PDGPCS
PDGPCS predicts personalized cancer driver genes by integrating patient-specific gene expression, gene mutation data, and pathway information using the Prize-Collecting Steiner Tree model.
Key Features:
- Integration of Personalized Data: PDGPCS constructs a personalized weighted gene interaction network by integrating patient-specific gene expression data with known gene/protein interactions.
- Incorporation of Edge Weight Information: PDGPCS incorporates personalized edge weight information within the gene interaction network to capture patient-specific interaction strengths.
- Prize-Collecting Steiner Tree Model: PDGPCS applies the Prize-Collecting Steiner Tree model to quantify the impact of each mutant gene on dysregulated pathways and aggregate influence scores across pathways.
- Validation on TCGA datasets: Experimental validation on four TCGA cancer datasets demonstrated improved performance compared with other personalized driver gene prediction methods.
Scientific Applications:
- Personalized medicine and therapy prioritization: Identification of individualized cancer drivers to inform diagnosis and targeted therapy strategies for individual patients.
Methodology:
A personalized weighted gene interaction network is built from patient-specific gene expression data and known gene/protein interactions; gene mutation data and pathway information are integrated and the Prize-Collecting Steiner Tree model is used to quantify the impact of each mutant gene on dysregulated pathways; mutant genes are ranked by aggregated impact scores across affected pathways.
Topics
Details
- License:
- Not licensed
- Cost:
- Free of charge
- Tool Type:
- command-line tool
- Operating Systems:
- Mac, Linux, Windows
- Programming Languages:
- MATLAB
- Added:
- 10/10/2022
- Last Updated:
- 11/24/2024
Operations
Publications
Zhang S, Wang Z, Li Y, Guo W. Prioritization of cancer driver gene with prize-collecting steiner tree by introducing an edge weighted strategy in the personalized gene interaction network. BMC Bioinformatics. 2022;23(1). doi:10.1186/s12859-022-04802-y. PMID:35974311. PMCID:PMC9380343.