|
CA2445204C
(en)
|
2002-10-16 |
2014-08-12 |
Streck Laboratories, Inc. |
Method and device for collecting and preserving cells for analysis
|
|
US7169560B2
(en)
|
2003-11-12 |
2007-01-30 |
Helicos Biosciences Corporation |
Short cycle methods for sequencing polynucleotides
|
|
EP1716254B1
(en)
*
|
2004-02-19 |
2010-04-07 |
Helicos Biosciences Corporation |
Methods for analyzing polynucleotide sequences
|
|
DE602005009324D1
(de)
|
2005-04-06 |
2008-10-09 |
Maurice Stroun |
Methode zur Krebsdiagnose mittels Nachweis von DNA und RNA im Kreislauf
|
|
US10081839B2
(en)
|
2005-07-29 |
2018-09-25 |
Natera, Inc |
System and method for cleaning noisy genetic data and determining chromosome copy number
|
|
US11111544B2
(en)
|
2005-07-29 |
2021-09-07 |
Natera, Inc. |
System and method for cleaning noisy genetic data and determining chromosome copy number
|
|
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
|
|
US20070178501A1
(en)
*
|
2005-12-06 |
2007-08-02 |
Matthew Rabinowitz |
System and method for integrating and validating genotypic, phenotypic and medical information into a database according to a standardized ontology
|
|
US20070027636A1
(en)
*
|
2005-07-29 |
2007-02-01 |
Matthew Rabinowitz |
System and method for using genetic, phentoypic and clinical data to make predictions for clinical or lifestyle decisions
|
|
US11111543B2
(en)
|
2005-07-29 |
2021-09-07 |
Natera, Inc. |
System and method for cleaning noisy genetic data and determining chromosome copy number
|
|
EP3002338B1
(en)
*
|
2006-02-02 |
2019-05-08 |
The Board of Trustees of The Leland Stanford Junior University |
Non-invasive fetal genetic screening by digital analysis
|
|
US8137912B2
(en)
|
2006-06-14 |
2012-03-20 |
The General Hospital Corporation |
Methods for the diagnosis of fetal abnormalities
|
|
US8372584B2
(en)
|
2006-06-14 |
2013-02-12 |
The General Hospital Corporation |
Rare cell analysis using sample splitting and DNA tags
|
|
EP2029779A4
(en)
|
2006-06-14 |
2010-01-20 |
Living Microsystems Inc |
HIGHLY PARALLEL SNP GENOTYPING UTILIZATION FOR FETAL DIAGNOSIS
|
|
US20080050739A1
(en)
|
2006-06-14 |
2008-02-28 |
Roland Stoughton |
Diagnosis of fetal abnormalities using polymorphisms including short tandem repeats
|
|
US12180549B2
(en)
|
2007-07-23 |
2024-12-31 |
The Chinese University Of Hong Kong |
Diagnosing fetal chromosomal aneuploidy using genomic sequencing
|
|
KR20220146689A
(ko)
|
2007-07-23 |
2022-11-01 |
더 차이니즈 유니버시티 오브 홍콩 |
핵산 서열 불균형의 결정
|
|
CN104732118B
(zh)
|
2008-08-04 |
2017-08-22 |
纳特拉公司 |
等位基因调用和倍性调用的方法
|
|
EP3216874A1
(en)
|
2008-09-05 |
2017-09-13 |
TOMA Biosciences, Inc. |
Methods for stratifying and annotating cancer drug treatment options
|
|
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
|
|
US11634747B2
(en)
*
|
2009-01-21 |
2023-04-25 |
Streck Llc |
Preservation of fetal nucleic acids in maternal plasma
|
|
DK2398912T3
(en)
|
2009-02-18 |
2017-10-30 |
Streck Inc |
Conservation of cell-free nucleic acids
|
|
JP2012525147A
(ja)
|
2009-04-30 |
2012-10-22 |
グッド スタート ジェネティクス, インコーポレイテッド |
遺伝マーカーを評価するための方法および組成物
|
|
US12129514B2
(en)
|
2009-04-30 |
2024-10-29 |
Molecular Loop Biosolutions, Llc |
Methods and compositions for evaluating genetic markers
|
|
US20120185176A1
(en)
|
2009-09-30 |
2012-07-19 |
Natera, Inc. |
Methods for Non-Invasive Prenatal Ploidy Calling
|
|
US9315857B2
(en)
|
2009-12-15 |
2016-04-19 |
Cellular Research, Inc. |
Digital counting of individual molecules by stochastic attachment of diverse label-tags
|
|
US8835358B2
(en)
|
2009-12-15 |
2014-09-16 |
Cellular Research, Inc. |
Digital counting of individual molecules by stochastic attachment of diverse labels
|
|
EP2516680B1
(en)
|
2009-12-22 |
2016-04-06 |
Sequenom, Inc. |
Processes and kits for identifying aneuploidy
|
|
US10388403B2
(en)
|
2010-01-19 |
2019-08-20 |
Verinata Health, Inc. |
Analyzing copy number variation in the detection of cancer
|
|
WO2011091063A1
(en)
|
2010-01-19 |
2011-07-28 |
Verinata Health, Inc. |
Partition defined detection methods
|
|
WO2011090556A1
(en)
|
2010-01-19 |
2011-07-28 |
Verinata Health, Inc. |
Methods for determining fraction of fetal nucleic acid in maternal samples
|
|
US9323888B2
(en)
|
2010-01-19 |
2016-04-26 |
Verinata Health, Inc. |
Detecting and classifying copy number variation
|
|
US9260745B2
(en)
|
2010-01-19 |
2016-02-16 |
