|
US4683202A
(en)
|
1985-03-28 |
1987-07-28 |
Cetus Corporation |
Process for amplifying nucleic acid sequences
|
|
US4683195A
(en)
|
1986-01-30 |
1987-07-28 |
Cetus Corporation |
Process for amplifying, detecting, and/or-cloning nucleic acid sequences
|
|
US5720928A
(en)
|
1988-09-15 |
1998-02-24 |
New York University |
Image processing and analysis of individual nucleic acid molecules
|
|
US5075212A
(en)
|
1989-03-27 |
1991-12-24 |
University Of Patents, Inc. |
Methods of detecting picornaviruses in biological fluids and tissues
|
|
US5143854A
(en)
|
1989-06-07 |
1992-09-01 |
Affymax Technologies N.V. |
Large scale photolithographic solid phase synthesis of polypeptides and receptor binding screening thereof
|
|
US5641628A
(en)
|
1989-11-13 |
1997-06-24 |
Children's Medical Center Corporation |
Non-invasive method for isolation and detection of fetal DNA
|
|
DE69133566T2
(de)
|
1990-01-12 |
2007-12-06 |
Amgen Fremont Inc. |
Bildung von xenogenen Antikörpern
|
|
US5091652A
(en)
|
1990-01-12 |
1992-02-25 |
The Regents Of The University Of California |
Laser excited confocal microscope fluorescence scanner and method
|
|
US5432054A
(en)
|
1994-01-31 |
1995-07-11 |
Applied Imaging |
Method for separating rare cells from a population of cells
|
|
CA2157219C
(en)
|
1994-08-31 |
2010-10-05 |
Munehiro Noda |
Process for purifying recombinant human serum albumin
|
|
US5846719A
(en)
|
1994-10-13 |
1998-12-08 |
Lynx Therapeutics, Inc. |
Oligonucleotide tags for sorting and identification
|
|
CA2207952A1
(en)
|
1994-12-23 |
1996-07-04 |
David Thornley |
Automated dna sequencing
|
|
US5795782A
(en)
|
1995-03-17 |
1998-08-18 |
President & Fellows Of Harvard College |
Characterization of individual polymer molecules based on monomer-interface interactions
|
|
US5670325A
(en)
|
1996-08-14 |
1997-09-23 |
Exact Laboratories, Inc. |
Method for the detection of clonal populations of transformed cells in a genomically heterogeneous cellular sample
|
|
CA2253710A1
(en)
|
1996-04-25 |
1997-10-30 |
Spectrametrix Inc. |
Analyte assay using particulate labels
|
|
US5786146A
(en)
|
1996-06-03 |
1998-07-28 |
The Johns Hopkins University School Of Medicine |
Method of detection of methylated nucleic acid using agents which modify unmethylated cytosine and distinguishing modified methylated and non-methylated nucleic acids
|
|
US5928870A
(en)
|
1997-06-16 |
1999-07-27 |
Exact Laboratories, Inc. |
Methods for the detection of loss of heterozygosity
|
|
US6100029A
(en)
|
1996-08-14 |
2000-08-08 |
Exact Laboratories, Inc. |
Methods for the detection of chromosomal aberrations
|
|
US6300077B1
(en)
|
1996-08-14 |
2001-10-09 |
Exact Sciences Corporation |
Methods for the detection of nucleic acids
|
|
US6403311B1
(en)
|
1997-02-12 |
2002-06-11 |
Us Genomics |
Methods of analyzing polymers using ordered label strategies
|
|
GB9704444D0
(en)
|
1997-03-04 |
1997-04-23 |
Isis Innovation |
Non-invasive prenatal diagnosis
|
|
US6566101B1
(en)
|
1997-06-16 |
2003-05-20 |
Anthony P. Shuber |
