Support Vector Machines with L1 penalty for detecting gene-gene interactions Online publication date: Wed, 17-Dec-2014
by Yuanyuan Shen; Zhe Liu; Jurg Ott
International Journal of Data Mining and Bioinformatics (IJDMB), Vol. 6, No. 5, 2012
Abstract: Interactions among genetic variants are likely to affect risk for human complex diseases, and their identification should increase the power to detect disease-associated variants and elucidate biological pathways underlying diseases. We propose a two-stage approach: 1) model selection with Support Vector Machines identifies the most promising Single Nucleotide Polymorphisms and interactions; 2) logistic regression ensures a valid type I error by excluding non-significant candidates after Bonferroni correction. Simulation studies for case-control data suggest that our method powerfully detects gene-gene interactions. We analyze a published genome-wide case-control dataset, where our method successfully identifies an interaction term, which was missed in previous studies.
Existing subscribers:
Go to Inderscience Online Journals to access the Full Text of this article.
If you are not a subscriber and you just want to read the full contents of this article, buy online access here.Complimentary Subscribers, Editors or Members of the Editorial Board of the International Journal of Data Mining and Bioinformatics (IJDMB):
Login with your Inderscience username and password:
Want to subscribe?
A subscription gives you complete access to all articles in the current issue, as well as to all articles in the previous three years (where applicable). See our Orders page to subscribe.
If you still need assistance, please email subs@inderscience.com