Verinata Health, Inc. |
Detecting and classifying copy number variation
|
|
US20120100548A1
(en)
|
2010-10-26 |
2012-04-26 |
Verinata Health, Inc. |
Method for determining copy number variations
|
|
ES2704701T3
(es)
|
2010-01-19 |
2019-03-19 |
Verinata Health Inc |
Nuevo protocolo de preparación de bibliotecas de secuenciación
|
|
US10662474B2
(en)
|
2010-01-19 |
2020-05-26 |
Verinata Health, Inc. |
Identification of polymorphic sequences in mixtures of genomic DNA by whole genome sequencing
|
|
US20110312503A1
(en)
|
2010-01-23 |
2011-12-22 |
Artemis Health, Inc. |
Methods of fetal abnormality detection
|
|
US11408031B2
(en)
|
2010-05-18 |
2022-08-09 |
Natera, Inc. |
Methods for non-invasive prenatal paternity testing
|
|
US10316362B2
(en)
|
2010-05-18 |
2019-06-11 |
Natera, Inc. |
Methods for simultaneous amplification of target loci
|
|
US12221653B2
(en)
|
2010-05-18 |
2025-02-11 |
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
|
|
US11939634B2
(en)
|
2010-05-18 |
2024-03-26 |
Natera, Inc. |
Methods for simultaneous amplification of target loci
|
|
US12152275B2
(en)
|
2010-05-18 |
2024-11-26 |
Natera, Inc. |
Methods for non-invasive prenatal ploidy calling
|
|
US11326208B2
(en)
|
2010-05-18 |
2022-05-10 |
Natera, Inc. |
Methods for nested PCR amplification of cell-free DNA
|
|
US11332793B2
(en)
|
2010-05-18 |
2022-05-17 |
Natera, Inc. |
Methods for simultaneous amplification of target loci
|
|
CA3037126C
(en)
|
2010-05-18 |
2023-09-12 |
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
|
|
US11339429B2
(en)
|
2010-05-18 |
2022-05-24 |
Natera, Inc. |
Methods for non-invasive prenatal ploidy calling
|
|
US20190010543A1
(en)
|
2010-05-18 |
2019-01-10 |
Natera, Inc. |
Methods for simultaneous amplification of target loci
|
|
US9677118B2
(en)
|
2014-04-21 |
2017-06-13 |
Natera, Inc. |
Methods for simultaneous amplification of target loci
|
|
US11322224B2
(en)
|
2010-05-18 |
2022-05-03 |
Natera, Inc. |
Methods for non-invasive prenatal ploidy calling
|
|
ES2595433T3
(es)
|
2010-09-21 |
2016-12-30 |
Population Genetics Technologies Ltd. |
Aumento de la confianza en las identificaciones de alelos con el recuento molecular
|
|
EP3572528A1
(en)
|
2010-09-24 |
2019-11-27 |
The Board of Trustees of the Leland Stanford Junior University |
Direct capture, amplification and sequencing of target dna using immobilized primers
|
|
EP2633311A4
(en)
*
|
2010-10-26 |
2014-05-07 |
Univ Stanford |
NONINVASIVE FETAL GENETIC SCREENING THROUGH SEQUENCING ANALYSIS
|
|
BR112013016193B1
(pt)
*
|
2010-12-22 |
2019-10-22 |
Natera, Inc. |
método ex vivo para determinar se um suposto pai é o pai biológico de um feto que está em gestação em uma gestante e relatório
|
|
WO2012088348A2
(en)
*
|
2010-12-23 |
2012-06-28 |
Sequenom, Inc. |
Fetal genetic variation detection
|
|
US9163281B2
(en)
|
2010-12-23 |
2015-10-20 |
Good Start Genetics, Inc. |
Methods for maintaining the integrity and identification of a nucleic acid template in a multiplex sequencing reaction
|
|
US10131947B2
(en)
*
|
2011-01-25 |
2018-11-20 |
Ariosa Diagnostics, Inc. |
Noninvasive detection of fetal aneuploidy in egg donor pregnancies
|
|
BR112013020220B1
(pt)
|
2011-02-09 |
2020-03-17 |
Natera, Inc. |
Método para determinar o estado de ploidia de um cromossomo em um feto em gestação
|
|
CA2827873C
(en)
*
|
2011-02-24 |
2022-08-16 |
The Chinese University Of Hong Kong |
Molecular testing of multiple pregnancies
|
|
WO2012129363A2
(en)
|
2011-03-24 |
2012-09-27 |
President And Fellows Of Harvard College |
Single cell nucleic acid detection and analysis
|
|
RS63008B1
(sr)
*
|
2011-04-12 |
2022-03-31 |
Verinata Health Inc |
Rešavanje frakcija genoma koristeći brojanje polimorfizma
|
|
GB2484764B
(en)
|
2011-04-14 |
2012-09-05 |
Verinata Health Inc |
Normalizing chromosomes for the determination and verification of common and rare chromosomal aneuploidies
|
|
CN102985561B
(zh)
*
|
2011-04-14 |
2015-04-01 |
维里纳塔健康公司 |
用于确定并且验证常见的和罕见的染色体非整倍性的归一化染色体
|
|
US9411937B2
(en)
|
2011-04-15 |
2016-08-09 |
Verinata Health, Inc. |
Detecting and classifying copy number variation
|
|
US9956281B2
(en)
|
2011-05-04 |
2018-05-01 |
Streck, Inc. |
Inactivated virus compositions and methods of preparing such compositions
|
|
WO2012162884A1
(zh)
*
|
2011-05-31 |
2012-12-06 |
北京贝瑞和康生物技术有限公司 |
检测胚胎或肿瘤染色体拷贝数的试剂盒、装置和方法
