EA035451B9 - Способ диагностики рака с использованием геномного секвенирования - Google Patents
Способ диагностики рака с использованием геномного секвенированияInfo
- Publication number
- EA035451B9 EA035451B9 EA201600280A EA201600280A EA035451B9 EA 035451 B9 EA035451 B9 EA 035451B9 EA 201600280 A EA201600280 A EA 201600280A EA 201600280 A EA201600280 A EA 201600280A EA 035451 B9 EA035451 B9 EA 035451B9
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- biological sample
- cancer
- dna fragments
- malignant tumor
- amount
- Prior art date
Links
- 201000011510 cancer Diseases 0.000 title abstract 5
- 206010028980 Neoplasm Diseases 0.000 title abstract 3
- 238000000034 method Methods 0.000 title abstract 3
- 238000012163 sequencing technique Methods 0.000 title abstract 2
- 239000012472 biological sample Substances 0.000 abstract 4
- 208000031404 Chromosome Aberrations Diseases 0.000 abstract 2
- 231100000005 chromosome aberration Toxicity 0.000 abstract 2
- 239000012634 fragment Substances 0.000 abstract 2
- 210000004027 cell Anatomy 0.000 abstract 1
- 210000002381 plasma Anatomy 0.000 abstract 1
- 210000003296 saliva Anatomy 0.000 abstract 1
- 210000002966 serum Anatomy 0.000 abstract 1
- 210000004881 tumor cell Anatomy 0.000 abstract 1
- 210000002700 urine Anatomy 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6809—Methods for determination or identification of nucleic acids involving differential detection
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6813—Hybridisation assays
- C12Q1/6827—Hybridisation assays for detection of mutation or polymorphism
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6869—Methods for sequencing
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6876—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
- C12Q1/6883—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6876—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
- C12Q1/6888—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for detection or identification of organisms
-
- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16B—BIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
- G16B20/00—ICT specially adapted for functional genomics or proteomics, e.g. genotype-phenotype associations
-
- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16B—BIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
- G16B20/00—ICT specially adapted for functional genomics or proteomics, e.g. genotype-phenotype associations
- G16B20/10—Ploidy or copy number detection
-
- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16B—BIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
- G16B20/00—ICT specially adapted for functional genomics or proteomics, e.g. genotype-phenotype associations
- G16B20/20—Allele or variant detection, e.g. single nucleotide polymorphism [SNP] detection
-
- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16B—BIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
- G16B30/00—ICT specially adapted for sequence analysis involving nucleotides or amino acids
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q2600/00—Oligonucleotides characterized by their use
- C12Q2600/112—Disease subtyping, staging or classification
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q2600/00—Oligonucleotides characterized by their use
- C12Q2600/154—Methylation markers
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q2600/00—Oligonucleotides characterized by their use
- C12Q2600/156—Polymorphic or mutational markers
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2800/00—Detection or diagnosis of diseases
- G01N2800/38—Pediatrics
- G01N2800/385—Congenital anomalies
- G01N2800/387—Down syndrome; Trisomy 18; Trisomy 13
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A90/00—Technologies having an indirect contribution to adaptation to climate change
- Y02A90/10—Information and communication technologies [ICT] supporting adaptation to climate change, e.g. for weather forecasting or climate simulation
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Analytical Chemistry (AREA)
- Genetics & Genomics (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Biotechnology (AREA)
- General Health & Medical Sciences (AREA)
- Biophysics (AREA)
- Molecular Biology (AREA)
- General Engineering & Computer Science (AREA)
- Immunology (AREA)
- Microbiology (AREA)
- Biochemistry (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Theoretical Computer Science (AREA)
- Medical Informatics (AREA)
- Evolutionary Biology (AREA)
- Bioinformatics & Computational Biology (AREA)
- Pathology (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Investigating Or Analysing Biological Materials (AREA)
- Apparatus Associated With Microorganisms And Enzymes (AREA)
- Crystallography & Structural Chemistry (AREA)
- Saccharide Compounds (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US95143807P | 2007-07-23 | 2007-07-23 | |
| US60/951,438 | 2007-07-23 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| EA201600280A1 EA201600280A1 (ru) | 2016-07-29 |
| EA035451B1 EA035451B1 (ru) | 2020-06-18 |
| EA035451B9 true EA035451B9 (ru) | 2020-09-09 |
Family
ID=39798126
Family Applications (6)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EA201600280A EA035451B9 (ru) | 2007-07-23 | 2008-07-23 | Способ диагностики рака с использованием геномного секвенирования |
| EA201201551A EA201201551A1 (ru) | 2007-07-23 | 2008-07-23 | Способ диагностики рака с использованием геномного секвенирования |
| EA201300072A EA028642B1 (ru) | 2007-07-23 | 2008-07-23 | Способ пренатальной диагностики фетальной хромосомной анэуплоидии |
| EA201791612A EA039167B1 (ru) | 2007-07-23 | 2008-07-23 | Диагностика фетальной хромосомной анэуплоидии с использованием геномного секвенирования |
| EA202192446A EA202192446A1 (ru) | 2007-07-23 | 2008-07-23 | Диагностика фетальной хромосомной анэуплоидии с использованием геномного секвенирования |
| EA201000231A EA017966B1 (ru) | 2007-07-23 | 2008-07-23 | Диагностика фетальной хромосомной анэуплоидии с использованием геномного секвенирования |
Family Applications After (5)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EA201201551A EA201201551A1 (ru) | 2007-07-23 | 2008-07-23 | Способ диагностики рака с использованием геномного секвенирования |
| EA201300072A EA028642B1 (ru) | 2007-07-23 | 2008-07-23 | Способ пренатальной диагностики фетальной хромосомной анэуплоидии |
| EA201791612A EA039167B1 (ru) | 2007-07-23 | 2008-07-23 | Диагностика фетальной хромосомной анэуплоидии с использованием геномного секвенирования |
| EA202192446A EA202192446A1 (ru) | 2007-07-23 | 2008-07-23 | Диагностика фетальной хромосомной анэуплоидии с использованием геномного секвенирования |
| EA201000231A EA017966B1 (ru) | 2007-07-23 | 2008-07-23 | Диагностика фетальной хромосомной анэуплоидии с использованием геномного секвенирования |
Country Status (26)
| Country | Link |
|---|---|
| US (13) | US8706422B2 (enExample) |
| EP (15) | EP2557518B1 (enExample) |
| JP (18) | JP5519500B2 (enExample) |
| KR (25) | KR20160113145A (enExample) |
| CN (11) | CN103849684A (enExample) |
| AU (1) | AU2008278839B2 (enExample) |
| BR (1) | BRPI0814670B8 (enExample) |
| CA (10) | CA3200589A1 (enExample) |
| CY (3) | CY1114773T1 (enExample) |
| DK (6) | DK2514842T3 (enExample) |
| EA (6) | EA035451B9 (enExample) |
| ES (7) | ES2571738T3 (enExample) |
| FI (1) | FI2557517T3 (enExample) |
| HK (2) | HK1199067A1 (enExample) |
| HR (5) | HRP20251164T3 (enExample) |
| HU (3) | HUE061020T2 (enExample) |
| IL (2) | IL203311A (enExample) |
| LT (2) | LT2557520T (enExample) |
| MX (3) | MX341573B (enExample) |
| NZ (2) | NZ600407A (enExample) |
| PL (5) | PL2514842T3 (enExample) |
| PT (3) | PT2557517T (enExample) |
| SG (1) | SG183062A1 (enExample) |
| SI (4) | SI2557517T1 (enExample) |
| WO (2) | WO2009013496A1 (enExample) |
| ZA (1) | ZA201000524B (enExample) |
Families Citing this family (303)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
| ES2313143T3 (es) | 2005-04-06 | 2009-03-01 | Maurice Stroun | Metodo para el diagnostico de cancer mediante la deteccion de adn y arn circulantes. |
| US20090317798A1 (en) * | 2005-06-02 | 2009-12-24 | Heid Christian A | Analysis using microfluidic partitioning devices |
| US8515679B2 (en) | 2005-12-06 | 2013-08-20 | Natera, Inc. | System and method for cleaning noisy genetic data and determining chromosome copy number |
| US10083273B2 (en) | 2005-07-29 | 2018-09-25 | Natera, Inc. | System and method for cleaning noisy genetic data and determining chromosome copy number |
| 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 |
| US8532930B2 (en) * | 2005-11-26 | 2013-09-10 | Natera, Inc. | Method for determining the number of copies of a chromosome in the genome of a target individual using genetic data from genetically related individuals |
| US10081839B2 (en) | 2005-07-29 | 2018-09-25 | Natera, Inc | System and method for cleaning noisy genetic data and determining chromosome copy number |
| US11111543B2 (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 |
