAAAATCC CAAGAAACTAATTAC CT
    AGAACATTTGTAACAAAAACTAGTGTTAATTTAT
    TTCCATTTATC CC TTTTC TCTC TGCTTTATTTRTGG
    GAWGCTATAAAGAACGCTCTTCTCTCCTGAAAAT
    Gm08:831 TGCTMATTTAAGAAATTATTTTCGAAGGA[A/C]C
    8316899 [C/A] 150 333 0.895 0.737
    6899 ACATTTTAATCTGTTAGAAATAGCCMAAAAAAA
    ATAGACAGAAAAATTACTCTAATTTTTTTTTTTTT
    TKGAATGATTGACTAGTCAAATTAACTCCAGTAA
    ACAAACAAGCAGCGGCGGGTTGAACATGAATAA
    CTTTCAATATGCC CC TTTGTTAAGCTAAAAGATT
    AC CC TAACATGGAAGTTTATGC TACATATA
    CATTTTGTCATTATACTTTGCACGAAGTGGGTCAT
    TGTAAGTCCACCTGTATTACAATTCAACAATAAC
    AAGAATGTCGAATAATTTTAGTATTTTACAGCAG
    TTAATATGTAAGTATAAAATGCTACTTGCAGTAG
    AAGAAAC CC TTTTTTCAGGGGAAGGGGAGGTC TG
    Gm08:831 GAC TC TGGAGGTTAGTTGCAC GTTAAGCA[A/G] A
    8317852 [A/G] 151 334 0.924 0.776
    7852 ATGAATC SC TATCATCAATGTGTTAACAAATCCA
    AAATTCTTGGTAAGGGAGAAATATCGGACAGAA
    AAAAAATTAAGATGTCAGAAAGCCAATGCAGAA
    TTTTCTCAGCAAATACATTGAATGCTGCCTTAAC
    ATACTAAAAC CC CATTATTC GAAAGATGATTATC
    AATATTTAATARCATGACTGCAAGCCTATCA
    ATTATACTTTGCACGAAGTGGGTCATTGTAAGTC
    CACCTGTATTACAATTCAACAATAACAAGAATGT
    CGAATAATTTTAGTATTTTACAGCAGTTAATATG
    TAAGTATAAAATGCTACTTGCAGTAGAAGAAACC
    CTTTTTTCAGGGGAAGGGGAGGTCTGGACTCTGG
    Gm08:831 [C/G] 152 335 0.924 0.923 AGGTTAGTTGCACGTTAAGCARAATGAATC [C/G]
    8317861
    7861 CTATCATCAATGTGTTAACAAATCCAAAATTCTT
    GGTAAGGGAGAAATATCGGACAGAAAAAAAATT
    AAGATGTCAGAAAGCCAATGCAGAATTTTCTCAG
    CAAATACATTGAATGCTGCCTTAACATACTAAAA
    CCCCATTATTCGAAAGATGATTATCAATATTTAA
    TARCATGACTGCAAGCCTATCAACCAACAAT
    GTTAGTTGCAC GTTAAGCARAATGAATC SC TATC
    ATCAATGTGTTAACAAATCCAAAATTCTTGGTAA
    GGGAGAAATATCGGACAGAAAAAAAATTAAGAT
    GTCAGAAAGCCAATGCAGAATTTTCTCAGCAAAT
    ACATTGAATGC TGCC TTAACATACTAAAAC CC CA
    Gm08:831 8318033 [A/G] 153 336 0.912 0.809 TTATTC GAAAGATGATTATCAATATTTAATA [A/G]
    8033 CATGACTGCAAGCCTATCAACCAACAATACATGA
    AAAAATTCTGGTGTGATAAAAAAAATTGTGTAGA
    CTCCTTTTAATGTCATAAAATCAGAAGTGTGGCA
    GAATCAGTCTAACATGTTACATCAACATTGAAAA
    CATAAACAGATTCAGGACTCTGTAGATAATAAAT
    GTAGCATTTCAGATATTCTCAGAACAGAGA
    AACCCAAAAGTACTATGAAAACAGATGAGCATA
    AC TCATGAGCATGCACTTTTGTCAAGATCTCAAA
    CCATATCAAGGGCTGCTAATAAACAACTCATTTA
    AATTGTGAGTTGTGACATGCAATATGATCCCTTC
    TTACTGTCCAGCTAAATTCACATAGAAGTCAAGG
    Gm08:831 GAGTCAGGGTAAAGTTGACAAACTAAGAACG+C/
    8319087 [C/T] 154 337 1 0.857
    9087 T+TGTAAACAATAAACTTCAAGCCAAGTACATAT
    TTCTACAAAATGAATGCCAAAAAAATAAAATAA
    GATTTGTGAGATGGCATAATTATGCTTACTCTAA
    ATGAAATATGTCTTTTAACTATATTCCTTCCAATC
    AACTCTCCCTCTTGAACCTCAATCTCACCCACAA
    TCAAATTCCTAAATAAGCAAAATGATAGGTAC
    TTCTCCCAGCCCAAGCCTAATTCCACCCTACCTTG
    TACACAC CC TTCTC GGGCTAATGTTCTC TGTC TTC
    TTACAACAAGCCCACATGCACTCCTCCCATGCTC
    TGCTACAGGGTTGACAGTTGGTTATATCTCTCTCC
    TAAAATTGATCAAGTGAACCTTTTGCCTATCCTT
    Gm08:831 ACATACACCTTATTTTGTGATCTTGGG[C/T]CTTG
    8319642 [C/T] 155 338 0.853 0.531
    9642 RGGCCTCCATCASAAAACCATTCTTCATAAAAAC
    TCTCATTTCACTCTTCTGATGACTAATAGCAGAA
    AATTTTTTAGATAACAAGAGAAAAAGAAATCTTA
    AATGAACATTTCACTATTGRCATGAGCATCTCAA
    TATCATCACATGAATC CGAGATCATTTTGGAC CA
    GTGCCATAGCAGATGAACTTCATAAG
    CCAGCCCAAGCCTAATTCCACCCTACCTTGTACA
    CACCCTTCTCGGGCTAATGTTCTCTGTCTTCTTAC
    AACAAGCCCACATGCACTCCTCCCATGCTCTGCT
    ACAGGGTTGACAGTTGGTTATATCTCTCTCCTAA
    AATTGATCAAGTGAACCTTTTGCCTATCCTTACAT
    Gm08:831 ACACCTTATTTTGTGATCTTGGGYCTTG[A/G]GGC
    8319647 [G/A] 156 339 0.853 0.587
    9647 CTCCATCASAAAACCATTCTTCATAAAAACTCTC
    ATTTCACTCTTCTGATGACTAATAGCAGAAAATT
    TTTTAGATAACAAGAGAAAAAGAAATCTTAAAT
    GAACATTTCACTATTGRCATGAGCATCTCAATAT
    CATCACATGAATCCGAGATCATTTTGGACCAGTG
    CCATAGCAGATGAACTTCATAAGTAAAT
    TTTTTCTCAGGATAAAACAACAAAAAACTAATAC
    CAAAGAATAGAATAAACAATCTACCACTATTCTT
    GAAACCGAAAGATATAGAACATAGGAGAAATTG
    AACTTACGGGTTATTCCAATCAGTAGTATCCTCA
    TTGACAAGATGGGTCCACTTGGTTCTTCCACTAC
    Gm08:832 GACCAAAGTGCTTAACTTGCATAACCTTTGG[C/T]
    8320068 [C/T] 157 340 1 0.837
    0068 AATATTGTCTTGTCCATTTTATCCTCCCCAGTTGG
    GGCAGAGAAATCACGAGCGAAAATACCATCAGA
    TCCAACGGTGGCAGCTCGGTCATCAGATTCATTC
    TGGAAGAAAGCACCTTTGTGATAGTATTTCTGCA
    TAAATCTCCATTTCTGCTTTGGTGGTGGAGCAGG
    TTTGGGATTCCTCCTTTCCCACTCCCTCCT
    TCATCAGCCCATTCAGGAACTTTACCGGGCCAAT
    AACGCTTAACTTTAGTTTGGCCAATTTTACCTCTG
    AGCTTATCCCTAATGGCTATTACAGTATCACTAA
    CACCCGCTGTCACCGACATTGTTCTTCCTCAATTG
    AACGCCAAACCCTATATTGCACAGATGCATAGTA
    Gm08:832 8321253 [C/A] 158 341 0.919 0.773 AATCGGTAAAATGTTTGTTTACACAGCA[A/C]AG
    1253 AAACAGAAGATTCCAGATTAAATAGCAAGAAAA
    TAAATAAATGAATCAAGAAACACAGAAAGATCA
    ATAGTGAATGATAAATTTTGATATGCGAAACATT
    GGAAGGGTTTGTGTTCSAAACACTAACACTTGAA
    TTGTTAGAGAGAATAGAAGAAAAGTTWGAAGGA
    CTTACAATTACAGCGACCGGAAGGAACCCTC
    CCCTCTCTGTCTCTGTCCCGTTCCAGGCAGCGCGT
    CGCCCCACCCCAGCTTGTTCTGTGAACTTTTATTT
    GATTTACTTTCTATAGTATTTATTTTTGTTTTTATG
    AGTATGTAAATGACATCTTTATACGAATATTATG
    TTTTCATTAAATAATAATAATAATAAATTTCTTAA
    Gm08:832 AATTAAATATATATACACTAATGCT[A/C]ATAAA
    8321649 [C/A] 159 342 1 1
    1649 AAAATTGAACGAATATCATATTTATTAAAACTAA
    TTTTTTTATACTAAACTAAAAATAATTTAAAATTT
    ATTATTATTATTATTATAAAGATATTTAAATTTTA
    TATTTTGGAATTGTATATATAAGATAAAATACAT
    TTAAGTTTCCTAAGTTACAACTTTCGCATCGGTTA
    CATTTTAMAGGWTATATATATA
    ATGTCTTTGTCCAAGGCTTGCTAACAAAAAAGGA
    GATTGCAAGATCAATAAAATACCTTACAATAATG
    AGAGACAAAGGGTTTTCAGTAGATGCTGCTACCA
    CAGAAATTACTATCAACTACTTATCTACTAATGA
    AGGAGACACCAGAATTCGAGAATTTTTTTTTCCA
    Gm08:832 AAA AGATAGCAAATGCCAAGAGTTTCACTT[A/G]
    8323937 [G/A] 160 343 1 0.918
    3937 GACATTTATTCAAATCCTGACTCTCAATTCATCCA
    TGTTCCACAATCCTATAGGACCCCATAGAGAGAA
    CTGGCATAGGCTTCAGAACTTACMATTTGTTAAA
    TATATAAAATCATTACCATTCAAGTGCWTCCACC
    TGACAATTTATGTGATTAGGAGAGTTGGTCCTTA
    ACAGGTATCACAACCTTTAAGAAATTATG
    TTGATCCTTGTTGCTTCTCTTCTTCATAATTAACT
    TATATTTGAGCCCAAGGTAAAGTGGGTTTGTGCA
    TTGTCCRCACTTCAAGCTCAAAAAGCTCTGTTTTA
    AGGGGGTCTTAGATATAAATCTTTCTTAGCTCCA
    CCAATCAGCTTAAGCTGTGAATAGAATTGTTC CT
    Gm08:832 TGACATTTTTAGTGGTAAGTATTTTCAC +A/C + TC T
    8324341 [C/A] 161 344 0.929 0.787
    4341 GC TTGCACATTTATTTTGATATAACC TCAAGTTAT
    TAAAATAGCTTAAAAAAATAGACCTATATACAAT
    TTAGAAATTGTGCTGTATCCTTGCATTTTTATGGA
    AC TGAGTAATTTTTTAC TTATGTATATTTGC CTTC
    AAGTAAGTTTAATAATGAAGCAAGTTGCATTAGG
    GATAAGCCAATCAATATTGCTAGT
    TGTTATTTTATATTTTGTTTCCTTTCTTGTGTATTT
    TACTTTTCTGTTTTAGGAGGATTCCTGATCCTTCT
    GCACTGTACTCCTTTTCTCTCCTAGTTCATTGTTT
    GTGATGGGAAWTTTTTTTCCATATTTATTACCTGT
    TAGGAGACGAAAATCTAAGATCTAATTTATGGAT
    Gm08:832 GC TTGC TGTC CTTTC TGCAAAC GTN[A/T] TTTTTTT
    8325127 162 345 0.829 0.706
    5127 TTTTTAC TTTTGACAGTTTTCC CC CCATTTAAAAT
    AACAGTTTGACTTCATGGTTCTTGGTTTGCAGATT
    GAAATCACTYTATGCACTCATTTTGTTATAACTTA
    TGTGCGAGGAAGACCGCAAATAGTTCAGCGATG
    GATCATAGAAGGTTAGTCAAACATTTTTTCTTTG
    CAATATCTGCTCAGCTTGTTT
    CTCTCCTAGTTCATTGTTTGTGATGGGAAWTTTTT
    TTCCATATTTATTACCTGTTAGGAGACGAAAATC
    TAAGATCTAATTTATGGATGCTTGCTGTCCTTTCT
    GCAAACGTNWTTTTTTTTTTTTACTTTTGACAGTT
    TTCC CC CCATTTAAAATAACAGTTTGAC TTCATG
    Gm08:832 8325214 163 346 0.929 0.837 GTTCTTGGTTTGCAGATTGAAATCACT[C/T]TATG
    5214 CACTCATTTTGTTATAACTTATGTGCGAGGAAGA
    CC GCAAATAGTTCAGC GATGGATCATAGAAGGTT
    AGTCAAACATTTTTTCTTTGCAATATCTGCTCAGC
    TTGTTTTTTGTAATTCAAATTTTTTAGCATCATAA
    GTTGTTCGTTTGAAATTTTGAATGAATATTTATCT
    GTTAAGTTATATTTCACTTTTCT
    AATATATTTATCTCAGAATAATGCTTTGACTTTTA
    CAATGTTCC CC TCACAAAATTGATC TCTTTAAAA
    AATAAAAAATAAAAACTTTGGAGTTTGTCCAGCT
    TGGCTCCAATCTTAACCAAAGCAGCATTAAAGCT
    TTGAAGTATAGAGCAAAAGTACACCATATTAGGC
    Gm08:832 TAATCAATGAAAAGGTACAAAGCTC CC GT [C/T]A
    832606 [C/T] 164 347 1 0.768
    6696 GATTTTGAACTAGRCAGATAACTAAGNGAGTGTT
    TAGTTTGGTTGTTTTTTGATTTTATTTTCACTGAA
    AATARAAAACGGTGATGAAAATGTGTTTGGTTTG
    ATTTCTGAAAACATTTTCRGTAAAAATGAAAACA
    GTAAACAACTAGAAAATGAAAACAAAAAATTTT
    CGTTTTCAGWATTTTCAGTTGAGAACAGA
    AAAGGTACAAAGC TC CC GTYAGATTTTGAAC TAG
    RCAGATAACTAAGNGAGTGTTTAGTTTGGTTGTT
    TTTTGATTTTATTTTCACTGAAAATARAAAACGGT
    GATGAAAATGTGTTTGGTTTGATTTCTGAAAACA
    TTTTCRGTAAAAATGAAAACAGTAAACAACTAGA
    Gm08:832 AAATGAAAACAAAAAATTTTC GTTTTCAG[A/T] AT
    8326877 165 348 0.884 0.808
    6877 TTTCAGTTGAGAACAGAAACCTCATTTTGGTTAA
    AATGAAATTGYGGTGACAATAAATGTAGTTTTAA
    RCAAATCTAAAAATACAAAAAGACAATAAGTCA
    ATATATCATAAATTTTCAGTATTTTTATTTCATRA
    AAACAGAAAACAAGAAATCAAACCAAACATRTT
    TTCAGAATTTAAATCTTTTGAAAATAAAA
    TCTCTTCAAAAGCCAAGTCCTTGGTTAGGACAGT
    GGTACTTAACATGGTTAATGCAAATGGTTTGTWG
    CAAATTCATAATAGACCTTTCAACCAGCTTTTGG
    CTCATTTTATTGCATTAGTCTTATTTGTTTTGGAG
    AATTTCTTTTATTTTTTTGGTAACTAGCAGATTTC
    Gm08:832 TTATC CTC CTC CTAGTTGTGC TTCTC TT [A/T] TC TC
    8328633 166 349 0.919 0.651 TTTAATGAATTTCCTCCTATGTAAAAAGCAATAG
    8633 AAAAAGAAAACCAGTTTTAAAAAAATAAAATAA
    AAGAACTAATTTCAGGTACCTTCTTCCATTTTGCA
    ATTAGATTGCGGTCAGCATATCCTTGATCTAAAC
    AGAATTCATACAGTTCTTTAGAAATTTCCTTCCTC
    CGATGGTATAGATCAAATATGTAGC
    TAAGTAAATCTAGAAAATATATAACTTTTGACAA
    AAAAATTATATCACTATTTAAATATATCTTTTTTC
    CTTTGTTTCTTATTTCCTAAATAAATTTTTTTATTA
    AATTTATTAACAAAAATTTCTCATAATTAACGAA
    TGAGGTTAAAAATAATAAAAAAATGAYAAATAT
    AATAAAAACAAATTAAATTTAAAGAC TT [A/G] AA
    Gm08:833
    8330929 [G/A] 167 350 1 0.789 ACATAATTTTTKTGTCWCATGAAAATATTTTTTTT
    0929 ATTCTAAACAAATTGTTTAAAGATAATRAAAATA
    TCATTTTTTTAAATCCTAWAAATATACCARATAA
    CTATAATTATTTAAATTAAATCACTCTAGCATAT
    ATTTTTAATAAATCAAATTAATATATACAAATAT
    TTTAATTTACTTTAAATTTAAAGATAA
    ACATAATTTTTKTGTCWCATGAAAATATTTTTTTT
    ATTCTAAACAAATTGTTTAAAGATAATRAAAATA
    TCATTTTTTTAAATCCTAWAAATATACCARATAA
    CTATAATTATTTAAATTAAATCACTCTAGCATAT
    ATTTTTAATAAATCAAATTAATATATACAAATAT
    Gm08:833 8331132 [C/T] 168 351 1 0.657 TTTAATTTACTTTAAATTTAAAGATAATA[C/T] GA
    1132 TAATATAAATATAGTAAAATTTTATAGAATTTTT
    AAACAATATTTTYCATTTATCTTTTTTTTTTCTTTT
    ATCTCTCTAGTTGCATGGAGCATGAGCCAACTTC
    CTAGTTTATTGTATATTTTCGTGATAATGTTGTGG
    CATTTGTTAGACATTTTAAAATATTAAATCTTATT
    AATTATTTTWAAATCATATTTATA
    GTTTAAAGATAATRAAAATATCATTTTTTTAAAT
    CC TAWAAATATACCARATAAC TATAATTATTTAA
    ATTAAATCACTCTAGCATATATTTTTAATAAATC
    AAATTAATATATACAAATATTTTAATTTACTTTAA
    ATTTAAAGATAATAYGATAATATAAATATAGTAA
    Gm08:833 AATTTTATAGAATTTTTAAACAATATTTT[C/T] CA
    8331181 [C/T] 10 352 0.87 0.612
    1181 TTTATCTTTTTTTTTTCTTTTATCTCTCTAGTTGCA
    TGGAGCATGAGCCAACTTCCTAGTTTATTGTATA
    TTTTCGTGATAATGTTGTGGCATTTGTTAGACATT
    TTAAAATATTAAATCTTATTAATTATTTTWAAAT
    CATATTTATATGAAAAATATGATTTTTTATTTAAT
    CTTTCTAGAAAAATCTTAATGTAT
    TCTCTAGTTGCATGGAGCATGAGCCAACTTCCTA
    GTTTATTGTATATTTTCGTGATAATGTTGTGGCAT
    TTGTTAGACATTTTAAAATATTAAATCTTATTAAT
    TATTTTWAAATCATATTTATATGAAAAATATGAT
    TTTTTATTTAATCTTTCTAGAAAAATCTTAATGTA
    Gm08:833 TCCACTTCCAACTTTTACATTTAAAAT[C/T]CCATT
    8331408 [C/T] 170 353 0.842 0.771
    1408 ATATATTTTTTTTCTAATTAACCTTCTCTAACAAT
    TGTTCAACACTTTCTTCCTAAACCTCTATTTCAGT
    TTC TCTC CC TCTTC GGTC TTCC CATTGAATTC CAG
    GATTTTACATACAAAAAATTTGWTAGTTTTGTTG
    TCTTGACAAGTTTTCGGAGGATTTGTTAAATTC TA
    AAGGACTTATGCACTACGTTG
    CGTGATGTCACTCATCTCATATTATCTATTTTGTG
    AC TAAC TCATGAATTTATGATAGATTGATGATCG
    GTGATTTTGGCCTACTACAATAACAATTTTAACTT
    TTAAGGAATAATC CC GAC CACTTTAAGGTATATT
    AATATATTAATTATTTTTTTCTCCAATCTTAATTT
    Gm08:833 AATTTGTTTGATGGTAATGAATCAGAT +A/C +AAC G
    8331827 [C/A] 171 354 0.838 0.772
    1827 ATTTTGGGACTGTTGTTGTTGTTCCATTTTCAGTT
    TTTTATTTTGTTTATGACTAGTTGAGTTTGYAATC
    GGTTCTTGCTCGGTGATTTTAGAGGTTTTGGACAT
    GATTTTAGAGTATGTTGTATTGTGTAAAACTTTGT
    TGCAATCTCGTGTGGTTAAATGGGTGTTAGGATG
    TGAAAATTTTATGTCTAAAATT
    AATACACTTGTGCATTCAAATATCCATAATAGTT
    AATAACAACAACTTATTCAATATACTATATTATC
    TAGGGTCACTAGATTAAACCCACTTCTAAAAAAA
    TCTTAAAACATCCAAATTTTATTAATACGTTATCT
    TGAACATACTTTCTTCTATAAATGTTAAAATTTAT
    Gm08:833 TTGAAAATTTGAAATCTTAGAAGGTCTC [A/G] TAC
    8332651 [A/G] 172 355 1 0.836
    2651 TTTAATTAATAAATATCTTTTATAATTTTTMATGA
    ATAGTACAATCAAGTGTGTTAAAAAATATTTTCT
    TGAAACTCCTCTAAATTTAATGCTACAAAAATTA
    CTTTTTCTTGCTTTCTCTTCAAACTTAGTGAGCAT
    TTTTGCACTCTTAAATTATGTTTGTCAAAATATTT
    GAATTGATTTTTAGTTTTTTTATT
    AATAACAACAACTTATTCAATATACTATATTATC
    TAGGGTCACTAGATTAAACCCACTTCTAAAAAAA
    TCTTAAAACATCCAAATTTTATTAATACGTTATCT
    TGAACATACTTTCTTCTATAAATGTTAAAATTTAT
    TTGAAAATTTGAAATC TTAGAAGGTCTC RTAC TT
    Gm08:833 8332685 [C/A] 173 356 0.857 0.772 TAATTAATAAATATC TTTTATAATTTTT [A/C] ATG
    2685 AATAGTACAATCAAGTGTGTTAAAAAATATTTTC
    TTGAAACTCCTCTAAATTTAATGCTACAAAAATT
    ACTTTTTCTTGCTTTCTCTTCAAACTTAGTGAGCA
    TTTTTGCACTCTTAAATTATGTTTGTCAAAATATT
    TGAATTGATTTTTAGTTTTTTTATTAACAGAAAAG
    TTTATTTAGTTGTTTGATAAAGAA
    ACTTTTTCTTGCTTTCTCTTCAAACTTAGTGAGCA
    TTTTTGCACTCTTAAATTATGTTTGTCAAAATATT
    TGAATTGATTTTTAGTTTTTTTATTAACAGAAAAG
    TTTATTTAGTTGTTTGATAAAGAAGTTTTTTAAAT
    AATTTTTAACATTTTTTTAAACACTACTTCAAGTA
    Gm08:833 ATATTTTTWAAAATATTATTTATTT[C/T] TTCATAT
    8332957 174 357 0.902 0.787
    2957 ATTCTYTTTTTATTTATTTTTAATATATTTATCAA
    ATTTATTATTTATCCTTTTTAAGCAAATCATTATT
    TTATTATTTTWAAGTTATTTTATATTTTTTAAC TA
    TTTCAAAAACTAATTTTATCACACACTTAATTTTA
    ATAAATTAATTTTTTAACTTCCAACTAATTTATTA
    GTTTTCAGCTAATTTTAT
    TGATTTTTCTGCATCTGAAACAATTTGAAATTTCA
    AAATTTCTCTTTTCTTTACGAGGTCATCAAAGCAC
