US10966421B2
(en)
|
2002-10-16 |
2021-04-06 |
Streck, 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
|
ATE463584T1
(de)
*
|
2004-02-19 |
2010-04-15 |
Helicos Biosciences Corp |
Verfahren zur analyse von polynukleotidsequenzen
|
ES2313143T3
(es)
|
2005-04-06 |
2009-03-01 |
Maurice Stroun |
Metodo para el diagnostico de cancer mediante la deteccion de adn y arn circulantes.
|
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
|
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
|
US11111543B2
(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
|
PT2385143T
(pt)
|
2006-02-02 |
2016-10-18 |
Univ Leland Stanford Junior |
Rastreio genético fetal não-invasivo por análise digital
|
US8137912B2
(en)
|
2006-06-14 |
2012-03-20 |
The General Hospital Corporation |
Methods for the diagnosis of fetal abnormalities
|
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
|
EP2589668A1
(en)
|
2006-06-14 |
2013-05-08 |
Verinata Health, Inc |
Rare cell analysis using sample splitting and DNA tags
|
US20100112590A1
(en)
|
2007-07-23 |
2010-05-06 |
The Chinese University Of Hong Kong |
Diagnosing Fetal Chromosomal Aneuploidy Using Genomic Sequencing With Enrichment
|
CA2694007C
(en)
*
|
2007-07-23 |
2019-02-26 |
The Chinese University Of Hong Kong |
Determining a nucleic acid sequence imbalance
|
CA2731991C
(en)
|
2008-08-04 |
2021-06-08 |
Gene Security Network, Inc. |
Methods for allele calling and ploidy calling
|
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
|
DK3290530T3
(da)
|
2009-02-18 |
2020-12-07 |
Streck Inc |
Konservering af cellefrie nukleinsyrer
|
AU2010242073C1
(en)
|
2009-04-30 |
2015-12-24 |
Good Start Genetics, Inc. |
Methods and compositions for evaluating genetic markers
|
US8825412B2
(en)
|
2010-05-18 |
2014-09-02 |
Natera, Inc. |
Methods for non-invasive prenatal ploidy calling
|
WO2011041485A1
(en)
|
2009-09-30 |
2011-04-07 |
Gene Security Network, 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
|
US9926593B2
(en)
|
2009-12-22 |
2018-03-27 |
Sequenom, Inc. |
Processes and kits for identifying aneuploidy
|
US9260745B2
(en)
|
2010-01-19 |
2016-02-16 |
Verinata Health, Inc. |
Detecting and classifying copy number variation
|
EP2526415B1
(en)
|
2010-01-19 |
2017-05-03 |
Verinata Health, Inc |
Partition defined detection methods
|
ES2704701T3
(es)
|
2010-01-19 |
2019-03-19 |
Verinata Health Inc |
Nuevo protocolo de preparación de bibliotecas de secuenciación
|
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
|
US20120100548A1
(en)
|
2010-10-26 |
2012-04-26 |
Verinata Health, Inc. |
Method for determining copy number variations
|
EP2513341B1
(en)
*
|
2010-01-19 |
2017-04-12 |
Verinata Health, Inc |
Identification of polymorphic sequences in mixtures of genomic dna by whole genome sequencing
|
US20120010085A1
(en)
|
2010-01-19 |
2012-01-12 |
Rava Richard P |
Methods for determining fraction of fetal nucleic acids in maternal samples
|
US20110312503A1
(en)
|
2010-01-23 |
2011-12-22 |
Artemis Health, Inc. |
Methods of fetal abnormality detection
|
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
|
US10316362B2
(en)
|
2010-05-18 |
2019-06-11 |
Natera, Inc. |
Methods for simultaneous amplification of target loci
