Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits.

Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits.
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DOI:
10.1038/ng.2213
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发表时间:
2012-03-18
期刊:
影响因子:
30.8
通讯作者:
Visscher, Peter M.
Visscher, Peter M.
中科院分区:
生物学1区
文献类型:
--
作者:
Yang, Jian;Ferreira, Teresa;Morris, Andrew P.;Medland, Sarah E.;Madden, Pamela A. F.;Heath, Andrew C.;Martin, Nicholas G.;Montgomery, Grant W.;Weedon, Michael N.;Loos, Ruth J.;Frayling, Timothy M.;McCarthy, Mark I.;Hirschhorn, Joel N.;Goddard, Michael E.;Visscher, Peter M.

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我们提出了一个近似的条件和联合关联分析,可以使用来自全基因组关联研究(GWAS)的荟萃分析的汇总水平统计数据和来自个体水平基因型数据的参考样本的估计连锁不平衡(LD)。使用这种方法,我们分析了来自GIANT Consortium的身高和体重指数(BMI)的荟萃分析汇总数据,并从两个独立队列的基因型数据中估计了LD结构。我们通过全基因组SNP选择程序鉴定了36个具有多个身高相关变异的基因座(38个前导和49个额外的SNP,总共87个)。这49个新的SNP解释了大约1.3%的变异,几乎是36个位点解释的遗传力的两倍。我们没有发现任何位点显示BMI的多个相关SNP。我们提出的方法是计算速度快,也适用于病例对照数据,我们证明了一个例子,从2型糖尿病的荟萃分析的DIAGRAM联盟。
We present an approximate conditional and joint association analysis that can use summary-level statistics from a meta-analysis of genome-wide association studies (GWAS) and estimated linkage disequilibrium (LD) from a reference sample with individual-level genotype data. Using this method, we analyzed meta-analysis summary data from the GIANT Consortium for height and body mass index (BMI), with the LD structure estimated from genotype data in two independent cohorts. We identified 36 loci with multiple associated variants for height (38 leading and 49 additional SNPs, 87 in total) via a genome-wide SNP selection procedure. The 49 new SNPs explain approximately 1.3% of variance, nearly doubling the heritability explained at the 36 loci. We did not find any locus showing multiple associated SNPs for BMI. The method we present is computationally fast and is also applicable to case-control data, which we demonstrate in an example from meta-analysis of type 2 diabetes by the DIAGRAM Consortium.
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