| 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 |
| EP2363205A3 (en) | 2006-01-11 | 2014-06-04 | Raindance Technologies, Inc. | Microfluidic Devices And Methods Of Use In The Formation And Control Of Nanoreactors |
| HUE030215T2 (en) | 2006-02-02 | 2017-04-28 | Univ Leland Stanford Junior | Non-invasive fetal genetic screening by digital analysis |
| US9562837B2 (en) | 2006-05-11 | 2017-02-07 | Raindance Technologies, Inc. | Systems for handling microfludic droplets |
| US20080050739A1 (en) * | 2006-06-14 | 2008-02-28 | Roland Stoughton | Diagnosis of fetal abnormalities using polymorphisms including short tandem repeats |
| EP2589668A1 (en) | 2006-06-14 | 2013-05-08 | Verinata Health, Inc | Rare cell analysis using sample splitting and DNA tags |
| 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 |
| HUE061020T2 (hu) | 2007-07-23 | 2023-05-28 | Univ Hong Kong Chinese | Nukleinsav-szekvencia kiegyensúlyozatlanságának meghatározására |
| US12180549B2 (en) | 2007-07-23 | 2024-12-31 | The Chinese University Of Hong Kong | Diagnosing fetal chromosomal aneuploidy using genomic sequencing |
| US7888127B2 (en) | 2008-01-15 | 2011-02-15 | Sequenom, Inc. | Methods for reducing adduct formation for mass spectrometry analysis |
| WO2009105531A1 (en) * | 2008-02-19 | 2009-08-27 | Gene Security Network, Inc. | Methods for cell genotyping |
| WO2009114543A2 (en) * | 2008-03-11 | 2009-09-17 | Sequenom, Inc. | Nucleic acid-based tests for prenatal gender determination |
| DE102008019132A1 (de) * | 2008-04-16 | 2009-10-22 | Olympus Life Science Research Europa Gmbh | Verfahren zur quantitativen Bestimmung der Kopienzahl einer vorbestimmten Sequenz in einer Probe |
| US20110092763A1 (en) * | 2008-05-27 | 2011-04-21 | Gene Security Network, Inc. | Methods for Embryo Characterization and Comparison |
| US12038438B2 (en) | 2008-07-18 | 2024-07-16 | Bio-Rad Laboratories, Inc. | Enzyme quantification |
| WO2010009365A1 (en) | 2008-07-18 | 2010-01-21 | Raindance Technologies, Inc. | Droplet libraries |
| US20110178719A1 (en) * | 2008-08-04 | 2011-07-21 | Gene Security Network, Inc. | Methods for Allele Calling and Ploidy Calling |
| US8583380B2 (en) | 2008-09-05 | 2013-11-12 | Aueon, Inc. | Methods for stratifying and annotating cancer drug treatment options |
| 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 |
| ES2620012T3 (es) | 2008-09-20 | 2017-06-27 | The Board Of Trustees Of The Leland Stanford Junior University | Diagnóstico no invasivo de la aneuploidia fetal por secuenciación |
| AU2015202167B2 (en) * | 2008-09-20 | 2017-12-21 | The Board Of Trustees Of The Leland Stanford Junior University | Noninvasive diagnosis of fetal aneuploidy by sequencing |
| US8563242B2 (en) * | 2009-08-11 | 2013-10-22 | The Chinese University Of Hong Kong | Method for detecting chromosomal aneuploidy |
| EP2473638B1 (en) | 2009-09-30 | 2017-08-09 | Natera, Inc. | Methods for non-invasive prenatal ploidy calling |
| AU2010311535B2 (en) * | 2009-10-26 | 2015-05-21 | Lifecodexx Ag | Means and methods for non-invasive diagnosis of chromosomal aneuploidy |
| WO2011053790A2 (en) * | 2009-10-30 | 2011-05-05 | Fluidigm Corporation | Assay of closely linked targets in fetal diagnosis and coincidence detection assay for genetic analysis |
| SMT202300034T1 (it) | 2009-11-05 | 2023-03-17 | Sequenom Inc | Analisi genomica fetale da un campione biologico materno |
| 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 |
| US8932812B2 (en) * | 2009-12-17 | 2015-01-13 | Keygene N.V. | Restriction enzyme based whole genome sequencing |
| DK2516680T3 (en) | 2009-12-22 | 2016-05-02 | Sequenom Inc | Method and kits to identify aneuploidy |
| AU2011207561B2 (en) | 2010-01-19 | 2014-02-20 | Verinata Health, Inc. | Partition defined detection methods |
| US9260745B2 (en) | 2010-01-19 | 2016-02-16 | Verinata Health, Inc. | Detecting and classifying copy number variation |
| AU2015203579B2 (en) * | 2010-01-19 | 2017-12-21 | Verinata Health, Inc. | Sequencing methods and compositions for prenatal diagnoses |
| AU2010343277B2 (en) | 2010-01-19 | 2015-05-28 | Verinata Health, Inc. | Method for determining copy number variations |
| AU2015204302B2 (en) * | 2010-01-19 | 2017-10-05 | Verinata Health, Inc. | Method for determining copy number variations |
| WO2012135730A2 (en) * | 2011-03-30 | 2012-10-04 | Verinata Health, Inc. | Method for verifying bioassay samples |
| US20120100548A1 (en) | 2010-10-26 | 2012-04-26 | Verinata Health, Inc. | Method for determining copy number variations |
| US9323888B2 (en) | 2010-01-19 | 2016-04-26 | Verinata Health, Inc. | Detecting and classifying copy number variation |
| US20120010085A1 (en) | 2010-01-19 | 2012-01-12 | Rava Richard P | Methods for determining fraction of fetal nucleic acids in maternal samples |
| WO2011091046A1 (en) | 2010-01-19 | 2011-07-28 | Verinata Health, Inc. | Identification of polymorphic sequences in mixtures of genomic dna by whole genome sequencing |
| US10388403B2 (en) | 2010-01-19 | 2019-08-20 | Verinata Health, Inc. | Analyzing copy number variation in the detection of cancer |
| US20110312503A1 (en) | 2010-01-23 | 2011-12-22 | Artemis Health, Inc. | Methods of fetal abnormality detection |
| DK2529032T3 (en) | 2010-01-26 | 2017-05-01 | Nipd Genetics Ltd | METHODS AND COMPOSITIONS FOR NON-INVASIVE PRE-NATIONAL DIAGNOSTICATION OF Fetal ANEUPLOIDITIES |
| US9399797B2 (en) | 2010-02-12 | 2016-07-26 | Raindance Technologies, Inc. | Digital analyte analysis |
| JP5934657B2 (ja) * | 2010-02-12 | 2016-06-15 | レインダンス テクノロジーズ, インコーポレイテッド | デジタル検体分析 |
| CN102753703B (zh) * | 2010-04-23 | 2014-12-24 | 深圳华大基因健康科技有限公司 | 胎儿染色体非整倍性的检测方法 |
| US12545960B2 (en) | 2010-05-18 | 2026-02-10 | 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 |
| US9677118B2 (en) | 2014-04-21 | 2017-06-13 | 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 |
| US20190010543A1 (en) | 2010-05-18 | 2019-01-10 | Natera, Inc. | Methods for simultaneous amplification of target loci |
| US12221653B2 (en) | 2010-05-18 | 2025-02-11 | Natera, Inc. | Methods for simultaneous amplification of target loci |
| US11339429B2 (en) | 2010-05-18 | 2022-05-24 | Natera, Inc. | Methods for non-invasive prenatal ploidy calling |
| US8825412B2 (en) | 2010-05-18 | 2014-09-02 | Natera, Inc. | Methods for non-invasive prenatal ploidy calling |
| US11408031B2 (en) | 2010-05-18 | 2022-08-09 | Natera, Inc. | Methods for non-invasive prenatal paternity testing |
| US12152275B2 (en) | 2010-05-18 | 2024-11-26 | 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 |
| WO2013052557A2 (en) * | 2011-10-03 | 2013-04-11 | Natera, Inc. | Methods for preimplantation genetic diagnosis by sequencing |
| 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 |
| US11322224B2 (en) | 2010-05-18 | 2022-05-03 | Natera, Inc. | Methods for non-invasive prenatal ploidy calling |
| CN103069006A (zh) * | 2010-07-23 | 2013-04-24 | 艾索特里克斯遗传实验室有限责任公司 | 区别表达的胚胎或母源基因组区的鉴定及其用途 |
| US20130040375A1 (en) | 2011-08-08 | 2013-02-14 | Tandem Diagnotics, Inc. | Assay systems for genetic analysis |
| 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 |
| US20140342940A1 (en) | 2011-01-25 | 2014-11-20 | Ariosa Diagnostics, Inc. | Detection of Target Nucleic Acids using Hybridization |
| US20120077185A1 (en) * | 2010-08-06 | 2012-03-29 | Tandem Diagnostics, Inc. | Detection of genetic abnormalities and infectious disease |
| US11031095B2 (en) | 2010-08-06 | 2021-06-08 | Ariosa Diagnostics, Inc. | Assay systems for determination of fetal copy number variation |
| US20120034603A1 (en) * | 2010-08-06 | 2012-02-09 | Tandem Diagnostics, Inc. | Ligation-based detection of genetic variants |
| US20130261003A1 (en) | 2010-08-06 | 2013-10-03 | Ariosa Diagnostics, In. | Ligation-based detection of genetic variants |
| US11203786B2 (en) | 2010-08-06 | 2021-12-21 | Ariosa Diagnostics, Inc. | Detection of target nucleic acids using hybridization |
| US10167508B2 (en) | 2010-08-06 | 2019-01-01 | Ariosa Diagnostics, Inc. | Detection of genetic abnormalities |
| CN103069004B (zh) * | 2010-08-13 | 2015-03-11 | 深圳华大基因医学有限公司 | 一种细胞染色体分析方法 |
| RU2565550C2 (ru) | 2010-09-24 | 2015-10-20 | Те Борд Оф Трастиз Оф Те Лилэнд Стэнфорд Джуниор Юниверсити | Прямой захват, амплификация и секвенирование днк-мишени с использованием иммобилизированных праймеров |
| EP2633311A4 (en) * | 2010-10-26 | 2014-05-07 | Univ Stanford | NONINVASIVE FETAL GENETIC SCREENING THROUGH SEQUENCING ANALYSIS |
| SG10202008532PA (en) * | 2010-11-30 | 2020-10-29 | Univ Hong Kong Chinese | Detection of genetic or molecular aberrations associated with cancer |
| CN103620055A (zh) | 2010-12-07 | 2014-03-05 | 利兰·斯坦福青年大学托管委员会 | 在全基因组规模非侵入性确定亲本单倍型的胎儿遗传 |
| EP2656263B1 (en) | 2010-12-22 | 2019-11-06 | Natera, Inc. | Methods for non-invasive prenatal paternity testing |
| JP6105485B2 (ja) * | 2011-01-05 | 2017-04-05 | 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 Hong Kong | 胎児の性染色体遺伝子型の非侵襲的出生前同定 |
