US4040785A
(en)
|
1976-10-18 |
1977-08-09 |
Technicon Instruments Corporation |
Lysable blood preservative composition
|
US5242794A
(en)
|
1984-12-13 |
1993-09-07 |
Applied Biosystems, Inc. |
Detection of specific sequences in nucleic acids
|
US4683195A
(en)
|
1986-01-30 |
1987-07-28 |
Cetus Corporation |
Process for amplifying, detecting, and/or-cloning nucleic acid sequences
|
US4935342A
(en)
|
1986-12-01 |
1990-06-19 |
Syngene, Inc. |
Method of isolating and purifying nucleic acids from biological samples
|
US4942124A
(en)
|
1987-08-11 |
1990-07-17 |
President And Fellows Of Harvard College |
Multiplex sequencing
|
US5153117A
(en)
|
1990-03-27 |
1992-10-06 |
Genetype A.G. |
Fetal cell recovery method
|
US6582908B2
(en)
|
1990-12-06 |
2003-06-24 |
Affymetrix, Inc. |
Oligonucleotides
|
US5262329A
(en)
|
1991-06-13 |
1993-11-16 |
Carver Jr Edward L |
Method for improved multiple species blood analysis
|
IL103935A0
(en)
|
1991-12-04 |
1993-05-13 |
Du Pont |
Method for the identification of microorganisms by the utilization of directed and arbitrary dna amplification
|
US5965362A
(en)
|
1992-03-04 |
1999-10-12 |
The Regents Of The University Of California |
Comparative genomic hybridization (CGH)
|
GB9305984D0
(en)
|
1993-03-23 |
1993-05-12 |
Royal Free Hosp School Med |
Predictive assay
|
CA2166729A1
(fr)
|
1993-07-05 |
1995-01-19 |
Vivian Granger |
Preparation et stabilisation de cellules
|
WO1995006137A1
(fr)
|
1993-08-27 |
1995-03-02 |
Australian Red Cross Society |
Detection de genes
|
CH686982A5
(fr)
|
1993-12-16 |
1996-08-15 |
Maurice Stroun |
Méthode pour le diagnostic de cancers.
|
SE9400522D0
(sv)
|
1994-02-16 |
1994-02-16 |
Ulf Landegren |
Method and reagent for detecting specific nucleotide sequences
|
US5716776A
(en)
|
1994-03-04 |
1998-02-10 |
Mark H. Bogart |
Enrichment by preferential mitosis of fetal lymphocytes from a maternal blood sample
|
US5891734A
(en)
|
1994-08-01 |
1999-04-06 |
Abbott Laboratories |
Method for performing automated analysis
|
US6025128A
(en)
|
1994-09-29 |
2000-02-15 |
The University Of Tulsa |
Prediction of prostate cancer progression by analysis of selected predictive parameters
|
US6479235B1
(en)
|
1994-09-30 |
2002-11-12 |
Promega Corporation |
Multiplex amplification of short tandem repeat loci
|
US5648220A
(en)
|
1995-02-14 |
1997-07-15 |
New England Medical Center Hospitals, Inc. |
Methods for labeling intracytoplasmic molecules
|
CA2221454A1
(fr)
|
1995-05-19 |
1996-11-21 |
Abbott Laboratories |
Procede de detection d'acides nucleiques a large plage dynamique, utilisant une serie complexe d'amorces
|
US6720140B1
(en)
|
1995-06-07 |
2004-04-13 |
Invitrogen Corporation |
Recombinational cloning using engineered recombination sites
|
US5733729A
(en)
|
1995-09-14 |
1998-03-31 |
Affymetrix, Inc. |
Computer-aided probability base calling for arrays of nucleic acid probes on chips
|
US5854033A
(en)
|
1995-11-21 |
1998-12-29 |
Yale University |
Rolling circle replication reporter systems
|
US6852487B1
(en)
|
1996-02-09 |
2005-02-08 |
Cornell Research Foundation, Inc. |
Detection of nucleic acid sequence differences using the ligase detection reaction with addressable arrays
|
US6156504A
(en)
|
1996-03-15 |
2000-12-05 |
The Penn State Research Foundation |
Detection of extracellular tumor-associated nucleic acid in blood plasma or serum using nucleic acid amplification assays
|
DK0938320T3
(da)
|
1996-03-26 |
2010-10-18 |
Michael S Kopreski |
Metode til at ud af plasma eller serum tilvejebringe ekstraheret ekstracellulært RNA for at detektere, overvåge eller vurdere cancer
|
US6108635A
(en)
|
1996-05-22 |
2000-08-22 |
Interleukin Genetics, Inc. |
Integrated disease information system
|
US6300077B1
(en)
|
1996-08-14 |
2001-10-09 |
Exact Sciences Corporation |
Methods for the detection of nucleic acids
|
US6100029A
(en)
|
1996-08-14 |
2000-08-08 |
Exact Laboratories, Inc. |
Methods for the detection of chromosomal aberrations
|
US6221654B1
(en)
|
1996-09-25 |
2001-04-24 |
California Institute Of Technology |
Method and apparatus for analysis and sorting of polynucleotides based on size
|
US5860917A
(en)
|
1997-01-15 |
1999-01-19 |
Chiron Corporation |
Method and apparatus for predicting therapeutic outcomes
|
US5824467A
(en)
|
1997-02-25 |
1998-10-20 |
Celtrix Pharmaceuticals |
Methods for predicting drug response
|
US20010051341A1
(en)
|
1997-03-04 |
2001-12-13 |
Isis Innovation Limited |
Non-invasive prenatal diagnosis
|
GB9704444D0
(en)
|
1997-03-04 |
1997-04-23 |
Isis Innovation |
Non-invasive prenatal diagnosis
|
DK0866071T3
(da)
|
1997-03-20 |
2005-01-17 |
Hoffmann La Roche |
Modificerede primere
|
DE69837913T2
(de)
|
1997-04-01 |
2008-02-07 |
Solexa Ltd., Saffron Walden |
Verfahren zur vervielfältigung von nukleinsäure
|
US6143496A
(en)
|
1997-04-17 |
2000-11-07 |
Cytonix Corporation |
Method of sampling, amplifying and quantifying segment of nucleic acid, polymerase chain reaction assembly having nanoliter-sized sample chambers, and method of filling assembly
|
US20020119478A1
(en)
|
1997-05-30 |
2002-08-29 |
Diagen Corporation |
Methods for detection of nucleic acid sequences in urine
|
US5994148A
(en)
|
1997-06-23 |
1999-11-30 |
The Regents Of University Of California |
Method of predicting and enhancing success of IVF/ET pregnancy
|
US6833242B2
(en)
|
1997-09-23 |
2004-12-21 |
California Institute Of Technology |
Methods for detecting and sorting polynucleotides based on size
|
US6124120A
(en)
|
1997-10-08 |
2000-09-26 |
Yale University |
Multiple displacement amplification
|
AR021833A1
(es)
|
1998-09-30 |
2002-08-07 |
Applied Research Systems |
Metodos de amplificacion y secuenciacion de acido nucleico
|
US6794140B1
(en)
|
1999-04-30 |
2004-09-21 |
Andrew Simon Goldsborough |
Isolation of nucleic acid
|
US6180349B1
(en)
|
1999-05-18 |
2001-01-30 |
The Regents Of The University Of California |
Quantitative PCR method to enumerate DNA copy number
|
US7058517B1
(en)
|
1999-06-25 |
2006-06-06 |
Genaissance Pharmaceuticals, Inc. |
Methods for obtaining and using haplotype data
|
US6964847B1
(en)
*
|
1999-07-14 |
2005-11-15 |
Packard Biosciences Company |
Derivative nucleic acids and uses thereof
|
GB9917307D0
(en)
|
1999-07-23 |
1999-09-22 |
Sec Dep Of The Home Department |
Improvements in and relating to analysis of DNA
|
ATE368125T1
(de)
|
1999-07-23 |
2007-08-15 |
Forensic Science Service Ltd |
Verfahren zur erkennung von einzel-nukleotid- polymorphismen
|
US6440706B1
(en)
|
1999-08-02 |
2002-08-27 |
Johns Hopkins University |
Digital amplification
|
US6251604B1
(en)
|
1999-08-13 |
2001-06-26 |
Genopsys, Inc. |
Random mutagenesis and amplification of nucleic acid
|
WO2001034844A1
(fr)
|
1999-11-10 |
2001-05-17 |
Ligochem, Inc. |
Methode permettant d'isoler un adn d'un milieu proteique et trousse utilisee pour realiser cette methode
|
US6221603B1
(en)
|
2000-02-04 |
2001-04-24 |
Molecular Dynamics, Inc. |
Rolling circle amplification assay for nucleic acid analysis
|
US7955794B2
(en)
|
2000-09-21 |
2011-06-07 |
Illumina, Inc. |
Multiplex nucleic acid reactions
|
AU2001238068A1
(en)
|
2000-02-07 |
2001-08-14 |
Illumina, Inc. |
Nucleic acid detection methods using universal priming
|
US7510834B2
(en)
|
2000-04-13 |
2009-03-31 |
Hidetoshi Inoko |
Gene mapping method using microsatellite genetic polymorphism markers
|
GB0009179D0
(en)
|
2000-04-13 |
2000-05-31 |
Imp College Innovations Ltd |
Non-invasive prenatal diagnosis
|
US6828098B2
(en)
|
2000-05-20 |
2004-12-07 |
The Regents Of The University Of Michigan |
Method of producing a DNA library using positional amplification based on the use of adaptors and nick translation
|
CA2409774A1
(fr)
|
2000-05-23 |
2001-11-29 |
Variagenics, Inc. |
Methodes d'analyse genetique d'adn servant a detecter des variances de sequence
|
US6605451B1
(en)
|
2000-06-06 |
2003-08-12 |
Xtrana, Inc. |
Methods and devices for multiplexing amplification reactions
|
US7087414B2
(en)
|
2000-06-06 |
2006-08-08 |
Applera Corporation |
Methods and devices for multiplexing amplification reactions
|
EP1356088A2
(fr)
|
2000-06-07 |
2003-10-29 |
Baylor College of Medicine |
Compositions et methodes d'hybridation d'acides nucleiques a partir de jeux d'echantillons
|
US7058616B1
(en)
|
2000-06-08 |
2006-06-06 |
