DK1951897T3 - Kromosomanalyse ved molekylær karyotype-bestemmelse - Google Patents

Kromosomanalyse ved molekylær karyotype-bestemmelse

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Publication number
DK1951897T3
DK1951897T3 DK06808513.3T DK06808513T DK1951897T3 DK 1951897 T3 DK1951897 T3 DK 1951897T3 DK 06808513 T DK06808513 T DK 06808513T DK 1951897 T3 DK1951897 T3 DK 1951897T3
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DK
Denmark
Prior art keywords
target cell
origin
paternal
chromosomes
chromosome
Prior art date
Application number
DK06808513.3T
Other languages
English (en)
Inventor
Alan Handyside
Original Assignee
Bluegnome Ltd
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
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Application granted granted Critical
Publication of DK1951897T3 publication Critical patent/DK1951897T3/da

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Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING 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
    • C12Q1/00Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6813Hybridisation assays
    • C12Q1/6827Hybridisation assays for detection of mutation or polymorphism

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Microbiology (AREA)
  • Biochemistry (AREA)
  • Physics & Mathematics (AREA)
  • Molecular Biology (AREA)
  • Biotechnology (AREA)
  • Biophysics (AREA)
  • Analytical Chemistry (AREA)
  • Immunology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Investigating Or Analysing Biological Materials (AREA)
  • Primary Cells (AREA)
DK06808513.3T 2005-11-15 2006-11-13 Kromosomanalyse ved molekylær karyotype-bestemmelse DK1951897T3 (da)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB0523276.4A GB0523276D0 (en) 2005-11-15 2005-11-15 Chromosomal analysis by molecular karyotyping
PCT/GB2006/004221 WO2007057647A1 (en) 2005-11-15 2006-11-13 Chromosomal analysis by molecular karyotyping

Publications (1)

Publication Number Publication Date
DK1951897T3 true DK1951897T3 (da) 2011-05-02

Family

ID=35516981

Family Applications (1)

Application Number Title Priority Date Filing Date
DK06808513.3T DK1951897T3 (da) 2005-11-15 2006-11-13 Kromosomanalyse ved molekylær karyotype-bestemmelse

Country Status (9)

Country Link
US (2) US11214826B2 (da)
EP (1) EP1951897B8 (da)
JP (1) JP5178525B2 (da)
AT (1) ATE497021T1 (da)
DE (1) DE602006019898D1 (da)
DK (1) DK1951897T3 (da)
ES (1) ES2360085T3 (da)
GB (1) GB0523276D0 (da)
WO (1) WO2007057647A1 (da)

