MX363345B - Determinación de genomas fetales para embarazos de múltiples fetos. - Google Patents

Determinación de genomas fetales para embarazos de múltiples fetos.

Info

Publication number
MX363345B
MX363345B MX2015010785A MX2015010785A MX363345B MX 363345 B MX363345 B MX 363345B MX 2015010785 A MX2015010785 A MX 2015010785A MX 2015010785 A MX2015010785 A MX 2015010785A MX 363345 B MX363345 B MX 363345B
Authority
MX
Mexico
Prior art keywords
maternal
inheritance
paternal
loci
haplotype
Prior art date
Application number
MX2015010785A
Other languages
English (en)
Spanish (es)
Other versions
MX2015010785A (es
Inventor
Ming Dennis Lo Yuk
Kwun Rossa Chiu Wai
Chee Chan Kwan
Original Assignee
Univ Hong Kong Chinese
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Univ Hong Kong Chinese filed Critical Univ Hong Kong Chinese
Publication of MX2015010785A publication Critical patent/MX2015010785A/es
Publication of MX363345B publication Critical patent/MX363345B/es

Links

Classifications

    • 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
    • G—PHYSICS
    • G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16B—BIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
    • G16B30/00—ICT specially adapted for sequence analysis involving nucleotides or amino acids
    • G16B30/10—Sequence alignment; Homology search
    • 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
    • C12Q1/6883—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
    • 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
    • G—PHYSICS
    • G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16B—BIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
    • G16B30/00—ICT specially adapted for sequence analysis involving nucleotides or amino acids

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Analytical Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • Genetics & Genomics (AREA)
  • Biophysics (AREA)
  • Biotechnology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Health & Medical Sciences (AREA)
  • Molecular Biology (AREA)
  • Immunology (AREA)
  • Biochemistry (AREA)
  • General Engineering & Computer Science (AREA)
  • Microbiology (AREA)
  • Pathology (AREA)
  • Bioinformatics & Computational Biology (AREA)
  • Evolutionary Biology (AREA)
  • Medical Informatics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Theoretical Computer Science (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Management, Administration, Business Operations System, And Electronic Commerce (AREA)
  • Investigating Or Analysing Biological Materials (AREA)
MX2015010785A 2013-03-15 2014-03-17 Determinación de genomas fetales para embarazos de múltiples fetos. MX363345B (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201361789992P 2013-03-15 2013-03-15
PCT/CN2014/073506 WO2014139477A1 (en) 2013-03-15 2014-03-17 Determining fetal genomes for multiple fetus pregnancies

Publications (2)

Publication Number Publication Date
MX2015010785A MX2015010785A (es) 2015-11-26
MX363345B true MX363345B (es) 2019-03-20

Family

ID=51535879

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2015010785A MX363345B (es) 2013-03-15 2014-03-17 Determinación de genomas fetales para embarazos de múltiples fetos.

Country Status (11)

Country Link
US (1) US10106836B2 (enExample)
EP (2) EP3434790A1 (enExample)
JP (1) JP2016518811A (enExample)
KR (1) KR20150132216A (enExample)
CN (1) CN105121660B (enExample)
AU (1) AU2014231358A1 (enExample)
CA (1) CA2901773A1 (enExample)
EA (1) EA201500939A1 (enExample)
MX (1) MX363345B (enExample)
TW (1) TWI637058B (enExample)
WO (1) WO2014139477A1 (enExample)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
LT3241914T (lt) 2009-11-05 2019-04-25 The Chinese University Of Hong Kong Vaisiaus genomo analizė iš motinos biologinio mėginio
EP3202921B1 (en) 2011-02-24 2019-02-13 The Chinese University of Hong Kong Molecular testing of multiple pregnancies
CN105121660B (zh) 2013-03-15 2018-09-28 香港中文大学 确定多胎妊娠的胎儿基因组
WO2017012544A1 (en) 2015-07-20 2017-01-26 The Chinese University Of Hong Kong Methylation pattern analysis of haplotypes in tissues in dna mixture

