ArticleGenetic epidemiology2009
A computationally efficient hypothesis testing method for epistasis analysis using multifactor dimensionality reduction.
Article in Genetic epidemiology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.
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Who cites it
48 citing papers in PubMed.
- Association between single nucleotides polymorphisms in the DR2D, ANKK1, COMT, and 5-HTT genes with temporomandibular disorder.Journal of applied oral science : revista FOB · 2025Article
- Considerations in the search for epistasis.Genome biology · 2024Review
- Searching for gene-gene interactions through variance quantitative trait loci of 29 continuous Taiwan Biobank phenotypes.Frontiers in genetics · 2024Article
- How National Culture Influences the Speed of COVID-19 Spread: Three Cross-Cultural Studies.Cross-cultural research : official journal of the Society for Cross-Cultural Research · 2023Article
- Association of Interactions between Metabolic 'Caretaker' Genes, p53, MDM2, and Tobacco Use with the Risk of Oral Cancer: A Multifactor Dimensionality Reduction Approach.Asian Pacific journal of cancer prevention : APJCP · 2023Article
- Article
- Genetic interactions effects for cancer disease identification using computational models: a review.Medical & biological engineering & computing · 2021Review
- SNCA and mTOR Pathway Single Nucleotide Polymorphisms Interact to Modulate the Age at Onset of Parkinson's Disease.Movement disorders : official journal of the Movement Disorder Society · 2019Article
- Association of nineteen polymorphisms from seven DNA repair genes and the risk for bladder cancer in Gansu province of China.Oncotarget · 2016Article
- A roadmap to multifactor dimensionality reduction methods.Briefings in bioinformatics · 2016Review
- An efficiency analysis of high-order combinations of gene-gene interactions using multifactor-dimensionality reduction.BMC genomics · 2015Article
- gammaMAXT: a fast multiple-testing correction algorithm.BioData mining · 2015Article
- Data-driven encoding for quantitative genetic trait prediction.BMC bioinformatics · 2015Article
- Tag polymorphisms of solute carrier family 12 member 3 gene modify the risk of hypertension in northeastern Han Chinese.Journal of human hypertension · 2014Article
- Weighted risk score-based multifactor dimensionality reduction to detect gene-gene interactions in nasopharyngeal carcinoma.International journal of molecular sciences · 2014Article
- Interactive contribution of serine/threonine kinase 39 gene multiple polymorphisms to hypertension among northeastern Han Chinese.Scientific reports · 2014Article
- The relationship between RAGE gene four common polymorphisms and breast cancer risk in northeastern Han Chinese.Scientific reports · 2014Article
- Synergistic association between two alcohol metabolism relevant genes and coronary artery disease among Chinese hypertensive patients.PloS one · 2014Article
- The contributory role of angiotensin receptor-like 1 gene multiple polymorphisms in hypertension among northeastern Han Chinese.PloS one · 2014Article
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9 authors.
Funding
Abstract
Multifactor dimensionality reduction (MDR) was developed as a nonparametric and model-free data mining method for detecting, characterizing, and interpreting epistasis in the absence of significant main effects in genetic and epidemiologic studies of complex traits such as disease susceptibility. The goal of MDR is to change the representation of the data using a constructive induction algorithm to make nonadditive interactions easier to detect using any classification method such as naïve Bayes or logistic regression. Traditionally, MDR constructed variables have been evaluated with a naïve Bayes classifier that is combined with 10-fold cross validation to obtain an estimate of predictive accuracy or generalizability of epistasis models. Traditionally, we have used permutation testing to statistically evaluate the significance of models obtained through MDR. The advantage of permutation testing is that it controls for false positives due to multiple testing. The disadvantage is that permutation testing is computationally expensive. This is an important issue that arises in the context of detecting epistasis on a genome-wide scale. The goal of the present study was to develop and evaluate several alternatives to large-scale permutation testing for assessing the statistical significance of MDR models. Using data simulated from 70 different epistasis models, we compared the power and type I error rate of MDR using a 1,000-fold permutation test with hypothesis testing using an extreme value distribution (EVD). We find that this new hypothesis testing method provides a reasonable alternative to the computationally expensive 1,000-fold permutation test and is 50 times faster. We then demonstrate this new method by applying it to a genetic epidemiology study of bladder cancer susceptibility that was previously analyzed using MDR and assessed using a 1,000-fold permutation test.
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