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
Publication of JP2017526347A publication Critical patent/JP2017526347A/ja
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 (enExample) 2018-11-22
JP6793112B2 JP6793112B2 (ja) 2020-12-02

Family

ID=55218263

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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 (enExample)
JP (1) JP6793112B2 (enExample)
KR (1) KR20170036727A (enExample)
CN (1) CN106537142B (enExample)
AU (1) AU2015296602B2 (enExample)
CA (1) CA2955740A1 (enExample)
ES (1) ES2752237T3 (enExample)
MX (1) MX376755B (enExample)
SG (1) SG11201700765WA (enExample)
WO (1) WO2016018986A1 (enExample)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8700338B2 (en) 2011-01-25 2014-04-15 Ariosa Diagnosis, Inc. Risk calculation for evaluation of fetal aneuploidy
US20130261003A1 (en) 2010-08-06 2013-10-03 Ariosa Diagnostics, In. Ligation-based detection of genetic variants
US20120034603A1 (en) 2010-08-06 2012-02-09 Tandem Diagnostics, Inc. Ligation-based detection of genetic variants
US11203786B2 (en) 2010-08-06 2021-12-21 Ariosa Diagnostics, Inc. Detection of target nucleic acids using hybridization
US10533223B2 (en) 2010-08-06 2020-01-14 Ariosa Diagnostics, Inc. Detection of target nucleic acids using hybridization
US20140342940A1 (en) 2011-01-25 2014-11-20 Ariosa Diagnostics, Inc. Detection of Target Nucleic Acids using Hybridization
US20130040375A1 (en) 2011-08-08 2013-02-14 Tandem Diagnotics, Inc. Assay systems for genetic analysis
US10829816B2 (en) 2012-11-19 2020-11-10 Apton Biosystems, Inc. Methods of analyte detection
CN110283888B (zh) 2013-08-19 2021-06-22 卓异生物公司 用于单分子检测的测定及其应用
CN107735497B (zh) 2015-02-18 2021-08-20 卓异生物公司 用于单分子检测的测定及其应用
WO2018175402A1 (en) * 2017-03-23 2018-09-27 Apton Biosystems, Inc. Polymorphism detection with increased accuracy
US11441174B2 (en) 2017-06-02 2022-09-13 Affymetrix, Inc. Array-based methods for analysing mixed samples using differently labelled allele-specific probes
CN110914448A (zh) * 2017-06-02 2020-03-24 昂飞股份有限公司 使用差异性标记的等位基因特异性探针分析混合样品的基于阵列的方法
US11535886B2 (en) 2017-06-02 2022-12-27 Affymetrix, Inc. Array-based methods for analysing mixed samples using different allele-specific labels, in particular for detection of fetal aneuploidies
DE112019005108T5 (de) * 2018-10-12 2021-07-15 Nantomics, Llc Pränatale Reinheitsbeurteilungen mit 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
US20050100939A1 (en) * 2003-09-18 2005-05-12 Eugeni Namsaraev System and methods for enhancing signal-to-noise ratios of microarray-based measurements
WO2005035725A2 (en) * 2003-10-08 2005-04-21 The Trustees Of Boston University Methods for prenatal diagnosis of chromosomal abnormalities
EP2767595B1 (en) * 2006-05-22 2018-09-19 Clinical Genomics Pty Ltd Detection method for characterising the anatomical origin of a cell
ES3026544T3 (en) * 2009-11-06 2025-06-11 Univ Hong Kong Chinese Size-based genomic analysis for prenatal diagnosis
JP2013511991A (ja) * 2009-11-25 2013-04-11 クアンタライフ, インコーポレイテッド 遺伝子材料を検出する方法および組成物
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
CA2824387C (en) * 2011-02-09 2019-09-24 Natera, Inc. Methods for non-invasive prenatal ploidy calling
EP2729580B1 (en) * 2011-07-08 2015-09-16 Keygene N.V. Sequence based genotyping based on oligonucleotide ligation assays
US10196681B2 (en) * 2011-10-06 2019-02-05 Sequenom, Inc. Methods and processes for non-invasive assessment of genetic variations
SG11201404899VA (en) * 2012-02-14 2014-10-30 Univ Cornell 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
CN104583421A (zh) * 2012-07-19 2015-04-29 阿瑞奥萨诊断公司 遗传变体的基于多重的顺序连接的检测

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