Virco Bvba |
Method and system for predicting resistance of a disease to a therapeutic agent using a neural network
|
GB0016742D0
(en)
|
2000-07-10 |
2000-08-30 |
Simeg Limited |
Diagnostic method
|
AU2002246612B2
(en)
|
2000-10-24 |
2007-11-01 |
The Board Of Trustees Of The Leland Stanford Junior University |
Direct multiplex characterization of genomic DNA
|
US20020107640A1
(en)
|
2000-11-14 |
2002-08-08 |
Ideker Trey E. |
Methods for determining the true signal of an analyte
|
CA2428757A1
(fr)
|
2000-11-15 |
2002-07-18 |
Roche Diagnostics Corporation |
Methodes et reactifs permettant d'identifier des cellules embryonnaires rares dans le systeme circulatoire maternel
|
WO2002044411A1
(fr)
|
2000-12-01 |
2002-06-06 |
Rosetta Inpharmatics, Inc. |
Utilisation de profils dans la detection de l'aneuploidie
|
US7218764B2
(en)
|
2000-12-04 |
2007-05-15 |
Cytokinetics, Inc. |
Ploidy classification method
|
AR031640A1
(es)
|
2000-12-08 |
2003-09-24 |
Applied Research Systems |
Amplificacion isotermica de acidos nucleicos en un soporte solido
|
US20020182622A1
(en)
|
2001-02-01 |
2002-12-05 |
Yusuke Nakamura |
Method for SNP (single nucleotide polymorphism) typing
|
JP2002300894A
(ja)
|
2001-02-01 |
2002-10-15 |
Inst Of Physical & Chemical Res |
一塩基多型タイピング方法
|
US7101663B2
(en)
|
2001-03-02 |
2006-09-05 |
University of Pittsburgh—of the Commonwealth System of Higher Education |
PCR method
|
WO2002073504A1
(fr)
|
2001-03-14 |
2002-09-19 |
Gene Logic, Inc. |
Systeme et procede d'extraction et d'utilisation de donnees d'expression genique provenant de multiples sources
|
WO2002076377A2
(fr)
|
2001-03-23 |
2002-10-03 |
Yoshiyuki Kanai |
Mononucleosome et son procede de production, methode d'analyse d'un anticorps specifique a un nucleosome, methode de diagnostic d'une maladie auto-immune, procede de production d'un adn nucleosomique, plaque d'adn et procede de production d'une plaque d'adn
|
US6489135B1
(en)
|
2001-04-17 |
2002-12-03 |
Atairgintechnologies, Inc. |
Determination of biological characteristics of embryos fertilized in vitro by assaying for bioactive lipids in culture media
|
FR2824144B1
(fr)
|
2001-04-30 |
2004-09-17 |
Metagenex S A R L |
Methode de diagnostic prenatal sur cellule foetale isolee du sang maternel
|
WO2002087431A1
(fr)
|
2001-05-01 |
2002-11-07 |
Structural Bioinformatics, Inc. |
Diagnostic de maladies inapparentes a partir de tests cliniques ordinaires utilisant l'analyse bayesienne
|
WO2002090505A2
(fr)
|
2001-05-09 |
2002-11-14 |
Virginia Commonwealth University |
Structures multiples de sequençage et de ligature pour analyse genomique
|
US20040126760A1
(en)
|
2001-05-17 |
2004-07-01 |
Natalia Broude |
Novel compositions and methods for carrying out multple pcr reactions on a single sample
|
US7026121B1
(en)
|
2001-06-08 |
2006-04-11 |
Expression Diagnostics, Inc. |
Methods and compositions for diagnosing and monitoring transplant rejection
|
JP2004531271A
(ja)
|
2001-06-22 |
2004-10-14 |
ユニバーシティ オブ ジュネーブ |
染色体不均衡により引き起こされる疾患を検出する方法
|
US20030101000A1
(en)
|
2001-07-24 |
2003-05-29 |
Bader Joel S. |
Family based tests of association using pooled DNA and SNP markers
|
ATE502119T1
(de)
|
2001-07-25 |
2011-04-15 |
Oncomedx Inc |
Verfahren zur bewertung pathologischer krankheitszustände unter verwendung extrazellulärer rna
|
US7297778B2
(en)
|
2001-07-25 |
2007-11-20 |
Affymetrix, Inc. |
Complexity management of genomic DNA
|
US6958211B2
(en)
|
2001-08-08 |
2005-10-25 |
Tibotech Bvba |
Methods of assessing HIV integrase inhibitor therapy
|
CN1571634A
(zh)
|
2001-08-23 |
2005-01-26 |
免疫公司 |
用于分析的细胞和生物学标本的稳定
|
US6807491B2
(en)
|
2001-08-30 |
2004-10-19 |
Hewlett-Packard Development Company, L.P. |
Method and apparatus for combining gene predictions using bayesian networks
|
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
|
AUPR749901A0
(en)
|
2001-09-06 |
2001-09-27 |
Monash University |
Method of identifying chromosomal abnormalities and prenatal diagnosis
|
US7153656B2
(en)
|
2001-09-11 |
2006-12-26 |
Los Alamos National Security, Llc |
Nucleic acid sequence detection using multiplexed oligonucleotide PCR
|
US8986944B2
(en)
|
2001-10-11 |
2015-03-24 |
Aviva Biosciences Corporation |
Methods and compositions for separating rare cells from fluid samples
|
WO2003031646A1
(fr)
*
|
2001-10-12 |
2003-04-17 |
The University Of Queensland |
Selection et amplification de marqueurs genetiques multiples
|
US7297485B2
(en)
|
2001-10-15 |
2007-11-20 |
Qiagen Gmbh |
Method for nucleic acid amplification that results in low amplification bias
|
US6617137B2
(en)
|
2001-10-15 |
2003-09-09 |
Molecular Staging Inc. |
Method of amplifying whole genomes without subjecting the genome to denaturing conditions
|
US20030119004A1
(en)
|
2001-12-05 |
2003-06-26 |
Wenz H. Michael |
Methods for quantitating nucleic acids using coupled ligation and amplification
|
US20050214758A1
(en)
|
2001-12-11 |
2005-09-29 |
Netech Inc. |
Blood cell separating system
|
US7198897B2
(en)
|
2001-12-19 |
2007-04-03 |
Brandeis University |
Late-PCR
|
DE60123448T2
(de)
|
2001-12-24 |
2007-08-23 |
Prof. Wolfgang Holzgreve |
Verfahren zur nicht-invasiven Diagnose von Transplantationen und Transfusionen
|
US20040115629A1
(en)
|
2002-01-09 |
2004-06-17 |
Panzer Scott R |
Molecules for diagnostics and therapeutics
|
WO2003062441A1
(fr)
|
2002-01-18 |
2003-07-31 |
Genzyme Corporation |
Procedes de detection d'adn foetal et de quantification d'alleles
|
EP1483720A1
(fr)
|
2002-02-01 |
2004-12-08 |
Rosetta Inpharmactis LLC. |
Systemes et procedes informatiques concus pour identifier des genes et determiner des voies associees a des caracteres
|
MXPA04008477A
(es)
|
2002-03-01 |
2005-10-26 |
Ravgen Inc |
Metodos para deteccion de trastornos geneticos.
|
US6977162B2
(en)
|
2002-03-01 |
2005-12-20 |
Ravgen, Inc. |
Rapid analysis of variations in a genome
|
US20060229823A1
(en)
|
2002-03-28 |
2006-10-12 |
Affymetrix, Inc. |
Methods and computer software products for analyzing genotyping data
|
US20040096874A1
(en)
|
2002-04-11 |
2004-05-20 |
Third Wave Technologies, Inc. |
Characterization of CYP 2D6 genotypes
|
IL164687A0
(en)
|
2002-05-02 |
2005-12-18 |
Univ North Carolina |
Cellular libraries and methods for the preparationthereof
|
US20070178478A1
(en)
|
2002-05-08 |
2007-08-02 |
Dhallan Ravinder S |
Methods for detection of genetic disorders
|
US7442506B2
(en)
|
2002-05-08 |
2008-10-28 |
Ravgen, Inc. |
Methods for detection of genetic disorders
|
US7727720B2
(en)
|
2002-05-08 |
2010-06-01 |
Ravgen, Inc. |
Methods for detection of genetic disorders
|
US20040009518A1
(en)
|
2002-05-14 |
2004-01-15 |
The Chinese University Of Hong Kong |
Methods for evaluating a disease condition by nucleic acid detection and fractionation
|
US20040229231A1
(en)
|
2002-05-28 |
2004-11-18 |
Frudakis Tony N. |
Compositions and methods for inferring ancestry
|
WO2003102595A1
(fr)
|
2002-05-31 |
2003-12-11 |
Genetype Pty Ltd |
Anticorps maternels servant de marqueurs de cellules foetales permettant d'identifier et d'enrichir les cellules foetales du sang maternel
|
WO2003106623A2
(fr)
|
2002-06-13 |
2003-12-24 |
New York University |
Teste precoce prenatal non effractif pour detecter des aneuploidies et des etats pathologiques hereditaires
|
US7108976B2
(en)
|
2002-06-17 |
2006-09-19 |
Affymetrix, Inc. |
Complexity management of genomic DNA by locus specific amplification
|
US7097976B2
(en)
|
2002-06-17 |
2006-08-29 |
Affymetrix, Inc. |
Methods of analysis of allelic imbalance
|
US20050009069A1
(en)
|
2002-06-25 |
2005-01-13 |
Affymetrix, Inc. |
Computer software products for analyzing genotyping
|
CN100354298C
(zh)
|
2002-06-28 |
2007-12-12 |
兰华生物科技公司 |
使用单核苷酸多态性组分析受损样品的方法和组合物
|
EP1388812A1
(fr)
|
2002-07-04 |
2004-02-11 |
Ronald E. Dr. Kates |
Procédé d'entraínement pour un système capable d'appentissage
|
UA53537C2
(en)
|
2002-07-15 |
2005-01-17 |
Amtech Ltd Ukrainian German Jo |
Injection syringe
|
US7459273B2
(en)
|
2002-10-04 |
2008-12-02 |
Affymetrix, Inc. |
Methods for genotyping selected polymorphism
|
AU2003285861A1
(en)
|
2002-10-07 |
2004-05-04 |
University Of Medicine And Dentistry Of New Jersey |
High throughput multiplex dna sequence amplifications
|
CA2505472A1
(fr)
|
2002-11-11 |
2004-05-27 |
