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
|
JP2005514956A
(ja)
*
|
2002-01-18 |
2005-05-26 |
ジェンザイム・コーポレーション |
胎児dnaの検出および対立遺伝子の定量化のための方法
|
WO2003074740A1
(en)
|
2002-03-01 |
2003-09-12 |
Ravgen, Inc. |
Rapid analysis of variations in a genome
|
US6977162B2
(en)
*
|
2002-03-01 |
2005-12-20 |
Ravgen, Inc. |
Rapid analysis of variations in a genome
|
ES2253461T3
(es)
*
|
2002-03-05 |
2006-06-01 |
Epigenomics Ag |
Procedimiento y dispositivo para la determinacion de la especificidad del tejido y del adn que flota libre en tejidos corporales.
|
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
|
US8394582B2
(en)
*
|
2003-03-05 |
2013-03-12 |
Genetic Technologies, Inc |
Identification of fetal DNA and fetal cell markers in maternal plasma or serum
|
AU2004274724B2
(en)
*
|
2003-09-22 |
2009-09-10 |
Trisogen Biotechnology Limited Partnership |
Methods and kits useful for detecting an alteration in a locus copy number
|
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
|
WO2005035725A2
(en)
*
|
2003-10-08 |
2005-04-21 |
The Trustees Of Boston University |
Methods for prenatal diagnosis of chromosomal abnormalities
|
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
|
US9186685B2
(en)
|
2012-01-13 |
2015-11-17 |
The University Of British Columbia |
Multiple arm apparatus and methods for separation of particles
|
EP1720636A4
(en)
|
2004-02-02 |
2012-06-20 |
Univ British Columbia |
SCODAPHORESIS, METHODS AND APPARATUS FOR DISPLACING AND CONCENTRATING PARTICLES
|
US7709194B2
(en)
*
|
2004-06-04 |
2010-05-04 |
The Chinese University Of Hong Kong |
Marker for prenatal diagnosis and monitoring
|
SI1871912T1
(sl)
|
2005-04-15 |
2012-06-29 |
Epigenomics Ag |
Postopek za določitev DNA metilacije v vzorcih krvi ali urina
|
EP2477029A1
(en)
*
|
2005-06-02 |
2012-07-18 |
Fluidigm Corporation |
Analysis using microfluidic partitioning devices
|
US11111543B2
(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
|
US11111544B2
(en)
*
|
2005-07-29 |
2021-09-07 |
Natera, Inc. |
System and method for cleaning noisy genetic data and determining chromosome copy number
|
EP2423334A3
(en)
|
2006-02-02 |
2012-04-18 |
The Board of Trustees of The Leland Stanford Junior University |
Non-invasive fetal genetic screening by digital analysis
|
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
|
US7901884B2
(en)
*
|
2006-05-03 |
2011-03-08 |
The Chinese University Of Hong Kong |
Markers for prenatal diagnosis and monitoring
|
US7754428B2
(en)
|
2006-05-03 |
2010-07-13 |
The Chinese University Of Hong Kong |
Fetal methylation markers
|
US8679741B2
(en)
*
|
2006-05-31 |
2014-03-25 |
Sequenom, Inc. |
Methods and compositions for the extraction and amplification of nucleic acid from a sample
|
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
|
EP2589668A1
(en)
|
2006-06-14 |
2013-05-08 |
Verinata Health, Inc |
Rare cell analysis using sample splitting and DNA tags
|
CN101153336B
(zh)
*
|
2006-09-27 |
2011-09-07 |
香港中文大学 |
检测dna甲基化程度的方法和试剂盒
|
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
|
DK2479289T3
(da)
|
2007-06-08 |
2016-05-02 |
Epigenomics Ag |
Fremgangsmåde til methyleringsanalyse
|
AU2013202157B2
(en)
*
|
2007-07-23 |
2015-04-30 |
The Chinese University Of Hong Kong |
Noninvasively determining a fetal genotype at a maternal heterozygous locus
|
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
|
WO2009032781A2
(en)
|
2007-08-29 |
2009-03-12 |
Sequenom, Inc. |
Methods and compositions for universal size-specific polymerase chain reaction
|
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
|
US8709726B2
(en)
*
|
2008-03-11 |
2014-04-29 |
Sequenom, Inc. |
Nucleic acid-based tests for prenatal gender determination
|
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
|
EP3103871B1
(en)
|
2008-09-16 |
2020-07-29 |
Sequenom, Inc. |
Processes for methylation-based enrichment of fetal nucleic acid from a maternal sample useful for fetal nucleic acid quantification
|
EP3751005A3
(en)
|
2008-09-20 |
2021-02-24 |
The Board of Trustees of the Leland Stanford Junior University |
