## Abstract A Bayesian modelβbased method for multilocus association analysis of quantitative and qualitative (binary) traits is presented. The method selects a traitβassociated subset of markers among candidates, and is equally applicable for analyzing wide chromosomal segments (genome scans) and
Analysis of multilocus models of association
β Scribed by B. Devlin; Kathryn Roeder; Larry Wasserman
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 163 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0741-0395
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β¦ Synopsis
Abstract
It is increasingly recognized that multiple genetic variants, within the same or different genes, combine to affect liability for many common diseases. Indeed, the variants may interact among themselves and with environmental factors. Thus realistic genetic/statistical models can include an extremely large number of parameters, and it is by no means obvious how to find the variants contributing to liability. For models of multiple candidate genes and their interactions, we prove that statistical inference can be based on controlling the false discovery rate (FDR), which is defined as the expected number of false rejections divided by the number of rejections. Controlling the FDR automatically controls the overall error rate in the special case that all the null hypotheses are true. So do more standard methods such as Bonferroni correction. However, when some null hypotheses are false, the goals of Bonferroni and FDR differ, and FDR will have better power. Model selection procedures, such as forward stepwise regression, are often used to choose important predictors for complex models. By analysis of simulations of such models, we compare a computationally efficient form of forward stepwise regression against the FDR methods. We show that model selection includes numerous genetic variants having no impact on the trait, whereas FDR maintains a falseβpositive rate very close to the nominal rate. With good control over false positives and better power than Bonferroni, the FDRβbased methods we introduce present a viable means of evaluating complex, multivariate genetic models. Naturally, as for any method seeking to explore complex genetic models, the power of the methods is limited by sample size and model complexity. Genet Epidemiol 25:36β47, 2003. Β© 2003 WileyβLiss, Inc.
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