|
|
US20140235474A1
(en)
|
2011-06-24 |
2014-08-21 |
Sequenom, Inc. |
Methods and processes for non invasive assessment of a genetic variation
|
|
SG191757A1
(en)
*
|
2011-06-29 |
2013-08-30 |
Bgi Health Service Co Ltd |
Noninvasive detection of fetal genetic abnormality
|
|
US20130157875A1
(en)
*
|
2011-07-20 |
2013-06-20 |
Anthony P. Shuber |
Methods for assessing genomic instabilities
|
|
US10196681B2
(en)
|
2011-10-06 |
2019-02-05 |
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
|
|
US9367663B2
(en)
|
2011-10-06 |
2016-06-14 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
|
EP2764458B1
(en)
|
2011-10-06 |
2021-04-07 |
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
|
|
US8688388B2
(en)
|
2011-10-11 |
2014-04-01 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
|
WO2013058907A1
(en)
|
2011-10-17 |
2013-04-25 |
Good Start Genetics, Inc. |
Analysis methods
|
|
PL2805280T3
(pl)
|
2012-01-20 |
2022-11-21 |
Sequenom, Inc. |
Procesy diagnostyczne będące czynnikiem warunków doświadczalnych
|
|
WO2013130512A2
(en)
|
2012-02-27 |
2013-09-06 |
The University Of North Carolina At Chapel Hill |
Methods and uses for molecular tags
|
|
ES2904816T3
(es)
|
2012-02-27 |
2022-04-06 |
Becton Dickinson Co |
Composiciones para recuento molecular
|
|
ES2741099T3
(es)
|
2012-02-28 |
2020-02-10 |
Agilent Technologies Inc |
Método de fijación de una secuencia de recuento para una muestra de ácido nucleico
|
|
US9605313B2
(en)
|
2012-03-02 |
2017-03-28 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
|
US8209130B1
(en)
|
2012-04-04 |
2012-06-26 |
Good Start Genetics, Inc. |
Sequence assembly
|
|
US10227635B2
(en)
|
2012-04-16 |
2019-03-12 |
Molecular Loop Biosolutions, Llc |
Capture reactions
|
|
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
|
|
US10497461B2
(en)
|
2012-06-22 |
2019-12-03 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
|
JP2015521862A
(ja)
|
2012-07-13 |
2015-08-03 |
セクエノム, インコーポレイテッド |
非侵襲性の出生前診断に有用な母体サンプル由来の胎児核酸のメチル化に基づく富化のためのプロセスおよび組成物
|
|
US9951386B2
(en)
|
2014-06-26 |
2018-04-24 |
10X Genomics, Inc. |
Methods and systems for processing polynucleotides
|
|
US10323279B2
(en)
|
2012-08-14 |
2019-06-18 |
10X Genomics, Inc. |
Methods and systems for processing polynucleotides
|
|
US9701998B2
(en)
|
2012-12-14 |
2017-07-11 |
10X Genomics, Inc. |
Methods and systems for processing polynucleotides
|
|
US10752949B2
(en)
|
2012-08-14 |
2020-08-25 |
10X Genomics, Inc. |
Methods and systems for processing polynucleotides
|
|
BR112015003354A8
(pt)
|
2012-08-14 |
2018-01-16 |
10X Genomics Inc |
métodos e composições de microcápsula
|
|
US11591637B2
(en)
|
2012-08-14 |
2023-02-28 |
10X Genomics, Inc. |
Compositions and methods for sample processing
|
|
US10273541B2
(en)
|
2012-08-14 |
2019-04-30 |
10X Genomics, Inc. |
Methods and systems for processing polynucleotides
|
|
US10584381B2
(en)
|
2012-08-14 |
2020-03-10 |
10X Genomics, Inc. |
Methods and systems for processing polynucleotides
|
|
US20140100126A1
(en)
|
2012-08-17 |
2014-04-10 |
Natera, Inc. |
Method for Non-Invasive Prenatal Testing Using Parental Mosaicism Data
|
|
US11913065B2
(en)
|
2012-09-04 |
2024-02-27 |
Guardent Health, Inc. |
Systems and methods to detect rare mutations and copy number variation
|
|
US20160040229A1
(en)
|
2013-08-16 |
2016-02-11 |
Guardant Health, Inc. |
Systems and methods to detect rare mutations and copy number variation
|
|
GB2533006B
(en)
|
2012-09-04 |
2017-06-07 |
Guardant Health Inc |
Systems and methods to detect copy number variation
|
|
US10876152B2
(en)
|
2012-09-04 |
2020-12-29 |
Guardant Health, Inc. |
Systems and methods to detect rare mutations and copy number variation
|
|
US10482994B2
(en)
|
2012-10-04 |
2019-11-19 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
|
TWI489305B
(zh)
*
|
2012-11-21 |
2015-06-21 |
Bgi Diagnosis Co Ltd |
對胎兒遺傳異常的無創性檢測
|
|
AU2013359165B2
(en)
|
2012-12-14 |
2019-09-12 |
10X Genomics, Inc. |
Methods and systems for processing polynucleotides
|
|
US10533221B2
(en)
|
2012-12-14 |
2020-01-14 |
10X Genomics, Inc. |
Methods and systems for processing polynucleotides
|
|
US20130309666A1
(en)
*
|
2013-01-25 |
2013-11-21 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
|
CA2900543C
(en)
|
2013-02-08 |
2023-01-31 |
10X Genomics, Inc. |
Partitioning and processing of analytes and other species