    AAAGC TAACAAATTC CC TAGAAGAGGGTGCATA
    AAACTCCAACCTGTTTCCTCTGTTTTTTCCCTTGC
    AATTATTACTCTTTTTTATTGRTAGAAATTGAATT
    Gm08:834 RTTGAARTATAAATGTGAAATAAAGTC [C/T] CAC
    8343167 [C/T] 175 358 0.904 0.883
    3167 ATCCAATAAAAATAAAAAAATTTAACATCATATA
    AGTAAAAATAACTAAATCTTAAAGTTTTTAAATT
    GC TATTCTC TTTCATGTAAAGATAAAACACATAA
    ATCTAACTCTTAAAGTCTCTTGATTACTATTTTTC
    ATCTTTCATGATATAAGTGATGATTTAGCCTCTA
    GATTTCATGGTGATTATAGAAGTGTA
    CAAGATAGGACCTTTTTACTTTGTTGGTCTATTAA
    TATCCAAGTTGTTCATGCTTATTTTCACACCTAAC
    ATTAGCTTATTCAAGATTCTTAATAAAATATTAG
    GGAAAATATCATGAAACTTTTATCAAAATTGTTT
    ATTTGTCGTTGACGTTTTTGGAAACATCTCAATA
    Gm08:834 GTGACTTGTTACTCAATCAATCTTTACT[A/G]GCA
    8345187 [A/G] 176 359 0.933 0.799
    5187 CTCTCATACTTGGTTTTCGTTATTCCTGTTTTCAA
    ACCACATACTTTGACTAATGGACTATGAATGAGG
    CTGCGTATAAAAATACAATTGGCGTATTCGAGAT
    GCAAATTGTGTTATTGGCCTCTTGTCCTTTTCCAG
    ATCAGTATTGAGAAGTTCAGGCAAGGCTTGTATT
    GAATCTGACTCTGACAGATACATAA
    ATACGACTTTTWCTTGTTGCCACTCTTTACCAAC
    AGCATTCAAGACGTACGTTAGGATATTCAAATCC
    AATGCGTCACTGAGGAACTTTTGCACTCATTTTTT
    CACGCAAAAACAGAGAATCATCCAGCACAGAGT
    CTTGCAAAAATTGATGTGAAACAAGAATGCTCTG
    Gm08:834 AGCCTAAATTGGATCAATGTGCATGCTAAA[A/G]
    8345720[A/G]177 360 0.871 0.587
    5720 TTTAGACCCATATMKTATKGGGAAGTTTTTATCC
    CTTAGTCGCTTTTGTCTTTTTCCTTTCCTTTTTCTA
    AGCAACAAACCATATTGTTTTATAATTTGGGCGA
    GGTCTAAATTCGTTTTATCATTGTAACAAAAACT
    AAAGAAATTAAAGCAAACGATTTCATAGGCTATT
    TGGGAGCTATGTTTTATGAGGTTAATAA
    AAATTCGTTTTATCATTGTAACAAAAACTAAAGA
    AATTAAAGCAAACGATTTCATAGGCTATTTGGGA
    GCTATGTTTTATGAGGTTAATAACAAAATAGGAA
    TCTCTTGATTTTAAGAATGAACAATTTTTTTTTCA
    CTATGAAAGGAGTCCTGAACATTATAATTGGATT
    Gm08:834 8346030 [C/G] 178 361 0.87 0.721 GGGTGTTAAGGAGAGAAATAGAAAGGAGA[C/G]
    6030 ATTTCACTCGATTGGTTCARAAAGAAATAAGAAC
    GAAATTGACAAATTCTGTGGGTTCATTTGGGAAA
    TTCTTCTCCATTGTTCATGATTGGAAATGATTTTG
    TGTATCTTCTTTTTTTTTCTTAATTTCTTTTTAAAA
    AATCAAATAATTTTTTTWAAAATAATTTCTTTATT
    AAAATACTTTTACTTTAYGATAAATA
    ACAAAAACTAAAGAAATTAAAGCAAACGATTTC
    ATAGGCTATTTGGGAGCTATGTTTTATGAGGTTA
    ATAACAAAATAGGAATCTCTTGATTTTAAGAATG
    AACAATTTTTTTTTCACTATGAAAGGAGTCCTGA
    ACATTATAATTGGATTGGGTGTTAAGGAGAGAAA
    Gm08:834 TAGAAAGGAGASATTTCACTCGATTGGTTCA[A/G]
    8346050 [A/G] 179 362 0.929 0.718
    6050 AAAGAAATAAGAACGAAATTGACAAATTCTGTG
    GGTTCATTTGGGAAATTCTTCTCCATTGTTCATGA
    TTGGAAATGATTTTGTGTATCTTCTTTTTTTTTCTT
    AATTTCTTTTTAAAAAATCAAATAATTTTTTTWA
    AAATAATTTCTTTATTAAAATACTTTTACTTTAYG
    ATAAATACTATGAATTAAAAAGATAAA
    CTTAATTTCTTTTTAAAAAATCAAATAATTTTTTT
    WAAAATAATTTCTTTATTAAAATACTTTTACTTT
    AYGATAAATACTATGAATTAAAAAGATAAATAT
    ATTCTCTTATTTTCTTATTTCTCTTCCAAGGATTGT
    CGAGATGGGAGAAGATTAACGTAAAGAATTTTT
    Gm08:834 ATTTTTTTATTAAAACAGCGAAAATATAG[G/T]GT
    8346352 180 363 0.936 0.841
    6352 ATATATATAAAAGGCACAAATGGGTGCCCCCAAT
    CAATTACAAAGTGGATAAAAGTCCAACAAAGAT
    AGTATACCTCGGTTACACCATATTAACAAAGGAG
    AGTAAATATAGTTTAACCAAGGCCAAAAACATC
    ACTCCTAGCCACACTCCAGTAAATATAGTTTAAC
    GTGAAGAATTTGATTCAACTTGTGAGAGCT
    AAGAATTTGATTCAACTTGTGAGAGCTTCACCCC
    TTAAGTTAATTCACCATATAGCTCAAATCGGATT
    AGTTGGAGAACTTAATTACCCTGATTGCCCTTTCT
    TAAAAATATTGCAGAAGCACCAAATAATACCAC
    AATGTGTCGATGTGTTTCCGAAACTAGATGATAG
    Gm08:834 ATGGGTAGGAATTTTTTTATTTTCTTTGAT[A/G]T
    8346726 [G/A] 181 364 0.87 0.8
    6726 ATTGAAAAGGCAGAAAGAAACACAAATTTTAGT
    ATTTAATAAAGCAAAATGCACACATCCCCCAAAC
    AAAACAAGCCTTATTCAACCCAAATTGGTTTCAT
    ATCACAGAAACCAACAGGATGCCGCCTTCCTCCT
    TACTGGTCCCACCCACTCGAACAAAAGTTSTACA
    GAAATAAAAATGGCTACAATTCTTCTACCA
    AGAGCCTGAAGGGCACAGATGGGATCAATCTCG
    GTCACGATGACACGAGCACCAGCCTGCTTCATTG
    CAGCAGCACAACCCTTGCCAACATCACCATATCC
    AGCCACAACAGCCACCTTTCCAGCAATCATAACA
    TCGGTAGCCCTCATGAGACCATCAGGGAGAGAG
    Gm08:834 TGACGGCACCCATACAAGTTGTCAAACTGTTA+A/
    8347799 [C/A] 182 365 0.919 0.757
    7799 C+AAAACCACAGATTAAAAGGTTAAACAAACAAA
    ACACAAGCAACAAAGCAAAATCCAATTATAATC
    AACTAGATCCATGACCAGCTAGTATAATGTCCTC
    AAAATCCAATCACCCACTTCTTACTTTCAATACC
    CTAATCAATAAACAACCCGTCACAAAAGACTCG
    GTTTGGATCAATGTTTGCAAAACCAATTTTGAAT
    AACAAACAAAACACAAGCAACAAAGCAAAATCC
    AATTATAATCAACTAGATCCATGACCAGCTAGTA
    TAATGTCCTCAAAATCCAATCACCCACTTCTTACT
    TTCAATACCCTAATCAATAAACAACCCGTCACAA
    AAGACTCGGTTTGGATCAATGTTTGCAAAACCAA
    Gm08:834 8348022183 366 0.854 0.848 TTTTGAATGAAAACGATTTCGAGTTAAAAT[A/T]G
    8022 ATTTYGAAACAACATGATTTATGTTTGAACATTT
    TTTTATTTTAAAACCAAAAACAGTAGTAAAATTC
    AGTATAATTTATTTTATCCTATCCAAAAGTAGCTT
    CAAATCAAAATGTGCACTCAGAATCAATTCCTTA
    TTTGTGTAATAAAACATGTGACCATTTACCTAAA
    GTCACGTTAGCAAGCAACTTACTAATGT
    CAAAACACAAGCAACAAAGCAAAATCCAATTAT
    AATCAACTAGATCCATGACCAGCTAGTATAATGT
    CCTCAAAATCCAATCACCCACTTCTTACTTTCAAT
    ACCCTAATCAATAAACAACCCGTCACAAAAGACT
    CGGTTTGGATCAATGTTTGCAAAACCAATTTTGA
    Gm08:834 ATGAAAACGATTTCGAGTTAAAATWGATTT[C/T]
    8348028 184 367 0.844 0.787
    8028 GAAACAACATGATTTATGTTTGAACATTTTTTTAT
    TTTAAAACCAAAAACAGTAGTAAAATTCAGTATA
    ATTTATTTTATCCTATCCAAAAGTAGCTTCAAATC
    AAAATGTGCACTCAGAATCAATTCCTTATTTGTG
    TAATAAAACATGTGACCATTTACCTAAAGTCACG
    TTAGCAAGCAACTTACTAATGTTCTGAC
    AMTATGAAAAATTATACTTCAAACAAGTCTCTCA
    TAAGAATGTTTATGGTCTCATACAGATGAATATT
    TTCACTTCGAATACACGTAAAACTAATATGAATT
    CACACAAGTGATTAAAGATCTAAAACTAACTTTT
    GTCTTCTTTTTTTTATAGATGTGGGTTTCATTCTCT
    Gm08:834 ATCATGCCACTAAAACTATCATCTAATA[G/T]ATT
    8349925 [G/T] 185 368 0.929 0.717
    9925 CTTTGACATCTAAGGACTAATTGAATAAATACAA
    TTAAGTAAAATTGTCTATGATTTAGGCCTGTGGA
    ATAATCCTTGAGTAAGCCTTTATTGACATCGCTA
    ACAAGTAGCATGTCATTAAGGTTTCATTCGATGG
    TATTGATCAGGCCTCTATAAAATTTTGTACATTTT
    AATATGCATCAAATGAGCATACKGGT
    ATAKATTCTTTGACATCTAAGGACTAATTGAATA
    AATACAATTAAGTAAAATTGTCTATGATTTAGGC
    CTGTGGAATAATCCTTGAGTAAGCCTTTATTGAC
    ATCGCTAACAAGTAGCATGTCATTAAGGTTTCAT
    TCGATGGTATTGATCAGGCCTCTATAAAATTTTG
    Gm08:835 TACATTTTAATATGCATCAAATGAGCATAC[G/T]G
    8350122 186 369 0.929 0.649
    0122 GTAAAGATTTCGGTGCTCAAGTTAATAGTTGGTA
    AAGTAAAAGCATTATATGTAAGATTTTCATGTAC
    TTGKTAAAGCTAAGGGACTATCGGAGATTGTTGA
    TAAGCATTTAAAAAACTCTCAACAATCTTCTATC
    TGCCTATAAAGTTTTCTYAAAAAGCATTTAAAAA
    ATTTATAGGTTAATTAGAGATTTGTTAGG
    CTCTATAAAATTTTGTACATTTTAATATGCATCAA
    ATGAGCATACKGGTAAAGATTTCGGTGCTCAAGT
    TAATAGTTGGTAAAGTAAAAGCATTATATGTAAG
    ATTTTCATGTACTTGKTAAAGCTAAGGGACTATC
    GGAGATTGTTGATAAGCATTTAAAAAACTCTCAA
    Gm08:835 CAATCTTCTATCTGCCTATAAAGTTTTCT[C/T]AA
    8350277 [C/T] 187 370 0.929 09 .0
    0277 AAAGCATTTAAAAAATTTATAGGTTAATTAGAGA
    TTTGTTAGGTAGGTTAACATACATGTAAAGATTT
    TTCTTTTTTTGGAAAATACATGTAAAGAGTTTTGT
    AAAAGTAGAACTTGTGAATACGTGATTTATAAGA
    CAATTCATATTCCTCCCAATCAGGTAATTTTGTGC
    AAAAAGTCTTATTAAGTTGGTGTGTA
    ATATTGTAAAACACAAAATATTTATATTCCAATC
    TTMAATGTTTTTATTTGACATTATAAATATTTAAA
    GGATAGAATCAATGTTAATCAAGTTAACATAAAA
    AATAAAAAATTACATAGCATTCAACATGTAGGTA
    TCAAATCTATGTTATAAAATGTTTATTAGATAGA
    Gm08:835 8351061 [G/A] 188 371 1 0.823 GAAAAATATTTGCTAAAATTTWGATAATT[A/G]T
    1061 GCTATGTTTATATGTTGAATGATGGGTAAAATAA
    AATGACGCATAATTAAGTAACATAAGTAAAATA
    AAAATTAAGTTTAATTTTTATGAATTATCAATAT
    AAAAAAATAAAATATATTCCTAACATTTCTCTTT
    CCTCTATTTTACATTCATTTTATTTTCTTAATTTTT
    TTCATTTTGATATCCTTTAATATAATAA
    CCCGGTCAAAATATAGGTTTAACAATTAGTCAAT
    TACTATATAAATAGGTTTTGTATTTGAATATGTTA
    GTAAAAAGTAGTTTTAATATATCTTATTCCAGTA
    AAATTATCAATTACTTTTAATAATAAAGTCATAC
    AAATTTGTATAAAACTATTTTCCCCCTACGATAA
    Gm08:835 AAGTTGTTTCGAAAAAAAAGTAAGTTGGA[A/G]A
    8351503 [A/G] 189 372 0.869 0.718
    1503 AATTTATTGAAGTGATGAAAACTATTTTTATGGT
    TATTTTTTATCACACAAATTAATTTTGGAATCTTA
    TAATTAGAAATGGTTGAATTTATATATTGGTTAA
    CTTTATTTTCTTATTTCGTCCACAGTAATGAATTG
    TTTCAAACAAAAAAAAAATCAATTAATATATATT
    TTATAATTTTACTATTGAAAAATACCT
    AGCATAATCACAATTATTGAGAAGATATTTTTAT
    TTTATTTTTACCGAATCGTCGCACGACTCGGCGT
    GTTGCAACCGCATTAAATCTTTGTGTTGGTCTCAC
    CCTGTCTTTTTGTGGATGATCGATCCTCTTGGATT
    GGTTTTTATAAAACTCAACTTCCCATCGGTGTTCT
    Gm08:835 TTAGTAATTGGAGTATCTTTGGATGTT[C/T]GTTA
    8352313 [C/T] 190 373 1 0.743
    2313 CATTTTATGATAAATTTAAATGATCCACAATCAC
    TAACTCAATTTTGCAAAGCAGGATTCTGAATGTT
    TTTGTAAATCTCGTTTTGTCCTAAAAGTTCGTCTA
    TAACAATAAAACAAACATGCACTTGGTTGTTTTT
    AAAATTGTCTCAAAACTCTGTTATAAAGAAATAA
    GACCTAAAGATATTTTTTACAAATT
    ATATCCTTAGATTAATTTATTTTSTTGATAAAAAA
    AAWKGATAAAAATTTCCATGCTTTAAATTTGTCA
    TTGGTC CATC TGATC GACTC TATACATCAAAC TT
    GAGTGTTATTTGCATACAAAAGGAAAACATCAG
    AGACATGACAGAGTAGGTTGCATTGGTGTTTAGT
    Gm08:835 TGACCTGATTAAGAAGTTACACACAAAGTG[C/T]
    8352743 [C/T] 191 374 0.843 0.72
    2743 TCC TCTATC TC CTC TTCAAGGTC CTC CTACC TATA
    GTCTTCTTGTACCTCTTATTATATGGATTAATTAG
    TGTAGAATTATTTCAACTTAATTAATAATTTTGAA
    TTTAAGTCATGAGAATGAGTATCAAAAYTTTTTC
    AC CTATAAAAATC GAATRTGCTTCAAATAAGATT
    GTCTCTAATAAATAATATGTGTTTAAT
    AAACCTATGTCGGTTGGTTCCTCTTTAAAGAAAA
    GAGAATAAAAATAACAAAGAAAAAAAAGTCGCC
    TTCCATTTCATTCGCATTCATAGTAAAAGAGTGA
    GC GATC CC GGGAAATGAATTAATATACGAC TAA
    AAAGATTTGAGAATTATAATAATTAATAATTAAT
    Gm08:835 AATTCTTTTTCAAAAGTAAAGTACAGTACTGC +A/
    8353341 [A/T] 192 375 0.812 0.774
    3341 T+GGAAACATGAGCATGTTCATAGATTAAAATTT
    AAAAGAATATTATCAGTAACAAAAAAATAAAAA
    TTAACCCATGCATCCAAGAAAGAAATACYCATGT
    GC TTCAGTTGTCC GC TGTC TGAGATGTGGTGACC
    TTTTTTCAAATGATCATAATAGTTACTTCATAATG
    AC GACATGCATCAAAC TATTTTTTC TTCAAAA
    TATCCCCCATGTTAATGAAGCAAGGTGTGGGGGA
    AGGAAAGAGTCAGCATCAGTGAAGTAGAGAGGG
    GGGTTGGTGATTTTGGTGGGAATAAATTGGCTAT
    ATTGC CC CCACCAACC TC GTTGC TAC CAAATAC C
    AACAACACTGACTCACTGAGAATTGGGAAAGAA
    Gm08:835 8355175 [C/T] 193 376 0.867 0.787 AC TTAAAAC CAAGTCTTGCAGTGAC GTACATG+C/
    5175 T+AGTGTGTGCATCACACATTCAGGTTTCCAGTCA
    AATTGTAGAACAAATGAATTTC TTGC TTTAAC TT
    AAGTTGAAGTTTAAGAAGTGAAGCTGATGCTTGT
    TTTTGAATGAAAAGCCTTTGATAGTTTGATGTAA
    GCATTTTCCAAATTTAACTCTTCCCATGCTTGACA
    GAGCCAATTAAGCTAACTGGTTTGATAACA
    CACCCCTCATTAGAGGCTTAGGATTTTTTTGAGTC
    CTAGAACACACATCTTATCTCAATAATGATTTCT
    ATCATTGCCAGAATTACAATTAAAAACTAAAATA
    TAATCAATTAGATTGAATTGAACTTCTACAGACC
    CCAAAGGCACTCGATGCATTTTCACTGTATGTGG
    Gm08:836 TTTGTCTTTC TGTAC TATAC TGCAC GCTT [A/G] GC
    8360133
    0133 [A/G] 194 377 1 0.773 AAAATAATCAGTAACACATGTTAAGAGAGCTTGC
    AC TTTATTTTTATC TTGTTGAC GGGTTTGTTGTCA
    TTGAAAACACATTATATTCAGAGGAATTTGACTC
    AACATGTTCAACCCACCAATTATCACATTTAAAC
    AAATYTAAATCAATCGCAAATCATATATATTCAG
    AATTTTACATATTAAATATTTCATATC
    AATAACATGGTTATGTTGAAAACAAAAGAAAAA
    AATATCAAATTTAATTCATGAATCTTTCAACTAA
    TTAAAAAATGACCAATCCTAACTAGTTGCAGAAG
    CTATTAATTAAATTTTTAAAAAAGTATATCTTTCT
    CTC TTATGAC TCACATAATTTATAKTC CC TATACT
    Gm08:836 CAAAGTCTCACATAATTTATACTACAAAA[A/T]CT
    8363193
    3193 195 378 1 0.703 TAGGTTTAATTTC GTACC TATTGTTAATGTTTC CT
    AATCGAAATTAGAATTTCACCCCGATAATTAAAA
    GTTTACATTAAAAAATTAYATAAATTACCGAAAT
    AAAACTCAAAATTTAGTCAAACAATAATGTAAGC
    AC TAAGCAGCAAC TAAGAAGC TATAAACAAAGT
    TTTGATAAATAGTTAAATTTATC CTC CA
    AAGTGGGGAACTGTCGATCCATGGTGCTGGCAGC
    AACCGTAACATGCCAGGGTGCGAGATTTTCCGCA
    GTGGCTTCC GC GGGCCCACTGTTGCCAGCAGAGC
    AAACCACCACAAC GCCAC GC TTGGCCGCATGGA
    AGGATCC GATGGCAACACTATCCTTGAAAAAC GT
    Gm08:836 GGAGGAAGAGCCACCGAGCGAGACGGAGAGG+A/
    3888 8363888 [A/G] 196 379 0.825 0.809 G+ CATCGACGCCGTCGTGGATGGCGAGGTCGAAG
    GCCGCCAAGATATCAGCGTCGAAGCACTCCTCGC
    CTCCGACGGGGGGCCAGCAGACCTTGTAGGCTGC
    CACACGTGCCATTGGTGAGCCACCCTTGGCTGTT
    CCC TGGCCC TGGCC GAAGAC GC TGACAC GTGC GA
    CCATGTTCCCGCCAGCTGTGGATAGGGTGTGG
    TGCCATTGGTGAGCCACCCTTGGCTGTTCCCTGG
    CCCTGGCCGAAGACGCTGACACGTGCGACCATGT
    TCCCGCCAGCTGTGGATAGGGTGTGGGTCCCGTG
    GCCCTCGTTGTCACGTGGCGAGTCAAAGGAGGA
    GTTCAGTGGGCCCGCCACTGAGGCGTAGCCCTTG
    Gm08:836 TTGAAGTACCTTGCCCCTATTAGCTTCCTGC [A/G]
    8364195 [A/G] 197 380 0.919 0.788
    4195 TTCAACATCTCCACTTAACGTTTCTTTAATTTWTC
    AAAACAAAATCATTGAAAGATTGGTCTGGTTGGT
    GTGAAAACACTAGTACTATAAAAGAATAAGATA
    AC GAAAGAAACATGTC TGC GTTCAAAGGAGTGC
    TTAACCCTTTCATTGTAGTATTCACCTAATAAAG
    AGTGCCAATTTAAAGGCATATGACTACAGAA
    R = Resistan;
    S = Susceptible
    *Liu et al. (2012). A soybean cyst nematode resistance gene points to a new mechanism of plant resistance to pathogens. Nature 492: 256-260.
  • TABLE 4 
    Non-limiting Examples of Amplicons Comprising the Various Marker Loci
    Provided Herein.
    Resistant
    Linkage (R) or
    Marker Group Susceptible SEQ Amplicon
    Name (ch) Primer 1 Primer 2 (S) Allele ID NO Amplicon Sequence Size (bp)
    S07160-1 A2 136868 136869 R 11 TGTGTTGTGTTTGACTG 118
    (Gm08) CCATAACATGATGTTTG
    GATTAAATATAAACAA
    TAATATC C TATGCAGTT
    AGTGAGGCTGTGATTT
    GGAAGACACTGTCTTA
    TCAAGAGGCTTGGGAA
    ATG
    S07160-1 A2 136868 136869 S 12 TGTGTTGTGTTTGACTG 118
    (Gm08) CCATAACATGATGTTTG
    GATTAAATATAAACAA
    TAATATC A TATGCAGTT
    AGTGAGGCTGTGATTT
    GGAAGACACTGTCTTA
    TCAAGAGGCTTGGGAA
    ATG
