JP2017526347A5 - - Google Patents

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Publication number
JP2017526347A5
JP2017526347A5 JP2017503992A JP2017503992A JP2017526347A5 JP 2017526347 A5 JP2017526347 A5 JP 2017526347A5 JP 2017503992 A JP2017503992 A JP 2017503992A JP 2017503992 A JP2017503992 A JP 2017503992A JP 2017526347 A5 JP2017526347 A5 JP 2017526347A5
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JP
Japan
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region
target genomic
fixed
cutting
assay method
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JP2017503992A
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English (en)
Japanese (ja)
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JP6793112B2 (ja
JP2017526347A (ja
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Priority claimed from US14/450,144 external-priority patent/US20140342940A1/en
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Priority claimed from PCT/US2015/042604 external-priority patent/WO2016018986A1/en
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Publication of JP2017526347A5 publication Critical patent/JP2017526347A5/ja
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JP2017503992A 2014-08-01 2015-07-29 胎児コピー数変異の統計的尤度を提供するアッセイ方法および胎児染色体異数性の尤度決定のためのアッセイ方法 Active JP6793112B2 (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US14/450,144 2014-08-01
US14/450,144 US20140342940A1 (en) 2011-01-25 2014-08-01 Detection of Target Nucleic Acids using Hybridization
US14/453,396 US9567639B2 (en) 2010-08-06 2014-08-06 Detection of target nucleic acids using hybridization
US14/453,396 2014-08-06
PCT/US2015/042604 WO2016018986A1 (en) 2014-08-01 2015-07-29 Detection of target nucleic acids using hybridization

Publications (3)

Publication Number Publication Date
JP2017526347A JP2017526347A (ja) 2017-09-14
JP2017526347A5 true JP2017526347A5 (cg-RX-API-DMAC7.html) 2018-11-22
JP6793112B2 JP6793112B2 (ja) 2020-12-02

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JP2017503992A Active JP6793112B2 (ja) 2014-08-01 2015-07-29 胎児コピー数変異の統計的尤度を提供するアッセイ方法および胎児染色体異数性の尤度決定のためのアッセイ方法

Country Status (10)

Country Link
EP (1) EP3175236B1 (cg-RX-API-DMAC7.html)
JP (1) JP6793112B2 (cg-RX-API-DMAC7.html)
KR (1) KR20170036727A (cg-RX-API-DMAC7.html)
CN (1) CN106537142B (cg-RX-API-DMAC7.html)
AU (1) AU2015296602B2 (cg-RX-API-DMAC7.html)
CA (1) CA2955740A1 (cg-RX-API-DMAC7.html)
ES (1) ES2752237T3 (cg-RX-API-DMAC7.html)
MX (1) MX376755B (cg-RX-API-DMAC7.html)
SG (1) SG11201700765WA (cg-RX-API-DMAC7.html)
WO (1) WO2016018986A1 (cg-RX-API-DMAC7.html)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20140342940A1 (en) 2011-01-25 2014-11-20 Ariosa Diagnostics, Inc. Detection of Target Nucleic Acids using Hybridization
US20120034603A1 (en) 2010-08-06 2012-02-09 Tandem Diagnostics, Inc. Ligation-based detection of genetic variants
US8700338B2 (en) 2011-01-25 2014-04-15 Ariosa Diagnosis, Inc. Risk calculation for evaluation of fetal aneuploidy
US20130040375A1 (en) 2011-08-08 2013-02-14 Tandem Diagnotics, Inc. Assay systems for genetic analysis
US11203786B2 (en) 2010-08-06 2021-12-21 Ariosa Diagnostics, Inc. Detection of target nucleic acids using hybridization
US20130261003A1 (en) 2010-08-06 2013-10-03 Ariosa Diagnostics, In. Ligation-based detection of genetic variants
US10533223B2 (en) 2010-08-06 2020-01-14 Ariosa Diagnostics, Inc. Detection of target nucleic acids using hybridization
US10829816B2 (en) 2012-11-19 2020-11-10 Apton Biosystems, Inc. Methods of analyte detection
AU2014308980C1 (en) 2013-08-19 2021-09-30 Invitae Corporation Assays for single molecule detection and use thereof
KR20170116157A (ko) 2015-02-18 2017-10-18 싱귤러 바이오, 인코포레이티드 단일분자 검출용 분석 및 그의 용도
EP3601599A4 (en) * 2017-03-23 2020-12-23 Apton Biosystems, Inc. POLYMORPHISM DETECTION WITH INCREASED ACCURACY
WO2018223055A1 (en) * 2017-06-02 2018-12-06 Affymetrix, Inc. Array-based methods for analysing mixed samples using differently labelled allele-specific probes
WO2018223057A1 (en) * 2017-06-02 2018-12-06 Affymetrix, Inc. Array-based methods for analysing mixed samples using different allele-specific labels, in particular for detection of fetal aneuploidies
WO2018223053A1 (en) * 2017-06-02 2018-12-06 Affymetrix, Inc. Array-based methods for analysing mixed samples using differently labelled allele-specific probes
US20210407621A1 (en) * 2018-10-12 2021-12-30 Nantomics, Llc Prenatal purity assessments using bambam

Family Cites Families (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6506594B1 (en) * 1999-03-19 2003-01-14 Cornell Res Foundation Inc Detection of nucleic acid sequence differences using the ligase detection reaction with addressable arrays
US20020042681A1 (en) * 2000-10-03 2002-04-11 International Business Machines Corporation Characterization of phenotypes by gene expression patterns and classification of samples based thereon
EP1685380A2 (en) * 2003-09-18 2006-08-02 Parallele Bioscience, Inc. System and methods for enhancing signal-to-noise ratios of microarray-based measurements
CA2541706C (en) * 2003-10-08 2014-02-18 The Trustees Of Boston University Methods for prenatal diagnosis of chromosomal abnormalities
CN101506379A (zh) * 2006-05-22 2009-08-12 临床基因组学有限公司 检测方法
US8620593B2 (en) * 2009-11-06 2013-12-31 The Chinese University Of Hong Kong Size-based genomic analysis
EP2504448B1 (en) * 2009-11-25 2016-10-19 Bio-Rad Laboratories, Inc. Methods and compositions for detecting genetic material
US20120034603A1 (en) * 2010-08-06 2012-02-09 Tandem Diagnostics, Inc. Ligation-based detection of genetic variants
US10131947B2 (en) * 2011-01-25 2018-11-20 Ariosa Diagnostics, Inc. Noninvasive detection of fetal aneuploidy in egg donor pregnancies
RU2671980C2 (ru) * 2011-02-09 2018-11-08 Натера, Инк. Способы неинвазивного пренатального установления плоидности
DK2729580T3 (en) * 2011-07-08 2015-12-14 Keygene Nv SEQUENCE BASED genotyping BASED ON OLIGONUKLEOTIDLIGERINGSASSAYS
US10196681B2 (en) * 2011-10-06 2019-02-05 Sequenom, Inc. Methods and processes for non-invasive assessment of genetic variations
US9598728B2 (en) * 2012-02-14 2017-03-21 Cornell University Method for relative quantification of nucleic acid sequence, expression, or copy changes, using combined nuclease, ligation, and polymerase reactions
WO2013192292A1 (en) * 2012-06-21 2013-12-27 Justin Lamb Massively-parallel multiplex locus-specific nucleic acid sequence analysis
AU2013292287A1 (en) * 2012-07-19 2015-02-19 Ariosa Diagnostics, Inc. Multiplexed sequential ligation-based detection of genetic variants

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