|
US9424392B2
(en)
|
2005-11-26 |
2016-08-23 |
Natera, Inc. |
System and method for cleaning noisy genetic data from target individuals using genetic data from genetically related individuals
|
|
US11111544B2
(en)
|
2005-07-29 |
2021-09-07 |
Natera, Inc. |
System and method for cleaning noisy genetic data and determining chromosome copy number
|
|
US10081839B2
(en)
|
2005-07-29 |
2018-09-25 |
Natera, Inc |
System and method for cleaning noisy genetic data and determining chromosome copy number
|
|
US11111543B2
(en)
|
2005-07-29 |
2021-09-07 |
Natera, Inc. |
System and method for cleaning noisy genetic data and determining chromosome copy number
|
|
US8532930B2
(en)
|
2005-11-26 |
2013-09-10 |
Natera, Inc. |
Method for determining the number of copies of a chromosome in the genome of a target individual using genetic data from genetically related individuals
|
|
US10083273B2
(en)
|
2005-07-29 |
2018-09-25 |
Natera, Inc. |
System and method for cleaning noisy genetic data and determining chromosome copy number
|
|
EP2351858B1
(en)
|
2006-02-28 |
2014-12-31 |
University of Louisville Research Foundation |
Detecting fetal chromosomal abnormalities using tandem single nucleotide polymorphisms
|
|
US8609338B2
(en)
|
2006-02-28 |
2013-12-17 |
University Of Louisville Research Foundation, Inc. |
Detecting fetal chromosomal abnormalities using tandem single nucleotide polymorphisms
|
|
US20080050739A1
(en)
|
2006-06-14 |
2008-02-28 |
Roland Stoughton |
Diagnosis of fetal abnormalities using polymorphisms including short tandem repeats
|
|
EP2029779A4
(en)
|
2006-06-14 |
2010-01-20 |
Living Microsystems Inc |
HIGHLY PARALLEL SNP GENOTYPING UTILIZATION FOR FETAL DIAGNOSIS
|
|
WO2009105531A1
(en)
*
|
2008-02-19 |
2009-08-27 |
Gene Security Network, Inc. |
Methods for cell genotyping
|
|
EP2271772B1
(en)
*
|
2008-03-11 |
2014-07-16 |
Sequenom, Inc. |
Nucleic acid-based tests for prenatal gender determination
|
|
WO2009146335A1
(en)
*
|
2008-05-27 |
2009-12-03 |
Gene Security Network, Inc. |
Methods for embryo characterization and comparison
|
|
EP2321642B1
(en)
*
|
2008-08-04 |
2017-01-11 |
Natera, Inc. |
Methods for allele calling and ploidy calling
|
|
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
|
|
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
|
|
US9524369B2
(en)
|
2009-06-15 |
2016-12-20 |
Complete Genomics, Inc. |
Processing and analysis of complex nucleic acid sequence data
|
|
WO2011041485A1
(en)
|
2009-09-30 |
2011-04-07 |
Gene Security Network, Inc. |
Methods for non-invasive prenatal ploidy calling
|
|
EP3783110B1
(en)
|
2009-11-05 |
2022-11-23 |
The Chinese University Of Hong Kong |
Fetal genomic analysis from a maternal biological sample
|
|
JP2013511991A
(ja)
*
|
2009-11-25 |
2013-04-11 |
クアンタライフ， インコーポレイテッド |
遺伝子材料を検出する方法および組成物
|
|
ES2577017T3
(es)
|
2009-12-22 |
2016-07-12 |
Sequenom, Inc. |
Procedimientos y kits para identificar la aneuploidia
|
|
US20120010085A1
(en)
|
2010-01-19 |
2012-01-12 |
Rava Richard P |
Methods for determining fraction of fetal nucleic acids in maternal samples
|
|
EP2513341B1
(en)
|
2010-01-19 |
2017-04-12 |
Verinata Health, Inc |
Identification of polymorphic sequences in mixtures of genomic dna by whole genome sequencing
|
|
US10388403B2
