LOTUS

LOTUS predicts cancer driver genes by integrating gene mutation and protein-protein interaction data with machine learning to identify oncogenes and tumor suppressor genes across cancer types.


Key Features:

  • Data integration: Integrates gene mutation and protein-protein interaction data using machine learning to inform driver gene prediction.
  • Multitask learning: Implements a multitask learning strategy to share information across different cancer types.
  • Prediction scope: Produces both pan-cancer predictions and cancer-type-specific analyses.
  • Driver types: Predicts oncogenes and tumor suppressor genes as candidate cancer drivers.
  • Framework: Uses a versatile framework to enhance prediction accuracy across diverse contexts.
  • Benchmarking: Demonstrates superiority over five other driver gene prediction methods in intrinsic consistency and prediction accuracy, including identification of novel cancer genes across multiple cancer types.

Scientific Applications:

  • Driver gene identification: Prioritizes candidate cancer driver genes for use as potential therapeutic targets or biomarkers.
  • Pan-cancer discovery: Identifies novel cancer genes across multiple cancer types.
  • Tumor biology insight: Supports analysis of mechanisms that confer selective growth advantages, including uncontrolled proliferation and evasion of apoptosis.

Methodology:

Applies machine learning to integrate gene mutation and protein-protein interaction data and employs a multitask learning strategy for pan-cancer and cancer-type-specific predictions, with performance evaluated by intrinsic consistency and prediction accuracy against five other methods.

Topics

Details

Tool Type:
command-line tool
Programming Languages:
R
Added:
1/9/2020
Last Updated:
12/22/2020

Operations

Publications

Collier O, Stoven V, Vert J. LOTUS: A single- and multitask machine learning algorithm for the prediction of cancer driver genes. PLOS Computational Biology. 2019;15(9):e1007381. doi:10.1371/journal.pcbi.1007381. PMID:31568528. PMCID:PMC6786659.

PMID: 31568528
PMCID: PMC6786659
Funding: - European Research Council: ERC-SMAC-280032