|
|
CN105229168B
(zh)
*
|
2013-02-20 |
2020-07-17 |
生物纳米基因有限公司 |
纳米流体中分子的表征
|
|
US11060145B2
(en)
|
2013-03-13 |
2021-07-13 |
Sequenom, Inc. |
Methods and compositions for identifying presence or absence of hypermethylation or hypomethylation locus
|
|
EP2971159B1
(en)
|
2013-03-14 |
2019-05-08 |
Molecular Loop Biosolutions, LLC |
Methods for analyzing nucleic acids
|
|
HUE061261T2
(hu)
|
2013-04-03 |
2023-05-28 |
Sequenom Inc |
Eljárások és folyamatok genetikai variánsok nem invazív értékelésére
|
|
IL309903A
(en)
|
2013-05-24 |
2024-03-01 |
Sequenom Inc |
Methods and processes for non-invasive assessment of genetic variations
|
|
AU2014284180B2
(en)
*
|
2013-06-21 |
2020-03-19 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
|
ES2938048T3
(es)
|
2013-07-24 |
2023-04-04 |
Streck Llc |
Composiciones y procedimientos para estabilizar las células tumorales circulantes
|
|
EP3480321B8
(en)
|
2013-08-28 |
2021-03-10 |
Becton, Dickinson and Company |
Massively parallel single cell analysis
|
|
US10395758B2
(en)
|
2013-08-30 |
2019-08-27 |
10X Genomics, Inc. |
Sequencing methods
|
|
WO2015035555A1
(zh)
*
|
2013-09-10 |
2015-03-19 |
深圳华大基因科技有限公司 |
用于确定胎儿是否存在性染色体数目异常的方法、系统和计算机可读介质
|
|
US10577655B2
(en)
|
2013-09-27 |
2020-03-03 |
Natera, Inc. |
Cell free DNA diagnostic testing standards
|
|
WO2015048535A1
(en)
|
2013-09-27 |
2015-04-02 |
Natera, Inc. |
Prenatal diagnostic resting standards
|
|
US10262755B2
(en)
|
2014-04-21 |
2019-04-16 |
Natera, Inc. |
Detecting cancer mutations and aneuploidy in chromosomal segments
|
|
PL3053071T3
(pl)
*
|
2013-10-04 |
2024-03-18 |
Sequenom, Inc. |
Metody i procesy nieinwazyjnej oceny zmienności genetycznych
|
|
CN105745528A
(zh)
|
2013-10-07 |
2016-07-06 |
赛卢拉研究公司 |
用于以数字方式对阵列上的特征进行计数的方法和系统
|
|
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
|
|
US10851414B2
(en)
|
2013-10-18 |
2020-12-01 |
Good Start Genetics, Inc. |
Methods for determining carrier status
|
|
CN105830077B
(zh)
|
2013-10-21 |
2019-07-09 |
维里纳塔健康公司 |
用于在确定拷贝数变异中改善检测的灵敏度的方法
|
|
US9824068B2
(en)
|
2013-12-16 |
2017-11-21 |
10X Genomics, Inc. |
Methods and apparatus for sorting data
|
|
EP3771745A1
(en)
|
2013-12-28 |
2021-02-03 |
Guardant Health, Inc. |
Methods and systems for detecting genetic variants
|
|
CN103824001A
(zh)
*
|
2014-02-27 |
2014-05-28 |
北京诺禾致源生物信息科技有限公司 |
染色体的检测方法和装置
|
|
EP3736344A1
(en)
|
2014-03-13 |
2020-11-11 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
|
DE202015009609U1
(de)
|
2014-04-10 |
2018-08-06 |
10X Genomics, Inc. |
Mikrofluidisches System zur Erzeugung von Emulsionen
|
|
US12492429B2
(en)
|
2014-04-21 |
2025-12-09 |
Natera, Inc. |
Detecting mutations and ploidy in chromosomal segments
|
|
CA2945962C
(en)
|
2014-04-21 |
2023-08-29 |
Natera, Inc. |
Detecting mutations and ploidy in chromosomal segments
|
|
US11053548B2
(en)
|
2014-05-12 |
2021-07-06 |
Good Start Genetics, Inc. |
Methods for detecting aneuploidy
|
|
BR112016027848A2
(pt)
|
2014-05-30 |
2017-08-22 |
Verinata Health Inc |
Método para avaliação de número de cópias de uma sequência de interesse, meio legível por máquina não transitória, e, sistema para avaliação de número de cópias de uma sequência de interesse
|
|
US20180173845A1
(en)
|
2014-06-05 |
2018-06-21 |
Natera, Inc. |
Systems and Methods for Detection of Aneuploidy
|
|
WO2015200893A2
(en)
|
2014-06-26 |
2015-12-30 |
10X Genomics, Inc. |
Methods of analyzing nucleic acids from individual cells or cell populations
|
|
AU2015279546B2
(en)
|
2014-06-26 |
2021-04-08 |
10X Genomics, Inc. |
Processes and systems for nucleic acid sequence assembly
|
|
CN106536756A
(zh)
*
|
2014-06-26 |
2017-03-22 |
10X基因组学有限公司 |
核酸序列的分析
|
|
US12312640B2
(en)
|
2014-06-26 |
2025-05-27 |
10X Genomics, Inc. |
Analysis of nucleic acid sequences
|
|
US11783911B2
(en)
|
2014-07-30 |
2023-10-10 |
Sequenom, Inc |
Methods and processes for non-invasive assessment of genetic variations
|
|
WO2016025818A1
(en)
|
2014-08-15 |
2016-02-18 |
Good Start Genetics, Inc. |
Systems and methods for genetic analysis
|
|
US11408024B2
(en)
|
2014-09-10 |
2022-08-09 |
Molecular Loop Biosciences, Inc. |
Methods for selectively suppressing non-target sequences
|
|
WO2016048829A1
(en)
|
2014-09-24 |
2016-03-31 |
Good Start Genetics, Inc. |
Process control for increased robustness of genetic assays
|
|
US10892035B2
(en)
*