Primer extension methods for detecting nucleic acids
|
|
US6570001B1
(en)
|
1997-06-20 |
2003-05-27 |
Institut Pasteur |
Polynucleotides and their use for detecting resistance to streptogramin A or to streptogramin B and related compounds
|
|
EP1105529B2
(en)
|
1998-07-30 |
2013-05-29 |
Illumina Cambridge Limited |
Arrayed biomolecules and their use in sequencing
|
|
US6263286B1
(en)
|
1998-08-13 |
2001-07-17 |
U.S. Genomics, Inc. |
Methods of analyzing polymers using a spatial network of fluorophores and fluorescence resonance energy transfer
|
|
US6818395B1
(en)
|
1999-06-28 |
2004-11-16 |
California Institute Of Technology |
Methods and apparatus for analyzing polynucleotide sequences
|
|
US20050287592A1
(en)
|
2000-08-29 |
2005-12-29 |
Yeda Research And Development Co. Ltd. |
Template-dependent nucleic acid polymerization using oligonucleotide triphosphates building blocks
|
|
EP1218543A2
(en)
|
1999-09-29 |
2002-07-03 |
Solexa Ltd. |
Polynucleotide sequencing
|
|
DE60027040T2
(de)
|
1999-10-29 |
2006-11-23 |
Stratagene California, La Jolla |
Zusammensetzungen und methoden zur verwendung von dna polymerasen
|
|
US20010049102A1
(en)
|
2000-02-24 |
2001-12-06 |
Huang Xiaohua C. |
Methods for determining single nucleotide variations
|
|
US6664056B2
(en)
|
2000-10-17 |
2003-12-16 |
The Chinese University Of Hong Kong |
Non-invasive prenatal monitoring
|
|
AU2002239284A1
(en)
*
|
2000-11-27 |
2002-06-03 |
The Regents Of The University Of California |
Methods and devices for characterizing duplex nucleic acid molecules
|
|
DE10112515B4
(de)
|
2001-03-09 |
2004-02-12 |
Epigenomics Ag |
Verfahren zum Nachweis von Cytosin-Methylierungsmustern mit hoher Sensitivität
|
|
CA2440754A1
(en)
|
2001-03-12 |
2002-09-19 |
Stephen Quake |
Methods and apparatus for analyzing polynucleotide sequences by asynchronous base extension
|
|
WO2003000920A2
(en)
|
2001-06-21 |
2003-01-03 |
President And Fellows Of Harvard College |
Methods for characterization of nucleic acid molecules
|
|
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
|
|
US20030157489A1
(en)
|
2002-01-11 |
2003-08-21 |
Michael Wall |
Recursive categorical sequence assembly
|
|
CA2476835A1
(en)
|
2002-02-20 |
2003-08-28 |
University Of Virginia Patent Foundation |
A non-invasive diagnostic test utilizing histone modification markers
|
|
US6977162B2
(en)
|
2002-03-01 |
2005-12-20 |
Ravgen, Inc. |
Rapid analysis of variations in a genome
|
|
DE60310697D1
(de)
|
2002-03-15 |
2007-02-08 |
Epigenomics Ag |
Entdeckungs- und diagnoseverfahren mit 5-methylcytosin-dna-glycosylase
|
|
US20040110208A1
(en)
|
2002-03-26 |
2004-06-10 |
Selena Chan |
Methods and device for DNA sequencing using surface enhanced Raman scattering (SERS)
|
|
US7744816B2
(en)
|
2002-05-01 |
2010-06-29 |
Intel Corporation |
Methods and device for biomolecule characterization
|
|
US20050019784A1
(en)
|
2002-05-20 |
2005-01-27 |
Xing Su |
Method and apparatus for nucleic acid sequencing and identification
|
|
US7005264B2
(en)
|
2002-05-20 |
2006-02-28 |
Intel Corporation |