  • In another embodiment, the method of detecting comprises DNA sequencing of at least one of the marker loci provided herein. As used herein, “sequencing” refers to sequencing methods for determining the order of nucleotides in a molecule of DNA. Any DNA sequencing method known in the art can be used in the methods provided herein. Non-limiting examples of DNA sequencing methods useful in the methods provided herein include Next Generation Sequencing (NGS) technologies, for example, as described in Egan, A. N, et al. (2012) American Journal of Botany 99(2):175-185; genotyping by sequencing (GBS) methods, for example, as described in Elshire, R. J., et al. (2011) PLoS ONE 6(5):e19379; Molecular Inversion Probe (MIP) genotyping, as described, for example, in Hardenbol, P., et al. (2003) Nature Biotechnology 21(6):673-678; or high throughput genotyping by whole-genome resequencing, as described, for example in Huang, X et al., (2009) Genome Research 19:1068-1076. Each of the above references is incorporated by reference in their entirety herein.
  • An active variant of any one of SEQ ID NOS: 1-380 can comprise a polynucleotide having at least 75%, 80% 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% sequence identity to SEQ ID NOS: 1-380 as long as it is capable of amplifying and/or detecting the marker locus of interest. By “fragment” is intended a portion of the polynucleotide. A fragment or portion can comprise at least 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 25, 30, 40, 50, 75, 100, 150, 200, 250, 300, 350, 400 contiguous nucleotides of SEQ ID NOS: 1-380 as long as it is capable of amplifying and/or detecting the marker locus of interest.
  • Unless otherwise stated, sequence identity/similarity values provided herein refer to the value obtained using GAP Version 10 using the following parameters: % identity and % similarity for a nucleotide sequence using GAP Weight of 50 and Length Weight of 3, and the nwsgapdna.cmp scoring matrix; or any equivalent program thereof. By “equivalent program” is intended any sequence comparison program that, for any two sequences in question, generates an alignment having identical nucleotide residue matches and an identical percent sequence identity when compared to the corresponding alignment generated by GAP Version 10.
  • Traits or markers are considered to be linked if they co-segregate. A 1/100 probability of recombination per generation is defined as a map distance of 1.0 centiMorgan (1.0 cM). Genetic elements or genes located on a single chromosome segment are physically linked. Two loci can be located in close proximity such that recombination between homologous chromosome pairs does not occur between the two loci during meiosis with high frequency, e.g., such that linked loci co-segregate at least about 90% of the time, e.g., 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, 99.5%, 99.75%, or more of the time. Genetic elements located within a chromosome segment are also genetically linked, typically within a genetic recombination distance of less than or equal to 50 centimorgans (cM), e.g., about 49, 40, 30, 20, 10, 5, 4, 3, 2, 1, 0.75, 0.5, or 0.25 cM or less. That is, two genetic elements within a single chromosome segment undergo recombination during meiosis with each other at a frequency of less than or equal to about 50%, e.g., about 49%, 40%, 30%, 20%, 10%, 5%, 4%, 3%, 2%, 1%, 0.75%, 0.5%, or 0.25% or less. Closely linked markers display a cross over frequency with a given marker of about 10% or less (the given marker is within about 10 cM of a closely linked marker). In specific embodiments, a closely linked marker is within 10 cM, 9 cM, 8 cM, 7 cM, 6 cM, 5 cM, 4 cM, 3 cM, 2 cM or 1 cM of any given marker disclosed herein. In further embodiments, a marker associated with one of the markers disclosed herein can be within 75 Kb, 60 Kb, 50 Kb, 40 Kb, 30 Kb, 20 K, 10 Kb, 5 Kb or less of the disclosed marker.
  • Put another way, closely linked loci co-segregate at least about 90% of the time. Genetic linkage as evaluated by recombination frequency is impacted by the chromatin structure of the region comprising the loci. Typically, the region is assumed to have a euchromatin structure during initial evaluations. However, some regions, such are regions closer to centrosomes, have a heterochromatin structure. Without further information, the predicted physical distance between genetic map positions is based on the assumption that the region is euchromatic, however if the region comprises heterochromatin the markers may be physically closer together. With regard to physical position on a chromosome, closely linked markers can be separated, for example, by about 1 megabase (Mb; 1 million nucleotides), about 500 kilobases (Kb; 1000 nucleotides), about 400 Kb, about 300 Kb, about 200 Kb, about 100 Kb, about 50 Kb, about 25 Kb, about 10 Kb, about 5 Kb, about 2 Kb, about 1 Kb, about 500 nucleotides, about 250 nucleotides, or less.
  • When referring to the relationship between two genetic elements, such as a genetic element contributing to resistance and a proximal marker, “coupling” phase linkage indicates the state where the “favorable” allele at the resistance locus is physically associated on the same chromosome strand as the “favorable” allele of the respective linked marker locus. In coupling phase, both favorable alleles are inherited together by progeny that inherit that chromosome strand. In “repulsion” phase linkage, the “favorable” allele at the locus of interest (e.g., a QTL for resistance) is physically linked with an “unfavorable” allele at the proximal marker locus, and the two “favorable” alleles are not inherited together (i.e., the two loci are “out of phase” with each other).
  • Markers are used to define a specific locus on the soybean genome. Each marker is therefore an indicator of a specific segment of DNA, having a unique nucleotide sequence. Map positions provide a measure of the relative positions of particular markers with respect to one another. When a trait is stated to be linked to a given marker it will be understood that the actual DNA segment whose sequence affects the trait generally co-segregates with the marker. More precise and definite localization of a trait can be obtained if markers are identified on both sides of the trait. By measuring the appearance of the marker(s) in progeny of crosses, the existence of the trait can be detected by relatively simple molecular tests without actually evaluating the appearance of the trait itself, which can be difficult and time-consuming because the actual evaluation of the trait requires growing plants to a stage and/or under environmental conditions where the trait can be expressed. Molecular markers have been widely used to determine genetic composition in soybeans.
  • Favorable genotypes associated with at least trait of interest may be identified by one or more methodologies. In some examples one or more markers are used, including but not limited to AFLPs, RFLPs, ASH, SSRs, SNPs, indels, padlock probes, molecular inversion probes, microarrays, sequencing, and the like. In some methods, a target nucleic acid is amplified prior to hybridization with a probe. In other cases, the target nucleic acid is not amplified prior to hybridization, such as methods using molecular inversion probes (see, for example Hardenbol et al. (2003) Nat Biotech 21:673-678). In some examples, the genotype related to a specific trait is monitored, while in other examples, a genome-wide evaluation including but not limited to one or more of marker panels, library screens, association studies, microarrays, gene chips, expression studies, or sequencing such as whole-genome resequencing and genotyping-by-sequencing (GBS) may be used. In some examples, no target-specific probe is needed, for example by using sequencing technologies, including but not limited to next-generation sequencing methods (see, for example, Metzker (2010) Nat Rev Genet 11:31-46; and, Egan et al. (2012) Am J Bot 99:175-185) such as sequencing by synthesis (e.g., Roche 454 pyrosequencing, Illumina Genome Analyzer, and Ion Torrent PGM or Proton systems), sequencing by ligation (e.g., SOLiD from Applied Biosystems, and Polnator system from Azco Biotech), and single molecule sequencing (SMS or third-generation sequencing) which eliminate template amplification (e.g., Helicos system, and PacBio RS system from Pacific BioSciences). Further technologies include optical sequencing systems (e.g., Starlight from Life Technologies), and nanopore sequencing (e.g., GridION from Oxford Nanopore Technologies). Each of these may be coupled with one or more enrichment strategies for organellar or nuclear genomes in order to reduce the complexity of the genome under investigation via PCR, hybridization, restriction enzyme (see, e.g., Elshire et al. (2011) PLoS ONE 6:e19379), and expression methods. In some examples, no reference genome sequence is needed in order to complete the analysis.
  • The use of marker assisted selection (MAS) to select a soybean plant or germplasm which has a certain marker locus, haplotype or marker profile is provided. For instance, in certain examples a soybean plant or germplasm possessing a certain predetermined favorable marker locus or haplotype will be selected via MAS. In certain other examples, a soybean plant or germplasm possessing a certain predetermined favorable marker profile will be selected via MAS.
  • Using MAS, soybean plants or germplasm can be selected for markers or marker alleles that positively correlate with soybean cyst nematode resistance, without actually raising soybean and measuring for resistance (or, contrawise, soybean plants can be selected against if they possess markers that negatively correlate with resistance). MAS is a powerful tool to select for desired phenotypes and for introgressing desired traits into cultivars of soybean (e.g., introgressing desired traits into elite lines). MAS is easily adapted to high throughput molecular analysis methods that can quickly screen large numbers of plant or germplasm genetic material for the markers of interest and is much more cost effective than raising and observing plants for visible traits.
  • In some embodiments, the molecular markers or marker loci are detected using a suitable amplification-based detection method. In these types of methods, nucleic acid primers are typically hybridized to the conserved regions flanking the polymorphic marker region. In certain methods, nucleic acid probes that bind to the amplified region are also employed. In general, synthetic methods for making oligonucleotides, including primers and probes, are well known in the art. For example, oligonucleotides can be synthesized chemically according to the solid phase phosphoramidite triester method described by Beaucage and Caruthers (1981) Tetrahedron Letts 22:1859-1862, e.g., using a commercially available automated synthesizer, e.g., as described in Needham-VanDevanter, et al. (1984) Nucleic Acids Res. 12:6159-6168. Oligonucleotides, including modified oligonucleotides, can also be ordered from a variety of commercial sources known to persons of skill in the art.
  • It will be appreciated that suitable primers and probes to be used can be designed using any suitable method. It is not intended that the invention be limited to any particular primer, primer pair or probe. For example, primers can be designed using any suitable software program, such as LASERGENE® or Primer3.
  • It is not intended that the primers be limited to generating an amplicon of any particular size. For example, the primers used to amplify the marker loci and alleles herein are not limited to amplifying the entire region of the relevant locus. In some embodiments, marker amplification produces an amplicon at least 20 nucleotides in length, or alternatively, at least 50 nucleotides in length, or alternatively, at least 100 nucleotides in length, or alternatively, at least 200 nucleotides in length.
  • Non-limiting examples of polynucleotide primers useful for detecting the marker loci provided herein are provided in Table 1 and include, for example, SEQ ID NOS: 1, 2, 3, 4, 5, 6, 7, 8 or variants or fragments thereof.
  • PCR, RT-PCR, and LCR are in particularly broad use as amplification and amplification-detection methods for amplifying nucleic acids of interest (e.g., those comprising marker loci), facilitating detection of the markers. Details regarding the use of these and other amplification methods are well known in the art and can be found in any of a variety of standard texts. Details for these techniques can also be found in numerous journal and patent references, such as Mullis, et al. (1987) U.S. Pat. No. 4,683,202; Arnheim & Levinson (Oct. 1, 1990) C&EN 36-47; Kwoh, et al. (1989) Proc. Natl. Acad. Sci. USA 86:1173; Guatelli, et al., (1990) Proc. Natl. Acad. Sci. USA 87:1874; Lomell, et al., (1989) J. Clin. Chem. 35:1826; Landegren, et al., (1988) Science 241:1077-1080; Van Brunt, (1990) Biotechnology 8:291-294; Wu and Wallace, (1989) Gene 4:560; Barringer, et al., (1990) Gene 89:117, and Sooknanan and Malek, (1995) Biotechnology 13:563-564.