Affymetrix, Inc. |
Procedes pour identifier des changements du nombre de copies adn
|
EP2031070B1
(fr)
|
2002-12-04 |
2013-07-17 |
Life Technologies Corporation |
Amplification multiplexe de polynucléotides
|
SI1583904T1
(sl)
|
2003-01-02 |
2013-12-31 |
Wobben Properties Gmbh |
Rotorska lopata vetrne turbine z zmanjšano emisijo zvoka
|
ATE435925T1
(de)
|
2003-01-17 |
2009-07-15 |
Univ Boston |
Haplotypanalyse
|
WO2004065628A1
(fr)
|
2003-01-21 |
2004-08-05 |
Guoliang Fu |
Detection multiplex quantitative d'acides nucleiques
|
DE602004024034D1
(de)
|
2003-01-29 |
2009-12-24 |
454 Corp |
Nukleinsäureamplifikation auf basis von kügelchenemulsion
|
US7575865B2
(en)
|
2003-01-29 |
2009-08-18 |
454 Life Sciences Corporation |
Methods of amplifying and sequencing nucleic acids
|
AU2004217872B2
(en)
|
2003-03-05 |
2010-03-25 |
Genetic Technologies Limited |
Identification of fetal DNA and fetal cell markers in maternal plasma or serum
|
US20040209299A1
(en)
|
2003-03-07 |
2004-10-21 |
Rubicon Genomics, Inc. |
In vitro DNA immortalization and whole genome amplification using libraries generated from randomly fragmented DNA
|
US20040197832A1
(en)
|
2003-04-03 |
2004-10-07 |
Mor Research Applications Ltd. |
Non-invasive prenatal genetic diagnosis using transcervical cells
|
CN1496413A
(zh)
|
2003-05-09 |
2004-05-12 |
清华大学 |
用于多重pcr条件优化的方法和组分
|
BRPI0410656A
(pt)
|
2003-05-28 |
2006-07-18 |
Pioneer Hi Bred Int |
método de melhoramento de planta e planta obtida
|
US20040259100A1
(en)
|
2003-06-20 |
2004-12-23 |
Illumina, Inc. |
Methods and compositions for whole genome amplification and genotyping
|
DE602004019941D1
(de)
|
2003-07-31 |
2009-04-23 |
Sequenom Inc |
Verfahren für multiplex-polymerasekettenreaktionen auf hohem niveau und homogenen massenverlängerungsreaktionen zur genotypisierung von polymorphismen
|
US8346482B2
(en)
|
2003-08-22 |
2013-01-01 |
Fernandez Dennis S |
Integrated biosensor and simulation system for diagnosis and therapy
|
AU2003263660A1
(en)
|
2003-08-29 |
2005-03-16 |
Pantarhei Bioscience B.V. |
Prenatal diagnosis of down syndrome by detection of fetal rna markers in maternal blood
|
AU2004270220B2
(en)
|
2003-09-05 |
2009-03-05 |
The Chinese University Of Hong Kong |
Method for non-invasive prenatal diagnosis
|
US20050053950A1
(en)
|
2003-09-08 |
2005-03-10 |
Enrique Zudaire Ubani |
Protocol and software for multiplex real-time PCR quantification based on the different melting temperatures of amplicons
|
WO2005028645A1
(fr)
*
|
2003-09-24 |
2005-03-31 |
Kyushu Tlo Company, Limited |
Snp dans la region regulatrice 5' du gene mdr1
|
WO2005030999A1
(fr)
|
2003-09-25 |
2005-04-07 |
Dana-Farber Cancer Institute, Inc |
Procedes permettant de detecter des cellules specifiques d'un lignage
|
WO2005035725A2
(fr)
|
2003-10-08 |
2005-04-21 |
The Trustees Of Boston University |
Methodes de diagnostic prenatal d'anomalies chromosomiques
|
CA2482097C
(fr)
|
2003-10-13 |
2012-02-21 |
F. Hoffmann-La Roche Ag |
Methodes pour isoler des acides nucleiques
|
DE60328193D1
(de)
|
2003-10-16 |
2009-08-13 |
Sequenom Inc |
Nicht invasiver Nachweis fötaler genetischer Merkmale
|
US20050221341A1
(en)
|
2003-10-22 |
2005-10-06 |
Shimkets Richard A |
Sequence-based karyotyping
|
EP1678329A4
(fr)
|
2003-10-30 |
2008-07-02 |
Tufts New England Medical Ct |
Diagnostic prenatal a l'aide d'adn foetal acellulaire dans le liquide amniotique
|
US20050164252A1
(en)
|
2003-12-04 |
2005-07-28 |
Yeung Wah Hin A. |
Methods using non-genic sequences for the detection, modification and treatment of any disease or improvement of functions of a cell
|
WO2005071078A1
(fr)
|
2004-01-12 |
2005-08-04 |
Nimblegen Systems Inc. |
Procede de mise en oeuvre d'une amplification en chaine par polymerase dans un micro-reseau
|
US20100216151A1
(en)
|
2004-02-27 |
2010-08-26 |
Helicos Biosciences Corporation |
Methods for detecting fetal nucleic acids and diagnosing fetal abnormalities
|
US20060046258A1
(en)
|
2004-02-27 |
2006-03-02 |
Lapidus Stanley N |
Applications of single molecule sequencing
|
US20100216153A1
(en)
|
2004-02-27 |
2010-08-26 |
Helicos Biosciences Corporation |
Methods for detecting fetal nucleic acids and diagnosing fetal abnormalities
|
US7035740B2
(en)
|
2004-03-24 |
2006-04-25 |
Illumina, Inc. |
Artificial intelligence and global normalization methods for genotyping
|
JP4437050B2
(ja)
|
2004-03-26 |
2010-03-24 |
株式会社日立製作所 |
診断支援システム、診断支援方法および診断支援サービスの提供方法
|
US7805282B2
(en)
*
|
2004-03-30 |
2010-09-28 |
New York University |
Process, software arrangement and computer-accessible medium for obtaining information associated with a haplotype
|
US7858757B2
(en)
|
2004-03-31 |
2010-12-28 |
Adnagen Ag |
Monoclonal antibodies with specificity for fetal erythroid cells
|
US7414118B1
(en)
|
2004-04-14 |
2008-08-19 |
Applied Biosystems Inc. |
Modified oligonucleotides and applications thereof
|
US7468249B2
(en)
|
2004-05-05 |
2008-12-23 |
Biocept, Inc. |
Detection of chromosomal disorders
|
US7709194B2
(en)
|
2004-06-04 |
2010-05-04 |
The Chinese University Of Hong Kong |
Marker for prenatal diagnosis and monitoring
|
KR20070034588A
(ko)
|
2004-06-14 |
2007-03-28 |
더 보오드 오브 트러스티스 오브 더 유니버시티 오브 일리노이즈 |
Cd34+/cd36+ 태아 세포에는 결합하지만 성체세포에는 결합하지 않는 항체
|
EP1786924A4
(fr)
|
2004-07-06 |
2008-10-01 |
Genera Biosystems Pty Ltd |
Procede de detection de l'aneuploidie
|
DE102004036285A1
(de)
|
2004-07-27 |
2006-02-16 |
Advalytix Ag |
Verfahren zum Bestimmen der Häufigkeit von Sequenzen einer Probe
|
JP5249581B2
(ja)
|
2004-08-09 |
2013-07-31 |
ジェネレイション バイオテック リミテッド ライアビリティ カンパニー |
核酸の単離および増幅方法
|
JP2008511058A
(ja)
|
2004-08-18 |
2008-04-10 |
アボツト・モレキユラー・インコーポレイテツド |
コンピュータシステムを用いるデータ品質および/または部分異数染色体の決定
|
US7634808B1
(en)
|
2004-08-20 |
2009-12-15 |
Symantec Corporation |
Method and apparatus to block fast-spreading computer worms that use DNS MX record queries
|
JP4810164B2
(ja)
|
2004-09-03 |
2011-11-09 |
富士フイルム株式会社 |
核酸分離精製方法
|
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
|
US20060088574A1
(en)
|
2004-10-25 |
2006-04-27 |
Manning Paul B |
Nutritional supplements
|
US20060134662A1
(en)
|
2004-10-25 |
2006-06-22 |
Pratt Mark R |
Method and system for genotyping samples in a normalized allelic space
|
US20060141499A1
(en)
|
2004-11-17 |
2006-06-29 |
Geoffrey Sher |
Methods of determining human egg competency
|
WO2006058236A2
(fr)
|
2004-11-24 |
2006-06-01 |
Neuromolecular Pharmaceuticals, Inc. |
Composition et methode pour traiter des affections neurologiques
|
US20070042384A1
(en)
|
2004-12-01 |
2007-02-22 |
Weiwei Li |
Method for isolating and modifying DNA from blood and body fluids
|
WO2006091979A2
(fr)
|
2005-02-25 |
2006-08-31 |
The Regents Of The University Of California |
Analyse complete de chromomes a cellule unique par caryotype
|
US7618777B2
(en)
|
2005-03-16 |
2009-11-17 |
Agilent Technologies, Inc. |
Composition and method for array hybridization
|
EP1859051A4
(fr)
|
2005-03-18 |
2009-08-05 |
Univ Hong Kong Chinese |
Marqueurs pour diagnostic et surveillance prénataux
|
AU2006224971B2
(en)
|
2005-03-18 |
2009-07-02 |
Boston University |
A method for the detection of chromosomal aneuploidies
|
US20060228721A1
(en)
|
2005-04-12 |
2006-10-12 |
Leamon John H |
Methods for determining sequence variants using ultra-deep sequencing
|
ES2404311T3
(es)
|
2005-04-12 |
2013-05-27 |
454 Life Sciences Corporation |
Métodos para determinar variantes de secuencias usando secuenciación ultraprofunda
|
EP1888786A4
(fr)
|
2005-05-27 |
2009-12-30 |
Wayne John Cancer Inst |
Utilisation d'adn en circulation libre pour le diagnostic, le pronostic et le traitement du cancer
|
AU2006341607B2
(en)
|
2005-05-31 |
2011-03-17 |
Applied Biosystems, Llc. |
Multiplexed amplification of short nucleic acids
|
WO2007145612A1
(fr)
|
2005-06-06 |
2007-12-21 |
454 Life Sciences Corporation |
Séquençage d'extrémités appariées
|
DK1907571T3
(en)
|
2005-06-15 |
2017-08-21 |
Complete Genomics Inc |
NUCLEIC ACID ANALYSIS USING INCIDENTAL MIXTURES OF NON-OVERLAPPING FRAGMENTS
|
EP2308990B1
(fr)
|
2005-07-15 |
2012-09-26 |
Life Technologies Corporation |
Analyse d'ARN messager et de micro-ARN dans le même mélange réactionnel
|
US20070020640A1
(en)
|
2005-07-21 |
2007-01-25 |
Mccloskey Megan L |
