US6927028B2
(en)
*
|
2001-08-31 |
2005-08-09 |
Chinese University Of Hong Kong |
Non-invasive methods for detecting non-host DNA in a host using epigenetic differences between the host and non-host DNA
|
US20030211522A1
(en)
*
|
2002-01-18 |
2003-11-13 |
Landes Gregory M. |
Methods for fetal DNA detection and allele quantitation
|
KR20040102024A
(ko)
*
|
2002-03-01 |
2004-12-03 |
라브겐, 인코퍼레이티드 |
유전적 장애의 검출 방법
|
US6977162B2
(en)
*
|
2002-03-01 |
2005-12-20 |
Ravgen, Inc. |
Rapid analysis of variations in a genome
|
EP1342794B1
(de)
*
|
2002-03-05 |
2005-12-14 |
Epigenomics AG |
Verfahren und Vorrichtung zur Bestimmung der Gewebespezifität von freier DNA in Körperflüssigkeiten
|
US7727720B2
(en)
*
|
2002-05-08 |
2010-06-01 |
Ravgen, Inc. |
Methods for detection of genetic disorders
|
US7442506B2
(en)
*
|
2002-05-08 |
2008-10-28 |
Ravgen, Inc. |
Methods for detection of genetic disorders
|
US20070178478A1
(en)
*
|
2002-05-08 |
2007-08-02 |
Dhallan Ravinder S |
Methods for detection of genetic disorders
|
AU2004217872B2
(en)
*
|
2003-03-05 |
2010-03-25 |
Genetic Technologies Limited |
Identification of fetal DNA and fetal cell markers in maternal plasma or serum
|
US20050282213A1
(en)
*
|
2003-09-22 |
2005-12-22 |
Trisogen Biotechnology Limited Partnership |
Methods and kits useful for detecting an alteration in a locus copy number
|
KR20060101470A
(ko)
*
|
2003-09-22 |
2006-09-25 |
트라이소겐 바이오테크놀로지 리미티드 파트너쉽 |
좌위 복제 수에서의 변동을 검출하기 위한 방법 및 이에유용한 키트
|
CN1930303B
(zh)
*
|
2003-10-08 |
2013-11-20 |
波士顿大学信托人 |
染色体异常的产前诊断试剂盒
|
US8529744B2
(en)
|
2004-02-02 |
2013-09-10 |
Boreal Genomics Corp. |
Enrichment of nucleic acid targets
|
JP2007526823A
(ja)
|
2004-02-02 |
2007-09-20 |
ザ ユニバーシティ オブ ブリティッシュ コロンビア |
粒子を運動および濃縮させるためのスコダ泳動ならびに方法および装置
|
US9186685B2
(en)
|
2012-01-13 |
2015-11-17 |
The University Of British Columbia |
Multiple arm apparatus and methods for separation of particles
|
US10337054B2
(en)
|
2004-02-02 |
2019-07-02 |
Quantum-Si Incorporated |
Enrichment of nucleic acid targets
|
US8518228B2
(en)
|
2011-05-20 |
2013-08-27 |
The University Of British Columbia |
Systems and methods for enhanced SCODA
|
US7709194B2
(en)
*
|
2004-06-04 |
2010-05-04 |
The Chinese University Of Hong Kong |
Marker for prenatal diagnosis and monitoring
|
CA2603815C
(en)
|
2005-04-15 |
2017-09-26 |
Epigenomics Ag |
A method for providing dna fragments derived from a remote sample
|
EP2477029A1
(de)
*
|
2005-06-02 |
2012-07-18 |
Fluidigm Corporation |
Auswertung mit mikrofluiden Aufteilungsvorrichtungen
|
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
|
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
|
TR201910868T4
(tr)
*
|
2006-02-02 |
2019-08-21 |
Univ Leland Stanford Junior |
Dijital analizle invazif olmayan fetal genetik tarama.
