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

被引:54
作者
Bush, William S. [1 ]
Edwards, Todd L. [1 ]
Dudek, Scott M. [1 ]
McKinney, Brett A. [2 ]
Ritchie, Marylyn D. [1 ]
机构
[1] Vanderbilt Univ, Med Ctr, Dept Mol Physiol & Biophys, Ctr Human Genet Res, Nashville, TN 37240 USA
[2] Univ Alabama Birmingham, Sch Med, Dept Genet, Birmingham, AL USA
基金
美国国家卫生研究院;
关键词
D O I
10.1186/1471-2105-9-238
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: Multifactor 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. Results: In 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 broadsense 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%. Conclusion: Of 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.
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页数:17
相关论文
共 41 条
[1]  
[Anonymous], 1994, SIGIR
[2]   Multifactor dimensionality reduction reveals gene-gene interactions associated with multiple sclerosis susceptibility in African Americans [J].
Brassat, D. ;
Motsinger, A. A. ;
Caillier, S. J. ;
Erlich, H. A. ;
Walker, K. ;
Steiner, L. L. ;
Cree, B. A. C. ;
Barcellos, L. F. ;
Pericak-Vance, M. A. ;
Schmidt, S. ;
Gregory, S. ;
Hauser, S. L. ;
Haines, J. L. ;
Oksenberg, J. R. ;
Ritchie, M. D. .
GENES AND IMMUNITY, 2006, 7 (04) :310-315
[3]   Genome-wide association study and mouse model identify interaction between RET and EDNRB pathways in Hirschsprung disease [J].
Carrasquillo, MM ;
McCallion, AS ;
Puffenberger, EG ;
Kashuk, CS ;
Nouri, N ;
Chakravarti, A .
NATURE GENETICS, 2002, 32 (02) :237-244
[4]   Tree and spline based association analysis of gene-gene interaction models for ischemic stroke [J].
Ccok, NR ;
Zee, RYL ;
Ridker, PM .
STATISTICS IN MEDICINE, 2004, 23 (09) :1439-1453
[5]   Multifactor-dimensionality reduction shows a two-locus interaction associated with Type 2 diabetes mellitus [J].
Cho, YM ;
Ritchie, MD ;
Moore, JH ;
Park, JY ;
Lee, KU ;
Shin, HD ;
Lee, HK ;
Park, KS .
DIABETOLOGIA, 2004, 47 (03) :549-554
[6]   Odds ratio based multifactor-dimensionality reduction method for detecting gene-gene interactions [J].
Chung, Yujin ;
Lee, Seung Yeoun ;
Elston, Robert C. ;
Park, Taesung .
BIOINFORMATICS, 2007, 23 (01) :71-76
[7]   Use of tree-based models to identify subgroups and increase power to detect linkage to cardiovascular disease traits [J].
Costello, TJ ;
Swartz, MD ;
Sabripour, M ;
Gu, XJ ;
Sharma, R ;
Etzel, CJ .
BMC GENETICS, 2003, 4 (Suppl 1)
[8]   Evidence for epistasis between SLC6A4 and ITGB3 in autism etiology and in the determination of platelet serotonin levels [J].
Coutinho, Ana M. ;
Sousa, Ines ;
Martins, Madalena ;
Correia, Catarina ;
Morgadinho, Teresa ;
Bento, Celeste ;
Marques, Carla ;
Ataide, Assuncao ;
Miguel, Teresa S. ;
Moore, Jason H. ;
Oliveira, Guiomar ;
Vicente, Astrid M. .
HUMAN GENETICS, 2007, 121 (02) :243-256
[9]   Detecting epistatic interactions contributing to quantitative traits [J].
Culverhouse, R ;
Klein, T ;
Shannon, W .
GENETIC EPIDEMIOLOGY, 2004, 27 (02) :141-152
[10]   A perspective on epistasis: Limits of models displaying no main effect [J].
Culverhouse, R ;
Suarez, BK ;
Lin, J ;
Reich, T .
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 70 (02) :461-471