Extension of multifactor dimensionality reduction for identifying multilocus effects in the GAW14 simulated data.

Journal Article (Journal Article)

The multifactor dimensionality reduction (MDR) is a model-free approach that can identify gene x gene or gene x environment effects in a case-control study. Here we explore several modifications of the MDR method. We extended MDR to provide model selection without crossvalidation, and use a chi-square statistic as an alternative to prediction error (PE). We also modified the permutation test to provide different levels of stringency. The extended MDR (EMDR) includes three permutation tests (fixed, non-fixed, and omnibus) to obtain p-values of multilocus models. The goal of this study was to compare the different approaches implemented in the EMDR method and evaluate the ability to identify genetic effects in the Genetic Analysis Workshop 14 simulated data. We used three replicates from the simulated family data, generating matched pairs from family triads. The results showed: 1) chi-square and PE statistics give nearly consistent results; 2) results of EMDR without cross-validation matched that of EMDR with 10-fold cross-validation; 3) the fixed permutation test reports false-positive results in data from loci unrelated to the disease, but the non-fixed and omnibus permutation tests perform well in preventing false positives, with the omnibus test being the most conservative. We conclude that the non-cross-validation test can provide accurate results with the advantage of high efficiency compared to 10-cross-validation, and the non-fixed permutation test provides a good compromise between power and false-positive rate.

Full Text

Duke Authors

Cited Authors

  • Mei, H; Ma, D; Ashley-Koch, A; Martin, ER

Published Date

  • December 30, 2005

Published In

Volume / Issue

  • 6 Suppl 1 /

Start / End Page

  • S145 -

PubMed ID

  • 16451605

Pubmed Central ID

  • PMC1866790

Electronic International Standard Serial Number (EISSN)

  • 1471-2156

Digital Object Identifier (DOI)

  • 10.1186/1471-2156-6-S1-S145


  • eng

Conference Location

  • England