Families Citing this family (61)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8024128B2 (en) 2004-09-07 2011-09-20 Gene Security Network, Inc. System and method for improving clinical decisions by aggregating, validating and analysing genetic and phenotypic data
US8515679B2 (en) 2005-12-06 2013-08-20 Natera, Inc. System and method for cleaning noisy genetic data and determining chromosome copy number
US11111544B2 (en) 2005-07-29 2021-09-07 Natera, Inc. System and method for cleaning noisy genetic data and determining chromosome copy number
US9424392B2 (en) 2005-11-26 2016-08-23 Natera, Inc. System and method for cleaning noisy genetic data from target individuals using genetic data from genetically related individuals
US10081839B2 (en) 2005-07-29 2018-09-25 Natera, Inc System and method for cleaning noisy genetic data and determining chromosome copy number
US11111543B2 (en) 2005-07-29 2021-09-07 Natera, Inc. System and method for cleaning noisy genetic data and determining chromosome copy number
US10083273B2 (en) 2005-07-29 2018-09-25 Natera, Inc. System and method for cleaning noisy genetic data and determining chromosome copy number
US8532930B2 (en) 2005-11-26 2013-09-10 Natera, Inc. Method for determining the number of copies of a chromosome in the genome of a target individual using genetic data from genetically related individuals
GB0523276D0 (en) * 2005-11-15 2005-12-21 London Bridge Fertility Chromosomal analysis by molecular karyotyping
SI2351858T1 (sl) * 2006-02-28 2015-06-30 University Of Louisville Research Foundation Med Center Three, Zaznavanje fetalnih kromosomskih nenormalnosti z uporabo tandema polimorfizmov posameznih nukleotidov
US8609338B2 (en) 2006-02-28 2013-12-17 University Of Louisville Research Foundation, Inc. Detecting fetal chromosomal abnormalities using tandem single nucleotide polymorphisms
US20100184043A1 (en) * 2006-02-28 2010-07-22 University Of Louisville Research Foundation Detecting Genetic Abnormalities
US20100184044A1 (en) * 2006-02-28 2010-07-22 University Of Louisville Research Foundation Detecting Genetic Abnormalities
US20080050739A1 (en) 2006-06-14 2008-02-28 Roland Stoughton Diagnosis of fetal abnormalities using polymorphisms including short tandem repeats
WO2007147074A2 (en) 2006-06-14 2007-12-21 Living Microsystems, Inc. Use of highly parallel snp genotyping for fetal diagnosis
EP2589668A1 (en) 2006-06-14 2013-05-08 Verinata Health, Inc Rare cell analysis using sample splitting and DNA tags
JP2010528629A (ja) 2007-06-07 2010-08-26 シモンズ ハプロミクス リミテッド 遺伝子地図作製及びハプロタイプ決定のための現場(insitu)法
AU2009279734A1 (en) 2008-08-04 2010-02-11 Natera, Inc. Methods for allele calling and ploidy calling
CA2641132A1 (en) * 2008-10-03 2010-04-03 Richard T. Scott, Jr. Improvements in in vitro fertilization
US20100206316A1 (en) * 2009-01-21 2010-08-19 Scott Jr Richard T Method for determining chromosomal defects in an ivf embryo
US20100317916A1 (en) * 2009-06-12 2010-12-16 Scott Jr Richard T Method for relative quantitation of chromosomal DNA copy number in single or few cells
WO2011041485A1 (en) 2009-09-30 2011-04-07 Gene Security Network, Inc. Methods for non-invasive prenatal ploidy calling
MX355132B (es) 2009-11-05 2018-04-06 Sequenom Inc Analisis genomico fetal de muestra biologica materna.
US8774488B2 (en) 2010-03-11 2014-07-08 Cellscape Corporation Method and device for identification of nucleated red blood cells from a maternal blood sample
US11939634B2 (en) 2010-05-18 2024-03-26 Natera, Inc. Methods for simultaneous amplification of target loci
US11339429B2 (en) 2010-05-18 2022-05-24 Natera, Inc. Methods for non-invasive prenatal ploidy calling
