|
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
|
|
EP1720636A4
(de)
|
2004-02-02 |
2012-06-20 |
Univ British Columbia |
Scodaphorese und verfahren und vorrichtungen zum bewegen und aufkonzentrieren von teilchen
|
|
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
|
|
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
|
|
WO2007044091A2
(en)
*
|
2005-06-02 |
2007-04-19 |
Fluidigm Corporation |
Analysis using microfluidic partitioning devices
|
|
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
|
|
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
|
|
US11111543B2
(en)
|
2005-07-29 |
2021-09-07 |
Natera, Inc. |
System and method for cleaning noisy genetic data and determining chromosome copy number
|
|
US8515679B2
(en)
|
2005-12-06 |
2013-08-20 |
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
|
|
US10083273B2
(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
|
|
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
|
|
US10081839B2
(en)
|
2005-07-29 |
2018-09-25 |
Natera, Inc |
System and method for cleaning noisy genetic data and determining chromosome copy number
|
|
US20070122823A1
(en)
*
|
2005-09-01 |
2007-05-31 |
Bianchi Diana W |
Amniotic fluid cell-free fetal DNA fragment size pattern for prenatal diagnosis
|
|
WO2007062164A2
(en)
*
|
2005-11-26 |
2007-05-31 |
Gene Security Network Llc |
System and method for cleaning noisy genetic data and using data to make predictions
|
|
EP3002338B1
(de)
|
2006-02-02 |
2019-05-08 |
The Board of Trustees of The Leland Stanford Junior University |
Nicht-invasives fötales genetisches screening mittels digitaler analyse
|
|
US20100184043A1
(en)
*
|
2006-02-28 |
2010-07-22 |
University Of Louisville Research Foundation |
Detecting Genetic Abnormalities
|
|
WO2007100911A2
(en)
*
|
2006-02-28 |
2007-09-07 |
University Of Louisville Research Foundation |
Detecting fetal chromosomal abnormalities using tandem single nucleotide polymorphisms
|
|
US20100184044A1
(en)
|
2006-02-28 |
2010-07-22 |
University Of Louisville Research Foundation |
Detecting Genetic Abnormalities
|
|
US8609338B2
(en)
|
2006-02-28 |
2013-12-17 |
University Of Louisville Research Foundation, Inc. |
Detecting fetal chromosomal abnormalities using tandem single nucleotide polymorphisms
|
|
AU2007223102A1
(en)
*
|
2006-03-06 |
2007-09-13 |
The Trustees Of Columbia University In The City Of New York |
Specific amplification of fetal DNA sequences from a mixed, fetal-maternal source
|
|
EP2602321B1
(de)
|
2006-05-31 |
2017-08-23 |
Sequenom, Inc. |
Verfahren und Zusammensetzungen zur Nukleinsäureextraktion und -verstärkung aus einer Probe
|
|
US8372584B2
(en)
|
2006-06-14 |
2013-02-12 |
The General Hospital Corporation |
Rare cell analysis using sample splitting and DNA tags
|
|
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
|
|
EP2029779A4
(de)
|
2006-06-14 |
2010-01-20 |
Living Microsystems Inc |
Verwendung hoch paralleler snp-genotypisierung zur fötalen diagnose
|
|
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
|
|
EP2140027B1
(de)
*
|
2006-12-07 |
2012-07-18 |
Novartis AG |
Nichtinvasiver pränataler genetischer screen-test
|
|
