HK1162056A1 - Identification method for genetic disease-related gene - Google Patents

Identification method for genetic disease-related gene

Info

Publication number
HK1162056A1
HK1162056A1 HK12102487.2A HK12102487A HK1162056A1 HK 1162056 A1 HK1162056 A1 HK 1162056A1 HK 12102487 A HK12102487 A HK 12102487A HK 1162056 A1 HK1162056 A1 HK 1162056A1
Authority
HK
Hong Kong
Prior art keywords
identification method
related gene
genetic disease
genetic
disease
Prior art date
Application number
HK12102487.2A
Other languages
Chinese (zh)
Inventor
張朋蘇政金鑫唐北沙王俊嶺翁翎
Original Assignee
深圳華大基因科技有限公司 廣東省深圳市 中南大學
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 深圳華大基因科技有限公司 廣東省深圳市 中南大學 filed Critical 深圳華大基因科技有限公司 廣東省深圳市 中南大學
Publication of HK1162056A1 publication Critical patent/HK1162056A1/en

Links

HK12102487.2A 2010-09-19 2012-03-12 Identification method for genetic disease-related gene HK1162056A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201010286309.3A CN102206701B (en) 2010-09-19 2010-09-19 Identification method for genetic disease-related gene

Publications (1)

Publication Number Publication Date
HK1162056A1 true HK1162056A1 (en) 2012-08-17

Family

ID=44695761

Family Applications (1)

Application Number Title Priority Date Filing Date
HK12102487.2A HK1162056A1 (en) 2010-09-19 2012-03-12 Identification method for genetic disease-related gene

Country Status (2)

Country Link
CN (1) CN102206701B (en)
HK (1) HK1162056A1 (en)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103509799B (en) * 2012-06-18 2016-03-23 深圳华大基因股份有限公司 Hypertrophic osteoarthropathy,primary Disease-causing gene
CN104178486B (en) * 2013-05-20 2017-12-15 中南大学湘雅医院 SACS gene mutant and application thereof
CN104178487B (en) * 2013-05-20 2017-09-19 中南大学湘雅医院 ATM gene mutant and application thereof
CN104862380B (en) * 2014-02-25 2018-04-13 绍兴市柯桥区基石生物科技有限公司 Family specificity hereditary disease associates allele monomer form variation label confirmation method
CN104946765A (en) * 2015-06-25 2015-09-30 华中农业大学 Somatic mutation site excavation method based on genomic sequencing
EP3356559A4 (en) * 2015-09-29 2019-03-06 Ludwig Institute for Cancer Research Ltd Typing and assembling discontinuous genomic elements
CN110268072B (en) * 2016-12-15 2023-11-07 Illumina公司 Method and system for determining paralogous genes
CN106834107A (en) * 2017-03-10 2017-06-13 首度生物科技（苏州）有限公司 A kind of prediction tumour system for being based on the sequencing of two generations
CN109994154B (en) * 2017-12-30 2021-07-13 安诺优达基因科技(北京)有限公司 Screening device for candidate pathogenic genes of monogenic recessive genetic disease
CN108913767A (en) * 2018-07-20 2018-11-30 中南大学湘雅医院 Parkinson disease pathogenic gene, kit and application
CN110468194A (en) * 2019-08-12 2019-11-19 广州万德基因医学科技有限公司 The multiple PCR primer group and kit in library are built for Inherited Metabolic Disorders high-flux sequence

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU785425B2 (en) * 2001-03-30 2007-05-17 Genetic Technologies Limited Methods of genomic analysis
WO2003074740A1 (en) * 2002-03-01 2003-09-12 Ravgen, Inc. Rapid analysis of variations in a genome

Also Published As

Publication number Publication date
CN102206701B (en) 2015-01-21
CN102206701A (en) 2011-10-05

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