AU2003254755B2
(en)
|
2002-10-16 |
2007-12-20 |
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
|
US7981604B2
(en)
*
|
2004-02-19 |
2011-07-19 |
California Institute Of Technology |
Methods and kits for analyzing polynucleotide sequences
|
EP1712639B1
(en)
|
2005-04-06 |
2008-08-27 |
Maurice Stroun |
Method for the diagnosis of cancer by detecting circulating DNA and RNA
|
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
|
US11111543B2
(en)
|
2005-07-29 |
2021-09-07 |
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
|
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
|
US10081839B2
(en)
|
2005-07-29 |
2018-09-25 |
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
|
ES2739483T3
(es)
*
|
2006-02-02 |
2020-01-31 |
Univ Leland Stanford Junior |
Detección genética fetal no invasiva mediante análisis digital
|
US20080050739A1
(en)
|
2006-06-14 |
2008-02-28 |
Roland Stoughton |
Diagnosis of fetal abnormalities using polymorphisms including short tandem repeats
|
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
|
US20080070792A1
(en)
|
2006-06-14 |
2008-03-20 |
Roland Stoughton |
Use of highly parallel snp genotyping for fetal diagnosis
|
US20100112590A1
(en)
|
2007-07-23 |
2010-05-06 |
The Chinese University Of Hong Kong |
Diagnosing Fetal Chromosomal Aneuploidy Using Genomic Sequencing With Enrichment
|
EA035451B9
(ru)
*
|
2007-07-23 |
2020-09-09 |
Те Чайниз Юниверсити Ов Гонконг |
Способ диагностики рака с использованием геномного секвенирования
|
ES2620431T3
(es)
|
2008-08-04 |
2017-06-28 |
Natera, Inc. |
Métodos para la determinación de alelos y de ploidía
|
US8583380B2
(en)
|
2008-09-05 |
2013-11-12 |
Aueon, 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
|
EP2425240A4
(en)
|
2009-04-30 |
2012-12-12 |
Good Start Genetics Inc |
METHOD AND COMPOSITION FOR EVALUATING GENETIC MARKERS
|
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
|
DK2516680T3
(en)
|
2009-12-22 |
2016-05-02 |
Sequenom Inc |
Method and kits to identify aneuploidy
|
US20120010085A1
(en)
|
2010-01-19 |
2012-01-12 |
Rava Richard P |
Methods for determining fraction of fetal nucleic acids in maternal samples
|
EP2526415B1
(en)
|
2010-01-19 |
2017-05-03 |
Verinata Health, Inc |
Partition defined detection methods
|
US10388403B2
(en)
|
2010-01-19 |
2019-08-20 |
Verinata Health, Inc. |
Analyzing copy number variation in the detection of cancer
|
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
|
AU2011207544A1
(en)
*
|
2010-01-19 |
2012-09-06 |
Verinata Health, Inc. |
Identification of polymorphic sequences in mixtures of genomic DNA by whole genome sequencing
|
US9323888B2
(en)
|
2010-01-19 |
2016-04-26 |
Verinata Health, Inc. |
Detecting and classifying copy number variation
|
EP2848704B1
(en)
|
2010-01-19 |
2018-08-29 |
Verinata Health, Inc |
Sequencing methods for prenatal diagnoses
|
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
|
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
|
EP2854058A3
(en)
|
2010-05-18 |
2015-10-28 |
Natera, Inc. |
Methods for non-invasive pre-natal ploidy calling
|
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
|
US11332793B2
(en)
|
2010-05-18 |
2022-05-17 |
Natera, Inc. |
Methods for simultaneous amplification of target loci
|
US11339429B2
(en)
|
2010-05-18 |
2022-05-24 |
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
|
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
|
EP2623613B8
(en)
|
2010-09-21 |
2016-09-07 |
Population Genetics Technologies Ltd. |
Increasing confidence of allele calls with molecular counting
|
CA2810931C
(en)
|
2010-09-24 |
2018-04-17 |
The Board Of Trustees Of The Leland Stanford Junior University |
