JP2014507134A5 - - Google Patents

Download PDF

Info

Publication number
JP2014507134A5
JP2014507134A5 JP2013547929A JP2013547929A JP2014507134A5 JP 2014507134 A5 JP2014507134 A5 JP 2014507134A5 JP 2013547929 A JP2013547929 A JP 2013547929A JP 2013547929 A JP2013547929 A JP 2013547929A JP 2014507134 A5 JP2014507134 A5 JP 2014507134A5
Authority
JP
Japan
Prior art keywords
shows
pregnant
fetus
mutations
present
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
Application number
JP2013547929A
Other languages
English (en)
Japanese (ja)
Other versions
JP2014507134A (ja
JP6105485B2 (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/IB2012/000015 external-priority patent/WO2012093331A1/en
Publication of JP2014507134A publication Critical patent/JP2014507134A/ja
Publication of JP2014507134A5 publication Critical patent/JP2014507134A5/ja
Application granted granted Critical
Publication of JP6105485B2 publication Critical patent/JP6105485B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2013547929A 2011-01-05 2012-01-05 胎児の性染色体遺伝子型の非侵襲的出生前同定 Active JP6105485B2 (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US201161430032P 2011-01-05 2011-01-05
US61/430,032 2011-01-05
US201161475632P 2011-04-14 2011-04-14
US61/475,632 2011-04-14
PCT/IB2012/000015 WO2012093331A1 (en) 2011-01-05 2012-01-05 Noninvasive prenatal genotyping of fetal sex chromosomes

Publications (3)

Publication Number Publication Date
JP2014507134A JP2014507134A (ja) 2014-03-27
JP2014507134A5 true JP2014507134A5 (https=) 2014-09-04
JP6105485B2 JP6105485B2 (ja) 2017-04-05

Family

ID=46457270

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2013547929A Active JP6105485B2 (ja) 2011-01-05 2012-01-05 胎児の性染色体遺伝子型の非侵襲的出生前同定

Country Status (7)

Country Link
US (3) US10152568B2 (https=)
EP (3) EP3680909B1 (https=)
JP (1) JP6105485B2 (https=)
CN (1) CN103459614B (https=)
AU (1) AU2012204748C1 (https=)
CA (1) CA2823618C (https=)
WO (1) WO2012093331A1 (https=)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10424394B2 (en) 2011-10-06 2019-09-24 Sequenom, Inc. Methods and processes for non-invasive assessment of genetic variations
US10482994B2 (en) 2012-10-04 2019-11-19 Sequenom, Inc. Methods and processes for non-invasive assessment of genetic variations
WO2014132244A1 (en) * 2013-02-28 2014-09-04 The Chinese University Of Hong Kong Maternal plasma transcriptome analysis by massively parallel rna sequencing
ES3037160T3 (en) 2013-06-21 2025-09-29 Sequenom Inc Methods and processes for non-invasive assessment of genetic variations
US10612080B2 (en) * 2014-09-22 2020-04-07 Roche Molecular Systems, Inc. Digital PCR for non-invasive prenatal testing
US10208339B2 (en) * 2015-02-19 2019-02-19 Takara Bio Usa, Inc. Systems and methods for whole genome amplification
US10689706B2 (en) * 2015-07-20 2020-06-23 The Chinese University Of Hong Kong Methylation pattern analysis of haplotypes in tissues in a DNA mixture
WO2018064486A1 (en) 2016-09-29 2018-04-05 Counsyl, Inc. Noninvasive prenatal screening using dynamic iterative depth optimization
IL266346B2 (en) * 2016-11-18 2024-07-01 Univ Hong Kong Chinese Universal haplotype-based noninvasive prenatal testing for single gene diseases
JP7370862B2 (ja) 2017-03-17 2023-10-30 セクエノム, インコーポレイテッド 遺伝子モザイク症のための方法およびプロセス
CN111526793A (zh) 2017-10-27 2020-08-11 朱诺诊断学公司 用于超低体积液体活检的设备、系统和方法
US12462935B2 (en) 2018-03-30 2025-11-04 Nucleix Ltd. Deep learning-based methods, devices, and systems for prenatal testing
EP3815092A2 (en) 2018-06-29 2021-05-05 F. Hoffmann-La Roche AG Detection of microsatellite instability
CN112889088B (zh) * 2018-10-31 2024-12-03 合同会社予幸集团中央研究所 可移动型记录介质、信息处理装置、信息处理方法、信息显示方法和学习模型的制造方法
KR102261474B1 (ko) * 2019-07-12 2021-06-07 주식회사 젠큐릭스 자동 경계화를 이용한 데이터 처리 방법 및 시스템
CN110993024B (zh) * 2019-12-20 2023-08-22 北京科迅生物技术有限公司 建立胎儿浓度校正模型的方法及装置与胎儿浓度定量的方法及装置
CN117711488B (zh) * 2023-11-29 2024-07-02 东莞博奥木华基因科技有限公司 一种基于长读长测序的基因单倍型检测方法及其应用
WO2025234041A1 (ja) * 2024-05-09 2025-11-13 株式会社日立ハイテク 対象核酸を検出する方法、および対象核酸検出システム

