Lower-order effects adjustment in quantitative traits model-based multifactor dimensionality reduction.

Identifying gene-gene interactions or gene-environment interactions in studies of human complex diseases remains a big challenge in genetic epidemiology. An additional challenge, often forgotten, is to account for important lower-order genetic effects. These may hamper the identification of genuine...

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Main Authors: Jestinah M Mahachie John, Tom Cattaert, François Van Lishout, Elena S Gusareva, Kristel Van Steen
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3252336?pdf=render
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spelling doaj-fdf7cb20fa834f029b1776d41c26599d2020-11-25T02:50:06ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0171e2959410.1371/journal.pone.0029594Lower-order effects adjustment in quantitative traits model-based multifactor dimensionality reduction.Jestinah M Mahachie JohnTom CattaertFrançois Van LishoutElena S GusarevaKristel Van SteenIdentifying gene-gene interactions or gene-environment interactions in studies of human complex diseases remains a big challenge in genetic epidemiology. An additional challenge, often forgotten, is to account for important lower-order genetic effects. These may hamper the identification of genuine epistasis. If lower-order genetic effects contribute to the genetic variance of a trait, identified statistical interactions may simply be due to a signal boost of these effects. In this study, we restrict attention to quantitative traits and bi-allelic SNPs as genetic markers. Moreover, our interaction study focuses on 2-way SNP-SNP interactions. Via simulations, we assess the performance of different corrective measures for lower-order genetic effects in Model-Based Multifactor Dimensionality Reduction epistasis detection, using additive and co-dominant coding schemes. Performance is evaluated in terms of power and familywise error rate. Our simulations indicate that empirical power estimates are reduced with correction of lower-order effects, likewise familywise error rates. Easy-to-use automatic SNP selection procedures, SNP selection based on "top" findings, or SNP selection based on p-value criterion for interesting main effects result in reduced power but also almost zero false positive rates. Always accounting for main effects in the SNP-SNP pair under investigation during Model-Based Multifactor Dimensionality Reduction analysis adequately controls false positive epistasis findings. This is particularly true when adopting a co-dominant corrective coding scheme. In conclusion, automatic search procedures to identify lower-order effects to correct for during epistasis screening should be avoided. The same is true for procedures that adjust for lower-order effects prior to Model-Based Multifactor Dimensionality Reduction and involve using residuals as the new trait. We advocate using "on-the-fly" lower-order effects adjusting when screening for SNP-SNP interactions using Model-Based Multifactor Dimensionality Reduction analysis.http://europepmc.org/articles/PMC3252336?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Jestinah M Mahachie John
Tom Cattaert
François Van Lishout
Elena S Gusareva
Kristel Van Steen
spellingShingle Jestinah M Mahachie John
Tom Cattaert
François Van Lishout
Elena S Gusareva
Kristel Van Steen
Lower-order effects adjustment in quantitative traits model-based multifactor dimensionality reduction.
PLoS ONE
author_facet Jestinah M Mahachie John
Tom Cattaert
François Van Lishout
Elena S Gusareva
Kristel Van Steen
author_sort Jestinah M Mahachie John
title Lower-order effects adjustment in quantitative traits model-based multifactor dimensionality reduction.
title_short Lower-order effects adjustment in quantitative traits model-based multifactor dimensionality reduction.
title_full Lower-order effects adjustment in quantitative traits model-based multifactor dimensionality reduction.
title_fullStr Lower-order effects adjustment in quantitative traits model-based multifactor dimensionality reduction.
title_full_unstemmed Lower-order effects adjustment in quantitative traits model-based multifactor dimensionality reduction.
title_sort lower-order effects adjustment in quantitative traits model-based multifactor dimensionality reduction.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description Identifying gene-gene interactions or gene-environment interactions in studies of human complex diseases remains a big challenge in genetic epidemiology. An additional challenge, often forgotten, is to account for important lower-order genetic effects. These may hamper the identification of genuine epistasis. If lower-order genetic effects contribute to the genetic variance of a trait, identified statistical interactions may simply be due to a signal boost of these effects. In this study, we restrict attention to quantitative traits and bi-allelic SNPs as genetic markers. Moreover, our interaction study focuses on 2-way SNP-SNP interactions. Via simulations, we assess the performance of different corrective measures for lower-order genetic effects in Model-Based Multifactor Dimensionality Reduction epistasis detection, using additive and co-dominant coding schemes. Performance is evaluated in terms of power and familywise error rate. Our simulations indicate that empirical power estimates are reduced with correction of lower-order effects, likewise familywise error rates. Easy-to-use automatic SNP selection procedures, SNP selection based on "top" findings, or SNP selection based on p-value criterion for interesting main effects result in reduced power but also almost zero false positive rates. Always accounting for main effects in the SNP-SNP pair under investigation during Model-Based Multifactor Dimensionality Reduction analysis adequately controls false positive epistasis findings. This is particularly true when adopting a co-dominant corrective coding scheme. In conclusion, automatic search procedures to identify lower-order effects to correct for during epistasis screening should be avoided. The same is true for procedures that adjust for lower-order effects prior to Model-Based Multifactor Dimensionality Reduction and involve using residuals as the new trait. We advocate using "on-the-fly" lower-order effects adjusting when screening for SNP-SNP interactions using Model-Based Multifactor Dimensionality Reduction analysis.
url http://europepmc.org/articles/PMC3252336?pdf=render
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