JP2017526347A5 - - Google Patents
Download PDFInfo
- 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
- Authority
- JP
- Japan
- Prior art keywords
- region
- target genomic
- fixed
- cutting
- assay method
- Prior art date
- Legal status (The legal status 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 status listed.)
- Granted
Links
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
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)
| 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 |
| US20120034603A1 (en) | 2010-08-06 | 2012-02-09 | Tandem Diagnostics, Inc. | Ligation-based detection of genetic variants |
| US20140342940A1 (en) | 2011-01-25 | 2014-11-20 | 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 |
| US11203786B2 (en) | 2010-08-06 | 2021-12-21 | 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 |
| 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 |
| CA2921628A1 (en) | 2013-08-19 | 2015-02-26 | Singular Bio, Inc. | Assays for single molecule detection and use thereof |
| WO2016134191A1 (en) | 2015-02-18 | 2016-08-25 | 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 |
| 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 |
| EP3631008B1 (en) * | 2017-06-02 | 2025-12-03 | Affymetrix, Inc. | Array-based methods for analysing mixed samples using differently labelled allele-specific probes |
| DE112019005108T5 (de) * | 2018-10-12 | 2021-07-15 | Nantomics, Llc | Pränatale Reinheitsbeurteilungen mit Bambam |
Family Cites Families (15)
| 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 |
| EP2395111B1 (en) * | 2003-10-08 | 2015-05-13 | Trustees of Boston University | Methods for prenatal diagnosis of chromosomal abnormalities |
| WO2007134395A1 (en) * | 2006-05-22 | 2007-11-29 | Clinical Genomics Pty Ltd | Detection method |
| US8620593B2 (en) * | 2009-11-06 | 2013-12-31 | The Chinese University Of Hong Kong | Size-based genomic analysis |
| WO2011066476A1 (en) * | 2009-11-25 | 2011-06-03 | Quantalife, 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 |
| CA2824387C (en) * | 2011-02-09 | 2019-09-24 | Natera, Inc. | Methods for non-invasive prenatal ploidy calling |
| 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 |
| US9206417B2 (en) * | 2012-07-19 | 2015-12-08 | Ariosa Diagnostics, Inc. | Multiplexed sequential ligation-based detection of genetic variants |
-
2015
- 2015-07-29 WO PCT/US2015/042604 patent/WO2016018986A1/en not_active Ceased
- 2015-07-29 CA CA2955740A patent/CA2955740A1/en active Pending
- 2015-07-29 SG SG11201700765WA patent/SG11201700765WA/en unknown
- 2015-07-29 EP EP15826681.7A patent/EP3175236B1/en active Active
- 2015-07-29 JP JP2017503992A patent/JP6793112B2/ja active Active
- 2015-07-29 KR KR1020177004719A patent/KR20170036727A/ko not_active Ceased
- 2015-07-29 MX MX2017001405A patent/MX376755B/es active IP Right Grant
- 2015-07-29 CN CN201580040576.3A patent/CN106537142B/zh active Active
- 2015-07-29 ES ES15826681T patent/ES2752237T3/es active Active
- 2015-07-29 AU AU2015296602A patent/AU2015296602B2/en not_active Ceased
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2017526347A5 (enExample) | ||
| US12180548B2 (en) | Detection of target nucleic acids using hybridization | |
| JP6793112B2 (ja) | 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 | |
| US9567639B2 (en) | Detection of target nucleic acids using hybridization | |
| EP1721014B1 (en) | Method for detecting and quantifying rare mutations/polymorphisms | |
| CA2528577A1 (en) | Methods and compositions for whole genome amplification and genotyping | |
| JP2014073134A5 (ja) | 標的増幅及びシークエンシングを使用した非侵襲的な胎児遺伝子型スクリーニング | |
| JP2014507141A5 (enExample) | ||
| JP2013039138A (ja) | ポリヌクレオチドの多重増幅 | |
| JP2013532494A5 (enExample) | ||
| JP2010519896A5 (enExample) | ||
| JP2013509871A5 (enExample) | ||
| JP2019500706A5 (enExample) | ||
| JP2010035532A (ja) | アレル特異的pcr法 | |
| US10533223B2 (en) | Detection of target nucleic acids using hybridization | |
| JP2007530026A (ja) | 核酸配列決定 | |
| WO2012032510A1 (en) | Primers for amplifying dna and methods of selecting same | |
| JP6728556B2 (ja) | 一塩基多型検出用キット及び方法 | |
| Smylie et al. | Analysis of sequence variations in several human genes using phosphoramidite bond DNA fragmentation and chip-based MALDI-TOF | |
| KR101856205B1 (ko) | 핵산의 대립형질 특이적 프라이머 및 이를 이용한 유전형 판별 방법 | |
| JP2003508074A5 (enExample) | ||
| Fahrenkrug et al. | Map assignments of 373 previously unreported porcine microsatellites. | |
| JP2015073506A (ja) | 遺伝子多型の判定方法 | |
| US20220127665A1 (en) | Elimination probe-based method for detecting numerical chromosomal abnormalities, and nucleic acid composition for detecting numerical chromosomal abnormalities | |
| KR101762486B1 (ko) | 한국인 모계 계통 분석용 마커 조성물 |