PL2716766T3 - Urządzenie do wykrywania liczby kopii chromosomów płodowych lub chromosomów komórek nowotworowych - Google Patents
Urządzenie do wykrywania liczby kopii chromosomów płodowych lub chromosomów komórek nowotworowychInfo
- Publication number
- PL2716766T3 PL2716766T3 PL11866914T PL11866914T PL2716766T3 PL 2716766 T3 PL2716766 T3 PL 2716766T3 PL 11866914 T PL11866914 T PL 11866914T PL 11866914 T PL11866914 T PL 11866914T PL 2716766 T3 PL2716766 T3 PL 2716766T3
- Authority
- PL
- Poland
- Prior art keywords
- chromosomes
- tumor cell
- copy number
- fetal
- detecting copy
- Prior art date
Links
- 210000000349 chromosome Anatomy 0.000 title 2
- 230000001605 fetal effect Effects 0.000 title 1
- 210000004881 tumor cell Anatomy 0.000 title 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
- C12Q1/6869—Methods for sequencing
- C12Q1/6874—Methods for sequencing involving nucleic acid arrays, e.g. sequencing by hybridisation
-
- 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
- G16B25/00—ICT specially adapted for hybridisation; ICT specially adapted for gene or protein expression
- G16B25/10—Gene or protein expression profiling; Expression-ratio estimation or normalisation
-
- 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
- C12Q1/6869—Methods for sequencing
-
- 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
- G16B25/00—ICT specially adapted for hybridisation; ICT specially adapted for gene or protein expression
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Genetics & Genomics (AREA)
- Physics & Mathematics (AREA)
- Analytical Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Molecular Biology (AREA)
- General Health & Medical Sciences (AREA)
- Biophysics (AREA)
- Biotechnology (AREA)
- General Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Immunology (AREA)
- Microbiology (AREA)
- Evolutionary Biology (AREA)
- Bioinformatics & Computational Biology (AREA)
- Medical Informatics (AREA)
- Theoretical Computer Science (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Apparatus Associated With Microorganisms And Enzymes (AREA)
- Investigating Or Analysing Biological Materials (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP11866914.2A EP2716766B1 (en) | 2011-05-31 | 2011-05-31 | A device for detecting copy number of fetal chromosomes or tumor cell chromosomes |
| PCT/CN2011/075037 WO2012162884A1 (zh) | 2011-05-31 | 2011-05-31 | 检测胚胎或肿瘤染色体拷贝数的试剂盒、装置和方法 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL2716766T3 true PL2716766T3 (pl) | 2017-09-29 |
Family
ID=47258277
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL11866914T PL2716766T3 (pl) | 2011-05-31 | 2011-05-31 | Urządzenie do wykrywania liczby kopii chromosomów płodowych lub chromosomów komórek nowotworowych |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US9885080B2 (pl) |
| EP (1) | EP2716766B1 (pl) |
| JP (1) | JP5926795B2 (pl) |
| CN (1) | CN103080336B (pl) |
| DK (1) | DK2716766T3 (pl) |
| ES (1) | ES2605372T3 (pl) |
| HU (1) | HUE031239T2 (pl) |
| PL (1) | PL2716766T3 (pl) |
| PT (1) | PT2716766T (pl) |
| RS (1) | RS55518B1 (pl) |
| WO (1) | WO2012162884A1 (pl) |
Families Citing this family (45)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2010242073C1 (en) | 2009-04-30 | 2015-12-24 | Good Start Genetics, Inc. | Methods and compositions for evaluating genetic markers |
| US12129514B2 (en) | 2009-04-30 | 2024-10-29 | Molecular Loop Biosolutions, Llc | Methods and compositions for evaluating genetic markers |
