HK1200934A1 - 用於遺傳變異的非侵入性評估的方法及過程 - Google Patents
用於遺傳變異的非侵入性評估的方法及過程Info
- Publication number
- HK1200934A1 HK1200934A1 HK15101188.3A HK15101188A HK1200934A1 HK 1200934 A1 HK1200934 A1 HK 1200934A1 HK 15101188 A HK15101188 A HK 15101188A HK 1200934 A1 HK1200934 A1 HK 1200934A1
- Authority
- HK
- Hong Kong
- Prior art keywords
- processes
- methods
- genetic variations
- invasive assessment
- invasive
- Prior art date
Links
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
- C12Q1/6813—Hybridisation assays
- C12Q1/6827—Hybridisation assays for detection of mutation or polymorphism
-
- 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
- G16B20/20—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
- G16B30/10—Sequence alignment; Homology search
-
- 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
- G16B30/20—Sequence assembly
-
- 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
- G16B40/00—ICT specially adapted for biostatistics; ICT specially adapted for bioinformatics-related machine learning or data mining, e.g. knowledge discovery or pattern finding
-
- 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
- G16B30/00—ICT specially adapted for sequence analysis involving nucleotides or amino acids
-
- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
- G16H50/00—ICT specially adapted for medical diagnosis, medical simulation or medical data mining; ICT specially adapted for detecting, monitoring or modelling epidemics or pandemics
- G16H50/20—ICT specially adapted for medical diagnosis, medical simulation or medical data mining; ICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for computer-aided diagnosis, e.g. based on medical expert systems
-
- 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
- Life Sciences & Earth Sciences (AREA)
- Physics & Mathematics (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical & Material Sciences (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Biophysics (AREA)
- Biotechnology (AREA)
- General Health & Medical Sciences (AREA)
- Medical Informatics (AREA)
- Analytical Chemistry (AREA)
- Theoretical Computer Science (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Evolutionary Biology (AREA)
- Bioinformatics & Computational Biology (AREA)
- Molecular Biology (AREA)
- Genetics & Genomics (AREA)
- Organic Chemistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Immunology (AREA)
- General Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Microbiology (AREA)
- Artificial Intelligence (AREA)
- Bioethics (AREA)
- Computer Vision & Pattern Recognition (AREA)
- Data Mining & Analysis (AREA)
- Databases & Information Systems (AREA)
- Epidemiology (AREA)
- Evolutionary Computation (AREA)
- Public Health (AREA)
- Software Systems (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Apparatus Associated With Microorganisms And Enzymes (AREA)
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201161544251P | 2011-10-06 | 2011-10-06 | |
US201261663477P | 2012-06-22 | 2012-06-22 | |
US201261709899P | 2012-10-04 | 2012-10-04 | |
PCT/US2012/059123 WO2013052913A2 (en) | 2011-10-06 | 2012-10-05 | Methods and processes for non-invasive assessment of genetic variations |
Publications (1)
Publication Number | Publication Date |
---|---|
HK1200934A1 true HK1200934A1 (zh) | 2015-08-14 |
Family
ID=47073532
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HK15101188.3A HK1200934A1 (zh) | 2011-10-06 | 2015-02-04 | 用於遺傳變異的非侵入性評估的方法及過程 |
Country Status (9)
Country | Link |
---|---|
US (1) | US20230112134A1 (zh) |
EP (2) | EP3922731A3 (zh) |
JP (3) | JP6073902B2 (zh) |
AU (1) | AU2012318371B2 (zh) |