EP2140031A4
(de)
|
2007-03-26 |
2011-04-20 |
Sequenom Inc |
Restriktionsendonukleaseverstärkte polymorphe sequenzerfassung
|
|
US12180549B2
(en)
|
2007-07-23 |
2024-12-31 |
The Chinese University Of Hong Kong |
Diagnosing fetal chromosomal aneuploidy using genomic sequencing
|
|
KR20220146689A
(ko)
|
2007-07-23 |
2022-11-01 |
더 차이니즈 유니버시티 오브 홍콩 |
핵산 서열 불균형의 결정
|
|
US20090053719A1
(en)
*
|
2007-08-03 |
2009-02-26 |
The Chinese University Of Hong Kong |
Analysis of nucleic acids by digital pcr
|
|
KR20180090396A
(ko)
|
2008-01-18 |
2018-08-10 |
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
|
|
EP2250497B1
(de)
*
|
2008-02-18 |
2014-09-10 |
Genetic Technologies Limited |
Zellprozessierungs- und/oder -anreicherungsverfahren
|
|
US20110033862A1
(en)
*
|
2008-02-19 |
2011-02-10 |
Gene Security Network, Inc. |
Methods for cell genotyping
|
|
AU2009223671B2
(en)
*
|
2008-03-11 |
2014-11-27 |
Sequenom, Inc. |
Nucleic acid-based tests for prenatal gender determination
|
|
WO2009120808A2
(en)
|
2008-03-26 |
2009-10-01 |
Sequenom, Inc. |
Restriction endonuclease enhanced polymorphic sequence detection
|
|
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
|
|
US20110262916A1
(en)
*
|
2008-07-18 |
2011-10-27 |
Wen-Hua Fan |
Non-invasive fetal rhd genotyping from maternal whole blood
|
|
CN104732118B
(zh)
*
|
2008-08-04 |
2017-08-22 |
纳特拉公司 |
等位基因调用和倍性调用的方法
|
|
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
|
|
CN102216456A
(zh)
|
2008-09-16 |
2011-10-12 |
塞昆纳姆股份有限公司 |
基于甲基化富集母体样品中胎儿核酸的非侵入性产前诊断用方法和组合物
|
|
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
|
|
ES2620012T3
(es)
|
2008-09-20 |
2017-06-27 |
The Board Of Trustees Of The Leland Stanford Junior University |
Diagnóstico no invasivo de la aneuploidia fetal por secuenciación
|
|
EP2414545B1
(de)
|
2009-04-03 |
2017-01-11 |
Sequenom, Inc. |
Zusammensetzungen und verfahren für die herstellung von nukleinsäuren
|
|
EP2421955A4
(de)
|
2009-04-21 |
2012-10-10 |
Genetic Technologies Ltd |
Verfahren zur gewinnung von fötalem genmaterial
|
|
US8877028B2
(en)
|
2009-04-21 |
2014-11-04 |
The University Of British Columbia |
System and methods for detection of particles
|
|
US20120185176A1
(en)
|
2009-09-30 |
2012-07-19 |
Natera, Inc. |
Methods for Non-Invasive Prenatal Ploidy Calling
|
|
PL2496717T3
(pl)
|
2009-11-05 |
2017-11-30 |
The Chinese University Of Hong Kong |
Analiza genomowa płodu z matczynej próbki biologicznej
|
|
MX357692B
(es)
|
2009-11-06 |
2018-07-19 |
Univ Hong Kong Chinese |
Analisis genomico a base de tamaño.
|
|
EP2516680B1
(de)
|
2009-12-22 |
2016-04-06 |
Sequenom, Inc. |
Verfahren und kits zur identifizierung von aneuploidie
|
|
US10662474B2
(en)
|
2010-01-19 |
2020-05-26 |
Verinata Health, Inc. |
Identification of polymorphic sequences in mixtures of genomic DNA by whole genome sequencing
|
|
WO2011090556A1
(en)
|
2010-01-19 |
2011-07-28 |
Verinata Health, Inc. |
Methods for determining fraction of fetal nucleic acid in maternal samples
|
|
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
|
|
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
|
|
US10316362B2
(en)
|
2010-05-18 |
2019-06-11 |