|
CN101421410A
(zh)
*
|
2006-03-06 |
2009-04-29 |
纽约市哥伦比亚大学托管会 |
从混合的胎儿-母体来源中特异性扩增胎儿dna序列
|
US7754428B2
(en)
|
2006-05-03 |
2010-07-13 |
The Chinese University Of Hong Kong |
Fetal methylation markers
|
US7901884B2
(en)
*
|
2006-05-03 |
2011-03-08 |
The Chinese University Of Hong Kong |
Markers for prenatal diagnosis and monitoring
|
EP2029777B1
(de)
|
2006-05-31 |
2017-03-08 |
Sequenom, Inc. |
Verfahren und zusammensetzungen zur nukleinsäureextraktion aus einer probe
|
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
|
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
|
TWI335354B
(en)
|
2006-09-27 |
2011-01-01 |
Univ Hong Kong Chinese |
Methods for the detection of the degree of the methylation of a target dna and kits
|
US7902345B2
(en)
|
2006-12-05 |
2011-03-08 |
Sequenom, Inc. |
Detection and quantification of biomolecules using mass spectrometry
|
JP5211790B2
(ja)
*
|
2007-03-26 |
2013-06-12 |
住友化学株式会社 |
Dnaメチル化測定方法
|
ITTO20070307A1
(it)
*
|
2007-05-04 |
2008-11-05 |
Silicon Biosystems Spa |
Metodo e dispositivo per la diagnosi prenatale non-invasiva
|
SI3101141T1
(sl)
|
2007-06-08 |
2020-03-31 |
Epigenomics Ag |
Postopek za metilacijsko analizo
|
AU2013202160B2
(en)
*
|
2007-07-23 |
2015-07-23 |
The Chinese University Of Hong Kong |
Determining percentage of fetal dna in maternal sample
|
US20100112590A1
(en)
|
2007-07-23 |
2010-05-06 |
The Chinese University Of Hong Kong |
Diagnosing Fetal Chromosomal Aneuploidy Using Genomic Sequencing With Enrichment
|
CA3176319A1
(en)
|
2007-07-23 |
2009-01-29 |
The Chinese University Of Hong Kong |
Analyzing tumor dna in a cell-free sample
|
EP2195452B1
(de)
|
2007-08-29 |
2012-03-14 |
Sequenom, Inc. |
Verfahren und zusammensetzungen für die universelle grössenspezifische polymerasekettenreaktion
|
AU2009205956B2
(en)
|
2008-01-18 |
2015-07-02 |
President And Fellows Of Harvard College |
Methods of detecting signatures of disease or conditions in bodily fluids
|
US8475641B2
(en)
|
2008-02-01 |
2013-07-02 |
The University Of British Columbia |
Methods and apparatus for particle introduction and recovery
|
EP2250497B1
(de)
*
|
2008-02-18 |
2014-09-10 |
Genetic Technologies Limited |
Zellprozessierungs- und/oder -anreicherungsverfahren
|
EP2271772B1
(de)
*
|
2008-03-11 |
2014-07-16 |
Sequenom, Inc. |
Tests auf nukleinsäurebasis zur pränatalen geschlechtsbestimmung
|
ES2599967T3
(es)
|
2008-09-16 |
2017-02-06 |
Sequenom, Inc. |
Procedimientos y composiciones para el enriquecimiento basado en metilación de ácido nucleico fetal de una muestra materna útiles para diagnósticos prenatales no invasivos
|
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
|
EP2334812B1
(de)
*
|
2008-09-20 |
2016-12-21 |
The Board of Trustees of The Leland Stanford Junior University |
Nichtinvasive diagnose von fötaler aneuploidie mittels sequenzieren
|
CN102428191A
(zh)
*
|
2009-03-18 |
2012-04-25 |
塞昆纳姆股份有限公司 |
热稳定性内切核酸酶在产生报道分子中的应用
|
US8771948B2
(en)
|
2009-04-03 |
2014-07-08 |
Sequenom, Inc. |
Nucleic acid preparation compositions and methods
|
WO2010121381A1
(en)
|
2009-04-21 |
2010-10-28 |
The University Of British Columbia |
System and methods for detection of particles
|
US9447467B2
(en)
|
2009-04-21 |
2016-09-20 |
Genetic Technologies Limited |
Methods for obtaining fetal genetic material
|
US9752191B2
(en)
|
2009-07-09 |
2017-09-05 |
The Scripps Research Institute |