US20190010543A1 (en) 2010-05-18 2019-01-10 Natera, Inc. Methods for simultaneous amplification of target loci
US11326208B2 (en) 2010-05-18 2022-05-10 Natera, Inc. Methods for nested PCR amplification of cell-free DNA
US10316362B2 (en) 2010-05-18 2019-06-11 Natera, Inc. Methods for simultaneous amplification of target loci
US11408031B2 (en) 2010-05-18 2022-08-09 Natera, Inc. Methods for non-invasive prenatal paternity testing
US11332793B2 (en) 2010-05-18 2022-05-17 Natera, Inc. Methods for simultaneous amplification of target loci
US11332785B2 (en) 2010-05-18 2022-05-17 Natera, Inc. Methods for non-invasive prenatal ploidy calling
US9677118B2 (en) 2014-04-21 2017-06-13 Natera, Inc. Methods for simultaneous amplification of target loci
US11322224B2 (en) 2010-05-18 2022-05-03 Natera, Inc. Methods for non-invasive prenatal ploidy calling
EP2854058A3 (en) 2010-05-18 2015-10-28 Natera, Inc. Methods for non-invasive pre-natal ploidy calling
GB201010232D0 (en) 2010-06-18 2010-07-21 Univ Leuven Kath Methods for haplotyping single cells
CA2821906C (en) 2010-12-22 2020-08-25 Natera, Inc. Methods for non-invasive prenatal paternity testing
JP6153874B2 (ja) 2011-02-09 2017-06-28 ナテラ, インコーポレイテッド 非侵襲的出生前倍数性呼び出しのための方法
CN103492588A (zh) * 2011-02-25 2014-01-01 伊路敏纳公司 用于单体型测定的方法和系统
US20140100126A1 (en) 2012-08-17 2014-04-10 Natera, Inc. Method for Non-Invasive Prenatal Testing Using Parental Mosaicism Data
MX363345B (es) 2013-03-15 2019-03-20 Univ Hong Kong Chinese Determinación de genomas fetales para embarazos de múltiples fetos.
WO2014155105A2 (en) * 2013-03-27 2014-10-02 Bluegnome Ltd Assessment of risk of aneuploidy
ES2775213T3 (es) * 2013-06-13 2020-07-24 Ariosa Diagnostics Inc Análisis estadístico para la determinación no invasiva de aneuploidías de los cromosomas sexuales
GB201318369D0 (en) * 2013-10-17 2013-12-04 Univ Leuven Kath Methods using BAF
WO2015048535A1 (en) 2013-09-27 2015-04-02 Natera, Inc. Prenatal diagnostic resting standards
US10262755B2 (en) 2014-04-21 2019-04-16 Natera, Inc. Detecting cancer mutations and aneuploidy in chromosomal segments
US10577655B2 (en) 2013-09-27 2020-03-03 Natera, Inc. Cell free DNA diagnostic testing standards
AU2015249846B2 (en) 2014-04-21 2021-07-22 Natera, Inc. Detecting mutations and ploidy in chromosomal segments
EP3294906B1 (en) 2015-05-11 2024-07-10 Natera, Inc. Methods for determining ploidy
CN105543372B (zh) * 2016-01-19 2017-04-19 北京中仪康卫医疗器械有限公司 一种检测染色体罗氏易位的方法
WO2018067517A1 (en) 2016-10-04 2018-04-12 Natera, Inc. Methods for characterizing copy number variation using proximity-litigation sequencing
US10011870B2 (en) 2016-12-07 2018-07-03 Natera, Inc. Compositions and methods for identifying nucleic acid molecules
CA3049139A1 (en) 2017-02-21 2018-08-30 Natera, Inc. Compositions, methods, and kits for isolating nucleic acids
US11866285B2 (en) 2017-07-04 2024-01-09 Tombow Pencil Co., Ltd. Coating film transfer tool
US12084720B2 (en) 2017-12-14 2024-09-10 Natera, Inc. Assessing graft suitability for transplantation
CA3090426A1 (en) 2018-04-14 2019-10-17 Natera, Inc. Methods for cancer detection and monitoring by means of personalized detection of circulating tumor dna
US11525159B2 (en) 2018-07-03 2022-12-13 Natera, Inc. Methods for detection of donor-derived cell-free DNA
ES2738176B2 (es) 2018-07-20 2021-01-11 Bioarray S L Metodo para el estudio de mutaciones en embriones en procesos de reproduccion in vitro
US20230162814A1 (en) * 2020-03-12 2023-05-25 Vrije Universiteit Brussel Method for the analysis of genetic material
JP7449032B2 (ja) 2020-12-10 2024-03-13 フジコピアン株式会社 塗膜転写具
CN116855617B (zh) * 2023-08-31 2024-08-02 安诺优达基因科技(北京)有限公司 基于核心家系的串联重复变异分型检测方法及其应用