|
2014-10-10 |
2021-01-12 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
|
MA40939A
(fr)
|
2014-12-12 |
2017-10-18 |
Verinata Health Inc |
Utilisation de la taille de fragments d'adn acellulaire pour déterminer les variations du nombre de copies
|
|
EP4095261B1
(en)
|
2015-01-06 |
2025-05-28 |
Molecular Loop Biosciences, Inc. |
Screening for structural variants
|
|
AU2016207023B2
(en)
|
2015-01-12 |
2019-12-05 |
10X Genomics, Inc. |
Processes and systems for preparing nucleic acid sequencing libraries and libraries prepared using same
|
|
WO2016115273A1
(en)
|
2015-01-13 |
2016-07-21 |
10X Genomics, Inc. |
Systems and methods for visualizing structural variation and phasing information
|
|
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
|
|
AU2016219480B2
(en)
|
2015-02-09 |
2021-11-11 |
10X Genomics, Inc. |
Systems and methods for determining structural variation and phasing using variant call data
|
|
US10697010B2
(en)
|
2015-02-19 |
2020-06-30 |
Becton, Dickinson And Company |
High-throughput single-cell analysis combining proteomic and genomic information
|
|
EP3262407B1
(en)
|
2015-02-24 |
2023-08-30 |
10X Genomics, Inc. |
Partition processing methods and systems
|
|
ES2836802T3
(es)
|
2015-02-27 |
2021-06-28 |
Becton Dickinson Co |
Códigos de barras moleculares espacialmente direccionables
|
|
US11168351B2
(en)
|
2015-03-05 |
2021-11-09 |
Streck, Inc. |
Stabilization of nucleic acids in urine
|
|
EP3274091B1
(en)
|
2015-03-23 |
2020-12-02 |
The University of North Carolina at Chapel Hill |
Universal molecular processor for precision medicine
|
|
WO2016154337A2
(en)
*
|
2015-03-23 |
2016-09-29 |
The University Of North Carolina At Chapel Hill |
Method for identification and enumeration of nucleic acid sequences, expression, splice variant, translocation, copy, or dna methylation changes using combined nuclease, ligase, polymerase, terminal transferase, and sequencing reactions
|
|
EP4180535A1
(en)
|
2015-03-30 |
2023-05-17 |
Becton, Dickinson and Company |
Methods and compositions for combinatorial barcoding
|
|
CN107580632B
(zh)
|
2015-04-23 |
2021-12-28 |
贝克顿迪金森公司 |
用于全转录组扩增的方法和组合物
|
|
WO2016183106A1
(en)
|
2015-05-11 |
2016-11-17 |
Natera, Inc. |
Methods and compositions for determining ploidy
|
|
WO2016196229A1
(en)
|
2015-06-01 |
2016-12-08 |
Cellular Research, Inc. |
Methods for rna quantification
|
|
AU2016293025A1
(en)
*
|
2015-07-13 |
2017-11-02 |
Agilent Technologies Belgium Nv |
System and methodology for the analysis of genomic data obtained from a subject
|
|
EP3118323A1
(en)
*
|
2015-07-13 |
2017-01-18 |
Cartagenia N.V. |
System and methodology for the analysis of genomic data obtained from a subject
|
|
BE1023266B1
(nl)
*
|
2015-07-13 |
2017-01-17 |
Cartagenia N.V. |
Systeem en methodologie voor de analyse van genomische gegevens die zijn verkregen van een onderwerp
|
|
US12540351B2
(en)
|
2015-09-02 |
2026-02-03 |
Guardant Health, Inc. |
Identification of somatic mutations versus germline variants for cell-free DNA variant calling applications
|
|
US11302416B2
(en)
|
2015-09-02 |
2022-04-12 |
Guardant Health |
Machine learning for somatic single nucleotide variant detection in cell-free tumor nucleic acid sequencing applications
|
|
JP6940484B2
(ja)
|
2015-09-11 |
2021-09-29 |
セルラー リサーチ, インコーポレイテッド |
ライブラリー正規化のための方法および組成物
|
|
US11371094B2
(en)
|
2015-11-19 |
2022-06-28 |
10X Genomics, Inc. |
Systems and methods for nucleic acid processing using degenerate nucleotides
|
|
US20170145475A1
(en)
|
2015-11-20 |
2017-05-25 |
Streck, Inc. |
Single spin process for blood plasma separation and plasma composition including preservative
|
|
EP3390668A4
(en)
|
2015-12-17 |
2020-04-01 |
Guardant Health, Inc. |
METHOD FOR DETERMINING THE TUMORGEN COPY NUMBER BY ANALYSIS OF CELL-FREE DNA
|
|
US10095831B2
(en)
|
2016-02-03 |
2018-10-09 |
Verinata Health, Inc. |
Using cell-free DNA fragment size to determine copy number variations
|
|
US11081208B2
(en)
|
2016-02-11 |
2021-08-03 |
10X Genomics, Inc. |
Systems, methods, and media for de novo assembly of whole genome sequence data
|
|
US12071669B2
(en)
*
|
2016-02-12 |
2024-08-27 |
Regeneron Pharmaceuticals, Inc. |
Methods and systems for detection of abnormal karyotypes
|
|
ES2913468T3
(es)
|
2016-04-15 |
2022-06-02 |
Natera Inc |
Métodos para la detección del cáncer de pulmón.