|
US11332785B2
(en)
|
2010-05-18 |
2022-05-17 |
Natera, Inc. |
Methods for non-invasive prenatal ploidy calling
|
US11408031B2
(en)
|
2010-05-18 |
2022-08-09 |
Natera, Inc. |
Methods for non-invasive prenatal paternity testing
|
US9677118B2
(en)
|
2014-04-21 |
2017-06-13 |
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
|
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
|
US11939634B2
(en)
|
2010-05-18 |
2024-03-26 |
Natera, Inc. |
Methods for simultaneous amplification of target loci
|
ES2523140T3
(es)
|
2010-09-21 |
2014-11-21 |
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
|
CN103534591B
(zh)
*
|
2010-10-26 |
2016-04-06 |
利兰·斯坦福青年大学托管委员会 |
通过测序分析进行的非侵入性胎儿遗传筛选
|
ES2770342T3
(es)
|
2010-12-22 |
2020-07-01 |
Natera Inc |
Procedimientos para pruebas prenatales no invasivas de paternidad
|
CN103384725A
(zh)
*
|
2010-12-23 |
2013-11-06 |
塞昆纳姆股份有限公司 |
胎儿遗传变异的检测
|
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
|
WO2012108920A1
(en)
|
2011-02-09 |
2012-08-16 |
Natera, Inc |
Methods for non-invasive prenatal ploidy calling
|
CA3160848A1
(en)
*
|
2011-02-24 |
2013-03-28 |
The Chinese University Of Hong Kong |
Molecular testing of multiple pregnancies
|
US9260753B2
(en)
|
2011-03-24 |
2016-02-16 |
President And Fellows Of Harvard College |
Single cell nucleic acid detection and analysis
|
CA2832468C
(en)
*
|
2011-04-12 |
2023-10-31 |
Verinata Health, Inc. |
Resolving genome fractions using polymorphism counts
|
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
|
WO2012151391A2
(en)
|
2011-05-04 |
2012-11-08 |
Streck, Inc. |
Inactivated virus compositions and methods of preparing such compositions
|
CN103080336B
(zh)
*
|
2011-05-31 |
2014-06-04 |
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
|
WO2012177792A2
(en)
|
2011-06-24 |
2012-12-27 |
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
|
US10424394B2
(en)
|
2011-10-06 |
2019-09-24 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
CA2850785C
(en)
|
2011-10-06 |
2022-12-13 |
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
|
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
|
US8688388B2
(en)
|
2011-10-11 |
2014-04-01 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
CA2852665A1
(en)
|
2011-10-17 |
2013-04-25 |
Good Start Genetics, Inc. |
Analysis methods
|
WO2013109981A1
(en)
*
|
2012-01-20 |
2013-07-25 |
Sequenom, Inc. |
Diagnostic processes that factor experimental conditions
|
ES2776673T3
(es)
|
2012-02-27 |
2020-07-31 |
Univ North Carolina Chapel Hill |
Métodos y usos para etiquetas moleculares
|
AU2013226081B2
(en)
|
2012-02-27 |
2018-06-14 |
Becton, Dickinson And Company |
Compositions and kits for molecular counting
|
WO2013128281A1
(en)
|
2012-02-28 |
2013-09-06 |
Population Genetics Technologies Ltd |
Method for attaching a counter sequence to a nucleic acid sample
|
ES2930180T3
(es)
|
2012-03-02 |
2022-12-07 |
Sequenom Inc |
Métodos para enriquecer ácido nucleico canceroso a partir de una muestra biológica
|
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
|
EP2872648B1
(en)
*
|
2012-07-13 |
2019-09-04 |
Sequenom, Inc. |
