MRC Biostatistics Unit, University of Cambridge, Cambridge, United Kingdom.
Cambridge Institute of Therapeutic Immunology and Infectious Disease, University of Cambridge, Cambridge, United Kingdom.
PLoS Genet. 2023 Aug 16;19(8):e1010852. doi: 10.1371/journal.pgen.1010852. eCollection 2023 Aug.
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.
评估两种表型之间的遗传相似性可以深入了解共同的遗传病因,并为使用多效性信息丰富的跨表型分析方法来识别新的遗传关联提供信息。遗传相关系数是一种用于量化和检验性状之间遗传相似性的常用方法,但它的估计值受到相对较大的抽样误差的影响。这使得它不适合在小样本情况下使用。我们讨论了使用先前发表的非参数遗传相似性检验方法来应用于 GWAS 汇总统计数据。我们确定,检验统计量的零分布通过极值分布来建模比通过标准指数分布的变换更好。我们通过模拟研究和来自英国生物库的 18 种表型的 GWAS 真实数据表明,当遗传效应较少且较大时,该检验在小样本量下更适用,特别是当遗传效应较少且较大时,表现优于遗传相关系数和另一种独立的非参数统计检验。我们发现该检验适用于罕见疾病情况下的遗传相似性检测。