(en)
|
2010-01-19 |
2019-08-20 |
Verinata Health, Inc. |
Analyzing copy number variation in the detection of cancer
|
|
US9323888B2
(en)
|
2010-01-19 |
2016-04-26 |
Verinata Health, Inc. |
Detecting and classifying copy number variation
|
|
WO2011091063A1
(en)
|
2010-01-19 |
2011-07-28 |
Verinata Health, Inc. |
Partition defined detection methods
|
|
EP2370599B1
(en)
|
2010-01-19 |
2015-01-21 |
Verinata Health, Inc |
Method for determining copy number variations
|
|
US20120100548A1
(en)
|
2010-10-26 |
2012-04-26 |
Verinata Health, Inc. |
Method for determining copy number variations
|
|
US9260745B2
(en)
|
2010-01-19 |
2016-02-16 |
Verinata Health, Inc. |
Detecting and classifying copy number variation
|
|
US20110312503A1
(en)
|
2010-01-23 |
2011-12-22 |
Artemis Health, Inc. |
Methods of fetal abnormality detection
|
|
US9677118B2
(en)
|
2014-04-21 |
2017-06-13 |
Natera, Inc. |
Methods for simultaneous amplification of target loci
|
|
WO2011146632A1
(en)
|
2010-05-18 |
2011-11-24 |
Gene Security Network Inc. |
Methods for non-invasive prenatal ploidy calling
|
|
US12152275B2
(en)
|
2010-05-18 |
2024-11-26 |
Natera, Inc. |
Methods for non-invasive prenatal ploidy calling
|
|
US10316362B2
(en)
|
2010-05-18 |
2019-06-11 |
Natera, Inc. |
Methods for simultaneous amplification of target loci
|
|
US11332793B2
(en)
|
2010-05-18 |
2022-05-17 |
Natera, Inc. |
Methods for simultaneous amplification of target loci
|
|
US20190010543A1
(en)
|
2010-05-18 |
2019-01-10 |
Natera, Inc. |
Methods for simultaneous amplification of target loci
|
|
US11326208B2
(en)
|
2010-05-18 |
2022-05-10 |
Natera, Inc. |
Methods for nested PCR amplification of cell-free DNA
|
|
US11408031B2
(en)
|
2010-05-18 |
2022-08-09 |
Natera, Inc. |
Methods for non-invasive prenatal paternity testing
|
|
US11339429B2
(en)
|
2010-05-18 |
2022-05-24 |
Natera, Inc. |
Methods for non-invasive prenatal ploidy calling
|
|
US11322224B2
(en)
|
2010-05-18 |
2022-05-03 |
Natera, Inc. |
Methods for non-invasive prenatal ploidy calling
|
|
US11332785B2
(en)
|
2010-05-18 |
2022-05-17 |
Natera, Inc. |
Methods for non-invasive prenatal ploidy calling
|
|
US12221653B2
(en)
|
2010-05-18 |
2025-02-11 |
Natera, Inc. |
Methods for simultaneous amplification of target loci
|
|
US11939634B2
(en)
|
2010-05-18 |
2024-03-26 |
Natera, Inc. |
Methods for simultaneous amplification of target loci
|
|
US12545960B2
(en)
|
2010-05-18 |
2026-02-10 |
Natera, Inc. |
Methods for simultaneous amplification of target loci
|
|
WO2012012703A2
(en)
*
|
2010-07-23 |
2012-01-26 |
Esoterix Genetic Laboratories, Llc |
Identification of differentially represented fetal or maternal genomic regions and uses thereof
|
|
US10167508B2
(en)
|
2010-08-06 |
2019-01-01 |
Ariosa Diagnostics, Inc. |
Detection of genetic abnormalities
|
|
US11031095B2
(en)
*
|
2010-08-06 |
2021-06-08 |
Ariosa Diagnostics, Inc. |
Assay systems for determination of fetal copy number variation
|
|
US20130040375A1
(en)
|
2011-08-08 |
2013-02-14 |
Tandem Diagnotics, Inc. |
Assay systems for genetic analysis
|
|
US20130261003A1
(en)
|
2010-08-06 |
2013-10-03 |
Ariosa Diagnostics, In. |
Ligation-based detection of genetic variants
|
|
US20140342940A1
(en)
|
2011-01-25 |
2014-11-20 |
Ariosa Diagnostics, Inc. |
