CN104968800A - 检测染色体异常的方法 - Google Patents
检测染色体异常的方法 Download PDFInfo
- Publication number
- CN104968800A CN104968800A CN201380056824.4A CN201380056824A CN104968800A CN 104968800 A CN104968800 A CN 104968800A CN 201380056824 A CN201380056824 A CN 201380056824A CN 104968800 A CN104968800 A CN 104968800A
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- nucleic acid
- sequence data
- sequence
- chromosome
- genome
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Classifications
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- 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
- C12Q1/6879—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for sex determination
-
- 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
- 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
-
- 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
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- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Health & Medical Sciences (AREA)
- Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- Analytical Chemistry (AREA)
- Organic Chemistry (AREA)
- Biophysics (AREA)
- Biotechnology (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Genetics & Genomics (AREA)
- Medical Informatics (AREA)
- Bioinformatics & Computational Biology (AREA)
- Evolutionary Biology (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Theoretical Computer Science (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Microbiology (AREA)
- General Engineering & Computer Science (AREA)
- Immunology (AREA)
- Pathology (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Investigating Or Analysing Biological Materials (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261695182P | 2012-08-30 | 2012-08-30 | |
| GB1215449.8 | 2012-08-30 | ||
| GBGB1215449.8A GB201215449D0 (en) | 2012-08-30 | 2012-08-30 | Method of detecting chromosonal abnormalities |
| US61/695182 | 2012-08-30 | ||
| PCT/GB2013/052261 WO2014033455A1 (en) | 2012-08-30 | 2013-08-29 | Method of detecting chromosomal abnormalities |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN104968800A true CN104968800A (zh) | 2015-10-07 |
Family
ID=47074981
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201380056824.4A Pending CN104968800A (zh) | 2012-08-30 | 2013-08-29 | 检测染色体异常的方法 |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US20150267255A1 (enExample) |
| EP (1) | EP2890813A1 (enExample) |
| JP (1) | JP2015526101A (enExample) |
| KR (1) | KR20150070111A (enExample) |
| CN (1) | CN104968800A (enExample) |
| CA (1) | CA2883464A1 (enExample) |
| GB (1) | GB201215449D0 (enExample) |
| HK (1) | HK1212391A1 (enExample) |
| IN (1) | IN2015MN00457A (enExample) |
| WO (1) | WO2014033455A1 (enExample) |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105926043A (zh) * | 2016-04-19 | 2016-09-07 | 苏州贝康医疗器械有限公司 | 一种提高孕妇血浆游离dna测序文库中胎儿游离dna占比的方法 |
| CN108268752A (zh) * | 2018-01-18 | 2018-07-10 | 东莞博奥木华基因科技有限公司 | 一种染色体异常检测装置 |
| CN108396058A (zh) * | 2018-01-19 | 2018-08-14 | 刘晓雯 | 检测染色体异常的产前诊断方法 |
| CN108604258A (zh) * | 2016-01-20 | 2018-09-28 | 伊万基因诊断中心有限公司 | 染色体异常判断方法 |
| CN109074427A (zh) * | 2015-12-22 | 2018-12-21 | 普瑞梅萨有限公司 | 染色体异常的检测 |
| CN109280702A (zh) * | 2017-07-21 | 2019-01-29 | 深圳华大基因研究院 | 确定个体染色体结构异常的方法和系统 |
| CN110033828A (zh) * | 2019-04-03 | 2019-07-19 | 北京各色科技有限公司 | 基于芯片检测dna数据的性别判断方法 |
| CN110914456A (zh) * | 2017-03-31 | 2020-03-24 | 普莱梅沙有限公司 | 检测胎儿染色体异常的方法 |
| US12221820B2 (en) * | 2021-10-12 | 2025-02-11 | Hyundai Motor Company | Vehicle hinge driving apparatus |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20130309666A1 (en) | 2013-01-25 | 2013-11-21 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| EP3149202A1 (en) * | 2014-05-26 | 2017-04-05 | Ebios Futura S.r.l. | Method of prenatal diagnosis |
| 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 |
| KR101638473B1 (ko) * | 2014-12-26 | 2016-07-12 | 연세대학교 산학협력단 | 차세대 염기서열 분석법을 기반으로 하는 결실 유전자군 검출 방법 |