Gene expression profiles associated with chronic allograft nephropathy
|
HUE034854T2
(en)
|
2009-11-05 |
2018-03-28 |
Univ Hong Kong Chinese |
Fetal genomic analysis from maternal biological samples
|
EP3406737B1
(de)
|
2009-11-06 |
2023-05-31 |
The Chinese University of Hong Kong |
Grössen-abhängige genomanalyse
|
PL2496720T3
(pl)
|
2009-11-06 |
2021-01-11 |
The Board Of Trustees Of The Leland Stanford Junior University |
Nieinwazyjna diagnoza odrzucenia przeszczepu u pacjentów z przeszczepem narządu
|
JP2013511991A
(ja)
*
|
2009-11-25 |
2013-04-11 |
クアンタライフ, インコーポレイテッド |
遺伝子材料を検出する方法および組成物
|
ES2577017T3
(es)
|
2009-12-22 |
2016-07-12 |
Sequenom, Inc. |
Procedimientos y kits para identificar la aneuploidia
|
EP2848703A1
(de)
|
2010-01-19 |
2015-03-18 |
Verinata Health, Inc |
Gleichzeitige Bestimmung von Aneupolidie- und Fötus-DNA-Fraktion
|
AU2011207561B2
(en)
|
2010-01-19 |
2014-02-20 |
Verinata Health, Inc. |
Partition defined detection methods
|
US9260745B2
(en)
|
2010-01-19 |
2016-02-16 |
Verinata Health, Inc. |
Detecting and classifying copy number variation
|
US9323888B2
(en)
|
2010-01-19 |
2016-04-26 |
Verinata Health, Inc. |
Detecting and classifying copy number variation
|
US20120010085A1
(en)
|
2010-01-19 |
2012-01-12 |
Rava Richard P |
Methods for determining fraction of fetal nucleic acids in maternal samples
|
AU2011207544A1
(en)
*
|
2010-01-19 |
2012-09-06 |
Verinata Health, Inc. |
Identification of polymorphic sequences in mixtures of genomic DNA by whole genome sequencing
|
US10388403B2
(en)
|
2010-01-19 |
2019-08-20 |
Verinata Health, Inc. |
Analyzing copy number variation in the detection of cancer
|
US20120100548A1
(en)
|
2010-10-26 |
2012-04-26 |
Verinata Health, Inc. |
Method for determining copy number variations
|
US20110312503A1
(en)
|
2010-01-23 |
2011-12-22 |
Artemis Health, Inc. |
Methods of fetal abnormality detection
|
US8774488B2
(en)
|
2010-03-11 |
2014-07-08 |
Cellscape Corporation |
Method and device for identification of nucleated red blood cells from a maternal blood sample
|
US11339429B2
(en)
|
2010-05-18 |
2022-05-24 |
Natera, Inc. |
Methods for non-invasive prenatal ploidy calling
|
US9677118B2
(en)
|
2014-04-21 |
2017-06-13 |
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
|
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
|
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
|
US11332793B2
(en)
|
2010-05-18 |
2022-05-17 |
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
|
EP2572003A4
(de)
|
2010-05-18 |
2016-01-13 |
Natera Inc |
Verfahren zur nichtinvasiven pränatalen ploidiezuordnung
|
US10316362B2
(en)
|
2010-05-18 |
2019-06-11 |
Natera, Inc. |
Methods for simultaneous amplification of target loci
|
SG10201505724SA
(en)
|
2010-07-23 |
2015-09-29 |
Harvard College |
Methods of detecting diseases or conditions using phagocytic cells
|
AU2011280997A1
(en)
|
2010-07-23 |
2013-02-28 |
President And Fellows Of Harvard College |
Methods of detecting autoimmune or immune-related diseases or conditions
|
EP2596353A4
(de)
|
2010-07-23 |
2014-01-15 |
Harvard College |
Verfahren zum nachweis pränataler oder schwangerschaftsvermittelter krankheiten oder leiden
|
MX361944B
(es)
|
2010-07-23 |
2018-12-19 |
President And Fellows Of Harvard College Star |
Metodos para detectar firmas de enfermedad o condiciones en fluidos corporales.
