stabJGL
stabJGL implements a stability-based penalty parameter selection to jointly reconstruct multiple Gaussian graphical models from high-dimensional omics data by selecting network sparsity and between-network similarity.
Key Features:
- Stability-Based Penalty Parameter Selection: Integrates model stability with likelihood-based similarity selection for tuning penalty parameters and addresses limitations of AIC-based criteria in high-dimensional settings.
- Joint Graphical Lasso Enhancement: Builds upon the joint graphical lasso framework to jointly estimate multiple inverse covariance matrices with tuned sparsity and similarity.
- Improved Performance: Demonstrates superior performance relative to the standard joint graphical lasso and other state-of-the-art methods across various performance metrics in high-dimensional data.
Scientific Applications:
- Network Modeling in Omics: Infers gene and protein association networks using Gaussian graphical models from the non-zero entries of inverse covariance matrices.
- Integrative Analysis of Multiple Conditions: Leverages similarities across multiple graphical structures for integrative analyses of complex high-dimensional biological datasets.
- Proteomic Pan-Cancer Analysis: Has been applied to a pan-cancer proteomic study to facilitate discovery of proteomic insights across cancer types.
Methodology:
Extends the joint graphical lasso by incorporating a stability approach to penalty parameter selection that integrates model stability with likelihood-based similarity selection and infers networks via Gaussian graphical models using non-zero entries of inverse covariance matrices.
Topics
Details
- License:
- MIT
- Cost:
- Free of charge
- Tool Type:
- library
- Operating Systems:
- Mac, Linux, Windows
- Programming Languages:
- R
- Added:
- 4/19/2024
- Last Updated:
- 11/24/2024
Operations
Publications
Lingjærde C, Richardson S. StabJGL: a stability approach to sparsity and similarity selection in multiple-network reconstruction. Bioinformatics Advances. 2023;3(1). doi:10.1093/bioadv/vbad185. PMID:38152341. PMCID:PMC10751232.