Family Cites Families (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3703890A (en) * 1970-08-10 1972-11-28 Milton A Saunders Jr Skin patch test device
US5271940A (en) * 1989-09-14 1993-12-21 Cygnus Therapeutic Systems Transdermal delivery device having delayed onset
US5736154A (en) * 1996-03-11 1998-04-07 Fuisz Technologies Ltd. Transdermal delivery system
US5985538A (en) 1997-08-01 1999-11-16 Saint Barnabas Medical Center Cryopreservation and cell culture medium comprising less than 50 mM sodium ions and greater than 100 mM choline salt
US6031098A (en) * 1997-08-11 2000-02-29 California Institute Of Technology Detection and treatment of duplex polynucleotide damage
US7399589B2 (en) 1998-02-06 2008-07-15 Digene Corporation Immunological detection of RNA:DNA hybrids on microarrays
CA2369485A1 (en) * 1999-06-25 2001-01-04 Genaissance Pharmaceuticals, Inc. Methods for obtaining and using haplotype data
US20050037388A1 (en) 2001-06-22 2005-02-17 University Of Geneva Method for detecting diseases caused by chromosomal imbalances
US20040197791A1 (en) * 2001-06-29 2004-10-07 Makarov Vladimir L. Methods of using nick translate libraries for snp analysis
US20030152951A1 (en) * 2001-07-20 2003-08-14 Mirel Daniel B. IL-4 receptor sequence variation associated with type 1 diabetes
US6979541B1 (en) 2001-07-26 2005-12-27 University Of Utah Research Foundation Methods for identifying chromosomal aneuploidy
AUPR749901A0 (en) * 2001-09-06 2001-09-27 Monash University Method of identifying chromosomal abnormalities and prenatal diagnosis
AU2002364945A1 (en) 2001-10-25 2003-07-09 Neurogenetics, Inc. Genes and polymorphisms on chromosome 10 associated with alzheimer's disease and other neurodegenerative diseases
CA2468601A1 (en) * 2001-12-03 2003-06-12 Dnaprint Genomics, Inc. Methods and apparatus for complex genetics classification based on correspondence analysis and linear/quadratic analysis
US6977162B2 (en) * 2002-03-01 2005-12-20 Ravgen, Inc. Rapid analysis of variations in a genome
US7727720B2 (en) * 2002-05-08 2010-06-01 Ravgen, Inc. Methods for detection of genetic disorders
EP2395111B1 (en) * 2003-10-08 2015-05-13 Trustees of Boston University Methods for prenatal diagnosis of chromosomal abnormalities
US7632640B2 (en) * 2003-12-08 2009-12-15 The Clinic For Special Children Association of TSPYL polymorphisms with SIDDT syndrome
US7226743B2 (en) * 2004-03-31 2007-06-05 University Of Saskatchewan CRH and POMC effects on animal growth
US8532930B2 (en) 2005-11-26 2013-09-10 Natera, Inc. Method for determining the number of copies of a chromosome in the genome of a target individual using genetic data from genetically related individuals
GB0523276D0 (en) * 2005-11-15 2005-12-21 London Bridge Fertility Chromosomal analysis by molecular karyotyping
EP1960929A4 (en) 2005-11-26 2009-01-28 Gene Security Network Llc SYSTEM AND METHOD FOR CLEANING RAISED GENETIC DATA AND USE OF DATA FOR PREDICTIONS
US20080085836A1 (en) 2006-09-22 2008-04-10 Kearns William G Method for genetic testing of human embryos for chromosome abnormalities, segregating genetic disorders with or without a known mutation and mitochondrial disorders following in vitro fertilization (IVF), embryo culture and embryo biopsy

Also Published As

Publication number Publication date
EP1951897A1 (en) 2008-08-06
DE602006019898D1 (de) 2011-03-10
US20190024151A1 (en) 2019-01-24
ES2360085T3 (es) 2011-05-31
ATE497021T1 (de) 2011-02-15
JP2009515544A (ja) 2009-04-16
GB0523276D0 (en) 2005-12-21
US11214826B2 (en) 2022-01-04
US20080318235A1 (en) 2008-12-25
EP1951897B8 (en) 2011-03-23
WO2007057647A1 (en) 2007-05-24
JP5178525B2 (ja) 2013-04-10
EP1951897B1 (en) 2011-01-26

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