Direct capture, amplification and sequencing of target dna using immobilized primers
|
WO2012058316A1
(en)
*
|
2010-10-26 |
2012-05-03 |
Stanford University |
Non-invasive fetal genetic screening by sequencing analysis
|
JP6328934B2
(ja)
|
2010-12-22 |
2018-05-23 |
ナテラ, インコーポレイテッド |
非侵襲性出生前親子鑑定法
|
AU2011348267A1
(en)
*
|
2010-12-23 |
2013-08-01 |
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
|
JP6153874B2
(ja)
|
2011-02-09 |
2017-06-28 |
ナテラ, インコーポレイテッド |
非侵襲的出生前倍数性呼び出しのための方法
|
EP3489368B1
(en)
|
2011-02-24 |
2020-09-09 |
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
|
DK2697392T3
(en)
*
|
2011-04-12 |
2016-03-29 |
Verinata Health Inc |
SOLUTION OF GENOME FRACTIONS USING Polymorphism COUNTS
|
AU2011365507A1
(en)
*
|
2011-04-14 |
2013-05-02 |
Verinata Health, Inc. |
Normalizing chromosomes for the determination and verification of common and rare chromosomal aneuploidies
|
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
|
US9956281B2
(en)
|
2011-05-04 |
2018-05-01 |
Streck, Inc. |
Inactivated virus compositions and methods of preparing such compositions
|
PT2716766T
(pt)
*
|
2011-05-31 |
2016-11-21 |
Berry Genomics Co Ltd |
Dispositivo para detectar o número de cópias de cromossomas fetais ou células tumorais
|
WO2012177792A2
(en)
|
2011-06-24 |
2012-12-27 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of a genetic variation
|
EP2561103B1
(en)
*
|
2011-06-29 |
2014-08-27 |
BGI Diagnosis 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
|
US9367663B2
(en)
|
2011-10-06 |
2016-06-14 |
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
|
WO2013052907A2
(en)
|
2011-10-06 |
2013-04-11 |
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
|
US8688388B2
(en)
|
2011-10-11 |
2014-04-01 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
EP2768983A4
(en)
|
2011-10-17 |
2015-06-03 |
Good Start Genetics Inc |
METHODS OF IDENTIFYING MUTATIONS ASSOCIATED WITH DISEASES
|
LT2805280T
(lt)
|
2012-01-20 |
2022-12-27 |
Sequenom, Inc. |
Diagnostikos būdai, kurie atsižvelgia į eksperimentines sąlygas
|
US11177020B2
(en)
|
2012-02-27 |
2021-11-16 |
The University Of North Carolina At Chapel Hill |
Methods and uses for molecular tags
|
GB2513024B
(en)
|
2012-02-27 |
2016-08-31 |
Cellular Res Inc |
A clonal amplification method
|
EP2820155B1
(en)
|
2012-02-28 |
2017-07-26 |
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
|
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
|
US11591637B2
(en)
|
2012-08-14 |
2023-02-28 |
10X Genomics, Inc. |
Compositions and methods for sample processing
|
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
|
CN113528634A
(zh)
|
2012-08-14 |
2021-10-22 |
10X基因组学有限公司 |
微胶囊组合物及方法
|
US9701998B2
(en)
|
2012-12-14 |
2017-07-11 |
10X Genomics, Inc. |
Methods and systems for processing polynucleotides
|
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
|
US10273541B2
(en)
|
2012-08-14 |
2019-04-30 |
10X Genomics, Inc. |
Methods and systems for processing polynucleotides
|
US10876152B2
(en)
|
2012-09-04 |
2020-12-29 |
Guardant Health, Inc. |
Systems and methods to detect rare mutations and copy number variation
|
EP2893040B1
(en)
|
2012-09-04 |
2019-01-02 |
Guardant Health, Inc. |
Methods to detect rare mutations and copy number variation
|
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
|
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
|
EP3567116A1
(en)
|
2012-12-14 |
2019-11-13 |
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
|
KR102190198B1
(ko)
|
2013-02-08 |
2020-12-14 |
10엑스 제노믹스, 인크. |
폴리뉴클레오티드 바코드 생성
|
CA2901460A1
(en)
*
|
2013-02-20 |
2014-08-28 |
Bionano Genomics, Inc. |
Characterization of molecules in nanofluidics
|
EP2971100A1
(en)
|
2013-03-13 |
