TY - JOUR
T1 - Power Analysis for Genetic Association Test (PAGEANT) provides insights to challenges for rare variant association studies
AU - Derkach, Andriy
AU - Zhang, Haoyu
AU - Chatterjee, Nilanjan
N1 - Funding Information:
A.D. was supported by the National Cancer Institute Intramural Research Program. The research of H.Z. and N.C. was supported by fund available through Bloomberg Distinguished Professorship Endowment at Johns Hopkins University.
Publisher Copyright:
© Published by Oxford University Press 2017. This work is written by US Government employees and is in the public domain in the US.
PY - 2018/5/1
Y1 - 2018/5/1
N2 - Motivation Genome-wide association studies are now shifting focus from analysis of common to rare variants. As power for association testing for individual rare variants may often be low, various aggregate level association tests have been proposed to detect genetic loci. Typically, power calculations for such tests require specification of large number of parameters, including effect sizes and allele frequencies of individual variants, making them difficult to use in practice. We propose to approximate power to a varying degree of accuracy using a smaller number of key parameters, including the total genetic variance explained by multiple variants within a locus. Results We perform extensive simulation studies to assess the accuracy of the proposed approximations in realistic settings. Using these simplified power calculations, we develop an analytic framework to obtain bounds on genetic architecture of an underlying trait given results from genome-wide association studies with rare variants. Finally, we provide insights into the required quality of annotation/functional information for identification of likely causal variants to make meaningful improvement in power. Availability and implementation A shiny application that allows a variety of Power Analysis of GEnetic AssociatioN Tests (PAGEANT), in R is made publicly available at https://andrewhaoyu.shinyapps.io/PAGEANT/. Contact nilanjan@jhu.edu Supplementary informationSupplementary dataare available at Bioinformatics online.
AB - Motivation Genome-wide association studies are now shifting focus from analysis of common to rare variants. As power for association testing for individual rare variants may often be low, various aggregate level association tests have been proposed to detect genetic loci. Typically, power calculations for such tests require specification of large number of parameters, including effect sizes and allele frequencies of individual variants, making them difficult to use in practice. We propose to approximate power to a varying degree of accuracy using a smaller number of key parameters, including the total genetic variance explained by multiple variants within a locus. Results We perform extensive simulation studies to assess the accuracy of the proposed approximations in realistic settings. Using these simplified power calculations, we develop an analytic framework to obtain bounds on genetic architecture of an underlying trait given results from genome-wide association studies with rare variants. Finally, we provide insights into the required quality of annotation/functional information for identification of likely causal variants to make meaningful improvement in power. Availability and implementation A shiny application that allows a variety of Power Analysis of GEnetic AssociatioN Tests (PAGEANT), in R is made publicly available at https://andrewhaoyu.shinyapps.io/PAGEANT/. Contact nilanjan@jhu.edu Supplementary informationSupplementary dataare available at Bioinformatics online.
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U2 - 10.1093/bioinformatics/btx770
DO - 10.1093/bioinformatics/btx770
M3 - Article
C2 - 29194474
AN - SCOPUS:85047063794
SN - 1367-4803
VL - 34
SP - 1506
EP - 1513
JO - Bioinformatics
JF - Bioinformatics
IS - 9
ER -