Natera, Inc. |
Methods for simultaneous amplification of target loci
|
|
US11939634B2
(en)
|
2010-05-18 |
2024-03-26 |
Natera, Inc. |
Methods for simultaneous amplification of target loci
|
|
US20190010543A1
(en)
|
2010-05-18 |
2019-01-10 |
Natera, Inc. |
Methods for simultaneous amplification of target loci
|
|
US12221653B2
(en)
|
2010-05-18 |
2025-02-11 |
Natera, Inc. |
Methods for simultaneous amplification of target loci
|
|
US11322224B2
(en)
|
2010-05-18 |
2022-05-03 |
Natera, Inc. |
Methods for non-invasive prenatal ploidy calling
|
|
US11332785B2
(en)
|
2010-05-18 |
2022-05-17 |
Natera, Inc. |
Methods for non-invasive prenatal ploidy calling
|
|
US11332793B2
(en)
|
2010-05-18 |
2022-05-17 |
Natera, Inc. |
Methods for simultaneous amplification of target loci
|
|
US12545960B2
(en)
|
2010-05-18 |
2026-02-10 |
Natera, Inc. |
Methods for simultaneous amplification of target loci
|
|
US12152275B2
(en)
|
2010-05-18 |
2024-11-26 |
Natera, Inc. |
Methods for non-invasive prenatal ploidy calling
|
|
US11326208B2
(en)
|
2010-05-18 |
2022-05-10 |
Natera, Inc. |
Methods for nested PCR amplification of cell-free DNA
|
|
CA3037126C
(en)
|
2010-05-18 |
2023-09-12 |
Natera, Inc. |
Methods for non-invasive prenatal ploidy calling
|
|
CN103069005A
(zh)
|
2010-06-07 |
2013-04-24 |
艾索特里克斯遗传实验室有限责任公司 |
核酸计数
|
|
EP2596134B1
(de)
|
2010-07-23 |
2020-04-08 |
President and Fellows of Harvard College |
Verfahren zur erkennung von erkrankungen oder leiden mit phagozytischen zellen
|
|
CA2806293A1
(en)
|
2010-07-23 |
2012-01-26 |
President And Fellows Of Harvard College |
Methods of detecting autoimmune or immune-related diseases or conditions
|
|
WO2012012717A1
(en)
|
2010-07-23 |
2012-01-26 |
President And Fellows Of Harvard College |
Methods of detecting prenatal or pregnancy-related diseases or conditions
|
|
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
|
|
US20120034603A1
(en)
*
|
2010-08-06 |
2012-02-09 |
Tandem Diagnostics, Inc. |
Ligation-based detection of genetic variants
|
|
EP2609219A4
(de)
*
|
2010-08-24 |
2014-03-26 |
Bio Dx Inc |
Festlegung von diagnose- und therapiezielen in konservierter frei fliessender fötus-dna im mütterlichen blutkreislauf
|
|
BR112013016193B1
(pt)
*
|
2010-12-22 |
2019-10-22 |
Natera, Inc. |
método ex vivo para determinar se um suposto pai é o pai biológico de um feto que está em gestação em uma gestante e relatório
|
|
US10131947B2
(en)
*
|
2011-01-25 |
2018-11-20 |
Ariosa Diagnostics, Inc. |
Noninvasive detection of fetal aneuploidy in egg donor pregnancies
|
|
BR112013020220B1
(pt)
|
2011-02-09 |
2020-03-17 |
Natera, Inc. |
Método para determinar o estado de ploidia de um cromossomo em um feto em gestação
|
|
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
|
|
CN103717750B
(zh)
|
2011-04-29 |
2017-03-08 |
塞昆纳姆股份有限公司 |
少数核酸物质的定量
|
|
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
|
|
SG191757A1
(en)
|
2011-06-29 |
2013-08-30 |
Bgi Health Service Co Ltd |
Noninvasive detection of fetal genetic abnormality
|
|
US10424394B2
(en)
|
2011-10-06 |
2019-09-24 |
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
|
|
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