2016-01-20 |
Sequenom, Inc. |
Primers for dna methylation analysis
|
WO2014152421A1
(en)
|
2013-03-14 |
2014-09-25 |
Good Start Genetics, Inc. |
Methods for analyzing nucleic acids
|
LT2981921T
(lt)
|
2013-04-03 |
2023-02-27 |
Sequenom, Inc. |
Neinvazinio genetinių variacijų vertinimo būdai ir procesai
|
IL309903A
(en)
|
2013-05-24 |
2024-03-01 |
Sequenom Inc |
Methods and processes for non-invasive evaluation of genetic variations
|
KR102299305B1
(ko)
*
|
2013-06-21 |
2021-09-06 |
시쿼넘, 인코포레이티드 |
유전적 변이의 비침습 평가를 위한 방법 및 프로세스
|
WO2015013244A1
(en)
|
2013-07-24 |
2015-01-29 |
Streck, Inc. |
Compositions and methods for stabilizing circulating tumor cells
|
GB2525104B
(en)
|
2013-08-28 |
2016-09-28 |
Cellular Res Inc |
Massively Parallel Single Cell Nucleic Acid 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
|
WO2015048535A1
(en)
|
2013-09-27 |
2015-04-02 |
Natera, Inc. |
Prenatal diagnostic resting standards
|
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
|
BR112016007401B1
(pt)
|
2013-10-04 |
2023-04-11 |
Sequenom, Inc. |
Método para determinar a presença ou ausência de uma aneuploidia cromossômica em uma amostra
|
JP2017504307A
(ja)
|
2013-10-07 |
2017-02-09 |
セルラー リサーチ, インコーポレイテッド |
アレイ上のフィーチャーをデジタルカウントするための方法およびシステム
|
CA2925111C
(en)
|
2013-10-07 |
2024-01-16 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of chromosome alterations
|
US10851414B2
(en)
|
2013-10-18 |
2020-12-01 |
Good Start Genetics, Inc. |
Methods for determining carrier status
|
CA2928185C
(en)
|
2013-10-21 |
2024-01-30 |
Verinata Health, Inc. |
Method for improving the sensitivity of detection in determining copy number variations
|
US9824068B2
(en)
|
2013-12-16 |
2017-11-21 |
10X Genomics, Inc. |
Methods and apparatus for sorting data
|
JP6571665B2
(ja)
|
2013-12-28 |
2019-09-04 |
ガーダント ヘルス, インコーポレイテッド |
遺伝的バリアントを検出するための方法およびシステム
|
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
|
US11365447B2
(en)
|
2014-03-13 |
2022-06-21 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
WO2015157567A1
(en)
|
2014-04-10 |
2015-10-15 |
10X Genomics, Inc. |
Fluidic devices, systems, and methods for encapsulating and partitioning reagents, and applications of same
|
EP3561075A1
(en)
|
2014-04-21 |
2019-10-30 |
Natera, Inc. |
Detecting mutations in tumour biopsies and cell-free samples
|
WO2015175530A1
(en)
*
|
2014-05-12 |
2015-11-19 |
Gore Athurva |
Methods for detecting aneuploidy
|
US10318704B2
(en)
|
2014-05-30 |
2019-06-11 |
Verinata Health, Inc. |
Detecting fetal sub-chromosomal aneuploidies
|
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
|
WO2015200869A1
(en)
*
|
2014-06-26 |
2015-12-30 |
10X Genomics, Inc. |
Analysis of nucleic acid sequences
|
EP3161160B1
(en)
|
2014-06-26 |
2021-10-13 |
10X Genomics, Inc. |
Methods of analyzing nucleic acids from individual cells or cell populations
|
EP3760739A1
(en)
|
2014-07-30 |
2021-01-06 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
WO2016040446A1
(en)
|
2014-09-10 |
2016-03-17 |
Good Start Genetics, Inc. |
Methods for selectively suppressing non-target sequences
|
CA2999708A1
(en)
|
2014-09-24 |
2016-03-31 |
Good Start Genetics, Inc. |
Process control for increased robustness of genetic assays
|
EP3567120B1
(en)
|
2014-12-12 |
2020-08-19 |
Verinata Health, Inc. |
Using cell-free dna fragment size to determine copy number variations
|
WO2016112073A1
(en)
|
2015-01-06 |
2016-07-14 |
Good Start Genetics, Inc. |
Screening for structural variants
|
SG11201705615UA
(en)
|
2015-01-12 |
2017-08-30 |
10X Genomics Inc |
Processes and systems for preparing nucleic acid sequencing libraries and libraries prepared using same
|
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
