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PMID: 17924337 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, Non-P.H.S.

Information-theoretic metrics for visualizing gene-environment interactions.

American journal of human genetics ·Vol. 81 ·No. 5 ·2007-11-00 ·Pages 939-63

Chanda P, Zhang A, Brazeau D, Sucheston L, Freudenheim JL, Ambrosone C, Ramanathan M

Abstract

The purpose of our work was to develop heuristics for visualizing and interpreting gene-environment interactions (GEIs) and to assess the dependence of candidate visualization metrics on biological and study-design factors. Two information-theoretic metrics, the k-way interaction information (KWII) and the total correlation information (TCI), were investigated. The effectiveness of the KWII and TCI to detect GEIs in a diverse range of simulated data sets and a Crohn disease data set was assessed. The sensitivity of the KWII and TCI spectra to biological and study-design variables was determined. Head-to-head comparisons with the relevance-chain, multifactor dimensionality reduction, and the pedigree disequilibrium test (PDT) methods were obtained. The KWII and TCI spectra, which are graphical summaries of the KWII and TCI for each subset of environmental and genotype variables, were found to detect each known GEI in the simulated data sets. The patterns in the KWII and TCI spectra were informative for factors such as case-control misassignment, locus heterogeneity, allele frequencies, and linkage disequilibrium. The KWII and TCI spectra were found to have excellent sensitivity for identifying the key disease-associated genetic variations in the Crohn disease data set. In head-to-head comparisons with the relevance-chain, multifactor dimensionality reduction, and PDT methods, the results from visual interpretation of the KWII and TCI spectra performed satisfactorily. The KWII and TCI are promising metrics for visualizing GEIs. They are capable of detecting interactions among numerous single-nucleotide polymorphisms and environmental variables for a diverse range of GEI models.

MeSH Terms
Chromosomes, Human, Pair 5/genetics Computer Simulation Crohn Disease/genetics Epistasis, Genetic Female Gene Frequency Humans Information Theory Linkage Disequilibrium/genetics Male Models, Genetic Pedigree Phenotype Polymorphism, Single Nucleotide/genetics Risk Factors Sample Size
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Chanda Pritam
Department of Computer Science and Engineering, State University of New York, Buffalo, NY 14260, USA.
Zhang Aidong
Brazeau Daniel
Sucheston Lara
Freudenheim Jo L
Ambrosone Christine
Ramanathan Murali
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Article Info
Journal
American journal of human genetics
Abbr.
Am J Hum Genet
ISSN
0002-9297
Published
2007-11-00
Epub
2007-00-03
Pages
939-63
Language
English
Region
United States
NLM ID
0370475
PMCID
PMC2265645
Subset
IM
Grants
CSR NIH HHS · RG3743 · United States
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