JP2013517789A5 - - Google Patents

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Publication number
JP2013517789A5
JP2013517789A5 JP2012550529A JP2012550529A JP2013517789A5 JP 2013517789 A5 JP2013517789 A5 JP 2013517789A5 JP 2012550529 A JP2012550529 A JP 2012550529A JP 2012550529 A JP2012550529 A JP 2012550529A JP 2013517789 A5 JP2013517789 A5 JP 2013517789A5
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JP
Japan
Prior art keywords
seq
base pair
dna
sample
chromosome
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Pending
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JP2012550529A
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English (en)
Japanese (ja)
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JP2013517789A (ja
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Priority claimed from PCT/IB2011/000217 external-priority patent/WO2011092592A2/en
Publication of JP2013517789A publication Critical patent/JP2013517789A/ja
Publication of JP2013517789A5 publication Critical patent/JP2013517789A5/ja
Pending legal-status Critical Current

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JP2012550529A 2010-01-26 2011-01-26 胎児異数性の非侵襲性出生前診断の方法および組成物 Pending JP2013517789A (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US29833910P 2010-01-26 2010-01-26
US61/298,339 2010-01-26
US40542110P 2010-10-21 2010-10-21
US61/405,421 2010-10-21
PCT/IB2011/000217 WO2011092592A2 (en) 2010-01-26 2011-01-26 Methods and compositions for noninvasive prenatal diagnosis of fetal aneuploidies

Publications (2)

Publication Number Publication Date
JP2013517789A JP2013517789A (ja) 2013-05-20
JP2013517789A5 true JP2013517789A5 (https=) 2014-03-13

Family

ID=44278821

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2012550529A Pending JP2013517789A (ja) 2010-01-26 2011-01-26 胎児異数性の非侵襲性出生前診断の方法および組成物

Country Status (17)

Country Link
US (1) US9249462B2 (https=)
EP (1) EP2529032B1 (https=)
JP (1) JP2013517789A (https=)
KR (1) KR20120107512A (https=)
CN (1) CN102892899A (https=)
AU (1) AU2011210255B2 (https=)
BR (1) BR112012018458A2 (https=)
CA (1) CA2786174A1 (https=)
CY (1) CY1118864T1 (https=)
DK (1) DK2529032T3 (https=)
EA (1) EA023565B1 (https=)
ES (1) ES2623156T3 (https=)
NZ (1) NZ601079A (https=)
PL (1) PL2529032T3 (https=)
PT (1) PT2529032T (https=)
SG (1) SG182322A1 (https=)
WO (1) WO2011092592A2 (https=)

