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Population genetic simulation study of power in association testing across genetic architectures and study designs
Author(s) -
Tong Dominic M. H.,
Hernandez Ryan D.
Publication year - 2020
Publication title -
genetic epidemiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.301
H-Index - 98
eISSN - 1098-2272
pISSN - 0741-0395
DOI - 10.1002/gepi.22264
Subject(s) - genetic architecture , statistical power , biology , genetic association , trait , quantitative trait locus , genome wide association study , imputation (statistics) , association mapping , genetics , population , genotyping , genetic variation , type i and type ii errors , computational biology , evolutionary biology , statistics , computer science , missing data , genotype , single nucleotide polymorphism , gene , mathematics , demography , sociology , programming language
While it is well established that genetics can be a major contributor to population variation of complex traits, the relative contributions of rare and common variants to phenotypic variation remains a matter of considerable debate. Here, we simulate genetic and phenotypic data across different case/control panel sampling strategies, sequencing methods, and genetic architecture models based on evolutionary forces to determine the statistical performance of rare variant association tests (RVATs) widely in use. We find that the highest statistical power of RVATs is achieved by sampling case/control individuals from the extremes of an underlying quantitative trait distribution. We also demonstrate that the use of genotyping arrays, in conjunction with imputation from a whole‐genome sequenced (WGS) reference panel, recovers the vast majority (90%) of the power that could be achieved by sequencing the case/control panel using current tools. Finally, we show that for dichotomous traits, the statistical performance of RVATs decreases as rare variants become more important in the trait architecture. Our results extend previous work to show that RVATs are insufficiently powered to make generalizable conclusions about the role of rare variants in dichotomous complex traits.