SA517380741B1 - طريقة ومعدة لتحليل جين - Google Patents
طريقة ومعدة لتحليل جينInfo
- Publication number
- SA517380741B1 SA517380741B1 SA517380741A SA517380741A SA517380741B1 SA 517380741 B1 SA517380741 B1 SA 517380741B1 SA 517380741 A SA517380741 A SA 517380741A SA 517380741 A SA517380741 A SA 517380741A SA 517380741 B1 SA517380741 B1 SA 517380741B1
- Authority
- SA
- Saudi Arabia
- Prior art keywords
- genes
- depths
- gene
- analyzing gene
- analyzed
- Prior art date
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- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biotechnology (AREA)
- Analytical Chemistry (AREA)
- Biophysics (AREA)
- Organic Chemistry (AREA)
- Bioinformatics & Computational Biology (AREA)
- Evolutionary Biology (AREA)
- Medical Informatics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Theoretical Computer Science (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Apparatus Associated With Microorganisms And Enzymes (AREA)
- Microbiology (AREA)
- Molecular Biology (AREA)
- Immunology (AREA)
- Biochemistry (AREA)
- General Engineering & Computer Science (AREA)
- Genetics & Genomics (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
Abstract
يتعلق الاختراع الحالي في هذه الوثيقة بتوفير طريقة ومعدة لتحليل جين gene. وفقاً للطريقة والمعدة، يتم توليد مجموعة بيانات مرجعية reference data set عن طريق تنفيذ تتالي عميق على الجينات المرجعية reference genes، يتم تحليل أعماق جينات خاضع عن طريق تنفيذ تتالي العمق على جينات الخاضع، ويتم تحديد وجود جين اختلاف عدد النسخ copy number variation (CNV) في جينات الخاضع عن طريق مقارنة الأعماق المحللة بأعماق الجينات المرجعية المضمنة في مجموعة البيانات المرجعية. شكل 1
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR20150089449 | 2015-06-24 | ||
KR1020150168833A KR101828052B1 (ko) | 2015-06-24 | 2015-11-30 | 유전자의 복제수 변이(cnv)를 분석하는 방법 및 장치 |
PCT/KR2015/012925 WO2016208827A1 (ko) | 2015-06-24 | 2015-11-30 | 유전자를 분석하는 방법 및 장치 |
Publications (1)
Publication Number | Publication Date |
---|---|
SA517380741B1 true SA517380741B1 (ar) | 2021-05-18 |
Family
ID=57797296
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SA517380741A SA517380741B1 (ar) | 2015-06-24 | 2017-01-18 | طريقة ومعدة لتحليل جين |
Country Status (4)
Country | Link |
---|---|
KR (1) | KR101828052B1 (ar) |
CN (1) | CN107408163B (ar) |
SA (1) | SA517380741B1 (ar) |
SG (1) | SG11201707649SA (ar) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101957909B1 (ko) | 2017-02-24 | 2019-03-15 | 에스디지노믹스 주식회사 | 복제수 변이 후보 우선순위 연산 방법 |
KR101943053B1 (ko) | 2017-02-24 | 2019-01-28 | 한림대학교 산학협력단 | 유전자 단위 반복 변이 검출 시스템 및 방법 |
KR101926977B1 (ko) * | 2017-05-29 | 2019-03-07 | 연세대학교 산학협력단 | 내포복제 판단을 위한 오토마타 생성 방법 |
KR102233740B1 (ko) * | 2017-09-27 | 2021-03-30 | 이화여자대학교 산학협력단 | Dna 복제수 변이 기반의 암 종 예측 방법 |
CN108647496B (zh) * | 2018-04-18 | 2019-07-02 | 成都仕康美生物科技有限公司 | 动态搜索变异基因的方法、装置及计算机可读存储介质 |
CN108920899B (zh) * | 2018-06-10 | 2022-02-08 | 杭州迈迪科生物科技有限公司 | 一种基于目标区域测序的单个外显子拷贝数变异预测方法 |
CN111383717A (zh) * | 2018-12-29 | 2020-07-07 | 北京安诺优达医学检验实验室有限公司 | 一种构建生物信息分析参照数据集的方法及系统 |
KR20210107492A (ko) * | 2020-02-24 | 2021-09-01 | (재)록원바이오융합연구재단 | 복제수 변이 검출용 표준화 유전자의 선별 방법 및 상기 방법에 의해서 선별된 c-Met 복제수 변이 검출용 조성물 |
KR102273257B1 (ko) * | 2020-11-16 | 2021-07-06 | 주식회사 엔젠바이오 | 리드 깊이 기반한 유전자 복제수 변이 검출 기법 및 분석장치 |
KR20230114952A (ko) * | 2022-01-26 | 2023-08-02 | 권창혁 | 암 판별 장치 및 암 판별 방법 |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7289911B1 (en) * | 2000-08-23 | 2007-10-30 | David Roth Rigney | System, methods, and computer program product for analyzing microarray data |
CN101374964B (zh) * | 2005-12-09 | 2013-07-17 | 贝勒研究院 | 外周血液白细胞转录模式的模块水平分析 |
EP2359284A2 (en) * | 2008-10-31 | 2011-08-24 | Abbott Laboratories | Method for genomic classification of malignant melanoma based on patterns of gene copy number alterations |
US8725422B2 (en) * | 2010-10-13 | 2014-05-13 | Complete Genomics, Inc. | Methods for estimating genome-wide copy number variations |
JP6420543B2 (ja) * | 2011-01-19 | 2018-11-07 | コーニンクレッカ フィリップス エヌ ヴェKoninklijke Philips N.V. | ゲノムデータ処理方法 |
CN102682224B (zh) * | 2011-03-18 | 2015-01-21 | 深圳华大基因科技服务有限公司 | 检测拷贝数变异的方法和装置 |
CN104136628A (zh) * | 2011-10-28 | 2014-11-05 | 深圳华大基因医学有限公司 | 一种检测染色体微缺失和微重复的方法 |
CN104428425A (zh) * | 2012-05-04 | 2015-03-18 | 考利达基因组股份有限公司 | 测定复杂肿瘤全基因组绝对拷贝数变异的方法 |
IL305303A (en) * | 2012-09-04 | 2023-10-01 | Guardant Health Inc | Systems and methods for detecting rare mutations and changes in number of copies |
CN104603284B (zh) * | 2012-09-12 | 2016-08-24 | 深圳华大基因研究院 | 利用基因组测序片段检测拷贝数变异的方法 |
US10482994B2 (en) * | 2012-10-04 | 2019-11-19 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
US20140222349A1 (en) * | 2013-01-16 | 2014-08-07 | Assurerx Health, Inc. | System and Methods for Pharmacogenomic Classification |
CN104298892B (zh) * | 2014-09-18 | 2017-05-10 | 天津诺禾致源生物信息科技有限公司 | 基因融合的检测装置和方法 |
-
2015
- 2015-11-30 SG SG11201707649SA patent/SG11201707649SA/en unknown
- 2015-11-30 CN CN201580078172.3A patent/CN107408163B/zh active Active
- 2015-11-30 KR KR1020150168833A patent/KR101828052B1/ko active IP Right Grant
-
2017
- 2017-01-18 SA SA517380741A patent/SA517380741B1/ar unknown
Also Published As
Publication number | Publication date |
---|---|
CN107408163A (zh) | 2017-11-28 |
SG11201707649SA (en) | 2017-10-30 |
KR101828052B1 (ko) | 2018-02-09 |
KR20170000744A (ko) | 2017-01-03 |
CN107408163B (zh) | 2021-03-05 |
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