TY - JOUR
T1 - Statistical tests for detecting variance effects in quantitative trait studies
AU - Dumitrascu, Bianca
AU - Darnell, Gregory
AU - Ayroles, Julien F.
AU - Engelhardt Martin, Barbara
N1 - Funding Information:
BEE was funded by NIH R01 MH101822, NIH R01 HL133218, NIH U01 HG007900, a Sloan Faculty Fellowship, and an NSF CAREER AWD1005627. BD was funded by NIH R01 HL133218, NIH U01 HG007900, and NSF CAREER AWD1005627.
Publisher Copyright:
© 2018 The Author(s).
PY - 2019/1/15
Y1 - 2019/1/15
N2 - Motivation Identifying variants, both discrete and continuous, that are associated with quantitative traits, or QTs, is the primary focus of quantitative genetics. Most current methods are limited to identifying mean effects, or associations between genotype or covariates and the mean value of a quantitative trait. It is possible, however, that a variant may affect the variance of the quantitative trait in lieu of, or in addition to, affecting the trait mean. Here, we develop a general methodology to identify covariates with variance effects on a quantitative trait using a Bayesian heteroskedastic linear regression model (BTH). We compare BTH with existing methods to detect variance effects across a large range of simulations drawn from scenarios common to the analysis of quantitative traits. Results We find that BTH and a double generalized linear model (dglm) outperform classical tests used for detecting variance effects in recent genomic studies. We show BTH and dglm are less likely to generate spurious discoveries through simulations and application to identifying methylation variance QTs and expression variance QTs. We identify four variance effects of sex in the Cardiovascular and Pharmacogenetics study. Our work is the first to offer a comprehensive view of variance identifying methodology. We identify shortcomings in previously used methodology and provide a more conservative and robust alternative. We extend variance effect analysis to a wide array of covariates that enables a new statistical dimension in the study of sex and age specific quantitative trait effects. Availability and implementation https://github.com/b2du/bth. Supplementary informationSupplementary dataare available at Bioinformatics online.
AB - Motivation Identifying variants, both discrete and continuous, that are associated with quantitative traits, or QTs, is the primary focus of quantitative genetics. Most current methods are limited to identifying mean effects, or associations between genotype or covariates and the mean value of a quantitative trait. It is possible, however, that a variant may affect the variance of the quantitative trait in lieu of, or in addition to, affecting the trait mean. Here, we develop a general methodology to identify covariates with variance effects on a quantitative trait using a Bayesian heteroskedastic linear regression model (BTH). We compare BTH with existing methods to detect variance effects across a large range of simulations drawn from scenarios common to the analysis of quantitative traits. Results We find that BTH and a double generalized linear model (dglm) outperform classical tests used for detecting variance effects in recent genomic studies. We show BTH and dglm are less likely to generate spurious discoveries through simulations and application to identifying methylation variance QTs and expression variance QTs. We identify four variance effects of sex in the Cardiovascular and Pharmacogenetics study. Our work is the first to offer a comprehensive view of variance identifying methodology. We identify shortcomings in previously used methodology and provide a more conservative and robust alternative. We extend variance effect analysis to a wide array of covariates that enables a new statistical dimension in the study of sex and age specific quantitative trait effects. Availability and implementation https://github.com/b2du/bth. Supplementary informationSupplementary dataare available at Bioinformatics online.
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U2 - 10.1093/bioinformatics/bty565
DO - 10.1093/bioinformatics/bty565
M3 - Article
C2 - 29982387
AN - SCOPUS:85058178392
SN - 1367-4803
VL - 35
SP - 200
EP - 210
JO - Bioinformatics
JF - Bioinformatics
IS - 2
ER -