  • Such nucleic acid amplification techniques can be applied to amplify and/or detect nucleic acids of interest, such as nucleic acids comprising marker loci. Amplification primers for amplifying useful marker loci and suitable probes to detect useful marker loci or to genotype SNP alleles are provided. For example, exemplary primers and probes are provided in SEQ ID NOS: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10 and in Tables 1 and 2, and the genomic loci comprising the various marker loci provided herein are provided in SEQ ID NOS: 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, 100, 101, 102, 103, 104, 105, 106, 107, 108, 109, 110, 111, 112, 113, 114, 115, 116, 117, 118, 119, 120, 121, 122, 123, 124, 125, 126, 127, 128, 129, 130, 131, 132, 133, 134, 135, 136, 137, 138, 139, 140, 141, 142, 143, 144, 145, 146, 147, 148, 149, 150, 151, 152, 153, 154, 155, 156, 157, 158, 159, 160, 161, 162, 163, 164, 165, 166, 167, 168, 169, 170, 171, 172, 173, 174, 175, 176, 177, 178, 179, 180, 181, 182, 183, 184, 185, 186, 187, 188, 189, 190, 191, 192, 193, 194, 195, 196, 197, 198, 199, 200, 201, 202, 203, 204, 205, 206, 207, 208, 209, 210, 211, 212, 213, 214, 215, 216, 217, 218, 219, 220, 221, 222, 223, 224, 225, 226, 227, 228, 229, 230, 231, 232, 233, 234, 235, 236, 237, 238, 239, 240, 241, 242, 243, 244, 245, 246, 247, 248, 249, 250, 251, 252, 253, 254, 255, 256, 257, 258, 259, 260, 261, 262, 263, 264, 265, 266, 267, 268, 269, 270, 271, 272, 273, 274, 275, 276, 277, 278, 279, 280, 281, 282, 283, 284, 285, 286, 287, 288, 289, 290, 291, 292, 293, 294, 295, 296, 297, 298, 299, 300, 301, 302, 303, 304, 305, 306, 307, 308, 309, 310, 311, 312, 313, 314, 315, 316, 317, 318, 319, 320, 321, 322, 323, 324, 325, 326, 327, 328, 329, 330, 331, 332, 333, 334, 335, 336, 337, 338, 339, 340, 341, 342, 343, 344, 345, 346, 347, 348, 349, 350, 351, 352, 353, 354, 355, 356, 357, 358, 359, 360, 361, 362, 363, 364, 365, 366, 367, 368, 369, 370, 371, 372, 373, 374, 375, 376, 377, 378, 379, 380 and in Tables 3A and 3B. Non-limiting examples of amplicon sequences comprising the marker loci provided herein are provided SEQ ID NOS: 11, 12 and in Table 4.
  • However, one of skill will immediately recognize that other primer and probe sequences could also be used. For instance primers to either side of the given primers can be used in place of the given primers, so long as the primers can amplify a region that includes the allele to be detected, as can primers and probes directed to other SNP marker loci. Further, it will be appreciated that the precise probe to be used for detection can vary, e.g., any probe that can identify the region of a marker amplicon to be detected can be substituted for those examples provided herein. Further, the configuration of the amplification primers and detection probes can, of course, vary. Thus, the compositions and methods are not limited to the primers and probes specifically recited herein.
  • In certain examples, probes will possess a detectable label. Any suitable label can be used with a probe. Detectable labels suitable for use with nucleic acid probes include, for example, any composition detectable by spectroscopic, radioisotopic, photochemical, biochemical, immunochemical, electrical, optical, or chemical means. Useful labels include biotin for staining with labeled streptavidin conjugate, magnetic beads, fluorescent dyes, radiolabels, enzymes, and colorimetric labels. Other labels include ligands, which bind to antibodies labeled with fluorophores, chemiluminescent agents, and enzymes. A probe can also constitute radiolabelled PCR primers that are used to generate a radiolabelled amplicon. Labeling strategies for labeling nucleic acids and corresponding detection strategies can be found, e.g., in Haugland (1996) Handbook of Fluorescent Probes and Research Chemicals Sixth Edition by Molecular Probes, Inc. (Eugene O R); or Haugland (2001) Handbook of Fluorescent Probes and Research Chemicals Eighth Edition by Molecular Probes, Inc. (Eugene O R).
  • Detectable labels may also include reporter-quencher pairs, such as are employed in Molecular Beacon and TaqMan™ probes. The reporter may be a fluorescent organic dye modified with a suitable linking group for attachment to the oligonucleotide, such as to the terminal 3′ carbon or terminal 5′ carbon. The quencher may also be an organic dye, which may or may not be fluorescent, depending on the embodiment. Generally, whether the quencher is fluorescent or simply releases the transferred energy from the reporter by non-radiative decay, the absorption band of the quencher should at least substantially overlap the fluorescent emission band of the reporter to optimize the quenching. Non-fluorescent quenchers or dark quenchers typically function by absorbing energy from excited reporters, but do not release the energy radiatively.
  • Selection of appropriate reporter-quencher pairs for particular probes may be undertaken in accordance with known techniques. Fluorescent and dark quenchers and their relevant optical properties from which exemplary reporter-quencher pairs may be selected are listed and described, for example, in Berlman, Handbook of Fluorescence Spectra of Aromatic Molecules, 2nd ed., Academic Press, New York, 1971, the content of which is incorporated herein by reference. Examples of modifying reporters and quenchers for covalent attachment via common reactive groups that can be added to an oligonucleotide in the present invention may be found, for example, in Haugland, Handbook of Fluorescent Probes and Research Chemicals, Molecular Probes of Eugene, Oreg., 1992, the content of which is incorporated herein by reference.
  • In certain examples, reporter-quencher pairs are selected from xanthene dyes including fluoresceins and rhodamine dyes. Many suitable forms of these compounds are available commercially with substituents on the phenyl groups, which can be used as the site for bonding or as the bonding functionality for attachment to an oligonucleotide. Another useful group of fluorescent compounds for use as reporters are the naphthylamines, having an amino group in the alpha or beta position. Included among such naphthylamino compounds are 1-dimethylaminonaphthyl-5 sulfonate, 1-anilino-8-naphthalene sulfonate and 2-p-touidinyl-6-naphthalene sulfonate. Other dyes include 3-phenyl-7-isocyanatocoumarin; acridines such as 9-isothiocyanatoacridine; N-(p-(2-benzoxazolyl)phenyl)maleimide; benzoxadiazoles; stilbenes; pyrenes and the like. In certain other examples, the reporters and quenchers are selected from fluorescein and rhodamine dyes. These dyes and appropriate linking methodologies for attachment to oligonucleotides are well known in the art.
  • Suitable examples of reporters may be selected from dyes such as SYBR green, 5-carboxyfluorescein (5-FAM™ available from Applied Biosystems of Foster City, Calif.), 6-carboxyfluorescein (6-FAM), tetrachloro-6-carboxyfluorescein (TET), 2,7-dimethoxy-4,5-dichloro-6-carboxyfluorescein, hexachloro-6-carboxyfluorescein (HEX), 6-carboxy-2′,4,7,7′-tetrachlorofluorescein (6-TET™ available from Applied Biosystems), carboxy-X-rhodamine (ROX), 6-carboxy-4′,5′-dichloro-2′,7′-dimethoxyfluorescein (6-JOE™ available from Applied Biosystems), VIC™ dye products available from Molecular Probes, Inc., NED™ dye products available from Applied Biosystems, and the like. Suitable examples of quenchers may be selected from 6-carboxy-tetramethyl-rhodamine, 4-(4-dimethylaminophenylazo) benzoic acid (DABYL), tetramethylrhodamine (TAMRA), BHQ-0™, BHQ-1™, BHQ-2™, and BHQ-3™, each of which are available from Biosearch Technologies, Inc. of Novato, Calif., QSY-7™, QSY-9™, QSY-21™ and QSY-35™, each of which are available from Molecular Probes, Inc., and the like.
  • In one aspect, real time PCR or LCR is performed on the amplification mixtures described herein, e.g., using molecular beacons or TaqMan™ probes. A molecular beacon (MB) is an oligonucleotide which, under appropriate hybridization conditions, self-hybridizes to form a stem and loop structure. The MB has a label and a quencher at the termini of the oligonucleotide; thus, under conditions that permit intra-molecular hybridization, the label is typically quenched (or at least altered in its fluorescence) by the quencher. Under conditions where the MB does not display intra-molecular hybridization (e.g., when bound to a target nucleic acid, such as to a region of an amplicon during amplification), the MB label is unquenched. Details regarding standard methods of making and using MBs are well established in the literature and MBs are available from a number of commercial reagent sources. See also, e.g., Leone, et al., (1995) Molecular beacon probes combined with amplification by NASBA enable homogenous real-time detection of RNA, Nucleic Acids Res. 26:2150-2155; Tyagi and Kramer, (1996) Molecular beacons: probes that fluoresce upon hybridization, Nature Biotechnology 14:303-308; Blok and Kramer, (1997) Amplifiable hybridization probes containing a molecular switch, Mol Cell Probes 11:187-194; Hsuih. et al., (1997) Novel, ligation-dependent PCR assay for detection of hepatitis C in serum, J Clin Microbiol 34:501-507; Kostrikis, et al., (1998) Molecular beacons: spectral genotyping of human alleles, Science 279:1228-1229; Sokol, et al., (1998) Real time detection of DNA:RNA hybridization in living cells, Proc. Natl. Acad. Sci. U.S.A. 95:11538-11543; Tyagi, et al., (1998) Multicolor molecular beacons for allele discrimination, Nature Biotechnology 16:49-53; Bonnet, et al., (1999) Thermodynamic basis of the chemical specificity of structured DNA probes, Proc. Natl. Acad. Sci. U.S.A. 96:6171-6176; Fang, et al. (1999) Designing a novel molecular beacon for surface-immobilized DNA hybridization studies, J. Am. Chem. Soc. 121:2921-2922; Marras, et al., (1999) Multiplex detection of single-nucleotide variation using molecular beacons, Genet. Anal. Biomol. Eng. 14:151-156; and Vet, et al., (1999) Multiplex detection of four pathogenic retroviruses using molecular beacons, Proc. Natl. Acad. Sci. U.S.A. 96:6394-6399. Additional details regarding MB construction and use is found in the patent literature, e.g., U.S. Pat. Nos. 5,925,517; 6,150,097; and 6,037,130.
  • Another real-time detection method is the 5′-exonuclease detection method, also called the TaqMan™ assay, as set forth in U.S. Pat. Nos. 5,804,375; 5,538,848; 5,487,972; and 5,210,015, each of which is hereby incorporated by reference in its entirety. In the TaqMan™ assay, a modified probe, typically 10-25 nucleic acids in length, is employed during PCR which binds intermediate to or between the two members of the amplification primer pair. The modified probe possesses a reporter and a quencher and is designed to generate a detectable signal to indicate that it has hybridized with the target nucleic acid sequence during PCR. As long as both the reporter and the quencher are on the probe, the quencher stops the reporter from emitting a detectable signal. However, as the polymerase extends the primer during amplification, the intrinsic 5′ to 3′ nuclease activity of the polymerase degrades the probe, separating the reporter from the quencher, and enabling the detectable signal to be emitted. Generally, the amount of detectable signal generated during the amplification cycle is proportional to the amount of product generated in each cycle.
  • It is well known that the efficiency of quenching is a strong function of the proximity of the reporter and the quencher, i.e., as the two molecules get closer, the quenching efficiency increases. As quenching is strongly dependent on the physical proximity of the reporter and quencher, the reporter and the quencher are preferably attached to the probe within a few nucleotides of one another, usually within 30 nucleotides of one another, more preferably with a separation of from about 6 to 16 nucleotides. Typically, this separation is achieved by attaching one member of a reporter-quencher pair to the 5′ end of the probe and the other member to a nucleotide about 6 to 16 nucleotides away, in some cases at the 3′ end of the probe.
  • Separate detection probes can also be omitted in amplification/detection methods, e.g., by performing a real time amplification reaction that detects product formation by modification of the relevant amplification primer upon incorporation into a product, incorporation of labeled nucleotides into an amplicon, or by monitoring changes in molecular rotation properties of amplicons as compared to unamplified precursors (e.g., by fluorescence polarization).
  • Further, it will be appreciated that amplification is not a requirement for marker detection—for example, one can directly detect unamplified genomic DNA simply by performing a Southern blot on a sample of genomic DNA. Procedures for performing Southern blotting, amplification e.g., (PCR, LCR, or the like), and many other nucleic acid detection methods are well established and are taught, e.g., in Sambrook, et al., Molecular Cloning—A Laboratory Manual (3d ed.), Vol. 1-3, Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y., 2000 (“Sambrook”); Current Protocols in Molecular Biology, F. M. Ausubel, et al., eds., Current Protocols, a joint venture between Greene Publishing Associates, Inc. and John Wiley & Sons, Inc., (supplemented through 2002) (“Ausubel”)) and PCR Protocols A Guide to Methods and Applications (Innis, et al., eds) Academic Press Inc. San Diego, Calif. (1990) (Innis). Additional details regarding detection of nucleic acids in plants can also be found, e.g., in Plant Molecular Biology (1993) Croy (ed.) BIOS Scientific Publishers, Inc.
  • Other techniques for detecting SNPs can also be employed, such as allele specific hybridization (ASH). ASH technology is based on the stable annealing of a short, single-stranded, oligonucleotide probe to a completely complementary single-stranded target nucleic acid. Detection is via an isotopic or non-isotopic label attached to the probe. For each polymorphism, two or more different ASH probes are designed to have identical DNA sequences except at the polymorphic nucleotides. Each probe will have exact homology with one allele sequence so that the range of probes can distinguish all the known alternative allele sequences. Each probe is hybridized to the target DNA. With appropriate probe design and hybridization conditions, a single-base mismatch between the probe and target DNA will prevent hybridization.
  • Real-time amplification assays, including MB or TaqMan™ based assays, are especially useful for detecting SNP alleles. In such cases, probes are typically designed to bind to the amplicon region that includes the SNP locus, with one allele-specific probe being designed for each possible SNP allele. For instance, if there are two known SNP alleles for a particular SNP locus, “A” or “C,” then one probe is designed with an “A” at the SNP position, while a separate probe is designed with a “C” at the SNP position. While the probes are typically identical to one another other than at the SNP position, they need not be. For instance, the two allele-specific probes could be shifted upstream or downstream relative to one another by one or more bases. However, if the probes are not otherwise identical, they should be designed such that they bind with approximately equal efficiencies, which can be accomplished by designing under a strict set of parameters that restrict the chemical properties of the probes. Further, a different detectable label, for instance a different reporter-quencher pair, is typically employed on each different allele-specific probe to permit differential detection of each probe. In certain examples, each allele-specific probe for a certain SNP locus is 11-20 nucleotides in length, dual-labeled with a florescence quencher at the 3′ end and either the 6-FAM (6-carboxyfluorescein) or VIC (4,7,2′-trichloro-7′-phenyl-6-carboxyfluorescein) fluorophore at the 5′ end.
  • To effectuate SNP allele detection, a real-time PCR reaction can be performed using primers that amplify the region including the SNP locus, for instance the sequences listed in Tables 3A and 3B, the reaction being performed in the presence of all allele-specific probes for the given SNP locus. By then detecting signal for each detectable label employed and determining which detectable label(s) demonstrated an increased signal, a determination can be made of which allele-specific probe(s) bound to the amplicon and, thus, which SNP allele(s) the amplicon possessed. For instance, when 6-FAM- and VIC-labeled probes are employed, the distinct emission wavelengths of 6-FAM (518 nm) and VIC (554 nm) can be captured. A sample that is homozygous for one allele will have fluorescence from only the respective 6-FAM or VIC fluorophore, while a sample that is heterozygous at the analyzed locus will have both 6-FAM and VIC fluorescence.
  • The KASPar® and Illumina® Detection Systems are additional examples of commercially-available marker detection systems. KASPar® is a homogeneous fluorescent genotyping system which utilizes allele specific hybridization and a unique form of allele specific PCR (primer extension) in order to identify genetic markers (e.g. a particular SNP locus associated with soybean cyst nematode resistance). Illumina® detection systems utilize similar technology in a fixed platform format. The fixed platform utilizes a physical plate that can be created with up to 384 markers. The Illumina® system is created with a single set of markers that cannot be changed and utilizes dyes to indicate marker detection.
  • These systems and methods represent a wide variety of available detection methods which can be utilized to detect markers associated with resistance or improved resistance to soybean cyst nematode, but any other suitable method could also be used.
  • Introgression of soybean cyst nematode resistance into non-resistant or less-resistant soybean germplasm is provided. Any method for introgressing one or more marker loci into soybean plants known to one of skill in the art can be used. Typically, a first soybean germplasm that contains soybean cyst nematode resistance derived from a particular marker locus, haplotype or marker profile and a second soybean germplasm that lacks such resistance derived from the marker locus, haplotype or marker profile are provided. The first soybean germplasm may be crossed with the second soybean germplasm to provide progeny soybean germplasm. These progeny germplasm are screened to determine the presence of soybean cyst nematode resistance derived from the marker locus, haplotype or marker profile, and progeny that tests positive for the presence of resistance derived from the marker locus, haplotype or marker profile are selected as being soybean germplasm into which the marker locus, haplotype or marker profile has been introgressed. Methods for performing such screening are well known in the art and any suitable method can be used.
  • One application of MAS is to use the resistance markers, haplotypes or marker profiles to increase the efficiency of an introgression or backcrossing effort aimed at introducing a resistance trait into a desired (typically high yielding) background. In marker assisted backcrossing of specific markers from a donor source, e.g., to an elite genetic background, one selects among backcross progeny for the donor trait and then uses repeated backcrossing to the elite line to reconstitute as much of the elite background's genome as possible.
  • Thus, the markers and methods can be utilized to guide marker assisted selection or breeding of soybean varieties with the desired complement (set) of allelic forms of chromosome segments associated with superior agronomic performance (resistance, along with any other available markers for yield, disease tolerance, etc.). Any of the disclosed marker loci, marker alleles, haplotypes, or marker profiles can be introduced into a soybean line via introgression, by traditional breeding (or introduced via transformation, or both) to yield a soybean plant with superior agronomic performance. The number of alleles associated with resistance that can be introduced or be present in a soybean plant ranges from 1 to the number of alleles disclosed herein, each integer of which is incorporated herein as if explicitly recited.
  • The markers and methods provided herein can also be utilized to guide marker assisted selection or breeding of soybean varieties comprising other soybean cyst nematode resistance markers or alleles to create a molecular stack for soybean cyst nematode resistance. For example, any of the marker loci provided herein can be introduced into a soybean line having one or more of the soybean cyst nematode resistance loci rhg1, rhg2, rhg3 or rhg5. In one embodiment, any one or more of the marker loci provided herein can be stacked with the rhg1 locus. In another embodiment, any one or more of the marker loci provided herein can be stacked with the rhg2 locus. In a further embodiment, any one or more of the marker loci provided herein can be stacked with the rhg1 and rhg2 loci.
  • This also provides a method of making a progeny soybean plant and these progeny soybean plants, per se. The method comprises crossing a first parent soybean plant with a second soybean plant and growing the female soybean plant under plant growth conditions to yield soybean plant progeny. Methods of crossing and growing soybean plants are well within the ability of those of ordinary skill in the art. Such soybean plant progeny can be assayed for alleles associated with resistance and, thereby, the desired progeny selected. Such progeny plants or seed can be sold commercially for soybean production, used for food, processed to obtain a desired constituent of the soybean, or further utilized in subsequent rounds of breeding. At least one of the first or second soybean plants is a soybean plant in that it comprises at least one of the marker loci or marker profiles, such that the progeny are capable of inheriting the marker locus or marker profile.
