Efficient Bayesian mixed-model analysis increases association power in large cohorts

混淆 遗传建筑学 统计能力 贝叶斯概率 遗传关联 混合模型 全基因组关联研究 生物 广义线性混合模型 统计 功率(物理) 计算机科学 计算生物学 单核苷酸多态性 无穷小 数学 遗传学 数量性状位点 基因型 物理 基因 数学分析 量子力学
作者
Po‐Ru Loh,George Tucker,Brendan Bulik‐Sullivan,Bjarni J. Vilhjálmsson,Hilary K. Finucane,Rany M. Salem,Daniel I. Chasman,Paul M. Ridker,Benjamin M. Neale,Bonnie Berger,Hon‐Cheong So,Alkes L. Price
出处
期刊:Nature Genetics [Nature Portfolio]
卷期号:47 (3): 284-290 被引量:1582
标识
DOI:10.1038/ng.3190
摘要

Alkes Price, Po-Ru Loh and colleagues report the BOLT-LMM method for mixed-model association. They apply their method to 9 quantitative traits in 23,294 samples and demonstrate that it provides improvements in computational efficiency as well as gains in power that increase with the size of the cohort, making it useful for the analysis of large cohorts. Linear mixed models are a powerful statistical tool for identifying genetic associations and avoiding confounding. However, existing methods are computationally intractable in large cohorts and may not optimize power. All existing methods require time cost O(MN2) (where N is the number of samples and M is the number of SNPs) and implicitly assume an infinitesimal genetic architecture in which effect sizes are normally distributed, which can limit power. Here we present a far more efficient mixed-model association method, BOLT-LMM, which requires only a small number of O(MN) time iterations and increases power by modeling more realistic, non-infinitesimal genetic architectures via a Bayesian mixture prior on marker effect sizes. We applied BOLT-LMM to 9 quantitative traits in 23,294 samples from the Women's Genome Health Study (WGHS) and observed significant increases in power, consistent with simulations. Theory and simulations show that the boost in power increases with cohort size, making BOLT-LMM appealing for genome-wide association studies in large cohorts.
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