| US20120190020A1 (en) * | 2011-01-25 | 2012-07-26 | Aria Diagnostics, Inc. | Detection of genetic abnormalities |
| US8756020B2 (en) | 2011-01-25 | 2014-06-17 | Ariosa Diagnostics, Inc. | Enhanced risk probabilities using biomolecule estimations |
| US10131947B2 (en) | 2011-01-25 | 2018-11-20 | Ariosa Diagnostics, Inc. | Noninvasive detection of fetal aneuploidy in egg donor pregnancies |
| US9994897B2 (en) | 2013-03-08 | 2018-06-12 | Ariosa Diagnostics, Inc. | Non-invasive fetal sex determination |
| US11270781B2 (en) | 2011-01-25 | 2022-03-08 | Ariosa Diagnostics, Inc. | Statistical analysis for non-invasive sex chromosome aneuploidy determination |
| EP2902500B1 (en) * | 2011-02-09 | 2017-01-11 | Natera, Inc. | Methods for non-invasive prenatal ploidy calling |
| JP6153874B2 (ja) | 2011-02-09 | 2017-06-28 | ナテラ, インコーポレイテッド | 非侵襲的出生前倍数性呼び出しのための方法 |
| EP2675819B1 (en) | 2011-02-18 | 2020-04-08 | Bio-Rad Laboratories, Inc. | Compositions and methods for molecular labeling |
| EP2682887A2 (en) * | 2011-02-24 | 2014-01-08 | The Chinese University Of Hong Kong | Determining fetal DNA percentage for twins |
| EP2689029A1 (en) * | 2011-03-22 | 2014-01-29 | Life Technologies Corporation | Identification of linkage using multiplex digital pcr |
| WO2012129363A2 (en) | 2011-03-24 | 2012-09-27 | President And Fellows Of Harvard College | Single cell nucleic acid detection and analysis |
| EP3456844B1 (en) | 2011-04-12 | 2020-06-10 | Verinata Health, Inc. | Resolving genome fractions using polymorphism counts |
| GB2484764B (en) * | 2011-04-14 | 2012-09-05 | Verinata Health Inc | Normalizing chromosomes for the determination and verification of common and rare chromosomal aneuploidies |
| US9411937B2 (en) | 2011-04-15 | 2016-08-09 | Verinata Health, Inc. | Detecting and classifying copy number variation |
| EP2702168B1 (en) | 2011-04-29 | 2018-01-17 | Sequenom, Inc. | Quantification of a minority nucleic acid species |
| US20140235474A1 (en) | 2011-06-24 | 2014-08-21 | Sequenom, Inc. | Methods and processes for non invasive assessment of a genetic variation |
| US9547748B2 (en) | 2011-06-29 | 2017-01-17 | Bgi Health Service Co., Ltd. | Method for determining fetal chromosomal abnormality |
| US20140141997A1 (en) * | 2011-06-30 | 2014-05-22 | National University Of Singapore | Foetal nucleated red blood cell detection |
| US20130157875A1 (en) * | 2011-07-20 | 2013-06-20 | Anthony P. Shuber | Methods for assessing genomic instabilities |
| CA2840418C (en) * | 2011-07-26 | 2019-10-29 | Verinata Health, Inc. | Method for determining the presence or absence of different aneuploidies in a sample |
| US8712697B2 (en) | 2011-09-07 | 2014-04-29 | Ariosa Diagnostics, Inc. | Determination of copy number variations using binomial probability calculations |
| US20130110407A1 (en) * | 2011-09-16 | 2013-05-02 | Complete Genomics, Inc. | Determining variants in genome of a heterogeneous sample |
| WO2013040773A1 (zh) * | 2011-09-21 | 2013-03-28 | 深圳华大基因科技有限公司 | 确定单细胞染色体非整倍性的方法和系统 |
| US10196681B2 (en) | 2011-10-06 | 2019-02-05 | 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 |
| EP3922731A3 (en) | 2011-10-06 | 2022-01-05 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| US9984198B2 (en) | 2011-10-06 | 2018-05-29 | Sequenom, Inc. | Reducing sequence read count error in assessment of complex genetic variations |
| US20140242588A1 (en) | 2011-10-06 | 2014-08-28 | 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 |
| CA2851537C (en) | 2011-10-11 | 2020-12-29 | 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 |
| CN102329876B (zh) * | 2011-10-14 | 2014-04-02 | 深圳华大基因科技有限公司 | 一种测定待检测样本中疾病相关核酸分子的核苷酸序列的方法 |
| WO2013057568A1 (en) | 2011-10-18 | 2013-04-25 | Multiplicom Nv | Fetal chromosomal aneuploidy diagnosis |
| WO2013062856A1 (en) | 2011-10-27 | 2013-05-02 | Verinata Health, Inc. | Set membership testers for aligning nucleic acid samples |
| EP2602733A3 (en) * | 2011-12-08 | 2013-08-14 | Koninklijke Philips Electronics N.V. | Biological cell assessment using whole genome sequence and oncological therapy planning using same |
| EP2805280B1 (en) | 2012-01-20 | 2022-10-05 | Sequenom, Inc. | Diagnostic processes that factor experimental conditions |
| US9605313B2 (en) | 2012-03-02 | 2017-03-28 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| US9892230B2 (en) | 2012-03-08 | 2018-02-13 | The Chinese University Of Hong Kong | Size-based analysis of fetal or tumor DNA fraction in plasma |
| US10053729B2 (en) | 2012-03-26 | 2018-08-21 | The Johns Hopkins University | Rapid aneuploidy detection |
| EP2834376B1 (en) * | 2012-04-06 | 2017-03-15 | The Chinese University Of Hong Kong | Noninvasive prenatal diagnosis of fetal trisomy by allelic ratio analysis using targeted massively parallel sequencing |
| AU2013249012B2 (en) * | 2012-04-19 | 2019-03-28 | The Medical College Of Wisconsin, Inc. | Highly sensitive surveillance using detection of cell free DNA |
| US10289800B2 (en) | 2012-05-21 | 2019-05-14 | Ariosa Diagnostics, Inc. | Processes for calculating phased fetal genomic sequences |
| US9840732B2 (en) | 2012-05-21 | 2017-12-12 | Fluidigm Corporation | Single-particle analysis of particle populations |
| ES2902401T3 (es) | 2012-05-21 | 2022-03-28 | Sequenom Inc | Métodos y procesos para la evaluación no invasiva de variaciones genéticas |
| US10504613B2 (en) | 2012-12-20 | 2019-12-10 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| US9920361B2 (en) | 2012-05-21 | 2018-03-20 | Sequenom, Inc. | Methods and compositions for analyzing nucleic acid |
| US11261494B2 (en) * | 2012-06-21 | 2022-03-01 | The Chinese University Of Hong Kong | Method of measuring a fractional concentration of tumor DNA |
| US10497461B2 (en) | 2012-06-22 | 2019-12-03 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| EP2872648B1 (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 |
| AU2013292287A1 (en) | 2012-07-19 | 2015-02-19 | Ariosa Diagnostics, Inc. | Multiplexed sequential ligation-based detection of genetic variants |
| US20140100126A1 (en) | 2012-08-17 | 2014-04-10 | Natera, Inc. | Method for Non-Invasive Prenatal Testing Using Parental Mosaicism Data |
| DE202013012824U1 (de) | 2012-09-04 | 2020-03-10 | Guardant Health, Inc. | Systeme zum Erfassen von seltenen Mutationen und einer Kopienzahlvariation |
| US10876152B2 (en) | 2012-09-04 | 2020-12-29 | Guardant Health, Inc. | Systems and methods to detect rare mutations and copy number variation |
| US20160040229A1 (en) | 2013-08-16 | 2016-02-11 | Guardant Health, Inc. | Systems and methods to detect rare mutations and copy number variation |
| US11913065B2 (en) | 2012-09-04 | 2024-02-27 | Guardent Health, Inc. | Systems and methods to detect rare mutations and copy number variation |
| PL3354747T3 (pl) | 2012-09-20 | 2021-07-26 | The Chinese University Of Hong Kong | Nieinwazyjne określanie metylomu guza z wykorzystaniem osocza |
| 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 |
| WO2014051522A1 (en) * | 2012-09-26 | 2014-04-03 | Agency For Science, Technology And Research | Biomarkers for down syndrome prenatal diagnosis |
| US10482994B2 (en) | 2012-10-04 | 2019-11-19 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| CA2887094C (en) | 2012-10-04 | 2021-09-07 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| DK2728014T3 (en) * | 2012-10-31 | 2016-01-25 | Genesupport Sa | A non-invasive method for the detection of fetal chromosomal aneuploidy |
| US10643738B2 (en) | 2013-01-10 | 2020-05-05 | The Chinese University Of Hong Kong | Noninvasive prenatal molecular karyotyping from maternal plasma |
| US20130309666A1 (en) | 2013-01-25 | 2013-11-21 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| WO2014130589A1 (en) * | 2013-02-20 | 2014-08-28 | Bionano Genomics, Inc. | Characterization of molecules in nanofluidics |
| WO2014133369A1 (ko) * | 2013-02-28 | 2014-09-04 | 주식회사 테라젠이텍스 | 유전체 서열분석을 이용한 태아 염색체 이수성의 진단 방법 및 장치 |
| ES2670544T3 (es) * | 2013-02-28 | 2018-05-30 | The Chinese University Of Hong Kong | Análisis de transcriptoma de plasma materno por secuenciación masiva en paralelo de ARN |
| US20130189684A1 (en) | 2013-03-12 | 2013-07-25 | Sequenom, Inc. | Quantification of cell-specific nucleic acid markers |
| US9305756B2 (en) | 2013-03-13 | 2016-04-05 | Agena Bioscience, Inc. | Preparation enhancements and methods of use for MALDI mass spectrometry |
| WO2014168711A1 (en) | 2013-03-13 | 2014-10-16 | Sequenom, Inc. | Primers for dna methylation analysis |
| KR20150132216A (ko) | 2013-03-15 | 2015-11-25 | 더 차이니즈 유니버시티 오브 홍콩 | 다태 임신에 대한 태아 게놈의 결정 |
| EP4187543A1 (en) | 2013-04-03 | 2023-05-31 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| WO2014182726A2 (en) | 2013-05-07 | 2014-11-13 | Sequenom, Inc. | Genetic markers for macular degeneration disorder treatment |
| US10699800B2 (en) | 2013-05-24 | 2020-06-30 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| CN112037860B (zh) * | 2013-06-13 | 2024-02-23 | 豪夫迈·罗氏有限公司 | 用于非入侵性性染色体非整倍性确定的统计分析 |
| KR102299305B1 (ko) | 2013-06-21 | 2021-09-06 | 시쿼넘, 인코포레이티드 | 유전적 변이의 비침습 평가를 위한 방법 및 프로세스 |