Processes and compositions for methylation-based enrichment of fetal nucleic acid from a maternal sample useful for non-invasive prenatal diagnoses
|
US9951386B2
(en)
|
2014-06-26 |
2018-04-24 |
10X Genomics, Inc. |
Methods and systems for processing polynucleotides
|
US10273541B2
(en)
|
2012-08-14 |
2019-04-30 |
10X Genomics, Inc. |
Methods and systems for processing polynucleotides
|
US9567631B2
(en)
|
2012-12-14 |
2017-02-14 |
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
|
US10752949B2
(en)
|
2012-08-14 |
2020-08-25 |
10X Genomics, Inc. |
Methods and systems for processing polynucleotides
|
US11591637B2
(en)
|
2012-08-14 |
2023-02-28 |
10X Genomics, Inc. |
Compositions and methods for sample processing
|
US9701998B2
(en)
|
2012-12-14 |
2017-07-11 |
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
|
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
|
US10876152B2
(en)
|
2012-09-04 |
2020-12-29 |
Guardant Health, Inc. |
Systems and methods to detect rare mutations and copy number variation
|
SG11201501662TA
(en)
|
2012-09-04 |
2015-05-28 |
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
|
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
|
CA2901460A1
(en)
*
|
2013-02-20 |
2014-08-28 |
Bionano Genomics, Inc. |
Characterization of molecules in nanofluidics
|
US11060145B2
(en)
|
2013-03-13 |
2021-07-13 |
Sequenom, Inc. |
Methods and compositions for identifying presence or absence of hypermethylation or hypomethylation locus
|
US8778609B1
(en)
|
2013-03-14 |
2014-07-15 |
Good Start Genetics, Inc. |
Methods for analyzing nucleic acids
|
WO2014165596A1
(en)
*
|
2013-04-03 |
2014-10-09 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
WO2014190286A2
(en)
|
2013-05-24 |
2014-11-27 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
DK3011051T3
(en)
|
2013-06-21 |
2019-04-23 |
Sequenom Inc |
Method for non-invasive evaluation of genetic variations
|
ES2938048T3
(es)
|
2013-07-24 |
2023-04-04 |
Streck Llc |
Composiciones y procedimientos para estabilizar las células tumorales circulantes
|
WO2015031691A1
(en)
|
2013-08-28 |
2015-03-05 |
Cellular Research, Inc. |
Massively parallel single cell analysis
|
US10395758B2
(en)
|
2013-08-30 |
2019-08-27 |
10X Genomics, Inc. |
Sequencing methods
|
CN104169929B
(zh)
*
|
2013-09-10 |
2016-12-28 |
深圳华大基因股份有限公司 |
用于确定胎儿是否存在性染色体数目异常的系统和装置
|
US10577655B2
(en)
|
2013-09-27 |
2020-03-03 |
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
|
WO2015048535A1
(en)
|
2013-09-27 |
2015-04-02 |
Natera, Inc. |
Prenatal diagnostic resting standards
|
ES2968644T3
(es)
|
2013-10-04 |
2024-05-13 |
Sequenom Inc |
Métodos y procedimientos para la evaluación no invasiva de variaciones genéticas
|
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
|
JP6680680B2
(ja)
|
2013-10-07 |
2020-04-15 |
セクエノム, インコーポレイテッド |
染色体変化の非侵襲性評価のための方法およびプロセス
|
US10851414B2
(en)
|
2013-10-18 |
2020-12-01 |
Good Start Genetics, Inc. |
Methods for determining carrier status
|
KR102429186B1
(ko)
|
2013-10-21 |
2022-08-03 |
베리나타 헬스, 인코포레이티드 |
사본수 변동을 결정함에 있어서 검출의 감수성을 향상시키기 위한 방법
|
US9824068B2
(en)
|
2013-12-16 |
2017-11-21 |
10X Genomics, Inc. |
Methods and apparatus for sorting data
|
EP3524694B1
(en)
|
2013-12-28 |
2020-07-15 |
