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韩国变异体档案(KOVA):韩国人群遗传变异的参考数据库。

Korean Variant Archive (KOVA): a reference database of genetic variations in the Korean population.

机构信息

Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul, 03080, Republic of Korea.

Ewha Research Center for Systems Biology (ERCSB), Ewha Womans University, Seoul, 03760, Republic of Korea.

出版信息

Sci Rep. 2017 Jun 27;7(1):4287. doi: 10.1038/s41598-017-04642-4.

Abstract

Despite efforts to interrogate human genome variation through large-scale databases, systematic preference toward populations of Caucasian descendants has resulted in unintended reduction of power in studying non-Caucasians. Here we report a compilation of coding variants from 1,055 healthy Korean individuals (KOVA; Korean Variant Archive). The samples were sequenced to a mean depth of 75x, yielding 101 singleton variants per individual. Population genetics analysis demonstrates that the Korean population is a distinct ethnic group comparable to other discrete ethnic groups in Africa and Europe, providing a rationale for such independent genomic datasets. Indeed, KOVA conferred 22.8% increased variant filtering power in addition to Exome Aggregation Consortium (ExAC) when used on Korean exomes. Functional assessment of nonsynonymous variant supported the presence of purifying selection in Koreans. Analysis of copy number variants detected 5.2 deletions and 10.3 amplifications per individual with an increased fraction of novel variants among smaller and rarer copy number variable segments. We also report a list of germline variants that are associated with increased tumor susceptibility. This catalog can function as a critical addition to the pre-existing variant databases in pursuing genetic studies of Korean individuals.

摘要

尽管通过大型数据库努力研究人类基因组变异,但系统地偏向白种人后裔导致在研究非白种人时无意降低了研究能力。在这里,我们报告了来自 1055 名健康韩国个体(KOVA;韩国变异档案)的编码变异的汇编。这些样本被测序到平均深度为 75x,每个个体产生 101 个单倍型变异。群体遗传学分析表明,韩国人群是一个独特的族群,与非洲和欧洲的其他离散族群相当,为这种独立的基因组数据集提供了合理的依据。实际上,当在韩国外显子组上使用时,KOVA 除了 Exome Aggregation Consortium (ExAC) 外,还增加了 22.8%的变异过滤能力。对非同义变异的功能评估支持韩国人群中存在纯化选择。拷贝数变异的分析检测到每个个体有 5.2 个缺失和 10.3 个扩增,较小和较罕见的拷贝数可变片段中存在更多的新变异。我们还报告了与增加的肿瘤易感性相关的种系变异列表。该目录可作为现有变异数据库的重要补充,用于开展韩国个体的遗传研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f99/5487339/a0171190a96c/41598_2017_4642_Fig1_HTML.jpg

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