| WO2015006932A1 (zh) * | 2013-07-17 | 2015-01-22 | 深圳华大基因科技有限公司 | 一种染色体非整倍性检测方法及装置 |
| 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 |
| US10577655B2 (en) | 2013-09-27 | 2020-03-03 | Natera, Inc. | Cell free DNA diagnostic testing standards |
| US10262755B2 (en) | 2014-04-21 | 2019-04-16 | Natera, Inc. | Detecting cancer mutations and aneuploidy in chromosomal segments |
| US9499870B2 (en) | 2013-09-27 | 2016-11-22 | Natera, Inc. | Cell free DNA diagnostic testing standards |
| DK3053071T3 (da) | 2013-10-04 | 2024-01-22 | Sequenom Inc | Fremgangsmåder og processer til ikke-invasiv bedømmelse af genetiske variationer |
| EP3495496B1 (en) | 2013-10-07 | 2020-11-25 | Sequenom, Inc. | Methods and processes for non-invasive assessment of chromosome alterations |
| JP6534191B2 (ja) * | 2013-10-21 | 2019-06-26 | ベリナタ ヘルス インコーポレイテッド | コピー数変動を決定することにおける検出の感度を向上させるための方法 |
| CN105765076B (zh) * | 2013-12-17 | 2019-07-19 | 深圳华大基因股份有限公司 | 一种染色体非整倍性检测方法及装置 |
| ES2660989T3 (es) | 2013-12-28 | 2018-03-27 | Guardant Health, Inc. | Métodos y sistemas para detectar variantes genéticas |
| US11365447B2 (en) | 2014-03-13 | 2022-06-21 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| CN113774132A (zh) | 2014-04-21 | 2021-12-10 | 纳特拉公司 | 检测染色体片段中的突变和倍性 |
| US12492429B2 (en) | 2014-04-21 | 2025-12-09 | Natera, Inc. | Detecting mutations and ploidy in chromosomal segments |
| RU2602366C2 (ru) * | 2014-05-21 | 2016-11-20 | Общество С Ограниченной Ответственностью "Тестген" | Способ получения днк-праймеров и зондов для малоинвазивной пренатальной пцр-диагностики трисомии 21-й хромосомы у плода по крови беременной женщины и диагностический набор для ее осуществления |
| KR101663171B1 (ko) * | 2014-05-27 | 2016-10-14 | 이원 다이애그노믹스 게놈센타(주) | 다운증후군 진단을 위한 바이오마커 및 그의 용도 |
| JP6659672B2 (ja) | 2014-05-30 | 2020-03-04 | ベリナタ ヘルス インコーポレイテッド | 胎児染色体部分異数性およびコピー数変動の検出 |
| US20180173846A1 (en) | 2014-06-05 | 2018-06-21 | Natera, Inc. | Systems and Methods for Detection of Aneuploidy |
| KR20160003547A (ko) * | 2014-07-01 | 2016-01-11 | 바이오코아 주식회사 | 디지털 pcr을 이용하여 임부의 혈액 또는 혈장으로부터 태아의 유전자 정보를 분석하는 방법 |
| TWI895765B (zh) | 2014-07-18 | 2025-09-01 | 香港中文大學 | Dna混合物中之組織甲基化模式分析 |
| KR20160010277A (ko) * | 2014-07-18 | 2016-01-27 | 에스케이텔레콤 주식회사 | 산모의 무세포 dna의 차세대 서열분석을 통한 태아의 단일유전자 유전변이의 예측방법 |
| WO2016010401A1 (ko) * | 2014-07-18 | 2016-01-21 | 에스케이텔레콘 주식회사 | 산모의 혈청 dna를 이용한 태아의 단일유전자 유전변이의 예측방법 |
| US20160026759A1 (en) * | 2014-07-22 | 2016-01-28 | Yourgene Bioscience | Detecting Chromosomal Aneuploidy |
| CA2956208C (en) | 2014-07-25 | 2025-07-08 | University Of Washington | METHODS FOR DETERMINING TISSUES AND/OR CELL TYPES RENDERING CELL-FREE DNA AND RELATED METHODS FOR DETERMINING A DISEASE OR DISORDER |
| EP3175000B1 (en) | 2014-07-30 | 2020-07-29 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| AU2015360298B2 (en) | 2014-12-12 | 2018-06-07 | Verinata Health, Inc. | Using cell-free DNA fragment size to determine copy number 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 |
| US10319463B2 (en) * | 2015-01-23 | 2019-06-11 | The Chinese University Of Hong Kong | Combined size- and count-based analysis of maternal plasma for detection of fetal subchromosomal aberrations |
| SG11201706529TA (en) | 2015-02-10 | 2017-09-28 | Univ Hong Kong Chinese | Detecting mutations for cancer screening and fetal analysis |
| CN104789686B (zh) * | 2015-05-06 | 2018-09-07 | 浙江安诺优达生物科技有限公司 | 检测染色体非整倍性的试剂盒和装置 |
| CN104789466B (zh) * | 2015-05-06 | 2018-03-13 | 安诺优达基因科技(北京)有限公司 | 检测染色体非整倍性的试剂盒和装置 |
| DK3294906T3 (en) | 2015-05-11 | 2024-08-05 | Natera Inc | Methods for determining ploidy |
| US10395759B2 (en) | 2015-05-18 | 2019-08-27 | Regeneron Pharmaceuticals, Inc. | Methods and systems for copy number variant detection |
| PT3666902T (pt) | 2015-05-22 | 2024-09-19 | Medicover Public Co Ltd | Análise paralela multiplexada de regiões genómicas alvo para testes pré-natais não invasivos |
| CN104951671B (zh) * | 2015-06-10 | 2017-09-19 | 东莞博奥木华基因科技有限公司 | 基于单样本外周血检测胎儿染色体非整倍性的装置 |
| US11795496B2 (en) * | 2015-06-24 | 2023-10-24 | Oxford BioDynamics PLC | Epigenetic chromosome interactions |
| EP3118323A1 (en) | 2015-07-13 | 2017-01-18 | Cartagenia N.V. | System and methodology for the analysis of genomic data obtained from a subject |
| AU2016293025A1 (en) | 2015-07-13 | 2017-11-02 | Agilent Technologies Belgium Nv | System and methodology for the analysis of genomic data obtained from a subject |
| DK3739061T3 (da) | 2015-07-20 | 2022-04-19 | Univ Hong Kong Chinese | Methyleringsmønsteranalyse af haplotyper i væv i DNA-blanding |
| US10453556B2 (en) | 2015-07-23 | 2019-10-22 | The Chinese University Of Hong Kong | Analysis of fragmentation patterns of cell-free DNA |
| CA2995422A1 (en) | 2015-08-12 | 2017-02-16 | The Chinese University Of Hong Kong | Single-molecule sequencing of plasma dna |
| EP3347466B9 (en) | 2015-09-08 | 2024-06-26 | Cold Spring Harbor Laboratory | Genetic copy number determination using high throughput multiplex sequencing of smashed nucleotides |
| US10774375B2 (en) | 2015-09-18 | 2020-09-15 | Agena Bioscience, Inc. | Methods and compositions for the quantitation of mitochondrial nucleic acid |
| WO2017051996A1 (ko) * | 2015-09-24 | 2017-03-30 | 에스케이텔레콤 주식회사 | 비침습적 태아 염색체 이수성 판별 방법 |
| CN105132572B (zh) * | 2015-09-25 | 2018-03-02 | 邯郸市康业生物科技有限公司 | 一种无创产前筛查21‑三体综合征试剂盒 |
| KR101848438B1 (ko) * | 2015-10-29 | 2018-04-13 | 바이오코아 주식회사 | 디지털 pcr을 이용한 산전진단 방법 |
| CN117174167A (zh) | 2015-12-17 | 2023-12-05 | 夸登特健康公司 | 通过分析无细胞dna确定肿瘤基因拷贝数的方法 |
| GB201522665D0 (en) * | 2015-12-22 | 2016-02-03 | Premaitha Ltd | Detection of chromosome abnormalities |
| KR101817180B1 (ko) * | 2016-01-20 | 2018-01-10 | 이원다이애그노믹스(주) | 염색체 이상 판단 방법 |
| US10095831B2 (en) | 2016-02-03 | 2018-10-09 | Verinata Health, Inc. | Using cell-free DNA fragment size to determine copy number variations |
| EP3414691A1 (en) | 2016-02-12 | 2018-12-19 | Regeneron Pharmaceuticals, Inc. | Methods and systems for detection of abnormal karyotypes |
| DK3443119T3 (da) | 2016-04-15 | 2022-05-23 | Natera Inc | Fremgangsmåde til bestemmelse af lunge cancer |
| WO2017192589A1 (en) | 2016-05-02 | 2017-11-09 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Neutralizing antibodies to influenza ha and their use and identification |
| KR101879329B1 (ko) * | 2016-06-13 | 2018-07-17 | 충북대학교 산학협력단 | 유전자 차별 발현 분석을 위한 RNA-seq 발현량 데이터 시뮬레이션 방법 및 이를 기록한 기록매체 |
| US11200963B2 (en) | 2016-07-27 | 2021-12-14 | Sequenom, Inc. | Genetic copy number alteration classifications |
| WO2018064486A1 (en) | 2016-09-29 | 2018-04-05 | Counsyl, Inc. | Noninvasive prenatal screening using dynamic iterative depth optimization |
| KR20240155386A (ko) | 2016-09-30 | 2024-10-28 | 가던트 헬쓰, 인크. | 무세포 핵산의 다중-해상도 분석 방법 |
| US9850523B1 (en) | 2016-09-30 | 2017-12-26 | Guardant Health, Inc. | Methods for multi-resolution analysis of cell-free nucleic acids |
| WO2018067517A1 (en) | 2016-10-04 | 2018-04-12 | Natera, Inc. | Methods for characterizing copy number variation using proximity-litigation sequencing |
| CA3041647A1 (en) | 2016-10-24 | 2018-05-03 | The Chinese University Of Hong Kong | Methods and systems for tumor detection |
| GB201618485D0 (en) | 2016-11-02 | 2016-12-14 | Ucl Business Plc | Method of detecting tumour recurrence |
| CA3039685A1 (en) | 2016-11-30 | 2018-06-07 | The Chinese University Of Hong Kong | Analysis of cell-free dna in urine and other samples |
| US10011870B2 (en) | 2016-12-07 | 2018-07-03 | Natera, Inc. | Compositions and methods for identifying nucleic acid molecules |
| BR112019014208A2 (pt) * | 2017-01-11 | 2020-03-17 | Quest Diagnostics Investments Llc | Métodos para detectar diagnóstico falso-positivo de aneuploidia cromossômica em um feto e para detectar diagnóstico aneuploidiadiagnóstico de aneuploidia cromossômica falso-positiva em um feto. |
| WO2018140521A1 (en) | 2017-01-24 | 2018-08-02 | Sequenom, Inc. | Methods and processes for assessment of genetic variations |
| ES2990117T3 (es) | 2017-01-25 | 2024-11-28 | Univ Hong Kong Chinese | Aplicaciones de diagnóstico que utilizan fragmentos de ácido nucleico |
| WO2018156418A1 (en) | 2017-02-21 | 2018-08-30 | Natera, Inc. | Compositions, methods, and kits for isolating nucleic acids |
| PT3596233T (pt) | 2017-03-17 | 2022-08-22 | Sequenom Inc | Métodos e processos para avaliação de mosaicismo genético |
| JP2020524519A (ja) | 2017-06-20 | 2020-08-20 | ザ 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The Medical College of Wisconsin, Inc. | 全セルフリーdnaによる移植合併症リスクの評価 |
| ES2959360T3 (es) | 2017-07-26 | 2024-02-23 | Univ Hong Kong Chinese | Mejora del cribado del cáncer mediante ácidos nucleicos víricos acelulares |
| HRP20210826T1 (hr) | 2017-07-26 | 2021-07-09 | Trisomytest, S.R.O. | Postupak neinvazivnog prenatalnog otkrivanja fetalnog kromosoma aneuploidija iz majčine krvi na temelju bayes mreže |
| EP3662479A1 (en) | 2017-08-04 | 2020-06-10 | Trisomytest, s.r.o. | A method for non-invasive prenatal detection of fetal sex chromosomal abnormalities and fetal sex determination for singleton and twin pregnancies |