|
US11203786B2
(en)
|
2010-08-06 |
2021-12-21 |
Ariosa Diagnostics, Inc. |
Detection of target nucleic acids using hybridization
|
US10167508B2
(en)
|
2010-08-06 |
2019-01-01 |
Ariosa Diagnostics, Inc. |
Detection of genetic abnormalities
|
US20130040375A1
(en)
|
2011-08-08 |
2013-02-14 |
Tandem Diagnotics, Inc. |
Assay systems for genetic analysis
|
US20140342940A1
(en)
|
2011-01-25 |
2014-11-20 |
Ariosa Diagnostics, Inc. |
Detection of Target Nucleic Acids using Hybridization
|
US8700338B2
(en)
|
2011-01-25 |
2014-04-15 |
Ariosa Diagnosis, Inc. |
Risk calculation for evaluation of fetal aneuploidy
|
US20130261003A1
(en)
|
2010-08-06 |
2013-10-03 |
Ariosa Diagnostics, In. |
Ligation-based detection of genetic variants
|
US11031095B2
(en)
|
2010-08-06 |
2021-06-08 |
Ariosa Diagnostics, Inc. |
Assay systems for determination of fetal copy number variation
|
US10533223B2
(en)
|
2010-08-06 |
2020-01-14 |
Ariosa Diagnostics, Inc. |
Detection of target nucleic acids using hybridization
|
US20120034603A1
(en)
|
2010-08-06 |
2012-02-09 |
Tandem Diagnostics, Inc. |
Ligation-based detection of genetic variants
|
EP2633311A4
(de)
|
2010-10-26 |
2014-05-07 |
Univ Stanford |
Nichtinvasives fötales genetisches screening durch sequenzierungsanalyse
|
US10131947B2
(en)
|
2011-01-25 |
2018-11-20 |
Ariosa Diagnostics, Inc. |
Noninvasive detection of fetal aneuploidy in egg donor pregnancies
|
US9994897B2
(en)
|
2013-03-08 |
2018-06-12 |
Ariosa Diagnostics, Inc. |
Non-invasive fetal sex determination
|
US8756020B2
(en)
|
2011-01-25 |
2014-06-17 |
Ariosa Diagnostics, Inc. |
Enhanced risk probabilities using biomolecule estimations
|
US11270781B2
(en)
|
2011-01-25 |
2022-03-08 |
Ariosa Diagnostics, Inc. |
Statistical analysis for non-invasive sex chromosome aneuploidy determination
|
JP2014506465A
(ja)
|
2011-02-09 |
2014-03-17 |
バイオ−ラド ラボラトリーズ,インコーポレイティド |
核酸の分析
|
CN103492589B
(zh)
|
2011-02-24 |
2016-06-15 |
香港中文大学 |
多胎妊娠的分子测试
|
CN103797129B
(zh)
*
|
2011-04-12 |
2016-08-17 |
维里纳塔健康公司 |
使用多态计数来解析基因组分数
|
US9411937B2
(en)
|
2011-04-15 |
2016-08-09 |
Verinata Health, Inc. |
Detecting and classifying copy number variation
|
US8450061B2
(en)
|
2011-04-29 |
2013-05-28 |
Sequenom, Inc. |
Quantification of a minority nucleic acid species
|
WO2012177792A2
(en)
|
2011-06-24 |
2012-12-27 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of a genetic variation
|
US8712697B2
(en)
|
2011-09-07 |
2014-04-29 |
Ariosa Diagnostics, Inc. |
Determination of copy number variations using binomial probability calculations
|
EP3922731A3
(de)
|
2011-10-06 |
2022-01-05 |
Sequenom, Inc. |
Verfahren und prozesse zur nichtinvasiven beurteilung genetischer variationen
|
US9367663B2
(en)
|
2011-10-06 |
2016-06-14 |
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
|
US10424394B2
(en)
|
2011-10-06 |
2019-09-24 |
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
|
US20140242588A1
(en)
|
2011-10-06 |
