ATE435301T1
(de)
*
|
2003-10-16 |
2009-07-15 |
Sequenom Inc |
Nicht invasiver nachweis fötaler genetischer merkmale
|
US9186685B2
(en)
|
2012-01-13 |
2015-11-17 |
The University Of British Columbia |
Multiple arm apparatus and methods for separation of particles
|
US8518228B2
(en)
|
2011-05-20 |
2013-08-27 |
The University Of British Columbia |
Systems and methods for enhanced SCODA
|
US10337054B2
(en)
|
2004-02-02 |
2019-07-02 |
Quantum-Si Incorporated |
Enrichment of nucleic acid targets
|
US8529744B2
(en)
|
2004-02-02 |
2013-09-10 |
Boreal Genomics Corp. |
Enrichment of nucleic acid targets
|
EP1720636A4
(de)
|
2004-02-02 |
2012-06-20 |
Univ British Columbia |
Scodaphorese und verfahren und vorrichtungen zum bewegen und aufkonzentrieren von teilchen
|
US20100216153A1
(en)
|
2004-02-27 |
2010-08-26 |
Helicos Biosciences Corporation |
Methods for detecting fetal nucleic acids and diagnosing fetal abnormalities
|
US8024128B2
(en)
*
|
2004-09-07 |
2011-09-20 |
Gene Security Network, Inc. |
System and method for improving clinical decisions by aggregating, validating and analysing genetic and phenotypic data
|
FR2880897B1
(fr)
*
|
2005-01-18 |
2010-12-17 |
Inst Nat Sante Rech Med |
Methode de detection, non invasive, prenatale, in vitro de l'etat sain normal, de l'etat de porteur sain ou de l'etat de porteur malade de la mucoviscidose
|
EP2477029A1
(de)
*
|
2005-06-02 |
2012-07-18 |
Fluidigm Corporation |
Auswertung mit mikrofluiden Aufteilungsvorrichtungen
|
US8515679B2
(en)
|
2005-12-06 |
2013-08-20 |
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
|
US10081839B2
(en)
|
2005-07-29 |
2018-09-25 |
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
|
US11111543B2
(en)
|
2005-07-29 |
2021-09-07 |
Natera, Inc. |
System and method for cleaning noisy genetic data and determining chromosome copy number
|
US10083273B2
(en)
|
2005-07-29 |
2018-09-25 |
Natera, Inc. |
System and method for cleaning noisy genetic data and determining chromosome copy number
|
US8532930B2
(en)
|
2005-11-26 |
2013-09-10 |
Natera, Inc. |
Method for determining the number of copies of a chromosome in the genome of a target individual using genetic data from genetically related individuals
|
US11111544B2
(en)
|
2005-07-29 |
2021-09-07 |
Natera, Inc. |
System and method for cleaning noisy genetic data and determining chromosome copy number
|
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
|
US20070122823A1
(en)
*
|
2005-09-01 |
2007-05-31 |
Bianchi Diana W |
Amniotic fluid cell-free fetal DNA fragment size pattern for prenatal diagnosis
|
EP2437191B1
(de)
*
|
2005-11-26 |
2017-04-26 |
Natera, Inc. |
Verfahren uns system zum nachweis chromosomaler anomalien
|
EP2423334A3
(de)
|
2006-02-02 |
2012-04-18 |
The Board of Trustees of The Leland Stanford Junior University |
Nicht-invasives fötales genetisches Screening mittels digitaler Analyse
|
US20100184044A1
(en)
*
|
2006-02-28 |
2010-07-22 |
University Of Louisville Research Foundation |
Detecting Genetic Abnormalities
|
SI1996728T1
(sl)
*
|
2006-02-28 |
2011-10-28 |
Univ Louisville Res Found |
Prepoznavanje kromosomskih nenormalnosti pri zarodku s pomočjo dvojnih mononukleotidnih polimorfizmov