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
|
CN106413896B
(zh)
|
2014-04-10 |
2019-07-05 |
10X基因组学有限公司 |
用于封装和分割试剂的流体装置、系统和方法及其应用
|
EP3957749A1
(en)
|
2014-04-21 |
2022-02-23 |
Natera, Inc. |
Detecting tumour specific mutations in biopsies with whole exome sequencing and in cell-free samples
|
US11053548B2
(en)
|
2014-05-12 |
2021-07-06 |
Good Start Genetics, Inc. |
Methods for detecting aneuploidy
|
EP3149199B1
(en)
|
2014-05-30 |
2020-03-25 |
Verinata Health, Inc. |
Detecting, optionally fetal, sub-chromosomal aneuploidies and copy number variations
|
JP6838969B2
(ja)
|
2014-06-26 |
2021-03-03 |
10エックス ジェノミクス, インコーポレイテッド |
個々の細胞または細胞集団由来の核酸の分析方法
|
EP3161162A4
(en)
*
|
2014-06-26 |
2018-01-10 |
10X Genomics, Inc. |
Analysis of nucleic acid sequences
|
CN110211637B
(zh)
|
2014-06-26 |
2023-10-27 |
10X基因组学有限公司 |
核酸序列装配的方法和系统
|
EP3175000B1
(en)
|
2014-07-30 |
2020-07-29 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
US11408024B2
(en)
|
2014-09-10 |
2022-08-09 |
Molecular Loop Biosciences, Inc. |
Methods for selectively suppressing non-target sequences
|
JP2017536087A
(ja)
|
2014-09-24 |
2017-12-07 |
グッド スタート ジェネティクス, インコーポレイテッド |
遺伝子アッセイのロバストネスを増大させるためのプロセス制御
|
US11072814B2
(en)
|
2014-12-12 |
2021-07-27 |
Verinata Health, Inc. |
Using cell-free DNA fragment size to determine copy number variations
|
US10066259B2
(en)
|
2015-01-06 |
2018-09-04 |
Good Start Genetics, Inc. |
Screening for structural variants
|
CN112126675B
(zh)
|
2015-01-12 |
2022-09-09 |
10X基因组学有限公司 |
用于制备核酸测序文库的方法和系统以及用其制备的文库
|
SG11201705425SA
(en)
|
2015-01-13 |
2017-08-30 |
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
|
CA2975529A1
(en)
|
2015-02-09 |
2016-08-18 |
10X Genomics, Inc. |
Systems and methods for determining structural variation and phasing using variant call data
|
EP3766988B1
(en)
|
2015-02-19 |
2024-02-14 |
Becton, Dickinson and Company |
High-throughput single-cell analysis combining proteomic and genomic information
|
EP4286516A3
(en)
|
2015-02-24 |
2024-03-06 |
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
|
US10393726B2
(en)
|
2015-03-23 |
2019-08-27 |
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
|
ES2934982T3
(es)
|
2015-03-30 |
2023-02-28 |
Becton Dickinson Co |
Métodos para la codificación con códigos de barras combinatorios
|
WO2016172373A1
(en)
|
2015-04-23 |
2016-10-27 |
Cellular Research, Inc. |
Methods and compositions for whole transcriptome amplification
|
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
|
EP3118323A1
(en)
*
|
2015-07-13 |
2017-01-18 |
Cartagenia N.V. |
System and methodology for the analysis of genomic data obtained from a subject
|
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
|
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
|
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. |
METHODS OF DETERMINING THE NUMBER OF TUMOR GENE COPIES BY ACELLULAR DNA ANALYSIS
|
US10095831B2
(en)
|
2016-02-03 |
2018-10-09 |
Verinata Health, Inc. |
Using cell-free DNA fragment size to determine copy number variations
|
JP6735348B2
(ja)
|
2016-02-11 |
2020-08-05 |
10エックス ジェノミクス, インコーポレイテッド |
全ゲノム配列データのデノボアセンブリのためのシステム、方法及び媒体
|
NZ745249A
(en)
*
|
2016-02-12 |
2021-07-30 |