2014-08-28 |
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
|
CA2851537C
(en)
|
2011-10-11 |
2020-12-29 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
EP2805280B1
(de)
|
2012-01-20 |
2022-10-05 |
Sequenom, Inc. |
Diagnostische verfahren zur evaluierung von versuchsbedingungen
|
EP3401399B1
(de)
|
2012-03-02 |
2020-04-22 |
Sequenom, Inc. |
Verfahren und prozesse zur nicht-invasiven beurteilung genetischer variationen
|
EP3573066B1
(de)
|
2012-03-13 |
2023-09-27 |
The Chinese University Of Hong Kong |
Verfahren zur analyse von massiv parallelen sequenzierungsdaten zur nichtinvasiven pränatalen diagnose
|
US9512477B2
(en)
|
2012-05-04 |
2016-12-06 |
Boreal Genomics Inc. |
Biomarker anaylsis using scodaphoresis
|
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
|
US9840732B2
(en)
|
2012-05-21 |
2017-12-12 |
Fluidigm Corporation |
Single-particle analysis of particle populations
|
US10289800B2
(en)
|
2012-05-21 |
2019-05-14 |
Ariosa Diagnostics, Inc. |
Processes for calculating phased fetal genomic sequences
|
CA2874195C
(en)
|
2012-05-21 |
2020-08-25 |
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
|
WO2014011928A1
(en)
|
2012-07-13 |
2014-01-16 |
Sequenom, Inc. |
Processes and compositions for methylation-based enrichment of fetal nucleic acid from a maternal sample useful for non-invasive prenatal diagnoses
|
JP2015522293A
(ja)
|
2012-07-19 |
2015-08-06 |
アリオサ ダイアグノスティックス インコーポレイテッドAriosa Diagnostics,Inc. |
多重化連続ライゲーションに基づく遺伝子変異体の検出
|
US10706957B2
(en)
|
2012-09-20 |
2020-07-07 |
The Chinese University Of Hong Kong |
Non-invasive determination of methylome of tumor from plasma
|
EP3354747B1
(de)
|
2012-09-20 |
2021-02-17 |
The Chinese University Of Hong Kong |
Nicht-invasive bestimmung des methyloms eines tumors aus plasma
|
US9732390B2
(en)
|
2012-09-20 |
2017-08-15 |
The Chinese University Of Hong Kong |
Non-invasive determination of methylome of fetus or tumor from plasma
|
US10482994B2
(en)
|
2012-10-04 |
2019-11-19 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
WO2014055790A2
(en)
|
2012-10-04 |
2014-04-10 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
US20130309666A1
(en)
|
2013-01-25 |
2013-11-21 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
US10494675B2
(en)
|
2013-03-09 |
2019-12-03 |
Cell Mdx, Llc |
Methods of detecting cancer
|
EP2965086A4
(de)
|
2013-03-09 |
2017-02-08 |
Harry Stylli |
Verfahren zum nachweis von prostatakrebs
|
US20130189684A1
(en)
|
2013-03-12 |
2013-07-25 |
Sequenom, Inc. |
Quantification of cell-specific nucleic acid markers
|
US11060145B2
(en)
|
2013-03-13 |
2021-07-13 |
Sequenom, Inc. |
Methods and compositions for identifying presence or absence of hypermethylation or hypomethylation locus
|
EP3415626B1
(de)
|
2013-03-15 |
2020-01-22 |
Lineage Biosciences, Inc. |
Verfahren und zusammensetzungen zum markieren und analysieren von proben
|
CN105121660B
(zh)
|
2013-03-15 |
2018-09-28 |
香港中文大学 |