|
US8609338B2
(en)
|
2006-02-28 |
2013-12-17 |
University Of Louisville Research Foundation, Inc. |
Detecting fetal chromosomal abnormalities using tandem single nucleotide polymorphisms
|
US20100184043A1
(en)
*
|
2006-02-28 |
2010-07-22 |
University Of Louisville Research Foundation |
Detecting Genetic Abnormalities
|
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
|
US8679741B2
(en)
*
|
2006-05-31 |
2014-03-25 |
Sequenom, Inc. |
Methods and compositions for the extraction and amplification of nucleic acid from a sample
|
US20080050739A1
(en)
|
2006-06-14 |
2008-02-28 |
Roland Stoughton |
Diagnosis of fetal abnormalities using polymorphisms including short tandem repeats
|
US20080070792A1
(en)
*
|
2006-06-14 |
2008-03-20 |
Roland Stoughton |
Use of highly parallel snp genotyping for fetal diagnosis
|
EP2589668A1
(de)
|
2006-06-14 |
2013-05-08 |
Verinata Health, Inc |
Analyse seltener Zellen mittels Probentrennung und DNA-Etiketten
|
US8137912B2
(en)
|
2006-06-14 |
2012-03-20 |
The General Hospital Corporation |
Methods for the diagnosis of fetal abnormalities
|
CN101501251A
(zh)
*
|
2006-06-16 |
2009-08-05 |
塞昆纳姆股份有限公司 |
扩增、检测和定量样品中核酸的方法和组合物
|
US20080176237A1
(en)
*
|
2006-12-07 |
2008-07-24 |
Biocept, Inc. |
Non-invasive prenatal genetic screen
|
AU2008230813B2
(en)
|
2007-03-26 |
2014-01-30 |
Sequenom, Inc. |
Restriction endonuclease enhanced polymorphic sequence detection
|
US20100112590A1
(en)
|
2007-07-23 |
2010-05-06 |
The Chinese University Of Hong Kong |
Diagnosing Fetal Chromosomal Aneuploidy Using Genomic Sequencing With Enrichment
|
EA028642B1
(ru)
|
2007-07-23 |
2017-12-29 |
Те Чайниз Юниверсити Ов Гонгконг |
Способ пренатальной диагностики фетальной хромосомной анэуплоидии
|
US20090053719A1
(en)
*
|
2007-08-03 |
2009-02-26 |
The Chinese University Of Hong Kong |
Analysis of nucleic acids by digital pcr
|
KR20180001596A
(ko)
|
2008-01-18 |
2018-01-04 |
프레지던트 앤드 펠로우즈 오브 하바드 칼리지 |
체액 내에서 질병 또는 병태의 시그너쳐의 검출 방법
|
CA2713313A1
(en)
|
2008-02-01 |
2009-08-06 |
The University Of British Columbia |
Methods and apparatus for particle introduction and recovery
|
WO2009103110A1
(en)
*
|
2008-02-18 |
2009-08-27 |
Genetic Technologies Limited |
Cell processing and/or enrichment methods
|
US20110033862A1
(en)
*
|
2008-02-19 |
2011-02-10 |
Gene Security Network, Inc. |
Methods for cell genotyping
|
US8709726B2
(en)
|
2008-03-11 |
2014-04-29 |
Sequenom, Inc. |
Nucleic acid-based tests for prenatal gender determination
|
EP2276858A4
(de)
|
2008-03-26 |
2011-10-05 |
Sequenom Inc |
Durch restriktionsendonuklease verbesserter nachweis polymorpher sequenzen
|
US20110092763A1
(en)
*
|
2008-05-27 |
2011-04-21 |
Gene Security Network, Inc. |
Methods for Embryo Characterization and Comparison
|
EP2128169A1
(de)
*
|
2008-05-30 |
2009-12-02 |
Qiagen GmbH |
Verfahren zur Isolierung von kurzkettigen Nukleinsäuren
|
JP2011528554A
(ja)
*
|
2008-07-18 |
2011-11-24 |
ノバルティス アーゲー |
母親の全血からの非侵襲的胎児RhDジェノタイピング
|
CA3116156C
(en)
*
|
2008-08-04 |
2023-08-08 |
Natera, Inc. |
Methods for allele calling and ploidy calling
|
EP3103871B1
(de)
|
2008-09-16 |
2020-07-29 |
Sequenom, Inc. |