| WO2019028462A1 (en) | 2017-08-04 | 2019-02-07 | Billiontoone, Inc. | TARGET-ASSOCIATED MOLECULES FOR CHARACTERIZATION ASSOCIATED WITH BIOLOGICAL TARGETS |
| US11519024B2 (en) | 2017-08-04 | 2022-12-06 | Billiontoone, Inc. | Homologous genomic regions for characterization associated with biological targets |
| SK862017A3 (sk) | 2017-08-24 | 2020-05-04 | Grendar Marian Doc Mgr Phd | Spôsob použitia fetálnej frakcie a chromozómovej reprezentácie pri určovaní aneuploidného stavu v neinvazívnom prenatálnom testovaní |
| WO2019043656A1 (en) | 2017-09-01 | 2019-03-07 | Genus Plc | METHODS AND SYSTEMS FOR ASSESSING AND / OR QUANTIFYING POPULATIONS OF SPERMATOZOIDS WITH SEXUAL ASYMMETRY |
| JP2021500883A (ja) | 2017-10-27 | 2021-01-14 | ジュノ ダイアグノスティックス,インク. | 超微量リキッドバイオプシーのためのデバイス、システム、および方法 |
| US11168356B2 (en) | 2017-11-02 | 2021-11-09 | The Chinese University Of Hong Kong | Using nucleic acid size range for noninvasive cancer detection |
| WO2019118926A1 (en) | 2017-12-14 | 2019-06-20 | Tai Diagnostics, Inc. | Assessing graft suitability for transplantation |
| CN112365927B (zh) * | 2017-12-28 | 2023-08-25 | 安诺优达基因科技(北京)有限公司 | Cnv检测装置 |
| SG11202006110UA (en) | 2018-01-05 | 2020-07-29 | Billiontoone Inc | Quality control templates for ensuring validity of sequencing-based assays |
| CN108282396B (zh) * | 2018-02-13 | 2022-02-22 | 湖南快乐阳光互动娱乐传媒有限公司 | 一种im集群中的多级消息广播方法及系统 |
| WO2019161244A1 (en) | 2018-02-15 | 2019-08-22 | Natera, Inc. | Methods for isolating nucleic acids with size selection |
| KR102099151B1 (ko) * | 2018-03-05 | 2020-04-10 | 서강대학교산학협력단 | 마이크로웰 어레이를 이용한 dPCR 분석방법 및 분석장치 |
| WO2019178289A1 (en) | 2018-03-13 | 2019-09-19 | Grail, Inc. | Method and system for selecting, managing, and analyzing data of high dimensionality |
| CA3095030A1 (en) | 2018-03-30 | 2019-10-03 | Juno Diagnostics, Inc. | Deep learning-based methods, devices, and systems for prenatal testing |
| CN110832086A (zh) | 2018-04-02 | 2020-02-21 | 伊鲁米那股份有限公司 | 用于制造用于基于序列的遗传检验的对照的组合物和方法 |
| JP7348603B2 (ja) | 2018-04-02 | 2023-09-21 | エニュメラ・モレキュラー・インコーポレイテッド | 核酸分子を計数するための方法、システム、および組成物 |
| DK3781714T3 (da) | 2018-04-14 | 2026-03-30 | Natera Inc | Fremgangsmåder til cancerpåvisning og -overvågning ved personlig påvisning af cirkulerende tumor-dna |
| EP3788172B1 (en) | 2018-05-03 | 2025-04-02 | The Chinese University Of Hong Kong | Size-tagged preferred ends and orientation-aware analysis for measuring properties of cell-free mixtures |
| CN112888459B (zh) | 2018-06-01 | 2023-05-23 | 格里尔公司 | 卷积神经网络系统及数据分类方法 |
| US12234509B2 (en) | 2018-07-03 | 2025-02-25 | Natera, Inc. | Methods for detection of donor-derived cell-free DNA |
| JP7637615B2 (ja) * | 2018-09-04 | 2025-02-28 | ガーダント ヘルス, インコーポレイテッド | 無細胞核酸試料におけるアレル不均衡を検出するための方法およびシステム |
| JP7485653B2 (ja) | 2018-09-07 | 2024-05-16 | セクエノム, インコーポレイテッド | 移植片拒絶を検出する方法およびシステム |
| US20210407621A1 (en) | 2018-10-12 | 2021-12-30 | Nantomics, Llc | Prenatal purity assessments using bambam |
| EP3874060B1 (en) * | 2018-10-31 | 2024-10-16 | Guardant Health, Inc. | Method and system for calibrating epigenetic partitioning assays |
| CN109545379B (zh) * | 2018-12-05 | 2021-11-09 | 易必祥 | 基于基因大数据的治疗系统 |
| US11581062B2 (en) | 2018-12-10 | 2023-02-14 | Grail, Llc | Systems and methods for classifying patients with respect to multiple cancer classes |
| JP6783437B2 (ja) * | 2019-01-04 | 2020-11-11 | 株式会社大一商会 | 遊技機 |
| JP2020108548A (ja) * | 2019-01-04 | 2020-07-16 | 株式会社大一商会 | 遊技機 |
| CA3126428A1 (en) | 2019-01-31 | 2020-08-06 | Guardant Health, Inc. | Compositions and methods for isolating cell-free dna |
| WO2020172164A1 (en) | 2019-02-19 | 2020-08-27 | Sequenom, Inc. | Compositions, methods, and systems to detect hematopoietic stem cell transplantation status |
| KR20200109544A (ko) * | 2019-03-13 | 2020-09-23 | 울산대학교 산학협력단 | 공통 유전자 추출에 의한 다중 암 분류 방법 |
| US12098429B2 (en) | 2019-03-25 | 2024-09-24 | The Chinese University Of Hong Kong | Determining linear and circular forms of circulating nucleic acids |
| EP3947718A4 (en) | 2019-04-02 | 2022-12-21 | Enumera Molecular, Inc. | METHODS, SYSTEMS AND COMPOSITIONS FOR COUNTING NUCLEIC ACID MOLECULES |
| US11931674B2 (en) | 2019-04-04 | 2024-03-19 | Natera, Inc. | Materials and methods for processing blood samples |
| US12497662B2 (en) | 2019-04-16 | 2025-12-16 | Grail, Inc. | Systems and methods for tumor fraction estimation from small variants |
| RU2717023C1 (ru) * | 2019-04-24 | 2020-03-17 | Общество с ограниченной ответственностью "ГЕНОТЕК ИТ" | Способ определения кариотипа плода беременной женщины на основании секвенирования гибридных прочтений, состоящих из коротких фрагментов внеклеточной ДНК |
| EP3980559A1 (en) | 2019-06-06 | 2022-04-13 | Natera, Inc. | Methods for detecting immune cell dna and monitoring immune system |
| TWI724710B (zh) * | 2019-08-16 | 2021-04-11 | 財團法人工業技術研究院 | 建構數位化疾病模組的方法及裝置 |
| SG11202101070QA (en) | 2019-08-16 | 2021-03-30 | Univ Hong Kong Chinese | Determination Of Base Modifications Of Nucleic Acids |
| CN114728069B (zh) * | 2019-09-30 | 2025-04-08 | 迈欧米公司 | 用于体外受精的多基因风险得分 |
| US20240093281A1 (en) * | 2019-10-16 | 2024-03-21 | Stilla Technologies | Determination of nucleic acid sequence concentrations |
| WO2021137770A1 (en) | 2019-12-30 | 2021-07-08 | Geneton S.R.O. | Method for fetal fraction estimation based on detection and interpretation of single nucleotide variants |
| WO2021139716A1 (en) * | 2020-01-08 | 2021-07-15 | The Chinese University Of Hong Kong | Biterminal dna fragment types in cell-free samples and uses thereof |
| US11211144B2 (en) | 2020-02-18 | 2021-12-28 | Tempus Labs, Inc. | Methods and systems for refining copy number variation in a liquid biopsy assay |
| US11475981B2 (en) | 2020-02-18 | 2022-10-18 | Tempus Labs, Inc. | Methods and systems for dynamic variant thresholding in a liquid biopsy assay |
| US11211147B2 (en) | 2020-02-18 | 2021-12-28 | Tempus Labs, Inc. | Estimation of circulating tumor fraction using off-target reads of targeted-panel sequencing |
| CA3173571A1 (en) | 2020-02-28 | 2021-09-02 | Laboratory Corporation Of America Holdings | Compositions, methods, and systems for paternity determination |
| US20220245934A1 (en) * | 2020-05-11 | 2022-08-04 | Nec Corporation | Determination device, determination method, and recording medium |
| US12412386B2 (en) | 2020-05-11 | 2025-09-09 | Nec Corporation | Determination device, determination method, and recording medium |
| WO2021229662A1 (ja) | 2020-05-11 | 2021-11-18 | 日本電気株式会社 | 判定装置、判定方法および記録媒体 |
| WO2021237105A1 (en) * | 2020-05-22 | 2021-11-25 | Invitae Corporation | Methods for determining a genetic variation |
| KR20230038263A (ko) * | 2020-07-13 | 2023-03-17 | 더 차이니즈 유니버시티 오브 홍콩 | 무세포 핵산에 대한 뉴클레아제 관련 말단 특징 분석 |
| JP2023552015A (ja) * | 2020-12-02 | 2023-12-14 | イルミナ ソフトウェア, インコーポレイテッド | 遺伝子変異を検出するためのシステム及び方法 |
| CN114645080A (zh) * | 2020-12-21 | 2022-06-21 | 高嵩 | 一种利用多态性位点和靶位点测序检测胎儿遗传变异的方法 |
| WO2022246291A1 (en) * | 2021-05-21 | 2022-11-24 | Invitae Corporation | Methods for determining a genetic variation |
| US12252745B2 (en) | 2021-09-02 | 2025-03-18 | Enumerix, Inc. | Detection and digital quantitation of multiple targets |
| CN113981062B (zh) * | 2021-10-14 | 2024-02-20 | 武汉蓝沙医学检验实验室有限公司 | 以非生父和母亲dna评估胎儿dna浓度的方法及应用 |
| AU2023240345A1 (en) | 2022-03-21 | 2024-10-10 | Billion Toone, Inc. | Molecule counting of methylated cell-free dna for treatment monitoring |
| US20260092314A1 (en) * | 2022-09-16 | 2026-04-02 | Myriad Women's Health, Inc. | Rna-facs for rare cell isolation and detection of genetic variants |
| US20240384334A1 (en) * | 2023-05-09 | 2024-11-21 | Centre For Novostics | Efficient digital measurement of long nucleic acid fragments |
| WO2024242641A1 (en) | 2023-05-25 | 2024-11-28 | Medirex Group Academy N.O. | Method for detection of samples with insufficient amount of fetal and circulating tumor dna fragments for non-invasive genetic testing |
| WO2024253600A1 (en) | 2023-06-07 | 2024-12-12 | Univerzita Komenského v Bratislave | Method for estimation of cell-free dna mixture proportions based on telomere-derived fragments |
| CN118098345B (zh) * | 2024-04-28 | 2024-08-09 | 深圳市真迈生物科技有限公司 | 一种染色体非整倍体的检测方法、装置、设备及存储介质 |
| WO2025234041A1 (ja) * | 2024-05-09 | 2025-11-13 | 株式会社日立ハイテク | 対象核酸を検出する方法、および対象核酸検出システム |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2249820C1 (ru) * | 2003-08-18 | 2005-04-10 | Лактионов Павел Петрович | Способ ранней диагностики заболеваний, связанных с нарушением функционирования генетического аппарата клетки |
Family Cites Families (110)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5641628A (en) * | 1989-11-13 | 1997-06-24 | Children's Medical Center Corporation | Non-invasive method for isolation and detection of fetal DNA |
| WO1993007296A1 (en) * | 1991-10-03 | 1993-04-15 | Indiana University Foundation | Method for screening for alzheimer's disease |
| US6100029A (en) * | 1996-08-14 | 2000-08-08 | Exact Laboratories, Inc. | Methods for the detection of chromosomal aberrations |