Regeneron Pharma |
Methods and systems for detection of abnormal karyotypes
|
JP7129343B2
(ja)
|
2016-05-02 |
2022-09-01 |
ベクトン・ディキンソン・アンド・カンパニー |
正確な分子バーコーディング
|
US10301677B2
(en)
|
2016-05-25 |
2019-05-28 |
Cellular Research, Inc. |
Normalization of nucleic acid libraries
|
JP7046007B2
(ja)
|
2016-05-26 |
2022-04-01 |
ベクトン・ディキンソン・アンド・カンパニー |
分子標識カウントの調節方法
|
US10640763B2
(en)
|
2016-05-31 |
2020-05-05 |
Cellular Research, Inc. |
Molecular indexing of internal sequences
|
US10202641B2
(en)
|
2016-05-31 |
2019-02-12 |
Cellular Research, Inc. |
Error correction in amplification of samples
|
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
|
SG11201901733PA
(en)
|
2016-09-26 |
2019-04-29 |
Cellular Res Inc |
Measurement of protein expression using reagents with barcoded oligonucleotide sequences
|
CA3037366A1
(en)
|
2016-09-29 |
2018-04-05 |
Myriad Women's Health, Inc. |
Noninvasive prenatal screening using dynamic iterative depth optimization
|
EP3461274B1
(en)
|
2016-09-30 |
2020-11-04 |
Guardant Health, Inc. |
Methods for multi-resolution analysis of cell-free nucleic acids
|
US9850523B1
(en)
|
2016-09-30 |
2017-12-26 |
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
|
US11608497B2
(en)
|
2016-11-08 |
2023-03-21 |
Becton, Dickinson And Company |
Methods for cell label classification
|
CN109952612B
(zh)
|
2016-11-08 |
2023-12-01 |
贝克顿迪金森公司 |
用于表达谱分类的方法
|
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
|
EP3571615B1
(en)
|
2017-01-20 |
2024-01-24 |
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
|
WO2018140966A1
(en)
|
2017-01-30 |
2018-08-02 |
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
|
EP3585889A1
(en)
|
2017-02-21 |
2020-01-01 |
Natera, Inc. |
Compositions, methods, and kits for isolating nucleic acids
|
WO2018178700A1
(en)
*
|
2017-03-31 |
2018-10-04 |
Premaitha Limited |
Method of detecting a fetal chromosomal abnormality
|
EP4230746A3
(en)
|
2017-05-26 |
2023-11-01 |
10X Genomics, Inc. |
Single cell analysis of transposase accessible chromatin
|
US10844372B2
(en)
|
2017-05-26 |
2020-11-24 |
10X Genomics, Inc. |
Single cell analysis of transposase accessible chromatin
|
US10676779B2
(en)
|
2017-06-05 |
2020-06-09 |
Becton, Dickinson And Company |
Sample indexing for single cells
|
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
|
WO2019084043A1
(en)
|
2017-10-26 |
2019-05-02 |
10X Genomics, Inc. |
METHODS AND SYSTEMS FOR NUCLEIC ACID PREPARATION AND CHROMATIN ANALYSIS
|
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
|
CA3080117A1
(en)
*
|
2017-10-27 |
2019-05-02 |
Juno Diagnostics, Inc. |
Devices, systems and methods for ultra-low volume liquid biopsy
|
SG11201913654QA
(en)
|
2017-11-15 |
2020-01-30 |
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
|
US11946095B2
(en)
|
2017-12-19 |
2024-04-02 |
Becton, Dickinson And Company |
Particles associated with oligonucleotides
|
EP3752832A1
(en)
|
2018-02-12 |
2020-12-23 |
10X Genomics, Inc. |
Methods characterizing multiple analytes from individual cells or cell populations
|
US11639928B2
(en)
|
2018-02-22 |
2023-05-02 |
10X Genomics, Inc. |
Methods and systems for characterizing analytes from individual cells or cell populations