Molecular encoding of nucleic acid templates for PCR and other forms of sequence analysis
|
RU2290078C1
(ru)
|
2005-07-25 |
2006-12-27 |
Евгений Владимирович Новичков |
Способ прогнозирования рецидива серозного рака яичников
|
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
|
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
|
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
|
US8515679B2
(en)
|
2005-12-06 |
2013-08-20 |
Natera, Inc. |
System and method for cleaning noisy genetic data and determining chromosome copy number
|
US10081839B2
(en)
|
2005-07-29 |
2018-09-25 |
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
|
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
|
US10083273B2
(en)
|
2005-07-29 |
2018-09-25 |
Natera, Inc. |
System and method for cleaning noisy genetic data and determining chromosome copy number
|
EP1924704B1
(fr)
|
2005-08-02 |
2011-05-25 |
Rubicon Genomics, Inc. |
Compositions et méthodes de traitement et d'amplification d'adn consistant à utiliser plusieurs enzymes dans une seule réaction
|
WO2007030680A2
(fr)
|
2005-09-07 |
2007-03-15 |
Rigel Pharmaceuticals, Inc. |
Derives de triazole utiles comme inhibiteurs d'axl
|
GB0522310D0
(en)
|
2005-11-01 |
2005-12-07 |
Solexa Ltd |
Methods of preparing libraries of template polynucleotides
|
GB0523276D0
(en)
|
2005-11-15 |
2005-12-21 |
London Bridge Fertility |
Chromosomal analysis by molecular karyotyping
|
EP3599609A1
(fr)
|
2005-11-26 |
2020-01-29 |
Natera, Inc. |
Système et procédé pour nettoyer des données génétiques bruyantes et au moyen de données pour faire des prédictions
|
US20070172853A1
(en)
|
2005-12-02 |
2007-07-26 |
The General Hospital Corporation |
Use of deletion polymorphisms to predict, prevent, and manage histoincompatibility
|
WO2007070482A2
(fr)
|
2005-12-14 |
2007-06-21 |
Xueliang Xia |
Procede de detection d'anormalites chromosomiques a l'aide de microreseaux pour le diagnostic genetique preimplantatoire
|
JP5198284B2
(ja)
|
2005-12-22 |
2013-05-15 |
キージーン ナムローゼ フェンノートシャップ |
高処理量配列決定技術を使用する転写産物の特徴づけのための改良された戦略
|
EP3591068A1
(fr)
|
2006-02-02 |
2020-01-08 |
The Board of Trustees of the Leland Stanford Junior University |
Dépistage génétique non invasif du f tus par analyse numérique
|
WO2007092538A2
(fr)
|
2006-02-07 |
2007-08-16 |
President And Fellows Of Harvard College |
Procédés de confection de sondes nucléotidiques pour séquençage et synthèse
|
WO2007091064A1
(fr)
|
2006-02-08 |
2007-08-16 |
Solexa Limited |
Modification terminale pour empêcher la surreprésentation de fragments
|
AU2007220991C1
(en)
|
2006-02-28 |
2013-08-15 |
University Of Louisville Research Foundation |
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
|
EP2007904A4
(fr)
|
2006-03-13 |
2009-06-10 |
Veridex Llc |
Propagation de cellules primaires
|
WO2007112418A2
(fr)
|
2006-03-28 |
2007-10-04 |
Baylor College Of Medicine |
Criblage du syndrome de down
|
JP2009072062A
(ja)
|
2006-04-07 |
2009-04-09 |
Institute Of Physical & Chemical Research |
核酸の5’末端を単離するための方法およびその適用
|
US20070243549A1
(en)
|
2006-04-12 |
2007-10-18 |
Biocept, Inc. |
Enrichment of circulating fetal dna
|
US7702468B2
(en)
|
2006-05-03 |
2010-04-20 |
Population Diagnostics, Inc. |
Evaluating genetic disorders
|
US7901884B2
(en)
|
2006-05-03 |
2011-03-08 |
The Chinese University Of Hong Kong |
Markers for prenatal diagnosis and monitoring
|
US8679741B2
(en)
|
2006-05-31 |
2014-03-25 |
Sequenom, Inc. |
Methods and compositions for the extraction and amplification of nucleic acid from a sample
|
US7981609B2
(en)
|
2006-06-09 |
2011-07-19 |
The Brigham And Women's Hospital, Inc. |
Methods for identifying and using SNP panels
|
US8137912B2
(en)
|
2006-06-14 |
2012-03-20 |
The General Hospital Corporation |
Methods for the diagnosis of fetal abnormalities
|
CA2655272C
(fr)
|
2006-06-14 |
2017-04-18 |
Living Microsystems, Inc. |
Analyse de cellules rares avec recours au fractionnement d'echantillons et a des marqueurs d'adn
|
WO2009035447A1
(fr)
|
2006-06-14 |
2009-03-19 |
Living Microsystems, Inc. |
Diagnostic d'anomalies fœtales par une analyse par hybridation génomique comparative
|
US8372584B2
(en)
|
2006-06-14 |
2013-02-12 |
The General Hospital Corporation |
Rare cell analysis using sample splitting and DNA tags
|
WO2007147074A2
(fr)
|
2006-06-14 |
2007-12-21 |
Living Microsystems, Inc. |
Utilisation de génotypage snp fortement parallèle pour diagnostic fœtal
|
WO2008111990A1
(fr)
|
2006-06-14 |
2008-09-18 |
Cellpoint Diagnostics, Inc. |
Analyse de cellules rares par division d'échantillon et utilisation de marqueurs d'adn
|
US20080050739A1
(en)
|
2006-06-14 |
2008-02-28 |
Roland Stoughton |
Diagnosis of fetal abnormalities using polymorphisms including short tandem repeats
|
DK2029778T3
(en)
|
2006-06-14 |
2018-08-20 |
Verinata Health Inc |
DIAGNOSIS OF Fetal ABNORMITIES
|
EP3406736B1
(fr)
|
2006-06-14 |
2022-09-07 |
Verinata Health, Inc. |
Procédés pour le diagnostic d'anomalies fétales
|
EP2035540A2
(fr)
|
2006-06-15 |
2009-03-18 |
Stratagene |
Système d'isolation de biomolécules d'un échantillon
|
WO2007147063A2
(fr)
|
2006-06-16 |
2007-12-21 |
Sequenom, Inc. |
Procédés et compositions destinés à l'amplification, la détection et la quantification d'acide nucléique issu d'un échantillon
|
WO2008019315A2
(fr)
|
2006-08-04 |
2008-02-14 |
Ikonisys, Inc. |
Test diagnostique génétique amélioré d'une pré-implantation
|
CA2661640A1
(fr)
|
2006-08-24 |
2008-02-28 |
University Of Massachusetts Medical School |
Cartographie d'interactions genomiques
|
AU2007353877B2
(en)
|
2006-09-14 |
2012-07-19 |
Ibis Biosciences, Inc. |
Targeted whole genome amplification method for identification of pathogens
|
US20080085836A1
(en)
|
2006-09-22 |
2008-04-10 |
Kearns William G |
Method for genetic testing of human embryos for chromosome abnormalities, segregating genetic disorders with or without a known mutation and mitochondrial disorders following in vitro fertilization (IVF), embryo culture and embryo biopsy
|
EP2094838A1
(fr)
|
2006-10-16 |
2009-09-02 |
Cellula, Inc. |
Procédés et compositions pour le développement différentiel de cellules foetales dans le sang maternel et leur utilisation
|
WO2008051928A2
(fr)
|
2006-10-23 |
2008-05-02 |
The Salk Institute For Biological Studies |
Amplification ciblée d'un génome entier d'acides nucléiques
|
KR100825367B1
(ko)
|
2006-11-07 |
2008-04-28 |
전남대학교산학협력단 |
표지자로서 미토콘드리아 유전자 과변이부위를 이용하는조혈모세포이식 후 생착능 평가방법 및 키트
|
WO2008069906A2
(fr)
|
2006-11-14 |
2008-06-12 |
The Regents Of The University Of California |
Expression numérisée de l'analyse génétique
|
WO2008059578A1
(fr)
|
2006-11-16 |
2008-05-22 |
Olympus Corporation |
Procédé d'amplification pcr multiplex
|
WO2008061213A2
(fr)
|
2006-11-16 |
2008-05-22 |
Genentech, Inc. |
Variations génétiques associées à des tumeurs
|
WO2008079374A2
(fr)
|
2006-12-21 |
2008-07-03 |
Wang Eric T |
Procédés et compositions pour sélectionner et utiliser des polymorphismes d'un nucléotide simple
|
WO2008081451A2
(fr)
|
2007-01-03 |
2008-07-10 |
Monaliza Medical Ltd. |
Méthode et trousse d'analyse du matériel génétique d'un foetus
|
US8642295B2
(en)
|
2007-01-11 |
2014-02-04 |
Erasmus University Medical Center |
Circular chromosome conformation capture (4C)
|
US20100129792A1
(en)
|
2007-02-06 |
2010-05-27 |
Gerassimos Makrigiorgos |
Direct monitoring and pcr amplification of the dosage and dosage difference between target genetic regions
|
WO2008098142A2
(fr)
|
2007-02-08 |
2008-08-14 |
Sequenom, Inc. |
Tests a base d'acide nucléique destinés au typage rhd, à la détermination du sexe et la quantification d'acide nucléique
|
CN101790731B
(zh)
|
2007-03-16 |
2013-11-06 |
纳特拉公司 |
用于清除遗传数据干扰并确定染色体拷贝数的系统和方法
|
EP2121984A2
(fr)
|
2007-03-16 |
2009-11-25 |
454 Life Sciences Corporation |
Système et procédé pour détecter des variants qui résistent à un médicament contre le vih
|
WO2008118988A1
(fr)
|
2007-03-26 |
2008-10-02 |
Sequenom, Inc. |
Détection de séquence polymorphe amplifiée par endonucléase de restriction
|
JP5262230B2
(ja)
|
2007-03-28 |
2013-08-14 |
独立行政法人理化学研究所 |
新規多型検出法
|
ITTO20070307A1
(it)
|
2007-05-04 |
2008-11-05 |
Silicon Biosystems Spa |
Metodo e dispositivo per la diagnosi prenatale non-invasiva
|
US20100248231A1
(en)
|
2007-05-31 |
2010-09-30 |
The Regents Of The University Of California |