| GB9704444D0 (en) * | 1997-03-04 | 1997-04-23 | Isis Innovation | Non-invasive prenatal diagnosis |
| US20010051341A1 (en) * | 1997-03-04 | 2001-12-13 | Isis Innovation Limited | Non-invasive prenatal diagnosis |
| 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 |
| US6558901B1 (en) * | 1997-05-02 | 2003-05-06 | Biomerieux Vitek | Nucleic acid assays |
| US6566101B1 (en) * | 1997-06-16 | 2003-05-20 | Anthony P. Shuber | Primer extension methods for detecting nucleic acids |
| US20030022207A1 (en) | 1998-10-16 | 2003-01-30 | Solexa, Ltd. | Arrayed polynucleotides and their use in genome analysis |
| ATE556149T1 (de) * | 1999-02-23 | 2012-05-15 | Caliper Life Sciences Inc | Manipulation von mikropartikeln in mikrofluidischen systemen |
| AUPQ008799A0 (en) * | 1999-04-30 | 1999-05-27 | Tillett, Daniel | Genome sequencing |
| US6818395B1 (en) * | 1999-06-28 | 2004-11-16 | California Institute Of Technology | Methods and apparatus for analyzing polynucleotide sequences |
| US6440706B1 (en) * | 1999-08-02 | 2002-08-27 | Johns Hopkins University | Digital amplification |
| JP2003519829A (ja) * | 1999-10-13 | 2003-06-24 | シークエノム・インコーポレーテツド | データベースを作成する方法および多型遺伝的マーカーを同定するためのデータベース |
| GB0009784D0 (en) * | 2000-04-20 | 2000-06-07 | Simeg Limited | Methods for clinical diagnosis |
| US20030087231A1 (en) | 2000-05-19 | 2003-05-08 | Albertson Donna G. | Methods and compositions for preparation of a polynucleotide array |
| GB0016742D0 (en) * | 2000-07-10 | 2000-08-30 | Simeg Limited | Diagnostic method |
| US6664056B2 (en) * | 2000-10-17 | 2003-12-16 | The Chinese University Of Hong Kong | Non-invasive prenatal monitoring |
| US8898021B2 (en) * | 2001-02-02 | 2014-11-25 | Mark W. Perlin | Method and system for DNA mixture analysis |
| JP2002272497A (ja) | 2001-03-15 | 2002-09-24 | Venture Link Co Ltd | 癌の診断方法、およびその診断用ベクター |
| EP1384022A4 (en) * | 2001-04-06 | 2004-08-04 | California Inst Of Techn | NUCLEIC ACID AMPLIFICATION USING MICROFLUID DEVICES |
| US20020164816A1 (en) * | 2001-04-06 | 2002-11-07 | California Institute Of Technology | Microfluidic sample separation device |
| US7118907B2 (en) * | 2001-06-06 | 2006-10-10 | Li-Cor, Inc. | Single molecule detection systems and methods |
| US20050037388A1 (en) * | 2001-06-22 | 2005-02-17 | University Of Geneva | Method for detecting diseases caused by chromosomal imbalances |
| 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 |
| GT200200183A (es) * | 2001-09-28 | 2003-05-23 | Procedimiento para preparar derivados de heterocicloalquilsulfonil pirazol | |
| MXPA04003266A (es) | 2001-10-05 | 2004-07-08 | Combinatorx Inc | Combinaciones para el tratamiento de desodrdenes inmuno-inflamatorios. |
| DE60232013D1 (de) * | 2001-11-20 | 2009-05-28 | Exact Sciences Corp | Automatische probenvorbereitungsverfahren und -vorrichtungen |
| US7691333B2 (en) * | 2001-11-30 | 2010-04-06 | Fluidigm Corporation | Microfluidic device and methods of using same |
| WO2003048295A1 (en) | 2001-11-30 | 2003-06-12 | Fluidigm Corporation | Microfluidic device and methods of using same |
| US20030180765A1 (en) | 2002-02-01 | 2003-09-25 | The Johns Hopkins University | Digital amplification for detection of mismatch repair deficient tumor cells |
| US6977162B2 (en) * | 2002-03-01 | 2005-12-20 | Ravgen, Inc. | Rapid analysis of variations in a genome |
| NZ535044A (en) | 2002-03-01 | 2008-12-24 | Ravgen Inc | Non-invasive method to determine the genetic sequence of foetal DNA from a sample from a pregnant female thereby detecting any alternation in gene sequence as compared with the wild type sequence |
| US7727720B2 (en) * | 2002-05-08 | 2010-06-01 | 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 |
| US7442506B2 (en) * | 2002-05-08 | 2008-10-28 | Ravgen, Inc. | Methods for detection of genetic disorders |
| EP1576131A4 (en) | 2002-08-15 | 2008-08-13 | Genzyme Corp | EXPRESSION PATTERN IN BRAIN DENTHELIC CELLS |
| KR100500697B1 (ko) | 2002-10-21 | 2005-07-12 | 한국에너지기술연구원 | 다단계 열회수형 물유동층 열교환기 |
| US7704687B2 (en) | 2002-11-15 | 2010-04-27 | The Johns Hopkins University | Digital karyotyping |
| WO2004065629A1 (en) | 2003-01-17 | 2004-08-05 | The Chinese University Of Hong Kong | Circulating mrna as diagnostic markers for pregnancy-related disorders |
| AU2003268333A1 (en) | 2003-02-28 | 2004-09-28 | Ravgen, Inc. | Methods for detection of genetic disorders |
| WO2004078999A1 (en) | 2003-03-05 | 2004-09-16 | Genetic Technologies Limited | Identification of fetal dna and fetal cell markers in maternal plasma or serum |
| EP1606417A2 (en) * | 2003-03-07 | 2005-12-21 | Rubicon Genomics Inc. | In vitro dna immortalization and whole genome amplification using libraries generated from randomly fragmented dna |
| WO2004083816A2 (en) | 2003-03-14 | 2004-09-30 | John Wayne Cancer Institute | Loss of heterozygosity of the dna markers in the 12q22-23 region |
| US7476363B2 (en) * | 2003-04-03 | 2009-01-13 | Fluidigm Corporation | Microfluidic devices and methods of using same |
| US20050145496A1 (en) * | 2003-04-03 | 2005-07-07 | Federico Goodsaid | Thermal reaction device and method for using the same |
| US7604965B2 (en) * | 2003-04-03 | 2009-10-20 | Fluidigm Corporation | Thermal reaction device and method for using the same |
| US20040197832A1 (en) * | 2003-04-03 | 2004-10-07 | Mor Research Applications Ltd. | Non-invasive prenatal genetic diagnosis using transcervical cells |
| WO2004089810A2 (en) * | 2003-04-03 | 2004-10-21 | Fluidigm Corp. | Microfluidic devices and methods of using same |
| EP1664077B1 (en) * | 2003-09-05 | 2016-04-13 | Trustees of Boston University | Method for non-invasive prenatal diagnosis |
| 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 |
| EP1689884A4 (en) | 2003-10-08 | 2007-04-04 | Univ Boston | PROCESS FOR THE PRENATAL DIAGNOSIS OF CHROMOSOMAL ABNORMALITIES |
| 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 |
| WO2005044086A2 (en) * | 2003-10-30 | 2005-05-19 | Tufts-New England Medical Center | Prenatal diagnosis using cell-free fetal dna in amniotic fluid |
| 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 |
| US20100216151A1 (en) * | 2004-02-27 | 2010-08-26 | Helicos Biosciences Corporation | Methods for detecting fetal nucleic acids and diagnosing fetal abnormalities |
| US7709194B2 (en) | 2004-06-04 | 2010-05-04 | The Chinese University Of Hong Kong | Marker for prenatal diagnosis and monitoring |
| DE102004036285A1 (de) * | 2004-07-27 | 2006-02-16 | Advalytix Ag | Verfahren zum Bestimmen der Häufigkeit von Sequenzen einer Probe |
| JP2008515393A (ja) * | 2004-09-20 | 2008-05-15 | ユニバーシティ オブ ピッツバーグ オブ ザ コモンウェルス システム オブ ハイヤー エデュケイション | 複数モードの多重化反応消去方法 |
| CN1779688A (zh) * | 2004-11-22 | 2006-05-31 | 寰硕数码股份有限公司 | 交互式医疗信息系统及方法 |
| CA2894337C (en) | 2005-03-18 | 2018-08-28 | The Chinese University Of Hong Kong | Markers for prenatal diagnosis of trisomy 18 |
| US7645576B2 (en) * | 2005-03-18 | 2010-01-12 | The Chinese University Of Hong Kong | Method for the detection of chromosomal aneuploidies |
| US20070196820A1 (en) | 2005-04-05 | 2007-08-23 | Ravi Kapur | Devices and methods for enrichment and alteration of cells and other particles |
| ES2313143T3 (es) | 2005-04-06 | 2009-03-01 | Maurice Stroun | Metodo para el diagnostico de cancer mediante la deteccion de adn y arn circulantes. |
| US20090317798A1 (en) | 2005-06-02 | 2009-12-24 | Heid Christian A | Analysis using microfluidic partitioning devices |
| WO2007001259A1 (en) * | 2005-06-16 | 2007-01-04 | Government Of The United States Of America, Represented By The Secretary, Department Of Health And Human Services | Methods and materials for identifying polymorphic variants, diagnosing susceptibilities, and treating disease |
| US20070059680A1 (en) * | 2005-09-15 | 2007-03-15 | Ravi Kapur | System for cell enrichment |
| US20070122823A1 (en) | 2005-09-01 | 2007-05-31 | Bianchi Diana W | Amniotic fluid cell-free fetal DNA fragment size pattern for prenatal diagnosis |
| US20070184511A1 (en) * | 2005-11-18 | 2007-08-09 | Large Scale Biology Corporation | Method for Diagnosing a Person Having Sjogren's Syndrome |
| EP3599609A1 (en) * | 2005-11-26 | 2020-01-29 | Natera, Inc. | System and method for cleaning noisy genetic data and using data to make predictions |
| HUE030215T2 (en) | 2006-02-02 | 2017-04-28 | Univ Leland Stanford Junior | Non-invasive fetal genetic screening by digital analysis |
| GB2449048A (en) | 2006-02-15 | 2008-11-05 | Agilent Technologies Inc | Normalization probes for comparative genome hybridization arrays |
| US7799531B2 (en) | 2006-02-28 | 2010-09-21 | University Of Louisville Research Foundation | Detecting fetal chromosomal abnormalities using tandem single nucleotide polymorphisms |
| US20080038733A1 (en) * | 2006-03-28 | 2008-02-14 | Baylor College Of Medicine | Screening for down syndrome |
| US8058055B2 (en) * | 2006-04-07 | 2011-11-15 | Agilent Technologies, Inc. | High resolution chromosomal mapping |
| 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 |
