JP2015501646A5 - - Google Patents

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JP2015501646A5
JP2015501646A5 JP2014546269A JP2014546269A JP2015501646A5 JP 2015501646 A5 JP2015501646 A5 JP 2015501646A5 JP 2014546269 A JP2014546269 A JP 2014546269A JP 2014546269 A JP2014546269 A JP 2014546269A JP 2015501646 A5 JP2015501646 A5 JP 2015501646A5
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JP2014546269A
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JP2015501646A (ja
JP6092891B2 (ja
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Priority claimed from PCT/CN2011/084165 external-priority patent/WO2013086744A1/zh
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**Nタグ付のプライマーの配列は、CAAGCAGAAGACGGCATACGAGATCGTGATGTGACTGGAGTTCAGACGTGTGCTCTTCCGATCTであった。
JP2014546269A 2011-12-17 2011-12-17 ゲノムの異常の有無を決定する方法及び判断するシステム Active JP6092891B2 (ja)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/CN2011/084165 WO2013086744A1 (zh) 2011-12-17 2011-12-17 确定基因组是否存在异常的方法及系统

Publications (3)

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JP2015501646A JP2015501646A (ja) 2015-01-19
JP2015501646A5 true JP2015501646A5 (ja) 2015-07-02
JP6092891B2 JP6092891B2 (ja) 2017-03-15

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ID=48611840

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JP2014546269A Active JP6092891B2 (ja) 2011-12-17 2011-12-17 ゲノムの異常の有無を決定する方法及び判断するシステム

Country Status (8)

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US (1) US20140336075A1 (ja)
EP (1) EP2792751B1 (ja)
JP (1) JP6092891B2 (ja)
CN (1) CN103987856B (ja)
ES (1) ES2699743T3 (ja)
HK (1) HK1196857A1 (ja)
RU (1) RU2599419C2 (ja)
WO (1) WO2013086744A1 (ja)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2016042830A1 (ja) * 2014-09-16 2016-03-24 富士フイルム株式会社 胎児染色体の解析方法
WO2016052405A1 (ja) * 2014-09-29 2016-04-07 富士フイルム株式会社 胎児の染色体異数性の非侵襲的判別方法および判別システム
JP2016067268A (ja) * 2014-09-29 2016-05-09 富士フイルム株式会社 胎児の染色体異数性の非侵襲的判別方法
WO2016160965A1 (en) * 2015-03-30 2016-10-06 Rubicon Genomics, Inc. Methods and compositions for repair of dna ends by multiple enzymatic activities
US10167502B2 (en) 2015-04-03 2019-01-01 Fluxion Biosciences, Inc. Molecular characterization of single cells and cell populations for non-invasive diagnostics
CN104894268B (zh) * 2015-06-05 2018-02-09 上海美吉生物医药科技有限公司 定量样本中源自细胞凋亡的dna浓度的方法及其应用
CN105019034A (zh) * 2015-07-11 2015-11-04 浙江大学 高通量转录组文库构建方法
CN108073790B (zh) * 2016-11-10 2022-03-01 安诺优达基因科技(北京)有限公司 一种染色体变异检测装置
WO2018148903A1 (zh) * 2017-02-16 2018-08-23 上海亿康医学检验所有限公司 泌尿系统肿瘤的辅助诊断方法
CN108660197A (zh) * 2017-04-01 2018-10-16 深圳华大基因科技服务有限公司 一种二代序列基因组重叠群的组装方法和系统
CN107217308A (zh) * 2017-06-21 2017-09-29 北京贝瑞和康生物技术股份有限公司 一种用于检测染色体拷贝数变异的测序文库构建方法和试剂盒
CN109402247B (zh) * 2018-11-06 2020-04-07 苏州首度基因科技有限责任公司 一种基于dna变异计数的胎儿染色体检测系统
DE102020116178A1 (de) * 2020-06-18 2021-12-23 Analytik Jena Gmbh Verfahren zum Erkennen einer Amplifikationsphase in einer Amplifikation

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH10507632A (ja) * 1994-09-20 1998-07-28 ミルテニー バイオテック,インコーポレイティド 母体からの胎児血液の濃縮
US20050277147A1 (en) * 2004-06-11 2005-12-15 Ameet Patki Identifying chromosomal abnormalities in cells obtained from follicular fluid
JP2009511001A (ja) * 2005-09-15 2009-03-19 アルテミス ヘルス,インク. 細胞及びその他の粒子を磁気濃縮するためのデバイス並びに方法
US8372584B2 (en) * 2006-06-14 2013-02-12 The General Hospital Corporation Rare cell analysis using sample splitting and DNA tags
AU2007260676A1 (en) * 2006-06-14 2007-12-21 Artemis Health, Inc. Rare cell analysis using sample splitting and DNA tags
WO2008015396A2 (en) * 2006-07-31 2008-02-07 Solexa Limited Method of library preparation avoiding the formation of adaptor dimers
CA3069082C (en) * 2008-09-20 2022-03-22 The Board Of Trustees Of The Leland Stanford Junior University Noninvasive diagnosis of fetal aneuploidy by sequencing
CA2748030A1 (en) * 2008-12-22 2010-07-01 Arnold R. Oliphant Methods and genotyping panels for detecting alleles, genomes, and transcriptomes
US8700341B2 (en) * 2010-01-19 2014-04-15 Verinata Health, Inc. Partition defined detection methods

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