High specificity and high sensitivity detection based on steric hindrance & enzyme-related signal amplification
|
WO2008157264A2
(fr)
|
2007-06-15 |
2008-12-24 |
Sequenom, Inc. |
Procédés combinés pour la détection de l'aneuploïdie chromosomique
|
US20090023190A1
(en)
|
2007-06-20 |
2009-01-22 |
Kai Qin Lao |
Sequence amplification with loopable primers
|
US8460874B2
(en)
|
2007-07-03 |
2013-06-11 |
Genaphora Ltd. |
Use of RNA/DNA chimeric primers for improved nucleic acid amplification reactions
|
WO2009009769A2
(fr)
|
2007-07-11 |
2009-01-15 |
Artemis Health, Inc. |
Diagnostic d'anomalies fœtales au moyen d'hématies nucléées
|
US20100112590A1
(en)
|
2007-07-23 |
2010-05-06 |
The Chinese University Of Hong Kong |
Diagnosing Fetal Chromosomal Aneuploidy Using Genomic Sequencing With Enrichment
|
US20090029377A1
(en)
|
2007-07-23 |
2009-01-29 |
The Chinese University Of Hong Kong |
Diagnosing fetal chromosomal aneuploidy using massively parallel genomic sequencing
|
KR101376359B1
(ko)
|
2007-08-01 |
2014-03-27 |
다나-파버 캔서 인스티튜트 인크. |
표적 서열 강화
|
US8568994B2
(en)
|
2007-08-03 |
2013-10-29 |
Dkfz Deutsches Krebsforschungszentrum, Stiftung Des Offentlichen Rechts |
Method for prenatal diagnosis
|
US20090053719A1
(en)
|
2007-08-03 |
2009-02-26 |
The Chinese University Of Hong Kong |
Analysis of nucleic acids by digital pcr
|
ATE549419T1
(de)
|
2007-08-29 |
2012-03-15 |
Sequenom Inc |
Verfahren und zusammensetzungen für die universelle grössenspezifische polymerasekettenreaktion
|
WO2009032779A2
(fr)
|
2007-08-29 |
2009-03-12 |
Sequenom, Inc. |
Procédés et compositions utilisés dans la séparation, en fonction de sa taille, de l'acide nucléique d'un échantillon
|
US8748100B2
(en)
|
2007-08-30 |
2014-06-10 |
The Chinese University Of Hong Kong |
Methods and kits for selectively amplifying, detecting or quantifying target DNA with specific end sequences
|
JP5707132B2
(ja)
|
2007-09-07 |
2015-04-22 |
フルイダイム コーポレイション |
コピー数変動の決定、方法およびシステム
|
US20090081678A1
(en)
|
2007-09-21 |
2009-03-26 |
Streck, Inc. |
Nucleic acid isolation in preserved whole blood
|
EP2201143B2
(fr)
|
2007-09-21 |
2016-08-24 |
Katholieke Universiteit Leuven |
Outils et procédés pour tests génétiques ayant recours à un séquençage de dernière génération
|
US20100086914A1
(en)
|
2008-10-03 |
2010-04-08 |
Roche Molecular Systems, Inc. |
High resolution, high throughput hla genotyping by clonal sequencing
|
WO2009049889A1
(fr)
|
2007-10-16 |
2009-04-23 |
Roche Diagnostics Gmbh |
Génotypage hla à haute résolution et haut débit par séquençage clonal
|
WO2009064897A2
(fr)
|
2007-11-14 |
2009-05-22 |
Chronix Biomedical |
Détection de variations de séquences d'acides nucléiques dans l'acide nucléique circulant dans l'encéphalopathie spongiforme bovine
|
JP5726529B2
(ja)
|
2007-11-30 |
2015-06-03 |
ジーイー・ヘルスケア・バイオサイエンス・コーポレイション |
単一試料からのゲノムdna、rnaおよびタンパク質の単離方法
|
FR2925480B1
(fr)
|
2007-12-21 |
2011-07-01 |
Gervais Danone Sa |
Procede d'enrichissement d'une eau en oxygene par voie electrolytique, eau ou boisson enrichie en oxygene et utilisations
|
EP2077337A1
(fr)
|
2007-12-26 |
2009-07-08 |
Eppendorf Array Technologies SA |
Composition d'amplification et de détection, procédé et kit
|
WO2009092035A2
(fr)
|
2008-01-17 |
2009-07-23 |
Sequenom, Inc. |
Procédés et compositions pour l'analyse de molécules biologiques
|
EP2245191A1
(fr)
|
2008-01-17 |
2010-11-03 |
Sequenom, Inc. |
Procédés et compositions d'analyse de séquence d'acide nucléique à simple molécule
|
EP4219762A1
(fr)
|
2008-02-01 |
2023-08-02 |
The General Hospital Corporation |
Utilisation de microvésicules dans le diagnostic et le pronostic de maladies et d'états médicaux
|
WO2009099602A1
(fr)
|
2008-02-04 |
2009-08-13 |
Massachusetts Institute Of Technology |
Sélection d'acides nucléiques par hybridation en solution en amorces oligonucléotidiques
|
US20110033862A1
(en)
|
2008-02-19 |
2011-02-10 |
Gene Security Network, Inc. |
Methods for cell genotyping
|
US20090221620A1
(en)
|
2008-02-20 |
2009-09-03 |
Celera Corporation |
Gentic polymorphisms associated with stroke, methods of detection and uses thereof
|
AU2009223671B2
(en)
|
2008-03-11 |
2014-11-27 |
Sequenom, Inc. |
Nucleic acid-based tests for prenatal gender determination
|
US20090307179A1
(en)
|
2008-03-19 |
2009-12-10 |
Brandon Colby |
Genetic analysis
|
AU2009228312B2
(en)
|
2008-03-26 |
2015-05-21 |
Sequenom, Inc. |
Restriction endonuclease enhanced polymorphic sequence detection
|
EP2274446B1
(fr)
|
2008-03-31 |
2015-09-09 |
Pacific Biosciences of California, Inc. |
Systèmes et procédés d'enzyme polymérase à deux étapes lentes
|
JP5811483B2
(ja)
|
2008-04-03 |
2015-11-11 |
シービー バイオテクノロジーズ インコーポレイテッド |
多数の標的の増幅のためのアンプリコンレスキューマルチプレックスポリメラーゼ連鎖反応
|
US20110092763A1
(en)
|
2008-05-27 |
2011-04-21 |
Gene Security Network, Inc. |
Methods for Embryo Characterization and Comparison
|
EP2128169A1
(fr)
|
2008-05-30 |
2009-12-02 |
Qiagen GmbH |
Procédé d'isolation d'acides nucléiques à chaînes courtes
|
US20100041048A1
(en)
|
2008-07-31 |
2010-02-18 |
The Johns Hopkins University |
Circulating Mutant DNA to Assess Tumor Dynamics
|
CA2731991C
(fr)
|
2008-08-04 |
2021-06-08 |
Gene Security Network, Inc. |
Procedes pour une classification d'allele et une classification de ploidie
|
WO2010027870A2
(fr)
|
2008-08-26 |
2010-03-11 |
Fluidigm Corporation |
Procédés de dosage pour un débit amélioré d'échantillons et/ou de cibles
|
DE102008045705A1
(de)
|
2008-09-04 |
2010-04-22 |
Macherey, Nagel Gmbh & Co. Kg Handelsgesellschaft |
Verfahren zur Gewinnung von kurzer RNA sowie Kit hierfür
|
US8586310B2
(en)
|
2008-09-05 |
2013-11-19 |
Washington University |
Method for multiplexed nucleic acid patch polymerase chain reaction
|
EP3103871B1
(fr)
|
2008-09-16 |
2020-07-29 |
Sequenom, Inc. |
Procédés pour l'enrichissiment en acide nucleic fétal d'un échantillon maternel, basé sur la méthylation et utilisation pour la quantification de l'acide nucleique fétal
|
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
|
US20110172405A1
(en)
|
2008-09-17 |
2011-07-14 |
Ge Healthcare Bio-Sciences Corp. |
Method for small rna isolation
|
CA3069081C
(fr)
|
2008-09-20 |
2023-05-23 |
The Board Of Trustees Of The Leland Stanford Junior University |
Diagnostic non effractif d'aneuploidie foetale par sequencage
|
US9156010B2
(en)
|
2008-09-23 |
2015-10-13 |
Bio-Rad Laboratories, Inc. |
Droplet-based assay system
|
US20110301221A1
(en)
|
2008-10-10 |
2011-12-08 |
Swedish Health Services |
Diagnosis, prognosis and treatment of glioblastoma multiforme
|
WO2010045617A2
(fr)
|
2008-10-17 |
2010-04-22 |
University Of Louisville Research Foundation |
Détection d'anomalies génétiques
|
US9506119B2
(en)
|
2008-11-07 |
2016-11-29 |
Adaptive Biotechnologies Corp. |
Method of sequence determination using sequence tags
|
US8748103B2
(en)
|
2008-11-07 |
2014-06-10 |
Sequenta, Inc. |
Monitoring health and disease status using clonotype profiles
|
EP2719774B8
(fr)
|
2008-11-07 |
2020-04-22 |
Adaptive Biotechnologies Corporation |
Procédés de surveillance de maladies par l'analyse de séquence
|
SG10201501804WA
(en)
|
2008-12-22 |
2015-05-28 |
Celula Inc |
Methods and genotyping panels for detecting alleles, genomes, and transcriptomes
|
US11634747B2
(en)
|
2009-01-21 |
2023-04-25 |
Streck Llc |
Preservation of fetal nucleic acids in maternal plasma
|
WO2010088288A2
(fr)
|
2009-01-28 |
2010-08-05 |
Fluidigm Corporation |
Détermination de différences du nombre de copies par amplification
|
NO2398912T3
(fr)
|
2009-02-18 |
2018-02-10 |
|
|
EP3249053A1
(fr)
|
2009-03-27 |
2017-11-29 |
Life Technologies Corporation |
Procédés, compositions et kits de détection de variants alléliques
|
US20100285537A1
(en)
|
2009-04-02 |
2010-11-11 |
Fluidigm Corporation |
Selective tagging of short nucleic acid fragments and selective protection of target sequences from degradation
|
US8691509B2
(en)
|
2009-04-02 |
2014-04-08 |
Fluidigm Corporation |
Multi-primer amplification method for barcoding of target nucleic acids
|
EP3211095B1
(fr)
|
2009-04-03 |
2019-01-02 |
Sequenom, Inc. |
Compositions et procédés de préparation d'acides nucléiques
|
US20120164638A1
(en)
|
2009-04-06 |
2012-06-28 |
Case Western Reserve University |
Digital Quantification of DNA Methylation
