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.

Documentation