BFRM
BFRM models sparse latent factors in large-scale gene expression datasets using Bayesian factor regression to infer pathway activity and support predictive molecular profiling.
Key Features:
- Sparse Latent Factor Models: Employs sparse latent factor models to decompose gene expression data into interpretable components representing underlying biological pathways.
- Pathway Analysis: Identifies and characterizes heterogeneity within oncogenic pathways and links factor structure to clinical biomarkers.
- Hierarchical Sparsity Priors: Uses hierarchical sparsity priors to perform dimension reduction and address multiple comparisons in high-dimensional data.
- Non-Gaussian/Nonparametric Components: Incorporates non-Gaussian and nonparametric model components to capture complex multivariate expression patterns.
Scientific Applications:
- Cancer Pathway Analysis: Applied to breast cancer studies to investigate the structure and activity of oncogenic pathways and their relation to clinical outcomes.
- Molecular Profiling and Predictive Modeling: Enables molecular profiling and development of predictive models from large-scale gene expression data.
- Biological Activity Interpretation: Supports overlaying statistical factors onto known biological activities to interpret disease mechanisms and biomarker associations.
Methodology:
Applies sparsity modeling techniques to multivariate regression, ANOVA, and latent factor models, employs hierarchical sparsity priors and non-Gaussian/nonparametric components, and performs model search and fitting using stochastic simulation and evolutionary stochastic search methods.
Topics
Details
- Tool Type:
- command-line tool
- Operating Systems:
- Linux, Windows, Mac
- Programming Languages:
- MATLAB
- Added:
- 12/18/2017
- Last Updated:
- 11/25/2024
Operations
Publications
Carvalho CM, Chang J, Lucas JE, Nevins JR, Wang Q, West M. High-Dimensional Sparse Factor Modeling: Applications in Gene Expression Genomics. Journal of the American Statistical Association. 2008;103(484):1438-1456. doi:10.1198/016214508000000869. PMID:21218139. PMCID:PMC3017385.