Method and apparatus for nucleic acid sequencing and identification
|
|
US6952651B2
(en)
|
2002-06-17 |
2005-10-04 |
Intel Corporation |
Methods and apparatus for nucleic acid sequencing by signal stretching and data integration
|
|
CA2497988C
(en)
|
2002-09-06 |
2011-03-29 |
The Trustees Of Boston University |
Quantification of gene expression
|
|
US7820378B2
(en)
|
2002-11-27 |
2010-10-26 |
Sequenom, Inc. |
Fragmentation-based methods and systems for sequence variation detection and discovery
|
|
WO2005010145A2
(en)
|
2003-07-05 |
2005-02-03 |
The Johns Hopkins University |
Method and compositions for detection and enumeration of genetic variations
|
|
US20070026406A1
(en)
*
|
2003-08-13 |
2007-02-01 |
Iconix Pharmaceuticals, Inc. |
Apparatus and method for classifying multi-dimensional biological data
|
|
US7846738B2
(en)
|
2003-08-15 |
2010-12-07 |
President And Fellows Of Harvard College |
Study of polymer molecules and conformations with a nanopore
|
|
AU2004270220B2
(en)
|
2003-09-05 |
2009-03-05 |
The Chinese University Of Hong Kong |
Method for non-invasive prenatal diagnosis
|
|
ATE435301T1
(de)
|
2003-10-16 |
2009-07-15 |
Sequenom Inc |
Nicht invasiver nachweis fötaler genetischer merkmale
|
|
US20050095599A1
(en)
|
2003-10-30 |
2005-05-05 |
Pittaro Richard J. |
Detection and identification of biopolymers using fluorescence quenching
|
|
US7169560B2
(en)
|
2003-11-12 |
2007-01-30 |
Helicos Biosciences Corporation |
Short cycle methods for sequencing polynucleotides
|
|
US20050147980A1
(en)
|
2003-12-30 |
2005-07-07 |
Intel Corporation |
Nucleic acid sequencing by Raman monitoring of uptake of nucleotides during molecular replication
|
|
US20100216151A1
(en)
|
2004-02-27 |
2010-08-26 |
Helicos Biosciences Corporation |
Methods for detecting fetal nucleic acids and diagnosing fetal abnormalities
|
|
US20100216153A1
(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
|
|
US7279337B2
(en)
|
2004-03-10 |
2007-10-09 |
Agilent Technologies, Inc. |
Method and apparatus for sequencing polymers through tunneling conductance variation detection
|
|
WO2006028508A2
(en)
|
2004-03-23 |
2006-03-16 |
President And Fellows Of Harvard College |
Methods and apparatus for characterizing polynucleotides
|
|
EP1784754A4
(en)
|
2004-08-13 |
2009-05-27 |
Harvard College |
OPTI-NANOPORE DNA READING PLATFORM WITH ULTRAHOLE THROUGHPUT
|
|
AU2005308918B2
(en)
|
2004-11-29 |
2012-09-27 |
Sequenom, Inc. |
Means and methods for detecting methylated DNA
|
|
US7645576B2
(en)
|
2005-03-18 |
2010-01-12 |
The Chinese University Of Hong Kong |
Method for the detection of chromosomal aneuploidies
|
|
EP3599609A1
(en)
*
|
2005-11-26 |
2020-01-29 |
Natera, Inc. |
System and method for cleaning noisy genetic data and using data to make predictions
|
|
US7960105B2
(en)
|
2005-11-29 |
2011-06-14 |
National Institutes Of Health |
Method of DNA analysis using micro/nanochannel
|
|
TR201910868T4
(tr)
|
2006-02-02 |
2019-08-21 |
Univ Leland Stanford Junior |
Dijital analizle invazif olmayan fetal genetik tarama.