|
|
EP2764458B1
(de)
|
2011-10-06 |
2021-04-07 |
Sequenom, Inc. |
Verfahren und prozesse zur nicht-invasiven beurteilung genetischer variationen
|
|
EP2780465A4
(de)
*
|
2011-11-17 |
2015-06-03 |
Cellscape Corp |
Verfahren, vorrichtungen und kits zur gewinnung und analyse von zellen
|
|
PL2805280T3
(pl)
|
2012-01-20 |
2022-11-21 |
Sequenom, Inc. |
Procesy diagnostyczne będące czynnikiem warunków doświadczalnych
|
|
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
|
|
WO2013166444A2
(en)
|
2012-05-04 |
2013-11-07 |
Boreal Genomics Corp. |
Biomarker analysis using scodaphoresis
|
|
CA2874343C
(en)
|
2012-05-21 |
2021-11-09 |
Fluidigm Corporation |
Single-particle analysis of particle populations
|
|
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
|
|
JP2015521862A
(ja)
|
2012-07-13 |
2015-08-03 |
セクエノム, インコーポレイテッド |
非侵襲性の出生前診断に有用な母体サンプル由来の胎児核酸のメチル化に基づく富化のためのプロセスおよび組成物
|
|
US20140100126A1
(en)
|
2012-08-17 |
2014-04-10 |
Natera, Inc. |
Method for Non-Invasive Prenatal Testing Using Parental Mosaicism Data
|
|
US11913065B2
(en)
|
2012-09-04 |
2024-02-27 |
Guardent Health, Inc. |
Systems and methods to detect rare mutations and copy number variation
|
|
US10876152B2
(en)
|
2012-09-04 |
2020-12-29 |
Guardant Health, Inc. |
Systems and methods to detect rare mutations and copy number variation
|
|
GB2533006B
(en)
|
2012-09-04 |
2017-06-07 |
Guardant Health Inc |
Systems and methods to detect copy number variation
|
|
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
|
|
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
|
|
US11060145B2
(en)
|
2013-03-13 |
2021-07-13 |
Sequenom, Inc. |
Methods and compositions for identifying presence or absence of hypermethylation or hypomethylation locus
|
|
US9340835B2
(en)
|
2013-03-15 |
2016-05-17 |
Boreal Genomics Corp. |
Method for separating homoduplexed and heteroduplexed nucleic acids
|
|
KR20150132216A
(ko)
|
2013-03-15 |
2015-11-25 |
더 차이니즈 유니버시티 오브 홍콩 |
다태 임신에 대한 태아 게놈의 결정
|
|
HUE061261T2
(hu)
|
2013-04-03 |
2023-05-28 |
Sequenom Inc |
Eljárások és folyamatok genetikai variánsok nem invazív értékelésére
|
|
IL309903A
(en)
|
2013-05-24 |
2024-03-01 |
Sequenom Inc |
Methods and processes for non-invasive assessment of genetic variations
|
|
AU2014284180B2
(en)
|
2013-06-21 |
2020-03-19 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
|
WO2015026873A1
(en)
|
2013-08-19 |
2015-02-26 |
Singular Bio, Inc. |
Assays for single molecule detection and use thereof
|
|
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
|
|
PL3053071T3
(pl)
|
2013-10-04 |
2024-03-18 |
Sequenom, Inc. |
Metody i procesy nieinwazyjnej oceny zmienności genetycznych
|
|
CN105874082B
(zh)
|
2013-10-07 |
2020-06-02 |
塞昆纳姆股份有限公司 |
用于非侵入性评估染色体改变的方法和过程
|
|
EP3771745A1
(de)
|
2013-12-28 |
2021-02-03 |
Guardant Health, Inc. |
Verfahren und systeme für den nachweis genetischer varianten
|
|
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
|
|
EP3736344A1
(de)
|
2014-03-13 |
2020-11-11 |
Sequenom, Inc. |
Verfahren und prozesse zur nichtinvasiven beurteilung genetischer variationen
|
|
CA2945962C
(en)
|
2014-04-21 |
2023-08-29 |
Natera, Inc. |