Verfahren zur methylierungsbasierten anreicherung fetaler nukleinsäure aus einer mütterlichen probe für fetale nukleinsäure quantifizierung
|
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
|
EP3751005A3
(de)
|
2008-09-20 |
2021-02-24 |
The Board of Trustees of the Leland Stanford Junior University |
Nicht invasive diagnose von fötaler aneuploidie durch sequenzierung
|
WO2010115016A2
(en)
|
2009-04-03 |
2010-10-07 |
Sequenom, Inc. |
Nucleic acid preparation compositions and methods
|
US8877028B2
(en)
|
2009-04-21 |
2014-11-04 |
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
|
WO2011041485A1
(en)
|
2009-09-30 |
2011-04-07 |
Gene Security Network, Inc. |
Methods for non-invasive prenatal ploidy calling
|
CN102770558B
(zh)
|
2009-11-05 |
2016-04-06 |
香港中文大学 |
由母本生物样品进行胎儿基因组的分析
|
EA034241B1
(ru)
|
2009-11-06 |
2020-01-21 |
Те Чайниз Юниверсити Ов Гонконг |
Способ пренатальной диагностики дисбаланса последовательности
|
US9926593B2
(en)
|
2009-12-22 |
2018-03-27 |
Sequenom, Inc. |
Processes and kits for identifying aneuploidy
|
EP2513341B1
(de)
|
2010-01-19 |
2017-04-12 |
Verinata Health, Inc |
Identifizierung von polymorphen sequenzen in mischungen aus genomischer dna durch gesamtgenomsequenzierung
|
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
|
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
|
EP2854057B1
(de)
|
2010-05-18 |
2018-03-07 |
Natera, Inc. |
Verfahren zur nichtinvasiven pränatalen Ploidiezuordnung
|
US11326208B2
(en)
|
2010-05-18 |
2022-05-10 |
Natera, Inc. |
Methods for nested PCR amplification of cell-free DNA
|
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
|
US11332793B2
(en)
|
2010-05-18 |
2022-05-17 |
Natera, Inc. |
Methods for simultaneous amplification of target loci
|
US11408031B2
(en)
|
2010-05-18 |
2022-08-09 |
Natera, Inc. |
Methods for non-invasive prenatal paternity testing
|
US11339429B2
(en)
|
2010-05-18 |
2022-05-24 |
Natera, Inc. |
Methods for non-invasive prenatal ploidy calling
|
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
|
CA2801039A1
(en)
|
2010-06-07 |
2011-12-15 |
Esoterix Genetic Laboratories, Llc |
Enumeration of nucleic acids
|
EP4303584A3
(de)
|
2010-07-23 |
2024-04-03 |
President and Fellows of Harvard College |
Verfahren zur erkennung von anzeichen für krankheiten oder leiden in körperflüssigkeiten
|
AU2011280936A1
(en)
|
2010-07-23 |
2013-02-28 |
President And Fellows Of Harvard College |
Methods of detecting prenatal or pregnancy-related diseases or conditions
|
SG10201505724SA
(en)
|
2010-07-23 |
2015-09-29 |
Harvard College |
Methods of detecting diseases or conditions using phagocytic cells
|
WO2012012694A2
(en)
|
2010-07-23 |
2012-01-26 |
President And Fellows Of Harvard College |
Methods of detecting autoimmune or immune-related diseases or conditions
|
US20120034603A1
(en)
*
|
2010-08-06 |
2012-02-09 |
Tandem Diagnostics, Inc. |
Ligation-based detection of genetic variants
|
WO2012027483A2
(en)
*
|
2010-08-24 |
2012-03-01 |
Bio Dx, Inc. |
Defining diagnostic and therapeutic targets of conserved free floating fetal dna in maternal circulating blood
|
RU2620959C2
(ru)
|
2010-12-22 |
2017-05-30 |
Натера, Инк. |