Detection of Target Nucleic Acids using Hybridization
|
|
US10533223B2
(en)
|
2010-08-06 |
2020-01-14 |
Ariosa Diagnostics, Inc. |
Detection of target nucleic acids using hybridization
|
|
US11203786B2
(en)
|
2010-08-06 |
2021-12-21 |
Ariosa Diagnostics, Inc. |
Detection of target nucleic acids using hybridization
|
|
US8700338B2
(en)
|
2011-01-25 |
2014-04-15 |
Ariosa Diagnosis, Inc. |
Risk calculation for evaluation of fetal aneuploidy
|
|
US20120034603A1
(en)
|
2010-08-06 |
2012-02-09 |
Tandem Diagnostics, Inc. |
Ligation-based detection of genetic variants
|
|
CN105243295B
(zh)
|
2010-11-30 |
2018-08-17 |
香港中文大学 |
与癌症相关的遗传或分子畸变的检测
|
|
CN103620055A
(zh)
|
2010-12-07 |
2014-03-05 |
利兰·斯坦福青年大学托管委员会 |
在全基因组规模非侵入性确定亲本单倍型的胎儿遗传
|
|
CN103608466B
(zh)
|
2010-12-22 |
2020-09-18 |
纳特拉公司 |
非侵入性产前亲子鉴定方法
|
|
US9994897B2
(en)
|
2013-03-08 |
2018-06-12 |
Ariosa Diagnostics, Inc. |
Non-invasive fetal sex determination
|
|
US20120190020A1
(en)
*
|
2011-01-25 |
2012-07-26 |
Aria Diagnostics, Inc. |
Detection of genetic abnormalities
|
|
US8756020B2
(en)
*
|
2011-01-25 |
2014-06-17 |
Ariosa Diagnostics, Inc. |
Enhanced risk probabilities using biomolecule estimations
|
|
US10131947B2
(en)
|
2011-01-25 |
2018-11-20 |
Ariosa Diagnostics, Inc. |
Noninvasive detection of fetal aneuploidy in egg donor pregnancies
|
|
US11270781B2
(en)
|
2011-01-25 |
2022-03-08 |
Ariosa Diagnostics, Inc. |
Statistical analysis for non-invasive sex chromosome aneuploidy determination
|
|
AU2012214312A1
(en)
|
2011-02-09 |
2013-08-22 |
Bio-Rad Laboratories, Inc. |
Analysis of nucleic acids
|
|
RU2671980C2
(ru)
|
2011-02-09 |
2018-11-08 |
Натера, Инк. |
Способы неинвазивного пренатального установления плоидности
|
|
CA2827873C
(en)
|
2011-02-24 |
2022-08-16 |
The Chinese University Of Hong Kong |
Molecular testing of multiple pregnancies
|
|
RS57837B1
(sr)
*
|
2011-04-12 |
2018-12-31 |
Verinata Health Inc |
Razrešavanje genomskih frakcija upotrebom broja kopija polimorfizama
|
|
GB2484764B
(en)
|
2011-04-14 |
2012-09-05 |
Verinata Health Inc |
Normalizing chromosomes for the determination and verification of common and rare chromosomal aneuploidies
|
|
US9411937B2
(en)
|
2011-04-15 |
2016-08-09 |
Verinata Health, Inc. |
Detecting and classifying copy number variation
|
|
US20140235474A1
(en)
|
2011-06-24 |
2014-08-21 |
Sequenom, Inc. |
Methods and processes for non invasive assessment of a genetic variation
|
|
US8880456B2
(en)
|
2011-08-25 |
2014-11-04 |
Complete Genomics, Inc. |
Analyzing genome sequencing information to determine likelihood of co-segregating alleles on haplotypes
|
|
US8712697B2
(en)
|
2011-09-07 |
2014-04-29 |
Ariosa Diagnostics, Inc. |
Determination of copy number variations using binomial probability calculations
|
|
US9367663B2
(en)
|
2011-10-06 |
2016-06-14 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
|
US9984198B2
(en)
|
2011-10-06 |
2018-05-29 |
Sequenom, Inc. |
Reducing sequence read count error in assessment of complex genetic variations
|
|
WO2013052907A2
(en)
|
2011-10-06 |
2013-04-11 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
|
US10424394B2
(en)
|
2011-10-06 |
2019-09-24 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
|
US10196681B2
(en)
|
2011-10-06 |