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TWI335354B (en) 2006-09-27 2011-01-01 Univ Hong Kong Chinese Methods for the detection of the degree of the methylation of a target dna and kits
US8476013B2 (en) 2008-09-16 2013-07-02 Sequenom, Inc. Processes and compositions for methylation-based acid enrichment of fetal nucleic acid from a maternal sample useful for non-invasive prenatal diagnoses
US8962247B2 (en) 2008-09-16 2015-02-24 Sequenom, Inc. Processes and compositions for methylation-based enrichment of fetal nucleic acid from a maternal sample useful for non invasive prenatal diagnoses
ES2577017T3 (es) 2009-12-22 2016-07-12 Sequenom, Inc. Procedimientos y kits para identificar la aneuploidia
EP2820129A1 (en) 2012-03-02 2015-01-07 Sequenom, Inc. Methods and processes for non-invasive assessment of genetic variations
US9920361B2 (en) 2012-05-21 2018-03-20 Sequenom, Inc. Methods and compositions for analyzing nucleic acid
US10504613B2 (en) 2012-12-20 2019-12-10 Sequenom, Inc. Methods and processes for non-invasive assessment of genetic variations
US20140093873A1 (en) 2012-07-13 2014-04-03 Sequenom, Inc. Processes and compositions for methylation-based enrichment of fetal nucleic acid from a maternal sample useful for non-invasive prenatal diagnoses
SI4056712T1 (sl) * 2012-09-20 2024-10-30 The Chinese University Of Hong Kong Neinvazivno določanje metiloma tumorja iz plazme
US9732390B2 (en) 2012-09-20 2017-08-15 The Chinese University Of Hong Kong Non-invasive determination of methylome of fetus or tumor from plasma
US10706957B2 (en) 2012-09-20 2020-07-07 The Chinese University Of Hong Kong Non-invasive determination of methylome of tumor from plasma
WO2014051522A1 (en) * 2012-09-26 2014-04-03 Agency For Science, Technology And Research Biomarkers for down syndrome prenatal diagnosis
US11060145B2 (en) 2013-03-13 2021-07-13 Sequenom, Inc. Methods and compositions for identifying presence or absence of hypermethylation or hypomethylation locus
KR20140118682A (ko) 2013-03-29 2014-10-08 (주)셀트리온 2 이상의 인플루엔자 a 바이러스 중화 결합 분자를 포함하는 조성물
EP3736344A1 (en) * 2014-03-13 2020-11-11 Sequenom, Inc. Methods and processes for non-invasive assessment of genetic variations
RU2583830C2 (ru) * 2014-04-21 2016-05-10 Закрытое акционерное общество "Геноаналитика" Способ неинвазивной пренатальной диагностики анеуплоидий плода
EP2942401A1 (en) 2014-05-09 2015-11-11 Lifecodexx AG Detection of DNA that originates from a specific cell-type
EP2942400A1 (en) 2014-05-09 2015-11-11 Lifecodexx AG Multiplex detection of DNA that originates from a specific cell-type
JP6681841B2 (ja) 2014-05-09 2020-04-15 ライフコーデックス アーゲー 特別な細胞タイプに由来するdnaの検出とそれに関連する方法
US20180187267A1 (en) * 2017-01-05 2018-07-05 Michael J. Powell Method for conducting early detection of colon cancer and/or of colon cancer precursor cells and for monitoring colon cancer recurrence
US10174383B2 (en) * 2014-08-13 2019-01-08 Vanadis Diagnostics Method of estimating the amount of a methylated locus in a sample
WO2016176846A1 (zh) * 2015-05-06 2016-11-10 安诺优达基因科技(北京)有限公司 检测染色体非整倍性的试剂盒、装置和方法
EP3666902B1 (en) 2015-05-22 2024-07-03 Medicover Public Co Ltd Multiplexed parallel analysis of targeted genomic regions for non-invasive prenatal testing
HUE050491T2 (hu) 2015-11-10 2020-12-28 Eurofins Lifecodexx Gmbh Magzati kromoszomális aneuploidiák kimutatása olyan DNS régiókat alkalmazva, amelyek különbözõképpen vannak metilezve a magzat és a terhes nõstény között
WO2017094941A1 (ko) * 2015-12-04 2017-06-08 주식회사 녹십자지놈 핵산의 혼합물을 포함하는 샘플에서 복제수 변이를 결정하는 방법
KR101817180B1 (ko) * 2016-01-20 2018-01-10 이원다이애그노믹스(주) 염색체 이상 판단 방법
EP3885447B1 (en) 2016-05-30 2024-01-10 The Chinese University Of Hong Kong Detecting hematological disorders using cell-free dna in blood
CN109112209B (zh) * 2017-06-25 2022-06-24 国家卫生计生委科学技术研究所 用于无创产前检测胎儿非整倍体染色体的参考品
AU2019234843B2 (en) 2018-03-13 2025-12-04 Grail, Inc. Anomalous fragment detection and classification
KR20200060969A (ko) 2018-11-23 2020-06-02 (주)셀트리온 인플루엔자 바이러스 질환을 치료하기 위한 투여 요법
US12234514B2 (en) 2018-12-21 2025-02-25 Grail, Inc. Source of origin deconvolution based on methylation fragments in cell-free DNA samples
US20230151409A1 (en) * 2020-03-30 2023-05-18 Vilnius University Methods and compositions for noninvasive prenatal diagnosis through targeted covalent labeling of genomic sites
US12592321B2 (en) 2020-06-19 2026-03-31 University Health Network Cancer detection and classification using methylome analysis
KR102332540B1 (ko) * 2020-07-02 2021-11-29 의료법인 성광의료재단 다운증후군 특이적인 후성학적 마커를 이용한 다운증후군 진단 방법
US20250079015A1 (en) * 2022-01-10 2025-03-06 Washington State University Dna methylation biomarkers for preterm birth
EP4695417A1 (en) * 2023-04-14 2026-02-18 Adela, Inc. Methods and systems for cell-free nucleic acid processing
WO2025179073A1 (en) * 2024-02-21 2025-08-28 Adela, Inc. Methods and systems for tissue informed differentially methylated region analysis

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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
WO2005028674A2 (en) 2003-09-22 2005-03-31 Trisogen Biotechnology Limited Partnership Methods and kits useful for detecting an alteration in a locus copy number
GB0413688D0 (en) 2004-06-18 2004-07-21 Novartis Forschungsstiftung Analysis of methylated nucleic acid
JP5149013B2 (ja) 2004-11-29 2013-02-20 セクエノム,インコーポレイティド メチル化dnaを検出する手段、及び方法
US20090042195A1 (en) 2005-10-07 2009-02-12 Bradford Coffee Methods and systems for screening for and diagnosing dna methylation associated abnormalities and sex chromosome aneuploidies
US7901884B2 (en) * 2006-05-03 2011-03-08 The Chinese University Of Hong Kong Markers for prenatal diagnosis and monitoring
PL2557520T3 (pl) * 2007-07-23 2021-10-11 The Chinese University Of Hong Kong Określanie zaburzenia równowagi sekwencji kwasu nukleinowego
JP5322471B2 (ja) 2008-03-27 2013-10-23 シスメックス株式会社 メチル化dnaの解析方法及びプライマーセット
US8476013B2 (en) * 2008-09-16 2013-07-02 Sequenom, Inc. Processes and compositions for methylation-based acid enrichment of fetal nucleic acid from a maternal sample useful for non-invasive prenatal diagnoses

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