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11,670 whole-genome sequences representative of the Han Chinese population from the CONVERGE project.
Cai, Na; Bigdeli, Tim B; Kretzschmar, Warren W; Li, Yihan; Liang, Jieqin; Hu, Jingchu; Peterson, Roseann E; Bacanu, Silviu; Webb, Bradley Todd; Riley, Brien; Li, Qibin; Marchini, Jonathan; Mott, Richard; Kendler, Kenneth S; Flint, Jonathan.
Afiliación
  • Cai N; Wellcome Trust Centre for Human Genetics, OX3 7BN Oxford, UK.
  • Bigdeli TB; Wellcome Trust Sanger Institute, Wellcome Genome Campus, CB10 1SA Hinxton, Cambridge, UK.
  • Kretzschmar WW; European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, CB10 1SD Hinxton, Cambridge, UK.
  • Li Y; Virginia Institute for Psychiatric and Behavioral Genetics, Virginia Commonwealth University, Richmond, Virginia 23298, USA.
  • Liang J; Wellcome Trust Centre for Human Genetics, OX3 7BN Oxford, UK.
  • Hu J; Wellcome Trust Centre for Human Genetics, OX3 7BN Oxford, UK.
  • Peterson RE; BGI-Shenzhen, Shenzhen, Guangdong 518083, China.
  • Bacanu S; BGI-Shenzhen, Shenzhen, Guangdong 518083, China.
  • Webb BT; Virginia Institute for Psychiatric and Behavioral Genetics, Virginia Commonwealth University, Richmond, Virginia 23298, USA.
  • Riley B; Virginia Institute for Psychiatric and Behavioral Genetics, Virginia Commonwealth University, Richmond, Virginia 23298, USA.
  • Li Q; Virginia Institute for Psychiatric and Behavioral Genetics, Virginia Commonwealth University, Richmond, Virginia 23298, USA.
  • Marchini J; Virginia Institute for Psychiatric and Behavioral Genetics, Virginia Commonwealth University, Richmond, Virginia 23298, USA.
  • Mott R; BGI-Shenzhen, Shenzhen, Guangdong 518083, China.
  • Kendler KS; Department of Statistics, University of Oxford, Oxford OX1 3TG, UK.
  • Flint J; Wellcome Trust Centre for Human Genetics, OX3 7BN Oxford, UK.
Sci Data ; 4: 170011, 2017 02 14.
Article en En | MEDLINE | ID: mdl-28195579
ABSTRACT
The China, Oxford and Virginia Commonwealth University Experimental Research on Genetic Epidemiology (CONVERGE) project on Major Depressive Disorder (MDD) sequenced 11,670 female Han Chinese at low-coverage (1.7X), providing the first large-scale whole genome sequencing resource representative of the largest ethnic group in the world. Samples are collected from 58 hospitals from 23 provinces around China. We are able to call 22 million high quality single nucleotide polymorphisms (SNP) from the nuclear genome, representing the largest SNP call set from an East Asian population to date. We use these variants for imputation of genotypes across all samples, and this has allowed us to perform a successful genome wide association study (GWAS) on MDD. The utility of these data can be extended to studies of genetic ancestry in the Han Chinese and evolutionary genetics when integrated with data from other populations. Molecular phenotypes, such as copy number variations and structural variations can be detected, quantified and analysed in similar ways.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Genoma Humano Límite: Female / Humans País/Región como asunto: Asia Idioma: En Revista: Sci Data Año: 2017 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Genoma Humano Límite: Female / Humans País/Región como asunto: Asia Idioma: En Revista: Sci Data Año: 2017 Tipo del documento: Article País de afiliación: Reino Unido