|
CN112262218A
(zh)
|
2018-04-06 |
2021-01-22 |
10X基因组学有限公司 |
用于单细胞处理中的质量控制的系统和方法
|
EP3788171B1
(en)
|
2018-05-03 |
2023-04-05 |
Becton, Dickinson and Company |
High throughput multiomics sample analysis
|
US11365409B2
(en)
|
2018-05-03 |
2022-06-21 |
Becton, Dickinson And Company |
Molecular barcoding on opposite transcript ends
|
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
|
US11525159B2
(en)
|
2018-07-03 |
2022-12-13 |
Natera, Inc. |
Methods for detection of donor-derived cell-free DNA
|
US20200032335A1
(en)
|
2018-07-27 |
2020-01-30 |
10X Genomics, Inc. |
Systems and methods for metabolome analysis
|
US11639517B2
(en)
|
2018-10-01 |
2023-05-02 |
Becton, Dickinson And Company |
Determining 5′ transcript sequences
|
WO2020097315A1
(en)
|
2018-11-08 |
2020-05-14 |
Cellular Research, Inc. |
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
|
WO2020123384A1
(en)
|
2018-12-13 |
2020-06-18 |
Cellular Research, Inc. |
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
|
US11845983B1
(en)
|
2019-01-09 |
2023-12-19 |
10X Genomics, Inc. |
Methods and systems for multiplexing of droplet based assays
|
US11371076B2
(en)
|
2019-01-16 |
2022-06-28 |
Becton, Dickinson And Company |
Polymerase chain reaction normalization through primer titration
|
ES2945227T3
(es)
|
2019-01-23 |
2023-06-29 |
Becton Dickinson Co |
Oligonucleótidos asociados con anticuerpos
|
US11643693B2
(en)
|
2019-01-31 |
2023-05-09 |
Guardant Health, Inc. |
Compositions and methods for isolating cell-free DNA
|
US11467153B2
(en)
|
2019-02-12 |
2022-10-11 |
10X Genomics, Inc. |
Methods for processing nucleic acid molecules
|
SG11202108788TA
(en)
|
2019-02-12 |
2021-09-29 |
10X Genomics Inc |
Methods for processing nucleic acid molecules
|
US11851683B1
(en)
|
2019-02-12 |
2023-12-26 |
10X Genomics, Inc. |
Methods and systems for selective analysis of cellular samples
|
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
|
US11965208B2
(en)
|
2019-04-19 |
2024-04-23 |
Becton, Dickinson And Company |
Methods of associating phenotypical data and single cell sequencing data
|
EP4004231A1
(en)
|
2019-07-22 |
2022-06-01 |
Becton, Dickinson and Company |
Single cell chromatin immunoprecipitation sequencing assay
|
CN112634986A
(zh)
*
|
2019-09-24 |
2021-04-09 |
厦门希吉亚生物科技有限公司 |
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
|
CN115244184A
(zh)
|
2020-01-13 |
2022-10-25 |
贝克顿迪金森公司 |
用于定量蛋白和rna的方法和组合物
|
US11851700B1
(en)
|
2020-05-13 |
2023-12-26 |
10X Genomics, Inc. |
Methods, kits, and compositions for processing extracellular molecules
|
EP4150118A1
(en)
|
2020-05-14 |
2023-03-22 |
Becton Dickinson and Company |
Primers for immune repertoire profiling
|
US11932901B2
(en)
|
2020-07-13 |
2024-03-19 |
Becton, Dickinson And Company |
Target enrichment using nucleic acid probes for scRNAseq
|
EP4247967A1
(en)
|
2020-11-20 |
2023-09-27 |
Becton, Dickinson and Company |
Profiling of highly expressed and lowly expressed proteins
|
CN114645078A
(zh)
*
|
2020-12-17 |
2022-06-21 |
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
|
AU2022227563A1
(en)
|
2021-02-23 |
2023-08-24 |
10X Genomics, Inc. |
Probe-based analysis of nucleic acids and proteins
|