BACKGROUND: Detecting single nucleotide polymorphism (SNP) interactions is an important and challenging task in genome-wide association studies (GWAS). Various efforts have been devoted to detect SNP interactions. However, the large volume of SNP datasets results in such a big number of high-order SNP combinations that restrict the power of detecting interactions. METHODS: In this paper, to combat with this challenge, we propose a two-stage approach (called HiSSI) to detect high-order SNP-SNP interactions. In the screening stage, HiSSI employs a statistically significant pattern that takes into account family wise error rate, to control false positives and to effectively screen two-locus combinations candidate set. In the searching stage, HiSSI applies two different search strategies (exhaustive search and heuristic search based on differential evolution along with Ï(2)-test) on candidate pairwise SNP combinations to detect high-order SNP interactions. RESULTS: Extensive experiments on simulated datasets are conducted to evaluate HiSSI and recently proposed and related approaches on both two-locus and three-locus disease models. A real genome-wide dataset: breast cancer dataset collected from the Wellcome Trust Case Control Consortium (WTCCC) is also used to test HiSSI. CONCLUSIONS: Simulated experiments on both two-locus and three-locus disease models show that HiSSI is more powerful than other related approaches. Real experiment on breast cancer dataset, in which HiSSI detects some significantly two-locus and three-locus interactions associated with breast cancer, again corroborate the effectiveness of HiSSI in high-order SNP-SNP interaction identification.
HiSSI: high-order SNP-SNP interactions detection based on efficient significant pattern and differential evolution.
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作者:Cao Xia, Liu Jie, Guo Maozu, Wang Jun
| 期刊: | BMC Medical Genomics | 影响因子: | 2.000 |
| 时间: | 2019 | 起止号: | 2019 Dec 30; 12(Suppl 7):139 |
| doi: | 10.1186/s12920-019-0584-6 | ||
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