|
|
WO2007100911A2
(en)
|
2006-02-28 |
2007-09-07 |
University Of Louisville Research Foundation |
Detecting fetal chromosomal abnormalities using tandem single nucleotide polymorphisms
|
|
TW200741192A
(en)
|
2006-03-10 |
2007-11-01 |
Koninkl Philips Electronics Nv |
Methods and systems for identification of DNA patterns through spectral analysis
|
|
WO2007121276A2
(en)
|
2006-04-12 |
2007-10-25 |
Biocept, Inc. |
Enrichment of circulating fetal dna
|
|
US7282337B1
(en)
|
2006-04-14 |
2007-10-16 |
Helicos Biosciences Corporation |
Methods for increasing accuracy of nucleic acid sequencing
|
|
US20090075252A1
(en)
|
2006-04-14 |
2009-03-19 |
Helicos Biosciences Corporation |
Methods for increasing accuracy of nucleic acid sequencing
|
|
WO2007140417A2
(en)
|
2006-05-31 |
2007-12-06 |
Sequenom, Inc. |
Methods and compositions for the extraction and amplification of nucleic acid from a sample
|
|
EP2029779A4
(en)
|
2006-06-14 |
2010-01-20 |
Living Microsystems Inc |
HIGHLY PARALLEL SNP GENOTYPING UTILIZATION FOR FETAL DIAGNOSIS
|
|
US8137912B2
(en)
|
2006-06-14 |
2012-03-20 |
The General Hospital Corporation |
Methods for the diagnosis of fetal abnormalities
|
|
AU2007260750A1
(en)
|
2006-06-16 |
2007-12-21 |
Sequenom, Inc. |
Methods and compositions for the amplification, detection and quantification of nucleic acid from a sample
|
|
US20080081330A1
(en)
|
2006-09-28 |
2008-04-03 |
Helicos Biosciences Corporation |
Method and devices for analyzing small RNA molecules
|
|
EP2081442B1
(en)
|
2006-10-10 |
2016-08-10 |
TrovaGene, Inc. |
Compositions, methods and kits for isolating nucleic acids from body fluids using anion exchange media
|
|
US8262900B2
(en)
|
2006-12-14 |
2012-09-11 |
Life Technologies Corporation |
Methods and apparatus for measuring analytes using large scale FET arrays
|
|
EP1944273A1
(en)
|
2007-01-15 |
2008-07-16 |
Rockwool International A/S |
Process and apparatus for making mineral fibers
|
|
US8003319B2
(en)
|
2007-02-02 |
2011-08-23 |
International Business Machines Corporation |
Systems and methods for controlling position of charged polymer inside nanopore
|
|
US8722327B2
(en)
|
2007-03-28 |
2014-05-13 |
Bionano Genomics, Inc. |
Methods of macromolecular analysis using nanochannel arrays
|
|
AU2008236694B2
(en)
|
2007-04-04 |
2014-01-23 |
The Regents Of The University Of California |
Compositions, devices, systems, and methods for using a nanopore
|
|
GB0713143D0
(en)
|
2007-07-06 |
2007-08-15 |
Ucl Business Plc |
Nucleic acid detection method
|
|
EP3892736A1
(en)
|
2007-07-23 |
2021-10-13 |
The Chinese University of Hong Kong |
Determining a nucleic acid sequence imbalance
|
|
US12180549B2
(en)
|
2007-07-23 |
2024-12-31 |
The Chinese University Of Hong Kong |
Diagnosing fetal chromosomal aneuploidy using genomic sequencing
|
|
EP2195452B1
(en)
|
2007-08-29 |
2012-03-14 |
Sequenom, Inc. |
Methods and compositions for universal size-specific polymerase chain reaction
|
|
WO2009032779A2
(en)
|
2007-08-29 |
2009-03-12 |
Sequenom, Inc. |
Methods and compositions for the size-specific seperation of nucleic acid from a sample
|
|
WO2009046445A1
(en)
|
2007-10-04 |
2009-04-09 |
Halcyon Molecular |
Sequencing nucleic acid polymers with electron microscopy
|
|
US7767400B2
(en)
|
2008-02-03 |
2010-08-03 |
Helicos Biosciences Corporation |
Paired-end reads in sequencing by synthesis
|
|