| BE1022789B1 (nl) | 2015-07-17 | 2016-09-06 | Multiplicom Nv | Werkwijze en systeem voor geslachtsinschatting van een foetus van een zwangere vrouw |
| KR101817785B1 (ko) * | 2015-08-06 | 2018-01-11 | 이원다이애그노믹스(주) | 다양한 플랫폼에서 태아의 성별과 성염색체 이상을 구분할 수 있는 새로운 방법 |
| IL285795B (en) * | 2015-08-12 | 2022-07-01 | Univ Hong Kong Chinese | Single-molecule sequencing of plasma dna |
| KR101686146B1 (ko) * | 2015-12-04 | 2016-12-13 | 주식회사 녹십자지놈 | 핵산의 혼합물을 포함하는 샘플에서 복제수 변이를 결정하는 방법 |
| JP2019500901A (ja) * | 2015-12-04 | 2019-01-17 | グリーン クロス ゲノム コーポレーションGreen Cross Genome Corporation | 核酸の混合物を含むサンプルでコピー数異常を決定する方法 |
| KR101721480B1 (ko) | 2016-06-02 | 2017-03-30 | 주식회사 랩 지노믹스 | 염색체 이상 검사 방법 및 시스템 |
| US20230028790A1 (en) * | 2019-11-29 | 2023-01-26 | GC Genome Corporation | Artificial intelligence-based chromosomal abnormality detection method |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2485635A (en) * | 2011-07-26 | 2012-05-23 | Verinata Health Inc | Chromosomal aneuploidy detection by mass sequencing and analysis against whole or segment of normalising chromosome. |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2011054936A1 (en) * | 2009-11-06 | 2011-05-12 | The Chinese University Of Hong Kong | Size-based genomic analysis |
| WO2012135730A2 (en) * | 2011-03-30 | 2012-10-04 | Verinata Health, Inc. | Method for verifying bioassay samples |
-
2012
- 2012-08-30 GB GBGB1215449.8A patent/GB201215449D0/en not_active Ceased
-
2013
- 2013-08-29 US US14/424,805 patent/US20150267255A1/en not_active Abandoned
- 2013-08-29 CN CN201380056824.4A patent/CN104968800A/zh active Pending
- 2013-08-29 CA CA2883464A patent/CA2883464A1/en not_active Abandoned
- 2013-08-29 HK HK16100149.2A patent/HK1212391A1/xx unknown
- 2013-08-29 EP EP13759286.1A patent/EP2890813A1/en not_active Ceased
- 2013-08-29 JP JP2015529121A patent/JP2015526101A/ja active Pending
- 2013-08-29 WO PCT/GB2013/052261 patent/WO2014033455A1/en not_active Ceased
- 2013-08-29 KR KR1020157007576A patent/KR20150070111A/ko not_active Withdrawn
- 2013-08-29 IN IN457MUN2015 patent/IN2015MN00457A/en unknown
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2485635A (en) * | 2011-07-26 | 2012-05-23 | Verinata Health Inc | Chromosomal aneuploidy detection by mass sequencing and analysis against whole or segment of normalising chromosome. |
Non-Patent Citations (1)
| Title |
|---|
| BEN LANGMEAD ETAL: "fast gapped-read alignment with Bowtie2", 《NATURE METHODS》 * |
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN109074427A (zh) * | 2015-12-22 | 2018-12-21 | 普瑞梅萨有限公司 | 染色体异常的检测 |
| CN108604258A (zh) * | 2016-01-20 | 2018-09-28 | 伊万基因诊断中心有限公司 | 染色体异常判断方法 |
| CN108604258B (zh) * | 2016-01-20 | 2022-05-13 | 伊万基因诊断中心有限公司 | 染色体异常判断方法 |
| CN105926043A (zh) * | 2016-04-19 | 2016-09-07 | 苏州贝康医疗器械有限公司 | 一种提高孕妇血浆游离dna测序文库中胎儿游离dna占比的方法 |
| CN110914456A (zh) * | 2017-03-31 | 2020-03-24 | 普莱梅沙有限公司 | 检测胎儿染色体异常的方法 |
| CN109280702A (zh) * | 2017-07-21 | 2019-01-29 | 深圳华大基因研究院 | 确定个体染色体结构异常的方法和系统 |
| CN108268752A (zh) * | 2018-01-18 | 2018-07-10 | 东莞博奥木华基因科技有限公司 | 一种染色体异常检测装置 |
| CN108396058A (zh) * | 2018-01-19 | 2018-08-14 | 刘晓雯 | 检测染色体异常的产前诊断方法 |
| CN110033828A (zh) * | 2019-04-03 | 2019-07-19 | 北京各色科技有限公司 | 基于芯片检测dna数据的性别判断方法 |
| CN110033828B (zh) * | 2019-04-03 | 2021-06-18 | 北京各色科技有限公司 | 基于芯片检测dna数据的性别判断方法 |
| US12221820B2 (en) * | 2021-10-12 | 2025-02-11 | Hyundai Motor Company | Vehicle hinge driving apparatus |
Also Published As
| Publication number | Publication date |
|---|---|
| US20150267255A1 (en) | 2015-09-24 |
| WO2014033455A1 (en) | 2014-03-06 |
| CA2883464A1 (en) | 2014-03-06 |
| KR20150070111A (ko) | 2015-06-24 |
| IN2015MN00457A (enExample) | 2015-09-04 |
| GB201215449D0 (en) | 2012-10-17 |
| HK1212391A1 (en) | 2016-06-10 |
| JP2015526101A (ja) | 2015-09-10 |
| EP2890813A1 (en) | 2015-07-08 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| WD01 | Invention patent application deemed withdrawn after publication |
Application publication date: 20151007 |
|
| WD01 | Invention patent application deemed withdrawn after publication |