HK1207701A1 - 無創評估遺傳變異的方法和流程 - Google Patents
無創評估遺傳變異的方法和流程Info
- Publication number
- HK1207701A1 HK1207701A1 HK15108082.5A HK15108082A HK1207701A1 HK 1207701 A1 HK1207701 A1 HK 1207701A1 HK 15108082 A HK15108082 A HK 15108082A HK 1207701 A1 HK1207701 A1 HK 1207701A1
- Authority
- HK
- Hong Kong
- Prior art keywords
- processes
- methods
- genetic variations
- invasive assessment
- invasive
- Prior art date
Links
Classifications
-
- 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
Landscapes
- Bioinformatics & Cheminformatics (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Biotechnology (AREA)
- Biophysics (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Chemical & Material Sciences (AREA)
- Bioinformatics & Computational Biology (AREA)
- Analytical Chemistry (AREA)
- Evolutionary Biology (AREA)
- General Health & Medical Sciences (AREA)
- Medical Informatics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Theoretical Computer Science (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Apparatus Associated With Microorganisms And Enzymes (AREA)
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201261709909P | 2012-10-04 | 2012-10-04 | |
US13/797,930 US9984198B2 (en) | 2011-10-06 | 2013-03-12 | Reducing sequence read count error in assessment of complex genetic variations |
US13/829,373 US10424394B2 (en) | 2011-10-06 | 2013-03-14 | Methods and processes for non-invasive assessment of genetic variations |
US13/829,164 US10196681B2 (en) | 2011-10-06 | 2013-03-14 | Methods and processes for non-invasive assessment of genetic variations |
PCT/US2013/063314 WO2014055790A2 (en) | 2012-10-04 | 2013-10-03 | Methods and processes for non-invasive assessment of genetic variations |
Publications (1)
Publication Number | Publication Date |
---|---|
HK1207701A1 true HK1207701A1 (zh) | 2016-02-05 |
Family
ID=49515465
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HK15108082.5A HK1207701A1 (zh) | 2012-10-04 | 2015-08-20 | 無創評估遺傳變異的方法和流程 |
Country Status (5)
Country | Link |
---|---|
EP (2) | EP2904534B1 (zh) |
AU (3) | AU2013326980B2 (zh) |
CA (2) | CA3120521A1 (zh) |
HK (1) | HK1207701A1 (zh) |
WO (1) | WO2014055790A2 (zh) |
Families Citing this family (28)
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US20140235474A1 (en) | 2011-06-24 | 2014-08-21 | Sequenom, Inc. | Methods and processes for non invasive assessment of a genetic variation |
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 |
US10196681B2 (en) | 2011-10-06 | 2019-02-05 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
US20140242588A1 (en) | 2011-10-06 | 2014-08-28 | 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 |
CA2861856C (en) | 2012-01-20 | 2020-06-02 | Sequenom, Inc. | Diagnostic processes that factor experimental conditions |
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 |
US10497461B2 (en) | 2012-06-22 | 2019-12-03 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
US10482994B2 (en) | 2012-10-04 | 2019-11-19 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
EP3561072A1 (en) | 2012-12-10 | 2019-10-30 | Resolution Bioscience, Inc. | Methods for targeted genomic analysis |
US20130309666A1 (en) | 2013-01-25 | 2013-11-21 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
FI2981921T3 (fi) | 2013-04-03 | 2023-03-09 | Sequenom Inc | Menetelmiä ja prosesseja geneettisten variaatioiden ei-invasiiviseen arviointiin |
KR102665592B1 (ko) | 2013-05-24 | 2024-05-21 | 시쿼넘, 인코포레이티드 | 유전적 변이의 비침습 평가를 위한 방법 및 프로세스 |
HUE042654T2 (hu) | 2013-06-21 | 2019-07-29 | Sequenom Inc | Eljárás genetikai variációk nem-invazív megállapítására |
MY181069A (en) | 2013-10-04 | 2020-12-17 | Sequenom Inc | Methods and processes for non-invasive assessment of genetic variations |
CN111863131A (zh) | 2013-10-07 | 2020-10-30 | 塞昆纳姆股份有限公司 | 用于非侵入性评估染色体改变的方法和过程 |
RU2583830C2 (ru) * | 2014-04-21 | 2016-05-10 | Закрытое акционерное общество "Геноаналитика" | Способ неинвазивной пренатальной диагностики анеуплоидий плода |
AU2015257654A1 (en) | 2014-05-09 | 2016-11-10 | Lifecodexx Ag | Detection of DNA that originates from a specific cell-type and related methods |
EP2942400A1 (en) | 2014-05-09 | 2015-11-11 | Lifecodexx AG | Multiplex detection of DNA that originates from a specific cell-type |
EP3760739A1 (en) | 2014-07-30 | 2021-01-06 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
HUE050491T2 (hu) | 2015-11-10 | 2020-12-28 | Eurofins Lifecodexx Gmbh | Magzati kromoszomális aneuploidiák kimutatása olyan DNS régiókat alkalmazva, amelyek különbözõképpen vannak metilezve a magzat és a terhes nõstény között |
