JP2016518811A5 - - Google Patents

Download PDF

Info

Publication number
JP2016518811A5
JP2016518811A5 JP2015561932A JP2015561932A JP2016518811A5 JP 2016518811 A5 JP2016518811 A5 JP 2016518811A5 JP 2015561932 A JP2015561932 A JP 2015561932A JP 2015561932 A JP2015561932 A JP 2015561932A JP 2016518811 A5 JP2016518811 A5 JP 2016518811A5
Authority
JP
Japan
Prior art keywords
allele
fetuses
ratio
cutoff value
determining
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.)
Pending
Application number
JP2015561932A
Other languages
English (en)
Japanese (ja)
Other versions
JP2016518811A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/CN2014/073506 external-priority patent/WO2014139477A1/en
Publication of JP2016518811A publication Critical patent/JP2016518811A/ja
Publication of JP2016518811A5 publication Critical patent/JP2016518811A5/ja
Pending legal-status Critical Current

Links

JP2015561932A 2013-03-15 2014-03-17 多胎妊娠における胎児ゲノムの決定 Pending JP2016518811A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201361789992P 2013-03-15 2013-03-15
US61/789,992 2013-03-15
PCT/CN2014/073506 WO2014139477A1 (en) 2013-03-15 2014-03-17 Determining fetal genomes for multiple fetus pregnancies

Publications (2)

Publication Number Publication Date
JP2016518811A JP2016518811A (ja) 2016-06-30
JP2016518811A5 true JP2016518811A5 (https=) 2017-04-13

Family

ID=51535879

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2015561932A Pending JP2016518811A (ja) 2013-03-15 2014-03-17 多胎妊娠における胎児ゲノムの決定

Country Status (11)

Country Link
US (1) US10106836B2 (https=)
EP (2) EP2971126B1 (https=)
JP (1) JP2016518811A (https=)
KR (1) KR20150132216A (https=)
CN (1) CN105121660B (https=)
AU (1) AU2014231358A1 (https=)
CA (1) CA2901773A1 (https=)
EA (1) EA201500939A1 (https=)
MX (1) MX363345B (https=)
TW (1) TWI637058B (https=)
WO (1) WO2014139477A1 (https=)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3783110B1 (en) 2009-11-05 2022-11-23 The Chinese University Of Hong Kong Fetal genomic analysis from a maternal biological sample
CA2827873C (en) 2011-02-24 2022-08-16 The Chinese University Of Hong Kong Molecular testing of multiple pregnancies
CN105121660B (zh) 2013-03-15 2018-09-28 香港中文大学 确定多胎妊娠的胎儿基因组
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

Family Cites Families (22)

* 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
US6927028B2 (en) 2001-08-31 2005-08-09 Chinese University Of Hong Kong Non-invasive methods for detecting non-host DNA in a host using epigenetic differences between the host and non-host DNA
US7727720B2 (en) 2002-05-08 2010-06-01 Ravgen, Inc. Methods for detection of genetic disorders
EP1599608A4 (en) 2003-03-05 2007-07-18 Genetic Technologies Ltd Identification of fetal DNA and fetal cell marker in maternal plasma or serum
ATE435301T1 (de) 2003-10-16 2009-07-15 Sequenom Inc Nicht invasiver nachweis fötaler genetischer merkmale
US7645576B2 (en) 2005-03-18 2010-01-12 The Chinese University Of Hong Kong Method for the detection of chromosomal aneuploidies
US20070122823A1 (en) 2005-09-01 2007-05-31 Bianchi Diana W Amniotic fluid cell-free fetal DNA fragment size pattern for prenatal diagnosis
GB0523276D0 (en) 2005-11-15 2005-12-21 London Bridge Fertility Chromosomal analysis by molecular karyotyping
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
EP2351858B1 (en) 2006-02-28 2014-12-31 University of Louisville Research Foundation Detecting fetal chromosomal abnormalities using tandem single nucleotide polymorphisms
EP2029779A4 (en) 2006-06-14 2010-01-20 Living Microsystems Inc HIGHLY PARALLEL SNP GENOTYPING UTILIZATION FOR FETAL DIAGNOSIS
PL2557520T3 (pl) 2007-07-23 2021-10-11 The Chinese University Of Hong Kong Określanie zaburzenia równowagi sekwencji kwasu nukleinowego
US12180549B2 (en) 2007-07-23 2024-12-31 The Chinese University Of Hong Kong Diagnosing fetal chromosomal aneuploidy using genomic sequencing
EP2321642B1 (en) 2008-08-04 2017-01-11 Natera, Inc. Methods for allele calling and ploidy calling
KR101781147B1 (ko) 2008-12-22 2017-10-10 셀루라 인코포레이티드 대립유전자, 게놈 및 전사체 검출을 위한 방법 및 유전자형 분석 패널
EP3783110B1 (en) * 2009-11-05 2022-11-23 The Chinese University Of Hong Kong Fetal genomic analysis from a maternal biological sample
CA2780016C (en) 2009-11-06 2017-09-19 The Chinese University Of Hong Kong Size-based genomic analysis
US9260745B2 (en) * 2010-01-19 2016-02-16 Verinata Health, Inc. Detecting and classifying copy number variation
WO2011146632A1 (en) 2010-05-18 2011-11-24 Gene Security Network Inc. Methods for non-invasive prenatal ploidy calling
US20120190020A1 (en) * 2011-01-25 2012-07-26 Aria Diagnostics, Inc. Detection of genetic abnormalities
CA2827873C (en) * 2011-02-24 2022-08-16 The Chinese University Of Hong Kong Molecular testing of multiple pregnancies
CN105121660B (zh) 2013-03-15 2018-09-28 香港中文大学 确定多胎妊娠的胎儿基因组

Similar Documents

Publication Publication Date Title
US20250027156A1 (en) Methods and systems for detection of abnormal karyotypes
CN106011237B (zh) 多胎妊娠的分子测试
TWI801188B (zh) 藉由大量平行rna定序之母體血漿轉錄體分析
CA2823618C (en) Noninvasive prenatal genotyping of fetal sex chromosomes
JP2014507158A5 (https=)
Ruano et al. Alternative splicing in normal and pathological human placentas is correlated to genetic variants
Çağlayan et al. ALPK3 gene mutation in a patient with congenital cardiomyopathy and dysmorphic features
Liu et al. A forward look at noninvasive prenatal testing
Russo et al. Comparative study of aCGH and Next Generation Sequencing (NGS) for chromosomal microdeletion and microduplication screening
TW202438680A (zh) 可實施2種以上檢測的遺傳學分析方法
JP2016518811A5 (https=)
US10106836B2 (en) Determining fetal genomes for multiple fetus pregnancies
Silveira et al. Genomic screening of testicular germ cell tumors from monozygotic twins
Kumasaka et al. PlatinumCNV: a Bayesian Gaussian mixture model for genotyping copy number polymorphisms using SNP array signal intensity data
HK40062687B (en) Noninvasive prenatal genotyping of fetal sex chromosomes
Han et al. Non‐invasive prenatal testing of monogenic fetal characteristics by maternal plasma DNA analysis
HK1260856A1 (en) Determining fetal genomes for multiple fetus pregnancies
AU2015227510A1 (en) Noninvasive prenatal genotyping of fetal sex chromosomes
HK1189393B (en) Noninvasive prenatal genotyping of fetal sex chromosomes
HK1189393A (en) Noninvasive prenatal genotyping of fetal sex chromosomes