  • Often, a method is applied to at least one related soybean plant such as from progenitor or descendant lines in the subject soybean plants pedigree such that inheritance of the desired resistance can be traced. The number of generations separating the soybean plants being subject to the methods provided herein will generally be from 1 to 20, commonly 1 to 5, and typically 1, 2, or 3 generations of separation, and quite often a direct descendant or parent of the soybean plant will be subject to the method (i.e., 1 generation of separation).
  • Genetic diversity is important for long term genetic gain in any breeding program. With limited diversity, genetic gain will eventually plateau when all of the favorable alleles have been fixed within the elite population. One objective is to incorporate diversity into an elite pool without losing the genetic gain that has already been made and with the minimum possible investment. MAS provides an indication of which genomic regions and which favorable alleles from the original ancestors have been selected for and conserved over time, facilitating efforts to incorporate favorable variation from exotic germplasm sources (parents that are unrelated to the elite gene pool) in the hopes of finding favorable alleles that do not currently exist in the elite gene pool.
  • For example, the markers, haplotypes, primers, probes, and marker profiles can be used for MAS in crosses involving elite x exotic soybean lines by subjecting the segregating progeny to MAS to maintain major yield alleles, along with the resistance marker alleles herein.
  • As an alternative to standard breeding methods of introducing traits of interest into soybean (e.g., introgression), transgenic approaches can also be used to create transgenic plants with the desired traits. In these methods, exogenous nucleic acids that encode a desired marker loci, marker profile or haplotype are introduced into target plants or germplasm. For example, a nucleic acid that codes for a resistance trait is cloned, e.g., via positional cloning, and introduced into a target plant or germplasm.
  • Experienced plant breeders can recognize resistant soybean plants in the field, and can select the resistant individuals or populations for breeding purposes or for propagation. In this context, the plant breeder recognizes “resistant” and “non-resistant” or “susceptible” soybean plants. However, plant resistance is a phenotypic spectrum consisting of extremes in resistance and susceptibility, as well as a continuum of intermediate resistance phenotypes. Evaluation of these intermediate phenotypes using reproducible assays are of value to scientists who seek to identify genetic loci that impart resistance, to conduct marker assisted selection for resistant populations, and to use introgression techniques to breed a resistance trait into an elite soybean line, for example.
  • By “improved resistance” is intended that the plants show a decrease in the disease symptoms that are the outcome of plant exposure to soybean cyst nematode. That is, the damage caused by soybean cyst nematode is prevented, or alternatively, the disease symptoms caused by soybean cyst nematode is minimized or lessened. Thus, improved resistance to soybean cyst nematode can result in reduction of the disease symptoms by at least about 2% to at least about 6%, at least about 5% to about 50%, at least about 10% to about 60%, at least about 30% to about 70%, at least about 40% to about 80%, or at least about 50% to about 90% or greater. Hence, the methods provided herein can be utilized to protect plants from soybean cyst nematode.
  • Screening and selection of soybean cyst nematode resistant soybean plants may be performed, for example, by exposing plants to soybean cyst nematode and selecting those plants showing resistance to soybean cyst nematode. Various assays can be used to measure resistance or improved resistance to soybean cyst nematode. For example, soybean cyst nematode resistance can be determined by visual observations after plant exposure to a particular race of soybean cyst nematode, such as race 1, 2, 3, 5 or 14. Scores range from 1 to 9 and indicate visual observations of resistance as compared to other genotypes in the test. A score of 1 indicates soybean cyst nematode are able to infect the plant and cause yield loss, while a score of 9 indicates soybean cyst nematode resistance. Preliminary scores are reported as double digits, for example, ‘55’ indicates a preliminary score of 5 on the scale of 1 to 9.
  • Non-limiting examples of soybean cyst nematode resistance phenotypic screening are described in detail below.
  • Multiple populations of Heterodera glycines are maintained and increased on host plants. These populations are used to identify, purify, and characterize elite soybean varieties for resistance to soybean cyst nematode. The following races of soybean cyst nematode are maintained: Race 1 (Type HG 2.5), Race 2 (Type HG 1.2.5.7), Race 3 (Type HG 0 or Type HG 7), Race 5 (Type HG 2.5.7), and Race 14 (Type HG 1.3.6.7).
  • Eggs or second stage juveniles (J2) are used to inoculate host plants to increase their population. Soybean cyst nematode infestation requires a minimum 35 days before the cysts reach maturity and can be used to inoculate soybean experiments. Cyst eggs/J2 inoculant is harvested through a series of washings, grindings, and screenings. Screens are used progressing from larger to smaller sizes, ending with a #500 (25 μm) screen.
  • Soybean plants are grown in cones. Cones are long containers approximately 12 inches long and 1.5 inches in diameter at the top (e.g., Ray Leach Cone-tainers™). The cone is designed to easily remove the root mass. Three to seven days after planting, an inoculum channel is made in the cone containing the experimental line by poking a 4 inch hole with a 10 ml pipette tip. One ml of inoculum is dispensed into the channel. The plants are watered manually for the duration of the test, with watering being moderately light during the first 3-5 days until J2 infects the roots.
  • Plants are scored approximately 28-35 days following inoculation when cyst reproduction on susceptible checks is sufficiently high. Plants are removed from their cones and the soil is removed from the roots by gently dipping the roots into a bucket of water. The plants are screened to identify native resistance to one or more of the five races of soybean cyst nematode inoculated using a combination of three methods (1) visual 9-6-1 score; (2) visual full count; and/or (3) microscope count score depending on the stage of the line when screened. In general, lines earlier in the development cycle (R1-R2) are screened by the visual 9-6-1 method, and lines that have progressed to later development phases (R3-R5) are screened by the visual full count and/or microscope count method(s).
  • One typical phenotyping method is a visual evaluation of the roots. Susceptible checks are first evaluated for the development of cysts on the root system. These counts are recorded and averaged across the experiment to determine the susceptible (SUS) check average. Roots from the test plants are then scored based on a comparison with the average of the susceptible checks as follows:
  • 9=0-15% of the susceptible checks average
  • 6=16-40% of the susceptible checks average
  • 1=≧41% of the susceptible checks average
  • Visual counts: In this method, known checks are counted and reported in full. Observed cysts on the test plants are counted for comparison to the susceptible check plant scores. Cyst counts are converted to 1-9 scores based on the female index (FI). The female index (FI) is the percentage of the number of females cysts produced on each experimental line divided by the number produced on a standard susceptible soybean check, then the result is multiplied by 100. A low FI (<10) means that the soybean cyst nematode population is not able to reproduce well on the test line, a high FI means that the soybean cyst nematode population is able to reproduce well on the test line.
    Microscope counts: Cysts counts for soybean cyst nematode assays for checks and experimental line are determined by washing cysts from roots and counting the number of cysts under the microscope.
  • At about 28-35 days after inoculation, roots from the susceptible check controls are examined for yellow cysts to assess whether to begin the process of evaluating the test. Experimental lines are compared with known standard checks. Once adequate levels of cysts are detected on the check varieties, plants from the test lines are removed from cones one at a time. Soil is removed from roots by gently dipping the roots into a bucket of water. The root tissue is placed on a 850 micron (#20) pore sieve stacked over a 250 micron (#60) pore sieve and sprayed with a jet of water to dislodge cysts from the roots. Collected cysts are rinsed from the #60 sieve into a clean labeled cup using no more than 30 mls of additional water.
  • Once all the samples are collected, each sample is counted using a gridded counting dish under a stereo microscope. The number of cysts counted are recorded for each sample. Cyst counts on the test plants are converted to the 1-9 scoring scale based on the female index (FI) described above.
  • The following exemplary soybean cyst nematode checks, provided in Table 5, can be planted and used to monitor cyst development:
  • TABLE 5
    Exemplary soybean cyst nematode checks.
    Race 1 Race 2 Race 3 Race 5 Race 14
    92B12 RES 95M60 RES 9182 RES 92B12 RES 9182 RES
    9281 SUS 9281 SUS 9281 SUS 9281 SUS 9281 SUS
    9234 RES PI437654 RES 9234 RES 9234 RES 9234 SUS
    9392 SUS 9392 SUS 9392 SUS 9392 SUS 9392 SUS
    91M12 MR 9234 MR 93B15 MR 91M12 SUS 93B15 MR
    RES = Resistant; SUS = Susceptible; and, MR = Moderately Resistant
  • In some examples, a kit or an automated system for detecting marker loci, haplotypes, and marker profiles, and/or correlating the marker loci, haplotypes, and marker profiles with a desired phenotype (e.g., soybean cyst nematode resistance) are provided. As used herein, “kit” refers to a set of reagents for the purpose of performing the various methods of detecting or identifying herein, more particularly, the identification and/or the detection of a soybean plant or germplasm having improved resistance to soybean cyst nematode.
  • In one embodiment, a kit for detecting or selecting at least one soybean plant or soybean germplasm with resistance or improved resistance to soybean cyst nematode is provided. Such a kit comprises (a) primers or probes for detecting one or more marker loci associated with resistance to soybean cyst nematode, wherein at least one of the primers and probes in the kit are capable of detecting a marker locus, wherein the marker locus is associated with the rhg4 locus on linkage group A2; and (b) instructions for using the primers or probes for detecting the one or more marker loci and correlating the detected marker loci with predicted resistance to soybean cyst nematode.
  • In a specific embodiment, the primers and probes of the kit are capable of detecting a marker locus comprising: (a) S07160-1 or a marker closely linked thereto on linkage group A2; or (ii) a marker locus comprising Gm08:8300131, Gm08:8257778, Gm08:8257785, Gm08:8258163, Gm08:8258688, Gm08:8258742, Gm08:8259928, Gm08:8260451, Gm08:8260590, Gm08:8261480, Gm08:8261684, Gm08:8262165, Gm08:8263213, Gm08:8263250, Gm08:8263611, Gm08:8264149, Gm08:8265227, Gm08:8265364, Gm08:8265614, Gm08:8266183, Gm08:8266185, Gm08:8266263, Gm08:8266350, Gm08:8266386, Gm08:8266473, Gm08:8266888, Gm08:8267085, Gm08:8267166, Gm08:8267721, Gm08:8267826, Gm08:8268336, Gm08:8268861, Gm08:8269148, Gm08:8269785, Gm08:8270037, Gm08:8270562, Gm08:8270652, Gm08:8271540, Gm08:8271591, Gm08:8271649, Gm08:8271672, Gm08:8271955, Gm08:8273257, Gm08:8273355, Gm08:8273979, Gm08:8275766, Gm08:8275780, Gm08:8275959, Gm08:8276701, Gm08:8276849, Gm08:8276913, Gm08:8277162, Gm08:8277227, Gm08:8277248, Gm08:8277381, Gm08:8277383, Gm08:8277542, Gm08:8277625, Gm08:8277643, Gm08:8277876, Gm08:8277880, Gm08:8277969, Gm08:8278001, Gm08:8278167, Gm08:8278274, Gm08:8278434, Gm08:8279165, Gm08:8279230, Gm08:8279854, Gm08:8280901, Gm08:8280937, Gm08:8281564, Gm08:8282902, Gm08:8284027, Gm08:8286864, Gm08:8287265, Gm08:8287278, Gm08:8287453, Gm08:8287459, Gm08:8288039, Gm08:8288141, Gm08:8288200, Gm08:8288470, Gm08:8288831, Gm08:8289392, Gm08:8290740, Gm08:8291682, Gm08:8292207, Gm08:8297064, Gm08:8299433, Gm08:8299672, Gm08:8301839, Gm08:8302134, Gm08:8303450, Gm08:8305237, Gm08:8305348, Gm08:8305905, Gm08:8306090, Gm08:8306141, Gm08:8306210, Gm08:8306492, Gm08:8306627, Gm08:8307172, Gm08:8307665, Gm08:8308019, Gm08:8308891, Gm08:8308917, Gm08:8309316, Gm08:8309423, Gm08:8309837, Gm08:8310383, Gm08:8310464, Gm08:8310503, Gm08:8310663, Gm08:8311631, Gm08:8311906, Gm08:8312536, Gm08:8312819, Gm08:8313273, Gm08:8313923, Gm08:8314010, Gm08:8314025, Gm08:8314208, Gm08:8314292, Gm08:8314295, Gm08:8314513, Gm08:8314736, Gm08:8314791, Gm08:8314860, Gm08:8315543, Gm08:8315644, Gm08:8316113, Gm08:8316689, Gm08:8316899, Gm08:8317852, Gm08:8317861, Gm08:8318033, Gm08:8319087, Gm08:8319642, Gm08:8319647, Gm08:8320068, Gm08:8321253, Gm08:8321649, Gm08:8323937, Gm08:8324341, Gm08:8325127, Gm08:8325214, Gm08:8326696, Gm08:8326877, Gm08:8328633, Gm08:8330929, Gm08:8331132, Gm08:8331181, Gm08:8331408, Gm08:8331827, Gm08:8332651, Gm08:8332685, Gm08:8332957, Gm08:8343167, Gm08:8345187, Gm08:8345720, Gm08:8346030, Gm08:8346050, Gm08:8346352, Gm08:8346726, Gm08:8347799, Gm08:8348022, Gm08:8348028, Gm08:8349925, Gm08:8350122, Gm08:8350277, Gm08:8351061, Gm08:8351503, Gm08:8352313, Gm08:8352743, Gm08:8353341, Gm08:8355175, Gm08:8360133, Gm08:8363193, Gm08:8363888, Gm08:8364195 or a marker closely linked thereto.
  • Thus, a typical kit or system can include a set of marker probes or primers configured to detect at least one favorable allele of one or more marker loci associated with resistance to soybean cyst nematode, for instance a favorable marker locus, haplotype or marker profile. These probes or primers can be configured, for example, to detect the marker loci noted in the tables and examples herein, e.g., using any available allele detection format, such as solid or liquid phase array based detection, microfluidic-based sample detection, etc. The systems and kits can further include packaging materials for packaging the probes, primers, or instructions, controls such as control amplification reactions that include probes, primers or template nucleic acids for amplifications, molecular size markers, or the like.
  • A typical system can also include a detector that is configured to detect one or more signal outputs from the set of marker probes or primers, or amplicon thereof, thereby identifying the presence or absence of the allele. A wide variety of signal detection apparatus are available, including photo multiplier tubes, spectrophotometers, CCD arrays, scanning detectors, phototubes and photodiodes, microscope stations, galvo-scans, microfluidic nucleic acid amplification detection appliances and the like. The precise configuration of the detector will depend, in part, on the type of label used to detect the marker allele, as well as the instrumentation that is most conveniently obtained for the user. Detectors that detect fluorescence, phosphorescence, radioactivity, pH, charge, absorbance, luminescence, temperature, magnetism or the like can be used. Typical detector examples include light (e.g., fluorescence) detectors or radioactivity detectors. For example, detection of a light emission (e.g., a fluorescence emission) or other probe label is indicative of the presence or absence of a marker allele. Fluorescent detection is generally used for detection of amplified nucleic acids (however, upstream and/or downstream operations can also be performed on amplicons, which can involve other detection methods). In general, the detector detects one or more label (e.g., light) emission from a probe label, which is indicative of the presence or absence of a marker allele. The detector(s) optionally monitors one or a plurality of signals from an amplification reaction. For example, the detector can monitor optical signals which correspond to “real time” amplification assay results.
  • System or kit instructions that describe how to use the system or kit or that correlate the presence or absence of the favorable allele with the predicted resistance are also provided. For example, the instructions can include at least one look-up table that includes a correlation between the presence or absence of the favorable alleles, haplotypes, or marker profiles and the predicted resistance. The precise form of the instructions can vary depending on the components of the system, e.g., they can be present as system software in one or more integrated unit of the system (e.g., a microprocessor, computer or computer readable medium), or can be present in one or more units (e.g., computers or computer readable media) operably coupled to the detector. As noted, in one typical example, the system instructions include at least one look-up table that includes a correlation between the presence or absence of the favorable alleles and predicted resistance. The instructions also typically include instructions providing a user interface with the system, e.g., to permit a user to view results of a sample analysis and to input parameters into the system.
  • Isolated polynucleotides comprising the nucleic acid sequences of the primers and probes provided herein are also encompassed herein. In one embodiment, the isolated polynucleotide comprises a polynucleotide capable of detecting a marker locus of the soybean genome comprising: (a) S07160-1, or a marker closely linked thereto on linkage group A2; or (b) Gm08:8300131, Gm08:8257778, Gm08:8257785, Gm08:8258163, Gm08:8258688, Gm08:8258742, Gm08:8259928, Gm08:8260451, Gm08:8260590, Gm08:8261480, Gm08:8261684, Gm08:8262165, Gm08:8263213, Gm08:8263250, Gm08:8263611, Gm08:8264149, Gm08:8265227, Gm08:8265364, Gm08:8265614, Gm08:8266183, Gm08:8266185, Gm08:8266263, Gm08:8266350, Gm08:8266386, Gm08:8266473, Gm08:8266888, Gm08:8267085, Gm08:8267166, Gm08:8267721, Gm08:8267826, Gm08:8268336, Gm08:8268861, Gm08:8269148, Gm08:8269785, Gm08:8270037, Gm08:8270562, Gm08:8270652, Gm08:8271540, Gm08:8271591, Gm08:8271649, Gm08:8271672, Gm08:8271955, Gm08:8273257, Gm08:8273355, Gm08:8273979, Gm08:8275766, Gm08:8275780, Gm08:8275959, Gm08:8276701, Gm08:8276849, Gm08:8276913, Gm08:8277162, Gm08:8277227, Gm08:8277248, Gm08:8277381, Gm08:8277383, Gm08:8277542, Gm08:8277625, Gm08:8277643, Gm08:8277876, Gm08:8277880, Gm08:8277969, Gm08:8278001, Gm08:8278167, Gm08:8278274, Gm08:8278434, Gm08:8279165, Gm08:8279230, Gm08:8279854, Gm08:8280901, Gm08:8280937, Gm08:8281564, Gm08:8282902, Gm08:8284027, Gm08:8286864, Gm08:8287265, Gm08:8287278, Gm08:8287453, Gm08:8287459, Gm08:8288039, Gm08:8288141, Gm08:8288200, Gm08:8288470, Gm08:8288831, Gm08:8289392, Gm08:8290740, Gm08:8291682, Gm08:8292207, Gm08:8297064, Gm08:8299433, Gm08:8299672, Gm08:8301839, Gm08:8302134, Gm08:8303450, Gm08:8305237, Gm08:8305348, Gm08:8305905, Gm08:8306090, Gm08:8306141, Gm08:8306210, Gm08:8306492, Gm08:8306627, Gm08:8307172, Gm08:8307665, Gm08:8308019, Gm08:8308891, Gm08:8308917, Gm08:8309316, Gm08:8309423, Gm08:8309837, Gm08:8310383, Gm08:8310464, Gm08:8310503, Gm08:8310663, Gm08:8311631, Gm08:8311906, Gm08:8312536, Gm08:8312819, Gm08:8313273, Gm08:8313923, Gm08:8314010, Gm08:8314025, Gm08:8314208, Gm08:8314292, Gm08:8314295, Gm08:8314513, Gm08:8314736, Gm08:8314791, Gm08:8314860, Gm08:8315543, Gm08:8315644, Gm08:8316113, Gm08:8316689, Gm08:8316899, Gm08:8317852, Gm08:8317861, Gm08:8318033, Gm08:8319087, Gm08:8319642, Gm08:8319647, Gm08:8320068, Gm08:8321253, Gm08:8321649, Gm08:8323937, Gm08:8324341, Gm08:8325127, Gm08:8325214, Gm08:8326696, Gm08:8326877, Gm08:8328633, Gm08:8330929, Gm08:8331132, Gm08:8331181, Gm08:8331408, Gm08:8331827, Gm08:8332651, Gm08:8332685, Gm08:8332957, Gm08:8343167, Gm08:8345187, Gm08:8345720, Gm08:8346030, Gm08:8346050, Gm08:8346352, Gm08:8346726, Gm08:8347799, Gm08:8348022, Gm08:8348028, Gm08:8349925, Gm08:8350122, Gm08:8350277, Gm08:8351061, Gm08:8351503, Gm08:8352313, Gm08:8352743, Gm08:8353341, Gm08:8355175, Gm08:8360133, Gm08:8363193, Gm08:8363888, Gm08:8364195 or a marker closely linked thereto.