确定多胎妊娠的胎儿基因组
|
US9340835B2
(en)
|
2013-03-15 |
2016-05-17 |
Boreal Genomics Corp. |
Method for separating homoduplexed and heteroduplexed nucleic acids
|
ES2939547T3
(es)
|
2013-04-03 |
2023-04-24 |
Sequenom Inc |
Métodos y procedimientos para la evaluación no invasiva de variaciones genéticas
|
AU2014268377B2
(en)
|
2013-05-24 |
2020-10-08 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
KR102299305B1
(ko)
|
2013-06-21 |
2021-09-06 |
시쿼넘, 인코포레이티드 |
유전적 변이의 비침습 평가를 위한 방법 및 프로세스
|
CN105555965B
(zh)
*
|
2013-07-30 |
2020-06-05 |
深圳华大基因股份有限公司 |
确定核酸混合物中核酸组成的方法
|
IL304949A
(en)
|
2013-10-04 |
2023-10-01 |
Sequenom Inc |
Methods and processes for non-invasive evaluation of genetic variations
|
US10438691B2
(en)
|
2013-10-07 |
2019-10-08 |
Sequenom, Inc. |
Non-invasive assessment of chromosome alterations using change in subsequence mappability
|
EP3736344A1
(de)
|
2014-03-13 |
2020-11-11 |
Sequenom, Inc. |
Verfahren und prozesse zur nichtinvasiven beurteilung genetischer variationen
|
CN106460070B
(zh)
|
2014-04-21 |
2021-10-08 |
纳特拉公司 |
检测染色体片段中的突变和倍性
|
EP2942400A1
(de)
|
2014-05-09 |
2015-11-11 |
Lifecodexx AG |
Multiplex-Nachweis von DNA, die aus einem spezifischen Zelltyp herrührt
|
CN107223159A
(zh)
|
2014-05-09 |
2017-09-29 |
科戴克斯生命股份公司 |
源自特定细胞类型的dna的检测及相关方法
|
US11104951B2
(en)
|
2014-05-22 |
2021-08-31 |
The Scripps Research Institute |
Molecular signatures for distinguishing liver transplant rejections or injuries
|
US10443100B2
(en)
|
2014-05-22 |
2019-10-15 |
The Scripps Research Institute |
Gene expression profiles associated with sub-clinical kidney transplant rejection
|
EP3598452B1
(de)
|
2014-05-30 |
2023-07-26 |
Sequenom, Inc. |
Chromosomendarstellungsbestimmungen
|
AU2015292311B2
(en)
|
2014-07-25 |
2022-01-20 |
University Of Washington |
Methods of determining tissues and/or cell types giving rise to cell-free DNA, and methods of identifying a disease or disorder using same
|
EP3175000B1
(de)
|
2014-07-30 |
2020-07-29 |
Sequenom, Inc. |
Verfahren und prozesse zur nicht-invasiven beurteilung genetischer variationen
|
WO2016040843A1
(en)
|
2014-09-11 |
2016-03-17 |
Harry Stylli |
Methods of detecting prostate cancer
|
CA2964158A1
(en)
|
2014-10-10 |
2016-04-14 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
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
|
WO2016183106A1
(en)
|
2015-05-11 |
2016-11-17 |
Natera, Inc. |
Methods and compositions for determining ploidy
|
WO2016185284A1
(en)
|
2015-05-20 |
2016-11-24 |
Boreal Genomics, Inc. |
Method for isolating target nucleic acid using heteroduplex binding proteins
|
CA2986200A1
(en)
|
2015-05-22 |
2016-12-01 |
Nipd Genetics Public Company Limited |
Multiplexed parallel analysis of targeted genomic regions for non-invasive prenatal testing
|
DK3168309T3
(da)
|
2015-11-10 |
2020-06-22 |
Eurofins Lifecodexx Gmbh |
Detektion af føtale kromosomale aneuploidier under anvendelse af dna-regioner med forskellig metylering mellem fosteret og det gravide hunkøn
