
Abstract Motivation Testing SNP–SNP interactions is considered as a key for overcoming bottlenecks of genetic association studies. However, related statistical methods for testing SNP–SNP interactions are underdeveloped. Results We propose the SNP Interaction Pattern Identifier (SIPI), which tests 45 biologically meaningful interaction patterns for a binary outcome. SIPI takes non-hierarchical models, inheritance modes and mode coding direction into consideration. The simulation results show that SIPI has higher power than MDR (Multifactor Dimensionality Reduction), AA_Full, Geno_Full (full interaction model with additive or genotypic mode) and SNPassoc in detecting interactions. Applying SIPI to the prostate cancer PRACTICAL consortium data with approximately 21 000 patients, the four SNP pairs in EGFR-EGFR, EGFR-MMP16 and EGFR-CSF1 were found to be associated with prostate cancer aggressiveness with the exact or similar pattern in the discovery and validation sets. A similar match for external validation of SNP–SNP interaction studies is suggested. We demonstrated that SIPI not only searches for more meaningful interaction patterns but can also overcome the unstable nature of interaction patterns. Availability and Implementation The SIPI software is freely available at http://publichealth.lsuhsc.edu/LinSoftware/. Supplementary information Supplementary data are available at Bioinformatics online.
Male, 570, Statistics as Topic, 610, Research Support, ta3111, Polymorphism, Single Nucleotide, N.I.H., Research Support, N.I.H., Extramural, Genetic, Models, Journal Article, PRACTICAL Consortium, Humans, Genetic Predisposition to Disease, Polymorphism, Genetic Association Studies, Epidermal Growth Factor, Models, Genetic, Extramural, Prostatic Neoplasms, 006, Epistasis, Genetic, Matrix Metalloproteinase 16, Single Nucleotide, Multicenter Study, ErbB Receptors, Epistasis, Receptor, Epidermal Growth Factor, Software, Receptor
Male, 570, Statistics as Topic, 610, Research Support, ta3111, Polymorphism, Single Nucleotide, N.I.H., Research Support, N.I.H., Extramural, Genetic, Models, Journal Article, PRACTICAL Consortium, Humans, Genetic Predisposition to Disease, Polymorphism, Genetic Association Studies, Epidermal Growth Factor, Models, Genetic, Extramural, Prostatic Neoplasms, 006, Epistasis, Genetic, Matrix Metalloproteinase 16, Single Nucleotide, Multicenter Study, ErbB Receptors, Epistasis, Receptor, Epidermal Growth Factor, Software, Receptor
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 15 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 10% | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Average | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Average |