  • In specific embodiments, the isolated polynucleotide comprises: (a) a polynucleotide comprising SEQ ID NOS: 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10; (c) a polynucleotide having at least 90% sequence identity to SEQ ID NOs: 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10; or (d) a polynucleotide comprising at least 10 contiguous nucleotides of SEQ ID NOs: 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10.
  • In certain embodiments, the isolated nucleic acids are capable of hybridizing under stringent conditions to nucleic acids of a soybean cultivar resistant to soybean cyst nematode, for instance to particular SNPs that comprise a marker locus, haplotype or marker profile.
  • As used herein, a substantially identical or complementary sequence is a polynucleotide that will specifically hybridize to the complement of the nucleic acid molecule to which it is being compared under high stringency conditions. A polynucleotide is said to be the “complement” of another polynucleotide if they exhibit complementarity. As used herein, molecules are said to exhibit “complete complementarity” when every nucleotide of one of the polynucleotide molecules is complementary to a nucleotide of the other. Two molecules are said to be “minimally complementary” if they can hybridize to one another with sufficient stability to permit them to remain annealed to one another under at least conventional “low-stringency” conditions. Similarly, the molecules are said to be “complementary” if they can hybridize to one another with sufficient stability to permit them to remain annealed to one another under conventional “high-stringency” conditions.
  • Appropriate stringency conditions which promote DNA hybridization, for example, 6× sodium chloride/sodium citrate (SSC) at about 45° C., followed by a wash of 2×SSC at 50° C., are known to those skilled in the art or can be found in Current Protocols in Molecular Biology, John Wiley & Sons, N.Y. (1989), 6.3.1-6.3.6. Typically, stringent conditions for hybridization and detection will be those in which the salt concentration is less than about 1.5 M Na ion, typically about 0.01 to 1.0 M Na ion concentration (or other salts) at pH 7.0 to 8.3 and the temperature is at least about 30° C. for short probes (e.g., 10 to 50 nucleotides) and at least about 60° C. for long probes (e.g., greater than 50 nucleotides). Stringent conditions may also be achieved with the addition of destabilizing agents such as formamide. Exemplary low stringency conditions include hybridization with a buffer solution of 30 to 35% formamide, 1 M NaCl, 1% SDS (sodium dodecyl sulphate) at 37° C., and a wash in 1× to 2×SSC (20×SSC=3.0 M NaCl/0.3 M trisodium citrate) at 50 to 55° C. Exemplary moderate stringency conditions include hybridization in 40 to 45% formamide, 1.0 M NaCl, 1% SDS at 37° C., and a wash in 0.5× to 1×SSC at 55 to 60° C. Exemplary high stringency conditions include hybridization in 50% formamide, 1 M NaCl, 1% SDS at 37° C., and a wash in 0.1×SSC at 60 to 65° C. Optionally, wash buffers may comprise about 0.1% to about 1% SDS. Duration of hybridization is generally less than about 24 hours, usually about 4 to about 12 hours. The duration of the wash time will be at least a length of time sufficient to reach equilibrium.
  • Non-limiting examples of methods and compositions disclosed herein are as follows:
  • 1. A method of identifying a first soybean plant or a first soybean germplasm that displays resistance or improved resistance to soybean cyst nematode, the method comprising detecting in the genome of said first soybean plant or in the genome of said first soybean germplasm at least one marker locus that is associated with the resistance, wherein the at least one marker locus comprises (a) S07160-1 or a marker closely linked thereto on linkage group A2; or (b) Gm08:8300131, Gm08:8257778, Gm08:8257785, Gm08:8258163, Gm08:8258688, Gm08:8258742, Gm08:8259928, Gm08:8260451, Gm08:8260590, Gm08:8261480, Gm08:8261684, Gm08:8262165, Gm08:8263213, Gm08:8263250, Gm08:8263611, Gm08:8264149, Gm08:8265227, Gm08:8265364, Gm08:8265614, Gm08:8266183, Gm08:8266185, Gm08:8266263, Gm08:8266350, Gm08:8266386, Gm08:8266473, Gm08:8266888, Gm08:8267085, Gm08:8267166, Gm08:8267721, Gm08:8267826, Gm08:8268336, Gm08:8268861, Gm08:8269148, Gm08:8269785, Gm08:8270037, Gm08:8270562, Gm08:8270652, Gm08:8271540, Gm08:8271591, Gm08:8271649, Gm08:8271672, Gm08:8271955, Gm08:8273257, Gm08:8273355, Gm08:8273979, Gm08:8275766, Gm08:8275780, Gm08:8275959, Gm08:8276701, Gm08:8276849, Gm08:8276913, Gm08:8277162, Gm08:8277227, Gm08:8277248, Gm08:8277381, Gm08:8277383, Gm08:8277542, Gm08:8277625, Gm08:8277643, Gm08:8277876, Gm08:8277880, Gm08:8277969, Gm08:8278001, Gm08:8278167, Gm08:8278274, Gm08:8278434, Gm08:8279165, Gm08:8279230, Gm08:8279854, Gm08:8280901, Gm08:8280937, Gm08:8281564, Gm08:8282902, Gm08:8284027, Gm08:8286864, Gm08:8287265, Gm08:8287278, Gm08:8287453, Gm08:8287459, Gm08:8288039, Gm08:8288141, Gm08:8288200, Gm08:8288470, Gm08:8288831, Gm08:8289392, Gm08:8290740, Gm08:8291682, Gm08:8292207, Gm08:8297064, Gm08:8299433, Gm08:8299672, Gm08:8301839, Gm08:8302134, Gm08:8303450, Gm08:8305237, Gm08:8305348, Gm08:8305905, Gm08:8306090, Gm08:8306141, Gm08:8306210, Gm08:8306492, Gm08:8306627, Gm08:8307172, Gm08:8307665, Gm08:8308019, Gm08:8308891, Gm08:8308917, Gm08:8309316, Gm08:8309423, Gm08:8309837, Gm08:8310383, Gm08:8310464, Gm08:8310503, Gm08:8310663, Gm08:8311631, Gm08:8311906, Gm08:8312536, Gm08:8312819, Gm08:8313273, Gm08:8313923, Gm08:8314010, Gm08:8314025, Gm08:8314208, Gm08:8314292, Gm08:8314295, Gm08:8314513, Gm08:8314736, Gm08:8314791, Gm08:8314860, Gm08:8315543, Gm08:8315644, Gm08:8316113, Gm08:8316689, Gm08:8316899, Gm08:8317852, Gm08:8317861, Gm08:8318033, Gm08:8319087, Gm08:8319642, Gm08:8319647, Gm08:8320068, Gm08:8321253, Gm08:8321649, Gm08:8323937, Gm08:8324341, Gm08:8325127, Gm08:8325214, Gm08:8326696, Gm08:8326877, Gm08:8328633, Gm08:8330929, Gm08:8331132, Gm08:8331181, Gm08:8331408, Gm08:8331827, Gm08:8332651, Gm08:8332685, Gm08:8332957, Gm08:8343167, Gm08:8345187, Gm08:8345720, Gm08:8346030, Gm08:8346050, Gm08:8346352, Gm08:8346726, Gm08:8347799, Gm08:8348022, Gm08:8348028, Gm08:8349925, Gm08:8350122, Gm08:8350277, Gm08:8351061, Gm08:8351503, Gm08:8352313, Gm08:8352743, Gm08:8353341, Gm08:8355175, Gm08:8360133, Gm08:8363193, Gm08:8363888, Gm08:8364195 or a marker closely linked thereto.
    2. The method of embodiment 1, wherein at least two marker loci are detected.
    3. The method of embodiment 2, wherein the at least two marker loci comprise a haplotype that is associated with said resistance.
    4. The method of embodiment 1, wherein the germplasm is a soybean variety.
    5. The method of embodiment 1, wherein the method further comprises selecting the first soybean plant or first soybean germplasm or a progeny thereof having the at least one marker locus.
    6. The method of embodiment 5, further comprising crossing the selected first soybean plant or first soybean germplasm with a second soybean plant or second soybean germplasm.
    7. The method of embodiment 6, wherein the second soybean plant or second soybean germplasm comprises an exotic soybean strain or an elite soybean strain.
    8. The method of embodiment 1, wherein the detecting comprises DNA sequencing of at least one of said marker loci.
    9. The method of embodiment 1, wherein the detecting comprises amplifying at least one of said marker loci and detecting the resulting amplified marker amplicon.
    10. The method of embodiment 9, wherein the amplifying comprises:
    (a) admixing an amplification primer or amplification primer pair for each marker locus being amplified with a nucleic acid isolated from the first soybean plant or the first soybean germplasm, wherein the primer or primer pair is complementary or partially complementary to a variant or fragment of the genomic locus comprising the marker locus, and is capable of initiating DNA polymerization by a DNA polymerase using the soybean nucleic acid as a template; and (b) extending the primer or primer pair in a DNA polymerization reaction comprising a DNA polymerase and a template nucleic acid to generate at least one amplicon.
    11. The method of embodiment 10, wherein said method comprises amplifying a variant or fragment of one or more polynucleotides comprising SEQ ID NOs: 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, 100, 101, 102, 103, 104, 105, 106, 107, 108, 109, 110, 111, 112, 113, 114, 115, 116, 117, 118, 119, 120, 121, 122, 123, 124, 125, 126, 127, 128, 129, 130, 131, 132, 133, 134, 135, 136, 137, 138, 139, 140, 141, 142, 143, 144, 145, 146, 147, 148, 149, 150, 151, 152, 153, 154, 155, 156, 157, 158, 159, 160, 161, 162, 163, 164, 165, 166, 167, 168, 169, 170, 171, 172, 173, 174, 175, 176, 177, 178, 179, 180, 181, 182, 183, 184, 185, 186, 187, 188, 189, 190, 191, 192, 193, 194, 195, 196, 197, 198, 199, 200, 201, 202, 203, 204, 205, 206, 207, 208, 209, 210, 211, 212, 213, 214, 215, 216, 217, 218, 219, 220, 221, 222, 223, 224, 225, 226, 227, 228, 229, 230, 231, 232, 233, 234, 235, 236, 237, 238, 239, 240, 241, 242, 243, 244, 245, 246, 247, 248, 249, 250, 251, 252, 253, 254, 255, 256, 257, 258, 259, 260, 261, 262, 263, 264, 265, 266, 267, 268, 269, 270, 271, 272, 273, 274, 275, 276, 277, 278, 279, 280, 281, 282, 283, 284, 285, 286, 287, 288, 289, 290, 291, 292, 293, 294, 295, 296, 297, 298, 299, 300, 301, 302, 303, 304, 305, 306, 307, 308, 309, 310, 311, 312, 313, 314, 315, 316, 317, 318, 319, 320, 321, 322, 323, 324, 325, 326, 327, 328, 329, 330, 331, 332, 333, 334, 335, 336, 337, 338, 339, 340, 341, 342, 343, 344, 345, 346, 347, 348, 349, 350, 351, 352, 353, 354, 355, 356, 357, 358, 359, 360, 361, 362, 363, 364, 365, 366, 367, 368, 369, 370, 371, 372, 373, 374, 375, 376, 377, 378, 379 or 380.
    12. The method of embodiment 10, wherein said primer or primer pair comprises a variant or fragment of one or more polynucleotides comprising SEQ ID NOs: 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, 100, 101, 102, 103, 104, 105, 106, 107, 108, 109, 110, 111, 112, 113, 114, 115, 116, 117, 118, 119, 120, 121, 122, 123, 124, 125, 126, 127, 128, 129, 130, 131, 132, 133, 134, 135, 136, 137, 138, 139, 140, 141, 142, 143, 144, 145, 146, 147, 148, 149, 150, 151, 152, 153, 154, 155, 156, 157, 158, 159, 160, 161, 162, 163, 164, 165, 166, 167, 168, 169, 170, 171, 172, 173, 174, 175, 176, 177, 178, 179, 180, 181, 182, 183, 184, 185, 186, 187, 188, 189, 190, 191, 192, 193, 194, 195, 196, 197, 198, 199, 200, 201, 202, 203, 204, 205, 206, 207, 208, 209, 210, 211, 212, 213, 214, 215, 216, 217, 218, 219, 220, 221, 222, 223, 224, 225, 226, 227, 228, 229, 230, 231, 232, 233, 234, 235, 236, 237, 238, 239, 240, 241, 242, 243, 244, 245, 246, 247, 248, 249, 250, 251, 252, 253, 254, 255, 256, 257, 258, 259, 260, 261, 262, 263, 264, 265, 266, 267, 268, 269, 270, 271, 272, 273, 274, 275, 276, 277, 278, 279, 280, 281, 282, 283, 284, 285, 286, 287, 288, 289, 290, 291, 292, 293, 294, 295, 296, 297, 298, 299, 300, 301, 302, 303, 304, 305, 306, 307, 308, 309, 310, 311, 312, 313, 314, 315, 316, 317, 318, 319, 320, 321, 322, 323, 324, 325, 326, 327, 328, 329, 330, 331, 332, 333, 334, 335, 336, 337, 338, 339, 340, 341, 342, 343, 344, 345, 346, 347, 348, 349, 350, 351, 352, 353, 354, 355, 356, 357, 358, 359, 360, 361, 362, 363, 364, 365, 366, 367, 368, 369, 370, 371, 372, 373, 374, 375, 376, 377, 378, 379, 380 or complements thereof.
    13. The method of embodiment 12, wherein said primer or primer pair comprises a nucleic acid sequence comprising SEQ ID NOs: 1, 2, 3, 4, 5, 6, 7, 8 or variants or fragments thereof.
    14. The method of embodiment 13, wherein said primer pair comprises SEQ ID NO: 1 and SEQ ID NO: 2.
    15. The method of embodiment 10, wherein the method further comprises providing one or more labeled nucleic acid probes suitable for detection of each marker locus being amplified.
    16. The method of embodiment 15, wherein said labeled nucleic acid probe comprises a nucleic acid sequence comprising a variant or fragment of one or more polynucleotides comprising SEQ ID NOs: 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, 100, 101, 102, 103, 104, 105, 106, 107, 108, 109, 110, 111, 112, 113, 114, 115, 116, 117, 118, 119, 120, 121, 122, 123, 124, 125, 126, 127, 128, 129, 130, 131, 132, 133, 134, 135, 136, 137, 138, 139, 140, 141, 142, 143, 144, 145, 146, 147, 148, 149, 150, 151, 152, 153, 154, 155, 156, 157, 158, 159, 160, 161, 162, 163, 164, 165, 166, 167, 168, 169, 170, 171, 172, 173, 174, 175, 176, 177, 178, 179, 180, 181, 182, 183, 184, 185, 186, 187, 188, 189, 190, 191, 192, 193, 194, 195, 196, 197, 198, 199, 200, 201, 202, 203, 204, 205, 206, 207, 208, 209, 210, 211, 212, 213, 214, 215, 216, 217, 218, 219, 220, 221, 222, 223, 224, 225, 226, 227, 228, 229, 230, 231, 232, 233, 234, 235, 236, 237, 238, 239, 240, 241, 242, 243, 244, 245, 246, 247, 248, 249, 250, 251, 252, 253, 254, 255, 256, 257, 258, 259, 260, 261, 262, 263, 264, 265, 266, 267, 268, 269, 270, 271, 272, 273, 274, 275, 276, 277, 278, 279, 280, 281, 282, 283, 284, 285, 286, 287, 288, 289, 290, 291, 292, 293, 294, 295, 296, 297, 298, 299, 300, 301, 302, 303, 304, 305, 306, 307, 308, 309, 310, 311, 312, 313, 314, 315, 316, 317, 318, 319, 320, 321, 322, 323, 324, 325, 326, 327, 328, 329, 330, 331, 332, 333, 334, 335, 336, 337, 338, 339, 340, 341, 342, 343, 344, 345, 346, 347, 348, 349, 350, 351, 352, 353, 354, 355, 356, 357, 358, 359, 360, 361, 362, 363, 364, 365, 366, 367, 368, 369, 370, 371, 372, 373, 374, 375, 376, 377, 378, 379, 380 or complements thereof.
    17. The method of embodiment 16, wherein the labeled nucleic acid probe comprises a nucleic acid sequence comprising SEQ ID NOs: 9 or 10.
    18. An isolated polynucleotide capable of detecting a marker locus of the soybean genome comprising (a) S07160-1 or a marker closely linked thereto on linkage group A2; or (b) Gm08:8300131, Gm08:8257778, Gm08:8257785, Gm08:8258163, Gm08:8258688, Gm08:8258742, Gm08:8259928, Gm08:8260451, Gm08:8260590, Gm08:8261480, Gm08:8261684, Gm08:8262165, Gm08:8263213, Gm08:8263250, Gm08:8263611, Gm08:8264149, Gm08:8265227, Gm08:8265364, Gm08:8265614, Gm08:8266183, Gm08:8266185, Gm08:8266263, Gm08:8266350, Gm08:8266386, Gm08:8266473, Gm08:8266888, Gm08:8267085, Gm08:8267166, Gm08:8267721, Gm08:8267826, Gm08:8268336, Gm08:8268861, Gm08:8269148, Gm08:8269785, Gm08:8270037, Gm08:8270562, Gm08:8270652, Gm08:8271540, Gm08:8271591, Gm08:8271649, Gm08:8271672, Gm08:8271955, Gm08:8273257, Gm08:8273355, Gm08:8273979, Gm08:8275766, Gm08:8275780, Gm08:8275959, Gm08:8276701, Gm08:8276849, Gm08:8276913, Gm08:8277162, Gm08:8277227, Gm08:8277248, Gm08:8277381, Gm08:8277383, Gm08:8277542, Gm08:8277625, Gm08:8277643, Gm08:8277876, Gm08:8277880, Gm08:8277969, Gm08:8278001, Gm08:8278167, Gm08:8278274, Gm08:8278434, Gm08:8279165, Gm08:8279230, Gm08:8279854, Gm08:8280901, Gm08:8280937, Gm08:8281564, Gm08:8282902, Gm08:8284027, Gm08:8286864, Gm08:8287265, Gm08:8287278, Gm08:8287453, Gm08:8287459, Gm08:8288039, Gm08:8288141, Gm08:8288200, Gm08:8288470, Gm08:8288831, Gm08:8289392, Gm08:8290740, Gm08:8291682, Gm08:8292207, Gm08:8297064, Gm08:8299433, Gm08:8299672, Gm08:8301839, Gm08:8302134, Gm08:8303450, Gm08:8305237, Gm08:8305348, Gm08:8305905, Gm08:8306090, Gm08:8306141, Gm08:8306210, Gm08:8306492, Gm08:8306627, Gm08:8307172, Gm08:8307665, Gm08:8308019, Gm08:8308891, Gm08:8308917, Gm08:8309316, Gm08:8309423, Gm08:8309837, Gm08:8310383, Gm08:8310464, Gm08:8310503, Gm08:8310663, Gm08:8311631, Gm08:8311906, Gm08:8312536, Gm08:8312819, Gm08:8313273, Gm08:8313923, Gm08:8314010, Gm08:8314025, Gm08:8314208, Gm08:8314292, Gm08:8314295, Gm08:8314513, Gm08:8314736, Gm08:8314791, Gm08:8314860, Gm08:8315543, Gm08:8315644, Gm08:8316113, Gm08:8316689, Gm08:8316899, Gm08:8317852, Gm08:8317861, Gm08:8318033, Gm08:8319087, Gm08:8319642, Gm08:8319647, Gm08:8320068, Gm08:8321253, Gm08:8321649, Gm08:8323937, Gm08:8324341, Gm08:8325127, Gm08:8325214, Gm08:8326696, Gm08:8326877, Gm08:8328633, Gm08:8330929, Gm08:8331132, Gm08:8331181, Gm08:8331408, Gm08:8331827, Gm08:8332651, Gm08:8332685, Gm08:8332957, Gm08:8343167, Gm08:8345187, Gm08:8345720, Gm08:8346030, Gm08:8346050, Gm08:8346352, Gm08:8346726, Gm08:8347799, Gm08:8348022, Gm08:8348028, Gm08:8349925, Gm08:8350122, Gm08:8350277, Gm08:8351061, Gm08:8351503, Gm08:8352313, Gm08:8352743, Gm08:8353341, Gm08:8355175, Gm08:8360133, Gm08:8363193, Gm08:8363888, Gm08:8364195 or a marker closely linked thereto.