|
|
EP4269616A3
(en)
|
2016-05-02 |
2024-02-14 |
Becton, Dickinson and Company |
Accurate molecular barcoding
|
|
US10301677B2
(en)
|
2016-05-25 |
2019-05-28 |
Cellular Research, Inc. |
Normalization of nucleic acid libraries
|
|
CN109074430B
(zh)
|
2016-05-26 |
2022-03-29 |
贝克顿迪金森公司 |
分子标记计数调整方法
|
|
US10202641B2
(en)
|
2016-05-31 |
2019-02-12 |
Cellular Research, Inc. |
Error correction in amplification of samples
|
|
US10640763B2
(en)
|
2016-05-31 |
2020-05-05 |
Cellular Research, Inc. |
Molecular indexing of internal sequences
|
|
EP3491560A1
(en)
|
2016-07-27 |
2019-06-05 |
Sequenom, Inc. |
Genetic copy number alteration classifications
|
|
WO2018022991A1
(en)
|
2016-07-29 |
2018-02-01 |
Streck, Inc. |
Suspension composition for hematology analysis control
|
|
CN109791157B
(zh)
|
2016-09-26 |
2022-06-07 |
贝克顿迪金森公司 |
使用具有条形码化的寡核苷酸序列的试剂测量蛋白质表达
|
|
WO2018064486A1
(en)
|
2016-09-29 |
2018-04-05 |
Counsyl, Inc. |
Noninvasive prenatal screening using dynamic iterative depth optimization
|
|
US9850523B1
(en)
|
2016-09-30 |
2017-12-26 |
Guardant Health, Inc. |
Methods for multi-resolution analysis of cell-free nucleic acids
|
|
AU2017336153B2
(en)
|
2016-09-30 |
2023-07-13 |
Guardant Health, Inc. |
Methods for multi-resolution analysis of cell-free nucleic acids
|
|
US11485996B2
(en)
|
2016-10-04 |
2022-11-01 |
Natera, Inc. |
Methods for characterizing copy number variation using proximity-litigation sequencing
|
|
GB201618485D0
(en)
|
2016-11-02 |
2016-12-14 |
Ucl Business Plc |
Method of detecting tumour recurrence
|
|
JP7228510B2
(ja)
|
2016-11-08 |
2023-02-24 |
ベクトン・ディキンソン・アンド・カンパニー |
細胞標識分類の方法
|
|
ES2980967T3
(es)
|
2016-11-08 |
2024-10-03 |
Becton Dickinson Co |
Métodos para la clasificación de perfiles de expresión
|
|
US10011870B2
(en)
|
2016-12-07 |
2018-07-03 |
Natera, Inc. |
Compositions and methods for identifying nucleic acid molecules
|
|
US10550429B2
(en)
|
2016-12-22 |
2020-02-04 |
10X Genomics, Inc. |
Methods and systems for processing polynucleotides
|
|
US10815525B2
(en)
|
2016-12-22 |
2020-10-27 |
10X Genomics, Inc. |
Methods and systems for processing polynucleotides
|
|
ES2961580T3
(es)
|
2017-01-13 |
2024-03-12 |
Cellular Res Inc |
Revestimiento hidrófilo de canales de fluidos
|
|
WO2018136888A1
(en)
|
2017-01-20 |
2018-07-26 |
Sequenom, Inc. |
Methods for non-invasive assessment of genetic alterations
|
|
WO2018140521A1
(en)
|
2017-01-24 |
2018-08-02 |
Sequenom, Inc. |
Methods and processes for assessment of genetic variations
|
|
US12264411B2
(en)
|
2017-01-30 |
2025-04-01 |
10X Genomics, Inc. |
Methods and systems for analysis
|
|
EP4029939B1
(en)
|
2017-01-30 |
2023-06-28 |
10X Genomics, Inc. |
Methods and systems for droplet-based single cell barcoding
|
|
CN110382708A
(zh)
|
2017-02-01 |
2019-10-25 |
赛卢拉研究公司 |
使用阻断性寡核苷酸进行选择性扩增
|
|
US10995333B2
(en)
|
2017-02-06 |
2021-05-04 |
10X Genomics, Inc. |
Systems and methods for nucleic acid preparation
|
|
US10894976B2
(en)
|
2017-02-21 |
2021-01-19 |
Natera, Inc. |
Compositions, methods, and kits for isolating nucleic acids
|
|
IL317916A
(en)
|
2017-03-17 |
2025-02-01 |
Sequenom Inc |
Methods and processes for assessing genetic mosaicism
|
|
CN110914456A
(zh)
*
|
2017-03-31 |
2020-03-24 |
普莱梅沙有限公司 |
检测胎儿染色体异常的方法
|
|
CN116064732A
(zh)
|
2017-05-26 |
2023-05-05 |
10X基因组学有限公司 |
转座酶可接近性染色质的单细胞分析
|
|
US10400235B2
(en)
|
2017-05-26 |
2019-09-03 |
10X Genomics, Inc. |
Single cell analysis of transposase accessible chromatin
|
|
KR102790050B1
(ko)
|
2017-06-05 |
2025-04-04 |
백톤 디킨슨 앤드 컴퍼니 |
단일 세포를 위한 샘플 인덱싱
|
|
CN109423510B
(zh)
*
|
2017-09-04 |
2022-08-30 |
深圳华大生命科学研究院 |
一种检测rca产物的方法及应用
|
|
US10837047B2
(en)
|
2017-10-04 |
2020-11-17 |
10X Genomics, Inc. |
Compositions, methods, and systems for bead formation using improved polymers
|
|
US12378543B2
(en)
|
2017-10-19 |
2025-08-05 |
Streck Llc |
Compositions for hemolysis and coagulation regulation and stabilization of extracellular vesicles
|
|
WO2019084043A1
(en)
|
2017-10-26 |
2019-05-02 |
10X Genomics, Inc. |
METHODS AND SYSTEMS FOR NUCLEIC ACID PREPARATION AND CHROMATIN ANALYSIS
|
|
TWI833715B
(zh)
*
|
2017-10-27 |
2024-03-01 |
美商奇諾診療公司 |
用於超低體積液體生物檢體之裝置、系統及方法
|
|
CN111479631B
(zh)
|
2017-10-27 |
2022-02-22 |
10X基因组学有限公司 |
用于样品制备和分析的方法和系统
|
|
WO2019099751A1
(en)
|
2017-11-15 |
2019-05-23 |
10X Genomics, Inc. |
Functionalized gel beads
|
|
US10829815B2
(en)
|
2017-11-17 |
2020-11-10 |
10X Genomics, Inc. |
Methods and systems for associating physical and genetic properties of biological particles
|
|
WO2019108851A1
(en)
|
2017-11-30 |
2019-06-06 |
10X Genomics, Inc. |