2019-02-05 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
|
CA2861856C
(en)
|
2012-01-20 |
2020-06-02 |
Sequenom, Inc. |
Diagnostic processes that factor experimental conditions
|
|
US9238836B2
(en)
|
2012-03-30 |
2016-01-19 |
Pacific Biosciences Of California, Inc. |
Methods and compositions for sequencing modified nucleic acids
|
|
WO2013130848A1
(en)
*
|
2012-02-29 |
2013-09-06 |
Natera, Inc. |
Informatics enhanced analysis of fetal samples subject to maternal contamination
|
|
EP2820129A1
(en)
*
|
2012-03-02 |
2015-01-07 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
|
US9892230B2
(en)
|
2012-03-08 |
2018-02-13 |
The Chinese University Of Hong Kong |
Size-based analysis of fetal or tumor DNA fraction in plasma
|
|
CA2866324C
(en)
|
2012-03-13 |
2019-01-15 |
The Chinese University Of Hong Kong |
Methods for analyzing massively parallel sequencing data for noninvasive prenatal diagnosis
|
|
US20150094210A1
(en)
|
2012-05-14 |
2015-04-02 |
Bgi Diagnosis Co., Ltd. |
Method, system and computer readable medium for determining base information in predetermined area of fetus genome
|
|
US10504613B2
(en)
|
2012-12-20 |
2019-12-10 |
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
|
|
US10289800B2
(en)
|
2012-05-21 |
2019-05-14 |
Ariosa Diagnostics, Inc. |
Processes for calculating phased fetal genomic sequences
|
|
US20150105267A1
(en)
*
|
2012-05-24 |
2015-04-16 |
University Of Washington Through Its Center For Commercialization |
Whole genome sequencing of a human fetus
|
|
US11261494B2
(en)
|
2012-06-21 |
2022-03-01 |
The Chinese University Of Hong Kong |
Method of measuring a fractional concentration of tumor DNA
|
|
US10497461B2
(en)
|
2012-06-22 |
2019-12-03 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
|
CN110777195A
(zh)
*
|
2012-07-13 |
2020-02-11 |
生命技术公司 |
采用一组snp的人身份识别
|
|
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
|
|
EP2875156A4
(en)
|
2012-07-19 |
2016-02-24 |
Ariosa Diagnostics Inc |
SEQUENTIAL LIGATION-BASED MULTIPLEX DETECTION OF GENETIC VARIANTS
|
|
US20140100126A1
(en)
|
2012-08-17 |
2014-04-10 |
Natera, Inc. |
Method for Non-Invasive Prenatal Testing Using Parental Mosaicism Data
|
|
US20140065621A1
(en)
*
|
2012-09-04 |
2014-03-06 |
Natera, Inc. |
Methods for increasing fetal fraction in maternal blood
|
|
CA2883245A1
(en)
*
|
2012-09-06 |
2014-03-13 |
Ancestry.Com Dna, Llc |
Using haplotypes to infer ancestral origins for recently admixed individuals
|
|
US10706957B2
(en)
|
2012-09-20 |
2020-07-07 |
The Chinese University Of Hong Kong |
Non-invasive determination of methylome of tumor from plasma
|
|
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
|
|
US10482994B2
(en)
*
|
2012-10-04 |
2019-11-19 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
|
US9213947B1
(en)
|
2012-11-08 |
2015-12-15 |
23Andme, Inc. |
Scalable pipeline for local ancestry inference
|
|
US9836576B1
(en)
|
2012-11-08 |
2017-12-05 |
23Andme, Inc. |
Phasing of unphased genotype data
|
|
US10643738B2
(en)
*
|
2013-01-10 |
2020-05-05 |
The Chinese University Of Hong Kong |
Noninvasive prenatal molecular karyotyping from maternal plasma
|
|
EP4414990A3
(en)
|
2013-01-17 |
2024-11-06 |
Personalis, Inc. |
Methods and systems for genetic analysis
|
|
US20130309666A1
