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 US20140342940A1 (en) 2011-01-25 2014-08-01 Detection of Target Nucleic Acids using Hybridization
US14/450,144 2014-08-01
US14/453,396 2014-08-06
US14/453,396 US9567639B2 (en) 2010-08-06 2014-08-06 Detection of target nucleic acids using hybridization
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

Family Applications (1)

Application Number Title Priority Date Filing Date
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)

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Publication number Priority date Publication date Assignee Title
US20130040375A1 (en) 2011-08-08 2013-02-14 Tandem Diagnotics, Inc. Assay systems for genetic analysis
US8700338B2 (en) 2011-01-25 2014-04-15 Ariosa Diagnosis, Inc. Risk calculation for evaluation of fetal aneuploidy
US10533223B2 (en) 2010-08-06 2020-01-14 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
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
US20140342940A1 (en) 2011-01-25 2014-11-20 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
MX371428B (es) 2013-08-19 2020-01-30 Singular Bio Inc Ensayos para la deteccion de una sola molecula y uso de los mismos.
AU2016219943A1 (en) 2015-02-18 2017-10-12 Singular Bio, Inc. Assays for single molecule detection and use thereof
EP3601599A4 (en) * 2017-03-23 2020-12-23 Apton Biosystems, Inc. POLYMORPHISM DETECTION WITH INCREASED ACCURACY
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
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
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
EP1689884A4 (en) * 2003-10-08 2007-04-04 Univ Boston PROCESS FOR THE PRENATAL DIAGNOSIS OF CHROMOSOMAL ABNORMALITIES
BRPI0713098A2 (pt) * 2006-05-22 2012-10-16 Clinical Genomics Pty Ltd método para determinar a origem anatÈmica de uma célula ou população celular derivada do intestino grosso de um indivìduo, método de detecção para determinar a origem anatÈmica de uma célula ou população celular derivada do intestino grosso de um indivìduo, sistema de detecção, meio de armazenagem legìvel por computador, arranjo de ácido nucleico, uso de um arranjo, método para determinar o inìcio ou predisposição para o inìcio de uma anormalidade celular ou uma condição destinguida por uma anormalidade celular no intestino grosso, kit de diagnóstico para ensaiar amostras biológicas
EA034241B1 (ru) * 2009-11-06 2020-01-21 Те Чайниз Юниверсити Ов Гонконг Способ пренатальной диагностики дисбаланса последовательности
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
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
AU2012281242B2 (en) * 2011-07-08 2016-12-22 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
JP2015508655A (ja) * 2012-02-14 2015-03-23 コーネル ユニバーシティー 組み合わせたヌクレアーゼ反応、連結反応、およびポリメラーゼ反応を用いて核酸配列、発現、またはコピー変化を相対的に定量するための方法
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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