EP2271772B1
(en)
|
2008-03-11 |
2014-07-16 |
Sequenom, Inc. |
Nucleic acid-based tests for prenatal gender determination
|
|
CA2718137A1
(en)
|
2008-03-26 |
2009-10-01 |
Sequenom, Inc. |
Restriction endonuclease enhanced polymorphic sequence detection
|
|
WO2011050147A1
(en)
|
2009-10-21 |
2011-04-28 |
Bionanomatrix, Inc . |
Methods and related devices for single molecule whole genome analysis
|
|
US8628919B2
(en)
|
2008-06-30 |
2014-01-14 |
Bionano Genomics, Inc. |
Methods and devices for single-molecule whole genome analysis
|
|
US20110229877A1
(en)
|
2008-07-07 |
2011-09-22 |
Oxford Nanopore Technologies Limited |
Enzyme-pore constructs
|
|
US9447152B2
(en)
|
2008-07-07 |
2016-09-20 |
Oxford Nanopore Technologies Limited |
Base-detecting pore
|
|
AU2009293232B2
(en)
|
2008-09-16 |
2015-05-14 |
Sequenom Center For Molecular Medicine |
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
|
|
HUE031848T2
(en)
|
2008-09-20 |
2017-08-28 |
Univ Leland Stanford Junior |
Non-invasive diagnosis of fetal aneuploidy by sequencing
|
|
GB2483810B
(en)
|
2008-11-07 |
2012-09-05 |
Sequenta Inc |
Methods for correlating clonotypes with diseases in a population
|
|
WO2010056728A1
(en)
|
2008-11-11 |
2010-05-20 |
Helicos Biosciences Corporation |
Nucleic acid encoding for multiplex analysis
|
|
JP5846703B2
(ja)
|
2008-11-18 |
2016-01-20 |
バイオナノ ジェノミックス、インク． |
ポリヌクレオチドのマッピング及び配列決定
|
|
WO2010065470A2
(en)
|
2008-12-01 |
2010-06-10 |
Consumer Genetics, Inc. |
Compositions and methods for detecting background male dna during fetal sex determination
|
|
CA2748030A1
(en)
|
2008-12-22 |
2010-07-01 |
Arnold R. Oliphant |
Methods and genotyping panels for detecting alleles, genomes, and transcriptomes
|
|
US8455260B2
(en)
|
2009-03-27 |
2013-06-04 |
Massachusetts Institute Of Technology |
Tagged-fragment map assembly
|
|
EP3211095B1
(en)
|
2009-04-03 |
2019-01-02 |
Sequenom, Inc. |
Nucleic acid preparation compositions and methods
|
|
US8246799B2
(en)
|
2009-05-28 |
2012-08-21 |
Nabsys, Inc. |
Devices and methods for analyzing biomolecules and probes bound thereto
|
|
US20100330557A1
(en)
|
2009-06-30 |
2010-12-30 |
Zohar Yakhini |
Genomic coordinate system
|
|
US9725315B2
(en)
|
2009-09-28 |
2017-08-08 |
Bionano Genomics, Inc. |
Nanochannel arrays and near-field illumination devices for polymer analysis and related methods
|
|
HUE061110T2
(hu)
|
2009-11-05 |
2023-05-28 |
Univ Hong Kong Chinese |
Magzati genomelemzés anyai biológiai mintából
|
|
EP2516680B1
(en)
|
2009-12-22 |
2016-04-06 |
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
|
|
EP4074838A1
(en)
|
2010-01-19 |
2022-10-19 |
Verinata Health, Inc. |
Novel protocol for preparing sequencing libraries
|
|
US9323888B2
(en)
|
2010-01-19 |
2016-04-26 |
Verinata Health, Inc. |
Detecting and classifying copy number variation
|
|
US20120270739A1
(en)
|
2010-01-19 |
2012-10-25 |
Verinata Health, Inc. |
Method for sample analysis of aneuploidies in maternal samples
|
|
US10662474B2
(en)
|
2010-01-19 |
2020-05-26 |
Verinata Health, Inc. |
Identification of polymorphic sequences in mixtures of genomic DNA by whole genome sequencing
|
|
US9260745B2
(en)
*
|
2010-01-19 |
2016-02-16 |
Verinata Health, Inc. |
Detecting and classifying copy number variation
|
|
WO2011090556A1
(en)
|
2010-01-19 |
2011-07-28 |
Verinata Health, Inc. |
Methods for determining fraction of fetal nucleic acid in maternal samples