Detecting mutations and ploidy in chromosomal segments
|
|
US12492429B2
(en)
|
2014-04-21 |
2025-12-09 |
Natera, Inc. |
Detecting mutations and ploidy in chromosomal segments
|
|
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
|
|
US20180173845A1
(en)
|
2014-06-05 |
2018-06-21 |
Natera, Inc. |
Systems and Methods for Detection of Aneuploidy
|
|
KR20160010277A
(ko)
|
2014-07-18 |
2016-01-27 |
에스케이텔레콤 주식회사 |
산모의 무세포 dna의 차세대 서열분석을 통한 태아의 단일유전자 유전변이의 예측방법
|
|
KR102696857B1
(ko)
|
2014-07-25 |
2024-08-19 |
유니버시티 오브 워싱톤 |
무세포 dna를 생성하는 조직 및/또는 세포 유형을 결정하는 방법 및 이를 사용하여 질환 또는 장애를 확인하는 방법
|
|
US11783911B2
(en)
|
2014-07-30 |
2023-10-10 |
Sequenom, Inc |
Methods and processes for non-invasive assessment of genetic variations
|
|
EP4428251A3
(de)
|
2014-09-11 |
2024-12-18 |
Immunis.AI, Inc. |
Verfahren zum nachweis von prostatakrebs
|
|
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
|
|
PT3256605T
(pt)
|
2015-02-10 |
2022-03-17 |
Univ Hong Kong Chinese |
Deteção de mutações para rastreio de cancro e análise fetal
|
|
KR20170116157A
(ko)
|
2015-02-18 |
2017-10-18 |
싱귤러 바이오, 인코포레이티드 |
단일분자 검출용 분석 및 그의 용도
|
|
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
|
|
US20180300449A1
(en)
*
|
2015-10-10 |
2018-10-18 |
Guardant Health, Inc. |
Methods and applications of gene fusion detection in cell-free dna analysis
|
|
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
|
|
EP3390668A4
(de)
|
2015-12-17 |
2020-04-01 |
Guardant Health, Inc. |
Verfahren zur bestimmung der tumorgenkopienzahl durch analyse von zellfreier dna
|
|
ES2913468T3
(es)
|
2016-04-15 |
2022-06-02 |
Natera Inc |
Métodos para la detección del cáncer de pulmón.
|
|
US11708574B2
(en)
|
2016-06-10 |
2023-07-25 |
Myriad Women's Health, 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
|
|
WO2018022991A1
(en)
|
2016-07-29 |
2018-02-01 |
Streck, Inc. |
Suspension composition for hematology analysis control
|
|
WO2018064486A1
(en)
|
2016-09-29 |
2018-04-05 |
Counsyl, Inc. |
Noninvasive prenatal screening using dynamic iterative depth optimization
|
|
US9850523B1
(en)
|
2016-09-30 |
2017-12-26 |
Guardant Health, Inc. |
Methods for multi-resolution analysis of cell-free nucleic acids
|
|
AU2017336153B2
(en)
|
2016-09-30 |
2023-07-13 |
Guardant Health, Inc. |
Methods for multi-resolution analysis of cell-free nucleic acids
|
|
US11485996B2
(en)
|
2016-10-04 |
2022-11-01 |
Natera, Inc. |
Methods for characterizing copy number variation using proximity-litigation sequencing
|
|
WO2018081130A1
(en)
|
2016-10-24 |
2018-05-03 |
The Chinese University Of Hong Kong |
Methods and systems for tumor detection
|
|
GB201618485D0
(en)
|
2016-11-02 |
2016-12-14 |
Ucl Business Plc |
Method of detecting tumour recurrence
|
|
US10011870B2
(en)
|
2016-12-07 |
2018-07-03 |
Natera, Inc. |
Compositions and methods for identifying nucleic acid molecules
|
|
WO2018140521A1
(en)
|
2017-01-24 |
2018-08-02 |
Sequenom, Inc. |
Methods and processes for assessment of genetic variations
|
|
EP4421489B1
(de)
|
2017-01-25 |
2026-03-11 |
The Chinese University of Hong Kong |
Diagnostische anwendungen unter verwendung von nukleinsäurefragmenten
|
|