Noninvasive diagnosis of fetal aneuploidy by sequencing
|
US20110159499A1
(en)
*
|
2009-11-25 |
2011-06-30 |
Quantalife, Inc. |
Methods and compositions for detecting genetic material
|
US20100279295A1
(en)
*
|
2009-03-18 |
2010-11-04 |
Sequenom, Inc. |
Use of thermostable endonucleases for generating reporter molecules
|
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
|
WO2011006119A2
(en)
|
2009-07-09 |
2011-01-13 |
The Scripps Research Institute |
Gene expression profiles associated with chronic allograft nephropathy
|
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
|
HUE052213T2
(hu)
*
|
2009-11-06 |
2021-04-28 |
Univ Leland Stanford Junior |
Grafitkilökõdés nem invazív diagnosztizálása szervátültetett betegekben
|
US9926593B2
(en)
|
2009-12-22 |
2018-03-27 |
Sequenom, Inc. |
Processes and kits for identifying aneuploidy
|
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
|
CA2786565C
(en)
|
2010-01-19 |
2017-04-25 |
Verinata Health, Inc. |
Partition defined detection methods
|
US20120010085A1
(en)
|
2010-01-19 |
2012-01-12 |
Rava Richard P |
Methods for determining fraction of fetal nucleic acids in maternal samples
|
US9323888B2
(en)
|
2010-01-19 |
2016-04-26 |
Verinata Health, Inc. |
Detecting and classifying copy number variation
|
EP2513341B1
(en)
*
|
2010-01-19 |
2017-04-12 |
Verinata Health, Inc |
Identification of polymorphic sequences in mixtures of genomic dna by whole genome sequencing
|
US20120100548A1
(en)
|
2010-10-26 |
2012-04-26 |
Verinata Health, Inc. |
Method for determining copy number variations
|
WO2011090558A1
(en)
|
2010-01-19 |
2011-07-28 |
Verinata Health, Inc. |
Simultaneous determination of aneuploidy and fetal fraction
|
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
|
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
|
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
|
US11322224B2
(en)
|
2010-05-18 |
2022-05-03 |
Natera, Inc. |
Methods for non-invasive prenatal ploidy calling
|
EP2854057B1
(en)
|
2010-05-18 |
2018-03-07 |
Natera, Inc. |
Methods for non-invasive pre-natal ploidy calling
|
US11408031B2
(en)
|
2010-05-18 |
2022-08-09 |
Natera, Inc. |
Methods for non-invasive prenatal paternity testing
|
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
|
US11332785B2
(en)
|
2010-05-18 |
2022-05-17 |
Natera, Inc. |
Methods for non-invasive prenatal ploidy calling
|
US11339429B2
(en)
|
2010-05-18 |
2022-05-24 |
Natera, Inc. |
Methods for non-invasive prenatal ploidy calling
|
AU2011280936A1
(en)
|
2010-07-23 |
2013-02-28 |
President And Fellows Of Harvard College |
Methods of detecting prenatal or pregnancy-related diseases or conditions
|
WO2012012694A2
(en)
|
2010-07-23 |
2012-01-26 |
President And Fellows Of Harvard College |
Methods of detecting autoimmune or immune-related diseases or conditions
|
EP4303584A3
(en)
|
2010-07-23 |
2024-04-03 |
President and Fellows of Harvard College |
Methods for detecting signatures of disease or conditions in bodily fluids
|
SG10201505724SA
(en)
|
2010-07-23 |
2015-09-29 |
Harvard College |
Methods of detecting diseases or conditions using phagocytic cells
|
US20130040375A1
(en)
|
2011-08-08 |
2013-02-14 |
Tandem Diagnotics, Inc. |
Assay systems for genetic analysis
|
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
|
US10167508B2
(en)
|
2010-08-06 |
2019-01-01 |
Ariosa Diagnostics, Inc. |
Detection of genetic abnormalities
|
US11203786B2
(en)
|
2010-08-06 |
2021-12-21 |
Ariosa Diagnostics, Inc. |
Detection of target nucleic acids using hybridization
|
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
|
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
(en)
|
2010-10-26 |
2014-05-07 |
Univ Stanford |
NON-INVASIVE F TAL GENE SCREENING BY SEQUENCING ANALYSIS
|
US9994897B2
(en)
|
2013-03-08 |
2018-06-12 |
Ariosa Diagnostics, Inc. |
Non-invasive fetal sex determination
|
US10131947B2
(en)
|
2011-01-25 |
2018-11-20 |
Ariosa Diagnostics, Inc. |
Noninvasive detection of fetal aneuploidy in egg donor pregnancies
|
US11270781B2
(en)
|
2011-01-25 |
2022-03-08 |
Ariosa Diagnostics, Inc. |