Systems and methods for nucleic acid preparation and analysis
|
|
WO2019118355A1
(en)
|
2017-12-12 |
2019-06-20 |
10X Genomics, Inc. |
Systems and methods for single cell processing
|
|
CA3085933A1
(en)
|
2017-12-14 |
2019-06-20 |
Tai Diagnostics, Inc. |
Assessing graft suitability for transplantation
|
|
CN111492068B
(zh)
|
2017-12-19 |
2025-03-21 |
贝克顿迪金森公司 |
与寡核苷酸相关联的颗粒
|
|
CN118547046A
(zh)
|
2017-12-22 |
2024-08-27 |
10X基因组学有限公司 |
用于处理来自一个或多个细胞的核酸分子的系统和方法
|
|
CN112005115A
(zh)
|
2018-02-12 |
2020-11-27 |
10X基因组学有限公司 |
表征来自单个细胞或细胞群体的多种分析物的方法
|
|
WO2019161244A1
(en)
|
2018-02-15 |
2019-08-22 |
Natera, Inc. |
Methods for isolating nucleic acids with size selection
|
|
US11639928B2
(en)
|
2018-02-22 |
2023-05-02 |
10X Genomics, Inc. |
Methods and systems for characterizing analytes from individual cells or cell populations
|
|
WO2019169028A1
(en)
|
2018-02-28 |
2019-09-06 |
10X Genomics, Inc. |
Transcriptome sequencing through random ligation
|
|
EP3775271B1
(en)
|
2018-04-06 |
2025-03-12 |
10X Genomics, Inc. |
Systems and methods for quality control in single cell processing
|
|
EP3781714B1
(en)
|
2018-04-14 |
2026-01-07 |
Natera, Inc. |
Methods for cancer detection and monitoring by means of personalized detection of circulating tumor dna
|
|
EP3788170B1
(en)
|
2018-05-03 |
2025-01-01 |
Becton, Dickinson and Company |
Molecular barcoding on opposite transcript ends
|
|
US11773441B2
(en)
|
2018-05-03 |
2023-10-03 |
Becton, Dickinson And Company |
High throughput multiomics sample analysis
|
|
WO2019217758A1
(en)
|
2018-05-10 |
2019-11-14 |
10X Genomics, Inc. |
Methods and systems for molecular library generation
|
|
US11932899B2
(en)
|
2018-06-07 |
2024-03-19 |
10X Genomics, Inc. |
Methods and systems for characterizing nucleic acid molecules
|
|
US11703427B2
(en)
|
2018-06-25 |
2023-07-18 |
10X Genomics, Inc. |
Methods and systems for cell and bead processing
|
|
US12234509B2
(en)
|
2018-07-03 |
2025-02-25 |
Natera, Inc. |
Methods for detection of donor-derived cell-free DNA
|
|
US12188014B1
(en)
|
2018-07-25 |
2025-01-07 |
10X Genomics, Inc. |
Compositions and methods for nucleic acid processing using blocking agents
|
|
US20200032335A1
(en)
|
2018-07-27 |
2020-01-30 |
10X Genomics, Inc. |
Systems and methods for metabolome analysis
|
|
EP3830289B1
(en)
|
2018-08-03 |
2026-02-11 |
10X Genomics, Inc. |
Methods to minimize barcode exchange
|
|
WO2020041148A1
(en)
|
2018-08-20 |
2020-02-27 |
10X Genomics, Inc. |
Methods and systems for detection of protein-dna interactions using proximity ligation
|
|
US12065688B2
(en)
|
2018-08-20 |
2024-08-20 |
10X Genomics, Inc. |
Compositions and methods for cellular processing
|
|
US20200075123A1
(en)
|
2018-08-31 |
2020-03-05 |
Guardant Health, Inc. |
Genetic variant detection based on merged and unmerged reads
|
|
US11639517B2
(en)
|
2018-10-01 |
2023-05-02 |
Becton, Dickinson And Company |
Determining 5′ transcript sequences
|
|
EP3877520B1
(en)
|
2018-11-08 |
2025-03-19 |
Becton, Dickson And Company |
Whole transcriptome analysis of single cells using random priming
|
|
US11459607B1
(en)
|
2018-12-10 |
2022-10-04 |
10X Genomics, Inc. |
Systems and methods for processing-nucleic acid molecules from a single cell using sequential co-partitioning and composite barcodes
|
|
US11492660B2
(en)
|
2018-12-13 |
2022-11-08 |
Becton, Dickinson And Company |
Selective extension in single cell whole transcriptome analysis
|
|
CN109637586B
(zh)
*
|
2018-12-27 |
2020-11-17 |
北京优迅医学检验实验室有限公司 |
测序深度的矫正方法及装置
|
|
US12169198B2
(en)
|
2019-01-08 |
2024-12-17 |
10X Genomics, Inc. |
Systems and methods for sample analysis
|
|
US11845983B1
(en)
|
2019-01-09 |
2023-12-19 |
10X Genomics, Inc. |
Methods and systems for multiplexing of droplet based assays
|
|
WO2020150356A1
(en)
|
2019-01-16 |
2020-07-23 |
Becton, Dickinson And Company |
Polymerase chain reaction normalization through primer titration
|
|
US11661631B2
(en)
|
2019-01-23 |
2023-05-30 |
Becton, Dickinson And Company |
Oligonucleotides associated with antibodies
|
|
ES3013495T3
(en)
|
2019-01-31 |
2025-04-14 |
Guardant Health Inc |
Method for isolating and sequencing cell-free dna
|
|
WO2020167866A1
(en)
|
2019-02-12 |
2020-08-20 |
10X Genomics, Inc. |
Systems and methods for transposon loading
|
|
WO2020167862A1
(en)
|
2019-02-12 |
2020-08-20 |
10X Genomics, Inc. |
Systems and methods for transfer of reagents between droplets
|
|
US12305239B2
(en)
|
2019-02-12 |
2025-05-20 |
10X Genomics, Inc. |
Analysis of nucleic acid sequences
|
|
US11467153B2
(en)
|
2019-02-12 |
2022-10-11 |
10X Genomics, Inc. |
Methods for processing nucleic acid molecules
