Odds ratio based multifactor-dimensionality reduction method for detecting gene–gene interactions
Open Access
- 8 November 2006
- journal article
- research article
- Published by Oxford University Press (OUP) in Bioinformatics
- Vol. 23 (1) , 71-76
- https://doi.org/10.1093/bioinformatics/btl557
Abstract
Motivation: The identification and characterization of genes that increase the susceptibility to common complex multifactorial diseases is a challenging task in genetic association studies. The multifactor dimensionality reduction (MDR) method has been proposed and implemented by Ritchie et al. (2001) to identify the combinations of multilocus genotypes and discrete environmental factors that are associated with a particular disease. However, the original MDR method classifies the combination of multilocus genotypes into high-risk and low-risk groups in an ad hoc manner based on a simple comparison of the ratios of the number of cases and controls. Hence, the MDR approach is prone to false positive and negative errors when the ratio of the number of cases and controls in a combination of genotypes is similar to that in the entire data, or when both the number of cases and controls is small. Hence, we propose the odds ratio based multifactor dimensionality reduction (OR MDR) method that uses the odds ratio as a new quantitative measure of disease risk. Results: While the original MDR method provides a simple binary measure of risk, the OR MDR method provides not only the odds ratio as a quantitative measure of risk but also the ordering of the multilocus combinations from the highest risk to lowest risk groups. Furthermore, the OR MDR method provides a confidence interval for the odds ratio for each multilocus combination, which is extremely informative in judging its importance as a risk factor. The proposed OR MDR method is illustrated using the dataset obtained from the CDC Chronic Fatigue Syndrome Research Group. Availability: The program written in R is available. Contact:tspark@snu.ac.krKeywords
This publication has 10 references indexed in Scilit:
- Polymorphisms in Genes Regulating the HPA Axis Associated with Empirically Delineated Classes of Unexplained Chronic FatiguePharmacogenomics, 2006
- Combinations of single nucleotide polymorphisms in neuroendocrine effector and receptor genes predict chronic fatigue syndromePharmacogenomics, 2006
- Serotonin transporter: Evolution and impact of polymorphic transcriptional regulationAmerican Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, 2005
- Fatigue in neurological disordersThe Lancet, 2004
- Multifactor dimensionality reduction software for detecting gene–gene and gene–environment interactionsBioinformatics, 2003
- Power of multifactor dimensionality reduction for detecting gene‐gene interactions in the presence of genotyping error, missing data, phenocopy, and genetic heterogeneityGenetic Epidemiology, 2003
- Symbolic discriminant analysis of microarray data in autoimmune diseaseGenetic Epidemiology, 2002
- New strategies for identifying gene-gene interactions in hypertensionAnnals of Medicine, 2002
- Genomewide Scans of Complex Human Diseases: True Linkage Is Hard to FindAmerican Journal of Human Genetics, 2001
- Multifactor-Dimensionality Reduction Reveals High-Order Interactions among Estrogen-Metabolism Genes in Sporadic Breast CancerAmerican Journal of Human Genetics, 2001