| EP2029779A4 (en) * | 2006-06-14 | 2010-01-20 | Living Microsystems Inc | HIGHLY PARALLEL SNP GENOTYPING UTILIZATION FOR FETAL DIAGNOSIS |
| EP2589668A1 (en) * | 2006-06-14 | 2013-05-08 | Verinata Health, Inc | Rare cell analysis using sample splitting and DNA tags |
| US20080026390A1 (en) * | 2006-06-14 | 2008-01-31 | Roland Stoughton | Diagnosis of Fetal Abnormalities by Comparative Genomic Hybridization Analysis |
| US20080050739A1 (en) * | 2006-06-14 | 2008-02-28 | Roland Stoughton | Diagnosis of fetal abnormalities using polymorphisms including short tandem repeats |
| US20080124721A1 (en) * | 2006-06-14 | 2008-05-29 | Martin Fuchs | Analysis of rare cell-enriched samples |
| EP3425058A1 (en) | 2006-06-14 | 2019-01-09 | Verinata Health, Inc | 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 |
| EP2548972A1 (en) | 2006-06-14 | 2013-01-23 | Verinata Health, Inc | 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 |
| WO2008014516A2 (en) * | 2006-07-28 | 2008-01-31 | Living Microsystems, Inc. | Selection of cells using biomarkers |
| JP4379742B2 (ja) | 2006-10-23 | 2009-12-09 | ソニー株式会社 | 再生装置および再生方法、並びにプログラム |
| SG177986A1 (en) * | 2007-01-30 | 2012-02-28 | Interdigital Tech Corp | Implicit drx cycle length adjustment control in lte_active mode |
| CA2677517C (en) * | 2007-02-08 | 2015-11-03 | Sequenom, Inc. | Nucleic acid-based tests for rhd typing, gender determination and nucleic acid quantification |
| WO2008135986A2 (en) * | 2007-05-04 | 2008-11-13 | Mor Research Applications Ltd | System, method and device for comprehensive individualized genetic information or genetic counseling |
| AU2008260651B2 (en) | 2007-05-24 | 2014-06-12 | Apceth Gmbh & Co. Kg | CD34 stem cell-related methods and compositions |
| US12180549B2 (en) | 2007-07-23 | 2024-12-31 | The Chinese University Of Hong Kong | Diagnosing fetal chromosomal aneuploidy using genomic sequencing |
| HUE061020T2 (hu) | 2007-07-23 | 2023-05-28 | Univ Hong Kong Chinese | Nukleinsav-szekvencia kiegyensúlyozatlanságának meghatározására |
| US20090053719A1 (en) | 2007-08-03 | 2009-02-26 | The Chinese University Of Hong Kong | Analysis of nucleic acids by digital pcr |
| KR101738323B1 (ko) | 2007-09-19 | 2017-05-19 | 플루리스템 리미티드 | 지방 또는 태반 조직 유래의 부착 세포 및 이의 치료 용도 |
| WO2009051842A2 (en) | 2007-10-18 | 2009-04-23 | The Johns Hopkins University | Detection of cancer by measuring genomic copy number and strand length in cell-free dna |
| US20100000804A1 (en) | 2008-07-02 | 2010-01-07 | Ming-Hsiang Yeh | Solar vehicle |
| ES2620012T3 (es) * | 2008-09-20 | 2017-06-27 | The Board Of Trustees Of The Leland Stanford Junior University | Diagnóstico no invasivo de la aneuploidia fetal por secuenciación |
| EA034241B1 (ru) | 2009-11-06 | 2020-01-21 | Те Чайниз Юниверсити Ов Гонконг | Способ пренатальной диагностики дисбаланса последовательности |
| KR20110072531A (ko) | 2009-12-23 | 2011-06-29 | 재단법인대구경북과학기술원 | 전력 거래 서비스 방법 및 시스템 |
| US20140186827A1 (en) | 2010-05-14 | 2014-07-03 | Fluidigm, Inc. | Assays for the detection of genotype, mutations, and/or aneuploidy |
| SG10202008532PA (en) | 2010-11-30 | 2020-10-29 | Univ Hong Kong Chinese | Detection of genetic or molecular aberrations associated with cancer |
| JP2012128587A (ja) | 2010-12-14 | 2012-07-05 | Mitsubishi Electric Corp | 救援システム及び救援指示装置及び救援装置及び対象装置及びコンピュータプログラム及び救援指示方法 |
| CA2840418C (en) | 2011-07-26 | 2019-10-29 | Verinata Health, Inc. | Method for determining the presence or absence of different aneuploidies in a sample |
| US11261494B2 (en) | 2012-06-21 | 2022-03-01 | The Chinese University Of Hong Kong | Method of measuring a fractional concentration of tumor DNA |
| JP2016131552A (ja) | 2015-01-22 | 2016-07-25 | クラシエフーズ株式会社 | 即席泡状固形ゼリーデザート用粉末 |
| CN107867186B (zh) | 2016-09-27 | 2021-02-23 | 华为技术有限公司 | 电动汽车以及电动汽车之间充电的方法 |
-
2008
- 2008-07-23 HU HUE12180122A patent/HUE061020T2/hu unknown
- 2008-07-23 WO PCT/GB2008/002530 patent/WO2009013496A1/en not_active Ceased
- 2008-07-23 CA CA3200589A patent/CA3200589A1/en active Pending
- 2008-07-23 KR KR1020167021211A patent/KR20160113145A/ko not_active Ceased
- 2008-07-23 PT PT121801229T patent/PT2557517T/pt unknown
- 2008-07-23 WO PCT/GB2008/002524 patent/WO2009013492A1/en not_active Ceased
- 2008-07-23 CA CA3176319A patent/CA3176319A1/en active Pending
- 2008-07-23 ES ES12175754T patent/ES2571738T3/es active Active
- 2008-07-23 BR BRPI0814670A patent/BRPI0814670B8/pt active Search and Examination
- 2008-07-23 EP EP12180129.4A patent/EP2557518B1/en active Active
- 2008-07-23 KR KR1020167021213A patent/KR101896167B1/ko active Active
- 2008-07-23 PT PT87760435T patent/PT2183693E/pt unknown
- 2008-07-23 EA EA201600280A patent/EA035451B9/ru not_active IP Right Cessation
- 2008-07-23 MX MX2014006579A patent/MX341573B/es unknown
- 2008-07-23 KR KR1020187029194A patent/KR102076438B1/ko active Active
- 2008-07-23 NZ NZ600407A patent/NZ600407A/en unknown
- 2008-07-23 KR KR1020227036245A patent/KR20220146689A/ko active Pending
- 2008-07-23 SI SI200832201T patent/SI2557517T1/sl unknown
- 2008-07-23 EA EA201201551A patent/EA201201551A1/ru unknown
- 2008-07-23 CN CN201410052009.7A patent/CN103849684A/zh active Pending
- 2008-07-23 CA CA2693081A patent/CA2693081C/en active Active
- 2008-07-23 EP EP16150714.0A patent/EP3067807A1/en not_active Ceased
- 2008-07-23 CN CN201710089366.4A patent/CN106676188A/zh active Pending
- 2008-07-23 JP JP2010517480A patent/JP5519500B2/ja active Active
- 2008-07-23 HR HRP20251164TT patent/HRP20251164T3/hr unknown
- 2008-07-23 EA EA201300072A patent/EA028642B1/ru unknown
- 2008-07-23 EP EP19153260.5A patent/EP3540739B1/en active Active
- 2008-07-23 EA EA201791612A patent/EA039167B1/ru unknown
- 2008-07-23 KR KR1020107003906A patent/KR101646978B1/ko active Active
- 2008-07-23 KR KR1020177032673A patent/KR101966262B1/ko active Active
- 2008-07-23 HR HRP20230033TT patent/HRP20230033T3/hr unknown
- 2008-07-23 EP EP08776038.5A patent/EP2183692B1/en active Active
- 2008-07-23 EP EP22187826.7A patent/EP4134960A1/en active Pending
- 2008-07-23 HR HRP20140009TT patent/HRP20140009T4/hr unknown
- 2008-07-23 KR KR1020227030988A patent/KR102516709B1/ko active Active
- 2008-07-23 CA CA3076142A patent/CA3076142C/en active Active
- 2008-07-23 ES ES12180133T patent/ES2820866T3/es active Active
- 2008-07-23 KR KR1020187025118A patent/KR102060911B1/ko active Active
- 2008-07-23 EP EP08776043.5A patent/EP2183693B2/en active Active
- 2008-07-23 EP EP12173422.2A patent/EP2527471B1/en not_active Revoked
- 2008-07-23 ES ES08776043T patent/ES2441807T5/es active Active
- 2008-07-23 CN CN201710198531.XA patent/CN107083425B/zh active Active
- 2008-07-23 MX MX2014006501A patent/MX346069B/es unknown
- 2008-07-23 CN CN201710103299.7A patent/CN106834481A/zh active Pending
- 2008-07-23 SG SG2012054102A patent/SG183062A1/en unknown
- 2008-07-23 KR KR1020167021212A patent/KR101829564B1/ko active Active
- 2008-07-23 KR KR1020197028750A patent/KR102222378B1/ko active Active
- 2008-07-23 US US12/178,116 patent/US8706422B2/en active Active
- 2008-07-23 EP EP12175754.6A patent/EP2514842B1/en active Active
- 2008-07-23 PL PL12175754T patent/PL2514842T3/pl unknown
- 2008-07-23 EA EA202192446A patent/EA202192446A1/ru unknown
- 2008-07-23 KR KR1020207037417A patent/KR102458210B1/ko active Active
- 2008-07-23 LT LTEP12180138.5T patent/LT2557520T/lt unknown
- 2008-07-23 US US12/178,181 patent/US12054776B2/en active Active
- 2008-07-23 DK DK12175754.6T patent/DK2514842T3/en active
- 2008-07-23 PL PL08776043T patent/PL2183693T5/pl unknown
- 2008-07-23 EP EP19215726.1A patent/EP3656870A1/en active Pending
- 2008-07-23 KR KR1020107003969A patent/KR101916456B1/ko active Active
- 2008-07-23 CN CN201710089357.5A patent/CN106834474B/zh active Active
- 2008-07-23 CA CA3127930A patent/CA3127930A1/en active Pending
- 2008-07-23 DK DK08776043.5T patent/DK2183693T5/en active
- 2008-07-23 KR KR1020197028752A patent/KR102128960B1/ko active Active
- 2008-07-23 PT PT121801385T patent/PT2557520T/pt unknown
- 2008-07-23 NZ NZ582702A patent/NZ582702A/xx unknown
- 2008-07-23 DK DK12180133.6T patent/DK2557519T3/da active
- 2008-07-23 SI SI200832168T patent/SI2557520T1/sl unknown
- 2008-07-23 JP JP2010517481A patent/JP5736170B2/ja active Active
- 2008-07-23 KR KR1020207013429A patent/KR102147626B1/ko active Active
- 2008-07-23 EP EP12180138.5A patent/EP2557520B1/en active Active
- 2008-07-23 KR KR1020267005284A patent/KR20260033624A/ko active Pending
- 2008-07-23 DK DK12180138.5T patent/DK2557520T3/da active
- 2008-07-23 CA CA2900927A patent/CA2900927C/en active Active
- 2008-07-23 SI SI200831133T patent/SI2183693T2/sl unknown
- 2008-07-23 KR KR1020197037904A patent/KR102197512B1/ko active Active
- 2008-07-23 ES ES19153260T patent/ES3040072T3/es active Active
- 2008-07-23 LT LTEP12180122.9T patent/LT2557517T/lt unknown
- 2008-07-23 CA CA3076159A patent/CA3076159C/en active Active
- 2008-07-23 EP EP21165151.8A patent/EP3892736A1/en active Pending
- 2008-07-23 CN CN200880108126.3A patent/CN101971178B/zh active Active
- 2008-07-23 DK DK12180122.9T patent/DK2557517T3/da active