|
US9085798B2
(en)
|
2009-04-30 |
2015-07-21 |
Prognosys Biosciences, Inc. |
Nucleic acid constructs and methods of use
|
US8481699B2
(en)
|
2009-07-14 |
2013-07-09 |
Academia Sinica |
Multiplex barcoded Paired-End ditag (mbPED) library construction for ultra high throughput sequencing
|
US20130196862A1
(en)
|
2009-07-17 |
2013-08-01 |
Natera, Inc. |
Informatics Enhanced Analysis of Fetal Samples Subject to Maternal Contamination
|
US8563242B2
(en)
|
2009-08-11 |
2013-10-22 |
The Chinese University Of Hong Kong |
Method for detecting chromosomal aneuploidy
|
CN101643904B
(zh)
|
2009-08-27 |
2011-04-27 |
北京北方微电子基地设备工艺研究中心有限责任公司 |
深硅刻蚀装置和深硅刻蚀设备的进气系统
|
WO2011032078A1
(fr)
|
2009-09-11 |
2011-03-17 |
Health Reseach Inc. |
Détection de souches x4 du vih-1 par test de suivi des hétéroduplexes
|
JP5926183B2
(ja)
|
2009-09-22 |
2016-05-25 |
エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft |
疾患関連kirハプロタイプの決定
|
WO2011037692A1
(fr)
|
2009-09-24 |
2011-03-31 |
Qiagen Gaithersburg Inc. |
Compositions, procédés, et kit d'isolement et d'analyse d'acides nucléiques en utilisant un matériau échangeur d'anions
|
ES2640776T3
(es)
|
2009-09-30 |
2017-11-06 |
Natera, Inc. |
Métodos para denominar de forma no invasiva ploidía prenatal
|
EP2494065B1
(fr)
|
2009-10-26 |
2015-12-23 |
Lifecodexx AG |
Moyens et procédés destinés au diagnostic non invasif d'une aneuploïdie chromosomale
|
FI3783110T3
(fi)
|
2009-11-05 |
2023-03-02 |
|
Fetaalisen genomin analyysi maternaalisesta biologisesta näytteestä
|
PT2496720T
(pt)
|
2009-11-06 |
2020-10-12 |
Univ Leland Stanford Junior |
Diagnóstico não-invasivo de rejeição de enxertos em pacientes sujeitos a transplantes de órgãos
|
EP2504448B1
(fr)
|
2009-11-25 |
2016-10-19 |
Bio-Rad Laboratories, Inc. |
Procédés et compositions destinés à détecter un matériel génétique
|
CN102802412A
(zh)
|
2009-12-08 |
2012-11-28 |
海玛奎斯特医药公司 |
用于治疗红细胞病症的方法及低剂量方案
|
US8835358B2
(en)
|
2009-12-15 |
2014-09-16 |
Cellular Research, Inc. |
Digital counting of individual molecules by stochastic attachment of diverse labels
|
US9315857B2
(en)
|
2009-12-15 |
2016-04-19 |
Cellular Research, Inc. |
Digital counting of individual molecules by stochastic attachment of diverse label-tags
|
US8574842B2
(en)
|
2009-12-22 |
2013-11-05 |
The Board Of Trustees Of The Leland Stanford Junior University |
Direct molecular diagnosis of fetal aneuploidy
|
EP3660165B1
(fr)
|
2009-12-22 |
2023-01-04 |
Sequenom, Inc. |
Procédés et kits pour identifier une aneuploïdie
|
US20130022973A1
(en)
|
2010-01-15 |
2013-01-24 |
Hansen Carl L G |
Multiplex Amplification for the Detection of Nucleic Acid Variations
|
US20120270739A1
(en)
|
2010-01-19 |
2012-10-25 |
Verinata Health, Inc. |
Method for sample analysis of aneuploidies in maternal samples
|
US10388403B2
(en)
|
2010-01-19 |
2019-08-20 |
Verinata Health, Inc. |
Analyzing copy number variation in the detection of cancer
|
US9323888B2
(en)
|
2010-01-19 |
2016-04-26 |
Verinata Health, Inc. |
Detecting and classifying copy number variation
|
ES2534758T3
(es)
|
2010-01-19 |
2015-04-28 |
Verinata Health, Inc. |
Métodos de secuenciación en diagnósticos prenatales
|
WO2011090556A1
(fr)
|
2010-01-19 |
2011-07-28 |
Verinata Health, Inc. |
Procédés pour déterminer une fraction d'acide nucléique fœtal dans des échantillons maternels
|
US20110312503A1
(en)
|
2010-01-23 |
2011-12-22 |
Artemis Health, Inc. |
Methods of fetal abnormality detection
|
EP2534263B1
(fr)
|
2010-02-09 |
2020-08-05 |
Unitaq Bio |
Procédés et compositions pour la détection universelle d'acides nucléiques
|
DK2539472T3
(da)
|
2010-02-26 |
2015-08-24 |
Hennessy Lori |
Hurtig pcr til str genotypebestemmelse
|
CA2791905A1
(fr)
|
2010-03-01 |
2011-09-09 |
Caris Life Sciences Luxembourg Holdings, S.A.R.L. |
Biomarqueurs pour theranostique
|
WO2011140433A2
(fr)
|
2010-05-07 |
2011-11-10 |
The Board Of Trustees Of The Leland Stanford Junior University |
Mesure et comparaison de diversité immunitaire par séquençage à haut débit
|
US11339429B2
(en)
|
2010-05-18 |
2022-05-24 |
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
|
US11326208B2
(en)
|
2010-05-18 |
2022-05-10 |
Natera, Inc. |
Methods for nested PCR amplification of cell-free DNA
|
US10316362B2
(en)
|
2010-05-18 |
2019-06-11 |
Natera, Inc. |
Methods for simultaneous amplification of target loci
|
US20190323076A1
(en)
|
2010-05-18 |
2019-10-24 |
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
|
US11408031B2
(en)
|
2010-05-18 |
2022-08-09 |
Natera, Inc. |
Methods for non-invasive prenatal paternity testing
|
AU2011255641A1
(en)
|
2010-05-18 |
2012-12-06 |
Natera, Inc. |
Methods for non-invasive prenatal ploidy calling
|
US20130123120A1
(en)
|
2010-05-18 |
2013-05-16 |
Natera, Inc. |
Highly Multiplex PCR Methods and Compositions
|
WO2013052557A2
(fr)
|
2011-10-03 |
2013-04-11 |
Natera, Inc. |
Procédés pour diagnostic génétique préimplantatoire par séquençage
|
US20140206552A1
(en)
|
2010-05-18 |
2014-07-24 |
Natera, Inc. |
Methods for preimplantation genetic diagnosis by sequencing
|
US20190284623A1
(en)
|
2010-05-18 |
2019-09-19 |
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
|
US20190309358A1
(en)
|
2010-05-18 |
2019-10-10 |
Natera, Inc. |
Methods for non-invasive prenatal ploidy calling
|
US11322224B2
(en)
|
2010-05-18 |
2022-05-03 |
Natera, Inc. |
Methods for non-invasive prenatal ploidy calling
|
US20190010543A1
(en)
|
2010-05-18 |
2019-01-10 |
Natera, Inc. |
Methods for simultaneous amplification of target loci
|
US20110301854A1
(en)
|
2010-06-08 |
2011-12-08 |
Curry Bo U |
Method of Determining Allele-Specific Copy Number of a SNP
|
US20120034603A1
(en)
|
2010-08-06 |
2012-02-09 |
Tandem Diagnostics, Inc. |
Ligation-based detection of genetic variants
|
US8700338B2
(en)
|
2011-01-25 |
2014-04-15 |
Ariosa Diagnosis, Inc. |
Risk calculation for evaluation of fetal aneuploidy
|
US20120190557A1
(en)
|
2011-01-25 |
2012-07-26 |
Aria Diagnostics, Inc. |
Risk calculation for evaluation of fetal aneuploidy
|
US20130040375A1
(en)
|
2011-08-08 |
2013-02-14 |
Tandem Diagnotics, Inc. |
Assay systems for genetic analysis
|
EP2426217A1
(fr)
|
2010-09-03 |
2012-03-07 |
Centre National de la Recherche Scientifique (CNRS) |
Procédés analytiques pour acides nucléiques libres dans les cellules et applications
|
WO2012042374A2
(fr)
|
2010-10-01 |
2012-04-05 |
Anssi Jussi Nikolai Taipale |
Procédé de détermination du nombre ou de la concentration de molécules
|
CN103534591B
(zh)
|
2010-10-26 |
2016-04-06 |
利兰·斯坦福青年大学托管委员会 |
通过测序分析进行的非侵入性胎儿遗传筛选
|
US9284602B2
(en)
|
2010-10-27 |
2016-03-15 |
President And Fellows Of Harvard College |
Compositions of toehold primer duplexes and methods of use
|
CN105243295B
(zh)
|
2010-11-30 |
2018-08-17 |
香港中文大学 |
与癌症相关的遗传或分子畸变的检测
|
WO2012078792A2
(fr)
|
2010-12-07 |
2012-06-14 |
Stanford University |
Détermination non invasive de l'héritage foetal des haplotypes parentaux à l'échelle du génome
|
WO2012083250A2
(fr)
|
2010-12-17 |
2012-06-21 |
Celula, Inc. |
Méthodes d'analyse et de diagnostic d'états génétiques
|
ES2770342T3
(es)
|
2010-12-22 |
2020-07-01 |
Natera Inc |
Procedimientos para pruebas prenatales no invasivas de paternidad
|
KR20230141927A
(ko)
|
2010-12-30 |
2023-10-10 |
파운데이션 메디신 인코포레이티드 |
종양 샘플의 다유전자 분석의 최적화
|
US20120190021A1
(en)
|
2011-01-25 |
2012-07-26 |
Aria Diagnostics, Inc. |
Detection of genetic abnormalities
|
EP3187597B1
(fr)
|
2011-02-09 |
2020-06-03 |
Natera, Inc. |
Procédés de classification de ploïdie prénatale non invasive
|
CA2824387C
(fr)
|
2011-02-09 |
2019-09-24 |
Natera, Inc. |
Procedes de classification de ploidie prenatale non invasive
|
GB2488358A
(en)
|
2011-02-25 |
2012-08-29 |
Univ Plymouth |
Enrichment of foetal DNA in maternal plasma
|
US9260753B2
(en)
|
2011-03-24 |
2016-02-16 |
President And Fellows Of Harvard College |
Single cell nucleic acid detection and analysis
|
SI3078752T1
(sl)
|
2011-04-12 |
2018-12-31 |
Verinata Health, Inc |
Razreševanje frakcij genoma z uporabo števila polimorfizmov
|
WO2012142531A2
(fr)
|
2011-04-14 |
2012-10-18 |
Complete Genomics, Inc. |
Traitement et analyse de données de séquences d'acides nucléiques complexes
|
US9411937B2
(en)
|
2011-04-15 |
2016-08-09 |
Verinata Health, Inc. |
Detecting and classifying copy number variation