(en)
|
2013-01-25 |
2013-11-21 |
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
|
|
US11060145B2
(en)
|
2013-03-13 |
2021-07-13 |
Sequenom, Inc. |
Methods and compositions for identifying presence or absence of hypermethylation or hypomethylation locus
|
|
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
|
|
US10930368B2
(en)
|
2013-04-03 |
2021-02-23 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
|
CA2909479A1
(en)
*
|
2013-05-09 |
2014-11-13 |
F. Hoffmann-La Roche Ag |
Method of determining the fraction of fetal dna in maternal blood using hla markers
|
|
KR102665592B1
(ko)
|
2013-05-24 |
2024-05-21 |
시쿼넘, 인코포레이티드 |
유전적 변이의 비침습 평가를 위한 방법 및 프로세스
|
|
ES3037160T3
(en)
|
2013-06-21 |
2025-09-29 |
Sequenom Inc |
Methods and processes for non-invasive assessment of genetic variations
|
|
US20150004601A1
(en)
*
|
2013-06-28 |
2015-01-01 |
Ariosa Diagnostics, Inc. |
Massively parallel sequencing of random dna fragments for determination of fetal fraction
|
|
GB201318369D0
(en)
*
|
2013-10-17 |
2013-12-04 |
Univ Leuven Kath |
Methods using BAF
|
|
WO2015031689A1
(en)
|
2013-08-30 |
2015-03-05 |
Personalis, Inc. |
Methods and systems for genomic analysis
|
|
US10577655B2
(en)
|
2013-09-27 |
2020-03-03 |
Natera, Inc. |
Cell free DNA diagnostic testing standards
|
|
US9499870B2
(en)
|
2013-09-27 |
2016-11-22 |
Natera, Inc. |
Cell free DNA diagnostic testing standards
|
|
US10262755B2
(en)
|
2014-04-21 |
2019-04-16 |
Natera, Inc. |
Detecting cancer mutations and aneuploidy in chromosomal segments
|
|
WO2015051275A1
(en)
|
2013-10-03 |
2015-04-09 |
Personalis, Inc. |
Methods for analyzing genotypes
|
|
KR102384620B1
(ko)
|
2013-10-04 |
2022-04-11 |
시쿼넘, 인코포레이티드 |
유전적 변이의 비침습 평가를 위한 방법 및 프로세스
|
|
CN105874082B
(zh)
|
2013-10-07 |
2020-06-02 |
塞昆纳姆股份有限公司 |
用于非侵入性评估染色体改变的方法和过程
|
|
EP3736344A1
(en)
|
2014-03-13 |
2020-11-11 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
|
CA2945962C
(en)
|
2014-04-21 |
2023-08-29 |
Natera, Inc. |
Detecting mutations and ploidy in chromosomal segments
|
|
US12492429B2
(en)
|
2014-04-21 |
2025-12-09 |
Natera, Inc. |
Detecting mutations and ploidy in chromosomal segments
|
|
US20180173846A1
(en)
|
2014-06-05 |
2018-06-21 |
Natera, Inc. |
Systems and Methods for Detection of Aneuploidy
|
|
EP3169803B1
(en)
|
2014-07-18 |
2019-11-20 |
Illumina, Inc. |
Non-invasive prenatal diagnosis of fetal genetic condition using cellular dna and cell free dna
|
|
US20160026759A1
(en)
*
|
2014-07-22 |
2016-01-28 |
Yourgene Bioscience |
Detecting Chromosomal Aneuploidy
|
|
EP4358097A1
(en)
|
2014-07-25 |
2024-04-24 |
University of Washington |
Methods of determining tissues and/or cell types giving rise to cell-free dna, and methods of identifying a disease or disorder using same
|
|
US11783911B2
(en)
|
2014-07-30 |
2023-10-10 |
Sequenom, Inc |
Methods and processes for non-invasive assessment of genetic variations
|
|
CN104182655B
(zh)
*
|
2014-09-01 |
2017-03-08 |
上海美吉生物医药科技有限公司 |
一种判断胎儿基因型的方法
|
|
CN104232778B
(zh)
*
|
2014-09-19 |
2016-08-17 |
天津华大基因科技有限公司 |
同时确定胎儿单体型及染色体非整倍性的方法及装置
|
|
US10612080B2
(en)
*
|
2014-09-22 |
2020-04-07 |
Roche Molecular Systems, Inc. |
Digital PCR for non-invasive prenatal testing
|
|
US10125399B2
(en)
|
2014-10-30 |
2018-11-13 |