Способы неинвазивного пренатального установления отцовства
|
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
|
GB2488358A
(en)
|
2011-02-25 |
2012-08-29 |
Univ Plymouth |
Enrichment of foetal DNA in maternal plasma
|
WO2012129363A2
(en)
|
2011-03-24 |
2012-09-27 |
President And Fellows Of Harvard College |
Single cell nucleic acid detection and analysis
|
CA2834218C
(en)
|
2011-04-29 |
2021-02-16 |
Sequenom, Inc. |
Quantification of a minority nucleic acid species using inhibitory oligonucleotides
|
US20140235474A1
(en)
|
2011-06-24 |
2014-08-21 |
Sequenom, Inc. |
Methods and processes for non invasive assessment of a genetic variation
|
WO2013002261A1
(ja)
*
|
2011-06-27 |
2013-01-03 |
オリンパス株式会社 |
標的粒子の検出方法
|
SI2561103T1
(sl)
|
2011-06-29 |
2014-11-28 |
Bgi Diagnosis Co., Ltd. |
Neinvazivna detekcija genetske anomalije ploda
|
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
|
US9984198B2
(en)
|
2011-10-06 |
2018-05-29 |
Sequenom, Inc. |
Reducing sequence read count error in assessment of complex genetic variations
|
US10196681B2
(en)
|
2011-10-06 |
2019-02-05 |
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
|
US20130130929A1
(en)
*
|
2011-11-17 |
2013-05-23 |
Bhairavi Parikh |
Methods, devices, and kits for obtaining and analyzing cells
|
WO2013109981A1
(en)
|
2012-01-20 |
2013-07-25 |
Sequenom, Inc. |
Diagnostic processes that factor experimental conditions
|
US9605313B2
(en)
|
2012-03-02 |
2017-03-28 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
US9892230B2
(en)
|
2012-03-08 |
2018-02-13 |
The Chinese University Of Hong Kong |
Size-based analysis of fetal or tumor DNA fraction in plasma
|
US9512477B2
(en)
|
2012-05-04 |
2016-12-06 |
Boreal Genomics Inc. |
Biomarker anaylsis using scodaphoresis
|
CN104471077B
(zh)
|
2012-05-21 |
2017-05-24 |
富鲁达公司 |
颗粒群的单颗粒分析
|
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
|
US11261494B2
(en)
|
2012-06-21 |
2022-03-01 |
The Chinese University Of Hong Kong |
Method of measuring a fractional concentration of tumor DNA
|
US10497461B2
(en)
|
2012-06-22 |
2019-12-03 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
EP2872648B1
(de)
|
2012-07-13 |
2019-09-04 |
Sequenom, Inc. |
Verfahren und zusammensetzungen zur methylierungsbasierten anreicherung fetaler nukleinsäure aus einer mütterlichen probe für nicht-invasive pränatale diagnosen
|
US20160040229A1
(en)
|
2013-08-16 |
2016-02-11 |
Guardant Health, Inc. |
Systems and methods to detect rare mutations and copy number variation
|
CN110872617A
(zh)
|
2012-09-04 |
2020-03-10 |
夸登特健康公司 |
检测稀有突变和拷贝数变异的系统和方法
|
US10876152B2
(en)
|
2012-09-04 |
2020-12-29 |
Guardant Health, Inc. |
Systems and 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
|
US10482994B2
(en)
|
2012-10-04 |
2019-11-19 |
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
|
EP2965077B1
(de)
|
2013-03-09 |
2022-07-13 |
Harry Stylli |
Verfahren zur krebserkennung
|
EP2965086A4
(de)
|
2013-03-09 |
2017-02-08 |
Harry Stylli |
Verfahren zum nachweis von prostatakrebs
|
EP3597774A1
(de)
|
2013-03-13 |
2020-01-22 |
Sequenom, Inc. |
Primer zur analyse der dna-methylierung
|
US9340835B2
(en)
|
2013-03-15 |
2016-05-17 |
