BHIT
BHIT detects high-order epistatic interactions among single nucleotide polymorphisms (SNPs) using a Bayesian partition model with Markov Chain Monte Carlo (MCMC) search to elucidate the genetic architecture of complex traits.
Key Features:
- Bayesian computational framework: Implements a Bayesian partition model capable of analyzing both continuous and discrete data types for case-control studies and quantitative phenotypes.
- High-order interaction detection: Detects complex interactions involving more than two SNPs to capture epistatic effects beyond additive single-marker associations in GWAS.
- MCMC search algorithm: Uses Markov Chain Monte Carlo search techniques to explore the large parameter space of possible interaction configurations.
- Cross-species pipeline: Provides a computational pipeline to apply the method across different species and research use cases.
Scientific Applications:
- Simulation and empirical validation: Applied to simulation data and empirical studies to assess detection of high-order SNP interactions.
- Soybean seed composition: Used to detect high-order interactions associated with soybean oil content and protein content.
- GWAS of complex traits: Applied to genome-wide association study data to investigate epistasis underlying complex traits and diseases, and to inform crop improvement research.
- Comparative performance: Demonstrated improved detection of high-order SNP interactions in comparative analyses versus other available tools.
Methodology:
Employs a Bayesian partition computational method combined with Markov Chain Monte Carlo (MCMC) search; supports analysis of continuous and discrete data for case-control and quantitative phenotypes.
Topics
Details
- Tool Type:
- command-line tool
- Operating Systems:
- Linux
- Programming Languages:
- C++
- Added:
- 8/3/2017
- Last Updated:
- 11/25/2024
Operations
Publications
Wang J, Joshi T, Valliyodan B, Shi H, Liang Y, Nguyen HT, Zhang J, Xu D. A Bayesian model for detection of high-order interactions among genetic variants in genome-wide association studies. BMC Genomics. 2015;16(1). doi:10.1186/s12864-015-2217-6. PMID:26607428. PMCID:PMC4660815.