Personalis, Inc. |
Methods for using mosaicism in nucleic acids sampled distal to their origin
|
|
CN105648045B
(zh)
*
|
2014-11-13 |
2019-10-11 |
天津华大基因科技有限公司 |
确定胎儿目标区域单体型的方法和装置
|
|
CN105648044B
(zh)
*
|
2014-11-13 |
2019-10-11 |
天津华大基因科技有限公司 |
确定胎儿目标区域单体型的方法和装置
|
|
CN104561311B
(zh)
*
|
2015-01-04 |
2016-08-17 |
北京大学第三医院 |
一种来自人辅助生殖胚胎发育早期出生安全性预测的试剂盒
|
|
CN104561309B
(zh)
*
|
2015-01-04 |
2017-04-19 |
北京积水潭医院 |
一种来自人辅助生殖囊胚植入前进行出生安全性预测的试剂盒
|
|
US10364467B2
(en)
|
2015-01-13 |
2019-07-30 |
The Chinese University Of Hong Kong |
Using size and number aberrations in plasma DNA for detecting cancer
|
|
CN107109324B
(zh)
*
|
2015-01-16 |
2019-11-08 |
深圳华大基因股份有限公司 |
确定胎儿核酸含量的方法和装置
|
|
HUE058263T2
(hu)
|
2015-02-10 |
2022-07-28 |
Univ Hong Kong Chinese |
Mutációk detektálása rákszûrési és magzatelemzési célból
|
|
US10424396B2
(en)
*
|
2015-03-27 |
2019-09-24 |
Sentieon Inc. |
Computation pipeline of location-dependent variant calls
|
|
US11479812B2
(en)
|
2015-05-11 |
2022-10-25 |
Natera, Inc. |
Methods and compositions for determining ploidy
|
|
JP6873921B2
(ja)
|
2015-05-18 |
2021-05-19 |
カリウス・インコーポレイテッド |
核酸の集団を濃縮するための組成物および方法
|
|
US12018314B2
(en)
|
2015-07-02 |
2024-06-25 |
Arima Genomics, Inc. |
Accurate molecular deconvolution of mixture samples
|
|
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
|
|
IL305462A
(en)
|
2015-07-23 |
2023-10-01 |
Univ Hong Kong Chinese |
DNA fragmentation pattern analysis suitable clean
|
|
CA2995422A1
(en)
|
2015-08-12 |
2017-02-16 |
The Chinese University Of Hong Kong |
Single-molecule sequencing of plasma dna
|
|
CN115035949A
(zh)
|
2015-09-22 |
2022-09-09 |
香港中文大学 |
通过母亲血浆dna的浅深度测序准确定量胎儿dna分数
|
|
GB201518665D0
(en)
|
2015-10-21 |
2015-12-02 |
Singapore Volition Pte Ltd |
Method for enrichment of cell free nucleosomes
|
|
CN105335625B
(zh)
*
|
2015-11-04 |
2018-02-16 |
和卓生物科技（上海）有限公司 |
胚胎植入前的遗传学检测装置
|
|
RU2760913C2
(ru)
|
2016-04-15 |
2021-12-01 |
Натера, Инк. |
Способы выявления рака легкого
|
|
CN105926043B
(zh)
*
|
2016-04-19 |
2018-08-28 |
苏州贝康医疗器械有限公司 |
一种提高孕妇血浆游离dna测序文库中胎儿游离dna占比的方法
|
|
WO2017193044A1
(en)
*
|
2016-05-06 |
2017-11-09 |
Counsyl, Inc. |
Noninvasive prenatal diagnostic
|
|
US11299783B2
(en)
|
2016-05-27 |
2022-04-12 |
Personalis, Inc. |
Methods and systems for genetic analysis
|
|
WO2018003220A1
(ja)
*
|
2016-06-29 |
2018-01-04 |
トヨタ自動車株式会社 |
Ｄｎａライブラリーの作製方法及びｄｎａライブラリーを用いたゲノムｄｎａ解析方法
|
|
CA3030890A1
(en)
|
2016-07-27 |
2018-02-01 |
Sequenom, Inc. |
Genetic copy number alteration classifications
|
|
WO2018064486A1
(en)
|
2016-09-29 |
2018-04-05 |
Counsyl, Inc. |
Noninvasive prenatal screening using dynamic iterative depth optimization
|
|
WO2018067517A1
(en)
|
2016-10-04 |
2018-04-12 |
Natera, Inc. |
Methods for characterizing copy number variation using proximity-litigation sequencing
|
|
WO2018081130A1
(en)
|
2016-10-24 |
2018-05-03 |
The Chinese University Of Hong Kong |
Methods and systems for tumor detection
|
|
GB201618485D0
(en)
|
2016-11-02 |
2016-12-14 |
Ucl Business Plc |
Method of detecting tumour recurrence
|
|
IL266346B2
(en)
*
|
2016-11-18 |
2024-07-01 |
Univ Hong Kong Chinese |
Universal haplotype-based noninvasive prenatal testing for single gene diseases
|
|
US10011870B2
(en)
|
2016-12-07 |
2018-07-03 |
