Evidence map›Paper›PMID 18485205›Full record

ArticleBMC bioinformatics2008

Alternative contingency table measures improve the power and detection of multifactor dimensionality reduction.

William S Bush, Todd L Edwards, Scott M Dudek, Brett A McKinney, Marylyn D Ritchie

Abstract read
In one paragraph

Article in BMC bioinformatics, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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3 · Its place in the literature

Who cites it

31 citing papers in PubMed.

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  19. Analysis of gene-gene interactions.Current protocols in human genetics · 2011
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

William S BushCenter for Human Genetics Research, Department of Molecular Physiology and Biophysics, Vanderbilt University Medical Center, Nashville, Tennessee, USA. wbush@chgr.mc.vanderbilt.edu
Todd L Edwards
Scott M Dudek
Brett A McKinney
Marylyn D Ritchie

Funding

Revealing Epistasis in Alzheimer DiseaseR01AG020135 · NIA · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI MARTIN, EDEN R. · 2002 to 2006
$2.7M
NIA NIH HHS AG20135NIA NIH HHS R01 AG020135
6 · The paper itself

Abstract

backgroundMultifactor Dimensionality Reduction (MDR) has been introduced previously as a non-parametric statistical method for detecting gene-gene interactions. MDR performs a dimensional reduction by assigning multi-locus genotypes to either high- or low-risk groups and measuring the percentage of cases and controls incorrectly labelled by this classification - the classification error. The combination of variables that produces the lowest classification error is selected as the best or most fit model. The correctly and incorrectly labelled cases and controls can be expressed as a two-way contingency table. We sought to improve the ability of MDR to detect gene-gene interactions by replacing classification error with a different measure to score model quality.

resultsIn this study, we compare the detection and power of MDR using a variety of measures for two-way contingency table analysis. We simulated 40 genetic models, varying the number of disease loci in the model (2 - 5), allele frequencies of the disease loci (.2/.8 or .4/.6) and the broad-sense heritability of the model (.05 - .3). Overall, detection using NMI was 65.36% across all models, and specific detection was 59.4% versus detection using classification error at 62% and specific detection was 52.2%.

conclusionOf the 10 measures evaluated, the likelihood ratio and normalized mutual information (NMI) are measures that consistently improve the detection and power of MDR in simulated data over using classification error. These measures also reduce the inclusion of spurious variables in a multi-locus model. Thus, MDR, which has already been demonstrated as a powerful tool for detecting gene-gene interactions, can be improved with the use of alternative fitness functions.

Indexed as

Models, GeneticBiasDiagnostic ErrorsGene FrequencyGene Regulatory NetworksGenetic MarkersGenotypeInformation Storage and RetrievalOdds RatioRisk AssessmentSensitivity and SpecificityStatistics, NonparametricWeights and MeasuresGenetic Markers

Identifiers

PMID18485205
PMCPMC2412877

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.