全基因组关联研究的集体排序方法。

Jie Liu, Humberto Vidaillet, Elizabeth Burnside, David Page
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引用次数: 0

摘要

全基因组关联研究(GWAS)分析整个人类基因组的遗传变异(SNPs),寻找与某些表型(最常见的疾病,如乳腺癌)相关的SNPs。在GWAS中,我们根据snp与给定表型的相关性寻求snp的排名。然而,由于已知某些snp在个体之间彼此高度相关,因此在排序时考虑这些相关性可能是有益的。如果一个SNP出现与表型相关,我们质疑这种关联是否真实,那么它的邻居(相关SNP)也出现相关的程度可以提供信息。因此,我们提出了CollectRank,这是一种允许snp通过相关结构相互加强的排序方法。CollectRank松散地类似于众所周知的PageRank算法。我们首先在不同设置下由各种遗传模型生成的合成数据上评估CollectRank。数值结果表明,CollectRank可以在少量额外计算的代价下显著优于常见的GWAS方法。我们进一步评估了CollectRank对乳腺癌和心房颤动/扑动的两项真实GWAS, CollectRank在两项研究中均表现良好。最后,我们提供了一个理论分析,也表明了CollectRank的优势。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Collective Ranking Method for Genome-wide Association Studies.

Genome-wide association studies (GWAS) analyze genetic variation (SNPs) across the entire human genome, searching for SNPs that are associated with certain phenotypes, most often diseases, such as breast cancer. In GWAS, we seek a ranking of SNPs in terms of their relevance to the given phenotype. However, because certain SNPs are known to be highly correlated with one another across individuals, it can be beneficial to take into account these correlations when ranking. If a SNP appears associated with the phenotype, and we question whether this association is real, the extent to which its neighbors (correlated SNPs) also appear associated can be informative. Therefore, we propose CollectRank, a ranking approach which allows SNPs to reinforce one another via the correlation structure. CollectRank is loosely analogous to the well-known PageRank algorithm. We first evaluate CollectRank on synthetic data generated from a variety of genetic models under different settings. The numerical results suggest CollectRank can significantly outperform common GWAS methods at the cost of a small amount of extra computation. We further evaluate CollectRank on two real-world GWAS on breast cancer and atrial fibrillation/flutter, and CollectRank performs well in both studies. We finally provide a theoretical analysis that also suggests CollectRank's advantages.

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