Natera, Inc. |
Compositions and methods for identifying nucleic acid molecules
|
|
CA3207879A1
(en)
|
2017-01-24 |
2018-08-02 |
Sequenom, Inc. |
Methods and processes for assessment of genetic variations
|
|
SG11201906397UA
(en)
|
2017-01-25 |
2019-08-27 |
Univ Hong Kong Chinese |
Diagnostic applications using nucleic acid fragments
|
|
WO2018156418A1
(en)
|
2017-02-21 |
2018-08-30 |
Natera, Inc. |
Compositions, methods, and kits for isolating nucleic acids
|
|
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
|
|
CA3057589A1
(en)
|
2017-03-24 |
2018-09-27 |
Myriad Women's Health, Inc. |
Copy number variant caller
|
|
WO2018209222A1
(en)
*
|
2017-05-12 |
2018-11-15 |
Massachusetts Institute Of Technology |
Systems and methods for crowdsourcing, analyzing, and/or matching personal data
|
|
JP7056012B2
(ja)
|
2017-05-19 |
2022-04-19 |
トヨタ自動車株式会社 |
ランダムプライマーセット、及びこれを用いたｄｎａライブラリーの作製方法
|
|
KR102145417B1
(ko)
*
|
2017-05-24 |
2020-08-19 |
지니너스 주식회사 |
무세포 핵산으로부터 수득된 서열 분석 데이터에 대한 배경 대립인자의 빈도 분포를 생성하는 방법 및 이를 이용하여 무세포 핵산으로부터 변이를 검출하는 방법
|
|
US11655498B2
(en)
*
|
2017-07-07 |
2023-05-23 |
Massachusetts Institute Of Technology |
Systems and methods for genetic identification and analysis
|
|
WO2019014455A2
(en)
*
|
2017-07-12 |
2019-01-17 |
Ande Corporation |
PATTERN RECOGNITION SYSTEM
|
|
CN109280697B
(zh)
*
|
2017-07-20 |
2022-04-26 |
天昊生物医药科技（苏州）有限公司 |
利用孕妇血浆游离dna进行胎儿基因型鉴定的方法
|
|
CN111051536A
(zh)
|
2017-07-26 |
2020-04-21 |
香港中文大学 |
利用不含细胞的病毒核酸改善癌症筛选
|
|
WO2019028462A1
(en)
|
2017-08-04 |
2019-02-07 |
Billiontoone, Inc. |
TARGET-ASSOCIATED MOLECULES FOR CHARACTERIZATION ASSOCIATED WITH BIOLOGICAL TARGETS
|
|
CN111094583A
(zh)
|
2017-08-04 |
2020-05-01 |
十亿至一公司 |
与生物靶相关的定量中利用靶相关分子的测序输出确定和分析
|
|
US11519024B2
(en)
|
2017-08-04 |
2022-12-06 |
Billiontoone, Inc. |
Homologous genomic regions for characterization associated with biological targets
|
|
CN107545153B
(zh)
*
|
2017-10-25 |
2021-06-11 |
桂林电子科技大学 |
一种基于卷积神经网络的核小体分类预测方法
|
|
US12084720B2
(en)
|
2017-12-14 |
2024-09-10 |
Natera, Inc. |
Assessing graft suitability for transplantation
|
|
JP7047373B2
(ja)
|
2017-12-25 |
2022-04-05 |
トヨタ自動車株式会社 |
次世代シーケンサー用プライマー並びにその製造方法、次世代シーケンサー用プライマーを用いたｄｎａライブラリー並びにその製造方法、及びｄｎａライブラリーを用いたゲノムｄｎａ解析方法
|
|
EP4650456A3
(en)
|
2018-01-05 |
2026-01-21 |
BillionToOne, Inc. |
Quality control templates for ensuring validity of sequencing-based assays
|
|
US12398389B2
(en)
|
2018-02-15 |
2025-08-26 |
Natera, Inc. |
Methods for isolating nucleic acids with size selection
|
|
US12024738B2
(en)
|
2018-04-14 |
2024-07-02 |
Natera, Inc. |
Methods for cancer detection and monitoring
|
|
EP3788172B1
(en)
|
2018-05-03 |
2025-04-02 |
The Chinese University Of Hong Kong |
Size-tagged preferred ends and orientation-aware analysis for measuring properties of cell-free mixtures
|
|
US11814750B2
(en)
|
2018-05-31 |
2023-11-14 |
Personalis, Inc. |
Compositions, methods and systems for processing or analyzing multi-species nucleic acid samples
|
|
US10801064B2
(en)
|
2018-05-31 |
2020-10-13 |
Personalis, Inc. |
Compositions, methods and systems for processing or analyzing multi-species nucleic acid samples
|
|
US12234509B2
(en)
|
2018-07-03 |
2025-02-25 |
Natera, Inc. |
Methods for detection of donor-derived cell-free DNA
|
|
EP3833776A4