Statistical analysis for non-invasive sex chromosome aneuploidy determination
|
US8756020B2
(en)
|
2011-01-25 |
2014-06-17 |
Ariosa Diagnostics, Inc. |
Enhanced risk probabilities using biomolecule estimations
|
WO2012108920A1
(en)
|
2011-02-09 |
2012-08-16 |
Natera, Inc |
Methods for non-invasive prenatal ploidy calling
|
EP3940084A1
(en)
|
2011-02-09 |
2022-01-19 |
Bio-Rad Laboratories, Inc. |
Analysis of nucleic acids
|
JP5837622B2
(ja)
|
2011-02-24 |
2015-12-24 |
ザ チャイニーズ ユニバーシティー オブ ホンコンThe Chinese University Of Hongkong |
多胎妊娠の分子検査
|
DK3456844T3
(da)
|
2011-04-12 |
2020-06-29 |
Verinata Health Inc |
Bestemmelse af genomfraktioner under anvendelse af polymorfisme-tællinger
|
US9411937B2
(en)
|
2011-04-15 |
2016-08-09 |
Verinata Health, Inc. |
Detecting and classifying copy number variation
|
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
|
US8712697B2
(en)
|
2011-09-07 |
2014-04-29 |
Ariosa Diagnostics, Inc. |
Determination of copy number variations using binomial probability calculations
|
US9984198B2
(en)
|
2011-10-06 |
2018-05-29 |
Sequenom, Inc. |
Reducing sequence read count error in assessment of complex genetic variations
|
CA2850785C
(en)
|
2011-10-06 |
2022-12-13 |
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
|
AU2012318371B2
(en)
|
2011-10-06 |
2018-03-22 |
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
|
US10196681B2
(en)
|
2011-10-06 |
2019-02-05 |
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
|
EP2766496B1
(en)
|
2011-10-11 |
2017-03-08 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
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
|
CA2866324C
(en)
|
2012-03-13 |
2019-01-15 |
The Chinese University Of Hong Kong |
Methods for analyzing massively parallel sequencing data for noninvasive prenatal diagnosis
|
US9512477B2
(en)
|
2012-05-04 |
2016-12-06 |
Boreal Genomics Inc. |
Biomarker anaylsis using scodaphoresis
|
US10289800B2
(en)
|
2012-05-21 |
2019-05-14 |
Ariosa Diagnostics, Inc. |
Processes for calculating phased fetal genomic sequences
|
US9920361B2
(en)
|
2012-05-21 |
2018-03-20 |
Sequenom, Inc. |
Methods and compositions for analyzing nucleic acid
|
EP3663409B1
(en)
|
2012-05-21 |
2021-10-06 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
US10504613B2
(en)
|
2012-12-20 |
2019-12-10 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
CN104471077B
(zh)
|
2012-05-21 |
2017-05-24 |
富鲁达公司 |
颗粒群的单颗粒分析
|
US10497461B2
(en)
|
2012-06-22 |
2019-12-03 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
EP2872648B1
(en)
|
2012-07-13 |
2019-09-04 |
Sequenom, Inc. |
Processes and compositions for methylation-based enrichment of fetal nucleic acid from a maternal sample useful for non-invasive prenatal diagnoses
|
US9206417B2
(en)
|
2012-07-19 |
2015-12-08 |
Ariosa Diagnostics, Inc. |
Multiplexed sequential ligation-based detection of genetic variants
|
KR102390711B1
(ko)
|
2012-09-20 |
2022-04-26 |
더 차이니즈 유니버시티 오브 홍콩 |
혈장으로부터 태아 또는 종양 메틸롬의 비침습적 결정
|
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
|
US10706957B2
(en)
|
2012-09-20 |
2020-07-07 |
The Chinese University Of Hong Kong |
Non-invasive determination of methylome of tumor from plasma
|
US10482994B2
(en)
|
2012-10-04 |
2019-11-19 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
EP4009329A1
(en)
|
2012-10-04 |
2022-06-08 |
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
(en)
|
2013-03-09 |
2022-07-13 |
Harry Stylli |
Methods of detecting cancer
|
EP2965086A4
(en)
|
2013-03-09 |
2017-02-08 |
Harry Stylli |
Methods of detecting prostate cancer
|
US20130189684A1
(en)
|
2013-03-12 |
2013-07-25 |
Sequenom, Inc. |
Quantification of cell-specific nucleic acid markers
|
EP3597774A1
(en)
|
2013-03-13 |
2020-01-22 |
Sequenom, Inc. |
Primers for dna methylation analysis
|
AU2014231358A1
(en)
|
2013-03-15 |
2015-09-24 |
The Chinese University Of Hong Kong |
Determining fetal genomes for multiple fetus pregnancies
|
US9340835B2
(en)
|
2013-03-15 |
2016-05-17 |
Boreal Genomics Corp. |
Method for separating homoduplexed and heteroduplexed nucleic acids
|
WO2014144822A2
