GWGGI: software for genome-wide gene-gene interaction analysis

被引:7
|
作者
Wei, Changshuai [1 ,2 ]
Lu, Qing [1 ]
机构
[1] Michigan State Univ, Dept Epidemiol & Biostat, E Lansing, MI 48824 USA
[2] Univ N Texas, Hlth Sci Ctr, Dept Epidemiol & Biostat, Ft Worth, TX 76107 USA
来源
BMC GENETICS | 2014年 / 15卷
关键词
Mann-whitney; Non-parametric statistic; Tree model; MANN-WHITNEY APPROACH; ASSOCIATION;
D O I
10.1186/s12863-014-0101-z
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background: While the importance of gene-gene interactions in human diseases has been well recognized, identifying them has been a great challenge, especially through association studies with millions of genetic markers and thousands of individuals. Computationally efficient and powerful tools are in great need for the identification of new gene-gene interactions in high-dimensional association studies. Result: We develop C++ software for genome-wide gene-gene interaction analyses (GWGGI). GWGGI utilizes tree-based algorithms to search a large number of genetic markers for a disease-associated joint association with the consideration of high-order interactions, and then uses non-parametric statistics to test the joint association. The package includes two functions, likelihood ratio Mann-Whitney (LRMW) and Tree Assembling Mann-Whitney (TAMW). We optimize the data storage and computational efficiency of the software, making it feasible to run the genome-wide analysis on a personal computer. The use of GWGGI was demonstrated by using two real data-sets with nearly 500 k genetic markers. Conclusion: Through the empirical study, we demonstrated that the genome-wide gene-gene interaction analysis using GWGGI could be accomplished within a reasonable time on a personal computer (i.e., similar to 3.5 hours for LRMW and similar to 10 hours for TAMW). We also showed that LRMW was suitable to detect interaction among a small number of genetic variants with moderate-to-strong marginal effect, while TAMW was useful to detect interaction among a larger number of low-marginal-effect genetic variants.
引用
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页数:6
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