|
|
US12275993B2
(en)
|
2019-02-12 |
2025-04-15 |
10X Genomics, Inc. |
Analysis of nucleic acid sequences
|
|
CN118979095A
(zh)
|
2019-02-12 |
2024-11-19 |
10X基因组学有限公司 |
用于加工核酸分子的方法
|
|
US11851683B1
(en)
|
2019-02-12 |
2023-12-26 |
10X Genomics, Inc. |
Methods and systems for selective analysis of cellular samples
|
|
US12071617B2
(en)
|
2019-02-14 |
2024-08-27 |
Becton, Dickinson And Company |
Hybrid targeted and whole transcriptome amplification
|
|
US11655499B1
(en)
|
2019-02-25 |
2023-05-23 |
10X Genomics, Inc. |
Detection of sequence elements in nucleic acid molecules
|
|
WO2020185791A1
(en)
|
2019-03-11 |
2020-09-17 |
10X Genomics, Inc. |
Systems and methods for processing optically tagged beads
|
|
WO2020214642A1
(en)
|
2019-04-19 |
2020-10-22 |
Becton, Dickinson And Company |
Methods of associating phenotypical data and single cell sequencing data
|
|
WO2020247263A1
(en)
|
2019-06-06 |
2020-12-10 |
Natera, Inc. |
Methods for detecting immune cell dna and monitoring immune system
|
|
EP4707405A2
(en)
|
2019-07-22 |
2026-03-11 |
Becton, Dickinson and Company |
Single cell chromatin immunoprecipitation sequencing assay
|
|
US12235262B1
(en)
|
2019-09-09 |
2025-02-25 |
10X Genomics, Inc. |
Methods and systems for single cell protein analysis
|
|
CN112634986B
(zh)
*
|
2019-09-24 |
2024-07-26 |
厦门赛尔吉亚医学检验所有限公司 |
一种基于孕妇外周血对双胞胎合子性质的无创鉴定方法
|
|
EP4055160B1
(en)
|
2019-11-08 |
2024-04-10 |
Becton Dickinson and Company |
Using random priming to obtain full-length v(d)j information for immune repertoire sequencing
|
|
WO2021137770A1
(en)
|
2019-12-30 |
2021-07-08 |
Geneton S.R.O. |
Method for fetal fraction estimation based on detection and interpretation of single nucleotide variants
|
|
WO2021146207A1
(en)
|
2020-01-13 |
2021-07-22 |
Becton, Dickinson And Company |
Methods and compositions for quantitation of proteins and rna
|
|
EP4097228B1
(en)
|
2020-01-29 |
2024-08-14 |
Becton, Dickinson and Company |
Barcoded wells for spatial mapping of single cells through sequencing
|
|
US12449419B1
(en)
|
2020-02-12 |
2025-10-21 |
10X Genomics, Inc. |
Methods for detecting binding of peptide-MHC monomers to T cells
|
|
WO2021163630A1
(en)
|
2020-02-13 |
2021-08-19 |
10X Genomics, Inc. |
Systems and methods for joint interactive visualization of gene expression and dna chromatin accessibility
|
|
WO2021173719A1
(en)
|
2020-02-25 |
2021-09-02 |
Becton, Dickinson And Company |
Bi-specific probes to enable the use of single-cell samples as single color compensation control
|
|
US11851700B1
(en)
|
2020-05-13 |
2023-12-26 |
10X Genomics, Inc. |
Methods, kits, and compositions for processing extracellular molecules
|
|
WO2021231779A1
(en)
|
2020-05-14 |
2021-11-18 |
Becton, Dickinson And Company |
Primers for immune repertoire profiling
|
|
ES2987035T3
(es)
|
2020-06-02 |
2024-11-13 |
Becton Dickinson Co |
Oligonucleótidos y perlas para el ensayo de expresión génica principal 5
|
|
US11932901B2
(en)
|
2020-07-13 |
2024-03-19 |
Becton, Dickinson And Company |
Target enrichment using nucleic acid probes for scRNAseq
|
|
WO2022026909A1
(en)
|
2020-07-31 |
2022-02-03 |
Becton, Dickinson And Company |
Single cell assay for transposase-accessible chromatin
|
|
US12480158B1
(en)
|
2020-11-05 |
2025-11-25 |
10X Genomics, Inc. |
Methods and systems for processing polynucleotides
|
|
US12084715B1
(en)
|
2020-11-05 |
2024-09-10 |
10X Genomics, Inc. |
Methods and systems for reducing artifactual antisense products
|
|
US11739443B2
(en)
|
2020-11-20 |
2023-08-29 |
Becton, Dickinson And Company |
Profiling of highly expressed and lowly expressed proteins
|
|
US12392771B2
(en)
|
2020-12-15 |
2025-08-19 |
Becton, Dickinson And Company |
Single cell secretome analysis
|
|
CN114645078B
(zh)
*
|
2020-12-17 |
2024-07-23 |
厦门大学 |
一种检测胎儿样品中母体细胞存在或比例的方法和试剂盒
|
|
US12398262B1
(en)
|
2021-01-22 |
2025-08-26 |
10X Genomics, Inc. |
Triblock copolymer-based cell stabilization and fixation system and methods of use thereof
|
|
EP4298244A1
(en)
|
2021-02-23 |
2024-01-03 |
10X Genomics, Inc. |
Probe-based analysis of nucleic acids and proteins
|
|
SK289398B6
(sk)
|
2023-05-25 |
2026-01-14 |
Medirex Group Academy N.O. |
Metóda detekcie vzoriek s nedostatočným množstvom fragmentov fetálnej a cirkulujúcej nádorovej DNA na neinvazívne genetické testovanie
|
|
WO2024253600A1
(en)
|
2023-06-07 |
2024-12-12 |
Univerzita Komenského v Bratislave |
Method for estimation of cell-free dna mixture proportions based on telomere-derived fragments
|
|
CN118711657B
(zh)
*
|
2024-08-30 |
2024-11-12 |
杭州杰毅生物技术有限公司 |
一种ngs测序中针对标签跳跃污染的假阳性排除方法及系统
|