    19. The isolated polynucleotide of embodiment 18, wherein the polynucleotide comprises: (a) a polynucleotide comprising SEQ ID NOs: 1, 2, 3, 4, 5, 6, 7, or 8; (b) a polynucleotide comprising SEQ ID NOs: 9 or 10; (c) a polynucleotide having at least 90% sequence identity to the polynucleotides set forth in parts (a) or (b); or (d) a polynucleotide comprising at least 10 contiguous nucleotides of the polynucleotides set forth in parts (a) or (b).
    20. A kit for detecting or selecting at least one soybean plant or soybean germplasm with resistance or improved resistance to soybean cyst nematode, the kit comprising:
    a) primers or probes for detecting one or more marker loci associated with resistance to soybean cyst nematode, wherein the primers or probes are capable of detecting a marker locus comprising (i) S07160-1 or a marker closely linked thereto; or (ii) Gm08:8300131, Gm08:8257778, Gm08:8257785, Gm08:8258163, Gm08:8258688, Gm08:8258742, Gm08:8259928, Gm08:8260451, Gm08:8260590, Gm08:8261480, Gm08:8261684, Gm08:8262165, Gm08:8263213, Gm08:8263250, Gm08:8263611, Gm08:8264149, Gm08:8265227, Gm08:8265364, Gm08:8265614, Gm08:8266183, Gm08:8266185, Gm08:8266263, Gm08:8266350, Gm08:8266386, Gm08:8266473, Gm08:8266888, Gm08:8267085, Gm08:8267166, Gm08:8267721, Gm08:8267826, Gm08:8268336, Gm08:8268861, Gm08:8269148, Gm08:8269785, Gm08:8270037, Gm08:8270562, Gm08:8270652, Gm08:8271540, Gm08:8271591, Gm08:8271649, Gm08:8271672, Gm08:8271955, Gm08:8273257, Gm08:8273355, Gm08:8273979, Gm08:8275766, Gm08:8275780, Gm08:8275959, Gm08:8276701, Gm08:8276849, Gm08:8276913, Gm08:8277162, Gm08:8277227, Gm08:8277248, Gm08:8277381, Gm08:8277383, Gm08:8277542, Gm08:8277625, Gm08:8277643, Gm08:8277876, Gm08:8277880, Gm08:8277969, Gm08:8278001, Gm08:8278167, Gm08:8278274, Gm08:8278434, Gm08:8279165, Gm08:8279230, Gm08:8279854, Gm08:8280901, Gm08:8280937, Gm08:8281564, Gm08:8282902, Gm08:8284027, Gm08:8286864, Gm08:8287265, Gm08:8287278, Gm08:8287453, Gm08:8287459, Gm08:8288039, Gm08:8288141, Gm08:8288200, Gm08:8288470, Gm08:8288831, Gm08:8289392, Gm08:8290740, Gm08:8291682, Gm08:8292207, Gm08:8297064, Gm08:8299433, Gm08:8299672, Gm08:8301839, Gm08:8302134, Gm08:8303450, Gm08:8305237, Gm08:8305348, Gm08:8305905, Gm08:8306090, Gm08:8306141, Gm08:8306210, Gm08:8306492, Gm08:8306627, Gm08:8307172, Gm08:8307665, Gm08:8308019, Gm08:8308891, Gm08:8308917, Gm08:8309316, Gm08:8309423, Gm08:8309837, Gm08:8310383, Gm08:8310464, Gm08:8310503, Gm08:8310663, Gm08:8311631, Gm08:8311906, Gm08:8312536, Gm08:8312819, Gm08:8313273, Gm08:8313923, Gm08:8314010, Gm08:8314025, Gm08:8314208, Gm08:8314292, Gm08:8314295, Gm08:8314513, Gm08:8314736, Gm08:8314791, Gm08:8314860, Gm08:8315543, Gm08:8315644, Gm08:8316113, Gm08:8316689, Gm08:8316899, Gm08:8317852, Gm08:8317861, Gm08:8318033, Gm08:8319087, Gm08:8319642, Gm08:8319647, Gm08:8320068, Gm08:8321253, Gm08:8321649, Gm08:8323937, Gm08:8324341, Gm08:8325127, Gm08:8325214, Gm08:8326696, Gm08:8326877, Gm08:8328633, Gm08:8330929, Gm08:8331132, Gm08:8331181, Gm08:8331408, Gm08:8331827, Gm08:8332651, Gm08:8332685, Gm08:8332957, Gm08:8343167, Gm08:8345187, Gm08:8345720, Gm08:8346030, Gm08:8346050, Gm08:8346352, Gm08:8346726, Gm08:8347799, Gm08:8348022, Gm08:8348028, Gm08:8349925, Gm08:8350122, Gm08:8350277, Gm08:8351061, Gm08:8351503, Gm08:8352313, Gm08:8352743, Gm08:8353341, Gm08:8355175, Gm08:8360133, Gm08:8363193, Gm08:8363888, Gm08:8364195 or a marker closely linked thereto; and b) instructions for using the primers or probes for detecting the one or more marker loci and correlating the detected marker loci with predicted resistance to soybean cyst nematode.
    • EXPERIMENTAL
  • The following examples are offered to illustrate, but not to limit the claimed invention. It is understood that the examples and embodiments described herein are for illustrative purposes only, and persons skilled in the art will recognize various reagents or parameters that can be altered without departing from the spirit of the invention or the scope of the appended claims.
    • Example 1 Marker Loci Associated with Soybean Cyst Nematode Resistance on Linkage Group A2
  • A SNP marker for the Rhg4 locus (Soybean Cyst Nematode Resistance) on Linkage Group A2 was developed for use in high throughput genotype screening, this marker, as well as markers genetically associated to this marker, are provided. Markers from this region are relevant to elite breeding populations and facilitate selection of soybean plants with resistance to SCN at the Rhg4 locus tracing back to PI437654 and Peking as well as stacks with other marker assisted traits, including yield genes.
  • S07160-1-Q1 was developed and optimized for high throughput PCR-based methods, such as Taqman™ assays. Optimization involved evaluation of amplification, Res, Sus, and heterozygous clustering, primer length, primer composition and the like. The marker distinguishes between the resistant allele from P1437654 or Peking (C) and a susceptible allele from BSR101 (A). Primers and probes useful for detecting the polymorphism are summarized below in Tables 6 and 7, respectively.
  • TABLE 6 
    Primers
    Oligo Product
    Primers: ID Sequence Size
    Primer 1 136868 TGTGTTGTGTTTGACTGCCATA
    (SEQ ID NO: 1)
    Primer 2 136869 CATTTCCCAAGCCTCTTGAT 117 bp
    (SEQ ID NO: 2)
  • TABLE 7 
    Probes
    Probes: Sequence
    102389 6FAM-ACTAACTGCATAaGATAT (SEQ ID NO: 9)
    102390 VIC-CTAACTGCATAcGATATT (SEQ ID NO: 10)
  • The marker was validated against a panel of 31 public or proprietary soybean lines comprising 2 resistant check lines, 27 susceptible lines, and 2 other lines. A summary of the rhg4 marker is provided below in Table 8.
  • Exemplary Amplification Mix
    H20 4.28 ul
    Hot Tub buffer 0.5 ul
    Rox Dye (50X) 0.075 ul
    DNTPs(24 mM each) 0.039 ul
    Primer(100 uM) 0.0375 ul
    Primer(100 uM) 0.0375 ul
    FAM Probe(100 uM 0.005 ul
    VIC Probe(100 uM 0.005 ul
    Hot Tub enzyme 0.025 ul
    Total volume 5.005 ul
  • TABLE 8
    Summary of rhg4 marker.
    Genetic
    Position Physical Pos_PHI
    Gene/ (genetic map); Map Allele Public Consensus
    locus Markers LG GmConsensus 4.0 Position (R/S) Source Name Map v1.1
    rhg4 S07160-1 A2 46.68 8300131 C/A Peking, pBLT65 51.42
    PI437654
    R = Resistant; S = Susceptible
    • Example 2 Identification of SNPs in Linkage Disequilibrium with Known Mutations at the Rhg4 Locus SUMMARY
  • The Rhg4 locus, which conditions resistance to soybean cyst nematode, has been cloned and found to encode a serine hydroxymethyltransferase (Liu et al. (2012). A soybean cyst nematode resistance gene points to a new mechanism of plant resistance to pathogens. Nature 492, 256-260). Two non-synonymous base substitutions that tightly correlate with SCN resistance were identified in the Rhg4 allele from the resistant source Forrest (Liu et al. Nature, 2012). Using SNP genotype data obtained from re-sequencing 385 Pioneer proprietary elite lines, 181 SNPs were identified that are in high linkage disequilibrium with the described mutations. These SNPs can be used for a variety of plant breeding efforts, including marker assisted selection of the Rhg4 locus.
    • Methods:
  • Linkage Disequilibrium was calculated using Haploview 4.2. 7810 SNP loci were evaluated across 385 elite lines. An interval of ˜1.2 mb or 6.5 cM (Gm08:7800225-8999989 bp; 48.26-54.80 cM) spanning the Rhg4 mutations was interrogated for SNP selection. An r2 above or equal to 0.8 is considered high for this analysis. Haploview settings were set as follows: Ignore Pairwise comparisons: >100 kb; HW p-value cutoff: 0.000; Min genotype %: 50; Max # mendel errors: 1; Min Minor Allele Frequency=0.01.
    • Results
  • The 181 Rhg4 SNPs in Linkage Disequilibrium with the described mutations (Liu et al. Nature, 2012) are summarized in Table 3B.
  • TABLE 9
    Summary of SEQ ID NOs.
    SEQ ID
    NO Description
    1 Primer 136868
    2 Primer 136869
    3 Primer 100532
    4 Primer 80588
    5 Primer 136870
    6 Primer 136871
    7 Primer 136872
    8 Primer 136873
    9 Probe 102389
    10 Probe 102390
    11 Amplicon comprising resistance allele
    12 Amplicon comprising susceptible allele
    13 Reference Sequence comprising S07160-1 resistance allele
    14 Reference Sequence comprising S07160-1 susceptible allele
    15-380 Consensus Reference Sequences comprising the various
    marker loci provided herein (see Table 3B)
  • All publications and patent applications mentioned in the specification are indicative of the level of those skilled in the art to which this invention pertains. All publications and patent applications are herein incorporated by reference to the same extent as if each individual publication or patent application was specifically and individually indicated to be incorporated by reference.
  • Although the foregoing invention has been described in some detail by way of illustration and example for purposes of clarity of understanding, it will be obvious that certain changes and modifications may be practiced within the scope of the appended claims.

Claims (20)

That which is claimed:
1. A method of identifying a first soybean plant or a first soybean germplasm that displays resistance or improved resistance to soybean cyst nematode, the method comprising detecting in the genome of said first soybean plant or in the genome of said first soybean germplasm at least one marker locus that is associated with the resistance, wherein the at least one marker locus comprises
(a) S07160-1 or a marker closely linked thereto on linkage group A2; or
(b) Gm08:8300131, Gm08:8257778, Gm08:8257785, Gm08:8258163, Gm08:8258688, Gm08:8258742, Gm08:8259928, Gm08:8260451, Gm08:8260590, Gm08:8261480, Gm08:8261684, Gm08:8262165, Gm08:8263213, Gm08:8263250, Gm08:8263611, Gm08:8264149, Gm08:8265227, Gm08:8265364, Gm08:8265614, Gm08:8266183, Gm08:8266185, Gm08:8266263, Gm08:8266350, Gm08:8266386, Gm08:8266473, Gm08:8266888, Gm08:8267085, Gm08:8267166, Gm08:8267721, Gm08:8267826, Gm08:8268336, Gm08:8268861, Gm08:8269148, Gm08:8269785, Gm08:8270037, Gm08:8270562, Gm08:8270652, Gm08:8271540, Gm08:8271591, Gm08:8271649, Gm08:8271672, Gm08:8271955, Gm08:8273257, Gm08:8273355, Gm08:8273979, Gm08:8275766, Gm08:8275780, Gm08:8275959, Gm08:8276701, Gm08:8276849, Gm08:8276913, Gm08:8277162, Gm08:8277227, Gm08:8277248, Gm08:8277381, Gm08:8277383, Gm08:8277542, Gm08:8277625, Gm08:8277643, Gm08:8277876, Gm08:8277880, Gm08:8277969, Gm08:8278001, Gm08:8278167, Gm08:8278274, Gm08:8278434, Gm08:8279165, Gm08:8279230, Gm08:8279854, Gm08:8280901, Gm08:8280937, Gm08:8281564, Gm08:8282902, Gm08:8284027, Gm08:8286864, Gm08:8287265, Gm08:8287278, Gm08:8287453, Gm08:8287459, Gm08:8288039, Gm08:8288141, Gm08:8288200, Gm08:8288470, Gm08:8288831, Gm08:8289392, Gm08:8290740, Gm08:8291682, Gm08:8292207, Gm08:8297064, Gm08:8299433, Gm08:8299672, Gm08:8301839, Gm08:8302134, Gm08:8303450, Gm08:8305237, Gm08:8305348, Gm08:8305905, Gm08:8306090, Gm08:8306141, Gm08:8306210, Gm08:8306492, Gm08:8306627, Gm08:8307172, Gm08:8307665, Gm08:8308019, Gm08:8308891, Gm08:8308917, Gm08:8309316, Gm08:8309423, Gm08:8309837, Gm08:8310383, Gm08:8310464, Gm08:8310503, Gm08:8310663, Gm08:8311631, Gm08:8311906, Gm08:8312536, Gm08:8312819, Gm08:8313273, Gm08:8313923, Gm08:8314010, Gm08:8314025, Gm08:8314208, Gm08:8314292, Gm08:8314295, Gm08:8314513, Gm08:8314736, Gm08:8314791, Gm08:8314860, Gm08:8315543, Gm08:8315644, Gm08:8316113, Gm08:8316689, Gm08:8316899, Gm08:8317852, Gm08:8317861, Gm08:8318033, Gm08:8319087, Gm08:8319642, Gm08:8319647, Gm08:8320068, Gm08:8321253, Gm08:8321649, Gm08:8323937, Gm08:8324341, Gm08:8325127, Gm08:8325214, Gm08:8326696, Gm08:8326877, Gm08:8328633, Gm08:8330929, Gm08:8331132, Gm08:8331181, Gm08:8331408, Gm08:8331827, Gm08:8332651, Gm08:8332685, Gm08:8332957, Gm08:8343167, Gm08:8345187, Gm08:8345720, Gm08:8346030, Gm08:8346050, Gm08:8346352, Gm08:8346726, Gm08:8347799, Gm08:8348022, Gm08:8348028, Gm08:8349925, Gm08:8350122, Gm08:8350277, Gm08:8351061, Gm08:8351503, Gm08:8352313, Gm08:8352743, Gm08:8353341, Gm08:8355175, Gm08:8360133, Gm08:8363193, Gm08:8363888, Gm08:8364195 or a marker closely linked thereto.
2. The method of claim 1, wherein at least two marker loci are detected.
3. The method of claim 2, wherein the at least two marker loci comprise a haplotype that is associated with said resistance.
4. The method of claim 1, wherein the germplasm is a soybean variety.
5. The method of claim 1, wherein the method further comprises selecting the first soybean plant or first soybean germplasm or a progeny thereof having the at least one marker locus.
6. The method of claim 5, further comprising crossing the selected first soybean plant or first soybean germplasm with a second soybean plant or second soybean germplasm.
7. The method of claim 6, wherein the second soybean plant or second soybean germplasm comprises an exotic soybean strain or an elite soybean strain.
8. The method of claim 1, wherein the detecting comprises DNA sequencing of at least one of said marker loci.
9. The method of claim 1, wherein the detecting comprises amplifying at least one of said marker loci and detecting the resulting amplified marker amplicon.
10. The method of claim 9, wherein the amplifying comprises:
a) admixing an amplification primer or amplification primer pair for each marker locus being amplified with a nucleic acid isolated from the first soybean plant or the first soybean germplasm, wherein the primer or primer pair is complementary or partially complementary to a variant or fragment of the genomic locus comprising the marker locus, and is capable of initiating DNA polymerization by a DNA polymerase using the soybean nucleic acid as a template; and
b) extending the primer or primer pair in a DNA polymerization reaction comprising a DNA polymerase and a template nucleic acid to generate at least one amplicon.
11. The method of claim 10, wherein said method comprises amplifying a variant or fragment of one or more polynucleotides comprising SEQ ID NOs: 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, 100, 101, 102, 103, 104, 105, 106, 107, 108, 109, 110, 111, 112, 113, 114, 115, 116, 117, 118, 119, 120, 121, 122, 123, 124, 125, 126, 127, 128, 129, 130, 131, 132, 133, 134, 135, 136, 137, 138, 139, 140, 141, 142, 143, 144, 145, 146, 147, 148, 149, 150, 151, 152, 153, 154, 155, 156, 157, 158, 159, 160, 161, 162, 163, 164, 165, 166, 167, 168, 169, 170, 171, 172, 173, 174, 175, 176, 177, 178, 179, 180, 181, 182, 183, 184, 185, 186, 187, 188, 189, 190, 191, 192, 193, 194, 195, 196, 197, 198, 199, 200, 201, 202, 203, 204, 205, 206, 207, 208, 209, 210, 211, 212, 213, 214, 215, 216, 217, 218, 219, 220, 221, 222, 223, 224, 225, 226, 227, 228, 229, 230, 231, 232, 233, 234, 235, 236, 237, 238, 239, 240, 241, 242, 243, 244, 245, 246, 247, 248, 249, 250, 251, 252, 253, 254, 255, 256, 257, 258, 259, 260, 261, 262, 263, 264, 265, 266, 267, 268, 269, 270, 271, 272, 273, 274, 275, 276, 277, 278, 279, 280, 281, 282, 283, 284, 285, 286, 287, 288, 289, 290, 291, 292, 293, 294, 295, 296, 297, 298, 299, 300, 301, 302, 303, 304, 305, 306, 307, 308, 309, 310, 311, 312, 313, 314, 315, 316, 317, 318, 319, 320, 321, 322, 323, 324, 325, 326, 327, 328, 329, 330, 331, 332, 333, 334, 335, 336, 337, 338, 339, 340, 341, 342, 343, 344, 345, 346, 347, 348, 349, 350, 351, 352, 353, 354, 355, 356, 357, 358, 359, 360, 361, 362, 363, 364, 365, 366, 367, 368, 369, 370, 371, 372, 373, 374, 375, 376, 377, 378, 379 or 380.