- 2008-07-23 AU AU2008278839A patent/AU2008278839B2/en active Active
- 2008-07-23 CN CN201410051659.XA patent/CN103902809B/zh active Active
- 2008-07-23 KR KR1020167005386A patent/KR101972994B1/ko active Active
- 2008-07-23 ES ES12173422T patent/ES2792802T3/es active Active
- 2008-07-23 PL PL12180138T patent/PL2557520T3/pl unknown
- 2008-07-23 FI FIEP12180122.9T patent/FI2557517T3/fi active
- 2008-07-23 CN CN200880108377A patent/CN101849236A/zh active Pending
- 2008-07-23 CA CA3009992A patent/CA3009992C/en active Active
- 2008-07-23 PL PL12180122.9T patent/PL2557517T3/pl unknown
- 2008-07-23 EP EP20187420.3A patent/EP3770275A1/en active Pending
- 2008-07-23 ES ES12180138T patent/ES2869347T3/es active Active
- 2008-07-23 KR KR1020237010459A patent/KR102930949B1/ko active Active
- 2008-07-23 KR KR1020217034197A patent/KR102561664B1/ko active Active
- 2008-07-23 CA CA2694007A patent/CA2694007C/en active Active
- 2008-07-23 KR KR1020187031541A patent/KR102112438B1/ko active Active
- 2008-07-23 EP EP12180122.9A patent/EP2557517B1/en active Active
- 2008-07-23 CN CN201710089355.6A patent/CN106886688B/zh active Active
- 2008-07-23 CN CN201410051950.7A patent/CN103853916B/zh active Active
- 2008-07-23 HU HUE12175754A patent/HUE030510T2/hu unknown
- 2008-07-23 CN CN201710197441.9A patent/CN107083424A/zh active Pending
- 2008-07-23 EP EP20179672.9A patent/EP3745405A1/en active Pending
- 2008-07-23 KR KR1020247040251A patent/KR20250002752A/ko active Pending
- 2008-07-23 KR KR1020217005667A patent/KR102443163B1/ko active Active
- 2008-07-23 ES ES12180122T patent/ES2933486T3/es active Active
- 2008-07-23 SI SI200831615A patent/SI2514842T1/sl unknown
- 2008-07-23 CA CA3029497A patent/CA3029497C/en active Active
- 2008-07-23 EA EA201000231A patent/EA017966B1/ru unknown
- 2008-07-23 DK DK12173422.2T patent/DK2527471T3/da active
- 2008-07-23 KR KR1020167021214A patent/KR101829565B1/ko active Active
- 2008-07-23 HU HUE12180138A patent/HUE054639T2/hu unknown
- 2008-07-23 KR KR1020207023505A patent/KR102339760B1/ko active Active
- 2008-07-23 KR KR1020237025635A patent/KR20230117256A/ko not_active Ceased
- 2008-07-23 MX MX2010000846A patent/MX2010000846A/es active IP Right Grant
- 2008-07-23 EP EP12180133.6A patent/EP2557519B1/en active Active
- 2008-07-23 PL PL19153260.5T patent/PL3540739T3/pl unknown
-
2010
- 2010-01-14 IL IL203311A patent/IL203311A/en active IP Right Grant
- 2010-01-22 ZA ZA2010/00524A patent/ZA201000524B/en unknown
-
2013
- 2013-09-18 US US14/030,904 patent/US10208348B2/en active Active
- 2013-10-18 US US14/057,689 patent/US20140256559A1/en not_active Abandoned
- 2013-11-22 US US14/087,525 patent/US20140256560A1/en not_active Abandoned
- 2013-12-25 JP JP2013267526A patent/JP2014073134A/ja active Pending
-
2014
- 2014-01-17 CY CY20141100042T patent/CY1114773T1/el unknown
- 2014-06-19 IL IL233261A patent/IL233261A/en active IP Right Grant
- 2014-07-18 US US14/335,477 patent/US9051616B2/en active Active - Reinstated
- 2014-07-18 US US14/335,374 patent/US8972202B2/en active Active
- 2014-12-10 HK HK14112444.1A patent/HK1199067A1/xx unknown
-
2015
- 2015-04-20 JP JP2015085723A patent/JP6151739B2/ja active Active
-
2016
- 2016-05-09 HR HRP20160493TT patent/HRP20160493T1/hr unknown
- 2016-05-18 CY CY20161100429T patent/CY1117525T1/el unknown
- 2016-07-01 JP JP2016131552A patent/JP6522554B2/ja active Active
- 2016-10-20 HK HK16112109.5A patent/HK1224033A1/en unknown
-
2017
- 2017-05-25 JP JP2017103772A patent/JP6383837B2/ja active Active
-
2018
- 2018-08-06 JP JP2018147642A patent/JP6695392B2/ja active Active
- 2018-10-05 JP JP2018190278A patent/JP6629940B2/ja active Active
-
2019
- 2019-01-11 US US16/246,420 patent/US11725245B2/en active Active
- 2019-10-31 US US16/670,981 patent/US12227804B2/en active Active
- 2019-12-05 JP JP2019220453A patent/JP7026303B2/ja active Active
- 2019-12-05 JP JP2019220507A patent/JP7081829B2/ja active Active
-
2020
- 2020-04-21 JP JP2020075630A patent/JP7490219B2/ja active Active
-
2021
- 2021-06-23 HR HRP20210983TT patent/HRP20210983T1/hr unknown
- 2021-07-02 CY CY20211100590T patent/CY1124357T1/el unknown
-
2022
- 2022-01-19 JP JP2022006135A patent/JP7381116B2/ja active Active
- 2022-05-19 JP JP2022082143A patent/JP7457399B2/ja active Active
- 2022-09-29 JP JP2022156687A patent/JP7634889B2/ja active Active
-
2023
- 2023-06-16 US US18/336,579 patent/US20230323462A1/en active Pending
- 2023-10-26 JP JP2023184105A patent/JP7761951B2/ja active Active
-
2024
- 2024-03-08 JP JP2024035749A patent/JP2024056078A/ja active Pending
- 2024-05-14 US US18/663,514 patent/US20250122566A1/en not_active Abandoned
- 2024-11-27 US US18/963,210 patent/US20250320558A1/en active Pending
-
2025
- 2025-01-14 US US19/021,066 patent/US20260009078A1/en active Pending
- 2025-02-04 JP JP2025017076A patent/JP2025069363A/ja active Pending
- 2025-10-09 JP JP2025171240A patent/JP2026012597A/ja active Pending
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2249820C1 (ru) * | 2003-08-18 | 2005-04-10 | Лактионов Павел Петрович | Способ ранней диагностики заболеваний, связанных с нарушением функционирования генетического аппарата клетки |
Non-Patent Citations (2)
| Title |
|---|
| TONG YK et al. "Noninvasive prenatal detection of fetal trisomy 18 by epigenetic allelic ratio analysis in maternal plasma: Theoretical and empirical considerations", Clin Chem, 2006 Dec; 52(12): 2194-202, (abstract) [online] [retrieved on 15.04.2013], Retrieved from the PubMed, PMID: 17040955 * |
| TONG YK et al. "Plasma epigenetic markers for cancer detection and prenatal diagnosis", Front Biosci, 2006 Sep. 1; 11: 2647-2656, (abstract) [online] [retrieved on 15.04.2013], Retrieved from the PubMed, PMID:16720341 * |
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Locke et al. | DNA methylation cancer biomarkers: translation to the clinic | |
| Bronkhorst et al. | The changing face of circulating tumor DNA (ctDNA) profiling: Factors that shape the landscape of methodologies, technologies, and commercialization | |
| Vriens et al. | MicroRNA expression profiling is a potential diagnostic tool for thyroid cancer | |
| Patel et al. | Association of plasma and urinary mutant DNA with clinical outcomes in muscle invasive bladder cancer | |
| Pu et al. | Tissue‐specific and plasma microRNA profiles could be promising biomarkers of histological classification and TNM stage in non‐small cell lung cancer | |
| Aisner et al. | Evaluation of EGFR mutation status in cytology specimens: an institutional experience | |
| Wu et al. | MSI status is associated with distinct clinicopathological features in BRAF mutation colorectal cancer: A systematic review and meta-analysis | |
| JP2020503003A (ja) | 尿および他のサンプルにおける無細胞dnaの分析 | |
| Koperski et al. | Next-generation sequencing reveals microRNA markers of adrenocortical tumors malignancy | |
| EA201201551A1 (ru) | Способ диагностики рака с использованием геномного секвенирования | |
| WO2008107134A3 (en) | A method for detection of liver cancer, risk of liver cancer, risk of recurrence of liver cancer, malignancy of liver cancer and progression of liver cancer with time by using the methylated cytosine in basp1 gene and/or srd5a2 gene | |
| Giaretti et al. | Chromosomal instability, aneuploidy and routine high-resolution DNA content analysis in oral cancer risk evaluation | |
| EP2966183B1 (en) | Method for obtaining information on lung cancer, and use of marker and determination device for obtaining information on lung cancer | |
| Song et al. | Application and development of noninvasive biomarkers for colorectal cancer screening: a systematic review | |
| Liu et al. | TERT promoter hypermethylation in gastrointestinal cancer: a potential stool biomarker | |
| Oh et al. | Exome and transcriptome sequencing identifies loss of PDLIM2 in metastatic colorectal cancers | |
| CA3159505A1 (en) | Methods and compositions for analyses of cancer | |
| Li et al. | Improvement in the risk assessment of oral leukoplakia through morphology-related copy number analysis | |
| Grahn et al. | Genomic profile–a possible diagnostic and prognostic marker in upper tract urothelial carcinoma | |
| Moldovan et al. | Genome-wide cell-free DNA termini in patients with cancer | |
| Miyake et al. | Association of GSTP1 methylation with aggressive phenotype in ER-positive breast cancer | |
| Lyman et al. | Systems-level liquid biopsy in advanced prostate cancer | |
| Shi et al. | Non-invasive genotyping of metastatic colorectal cancer using circulating cell free DNA | |
| Maansson et al. | Liquid biopsy epigenetics: establishing a molecular profile based on cell‐free DNA | |
| Perell et al. | Development and validation of a microRNA based diagnostic assay for primary tumor site classification of liver core biopsies |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| TH4A | Publication of the corrected specification to eurasian patent | ||
| MM4A | Lapse of a eurasian patent due to non-payment of renewal fees within the time limit in the following designated state(s) |
Designated state(s): MD |