BANDITS
BANDITS detects differential transcript usage and alternative splicing between conditions in RNA-seq data at gene and transcript levels using a Bayesian hierarchical model that accounts for sample-to-sample variability and mapping uncertainty.
Key Features:
- Implementation: Provided as an R/Bioconductor package for integration with Bioconductor workflows.
- Bayesian hierarchical framework: Models sample-specific proportions with a Dirichlet-Multinomial component to capture biological variability across samples.
- Latent variable modeling: Treats transcript allocation of reads as latent variables to account for mapping uncertainty of RNA fragments to transcripts.
- Markov Chain Monte Carlo (MCMC) inference: Uses MCMC techniques for parameter estimation and sampling from complex posterior distributions.
- Multivariate Wald test: Applies a multivariate Wald test on posterior densities of average relative transcript abundances to assess differential transcript usage.
Scientific Applications:
- Alternative splicing analysis: Identification of differential splicing events and differential transcript usage (DTU) between experimental conditions using RNA-seq data.
- Gene expression regulation studies: Investigation of transcript-level regulatory changes that affect gene expression profiles across conditions.
- Disease and developmental biology research: Detection of splicing alterations relevant to disease mechanisms and developmental processes.
Methodology:
BANDITS employs a Bayesian hierarchical model with a Dirichlet-Multinomial component for sample-specific proportions, treats read-to-transcript allocation as latent variables, performs parameter inference via MCMC, and assesses differential transcript usage using a multivariate Wald test on posterior densities of average relative transcript abundances.
Topics
Details
- License:
- GPL-3.0
- Programming Languages:
- R, C++
- Added:
- 11/14/2019
- Last Updated:
- 11/24/2024
Operations
Publications
Tiberi S, Robinson MD. BANDITS: Bayesian differential splicing accounting for sample-to-sample variability and mapping uncertainty. Genome Biology. 2020;21(1). doi:10.1186/s13059-020-01967-8. PMID:32178699. PMCID:PMC7075019.