论文标题

多特征自适应Fisher的全基因组关联研究方法

Multiple-trait Adaptive Fisher's Method for Genome-wide Association Studies

论文作者

Deng, Qiaolan, Song, Chi

论文摘要

在全基因组关联研究(GWASS)中,越来越需要检测遗传变异和多种性状之间的关联。在复杂疾病的研究中,通常在单个GWA中测量几种潜在的相关性状。尽管研究的多元性质,但基于单特征的方法仍然是最广泛的分析程序,这是由于它们的研究简单性,并具有多种性状作为结果。但是,遗传变异与单个特征之间的关联有时可能很弱,而忽略特征之间的实际相关性可能会失去权力。相反,多种特征分析,一种方法同时分析了一组特征,已通过合并相关性状的信息而被证明具有更大的功能。尽管已经针对多种特征开发了现有的方法,但几个缺点限制了其在GWASS中的广泛应用。在本文中,我们提出了一种多特征自适应Fisher(MTAF)方法,通过从每个性状中自适应地汇总证据来一次测试遗传变异和多个特征之间的关联。所提出的方法可以适应连续和二进制特征,并且在各种情况下具有可靠的性能。使用仿真研究,我们将我们提出的方法与几种现有方法进行了比较,并证明了它在I型错误控制和统计能力方面的竞争力。通过将方法应用于成瘾研究:遗传学和环境(SAGE)数据集,我们成功地鉴定了与物质依赖性相关的几个基因。

In genome-wide association studies (GWASs), there is an increasing need for detecting the associations between a genetic variant and multiple traits. In studies of complex diseases, it is common to measure several potentially correlated traits in a single GWAS. Despite the multivariate nature of the studies, single-trait-based methods remain the most widely-adopted analysis procedure, owing to their simplicity for studies with multiple traits as their outcome. However, the association between a genetic variant and a single trait sometimes can be weak, and ignoring the actual correlation among traits may lose power. On the contrary, multiple-trait analysis, a method analyzes a group of traits simultaneously, has been proven to be more powerful by incorporating information from the correlated traits. Although existing methods have been developed for multiple traits, several drawbacks limit their wide application in GWASs. In this paper, we propose a multiple-trait adaptive Fisher's (MTAF) method to test associations between a genetic variant and multiple traits at once, by adaptively aggregating evidence from each trait. The proposed method can accommodate both continuous and binary traits and it has reliable performance under various scenarios. Using a simulation study, we compared our proposed method with several existing methods and demonstrated its competitiveness in terms of type I error control and statistical power. By applying the method to the Study of Addiction: Genetics and Environment (SAGE) dataset, we successfully identified several genes associated with substance dependence.

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