| US9163281B2 (en) | 2010-12-23 | 2015-10-20 | Good Start Genetics, Inc. | Methods for maintaining the integrity and identification of a nucleic acid template in a multiplex sequencing reaction |
| US20140235474A1 (en) | 2011-06-24 | 2014-08-21 | Sequenom, Inc. | Methods and processes for non invasive assessment of a genetic variation |
| US9984198B2 (en) | 2011-10-06 | 2018-05-29 | Sequenom, Inc. | Reducing sequence read count error in assessment of complex genetic variations |
| US9367663B2 (en) | 2011-10-06 | 2016-06-14 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| US10424394B2 (en) | 2011-10-06 | 2019-09-24 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| EP2764458B1 (en) | 2011-10-06 | 2021-04-07 | 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 |
| CA2852665A1 (en) | 2011-10-17 | 2013-04-25 | Good Start Genetics, Inc. | Analysis methods |
| LT2805280T (lt) | 2012-01-20 | 2022-12-27 | Sequenom, Inc. | Diagnostikos būdai, kurie atsižvelgia į eksperimentines sąlygas |
| US8209130B1 (en) | 2012-04-04 | 2012-06-26 | Good Start Genetics, Inc. | Sequence assembly |
| US10227635B2 (en) | 2012-04-16 | 2019-03-12 | Molecular Loop Biosolutions, Llc | Capture reactions |
| US9920361B2 (en) | 2012-05-21 | 2018-03-20 | Sequenom, Inc. | Methods and compositions for analyzing nucleic acid |
| US10504613B2 (en) | 2012-12-20 | 2019-12-10 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| US10497461B2 (en) | 2012-06-22 | 2019-12-03 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| AU2013204615A1 (en) * | 2012-07-20 | 2014-02-06 | Verinata Health, Inc. | Detecting and classifying copy number variation in a fetal genome |
| US10482994B2 (en) | 2012-10-04 | 2019-11-19 | 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 |
| WO2014152421A1 (en) | 2013-03-14 | 2014-09-25 | Good Start Genetics, Inc. | Methods for analyzing nucleic acids |
| EP4187543A1 (en) | 2013-04-03 | 2023-05-31 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| EP3578670B1 (en) | 2013-05-24 | 2025-07-02 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| AU2014284180B2 (en) | 2013-06-21 | 2020-03-19 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| CN110176273B (zh) | 2013-10-04 | 2024-01-12 | 塞昆纳姆股份有限公司 | 遗传变异的非侵入性评估的方法和过程 |
| EP3851539B1 (en) | 2013-10-07 | 2026-01-07 | Sequenom, Inc. | Systems for non-invasive assessment of chromosome alterations |
| US10851414B2 (en) | 2013-10-18 | 2020-12-01 | Good Start Genetics, Inc. | Methods for determining carrier status |
| 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 |
| US11053548B2 (en) | 2014-05-12 | 2021-07-06 | Good Start Genetics, Inc. | Methods for detecting aneuploidy |
| JP7182353B2 (ja) * | 2014-05-30 | 2022-12-02 | セクエノム， インコーポレイテッド | 染色体提示の決定 |
| WO2015184404A1 (en) | 2014-05-30 | 2015-12-03 | Verinata Health, Inc. | Detecting fetal sub-chromosomal aneuploidies and copy number variations |
| US20160034640A1 (en) | 2014-07-30 | 2016-02-04 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| US20160048608A1 (en) | 2014-08-15 | 2016-02-18 | Good Start Genetics, Inc. | Systems and methods for genetic analysis |
| US11408024B2 (en) | 2014-09-10 | 2022-08-09 | Molecular Loop Biosciences, Inc. | Methods for selectively suppressing non-target sequences |
| EP3224595A4 (en) | 2014-09-24 | 2018-06-13 | Good Start Genetics, Inc. | Process control for increased robustness of genetic assays |