|
AU2016206706B2
(en)
|
2015-01-13 |
2021-10-07 |
10X Genomics, Inc. |
Systems and methods for visualizing structural variation and phasing information
|
WO2016130578A1
(en)
|
2015-02-09 |
2016-08-18 |
10X Genomics, Inc. |
Systems and methods for determining structural variation and phasing using variant call data
|
EP3259371B1
(en)
|
2015-02-19 |
2020-09-02 |
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
|
WO2016138496A1
(en)
|
2015-02-27 |
2016-09-01 |
Cellular Research, Inc. |
Spatially addressable molecular barcoding
|
US11168351B2
(en)
|
2015-03-05 |
2021-11-09 |
Streck, Inc. |
Stabilization of nucleic acids in urine
|
JP6811230B2
(ja)
|
2015-03-23 |
2021-01-13 |
ザ ユニバーシティ オブ ノース カロライナ アット チャペル ヒルThe University Of North Carolina At Chapel Hill |
精密医療のための汎用分子プロセッサ
|
EP3274293A4
(en)
*
|
2015-03-23 |
2018-08-22 |
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
|
US11535882B2
(en)
|
2015-03-30 |
2022-12-27 |
Becton, Dickinson And Company |
Methods and compositions for combinatorial barcoding
|
WO2016172373A1
(en)
|
2015-04-23 |
2016-10-27 |
Cellular Research, Inc. |
Methods and compositions for whole transcriptome amplification
|
EP3294906B1
(en)
|
2015-05-11 |
2024-07-10 |
Natera, Inc. |
Methods for determining ploidy
|
US11124823B2
(en)
|
2015-06-01 |
2021-09-21 |
Becton, Dickinson And Company |
Methods for RNA quantification
|
EP3636777A1
(en)
*
|
2015-07-13 |
2020-04-15 |
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
|
EP3118323A1
(en)
*
|
2015-07-13 |
2017-01-18 |
Cartagenia N.V. |
System and methodology for the analysis of genomic data obtained from a subject
|
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
|
EP3347465B1
(en)
|
2015-09-11 |
2019-06-26 |
Cellular Research, Inc. |
Methods and compositions for nucleic acid library normalization
|
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
|
WO2017106768A1
(en)
|
2015-12-17 |
2017-06-22 |
Guardant Health, Inc. |
Methods to determine tumor gene 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
|
WO2017138984A1
(en)
|
2016-02-11 |
2017-08-17 |
10X Genomics, Inc. |
Systems, methods, and media for de novo assembly of whole genome sequence data
|
NZ745249A
(en)
*
|
2016-02-12 |
2021-07-30 |
Regeneron Pharma |
Methods and systems for detection of abnormal karyotypes
|
EP3452614B1
(en)
|
2016-05-02 |
2023-06-28 |
Becton, Dickinson and Company |
Accurate molecular barcoding
|
US10301677B2
(en)
|
2016-05-25 |
2019-05-28 |
Cellular Research, Inc. |
Normalization of nucleic acid libraries
|
WO2017205691A1
(en)
|
2016-05-26 |
2017-11-30 |
Cellular Research, Inc. |
Molecular label counting adjustment methods
|
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
|
CA3034924A1
(en)
|
2016-09-26 |
2018-03-29 |
Cellular Research, 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
|
AU2017336153B2
(en)
|
2016-09-30 |
2023-07-13 |
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
|
WO2018067517A1
(en)
|
2016-10-04 |
2018-04-12 |
Natera, Inc. |
Methods for characterizing copy number variation using proximity-litigation sequencing
|
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
|
KR20190077061A
(ko)
|
2016-11-08 |
2019-07-02 |
셀룰러 리서치, 인크. |
세포 표지 분류 방법
|
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
|
WO2018132610A1
(en)
|
2017-01-13 |
2018-07-19 |
Cellular Research, Inc. |
Hydrophilic coating of fluidic channels
|
WO2018136888A1
(en)
|
2017-01-20 |
2018-07-26 |
Sequenom, Inc. |
Methods for non-invasive assessment of genetic alterations
|
US11694768B2
(en)
|
2017-01-24 |
2023-07-04 |
Sequenom, Inc. |
Methods and processes for assessment of genetic variations
|
CN117512066A
(zh)
|
2017-01-30 |
2024-02-06 |