ES2856598T3 (es) | 2015-11-11 | 2021-09-27 | Resolution Bioscience Inc | Construcción de alta eficiencia de bibliotecas de ADN |
CA3030890A1 (en) | 2016-07-27 | 2018-02-01 | Sequenom, Inc. | Genetic copy number alteration classifications |
RU2019108294A (ru) * | 2016-08-25 | 2020-09-25 | Резолюшн Байосайенс, Инк. | Способы обнаружения изменений количества геномных копий в образцах днк |
WO2018140521A1 (en) | 2017-01-24 | 2018-08-02 | Sequenom, Inc. | Methods and processes for assessment of genetic variations |
CN116246704B (zh) * | 2023-05-10 | 2023-08-15 | 广州精科生物技术有限公司 | 用于胎儿无创产前检测的系统 |
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US2187108A (en) | 1938-05-27 | 1940-01-16 | Du Pont | Process of purifying lead nitrate solutions |
US4683202A (en) | 1985-03-28 | 1987-07-28 | Cetus Corporation | Process for amplifying nucleic acid sequences |
US4683195A (en) | 1986-01-30 | 1987-07-28 | Cetus Corporation | Process for amplifying, detecting, and/or-cloning nucleic acid sequences |
US5605798A (en) | 1993-01-07 | 1997-02-25 | Sequenom, Inc. | DNA diagnostic based on mass spectrometry |
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CN100402850C (zh) | 1999-06-28 | 2008-07-16 | 加利福尼亚技术学院 | 微型制造的弹性体的阀和泵系统 |
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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 |
CN102344960B (zh) | 2002-09-06 | 2014-06-18 | 波士顿大学信托人 | 基因表达的定量 |
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 |
WO2005010145A2 (en) | 2003-07-05 | 2005-02-03 | The Johns Hopkins University | Method and compositions for detection and enumeration of genetic variations |
ATE425265T1 (de) | 2003-07-31 | 2009-03-15 | Sequenom Inc | Verfahren für multiplex- polymerasekettenreaktionen auf hohem niveau und homogenen massenverlängerungsreaktionen zur genotypisierung von polymorphismen |
EP1664077B1 (en) | 2003-09-05 | 2016-04-13 | Trustees of Boston University | Method for non-invasive prenatal diagnosis |
ATE443161T1 (de) | 2004-11-29 | 2009-10-15 | Univ Regensburg Klinikum | Mittel und verfahren für den nachweis von methylierter dna |
PT3002338T (pt) | 2006-02-02 | 2019-08-02 | Univ Leland Stanford Junior | Triagem genética não invasiva de fetos por análise digital |
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US20100112590A1 (en) * | 2007-07-23 | 2010-05-06 | The Chinese University Of Hong Kong | Diagnosing Fetal Chromosomal Aneuploidy Using Genomic Sequencing With Enrichment |
SI2183693T2 (sl) | 2007-07-23 | 2019-02-28 | The Chinese University Of Hong Kong Technology Licenising Office | Diagnosticiranje fetalne kromosomske anevploidije z uporabo genomskega sekvenciranja |
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ATE549419T1 (de) | 2007-08-29 | 2012-03-15 | Sequenom Inc | Verfahren und zusammensetzungen für die universelle grössenspezifische polymerasekettenreaktion |
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JP5727375B2 (ja) | 2008-09-16 | 2015-06-03 | セクエノム, インコーポレイテッド | 非侵襲性の出生前診断のために有用な、母体サンプル由来の胎児核酸のメチル化に基づく濃縮のためのプロセスおよび組成物 |
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ES2886508T3 (es) * | 2011-10-06 | 2021-12-20 | Sequenom Inc | Métodos y procedimientos para la evaluación no invasiva de variaciones genéticas |
US20140242588A1 (en) * | 2011-10-06 | 2014-08-28 | Sequenom, Inc | Methods and processes for non-invasive assessment of genetic variations |
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-
2013
- 2013-10-03 EP EP13785687.8A patent/EP2904534B1/en active Active
- 2013-10-03 WO PCT/US2013/063314 patent/WO2014055790A2/en active Application Filing
- 2013-10-03 CA CA3120521A patent/CA3120521A1/en active Pending
- 2013-10-03 CA CA2887094A patent/CA2887094C/en active Active
- 2013-10-03 EP EP21213023.1A patent/EP4009329A1/en active Pending
- 2013-10-03 AU AU2013326980A patent/AU2013326980B2/en active Active
-
2015
- 2015-08-20 HK HK15108082.5A patent/HK1207701A1/zh unknown
-
2019
- 2019-09-20 AU AU2019232913A patent/AU2019232913B2/en active Active
-
2021
- 2021-11-26 AU AU2021273631A patent/AU2021273631A1/en active Pending
Also Published As
Publication number | Publication date |
---|---|
AU2013326980A1 (en) | 2015-04-16 |
AU2013326980B2 (en) | 2019-08-15 |
EP2904534A2 (en) | 2015-08-12 |
AU2019232913A1 (en) | 2019-10-10 |
AU2019232913B2 (en) | 2021-10-21 |
AU2021273631A1 (en) | 2021-12-16 |
CA2887094C (en) | 2021-09-07 |
WO2014055790A2 (en) | 2014-04-10 |
CA2887094A1 (en) | 2014-04-10 |
EP2904534B1 (en) | 2021-12-15 |
EP4009329A1 (en) | 2022-06-08 |
WO2014055790A9 (en) | 2014-06-05 |
CA3120521A1 (en) | 2014-04-10 |
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