CA (1) | CA2850781C (zh) |
DK (1) | DK2764459T3 (zh) |
ES (1) | ES2886508T3 (zh) |
HK (1) | HK1200934A1 (zh) |
WO (1) | WO2013052913A2 (zh) |
Families Citing this family (74)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
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 |
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 |
WO2011087760A2 (en) | 2009-12-22 | 2011-07-21 | Sequenom, Inc. | Processes and kits for identifying aneuploidy |
TWI611186B (zh) * | 2011-02-24 | 2018-01-11 | 香港中文大學 | 多重妊娠之分子檢驗 |
US20140235474A1 (en) | 2011-06-24 | 2014-08-21 | Sequenom, Inc. | Methods and processes for non invasive assessment of a genetic variation |
US20140242588A1 (en) | 2011-10-06 | 2014-08-28 | 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 |
US9367663B2 (en) | 2011-10-06 | 2016-06-14 | 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 |
US10196681B2 (en) | 2011-10-06 | 2019-02-05 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
EP2805280B1 (en) | 2012-01-20 | 2022-10-05 | Sequenom, Inc. | Diagnostic processes that factor experimental conditions |
ES2930180T3 (es) | 2012-03-02 | 2022-12-07 | Sequenom Inc | Métodos para enriquecer ácido nucleico canceroso a partir de una muestra biológica |
US10504613B2 (en) | 2012-12-20 | 2019-12-10 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
DK3663409T3 (da) | 2012-05-21 | 2021-12-13 | Sequenom Inc | Fremgangsmåder og processer til ikke-invasiv bedømmelse af genetiske variationer |
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 |
CA2878979C (en) | 2012-07-13 | 2021-09-14 | Sequenom, Inc. | Processes and compositions for methylation-based enrichment of fetal nucleic acid from a maternal sample useful for non-invasive prenatal diagnoses |
US10482994B2 (en) * | 2012-10-04 | 2019-11-19 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
CA3120521A1 (en) * | 2012-10-04 | 2014-04-10 | 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 |
CA2901460A1 (en) | 2013-02-20 | 2014-08-28 | Bionano Genomics, Inc. | Characterization of molecules in nanofluidics |
WO2015130696A1 (en) | 2014-02-25 | 2015-09-03 | Bionano Genomics, Inc. | Reduction of bias in genomic coverage measurements |
US10844424B2 (en) | 2013-02-20 | 2020-11-24 | Bionano Genomics, Inc. | Reduction of bias in genomic coverage measurements |
WO2014168711A1 (en) | 2013-03-13 | 2014-10-16 | Sequenom, Inc. | Primers for dna methylation analysis |
HUE061261T2 (hu) | 2013-04-03 | 2023-05-28 | Sequenom Inc | Eljárások és folyamatok genetikai variánsok nem invazív értékelésére |
JP6561046B2 (ja) * | 2013-05-24 | 2019-08-14 | セクエノム, インコーポレイテッド | 遺伝子の変動の非侵襲性評価のための方法および処理 |
US20160117440A1 (en) * | 2013-05-30 | 2016-04-28 | Memorial Sloan-Kettering Cancer Center | System and method for automated prediction of vulnerabilities in biological samples |
SI3011051T1 (sl) * | 2013-06-21 | 2019-05-31 | Sequenom, Inc. | Postopek za neinvazivno oceno genetskih variacij |
CN104450872A (zh) * | 2013-09-25 | 2015-03-25 | 上海市肿瘤研究所 | 一种高通量多样本多靶点单碱基分辨率的甲基化水平检测方法 |
IL289974B (en) * | 2013-10-04 | 2022-09-01 | Sequenom Inc | Methods and processes for non-invasive evaluation of genetic variations |
JP6680680B2 (ja) | 2013-10-07 | 2020-04-15 | セクエノム, インコーポレイテッド | 染色体変化の非侵襲性評価のための方法およびプロセス |
US10851414B2 (en) * | 2013-10-18 | 2020-12-01 | Good Start Genetics, Inc. | Methods for determining carrier status |
WO2015061359A1 (en) | 2013-10-21 | 2015-04-30 | Verinata Health, Inc. | Method for improving the sensitivity of detection in determining copy number variations |
CN103540672B (zh) * | 2013-10-29 | 2015-04-08 | 中国科学技术大学 | 一种亲和核酸分子的快速鉴定和分离方法 |
