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PMID: 15107022 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Ideal discrimination of discrete clinical endpoints using multilocus genotypes.

In silico biology ·Vol. 4 ·No. 2 ·2004-00-00 ·Pages 183-94

Hahn LW, Moore JH

Abstract

Multifactor Dimensionality Reduction (MDR) is a method for the classification and prediction of discrete clinical endpoints using attributes constructed from multilocus genotype data. Empirical studies with both real and simulated data suggest that MDR has good power for detecting gene-gene interactions in the absence of independent main effects. The purpose of this study is to develop an objective, theory-driven approach to evaluate the strengths and limitations of MDR. To accomplish this goal, we borrow concepts from ideal observer analysis used in visual perception to evaluate the theoretical limits of classifying and predicting discrete clinical endpoints using multilocus genotype data. We conclude that MDR ideally discriminates between low risk and high risk subjects using attributes constructed from multilocus genotype data. We also how that the classification approach used once a multilocus attribute is constructed is similar to that of a naive Bayes classifier. This study provides a theoretical foundation for the continued development, evaluation, and application of the MDR as a data mining tool in the domain of statistical genetics and genetic epidemiology.

MeSH Terms
Animals Bayes Theorem Computational Biology/methods Epistasis, Genetic Genetic Predisposition to Disease Genetics Genotype Humans Models, Genetic Psychophysics Retina/physiology Vision, Ocular Visual Perception
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Hahn Lance W
Center for Human Genetics Research, 519 Light Hall, Vanderbilt University, Nashville, TN 37232-0700, USA.
Moore Jason H
Article Info
Journal
In silico biology
Abbr.
In Silico Biol
ISSN
1386-6338
Published
2004-00-00
Pages
183-94
Language
English
Region
Netherlands
NLM ID
9815902
Subset
IM
Grants
NIA NIH HHS · AG19085 · United States
NIA NIH HHS · AG20135 · United States
NIGMS NIH HHS · GM31304 · United States
NHLBI NIH HHS · HL65234 · United States
NHLBI NIH HHS · HL65962 · United States
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PubMed source
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