| EP3567120B1 (en) | 2014-12-12 | 2020-08-19 | Verinata Health, Inc. | Using cell-free dna fragment size to determine copy number variations |
| WO2016112073A1 (en) | 2015-01-06 | 2016-07-14 | Good Start Genetics, Inc. | Screening for structural variants |
| US10095831B2 (en) | 2016-02-03 | 2018-10-09 | Verinata Health, Inc. | Using cell-free DNA fragment size to determine copy number variations |
| US11200963B2 (en) | 2016-07-27 | 2021-12-14 | Sequenom, Inc. | Genetic copy number alteration classifications |
| WO2018140521A1 (en) | 2017-01-24 | 2018-08-02 | Sequenom, Inc. | Methods and processes for assessment of genetic variations |
| IL269202B2 (en) | 2017-03-17 | 2025-08-01 | Sequenom Inc | Methods and processes for assessment of genetic mosaicism |
| CN107217308A (zh) * | 2017-06-21 | 2017-09-29 | 北京贝瑞和康生物技术股份有限公司 | 一种用于检测染色体拷贝数变异的测序文库构建方法和试剂盒 |
| CN109112191A (zh) * | 2017-06-23 | 2019-01-01 | 沈阳精准医疗技术有限公司 | 一种肿瘤ctDNA的信息统计方法 |
| CN109136363A (zh) * | 2018-08-31 | 2019-01-04 | 领航基因科技（杭州）有限公司 | 一种检测胎儿染色体非整数倍的试剂盒和检测胎儿甲基化dna拷贝数的方法 |
| KR102532991B1 (ko) * | 2019-12-23 | 2023-05-18 | 주식회사 랩 지노믹스 | 태아의 염색체 이수성 검출방법 |
| CN113096728B (zh) * | 2021-06-10 | 2021-08-20 | 臻和(北京)生物科技有限公司 | 一种微小残余病灶的检测方法、装置、存储介质及设备 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4643023B2 (ja) * | 1999-05-04 | 2011-03-02 | オルソ−クリニカル ダイアグノスティクス，インコーポレイティド | 細胞溶解剤を使用せずに試料からｄｎａを迅速に効率よく捕捉する方法 |
| US20100216153A1 (en) | 2004-02-27 | 2010-08-26 | Helicos Biosciences Corporation | Methods for detecting fetal nucleic acids and diagnosing fetal abnormalities |
| US12180549B2 (en) | 2007-07-23 | 2024-12-31 | The Chinese University Of Hong Kong | Diagnosing fetal chromosomal aneuploidy using genomic sequencing |
| SMT201700149T1 (it) | 2008-09-20 | 2017-05-08 | Univ Leland Stanford Junior | Diagnosi non invasiva di aneuploidia fetale mediante sequenziamento |
| WO2011051283A1 (en) | 2009-10-26 | 2011-05-05 | Lifecodexx Ag | Means and methods for non-invasive diagnosis of chromosomal aneuploidy |
| CN102018406A (zh) | 2010-11-30 | 2011-04-20 | 赖新莲 | 一种治疗颈椎病的药枕 |
| CN102108406B (zh) * | 2010-12-20 | 2014-05-21 | 北京贝瑞和康生物技术有限公司 | 检测胚胎染色体拷贝数的试剂盒、装置和方法 |
-
2011
- 2011-05-31 PL PL11866914T patent/PL2716766T3/pl unknown
- 2011-05-31 CN CN201180035510.7A patent/CN103080336B/zh active Active
- 2011-05-31 US US13/811,634 patent/US9885080B2/en active Active
- 2011-05-31 DK DK11866914.2T patent/DK2716766T3/da active
- 2011-05-31 HU HUE11866914A patent/HUE031239T2/en unknown
- 2011-05-31 JP JP2014513025A patent/JP5926795B2/ja active Active
- 2011-05-31 EP EP11866914.2A patent/EP2716766B1/en active Active
- 2011-05-31 PT PT118669142T patent/PT2716766T/pt unknown
- 2011-05-31 ES ES11866914.2T patent/ES2605372T3/es active Active
- 2011-05-31 WO PCT/CN2011/075037 patent/WO2012162884A1/zh not_active Ceased
- 2011-05-31 RS RS20161036A patent/RS55518B1/sr unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP2716766A4 (en) | 2014-11-26 |
| EP2716766B1 (en) | 2016-09-28 |
| JP2014516541A (ja) | 2014-07-17 |
| EP2716766A1 (en) | 2014-04-09 |
| HUE031239T2 (en) | 2017-07-28 |
| WO2012162884A1 (zh) | 2012-12-06 |
| PT2716766T (pt) | 2016-11-21 |
| CN103080336A (zh) | 2013-05-01 |
| JP5926795B2 (ja) | 2016-05-25 |
| US20130130921A1 (en) | 2013-05-23 |
| US9885080B2 (en) | 2018-02-06 |
| CN103080336B (zh) | 2014-06-04 |
| ES2605372T3 (es) | 2017-03-14 |
| DK2716766T3 (da) | 2017-01-02 |
| RS55518B1 (sr) | 2017-05-31 |
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