KR101516976B1 (ko) * | 2013-10-30 | 2015-05-04 | 에스케이텔레콤 주식회사 | 표적 염기 서열 해독에서의 바이어스 제거 방법 |
EP3736344A1 (en) | 2014-03-13 | 2020-11-11 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
WO2015183872A1 (en) * | 2014-05-30 | 2015-12-03 | Sequenom, Inc. | Chromosome representation determinations |
EP3175000B1 (en) | 2014-07-30 | 2020-07-29 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
JP2016042836A (ja) * | 2014-08-25 | 2016-04-04 | 富士フイルム株式会社 | 検査通知出力装置、検査通知出力方法、検査通知出力プログラム、及び遺伝子染色体検査システム |
CA2970501C (en) | 2014-12-12 | 2020-09-15 | Verinata Health, Inc. | Using cell-free dna fragment size to determine copy number variations |
WO2016100049A1 (en) | 2014-12-18 | 2016-06-23 | Edico Genome Corporation | Chemically-sensitive field effect transistor |
US9857328B2 (en) | 2014-12-18 | 2018-01-02 | Agilome, Inc. | Chemically-sensitive field effect transistors, systems and methods for manufacturing and using the same |
US10006910B2 (en) | 2014-12-18 | 2018-06-26 | Agilome, Inc. | Chemically-sensitive field effect transistors, systems, and methods for manufacturing and using the same |
US9618474B2 (en) | 2014-12-18 | 2017-04-11 | Edico Genome, Inc. | Graphene FET devices, systems, and methods of using the same for sequencing nucleic acids |
US10020300B2 (en) | 2014-12-18 | 2018-07-10 | Agilome, Inc. | Graphene FET devices, systems, and methods of using the same for sequencing nucleic acids |
US9859394B2 (en) | 2014-12-18 | 2018-01-02 | Agilome, Inc. | Graphene FET devices, systems, and methods of using the same for sequencing nucleic acids |
HUE058263T2 (hu) | 2015-02-10 | 2022-07-28 | Univ Hong Kong Chinese | Mutációk detektálása rákszûrési és magzatelemzési célból |
EP3967775B1 (en) | 2015-07-23 | 2023-08-23 | The Chinese University Of Hong Kong | Analysis of fragmentation patterns of cell-free dna |
RU2613021C1 (ru) * | 2015-11-20 | 2017-03-14 | Общество С Ограниченной Ответственностью "Стриж Телематика" | Способ кодирования и декодирования сообщений |
US10095831B2 (en) | 2016-02-03 | 2018-10-09 | Verinata Health, Inc. | Using cell-free DNA fragment size to determine copy number variations |
WO2017201081A1 (en) | 2016-05-16 | 2017-11-23 | Agilome, Inc. | Graphene fet devices, systems, and methods of using the same for sequencing nucleic acids |
WO2017205826A1 (en) | 2016-05-27 | 2017-11-30 | Sequenom, Inc. | Methods for detecting genetic variations |
SG11201811556RA (en) * | 2016-07-06 | 2019-01-30 | Guardant Health Inc | Methods for fragmentome profiling of cell-free nucleic acids |
US11200963B2 (en) | 2016-07-27 | 2021-12-14 | Sequenom, Inc. | Genetic copy number alteration classifications |
WO2018022906A1 (en) | 2016-07-27 | 2018-02-01 | Sequenom, Inc. | Methods for non-invasive assessment of genomic instability |
RU2768718C2 (ru) * | 2016-09-22 | 2022-03-24 | Иллумина, Инк. | Обнаружение соматического варьирования числа копий |
CA3049457C (en) | 2017-01-20 | 2023-05-16 | Sequenom, Inc. | Methods for non-invasive assessment of copy number alterations |
CA3049455C (en) | 2017-01-20 | 2023-06-13 | Sequenom, Inc. | Sequencing adapter manufacture and use |
US11929145B2 (en) | 2017-01-20 | 2024-03-12 | Sequenom, Inc | Methods for non-invasive assessment of genetic alterations |
JP7237003B2 (ja) | 2017-01-24 | 2023-03-10 | セクエノム, インコーポレイテッド | 遺伝子片の評価のための方法およびプロセス |
TWI803477B (zh) | 2017-01-25 | 2023-06-01 | 香港中文大學 | 使用核酸片段之診斷應用 |
EP3998350A1 (en) | 2017-03-17 | 2022-05-18 | Sequenom, Inc. | Methods and processes for assessment of genetic mosaicism |
US11342047B2 (en) | 2017-04-21 | 2022-05-24 | Illumina, Inc. | Using cell-free DNA fragment size to detect tumor-associated variant |
