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.

Documentation

Links