|
WO2017205826A1
(en)
|
2016-05-27 |
2017-11-30 |
Sequenom, Inc. |
Methods for detecting genetic variations
|
WO2018013837A1
(en)
|
2016-07-15 |
2018-01-18 |
The Regents Of The University Of California |
Methods of producing nucleic acid libraries
|
CA3030894A1
(en)
|
2016-07-27 |
2018-02-01 |
Sequenom, Inc. |
Methods for non-invasive assessment of genomic instability
|
US11200963B2
(en)
|
2016-07-27 |
2021-12-14 |
Sequenom, Inc. |
Genetic copy number alteration classifications
|
WO2018064486A1
(en)
|
2016-09-29 |
2018-04-05 |
Counsyl, Inc. |
Noninvasive prenatal screening using dynamic iterative depth optimization
|
US11485996B2
(en)
|
2016-10-04 |
2022-11-01 |
Natera, Inc. |
Methods for characterizing copy number variation using proximity-litigation sequencing
|
US10011870B2
(en)
|
2016-12-07 |
2018-07-03 |
Natera, Inc. |
Compositions and methods for identifying nucleic acid molecules
|
EP3571614A1
(de)
|
2017-01-20 |
2019-11-27 |
Sequenom, Inc. |
Verfahren zur nichtinvasiven beurteilung von kopienzahländerungen
|
WO2018136881A1
(en)
|
2017-01-20 |
2018-07-26 |
Sequenom, Inc. |
Sequencing adapter manufacture and use
|
EP4235676A3
(de)
|
2017-01-20 |
2023-10-18 |
Sequenom, Inc. |
Verfahren zur nichtinvasiven beurteilung genetischer veränderungen
|
JP7237003B2
(ja)
|
2017-01-24 |
2023-03-10 |
セクエノム, インコーポレイテッド |
遺伝子片の評価のための方法およびプロセス
|
EP3596233B1
(de)
|
2017-03-17 |
2022-05-18 |
Sequenom, Inc. |
Verfahren und vorgänge zur beurteilung von genetischem mosaizismus
|
AU2019207900A1
(en)
|
2018-01-12 |
2020-07-09 |
Claret Bioscience, Llc |
Methods and compositions for analyzing nucleic acid
|
WO2019236726A1
(en)
|
2018-06-06 |
2019-12-12 |
The Regents Of The University Of California |
Methods of producing nucleic acid libraries and compositions and kits for practicing same
|
US11525159B2
(en)
|
2018-07-03 |
2022-12-13 |
Natera, Inc. |
Methods for detection of donor-derived cell-free DNA
|
SG11202110468YA
(en)
|
2019-04-05 |
2021-10-28 |
Claret Bioscience Llc |
Methods and compositions for analyzing nucleic acid
|
CN110734966B
(zh)
*
|
2019-09-19 |
2021-06-25 |
广州医科大学附属肿瘤医院 |
一种用于检测sav1基因启动子区甲基化位点的检测体系及试剂盒
|
AU2020363787A1
(en)
|
2019-10-09 |
2022-04-21 |
Claret Bioscience, Llc |
Methods and compositions for analyzing nucleic acid
|
EP4052259A1
(de)
|
2019-10-31 |
2022-09-07 |
Sequenom, Inc. |
Anwendung eines mosaikbildungsverhältnisses bei mehrlingsschwangerschaften und personalisierter risikobeurteilung
|
WO2021262805A1
(en)
|
2020-06-24 |
2021-12-30 |
Claret Bioscience, Llc |
Methods and compositions for analyzing nucleic acid
|
WO2022076574A1
(en)
|
2020-10-08 |
2022-04-14 |
Claret Bioscience, Llc |
Methods and compositions for analyzing nucleic acid
|
CA3209074A1
(en)
*
|
2021-03-09 |
2022-09-15 |
Andrew Kennedy |
Genomic library preparation and targeted epigenetic assays using cas-grna ribonucleoproteins
|