An integrated map of genetic variation from 1,092 human genomes.

An integrated map of genetic variation from 1,092 human genomes.
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来自1,092个人基因组的遗传变异的综合图。

DOI:
10.1038/nature11632
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发表时间:
2012-11-01
期刊:
影响因子:
64.8
通讯作者:
--
中科院分区:
综合性期刊1区
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--
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通过描述人类遗传变异的地理和功能谱,1000个基因组计划旨在建立一个资源,以帮助了解遗传对疾病的贡献。我们描述了来自14个群体的1,092个个体的基因组,使用低覆盖率全基因组和外显子组测序的组合构建。通过开发方法来整合多种算法和不同数据源的信息,我们提供了一个包含3800万个SNP、140万个插入缺失和超过14000个较大缺失的经验证的单倍型图谱。我们发现,来自不同人群的个体携带不同的罕见和常见的变异,低频变异表现出实质性的地理分化,这是进一步增加了纯化选择的作用。我们表明,进化保守性和编码结果是纯化选择强度的关键决定因素,稀有变异负载在生物学途径中变化很大,每个人在保守位点上都有数百种稀有非编码变异,如转录因子基序破坏变化。该资源在医学遗传学重点人群中以1%的频率捕获了高达98%的可访问SNP,能够分析来自不同人群(包括混合人群)的个体中的常见和低频变异。
Through characterising the geographic and functional spectrum of human genetic variation, the 1000 Genomes Project aims to build a resource to help understand the genetic contribution to disease. We describe the genomes of 1,092 individuals from 14 populations, constructed using a combination of low-coverage whole-genome and exome sequencing. By developing methodologies to integrate information across multiple algorithms and diverse data sources we provide a validated haplotype map of 38 million SNPs, 1.4 million indels and over 14 thousand larger deletions. We show that individuals from different populations carry different profiles of rare and common variants and that low-frequency variants show substantial geographic differentiation, which is further increased by the action of purifying selection. We show that evolutionary conservation and coding consequence are key determinants of the strength of purifying selection, that rare-variant load varies substantially across biological pathways and that each individual harbours hundreds of rare non-coding variants at conserved sites, such as transcription-factor-motif disrupting changes. This resource, which captures up to 98% of accessible SNPs at a frequency of 1% in populations of medical genetics focus, enables analysis of common and low-frequency variants in individuals from diverse, including admixed, populations.
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发表时间: 2012-08-23
期刊: NATURE
影响因子: 64.8
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影响因子: 64.8
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