mLASSO-Hum
mLASSO-Hum predicts protein subcellular localization and identifies explanatory Gene Ontology (GO) terms using a LASSO-based multi-label classification approach.
Key Features:
- Interpretable Predictions: Leverages a LASSO-based approach to produce sparse, interpretable models that highlight GO terms important for protein subcellular localization.
- Multi-Label Classification: Handles multi-label classification to assign multiple potential subcellular localizations to a single protein.
- Sparse Solutions: Employs one-vs-rest LASSO-based classifiers to reduce feature dimensionality and mitigate overfitting in high-dimensional feature vectors.
- Significant GO Terms Identification: From over 8,000 GO terms it identifies 87 essential terms implicated in subcellular localization, providing explanatory features.
- Utilization of Hierarchical Information: Incorporates hierarchical information derived from the depth distance of GO terms to enhance prediction accuracy.
- Comprehensive GO Term Utilization: Integrates GO terms from the cellular component category and other GO categories, contributing to superior performance relative to existing state-of-the-art predictors.
Scientific Applications:
- Disease Mechanism Elucidation: Accurate subcellular localization predictions assist in elucidating mechanisms underlying human diseases.
- Research and Development: Provides interpretable GO-term-based predictions to support proteomics research, experimental validation, and hypothesis generation.
Methodology:
Uses a LASSO-based multi-label classification framework with one-vs-rest classifiers to select sparse, interpretable GO-term features and integrates GO hierarchical information via depth distance.
Topics
Details
- Tool Type:
- web application
- Operating Systems:
- Linux, Windows, Mac
- Added:
- 5/6/2018
- Last Updated:
- 12/10/2018
Operations
Publications
Wan S, Mak M, Kung S. mLASSO-Hum: A LASSO-based interpretable human-protein subcellular localization predictor. Journal of Theoretical Biology. 2015;382:223-234. doi:10.1016/j.jtbi.2015.06.042. PMID:26164062.
PMID: 26164062