(en)
|
2013-03-15 |
2014-09-18 |
Immumetrix, Inc. |
Methods and compositions for tagging and analyzing samples
|
HUE061261T2
(hu)
|
2013-04-03 |
2023-05-28 |
Sequenom Inc |
Eljárások és folyamatok genetikai variánsok nem invazív értékelésére
|
EP3004383B1
(en)
|
2013-05-24 |
2019-04-24 |
Sequenom, Inc. |
Methods for non-invasive assessment of genetic variations using area-under-curve (auc) analysis
|
BR112015032031B1
(pt)
|
2013-06-21 |
2023-05-16 |
Sequenom, Inc |
Métodos e processos para avaliação não invasiva das variações genéticas
|
EP3029148B1
(en)
*
|
2013-07-30 |
2018-06-27 |
BGI Genomics Co., Limited |
Method for determining nucleic acid composition of nucleic acid mixture
|
AU2014329493B2
(en)
|
2013-10-04 |
2020-09-03 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
EP3495496B1
(en)
|
2013-10-07 |
2020-11-25 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of chromosome alterations
|
EP3117011B1
(en)
|
2014-03-13 |
2020-05-06 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
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
|
EP2942400A1
(en)
|
2014-05-09 |
2015-11-11 |
Lifecodexx AG |
Multiplex detection of DNA that originates from a specific cell-type
|
MA39951A
(fr)
|
2014-05-09 |
2017-03-15 |
Lifecodexx Ag |
Détection de l'adn provenant d'un type spécifique de cellule et méthodes associées
|
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
(en)
|
2014-05-30 |
2023-07-26 |
Sequenom, Inc. |
Chromosome representation determinations
|
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
|
EP3730629A1
(en)
|
2014-10-10 |
2020-10-28 |
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
|
WO2016189388A1
(en)
|
2015-05-22 |
2016-12-01 |
Nipd Genetics Ltd |
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
|
US20170342477A1
(en)
|
2016-05-27 |
2017-11-30 |
Sequenom, Inc. |
Methods for Detecting Genetic Variations
|
CA3030430A1
(en)
|
2016-07-15 |
2018-01-18 |
The Regents Of The University Of California |
Methods of producing nucleic acid libraries
|
EP3491561A1
(en)
|
2016-07-27 |
2019-06-05 |
Sequenom, Inc. |
Methods for non-invasive assessment of genomic instability
|
EP3491560A1
(en)
|
2016-07-27 |
2019-06-05 |
Sequenom, Inc. |
Genetic copy number alteration classifications
|
US11854666B2
(en)
|
2016-09-29 |
2023-12-26 |
Myriad Women's Health, Inc. |
Noninvasive prenatal screening using dynamic iterative depth optimization
|
WO2018067517A1
(en)
|
2016-10-04 |
2018-04-12 |
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
|
WO2018136882A1
(en)
|
2017-01-20 |
2018-07-26 |
Sequenom, Inc. |
Methods for non-invasive assessment of copy number alterations
|
CA3049455C
(en)
|
2017-01-20 |
2023-06-13 |
Sequenom, Inc. |
Sequencing adapter manufacture and use
|
US11929145B2
(en)
|
2017-01-20 |
2024-03-12 |
Sequenom, Inc |
Methods for non-invasive assessment of genetic alterations
|
CA3207879A1
(en)
|
2017-01-24 |
2018-08-02 |
Sequenom, Inc. |
Methods and processes for assessment of genetic variations
|
EP3596233B1
(en)
|
2017-03-17 |
2022-05-18 |
Sequenom, Inc. |
Methods and processes for assessment of genetic mosaicism
|
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
|
US11525159B2
(en)
|
2018-07-03 |
2022-12-13 |
Natera, Inc. |
Methods for detection of donor-derived cell-free DNA
|
US20220348906A1
(en)
|
2019-04-05 |
2022-11-03 |
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
|
WO2021072037A1
(en)
|
2019-10-09 |
2021-04-15 |
Claret Bioscience, Llc |
Methods and compositions for analyzing nucleic acid
|
WO2021086985A1
(en)
|
2019-10-29 |
2021-05-06 |
Quantum-Si Incorporated |
Peristaltic pumping of fluids and associated methods, systems, and devices
|
JP2022553829A
(ja)
|
2019-10-31 |
2022-12-26 |
セクエノム, インコーポレイテッド |
多胎児妊娠およびパーソナライズされたリスク評価におけるモザイク現象比の適用
|
EP4172357B1
(en)
|
2020-06-24 |
2024-05-15 |
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
|
BR112023018152A2
(pt)
*
|
2021-03-09 |
2023-10-31 |
Illumina Cambridge Ltd |
Preparação de biblioteca genômica e ensaios epigenéticos direcionados com o uso de ribonucleoproteínas de cas-grna
|