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.

PMID: 26607428
PMCID: PMC4660815
Funding: - National Natural Science Foundation of China: 61272207, 61472158 - Science-Technology Development Project from Jilin Province of China: 201201048 - National Institute of Child Health and Human Development: R01-GM10070

Documentation

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