Accurate detection of shared genetic architecture from GWAS summary statistics in the small-sample context.

IF 4.5 2区 生物学 Q1 Agricultural and Biological Sciences PLoS Genetics Pub Date : 2023-08-16 eCollection Date: 2023-08-01 DOI:10.1371/journal.pgen.1010852
Thomas W Willis, Chris Wallace
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Abstract

Assessment of the genetic similarity between two phenotypes can provide insight into a common genetic aetiology and inform the use of pleiotropy-informed, cross-phenotype analytical methods to identify novel genetic associations. The genetic correlation is a well-known means of quantifying and testing for genetic similarity between traits, but its estimates are subject to comparatively large sampling error. This makes it unsuitable for use in a small-sample context. We discuss the use of a previously published nonparametric test of genetic similarity for application to GWAS summary statistics. We establish that the null distribution of the test statistic is modelled better by an extreme value distribution than a transformation of the standard exponential distribution. We show with simulation studies and real data from GWAS of 18 phenotypes from the UK Biobank that the test is to be preferred for use with small sample sizes, particularly when genetic effects are few and large, outperforming the genetic correlation and another nonparametric statistical test of independence. We find the test suitable for the detection of genetic similarity in the rare disease context.

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在小样本背景下,从GWAS汇总统计数据中准确检测共享遗传结构。
评估两种表型之间的遗传相似性可以深入了解常见的遗传病因,并为使用多效性知情的跨表型分析方法来识别新的遗传关联提供信息。遗传相关性是量化和测试性状之间遗传相似性的一种众所周知的方法,但其估计值存在较大的抽样误差。这使得它不适合在小样本上下文中使用。我们讨论了先前发表的遗传相似性的非参数检验在GWAS汇总统计中的应用。我们确定,与标准指数分布的变换相比,通过极值分布更好地模拟测试统计量的零分布。我们通过模拟研究和英国生物库18种表型的GWAS的真实数据表明,该测试更适合用于小样本量的情况,特别是当遗传效应很少和很大时,优于遗传相关性和另一种非参数独立性统计测试。我们发现该测试适用于罕见病背景下的基因相似性检测。
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来源期刊
PLoS Genetics
PLoS Genetics 生物-遗传学
CiteScore
8.10
自引率
2.20%
发文量
438
审稿时长
1 months
期刊介绍: PLOS Genetics is run by an international Editorial Board, headed by the Editors-in-Chief, Greg Barsh (HudsonAlpha Institute of Biotechnology, and Stanford University School of Medicine) and Greg Copenhaver (The University of North Carolina at Chapel Hill). Articles published in PLOS Genetics are archived in PubMed Central and cited in PubMed.
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