|
|
EP2526415B1
(en)
|
2010-01-19 |
2017-05-03 |
Verinata Health, Inc |
Partition defined detection methods
|
|
US20110312503A1
(en)
|
2010-01-23 |
2011-12-22 |
Artemis Health, Inc. |
Methods of fetal abnormality detection
|
|
WO2011143659A2
(en)
|
2010-05-14 |
2011-11-17 |
Fluidigm Corporation |
Nucleic acid isolation methods
|
|
CA3207599A1
(en)
|
2010-05-18 |
2011-11-24 |
Natera, Inc. |
Methods for non-invasive prenatal ploidy calling
|
|
WO2012006291A2
(en)
|
2010-07-06 |
2012-01-12 |
Life Technologies Corporation |
Systems and methods to detect copy number variation
|
|
WO2012012703A2
(en)
|
2010-07-23 |
2012-01-26 |
Esoterix Genetic Laboratories, Llc |
Identification of differentially represented fetal or maternal genomic regions and uses thereof
|
|
US11031095B2
(en)
|
2010-08-06 |
2021-06-08 |
Ariosa Diagnostics, Inc. |
Assay systems for determination of fetal copy number variation
|
|
US8700338B2
(en)
*
|
2011-01-25 |
2014-04-15 |
Ariosa Diagnosis, Inc. |
Risk calculation for evaluation of fetal aneuploidy
|
|
SG190344A1
(en)
|
2010-11-30 |
2013-06-28 |
Univ Hong Kong Chinese |
Detection of genetic or molecular aberrations associated with cancer
|
|
US20150064695A1
(en)
|
2010-12-17 |
2015-03-05 |
Celula Inc. |
Methods for screening and diagnosing genetic conditions
|
|
BR112013016193B1
(pt)
|
2010-12-22 |
2019-10-22 |
Natera Inc |
método ex vivo para determinar se um suposto pai é o pai biológico de um feto que está em gestação em uma gestante e relatório
|
|
EP2655666A2
(en)
|
2010-12-23 |
2013-10-30 |
Sequenom, Inc. |
Fetal genetic variation detection
|
|
WO2012103031A2
(en)
|
2011-01-25 |
2012-08-02 |
Ariosa Diagnostics, Inc. |
Detection of genetic abnormalities
|
|
BR112013020220B1
(pt)
|
2011-02-09 |
2020-03-17 |
Natera, Inc. |
Método para determinar o estado de ploidia de um cromossomo em um feto em gestação
|
|
WO2012118745A1
(en)
|
2011-02-28 |
2012-09-07 |
Arnold Oliphant |
Assay systems for detection of aneuploidy and sex determination
|
|
LT3567124T
(lt)
|
2011-04-12 |
2022-04-11 |
Verinata Health, Inc. |
Genominių frakcijų paskirstymas, naudojant polimorfizmo skaičiavimo rezultatus
|
|
GB2484764B
(en)
|
2011-04-14 |
2012-09-05 |
Verinata Health Inc |
Normalizing chromosomes for the determination and verification of common and rare chromosomal aneuploidies
|
|
WO2014014498A1
(en)
|
2012-07-20 |
2014-01-23 |
Verinata Health, Inc. |
Detecting and classifying copy number variation in a fetal genome
|
|
US9411937B2
(en)
|
2011-04-15 |
2016-08-09 |
Verinata Health, Inc. |
Detecting and classifying copy number variation
|
|
PL2716766T3
(pl)
|
2011-05-31 |
2017-09-29 |
Berry Genomics Co., Ltd. |
Urządzenie do wykrywania liczby kopii chromosomów płodowych lub chromosomów komórek nowotworowych
|
|
US20140235474A1
(en)
|
2011-06-24 |
2014-08-21 |
Sequenom, Inc. |
Methods and processes for non invasive assessment of a genetic variation
|
|
KR101489568B1
(ko)
|
2011-06-29 |
2015-02-03 |
비지아이 헬스 서비스 코포레이션 리미티드 |
태아 유전학적 이상의 비침습성 검출
|
|
US9139874B2
(en)
|
2011-07-07 |
2015-09-22 |
Life Technologies Corporation |
Bi-directional sequencing compositions and methods
|
|
US9984198B2
(en)
|
2011-10-06 |
2018-05-29 |
Sequenom, Inc. |
Reducing sequence read count error in assessment of complex genetic variations
|
|
US10196681B2
(en)
|
2011-10-06 |