(en)
|
2018-08-06 |
2022-04-27 |
Billiontoone, Inc. |
DILUTION MARKER FOR QUANTIFICATION OF BIOLOGICAL TARGETS
|
|
WO2020049558A1
(en)
*
|
2018-09-03 |
2020-03-12 |
Ramot At Tel-Aviv University Ltd. |
Method and system for identifying gene disorder in maternal blood
|
|
US20210280270A1
(en)
*
|
2018-09-07 |
2021-09-09 |
Illumina, Inc. |
Method to determine if a circulating fetal cell isolated from a pregnant mother is from either the current or a historical pregnancy
|
|
JP2022519159A
(ja)
|
2018-12-17 |
2022-03-22 |
ナテラ， インコーポレイテッド |
循環細胞の分析方法
|
|
CN109887548B
(zh)
*
|
2019-01-18 |
2022-11-08 |
臻悦生物科技江苏有限公司 |
基于捕获测序的ctDNA占比的检测方法及检测装置
|
|
CN111560424A
(zh)
*
|
2019-02-13 |
2020-08-21 |
广州医科大学附属第一医院 |
可检测的目标核酸、探针、确定胎儿f8基因单体型的方法及应用
|
|
US12098429B2
(en)
|
2019-03-25 |
2024-09-24 |
The Chinese University Of Hong Kong |
Determining linear and circular forms of circulating nucleic acids
|
|
CN113692448A
(zh)
*
|
2019-04-22 |
2021-11-23 |
私人基因诊断公司 |
用于遗传分析的方法和系统
|
|
US12305235B2
(en)
|
2019-06-06 |
2025-05-20 |
Natera, Inc. |
Methods for detecting immune cell DNA and monitoring immune system
|
|
US20210020266A1
(en)
|
2019-07-19 |
2021-01-21 |
23Andme, Inc. |
Phase-aware determination of identity-by-descent dna segments
|
|
PL3916105T3
(pl)
*
|
2019-08-14 |
2023-06-26 |
Bgi Genomics Co., Limited |
Metoda i urządzenie do oznaczania stężenia płodowego kwasu nukleinowego we krwi kobiety w ciąży
|
|
SG11202101070QA
(en)
|
2019-08-16 |
2021-03-30 |
Univ Hong Kong Chinese |
Determination Of Base Modifications Of Nucleic Acids
|
|
CN112466397A
(zh)
*
|
2019-09-09 |
2021-03-09 |
深圳乐土生物科技有限公司 |
一种用于亲缘关系检测的方法和装置
|
|
JP7470787B2
(ja)
|
2019-11-05 |
2024-04-18 |
パーソナリス，インコーポレイティド |
単一試料からの腫瘍純度の推定
|
|
KR20220115952A
(ko)
*
|
2019-11-18 |
2022-08-19 |
엠바크 베터리너리, 인크. |
조상 근연도를 결정하기 위한 방법 및 시스템
|
|
IL303888B2
(en)
|
2020-02-05 |
2025-09-01 |
Univ Hong Kong Chinese |
Molecular testing using long cell-free fragments in pregnancy
|
|
CN111312332B
(zh)
*
|
2020-02-13 |
2020-10-30 |
国家卫生健康委科学技术研究所 |
基于hla基因的生物信息处理方法、装置及终端
|
|
US11817176B2
(en)
|
2020-08-13 |
2023-11-14 |
23Andme, Inc. |
Ancestry composition determination
|
|
US12322509B2
(en)
*
|
2020-11-08 |
2025-06-03 |
The Johns Hopkins University |
Methods and related aspects for analyzing chromosome number status
|
|
CN112575077A
(zh)
*
|
2020-12-23 |
2021-03-30 |
东莞市妇幼保健院 |
一种胎儿显性遗传病新发突变的无创基因检测方法及应用
|
|
WO2022225933A1
(en)
|
2021-04-22 |
2022-10-27 |
Natera, Inc. |
Methods for determining velocity of tumor growth
|
|
EP4381099A1
(en)
|
2021-08-02 |
2024-06-12 |
Natera, Inc. |
Methods for detecting neoplasm in pregnant women
|
|
WO2023059654A1
(en)
|
2021-10-05 |
2023-04-13 |
Personalis, Inc. |
Customized assays for personalized cancer monitoring
|
|
WO2023133131A1
(en)
|
2022-01-04 |
2023-07-13 |
Natera, Inc. |
Methods for cancer detection and monitoring
|
|
KR20250019610A
(ko)
|
2022-03-21 |
2025-02-10 |
빌리언투원, 인크. |
치료 모니터링을 위한 메틸화된 세포 유리 dna의 분자 계수
|
|
WO2025208288A1
(zh)
*
|
2024-04-01 |
2025-10-09 |
深圳华大生命科学研究院 |
基因预测方法、装置、计算机设备及计算机可读存储介质
|
|
CN119007813B
(zh)
*
|
2024-09-29 |
2025-11-07 |
漳州片仔癀药业股份有限公司 |
一种基于mtDNA的高海拔饲养林麝的种源鉴定及遴选方法
|
|
CN120412715B
(zh)
*
|
2025-03-17 |
2025-11-28 |
上海蓝沙生物科技有限公司 |
一种通过多态性位点连锁区域块评估孕期母本游离血液中胎儿DNA浓度（cffDNA）的方法
|