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11,670 whole-genome sequences representative of the Han Chinese population from the CONVERGE project

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 th...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5308202/
https://www.ncbi.nlm.nih.gov/pubmed/28195579
http://dx.doi.org/10.1038/sdata.2017.11
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author 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
author_facet 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
author_sort Cai, Na
collection PubMed
description 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.
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spelling pubmed-53082022017-02-17 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 Sci Data Data Descriptor 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. Nature Publishing Group 2017-02-14 /pmc/articles/PMC5308202/ /pubmed/28195579 http://dx.doi.org/10.1038/sdata.2017.11 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0 This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0 Metadata associated with this Data Descriptor is available at http://www.nature.com/sdata/ and is released under the CC0 waiver to maximize reuse.
spellingShingle Data Descriptor
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
11,670 whole-genome sequences representative of the Han Chinese population from the CONVERGE project
title 11,670 whole-genome sequences representative of the Han Chinese population from the CONVERGE project
title_full 11,670 whole-genome sequences representative of the Han Chinese population from the CONVERGE project
title_fullStr 11,670 whole-genome sequences representative of the Han Chinese population from the CONVERGE project
title_full_unstemmed 11,670 whole-genome sequences representative of the Han Chinese population from the CONVERGE project
title_short 11,670 whole-genome sequences representative of the Han Chinese population from the CONVERGE project
title_sort 11,670 whole-genome sequences representative of the han chinese population from the converge project
topic Data Descriptor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5308202/
https://www.ncbi.nlm.nih.gov/pubmed/28195579
http://dx.doi.org/10.1038/sdata.2017.11
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