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 (enExample) 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 (enExample)
EP (2) EP3434790A1 (enExample)
JP (1) JP2016518811A (enExample)
KR (1) KR20150132216A (enExample)
CN (1) CN105121660B (enExample)
AU (1) AU2014231358A1 (enExample)
CA (1) CA2901773A1 (enExample)
EA (1) EA201500939A1 (enExample)
MX (1) MX363345B (enExample)
TW (1) TWI637058B (enExample)
WO (1) WO2014139477A1 (enExample)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
HUE061110T2 (hu) 2009-11-05 2023-05-28 Univ Hong Kong Chinese Magzati genomelemzés anyai biológiai mintából
EP2678451B1 (en) 2011-02-24 2017-04-26 The Chinese University Of Hong Kong Molecular testing of multiple pregnancies
AU2014231358A1 (en) 2013-03-15 2015-09-24 The Chinese University Of Hong Kong Determining fetal genomes for multiple fetus pregnancies
EP3739061B1 (en) 2015-07-20 2022-03-23 The Chinese University Of Hong Kong Methylation pattern analysis of haplotypes in tissues in 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
TR201910868T4 (tr) 2006-02-02 2019-08-21 Univ Leland Stanford Junior Dijital analizle invazif olmayan fetal genetik tarama.
WO2007100911A2 (en) 2006-02-28 2007-09-07 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
EP3892736A1 (en) 2007-07-23 2021-10-13 The Chinese University of Hong Kong Determining a nucleic acid sequence imbalance
US12180549B2 (en) 2007-07-23 2024-12-31 The Chinese University Of Hong Kong Diagnosing fetal chromosomal aneuploidy using genomic sequencing
ES2620431T3 (es) 2008-08-04 2017-06-28 Natera, Inc. Métodos para la determinación de alelos y de ploidía
CA2748030A1 (en) 2008-12-22 2010-07-01 Arnold R. Oliphant Methods and genotyping panels for detecting alleles, genomes, and transcriptomes
HUE061110T2 (hu) 2009-11-05 2023-05-28 Univ Hong Kong Chinese Magzati genomelemzés anyai biológiai mintából
MX357692B (es) 2009-11-06 2018-07-19 Univ Hong Kong Chinese Analisis genomico a base de tamaño.
US9260745B2 (en) * 2010-01-19 2016-02-16 Verinata Health, Inc. Detecting and classifying copy number variation
CA3207599A1 (en) 2010-05-18 2011-11-24 Natera, Inc. Methods for non-invasive prenatal ploidy calling
WO2012103031A2 (en) * 2011-01-25 2012-08-02 Ariosa Diagnostics, Inc. Detection of genetic abnormalities
EP2678451B1 (en) 2011-02-24 2017-04-26 The Chinese University Of Hong Kong Molecular testing of multiple pregnancies
AU2014231358A1 (en) 2013-03-15 2015-09-24 The Chinese University Of Hong Kong Determining fetal genomes for multiple fetus pregnancies

Similar Documents

Publication Publication Date Title
Oliver et al. New insights into human nondisjunction of chromosome 21 in oocytes
CN106011237B (zh) 多胎妊娠的分子测试
US20250027156A1 (en) Methods and systems for detection of abnormal karyotypes
CA2823618C (en) Noninvasive prenatal genotyping of fetal sex chromosomes
JP2014507158A5 (enExample)
Çağlayan et al. ALPK3 gene mutation in a patient with congenital cardiomyopathy and dysmorphic features
Ruano et al. Alternative splicing in normal and pathological human placentas is correlated to genetic variants
Liu et al. A forward look at noninvasive prenatal testing
CN115035949A (zh) 通过母亲血浆dna的浅深度测序准确定量胎儿dna分数
Russo et al. Comparative study of aCGH and Next Generation Sequencing (NGS) for chromosomal microdeletion and microduplication screening
JP2016518811A5 (enExample)
TW202438680A (zh) 可實施2種以上檢測的遺傳學分析方法
US10106836B2 (en) Determining fetal genomes for multiple fetus pregnancies
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
AU2015227510B2 (en) Noninvasive prenatal genotyping of fetal sex chromosomes
Warden et al. Bioinformatics for copy number variation data
HK1260856A1 (en) Determining fetal genomes for multiple fetus pregnancies
HK1189393B (en) Noninvasive prenatal genotyping of fetal sex chromosomes
HK1189393A (en) Noninvasive prenatal genotyping of fetal sex chromosomes