Family Cites Families (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9704444D0 (en) 1997-03-04 1997-04-23 Isis Innovation Non-invasive prenatal diagnosis
US6927028B2 (en) 2001-08-31 2005-08-09 Chinese University Of Hong Kong Non-invasive methods for detecting non-host DNA in a host using epigenetic differences between the host and non-host DNA
US7727720B2 (en) 2002-05-08 2010-06-01 Ravgen, Inc. Methods for detection of genetic disorders
EP1599608A4 (en) 2003-03-05 2007-07-18 Genetic Technologies Ltd Identification of fetal DNA and fetal cell marker in maternal plasma or serum
DE60328193D1 (de) 2003-10-16 2009-08-13 Sequenom Inc Nicht invasiver Nachweis fötaler genetischer Merkmale
JP5219516B2 (ja) 2005-03-18 2013-06-26 ザ チャイニーズ ユニバーシティー オブ ホンコン 染色体異数性の検出方法
US20070122823A1 (en) 2005-09-01 2007-05-31 Bianchi Diana W Amniotic fluid cell-free fetal DNA fragment size pattern for prenatal diagnosis
GB0523276D0 (en) 2005-11-15 2005-12-21 London Bridge Fertility Chromosomal analysis by molecular karyotyping
WO2007092473A2 (en) 2006-02-02 2007-08-16 The Board Of Trustees Of The Leland Stanford Junior University Non-invasive fetal genetic screening by digital analysis
SI1996728T1 (sl) 2006-02-28 2011-10-28 Univ Louisville Res Found Prepoznavanje kromosomskih nenormalnosti pri zarodku s pomočjo dvojnih mononukleotidnih polimorfizmov
EP2029779A4 (en) 2006-06-14 2010-01-20 Living Microsystems Inc HIGHLY PARALLEL SNP GENOTYPING UTILIZATION FOR FETAL DIAGNOSIS
US12054776B2 (en) 2007-07-23 2024-08-06 The Chinese University Of Hong Kong Diagnosing fetal chromosomal aneuploidy using massively parallel genomic sequencing
US12180549B2 (en) 2007-07-23 2024-12-31 The Chinese University Of Hong Kong Diagnosing fetal chromosomal aneuploidy using genomic sequencing
CN104732118B (zh) 2008-08-04 2017-08-22 纳特拉公司 等位基因调用和倍性调用的方法
CN104531837A (zh) 2008-12-22 2015-04-22 赛卢拉有限公司 检测等位基因、基因组和转录物组的方法和基因型分析谱
LT3241914T (lt) 2009-11-05 2019-04-25 The Chinese University Of Hong Kong Vaisiaus genomo analizė iš motinos biologinio mėginio
CA2780016C (en) 2009-11-06 2017-09-19 The Chinese University Of Hong Kong Size-based genomic analysis
US9260745B2 (en) * 2010-01-19 2016-02-16 Verinata Health, Inc. Detecting and classifying copy number variation
EP2854058A3 (en) 2010-05-18 2015-10-28 Natera, Inc. Methods for non-invasive pre-natal ploidy calling
US20120190021A1 (en) 2011-01-25 2012-07-26 Aria Diagnostics, Inc. Detection of genetic abnormalities
EP3202921B1 (en) * 2011-02-24 2019-02-13 The Chinese University of Hong Kong Molecular testing of multiple pregnancies
CN105121660B (zh) 2013-03-15 2018-09-28 香港中文大学 确定多胎妊娠的胎儿基因组

Also Published As

Publication number Publication date
TW201441373A (zh) 2014-11-01
KR20150132216A (ko) 2015-11-25
CN105121660B (zh) 2018-09-28
JP2016518811A (ja) 2016-06-30
AU2014231358A1 (en) 2015-09-24
CN105121660A (zh) 2015-12-02
EA201500939A1 (ru) 2016-01-29
US20140315200A1 (en) 2014-10-23
TWI637058B (zh) 2018-10-01
EP3434790A1 (en) 2019-01-30
CA2901773A1 (en) 2014-09-18
US10106836B2 (en) 2018-10-23
MX2015010785A (es) 2015-11-26
EP2971126B1 (en) 2018-11-07
EP2971126A1 (en) 2016-01-20
WO2014139477A1 (en) 2014-09-18
EP2971126A4 (en) 2016-10-26

Similar Documents

Publication Publication Date Title
Docherty et al. Genome-wide DNA methylation analysis of patients with imprinting disorders identifies differentially methylated regions associated with novel candidate imprinted genes
Hanna et al. Pervasive polymorphic imprinted methylation in the human placenta
CY1125362T1 (el) Διαχωρισμος γονιδιωματικων κλασματων με χρηση των μετρησεων πολυμορφισμων
CY1121828T1 (el) Αναλυση βασει μεγεθους θραυσματος εμβρυϊκου dna στο μητρικο πλασμα
AU2010315037A8 (en) Fetal genomic analysis from a maternal biological sample
TW201129736A (en) Size-based genomic analysis
WO2010045617A9 (en) Detecting genetic abnormalities
MY208464A (en) Universal haplotype-based noninvasive prenatal testing for single gene diseases
MX2015010785A (es) Determinacion de genomas fetales para embarazos de multiples fetos.
Lim et al. Epigenetic state and expression of imprinted genes in umbilical cord correlates with growth parameters in human pregnancy
WO2013177581A3 (en) Whole genome sequencing of a human fetus
Çağlayan et al. ALPK3 gene mutation in a patient with congenital cardiomyopathy and dysmorphic features
WO2014165267A3 (en) Systems and methods for prenatal genetic analysis
JP2014507158A5 (enExample)
SA518391141B1 (ar) جزء جنيني من خلال تكوين متواليات ذات عمق سطحي
WO2012038382A3 (en) Markers for joint displasia, osteoarthritis and conditions secondary thereto
WO2014155105A3 (en) Assessment of risk of aneuploidy
JP2014513958A5 (enExample)
JP2016518811A5 (enExample)
Yin et al. Fine-mapping markers of lung cancer susceptibility in a sub-region of chromosome 19q13. 3 among Chinese
Duan et al. Association analysis of GWAS hits and non-syndromic cleft lip with/without palate with cleft alveolar in Han population of western China
Huang et al. Association between ERCC2 polymorphisms and glioma risk: a meta-analysis
Fulford et al. Progressive influence of body mass index-associated genetic markers in rural Gambians
Van Limbergen et al. Germline variants of IRGM in childhood-onset Crohn’s disease
WO2011127527A8 (en) Method and system for detecting regulatory single nucleotide polymorphisms