CA3107467A1 (en) | 2018-09-07 | 2020-03-12 | Sequenom, Inc. | Methods, and systems to detect transplant rejection |
CA3128894A1 (en) | 2019-02-19 | 2020-08-27 | Sequenom, Inc. | Compositions, methods, and systems to detect hematopoietic stem cell transplantation status |
KR102452413B1 (ko) * | 2019-08-19 | 2022-10-11 | 주식회사 지씨지놈 | 핵산 단편간 거리 정보를 이용한 염색체 이상 검출 방법 |
AU2020333348B2 (en) * | 2019-08-19 | 2023-11-23 | Green Cross Genome Corporation | Method for detecting chromosomal abnormality by using information about distance between nucleic acid fragments |
EP4035161A1 (en) | 2019-09-23 | 2022-08-03 | Grail, LLC | Systems and methods for diagnosing a disease condition using on-target and off-target sequencing data |
EP4052259A1 (en) | 2019-10-31 | 2022-09-07 | Sequenom, Inc. | Application of mosaicism ratio in multifetal gestations and personalized risk assessment |
WO2021107676A1 (ko) * | 2019-11-29 | 2021-06-03 | 주식회사 녹십자지놈 | 인공지능 기반 염색체 이상 검출 방법 |
EP4022646A4 (en) * | 2019-12-25 | 2022-11-02 | Idea Teknoloji Çözümleri Bilgisayar Sanayi ve Ticaret Anonim Sirketi | PRIORITY AND RATING PROCEDURE |
US20230120825A1 (en) | 2020-02-28 | 2023-04-20 | Laboratory Corporation Of America Holdings | Compositions, Methods, and Systems for Paternity Determination |
WO2024186778A1 (en) | 2023-03-03 | 2024-09-12 | Laboratory Corporation Of America Holdings | Methods and systems for positive cfdna screening on genetic variations using mosaicism ratio |
Family Cites Families (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
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 |
CA2497988C (en) | 2002-09-06 | 2011-03-29 | The Trustees Of Boston University | Quantification of gene expression |
CN1774511B (zh) | 2002-11-27 | 2013-08-21 | 斯昆诺有限公司 | 用于序列变异检测和发现的基于断裂的方法和系统 |
EP1641809B2 (en) | 2003-07-05 | 2018-10-03 | The Johns Hopkins University | Method and compositions for detection and enumeration of genetic variations |
CN101243191B (zh) | 2004-11-29 | 2014-04-16 | 塞昆纳姆股份有限公司 | 用于检测甲基化dna的手段和方法 |
US8679741B2 (en) | 2006-05-31 | 2014-03-25 | Sequenom, Inc. | Methods and compositions for the extraction and amplification of nucleic acid from a sample |
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 |
US8262900B2 (en) | 2006-12-14 | 2012-09-11 | Life Technologies Corporation | Methods and apparatus for measuring analytes using large scale FET arrays |
EP3770275A1 (en) | 2007-07-23 | 2021-01-27 | The Chinese University of Hong Kong | Determining a fetal aneuploidy |
WO2009032779A2 (en) | 2007-08-29 | 2009-03-12 | Sequenom, Inc. | Methods and compositions for the size-specific seperation of nucleic acid from a sample |
US9404150B2 (en) | 2007-08-29 | 2016-08-02 | Sequenom, Inc. | Methods and compositions for universal size-specific PCR |
CN101889074A (zh) | 2007-10-04 | 2010-11-17 | 哈尔西恩莫尔丘勒公司 | 采用电子显微镜对核酸聚合物测序 |
CA2718137A1 (en) | 2008-03-26 | 2009-10-01 | Sequenom, Inc. | Restriction endonuclease enhanced polymorphic sequence detection |
CN102245760A (zh) | 2008-07-07 | 2011-11-16 | 牛津纳米孔技术有限公司 | 酶-孔构建体 |
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 |
ES2599967T3 (es) | 2008-09-16 | 2017-02-06 | Sequenom, Inc. | Procedimientos y composiciones para el enriquecimiento basado en metilación de ácido nucleico fetal de una muestra materna útiles para diagnósticos prenatales no invasivos |
LT2562268T (lt) * | 2008-09-20 | 2017-04-25 | The Board Of Trustees Of The Leland Stanford Junior University | Neinvazinis fetalinės aneuploidijos diagnozavimas sekvenavimu |
EP3514244B1 (en) | 2009-04-03 | 2021-07-07 | Sequenom, Inc. | Nucleic acid preparation methods |