|
US9476095B2
(en)
|
2011-04-15 |
2016-10-25 |
The Johns Hopkins University |
Safe sequencing system
|
EP3495497B1
(fr)
|
2011-04-28 |
2021-03-24 |
Life Technologies Corporation |
Procédés et compositions pour pcr multiplexe
|
AU2012249531B2
(en)
|
2011-04-29 |
2017-06-29 |
Sequenom, Inc. |
Quantification of a minority nucleic acid species
|
CN102876660A
(zh)
|
2011-07-11 |
2013-01-16 |
三星电子株式会社 |
扩增靶核酸的方法和测定样品中的靶核酸的相对量的方法
|
US20130024127A1
(en)
|
2011-07-19 |
2013-01-24 |
John Stuelpnagel |
Determination of source contributions using binomial probability calculations
|
GB201115095D0
(en)
|
2011-09-01 |
2011-10-19 |
Singapore Volition Pte Ltd |
Method for detecting nucleosomes containing nucleotides
|
US8712697B2
(en)
|
2011-09-07 |
2014-04-29 |
Ariosa Diagnostics, Inc. |
Determination of copy number variations using binomial probability calculations
|
JP5536729B2
(ja)
|
2011-09-20 |
2014-07-02 |
株式会社ソニー・コンピュータエンタテインメント |
情報処理装置、アプリケーション提供システム、アプリケーション提供サーバ、アプリケーション提供方法、および情報処理方法
|
US10184145B2
(en)
|
2011-09-26 |
2019-01-22 |
Qiagen Gmbh |
Rapid method for isolating extracellular nucleic acids
|
US9984198B2
(en)
|
2011-10-06 |
2018-05-29 |
Sequenom, Inc. |
Reducing sequence read count error in assessment of complex genetic variations
|
US9367663B2
(en)
|
2011-10-06 |
2016-06-14 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
US20140234273A1
(en)
|
2011-10-07 |
2014-08-21 |
Muroch Children Research Institute |
Diagnostic assay for tissue transplantation status
|
WO2013078470A2
(fr)
|
2011-11-22 |
2013-05-30 |
MOTIF, Active |
Isolation multiplex d'acides nucléiques associés à des protéines
|
WO2013086464A1
(fr)
|
2011-12-07 |
2013-06-13 |
The Broad Institute, Inc. |
Marqueurs associés au pronostic et à l'évolution de la leucémie lymphocytaire chronique
|
US20130190653A1
(en)
|
2012-01-25 |
2013-07-25 |
Angel Gabriel Alvarez Ramos |
Device for blood collection from the placenta and the umbilical cord
|
ES2655509T3
(es)
|
2012-02-14 |
2018-02-20 |
Cornell University |
Método para la cuantificación relativa de la secuencia, la expresión o los cambios de copias de ácidos nucleicos, usando reacciones combinadas de polimerasa, ligadura y nucleasa
|
ES2741099T3
(es)
|
2012-02-28 |
2020-02-10 |
Agilent Technologies Inc |
Método de fijación de una secuencia de recuento para una muestra de ácido nucleico
|
WO2013130848A1
(fr)
|
2012-02-29 |
2013-09-06 |
Natera, Inc. |
Analyse améliorée par informatique d'échantillons de fœtus soumis à une contamination maternelle
|
US9862995B2
(en)
|
2012-03-13 |
2018-01-09 |
Abhijit Ajit Patel |
Measurement of nucleic acid variants using highly-multiplexed error-suppressed deep sequencing
|
CA3209140A1
(fr)
|
2012-04-19 |
2013-10-24 |
The Medical College Of Wisconsin, Inc. |
Surveillance hautement sensible utilisant une detection d'adn acellulaire
|
CN108018343B
(zh)
|
2012-05-10 |
2023-01-03 |
通用医疗公司 |
用于测定核苷酸序列的方法
|
US9968901B2
(en)
|
2012-05-21 |
2018-05-15 |
The Scripps Research Institute |
Methods of sample preparation
|
CN104350152B
(zh)
|
2012-06-01 |
2017-08-11 |
欧米伽生物技术公司 |
选择性核酸片段回收
|
WO2014004726A1
(fr)
|
2012-06-26 |
2014-01-03 |
Caifu Chen |
Procédés, compositions et kits pour le diagnostic, le pronostic et la surveillance d'un cancer
|
AU2013204615A1
(en)
|
2012-07-20 |
2014-02-06 |
Verinata Health, Inc. |
Detecting and classifying copy number variation in a fetal genome
|
RU2650790C2
(ru)
|
2012-07-24 |
2018-04-17 |
Натера, Инк. |
Способы и композиции для высокомультиплексной пцр
|
US10993418B2
(en)
|
2012-08-13 |
2021-05-04 |
Life Genetics Lab, Llc |
Method for measuring tumor burden in patient derived xenograft (PDX) mice
|
US20140051585A1
(en)
|
2012-08-15 |
2014-02-20 |
Natera, Inc. |
Methods and compositions for reducing genetic library contamination
|
US20140100126A1
(en)
|
2012-08-17 |
2014-04-10 |
Natera, Inc. |
Method for Non-Invasive Prenatal Testing Using Parental Mosaicism Data
|
CN105164509B
(zh)
|
2012-08-28 |
2018-02-23 |
阿科尼生物系统公司 |
用于纯化核酸的方法和试剂盒
|
US10876152B2
(en)
|
2012-09-04 |
2020-12-29 |
Guardant Health, Inc. |
Systems and methods to detect rare mutations and copy number variation
|
US20140065621A1
(en)
|
2012-09-04 |
2014-03-06 |
Natera, Inc. |
Methods for increasing fetal fraction in maternal blood
|
US20140066317A1
(en)
|
2012-09-04 |
2014-03-06 |
Guardant Health, Inc. |
Systems and methods to detect rare mutations and copy number variation
|
IL269097B2
(en)
|
2012-09-04 |
2024-01-01 |
Guardant Health Inc |
Systems and methods for detecting rare mutations and changes in number of copies
|
EP2728014B1
(fr)
|
2012-10-31 |
2015-10-07 |
Genesupport SA |
Procédé non invasif permettant de détecter une aneuploïdie chromosomique fétale
|
US9523121B2
(en)
|
2013-01-13 |
2016-12-20 |
Uni Taq Bio |
Methods and compositions for PCR using blocked and universal primers
|
EP2954054B1
(fr)
|
2013-02-08 |
2018-12-05 |
Qiagen GmbH |
Procédé pour séparer l'adn par taille
|
US9982255B2
(en)
|
2013-03-11 |
2018-05-29 |
Kailos Genetics, Inc. |
Capture methodologies for circulating cell free DNA
|
US10385394B2
(en)
|
2013-03-15 |
2019-08-20 |
The Translational Genomics Research Institute |
Processes of identifying and characterizing X-linked disorders
|
EP3882362B1
(fr)
|
2013-03-15 |
2024-05-08 |
Guardant Health, Inc. |
Procédés de séquençage de polynucleotides acellulaires
|
CA2902167A1
(fr)
|
2013-03-15 |
2014-09-25 |
Abbott Molecular Inc. |
Procede d'amplification et de dosage de variants de gene de fusion d'arn, procede de distinction de ceux-ci et amorces, sondes et trousses s'y rapportant
|
WO2014145078A1
(fr)
|
2013-03-15 |
2014-09-18 |
Verinata Health, Inc. |
Génération de bibliothèques d'adn acellulaire directement à partir du sang
|
CN105518151B
(zh)
|
2013-03-15 |
2021-05-25 |
莱兰斯坦福初级大学评议会 |
循环核酸肿瘤标志物的鉴别和用途
|
EP2971135A4
(fr)
|
2013-03-15 |
2016-11-09 |
Immucor Gti Diagnostics Inc |
Procédés et compositions pour estimer le statut rénal à l'aide de l'adn acellulaire de l'urine
|
US10072298B2
(en)
|
2013-04-17 |
2018-09-11 |
Life Technologies Corporation |
Gene fusions and gene variants associated with cancer
|
EP3004388B2
(fr)
|
2013-05-29 |
2023-05-31 |
Chronix Biomedical |
Détection et quantification d'adn libre en provenance de cellules du donneur dans la circulation sanguine de bénéficiaires d'une greffe d'organe
|
US10577655B2
(en)
|
2013-09-27 |
2020-03-03 |
Natera, Inc. |
Cell free DNA diagnostic testing standards
|
US9499870B2
(en)
|
2013-09-27 |
2016-11-22 |
Natera, Inc. |
Cell free DNA diagnostic testing standards
|
US11694764B2
(en)
|
2013-09-27 |
2023-07-04 |
University Of Washington |
Method for large scale scaffolding of genome assemblies
|
EP3077539B8
(fr)
|
2013-12-02 |
2018-10-10 |
Personal Genome Diagnostics Inc. |
Procédé d'évaluation de variants minoritaires dans un échantillon
|
CA2934822A1
(fr)
|
2013-12-28 |
2015-07-02 |
Guardant Health, Inc. |
Procedes et systemes de detection de variants genetiques
|
KR102433825B1
(ko)
|
2013-12-30 |
2022-08-31 |
아트레카, 인크. |
핵산 바코드를 이용하는 단일 세포와 관련된 핵산의 분석
|
CN106661612A
(zh)
|
2014-01-27 |
2017-05-10 |
通用医疗公司 |
制备用于测序的核酸的方法
|
ES2819277T3
(es)
|
2014-02-11 |
2021-04-15 |
Hoffmann La Roche |
Secuenciación dirigida y filtrado de UID
|
CN113528645A
(zh)
|
2014-03-14 |
2021-10-22 |
凯尔迪克斯公司 |
用于在移植受体中监测免疫抑制疗法的方法
|
WO2015148494A1
(fr)
|
2014-03-25 |
2015-10-01 |
Quest Diagnostics Investments Incorporated |
Détection de fusions de gènes par expression différentielle intragénique (ide) à l'aide de seuils de cycle moyen
|
RU2717641C2
(ru)
|
2014-04-21 |
2020-03-24 |
Натера, Инк. |
Обнаружение мутаций и плоидности в хромосомных сегментах
|
WO2015164432A1
(fr)
|
2014-04-21 |
2015-10-29 |
Natera, Inc. |
Détection de mutations et de la ploïdie dans des segments chromosomiques
|
US20180173845A1
(en)
|
2014-06-05 |
2018-06-21 |
Natera, Inc. |
Systems and Methods for Detection of Aneuploidy
|
ES2815349T3
(es)
|
2014-06-27 |
2021-03-29 |
Inst Nat Sante Rech Med |
Métodos que emplean ADN y miARN circulantes como biomarcadores para la infertilidad femenina
|
ES2810300T3
(es)
|
2014-07-03 |
2021-03-08 |
Rhodx Inc |
Etiquetado y evaluación de una secuencia diana
|
AU2015289027B2
(en)
|
2014-07-17 |
2021-08-19 |
Qiagen Gmbh |
Method for isolating RNA with high yield
