BioVNN
BioVNN predicts cancer dependencies by integrating biological pathway knowledge into a visible neural network architecture to provide interpretable, pathway-informed predictions.
Key Features:
- Pathway Knowledge Integration: BioVNN embeds detailed biological pathway information into its neural architecture and enables correlating predictions with neuron output states of relevant pathways.
- Interpretable Predictions: The model provides interpretability by correlating dependency predictions with neuron output states, allowing inference of pathway-level contributions to dependencies.
- Performance Efficiency: Despite using fewer parameters than conventional neural networks, BioVNN marginally outperforms traditional NNs and converges faster during training.
- Comparison with Randomized Pathways: In comparative analyses, BioVNN significantly outperforms a neural network based on randomized pathways.
- Feature Importance Analysis: Feature importance analysis recapitulates known reaction partners and proposes novel ones, expanding understanding of cancer dependency networks.
Scientific Applications:
- Oncology research: Identify potential drug targets by predicting cancer dependencies.
- Mechanistic exploration: Use interpretable neuron output states to explore mechanisms underlying cancer dependencies.
- Therapeutic development: Inform development of targeted therapies by linking dependencies to specific pathway components.
- Personalized medicine: Support tailoring predictions to specific cancers or individual patients.
Methodology:
BioVNN implements visible neural networks that incorporate pathway knowledge into the model architecture, and achieves interpretability by correlating dependency predictions with neuron output states.
Topics
Details
- License:
- MIT
- Tool Type:
- command-line tool
- Programming Languages:
- Python
- Added:
- 6/14/2021
- Last Updated:
- 11/24/2024
Operations
Publications
Lin C, Lichtarge O. Using interpretable deep learning to model cancer dependencies. Bioinformatics. 2021;37(17):2675-2681. doi:10.1093/bioinformatics/btab137. PMID:34042953. PMCID:PMC8428607.
PMID: 34042953
PMCID: PMC8428607
Funding: - National Institutes of Health: AG061105, NIH-GM066099, NIH-GM079656
Downloads
- Downloads pagehttp://static.lichtargelab.org/BioVNN/
Links
Issue tracker
https://github.com/LichtargeLab/BioVNN/issues