Boreal Genomics Corp. |
Method for separating homoduplexed and heteroduplexed nucleic acids
|
AU2014231358A1
(en)
|
2013-03-15 |
2015-09-24 |
The Chinese University Of Hong Kong |
Determining fetal genomes for multiple fetus pregnancies
|
HUE061261T2
(hu)
|
2013-04-03 |
2023-05-28 |
Sequenom Inc |
Eljárások és folyamatok genetikai variánsok nem invazív értékelésére
|
EP3004383B1
(de)
|
2013-05-24 |
2019-04-24 |
Sequenom, Inc. |
Auf fläche unter der kurve (auc) analyse basiertes verfahren zur nichtinvasiven beurteilung genetischer variationen
|
BR112015032031B1
(pt)
|
2013-06-21 |
2023-05-16 |
Sequenom, Inc |
Métodos e processos para avaliação não invasiva das variações genéticas
|
IL285521B2
(en)
|
2013-08-19 |
2023-03-01 |
Singular Bio Inc |
Methods for single molecule detection
|
US10262755B2
(en)
|
2014-04-21 |
2019-04-16 |
Natera, Inc. |
Detecting cancer mutations and aneuploidy in chromosomal segments
|
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
|
AU2014329493B2
(en)
|
2013-10-04 |
2020-09-03 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
EP3495496B1
(de)
|
2013-10-07 |
2020-11-25 |
Sequenom, Inc. |
Verfahren und prozesse zur nichtinvasiven beurteilung chromosomaler veränderungen
|
WO2015100427A1
(en)
|
2013-12-28 |
2015-07-02 |
Guardant Health, Inc. |
Methods and systems for detecting genetic variants
|
GB2524948A
(en)
*
|
2014-03-07 |
2015-10-14 |
Oxford Gene Technology Operations Ltd |
Detecting Increase or Decrease in the Amount of a Nucleic Acid having a Sequence of Interest
|
EP3117011B1
(de)
|
2014-03-13 |
2020-05-06 |
Sequenom, Inc. |
Verfahren und prozesse zur nicht-invasiven beurteilung genetischer variationen
|
CN109971852A
(zh)
|
2014-04-21 |
2019-07-05 |
纳特拉公司 |
检测染色体片段中的突变和倍性
|
MA39951A
(fr)
|
2014-05-09 |
2017-03-15 |
Lifecodexx Ag |
Détection de l'adn provenant d'un type spécifique de cellule et méthodes associées
|
EP2942400A1
(de)
|
2014-05-09 |
2015-11-11 |
Lifecodexx AG |
Multiplex-Nachweis von DNA, die aus einem spezifischen Zelltyp herrührt
|
KR20160010277A
(ko)
|
2014-07-18 |
2016-01-27 |
에스케이텔레콤 주식회사 |
산모의 무세포 dna의 차세대 서열분석을 통한 태아의 단일유전자 유전변이의 예측방법
|
KR102441391B1
(ko)
|
2014-07-25 |
2022-09-07 |
유니버시티 오브 워싱톤 |
무세포 dna를 생성하는 조직 및/또는 세포 유형을 결정하는 방법 및 이를 사용하여 질환 또는 장애를 확인하는 방법
|
US20160034640A1
(en)
|
2014-07-30 |
2016-02-04 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
WO2016040843A1
(en)
|
2014-09-11 |
2016-03-17 |
Harry Stylli |
Methods of detecting prostate cancer
|
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
|
CA2976303A1
(en)
|
2015-02-10 |
2016-08-18 |
The Chinese University Of Hong Kong |
Detecting mutations for cancer screening and fetal analysis
|
AU2016219943A1
(en)
|
2015-02-18 |
2017-10-12 |
Singular Bio, Inc. |
Assays for single molecule detection and use thereof
|
US11168351B2
(en)
|
2015-03-05 |
2021-11-09 |
Streck, Inc. |
Stabilization of nucleic acids in urine
|
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
|
CN117012283A
(zh)
*
|
2015-10-10 |
2023-11-07 |
夸登特健康公司 |
无细胞dna分析中基因融合检测的方法和应用
|
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
|
US20170145475A1
(en)
|
2015-11-20 |
2017-05-25 |
Streck, Inc. |