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9704444D0 (en) 1997-03-04 1997-04-23 Isis Innovation Non-invasive prenatal diagnosis
US6440706B1 (en) 1999-08-02 2002-08-27 Johns Hopkins University Digital amplification
JP2001269196A (ja) * 2000-03-24 2001-10-02 Hamamatsu Photonics Kk 被検体核酸の定量方法、および被検体核酸の分子数の計数方法
US20030180765A1 (en) 2002-02-01 2003-09-25 The Johns Hopkins University Digital amplification for detection of mismatch repair deficient tumor cells
US6977162B2 (en) 2002-03-01 2005-12-20 Ravgen, Inc. Rapid analysis of variations in a genome
US7727720B2 (en) 2002-05-08 2010-06-01 Ravgen, Inc. Methods for detection of genetic disorders
WO2005023091A2 (en) 2003-09-05 2005-03-17 The Trustees Of Boston University Method for non-invasive prenatal diagnosis
US20050282213A1 (en) * 2003-09-22 2005-12-22 Trisogen Biotechnology Limited Partnership Methods and kits useful for detecting an alteration in a locus copy number
EP3591068A1 (en) 2006-02-02 2020-01-08 The Board of Trustees of the Leland Stanford Junior University Non-invasive fetal genetic screening by digital analysis
PL2557520T3 (pl) 2007-07-23 2021-10-11 The Chinese University Of Hong Kong Określanie zaburzenia równowagi sekwencji kwasu nukleinowego
EP3663411B1 (en) 2008-08-12 2021-11-24 Stokes Bio Limited Methods for digital pcr
WO2011146632A1 (en) * 2010-05-18 2011-11-24 Gene Security Network Inc. Methods for non-invasive prenatal ploidy calling

Similar Documents

Publication Publication Date Title
JP2014507134A5 (https=)
JP6806854B2 (ja) 無細胞核酸の多重解像度分析のための方法
JP6725481B2 (ja) 母体血漿の無侵襲的出生前分子核型分析
CN104662168B (zh) 用于癌症检测的血浆dna突变分析
Hou et al. Single-cell exome sequencing and monoclonal evolution of a JAK2-negative myeloproliferative neoplasm
CN106886688B (zh) 用于分析癌症相关的遗传变异的系统
JP6618929B2 (ja) ウルトラディープシークエンシングにおける希少バリアントコール
TW202039860A (zh) 游離dna末端特徵
CA2986200C (en) Multiplexed parallel analysis of targeted genome regions for non-invasive prenatal testing
CN107849612A (zh) 比对和变体测序分析管线
US20220396838A1 (en) Cell-free dna methylation and nuclease-mediated fragmentation
CN105473741A (zh) 用于遗传变异的非侵入性评估的方法和过程
JP2019164830A (ja) ターゲットシークエンシングパネルから変異を見つける方法
AU2025203115A9 (en) Fragmentation for measuring methylation and disease
JP2015521028A (ja) 標的大規模並列配列決定法を使用した対立遺伝子比分析による胎児トリソミーの非侵襲的出生前診断
CN114303202A (zh) 用于确定胚胎中遗传模式的系统和方法
WO2018090991A1 (en) Universal haplotype-based noninvasive prenatal testing for single gene diseases
Deleye et al. Massively parallel sequencing of micro-manipulated cells targeting a comprehensive panel of disease-causing genes: A comparative evaluation of upstream whole-genome amplification methods
JP2020517304A (ja) Dna分析のためのオフターゲット配列の使用
JP2009518051A (ja) 異なる個体の核酸を含む生体試料から遺伝子型を決定する方法
Ip et al. Molecular Techniques in the Diagnosis and Monitoring of Acute and Chronic Leukaemias
Monaco et al. " Sequencing-grade" screening for BRCA1 variants by oligo-arrays
Vattathil Utilizing Haplotypes for Sensitive SNP Array-based Discovery of Somatic Chromosomal Mutations
HK40006642A (en) Universal haplotype-based noninvasive prenatal testing for single gene diseases
EA042093B1 (ru) Мутационный анализ днк в плазме для детектирования рака