10X基因组学有限公司 |
用于基于微滴的单细胞条形编码的方法和系统
|
US11319583B2
(en)
|
2017-02-01 |
2022-05-03 |
Becton, Dickinson And Company |
Selective amplification using blocking oligonucleotides
|
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
|
US10400235B2
(en)
|
2017-05-26 |
2019-09-03 |
10X Genomics, Inc. |
Single cell analysis of transposase accessible chromatin
|
CN109526228B
(zh)
|
2017-05-26 |
2022-11-25 |
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
|
AU2018281745B2
(en)
|
2017-06-05 |
2022-05-19 |
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
|
WO2019084165A1
(en)
|
2017-10-27 |
2019-05-02 |
10X Genomics, Inc. |
METHODS AND SYSTEMS FOR SAMPLE PREPARATION AND ANALYSIS
|
US20200299677A1
(en)
*
|
2017-10-27 |
2020-09-24 |
Juno Diagnostics, Inc. |
Devices, systems and methods for ultra-low volume liquid biopsy
|
EP3625361A1
(en)
|
2017-11-15 |
2020-03-25 |
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
|
JP2021506342A
(ja)
|
2017-12-14 |
2021-02-22 |
ティーエーアイ ダイアグノスティックス インコーポレイテッドTai Diagnostics,Inc. |
移植のための移植片適合性の評価
|
WO2019126209A1
(en)
|
2017-12-19 |
2019-06-27 |
Cellular Research, Inc. |
Particles associated with oligonucleotides
|
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
|
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
|
WO2019195166A1
(en)
|
2018-04-06 |
2019-10-10 |
10X Genomics, Inc. |
Systems and methods for quality control in single cell processing
|
CA3090426A1
(en)
|
2018-04-14 |
2019-10-17 |
Natera, Inc. |
Methods for cancer detection and monitoring by means of personalized detection of circulating tumor dna
|
WO2019213237A1
(en)
|
2018-05-03 |
2019-11-07 |
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
|
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
|
US12065688B2
(en)
|
2018-08-20 |
2024-08-20 |
10X Genomics, Inc. |
Compositions and methods for cellular processing
|
WO2020072380A1
(en)
|
2018-10-01 |
2020-04-09 |
Cellular Research, Inc. |
Determining 5' transcript sequences
|
US11932849B2
(en)
|
2018-11-08 |
2024-03-19 |
Becton, Dickinson 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
|
CN113195717A
(zh)
|
2018-12-13 |
2021-07-30 |
贝克顿迪金森公司 |
单细胞全转录组分析中的选择性延伸
|
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
|
WO2020160414A1
(en)
|
2019-01-31 |
2020-08-06 |
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
|
US11851683B1
(en)
|
2019-02-12 |
2023-12-26 |
10X Genomics, Inc. |
Methods and systems for selective analysis of cellular samples
|
EP3924505A1
(en)
|
2019-02-12 |
2021-12-22 |
10X Genomics, Inc. |
Methods for processing nucleic acid molecules
|
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
|
US11920183B2
(en)
|
2019-03-11 |
2024-03-05 |
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
|
CN114051534A
(zh)
|
2019-07-22 |
2022-02-15 |
贝克顿迪金森公司 |
单细胞染色质免疫沉淀测序测定
|
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
|
JP7522189B2
(ja)
|
2019-11-08 |
2024-07-24 |
ベクトン・ディキンソン・アンド・カンパニー |
免疫レパートリーシーケンシングのための完全長v(d)j情報を得るためのランダムプライミングの使用
|
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
|
EP4090763A1
(en)
|
2020-01-13 |
2022-11-23 |
Becton Dickinson and Company |
Methods and compositions for quantitation of proteins and rna
|
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
|
US12084715B1
(en)
|
2020-11-05 |
2024-09-10 |
10X Genomics, Inc. |
Methods and systems for reducing artifactual antisense products
|
EP4247967A1
(en)
|
2020-11-20 |
2023-09-27 |
Becton, Dickinson and Company |
Profiling of highly expressed and lowly expressed proteins
|
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
|
WO2022182682A1
(en)
|
2021-02-23 |
2022-09-01 |
10X Genomics, Inc. |
Probe-based analysis of nucleic acids and proteins
|