Identification of functional rare variants in genome-wide association studies using stability selection based on random collapsing

1Citations
Citations of this article
8Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Genome-wide association studies are a powerful approach used to identify common variants for complex disease. However, the traditional genome-wide association methods may not be optimal when they are applied to rare variants because of the rare variants low frequencies and weak signals. To alleviate the difficulty, investigators have proposed many methods that collapse rare variants. In this paper, we propose a novel ranking method, which we call stability selection based on random collapsing, to rank the candidate rare variants. We use the simulated mini-exome data sets of unrelated individuals from Genetic Analysis Workshop 17 for the analysis. The numerical results suggest that the selection based on a random collapsing method is promising for identifying functional rare variants in genome-wide association studies. Further research to examine the error control property of the proposed method is underway. © 2011 Huang et al; licensee BioMed Central Ltd.

Cite

CITATION STYLE

APA

Huang, X., Fang, Y., & Wang, J. (2011). Identification of functional rare variants in genome-wide association studies using stability selection based on random collapsing. In BMC Proceedings (Vol. 5). https://doi.org/10.1186/1753-6561-5-S9-S56

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free