|
CA2955367C
(fr)
|
2014-07-18 |
2021-11-30 |
Illumina, Inc. |
Diagnostic prenatal non invasif d'affection genetique foetale a l'aide d'adn cellulaire et d'adn acellulaire
|
CN113481281A
(zh)
|
2014-10-08 |
2021-10-08 |
康奈尔大学 |
一种用于鉴定样品中的含有靶核苷酸序列的一个或多个核酸分子的方法
|
WO2016063122A1
(fr)
|
2014-10-20 |
2016-04-28 |
INSERM (Institut National de la Santé et de la Recherche Médicale) |
Procédés de criblage d'un sujet pour dépister un cancer
|
WO2016065295A1
(fr)
|
2014-10-24 |
2016-04-28 |
Dae Hyun Kim |
Enrichissement de petits acides nucléiques
|
EP3218519B1
(fr)
|
2014-11-11 |
2020-12-02 |
BGI Shenzhen |
Séquençage en plusieurs passes
|
US11279974B2
(en)
|
2014-12-01 |
2022-03-22 |
The Broad Institute, Inc. |
Method for in situ determination of nucleic acid proximity
|
WO2016109604A2
(fr)
|
2014-12-29 |
2016-07-07 |
InnoGenomics Technologies, LLC |
Dosage multiplexé pour quantifier et évaluer l'intégrité de l'adn libre dans des fluides biologiques pour le diagnostic, le pronostic et la surveillance du cancer
|
GB201501907D0
(en)
|
2015-02-05 |
2015-03-25 |
Technion Res & Dev Foundation |
System and method for single cell genetic analysis
|
WO2016123698A1
(fr)
|
2015-02-06 |
2016-08-11 |
Uti Limited Partnership |
Test diagnostique pour l'évaluation posttransplantation du rejet potentiel d'organes de donneurs
|
WO2016138080A1
(fr)
|
2015-02-24 |
2016-09-01 |
Trustees Of Boston University |
Protection de codes à barres pendant une amplification d'adn au moyen d'épingles à cheveux moléculaires
|
WO2016138500A1
(fr)
|
2015-02-27 |
2016-09-01 |
Cellular Research, Inc. |
Procédés et compositions pour le marquage d'acides nucléiques au moyen de codes à barres en vue du séquençage
|
WO2016160844A2
(fr)
|
2015-03-30 |
2016-10-06 |
Cellular Research, Inc. |
Procédés et compositions pour codage à barres combinatoire
|
KR101850437B1
(ko)
|
2015-04-14 |
2018-04-20 |
이원다이애그노믹스(주) |
차세대 염기서열 분석기법을 이용한 장기 이식 거부 반응 예측 방법
|
US11390914B2
(en)
|
2015-04-23 |
2022-07-19 |
Becton, Dickinson And Company |
Methods and compositions for whole transcriptome amplification
|
US10844428B2
(en)
|
2015-04-28 |
2020-11-24 |
Illumina, Inc. |
Error suppression in sequenced DNA fragments using redundant reads with unique molecular indices (UMIS)
|
JP2018514219A
(ja)
|
2015-04-30 |
2018-06-07 |
メディカル カレッジ オブ ウィスコンシン インコーポレイテッド |
無細胞dnaを評価するための多重/最適化ミスマッチ増幅(moma)−リアルタイムpcr
|
WO2016183106A1
(fr)
|
2015-05-11 |
2016-11-17 |
Natera, Inc. |
Procédés et compositions pour la détermination de la ploïdie
|
WO2016193490A1
(fr)
|
2015-06-05 |
2016-12-08 |
Qiagen Gmbh |
Procédé de séparation d'adn selon la taille
|
US20160371428A1
(en)
|
2015-06-19 |
2016-12-22 |
Natera, Inc. |
Systems and methods for determining aneuploidy risk using sample fetal fraction
|
EP3317420B1
(fr)
|
2015-07-02 |
2021-10-20 |
Arima Genomics, Inc. |
Déconvolution moléculaire précise de mélanges échantillons
|
GB201516047D0
(en)
|
2015-09-10 |
2015-10-28 |
Cancer Rec Tech Ltd |
Method
|
CN108138231A
(zh)
|
2015-09-29 |
2018-06-08 |
路德维格癌症研究有限公司 |
分型和组装不连续基因组元件
|
CN108368542B
(zh)
|
2015-10-19 |
2022-04-08 |
多弗泰尔基因组学有限责任公司 |
用于基因组组装、单元型定相以及独立于靶标的核酸检测的方法
|
CN105986030A
(zh)
|
2016-02-03 |
2016-10-05 |
广州市基准医疗有限责任公司 |
甲基化dna检测方法
|
EP4071250A1
(fr)
|
2016-03-22 |
2022-10-12 |
Myriad Women's Health, Inc. |
Criblage combinatoire d'adn
|
US10781439B2
(en)
|
2016-03-30 |
2020-09-22 |
Covaris, Inc. |
Extraction of cfDNA from biological samples
|
EP3443066A4
(fr)
|
2016-04-14 |
2019-12-11 |
Guardant Health, Inc. |
Méthodes de détection précoce du cancer
|
AU2017249594B2
(en)
|
2016-04-15 |
2023-08-24 |
Natera, Inc. |
Methods for lung cancer detection
|
BR112018072196A2
(pt)
|
2016-04-29 |
2019-02-12 |
Medical College Wisconsin Inc |
amplificação de incompatibilidade otimizada multiplexadas (moma) - número do alvo
|
WO2017205540A1
(fr)
|
2016-05-24 |
2017-11-30 |
The Translational Genomics Research Institute |
Procédés de marquage moléculaire et bibliothèques de séquençage
|
US20170342477A1
(en)
|
2016-05-27 |
2017-11-30 |
Sequenom, Inc. |
Methods for Detecting Genetic Variations
|
AU2017290809A1
(en)
|
2016-07-01 |
2018-12-13 |
Natera, Inc. |
Compositions and methods for detection of nucleic acid mutations
|
WO2018009723A1
(fr)
|
2016-07-06 |
2018-01-11 |
Guardant Health, Inc. |
Procédés de profilage d'un fragmentome d'acides nucléiques sans cellule
|
US11485996B2
(en)
|
2016-10-04 |
2022-11-01 |
Natera, Inc. |
Methods for characterizing copy number variation using proximity-litigation sequencing
|
EP3535413A1
(fr)
|
2016-11-02 |
2019-09-11 |
The Medical College of Wisconsin, Inc. |
Procédés d'évaluation du risque à l'aide d'adn acellulaire total et spécifique
|
GB201618485D0
(en)
|
2016-11-02 |
2016-12-14 |
Ucl Business Plc |
Method of detecting tumour recurrence
|
SG11201903158RA
(en)
|
2016-11-08 |
2019-05-30 |
Cellular Res Inc |
Methods for cell label classification
|
US10011870B2
(en)
|
2016-12-07 |
2018-07-03 |
Natera, Inc. |
Compositions and methods for identifying nucleic acid molecules
|
EP4050113A1
(fr)
|
2017-01-17 |
2022-08-31 |
Life Technologies Corporation |
Compositions et méthodes destinées au séquençage de répertoire immunologique
|
EP3585889A1
(fr)
|
2017-02-21 |
2020-01-01 |
Natera, Inc. |
Compositions, procédés, et kits d'isolement d'acides nucléiques
|
CA3067634A1
(fr)
|
2017-06-20 |
2018-12-27 |
The Medical College Of Wisconsin, Inc. |
Evaluation de conditions chez des sujets greffes a l'aide d'adn acellulaire specifique d'un donneur
|
CA3067635A1
(fr)
|
2017-06-20 |
2018-12-27 |
The Medical College Of Wisconsin, Inc. |
Suivi de patient transplante avec de l'adn acellulaire
|
EP3642353A4
(fr)
|
2017-06-20 |
2021-02-24 |
The Medical College of Wisconsin, Inc. |
Évaluation du risque de complication d'une greffe avec l'adn acellulaire total
|
EP3665308A1
(fr)
|
2017-08-07 |
2020-06-17 |
The Johns Hopkins University |
Méthodes et substances pour l'évaluation et le traitement du cancer
|
CN111344416A
(zh)
|
2017-09-01 |
2020-06-26 |
生命技术公司 |
用于免疫组库测序的组合物和方法
|
US11091800B2
(en)
|
2017-09-20 |
2021-08-17 |
University Of Utah Research Foundation |
Size-selection of cell-free DNA for increasing family size during next-generation sequencing
|
CA3085933A1
(fr)
|
2017-12-14 |
2019-06-20 |
Tai Diagnostics, Inc. |
Evaluation de la compatibilite d'une greffe pour la transplantation
|
WO2019140298A1
(fr)
|
2018-01-12 |
2019-07-18 |
Natera, Inc. |
Nouvelles amorces et utilisations correspondantes
|
WO2019161244A1
(fr)
|
2018-02-15 |
2019-08-22 |
Natera, Inc. |
Procédés pour isoler des acides nucléiques avec sélection de taille
|
CA3090426A1
(fr)
|
2018-04-14 |
2019-10-17 |
Natera, Inc. |
Procedes de detection et de surveillance du cancer au moyen d'une detection personnalisee d'adn tumoral circulant
|
EP3807884A1
(fr)
|
2018-06-12 |
2021-04-21 |
Natera, Inc. |
Procédés et systèmes d'appel de mutations
|
US11525159B2
(en)
|
2018-07-03 |
2022-12-13 |
Natera, Inc. |
Methods for detection of donor-derived cell-free DNA
|
BR112020027023A2
(pt)
|
2018-07-03 |
2021-04-06 |
Natera, Inc. |
Métodos para detecção de dna livre de células derivado de doador
|
CN112639982A
(zh)
|
2018-07-17 |
2021-04-09 |
纳特拉公司 |
使用神经网络调用倍性状态的方法和系统
|
WO2020041449A1
(fr)
|
2018-08-21 |
2020-02-27 |
Zymo Research Corporation |
Procédés et compositions pour le suivi de la qualité d'un échantillon
|
US20200109449A1
(en)
|
2018-10-09 |
2020-04-09 |
Tai Diagnostics, Inc. |
Cell lysis assay for cell-free dna analysis
|
CN113227468A
(zh)
|
2018-11-21 |
2021-08-06 |
卡里乌斯公司 |
感染性疾病的检测和预测
|
CN113330121A
(zh)
|
2018-12-17 |
2021-08-31 |
纳特拉公司 |
用于循环细胞分析的方法
|
US11931674B2
(en)
|
2019-04-04 |
2024-03-19 |
Natera, Inc. |
Materials and methods for processing blood samples
|
CA3134519A1
(fr)
|
2019-04-15 |
2020-10-22 |
Natera, Inc. |
Biopsie liquide amelioree utilisant une selection de taille
|
EP3980559A1
(fr)
|
2019-06-06 |
2022-04-13 |
Natera, Inc. |
Procédés de détection d'adn de cellules immunitaires et de surveillance du système immunitaire
|
US20220340963A1
(en)
|
2019-09-20 |
2022-10-27 |
Natera, Inc. |
Methods for assessing graft suitability for transplantation
|
US20230203573A1
(en)
|
2020-05-29 |
2023-06-29 |
Natera, Inc. |
Methods for detection of donor-derived cell-free dna
|