US10894976B2
(en)
|
2017-02-21 |
2021-01-19 |
Natera, Inc. |
Compositions, methods, and kits for isolating nucleic acids
|
|
IL317916A
(en)
|
2017-03-17 |
2025-02-01 |
Sequenom Inc |
Methods and processes for assessing genetic mosaicism
|
|
EP3602359A4
(de)
|
2017-03-24 |
2021-01-06 |
Myriad Women's Health, Inc. |
Kopienzahlvariantencaller
|
|
KR20250171389A
(ko)
|
2017-07-26 |
2025-12-08 |
더 차이니즈 유니버시티 오브 홍콩 |
세포-무함유 바이러스 핵산을 사용하는 암 스크리닝의 증강
|
|
US12378543B2
(en)
|
2017-10-19 |
2025-08-05 |
Streck Llc |
Compositions for hemolysis and coagulation regulation and stabilization of extracellular vesicles
|
|
TWI833715B
(zh)
|
2017-10-27 |
2024-03-01 |
美商奇諾診療公司 |
用於超低體積液體生物檢體之裝置、系統及方法
|
|
CA3085933A1
(en)
|
2017-12-14 |
2019-06-20 |
Tai Diagnostics, Inc. |
Assessing graft suitability for transplantation
|
|
WO2019140201A1
(en)
|
2018-01-12 |
2019-07-18 |
Claret Bioscience, Llc |
Methods and compositions for analyzing nucleic acid
|
|
WO2019161244A1
(en)
|
2018-02-15 |
2019-08-22 |
Natera, Inc. |
Methods for isolating nucleic acids with size selection
|
|
WO2019191319A1
(en)
|
2018-03-30 |
2019-10-03 |
Juno Diagnostics, Inc. |
Deep learning-based methods, devices, and systems for prenatal testing
|
|
EP3781714B1
(de)
|
2018-04-14 |
2026-01-07 |
Natera, Inc. |
Verfahren zur krebserkennung und -überwachung durch personalisierte detektion zirkulierender tumor-dna
|
|
WO2019231259A1
(ko)
|
2018-06-01 |
2019-12-05 |
주식회사 제놉시 |
불안정한 세포유리 dna 검출 방법 및 이를 이용한 장치
|
|
JP7537748B2
(ja)
|
2018-06-06 |
2024-08-21 |
ザ リージェンツ オブ ザ ユニバーシティ オブ カリフォルニア |
核酸ライブラリを生成する方法ならびにそれを実施するための組成物およびキット
|
|
EP3806973B1
(de)
|
2018-06-18 |
2023-10-18 |
Takeda Pharmaceutical Company Limited |
Zusammenbau mit plattenabsetzvorrichtung und bodenabschnitt zur verbindung damit
|
|
US12234509B2
(en)
|
2018-07-03 |
2025-02-25 |
Natera, Inc. |
Methods for detection of donor-derived cell-free DNA
|
|
US20200075123A1
(en)
|
2018-08-31 |
2020-03-05 |
Guardant Health, Inc. |
Genetic variant detection based on merged and unmerged reads
|
|
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
|
|
ES3013495T3
(en)
|
2019-01-31 |
2025-04-14 |
Guardant Health Inc |
Method for isolating and sequencing cell-free dna
|
|
WO2020247263A1
(en)
|
2019-06-06 |
2020-12-10 |
Natera, Inc. |
Methods for detecting immune cell dna and monitoring immune system
|
|
EP3990632A1
(de)
|
2019-06-28 |
2022-05-04 |
QIAGEN GmbH |
Verfahren zur anreicherung von nukleinsäuren nach grösse
|
|
US12011716B2
(en)
|
2019-10-29 |
2024-06-18 |
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
|
|
US20230120825A1
(en)
*
|
2020-02-28 |
2023-04-20 |
Laboratory Corporation Of America Holdings |
Compositions, Methods, and Systems for Paternity Determination
|
|
EP4150074A1
(de)
|
2020-05-14 |
2023-03-22 |
Sequenom, Inc. |
Verfahren, systeme und zusammensetzungen zur analyse von zellfreien nukleinsäuren
|
|
EP4301499A4
(de)
|
2021-03-05 |
2025-01-22 |
Enumerix, Inc. |
Systeme und verfahren zur erzeugung von tröpfchen und zur durchführung digitaler analysen
|
|
US12252745B2
(en)
|
2021-09-02 |
2025-03-18 |
Enumerix, Inc. |
Detection and digital quantitation of multiple targets
|