Single spin process for blood plasma separation and plasma composition including preservative
|
CN117174167A
(zh)
|
2015-12-17 |
2023-12-05 |
夸登特健康公司 |
通过分析无细胞dna确定肿瘤基因拷贝数的方法
|
WO2017214557A1
(en)
|
2016-06-10 |
2017-12-14 |
Counsyl, Inc. |
Nucleic acid sequencing adapters and uses thereof
|
CA3030430A1
(en)
|
2016-07-15 |
2018-01-18 |
The Regents Of The University Of California |
Methods of producing nucleic acid libraries
|
EP3491560A1
(de)
|
2016-07-27 |
2019-06-05 |
Sequenom, Inc. |
Genkopienzahlvariationklassifizierungen
|
US11506655B2
(en)
|
2016-07-29 |
2022-11-22 |
Streck, Inc. |
Suspension composition for hematology analysis control
|
US11854666B2
(en)
|
2016-09-29 |
2023-12-26 |
Myriad Women's Health, Inc. |
Noninvasive prenatal screening using dynamic iterative depth optimization
|
KR102344635B1
(ko)
|
2016-09-30 |
2021-12-31 |
가던트 헬쓰, 인크. |
무세포 핵산의 다중-해상도 분석 방법
|
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
|
WO2018081130A1
(en)
|
2016-10-24 |
2018-05-03 |
The Chinese University Of Hong Kong |
Methods and systems for tumor detection
|
US10011870B2
(en)
|
2016-12-07 |
2018-07-03 |
Natera, Inc. |
Compositions and methods for identifying nucleic acid molecules
|
CA3207879A1
(en)
|
2017-01-24 |
2018-08-02 |
Sequenom, Inc. |
Methods and processes for assessment of genetic variations
|
TW202348802A
(zh)
|
2017-01-25 |
2023-12-16 |
香港中文大學 |
使用核酸片段之診斷應用
|
US10894976B2
(en)
|
2017-02-21 |
2021-01-19 |
Natera, Inc. |
Compositions, methods, and kits for isolating nucleic acids
|
WO2018175907A1
(en)
|
2017-03-24 |
2018-09-27 |
Counsyl, Inc. |
Copy number variant caller
|
AU2018355575A1
(en)
|
2017-10-27 |
2020-05-21 |
Juno Diagnostics, Inc. |
Devices, systems and methods for ultra-low volume liquid biopsy
|
US11584929B2
(en)
|
2018-01-12 |
2023-02-21 |
Claret Bioscience, Llc |
Methods and compositions for analyzing nucleic acid
|
JP2021520816A
(ja)
|
2018-04-14 |
2021-08-26 |
ナテラ, インコーポレイテッド |
循環腫瘍dnaの個別化された検出を用いる癌検出およびモニタリングの方法
|
KR20210016560A
(ko)
|
2018-06-06 |
2021-02-16 |
더 리젠츠 오브 더 유니버시티 오브 캘리포니아 |
핵산 라이브러리의 생성 방법 및 이를 실행하기 위한 조성물 및 키트
|
US11090583B2
(en)
|
2018-06-18 |
2021-08-17 |
Takeda Pharmaceutical Company Limited |
Bottom section for being connected to an assembly with plate settler, and assembly with plate settler
|
US11525159B2
(en)
|
2018-07-03 |
2022-12-13 |
Natera, Inc. |
Methods for detection of donor-derived cell-free DNA
|
TWI725686B
(zh)
|
2018-12-26 |
2021-04-21 |
財團法人工業技術研究院 |
用於產生液珠的管狀結構及液珠產生方法
|
JP2022519045A
(ja)
|
2019-01-31 |
2022-03-18 |
ガーダント ヘルス, インコーポレイテッド |
無細胞dnaを単離するための組成物および方法
|
US20220259637A1
(en)
|
2019-06-28 |
2022-08-18 |
Qiagen Gmbh |
Method for enriching nucleic acids by size
|
WO2021086985A1
(en)
|
2019-10-29 |
2021-05-06 |
Quantum-Si Incorporated |
Peristaltic pumping of fluids and associated methods, systems, and devices
|
TW202136283A
(zh)
|
2019-12-12 |
2021-10-01 |
日商武田藥品工業股份有限公司 |
連續性的蛋白質回收方法
|
JP2023516299A
(ja)
*
|
2020-02-28 |
2023-04-19 |
ラボラトリー コーポレイション オブ アメリカ ホールディングス |
父子判定のための組成物、方法、およびシステム
|
WO2021231912A1
(en)
|
2020-05-14 |
2021-11-18 |
Sequenom, Inc. |
Methods, systems, and compositions for the analysis of cell-free nucleic acids
|