12. The method of claim 10, wherein said primer or primer pair comprises a variant or fragment of one or more polynucleotides comprising SEQ ID NOs: 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, 100, 101, 102, 103, 104, 105, 106, 107, 108, 109, 110, 111, 112, 113, 114, 115, 116, 117, 118, 119, 120, 121, 122, 123, 124, 125, 126, 127, 128, 129, 130, 131, 132, 133, 134, 135, 136, 137, 138, 139, 140, 141, 142, 143, 144, 145, 146, 147, 148, 149, 150, 151, 152, 153, 154, 155, 156, 157, 158, 159, 160, 161, 162, 163, 164, 165, 166, 167, 168, 169, 170, 171, 172, 173, 174, 175, 176, 177, 178, 179, 180, 181, 182, 183, 184, 185, 186, 187, 188, 189, 190, 191, 192, 193, 194, 195, 196, 197, 198, 199, 200, 201, 202, 203, 204, 205, 206, 207, 208, 209, 210, 211, 212, 213, 214, 215, 216, 217, 218, 219, 220, 221, 222, 223, 224, 225, 226, 227, 228, 229, 230, 231, 232, 233, 234, 235, 236, 237, 238, 239, 240, 241, 242, 243, 244, 245, 246, 247, 248, 249, 250, 251, 252, 253, 254, 255, 256, 257, 258, 259, 260, 261, 262, 263, 264, 265, 266, 267, 268, 269, 270, 271, 272, 273, 274, 275, 276, 277, 278, 279, 280, 281, 282, 283, 284, 285, 286, 287, 288, 289, 290, 291, 292, 293, 294, 295, 296, 297, 298, 299, 300, 301, 302, 303, 304, 305, 306, 307, 308, 309, 310, 311, 312, 313, 314, 315, 316, 317, 318, 319, 320, 321, 322, 323, 324, 325, 326, 327, 328, 329, 330, 331, 332, 333, 334, 335, 336, 337, 338, 339, 340, 341, 342, 343, 344, 345, 346, 347, 348, 349, 350, 351, 352, 353, 354, 355, 356, 357, 358, 359, 360, 361, 362, 363, 364, 365, 366, 367, 368, 369, 370, 371, 372, 373, 374, 375, 376, 377, 378, 379, 380 or complements thereof.
13. The method of claim 12, wherein said primer or primer pair comprises a nucleic acid sequence comprising SEQ ID NOs: 1, 2, 3, 4, 5, 6, 7, 8 or variants or fragments thereof.
14. The method of claim 13, wherein said primer pair comprises SEQ ID NO: 1 and SEQ ID NO: 2.
15. The method of claim 10, wherein the method further comprises providing one or more labeled nucleic acid probes suitable for detection of each marker locus being amplified.
16. The method of claim 15, wherein said labeled nucleic acid probe comprises a nucleic acid sequence comprising a variant or fragment of one or more polynucleotides comprising SEQ ID NOs: 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, 100, 101, 102, 103, 104, 105, 106, 107, 108, 109, 110, 111, 112, 113, 114, 115, 116, 117, 118, 119, 120, 121, 122, 123, 124, 125, 126, 127, 128, 129, 130, 131, 132, 133, 134, 135, 136, 137, 138, 139, 140, 141, 142, 143, 144, 145, 146, 147, 148, 149, 150, 151, 152, 153, 154, 155, 156, 157, 158, 159, 160, 161, 162, 163, 164, 165, 166, 167, 168, 169, 170, 171, 172, 173, 174, 175, 176, 177, 178, 179, 180, 181, 182, 183, 184, 185, 186, 187, 188, 189, 190, 191, 192, 193, 194, 195, 196, 197, 198, 199, 200, 201, 202, 203, 204, 205, 206, 207, 208, 209, 210, 211, 212, 213, 214, 215, 216, 217, 218, 219, 220, 221, 222, 223, 224, 225, 226, 227, 228, 229, 230, 231, 232, 233, 234, 235, 236, 237, 238, 239, 240, 241, 242, 243, 244, 245, 246, 247, 248, 249, 250, 251, 252, 253, 254, 255, 256, 257, 258, 259, 260, 261, 262, 263, 264, 265, 266, 267, 268, 269, 270, 271, 272, 273, 274, 275, 276, 277, 278, 279, 280, 281, 282, 283, 284, 285, 286, 287, 288, 289, 290, 291, 292, 293, 294, 295, 296, 297, 298, 299, 300, 301, 302, 303, 304, 305, 306, 307, 308, 309, 310, 311, 312, 313, 314, 315, 316, 317, 318, 319, 320, 321, 322, 323, 324, 325, 326, 327, 328, 329, 330, 331, 332, 333, 334, 335, 336, 337, 338, 339, 340, 341, 342, 343, 344, 345, 346, 347, 348, 349, 350, 351, 352, 353, 354, 355, 356, 357, 358, 359, 360, 361, 362, 363, 364, 365, 366, 367, 368, 369, 370, 371, 372, 373, 374, 375, 376, 377, 378, 379, 380 or complements thereof.
17. The method of claim 16, wherein the labeled nucleic acid probe comprises a nucleic acid sequence comprising SEQ ID NOs: 9 or 10.
18. An isolated polynucleotide capable of detecting a marker locus of the soybean genome comprising
(a) S07160-1 or a marker closely linked thereto on linkage group A2; or
(b) Gm08:8300131, Gm08:8257778, Gm08:8257785, Gm08:8258163, Gm08:8258688, Gm08:8258742, Gm08:8259928, Gm08:8260451, Gm08:8260590, Gm08:8261480, Gm08:8261684, Gm08:8262165, Gm08:8263213, Gm08:8263250, Gm08:8263611, Gm08:8264149, Gm08:8265227, Gm08:8265364, Gm08:8265614, Gm08:8266183, Gm08:8266185, Gm08:8266263, Gm08:8266350, Gm08:8266386, Gm08:8266473, Gm08:8266888, Gm08:8267085, Gm08:8267166, Gm08:8267721, Gm08:8267826, Gm08:8268336, Gm08:8268861, Gm08:8269148, Gm08:8269785, Gm08:8270037, Gm08:8270562, Gm08:8270652, Gm08:8271540, Gm08:8271591, Gm08:8271649, Gm08:8271672, Gm08:8271955, Gm08:8273257, Gm08:8273355, Gm08:8273979, Gm08:8275766, Gm08:8275780, Gm08:8275959, Gm08:8276701, Gm08:8276849, Gm08:8276913, Gm08:8277162, Gm08:8277227, Gm08:8277248, Gm08:8277381, Gm08:8277383, Gm08:8277542, Gm08:8277625, Gm08:8277643, Gm08:8277876, Gm08:8277880, Gm08:8277969, Gm08:8278001, Gm08:8278167, Gm08:8278274, Gm08:8278434, Gm08:8279165, Gm08:8279230, Gm08:8279854, Gm08:8280901, Gm08:8280937, Gm08:8281564, Gm08:8282902, Gm08:8284027, Gm08:8286864, Gm08:8287265, Gm08:8287278, Gm08:8287453, Gm08:8287459, Gm08:8288039, Gm08:8288141, Gm08:8288200, Gm08:8288470, Gm08:8288831, Gm08:8289392, Gm08:8290740, Gm08:8291682, Gm08:8292207, Gm08:8297064, Gm08:8299433, Gm08:8299672, Gm08:8301839, Gm08:8302134, Gm08:8303450, Gm08:8305237, Gm08:8305348, Gm08:8305905, Gm08:8306090, Gm08:8306141, Gm08:8306210, Gm08:8306492, Gm08:8306627, Gm08:8307172, Gm08:8307665, Gm08:8308019, Gm08:8308891, Gm08:8308917, Gm08:8309316, Gm08:8309423, Gm08:8309837, Gm08:8310383, Gm08:8310464, Gm08:8310503, Gm08:8310663, Gm08:8311631, Gm08:8311906, Gm08:8312536, Gm08:8312819, Gm08:8313273, Gm08:8313923, Gm08:8314010, Gm08:8314025, Gm08:8314208, Gm08:8314292, Gm08:8314295, Gm08:8314513, Gm08:8314736, Gm08:8314791, Gm08:8314860, Gm08:8315543, Gm08:8315644, Gm08:8316113, Gm08:8316689, Gm08:8316899, Gm08:8317852, Gm08:8317861, Gm08:8318033, Gm08:8319087, Gm08:8319642, Gm08:8319647, Gm08:8320068, Gm08:8321253, Gm08:8321649, Gm08:8323937, Gm08:8324341, Gm08:8325127, Gm08:8325214, Gm08:8326696, Gm08:8326877, Gm08:8328633, Gm08:8330929, Gm08:8331132, Gm08:8331181, Gm08:8331408, Gm08:8331827, Gm08:8332651, Gm08:8332685, Gm08:8332957, Gm08:8343167, Gm08:8345187, Gm08:8345720, Gm08:8346030, Gm08:8346050, Gm08:8346352, Gm08:8346726, Gm08:8347799, Gm08:8348022, Gm08:8348028, Gm08:8349925, Gm08:8350122, Gm08:8350277, Gm08:8351061, Gm08:8351503, Gm08:8352313, Gm08:8352743, Gm08:8353341, Gm08:8355175, Gm08:8360133, Gm08:8363193, Gm08:8363888, Gm08:8364195 or a marker closely linked thereto.
19. The isolated polynucleotide of claim 18, wherein the polynucleotide comprises:
(a) a polynucleotide comprising SEQ ID NOs: 1, 2, 3, 4, 5, 6, 7, or 8;
(b) a polynucleotide comprising SEQ ID NOs: 9 or 10;
(c) a polynucleotide having at least 90% sequence identity to the polynucleotides set forth in parts (a) or (b); or
(d) a polynucleotide comprising at least 10 contiguous nucleotides of the polynucleotides set forth in parts (a) or (b).
20. A kit for detecting or selecting at least one soybean plant or soybean germplasm with resistance or improved resistance to soybean cyst nematode, the kit comprising:
a) primers or probes for detecting one or more marker loci associated with resistance to soybean cyst nematode, wherein the primers or probes are capable of detecting a marker locus comprising
(i) S07160-1 or a marker closely linked thereto; or
(ii) Gm08:8300131, Gm08:8257778, Gm08:8257785, Gm08:8258163, Gm08:8258688, Gm08:8258742, Gm08:8259928, Gm08:8260451, Gm08:8260590, Gm08:8261480, Gm08:8261684, Gm08:8262165, Gm08:8263213, Gm08:8263250, Gm08:8263611, Gm08:8264149, Gm08:8265227, Gm08:8265364, Gm08:8265614, Gm08:8266183, Gm08:8266185, Gm08:8266263, Gm08:8266350, Gm08:8266386, Gm08:8266473, Gm08:8266888, Gm08:8267085, Gm08:8267166, Gm08:8267721, Gm08:8267826, Gm08:8268336, Gm08:8268861, Gm08:8269148, Gm08:8269785, Gm08:8270037, Gm08:8270562, Gm08:8270652, Gm08:8271540, Gm08:8271591, Gm08:8271649, Gm08:8271672, Gm08:8271955, Gm08:8273257, Gm08:8273355, Gm08:8273979, Gm08:8275766, Gm08:8275780, Gm08:8275959, Gm08:8276701, Gm08:8276849, Gm08:8276913, Gm08:8277162, Gm08:8277227, Gm08:8277248, Gm08:8277381, Gm08:8277383, Gm08:8277542, Gm08:8277625, Gm08:8277643, Gm08:8277876, Gm08:8277880, Gm08:8277969, Gm08:8278001, Gm08:8278167, Gm08:8278274, Gm08:8278434, Gm08:8279165, Gm08:8279230, Gm08:8279854, Gm08:8280901, Gm08:8280937, Gm08:8281564, Gm08:8282902, Gm08:8284027, Gm08:8286864, Gm08:8287265, Gm08:8287278, Gm08:8287453, Gm08:8287459, Gm08:8288039, Gm08:8288141, Gm08:8288200, Gm08:8288470, Gm08:8288831, Gm08:8289392, Gm08:8290740, Gm08:8291682, Gm08:8292207, Gm08:8297064, Gm08:8299433, Gm08:8299672, Gm08:8301839, Gm08:8302134, Gm08:8303450, Gm08:8305237, Gm08:8305348, Gm08:8305905, Gm08:8306090, Gm08:8306141, Gm08:8306210, Gm08:8306492, Gm08:8306627, Gm08:8307172, Gm08:8307665, Gm08:8308019, Gm08:8308891, Gm08:8308917, Gm08:8309316, Gm08:8309423, Gm08:8309837, Gm08:8310383, Gm08:8310464, Gm08:8310503, Gm08:8310663, Gm08:8311631, Gm08:8311906, Gm08:8312536, Gm08:8312819, Gm08:8313273, Gm08:8313923, Gm08:8314010, Gm08:8314025, Gm08:8314208, Gm08:8314292, Gm08:8314295, Gm08:8314513, Gm08:8314736, Gm08:8314791, Gm08:8314860, Gm08:8315543, Gm08:8315644, Gm08:8316113, Gm08:8316689, Gm08:8316899, Gm08:8317852, Gm08:8317861, Gm08:8318033, Gm08:8319087, Gm08:8319642, Gm08:8319647, Gm08:8320068, Gm08:8321253, Gm08:8321649, Gm08:8323937, Gm08:8324341, Gm08:8325127, Gm08:8325214, Gm08:8326696, Gm08:8326877, Gm08:8328633, Gm08:8330929, Gm08:8331132, Gm08:8331181, Gm08:8331408, Gm08:8331827, Gm08:8332651, Gm08:8332685, Gm08:8332957, Gm08:8343167, Gm08:8345187, Gm08:8345720, Gm08:8346030, Gm08:8346050, Gm08:8346352, Gm08:8346726, Gm08:8347799, Gm08:8348022, Gm08:8348028, Gm08:8349925, Gm08:8350122, Gm08:8350277, Gm08:8351061, Gm08:8351503, Gm08:8352313, Gm08:8352743, Gm08:8353341, Gm08:8355175, Gm08:8360133, Gm08:8363193, Gm08:8363888, Gm08:8364195 or a marker closely linked thereto; and
b) instructions for using the primers or probes for detecting the one or more marker loci and correlating the detected marker loci with predicted resistance to soybean cyst nematode.
US13/781,963 2012-12-21 2013-03-01 Genetic loci associated with soybean cyst nematode resistance and methods of use Abandoned US20140178866A1 (en)

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US13/781,963 US20140178866A1 (en) 2012-12-21 2013-03-01 Genetic loci associated with soybean cyst nematode resistance and methods of use
BR112015015057-8A BR112015015057B1 (en) 2012-12-21 2013-12-18 SOYBEAN PLANT IDENTIFICATION METHOD
CA2893975A CA2893975C (en) 2012-12-21 2013-12-18 Genetic loci associated with soybean cyst nematode resistance and methods of use
PCT/US2013/076218 WO2014100229A1 (en) 2012-12-21 2013-12-18 Genetic loci associated with soybean cyst nematode resistance and methods of use
ARP130104971A AR094234A1 (en) 2012-12-21 2013-12-20 GENETIC LOCIES ASSOCIATED WITH THE NEMATOD RESISTANCE OF THE SOY BEAN CYST AND USE METHODS
ZA2015/03068A ZA201503068B (en) 2012-12-21 2015-05-05 Genetic loci associated with soybean cyst nematode resistance and methods of use
US15/001,290 US9994920B2 (en) 2012-12-21 2016-01-20 Genetic loci associated with soybean cyst nematode resistance and methods of use

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111471783A (en) * 2019-01-23 2020-07-31 东北农业大学 Screening method, molecular marker, primer and application of molecular marker linked with soybean cyst nematode resistance locus

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20140178866A1 (en) 2012-12-21 2014-06-26 Pioneer Hi-Bred International, Inc. Genetic loci associated with soybean cyst nematode resistance and methods of use
US11180795B1 (en) 2015-06-02 2021-11-23 Syngenta Participations Ag Nematode resistance alleles in soybean
BR112023002885A2 (en) 2020-08-18 2023-03-21 Pioneer Hi Bred Int MULTIPLE DISEASE RESISTANCE GENES AND THEIR GENOMIC STACKINGS

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030005491A1 (en) * 2000-01-07 2003-01-02 Monsanto Company Nucleic acid molecules and other molecules associated with soybean cyst nematode resistance
US20090241214A1 (en) * 2005-05-18 2009-09-24 Michigan State University Markers For Aphid Resistant Germplasm In Soybean Plants
US20100275286A1 (en) * 2007-05-31 2010-10-28 Monsanto Technology Llc Soybean Polymorphisms And Methods Of Genotyping
US20110083234A1 (en) * 2009-10-02 2011-04-07 Nguyen Henry T Quantitative Trait Loci Associated With Soybean Cyst Nematode Resistance And Methods Of Their Use

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5491081A (en) 1994-01-26 1996-02-13 Pioneer Hi-Bred International, Inc. Soybean cyst nematode resistant soybeans and methods of breeding and identifying resistant plants
US6162967A (en) 1994-01-26 2000-12-19 Pioneer Hi-Bred International, Inc. Positional cloning of soybean cyst nematode resistance genes
AR004095A1 (en) * 1995-10-24 1998-09-30 Pioneer Hi Bred Int METHOD FOR INTRODUCING IN A RELIABLE AND PREDICTABLE RESISTANCE TO THE CYSTIC NEMATODES OF SOYA, IN NON-RESISTANT SOYBEAN GERMPLASM, AND QUANTITATIVE LOCUSCARACTERISTIC ASSOCIATED WITH THE INTRODUCED RESISTANCE THROUGH SUCH A METHOD.
CA2192920A1 (en) 1995-12-15 1997-06-16 Richard A. Vierling Methods for conferring broad-based soybean cyst nematode resistance to asoybean line
US6300541B1 (en) 1997-01-14 2001-10-09 Southern Illinois University Soybean sudden death syndrome resistant soybeans, soybean cyst nematode resistant soybeans and methods of breeding and identifying resistant plants
CA2314992A1 (en) * 1997-12-19 1999-07-01 Pioneer Hi-Bred International, Inc. Nucleotide polymorphisms in soybean
US20020144310A1 (en) 2000-01-28 2002-10-03 Lightfoot David A. Isolated polynucleotides and polypeptides relating to loci underlying resistance to soybean cyst nematode and soybean sudden death syndrome and methods employing same
WO2009048847A1 (en) 2007-10-12 2009-04-16 Monsanto Technology Llc Methods and compositions for high yielding soybeans with nematode resistance
WO2012094529A2 (en) * 2011-01-05 2012-07-12 The Curators Of The University Of Missouri Genes implicated in resistance to soybean cyst nematode infection and methods of their use
US20140178866A1 (en) 2012-12-21 2014-06-26 Pioneer Hi-Bred International, Inc. Genetic loci associated with soybean cyst nematode resistance and methods of use

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030005491A1 (en) * 2000-01-07 2003-01-02 Monsanto Company Nucleic acid molecules and other molecules associated with soybean cyst nematode resistance
US20090241214A1 (en) * 2005-05-18 2009-09-24 Michigan State University Markers For Aphid Resistant Germplasm In Soybean Plants
US20100275286A1 (en) * 2007-05-31 2010-10-28 Monsanto Technology Llc Soybean Polymorphisms And Methods Of Genotyping
US20110083234A1 (en) * 2009-10-02 2011-04-07 Nguyen Henry T Quantitative Trait Loci Associated With Soybean Cyst Nematode Resistance And Methods Of Their Use

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
Batley and Edwards, 2007, In; Association Mapping in Plants, pp 95-102. *
Hyten et al., 2010, Crop Science 50: 960-968. *
Thomas, 1985, J. Opt. Soc. Am. 2: 1457-1467. *
Yue et al., 2000, Euphytica 116: 181-186. *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111471783A (en) * 2019-01-23 2020-07-31 东北农业大学 Screening method, molecular marker, primer and application of molecular marker linked with soybean cyst nematode resistance locus

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