VAECox
VAECox applies deep learning with a pre-trained variational autoencoder and transfer learning to improve survival prediction from cancer RNA-seq transcriptome data, mitigating overfitting when the number of genes exceeds available patient samples.
Key Features:
- Deep Learning Integration: Incorporates a variational autoencoder (VAE) and deep neural networks for survival prediction from RNA-seq transcriptome data.
- Transfer Learning Approach: Pre-trains the VAE on RNA-seq data from 20 TCGA datasets to capture shared pan-cancer transcriptomic features.
- Fine-Tuning Mechanism: Transfers learned VAE weights to a survival prediction model and fine-tunes those weights on individual cancer datasets.
- Performance and Robustness: Achieves a higher C-index than Cox Proportional Hazard with LASSO and ridge penalties and Cox-nnet on 7 of 10 TCGA datasets.
- Reduction of Overfitting: Mitigates overfitting in high-dimensional genomic settings (genes > samples) by leveraging shared information across cancers.
Scientific Applications:
- Survival Prediction and Risk Stratification: Improves survival prediction and risk stratification in oncology using cancer RNA-seq transcriptome data.
- Pan-cancer Feature Extraction: Extracts shared transcriptomic features from TCGA RNA-seq to inform models for specific cancer types.
- Model Benchmarking: Supports comparative evaluation against Cox Proportional Hazard models with LASSO/ridge penalties and Cox-nnet using the C-index.
Methodology:
Pre-trains a variational autoencoder (VAE) on RNA-seq from 20 TCGA datasets, transfers the learned weights to a survival prediction model, fine-tunes weights on individual cancer datasets, and evaluates performance using the C-index compared to Cox Proportional Hazard with LASSO and ridge penalties and Cox-nnet on 10 TCGA datasets.
Topics
Details
- Programming Languages:
- Python
- Added:
- 1/18/2021
- Last Updated:
- 3/10/2021
Operations
Publications
Kim S, Kim K, Choe J, Lee I, Kang J. Improved survival analysis by learning shared genomic information from pan-cancer data. Bioinformatics. 2020;36(Supplement_1):i389-i398. doi:10.1093/bioinformatics/btaa462. PMID:32657401. PMCID:PMC7355236.