Maximal conditional chi-square importance in random forests
Open Access
- 3 February 2010
- journal article
- research article
- Published by Oxford University Press (OUP) in Bioinformatics
- Vol. 26 (6) , 831-837
- https://doi.org/10.1093/bioinformatics/btq038
Abstract
Motivation: High-dimensional data are frequently generated in genome-wide association studies (GWAS) and other studies. It is important to identify features such as single nucleotide polymorphisms (SNPs) in GWAS that are associated with a disease. Random forests represent a very useful approach for this purpose, using a variable importance score. This importance score has several shortcomings. We propose an alternative importance measure to overcome those shortcomings. Results: We characterized the effect of multiple SNPs under various models using our proposed importance measure in random forests, which uses maximal conditional chi-square (MCC) as a measure of association between a SNP and the trait conditional on other SNPs. Based on this importance measure, we employed a permutation test to estimate empirical P-values of SNPs. Our method was compared to a univariate test and the permutation test using the Gini and permutation importance. In simulation, the proposed method performed consistently superior to the other methods in identifying of risk SNPs. In a GWAS of age-related macular degeneration, the proposed method confirmed two significant SNPs (at the genome-wide adjusted level of 0.05). Further analysis showed that these two SNPs conformed with a heterogeneity model. Compared with the existing importance measures, the MCC importance measure is more sensitive to complex effects of risk SNPs by utilizing conditional information on different SNPs. The permutation test with the MCC importance measure provides an efficient way to identify candidate SNPs in GWAS and facilitates the understanding of the etiology between genetic variants and complex diseases. Contact:heping.zhang@yale.edu Supplementary information: Supplementary data are available at Bioinformatics online.Keywords
This publication has 31 references indexed in Scilit:
- A permutation-based multiple testing method for time-course microarray experimentsBMC Bioinformatics, 2009
- The influence of carnosinase gene polymorphisms on diabetic nephropathy risk in African-AmericansHuman Genetics, 2009
- Performance of random forest when SNPs are in linkage disequilibriumBMC Bioinformatics, 2009
- A random forest approach to the detection of epistatic interactions in case-control studiesBMC Bioinformatics, 2009
- A forest-based approach to identifying gene and gene–gene interactionsProceedings of the National Academy of Sciences, 2007
- Genomewide Association Analysis of Coronary Artery DiseaseNew England Journal of Medicine, 2007
- A Common Allele on Chromosome 9 Associated with Coronary Heart DiseaseScience, 2007
- CFH haplotypes without the Y402H coding variant show strong association with susceptibility to age-related macular degenerationNature Genetics, 2006
- Complement Factor H Polymorphism in Age-Related Macular DegenerationScience, 2005
- Identifying SNPs predictive of phenotype using random forestsGenetic Epidemiology, 2004