US8574842B2 (en) * | 2009-12-22 | 2013-11-05 | The Board Of Trustees Of The Leland Stanford Junior University | Direct molecular diagnosis of fetal aneuploidy |
EP2526415B1 (en) * | 2010-01-19 | 2017-05-03 | Verinata Health, Inc | Partition defined detection methods |
ES2704701T3 (es) * | 2010-01-19 | 2019-03-19 | Verinata Health Inc | Nuevo protocolo de preparación de bibliotecas de secuenciación |
EP2569453B1 (en) | 2010-05-14 | 2015-12-16 | Fluidigm Corporation | Nucleic acid isolation methods |
-
2012
- 2012-10-05 JP JP2014534806A patent/JP6073902B2/ja active Active
- 2012-10-05 AU AU2012318371A patent/AU2012318371B2/en active Active
- 2012-10-05 EP EP21182355.4A patent/EP3922731A3/en active Pending
- 2012-10-05 EP EP12777999.9A patent/EP2764459B1/en active Active
- 2012-10-05 CA CA2850781A patent/CA2850781C/en active Active
- 2012-10-05 DK DK12777999.9T patent/DK2764459T3/da active
- 2012-10-05 ES ES12777999T patent/ES2886508T3/es active Active
- 2012-10-05 WO PCT/US2012/059123 patent/WO2013052913A2/en active Application Filing
-
2015
- 2015-02-04 HK HK15101188.3A patent/HK1200934A1/zh unknown
-
2016
- 2016-11-07 JP JP2016216922A patent/JP6227095B2/ja active Active
-
2017
- 2017-03-09 JP JP2017045068A patent/JP2017099419A/ja not_active Withdrawn
-
2022
- 2022-12-13 US US18/080,620 patent/US20230112134A1/en active Pending
Also Published As
Publication number | Publication date |
---|---|
JP6227095B2 (ja) | 2017-11-08 |
US20230112134A1 (en) | 2023-04-13 |
ES2886508T3 (es) | 2021-12-20 |
DK2764459T3 (da) | 2021-08-23 |
JP2017073144A (ja) | 2017-04-13 |
EP3922731A3 (en) | 2022-01-05 |
CA2850781A1 (en) | 2013-04-11 |
JP2014534507A (ja) | 2014-12-18 |
JP2017099419A (ja) | 2017-06-08 |
EP2764459A2 (en) | 2014-08-13 |
EP3922731A2 (en) | 2021-12-15 |
JP6073902B2 (ja) | 2017-02-01 |
CA2850781C (en) | 2020-09-01 |
WO2013052913A4 (en) | 2013-12-27 |
WO2013052913A2 (en) | 2013-04-11 |
WO2013052913A3 (en) | 2013-11-07 |
EP2764459B1 (en) | 2021-06-30 |
AU2012318371A1 (en) | 2014-04-17 |
AU2012318371B2 (en) | 2018-03-22 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
HK1246362B (zh) | 用於遺傳變異的非侵入性評估的方法及過程 | |
HK1200935A1 (zh) | 用於遺傳變異的非侵入性評估的方法及過程 | |
HK1200934A1 (zh) | 用於遺傳變異的非侵入性評估的方法及過程 | |
IL295860B1 (en) | Methods and processes for non-invasive evaluation of genetic variations | |
IL283586A (en) | Methods and processes for non-invasive evaluation of genetic variations | |
HK1207399A1 (zh) | 無創評估遺傳變異的方法和流程 | |
HK1206794A1 (zh) | 遺傳變異的無創評估方法和流程 | |
HK1205203A1 (zh) | 用於遺傳變異的非侵入性評估的方法及過程 | |
HK1206055A1 (zh) | 遺傳變異的無創評估方法和流程 | |
HK1207701A1 (zh) | 無創評估遺傳變異的方法和流程 | |
IL269567B1 (en) | Methods and processes for the non-invasive evaluation of genetic variations | |
HK1218173A1 (zh) | 無創檢測遺傳變異的方法和過程 | |
HK1214870A1 (zh) | 非侵入性遺傳變異評估的方法及流程 | |
WO2012177792A9 (en) | Methods and processes for non-invasive assessment of a genetic variation | |
HK1215284A1 (zh) | 位點特異性酶和使用方法 | |
GB201004895D0 (en) | Consumables and methods of production thereof | |
EP2672963A4 (en) | METHOD FOR THE TREATMENT OF MELANOMA | |
GB201004897D0 (en) | Consumables and methods of production thereof | |
ZA201207878B (en) | Consumables and methods of production thereof | |
EP2670245A4 (en) | ALPHA-CÉTOHÉTÉROCYCLES AND METHODS OF MAKING AND USING THEM | |
GB201004894D0 (en) | Consumables and methods of production thereof | |
PL2665602T3 (pl) | Ultraelastyczny materiał i sposób jego wytwarzania | |
EP2782670A4 (en) | COPPER ZIRCONIUM CATALYST AND METHOD FOR ITS USE AND MANUFACTURE | |
GB201004902D0 (en) | Consumables and methods of production thereof | |
EP2753708A4 (en) | SYSTEMS AND METHODS FOR BIOSIMILARITY ASSESSMENT |