2019-02-05 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
|
JP6073902B2
(ja)
*
|
2011-10-06 |
2017-02-01 |
セクエノム， インコーポレイテッド |
遺伝的変異の非侵襲的評価のための方法およびプロセス
|
|
US9367663B2
(en)
|
2011-10-06 |
2016-06-14 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
|
US10424394B2
(en)
|
2011-10-06 |
2019-09-24 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
|
CA2850785C
(en)
|
2011-10-06 |
2022-12-13 |
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
|
|
DK2766496T3
(en)
|
2011-10-11 |
2017-05-15 |
Sequenom Inc |
METHODS AND PROCESSES FOR NON-INVASIVE ASSESSMENT OF GENETIC VARIATIONS
|
|
CA2861856C
(en)
|
2012-01-20 |
2020-06-02 |
Sequenom, Inc. |
Diagnostic processes that factor experimental conditions
|
|
US9892230B2
(en)
|
2012-03-08 |
2018-02-13 |
The Chinese University Of Hong Kong |
Size-based analysis of fetal or tumor DNA fraction in plasma
|
|
EP3573066B1
(en)
|
2012-03-13 |
2023-09-27 |
The Chinese University Of Hong Kong |
Methods for analyzing massively parallel sequencing data for noninvasive prenatal diagnosis
|
|
US9920361B2
(en)
|
2012-05-21 |
2018-03-20 |
Sequenom, Inc. |
Methods and compositions for analyzing nucleic acid
|
|
US10504613B2
(en)
|
2012-12-20 |
2019-12-10 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
|
ES2902401T3
(es)
|
2012-05-21 |
2022-03-28 |
Sequenom Inc |
Métodos y procesos para la evaluación no invasiva de variaciones genéticas
|
|
US10497461B2
(en)
|
2012-06-22 |
2019-12-03 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
|
KR102393608B1
(ko)
|
2012-09-04 |
2022-05-03 |
가던트 헬쓰, 인크. |
희귀 돌연변이 및 카피수 변이를 검출하기 위한 시스템 및 방법
|
|
US10482994B2
(en)
|
2012-10-04 |
2019-11-19 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
|
AU2013326980B2
(en)
|
2012-10-04 |
2019-08-15 |
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
|
|
EP3409791B1
(en)
|
2013-03-15 |
2021-06-30 |
Verinata Health, Inc. |
Generating cell-free dna libraries directly from blood
|
|
EP4187543A1
(en)
|
2013-04-03 |
2023-05-31 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
|
WO2014190286A2
(en)
|
2013-05-24 |
2014-11-27 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
|
EP3011051B1
(en)
|
2013-06-21 |
2019-01-30 |
Sequenom, Inc. |
Method for non-invasive assessment of genetic variations
|
|
GB201318369D0
(en)
*
|
2013-10-17 |
2013-12-04 |
Univ Leuven Kath |
Methods using BAF
|
|
US10174375B2
(en)
|
2013-09-20 |
2019-01-08 |
The Chinese University Of Hong Kong |
Sequencing analysis of circulating DNA to detect and monitor autoimmune diseases
|
|
BR112016007401B1
(pt)
|
2013-10-04 |
2023-04-11 |
Sequenom, Inc. |
Método para determinar a presença ou ausência de uma aneuploidia cromossômica em uma amostra
|
|
EP3495496B1
(en)
|
2013-10-07 |
2020-11-25 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of chromosome alterations
|
|
GB201319779D0
(en)
*
|
2013-11-08 |
2013-12-25 |
Cartagenia N V |
Genetic analysis method
|
|
US20150347676A1
(en)
|
2014-05-30 |
2015-12-03 |
Sequenom, Inc. |
Chromosome representation determinations
|
|
WO2016019042A1
(en)
|
2014-07-30 |
2016-02-04 |
Sequenom, Inc. |
Methods and processes for non-invasive assessment of genetic variations
|
|
EP3491560A1
(en)
|
2016-07-27 |
2019-06-05 |
Sequenom, Inc. |
Genetic copy number alteration classifications
|
|
CA3207879A1
(en)
|
2017-01-24 |
2018-08-02 |
Sequenom, Inc. |
Methods and processes for assessment of genetic variations
|