CBNA
CBNA identifies coding and non-coding cancer drivers, including miRNA drivers, by analyzing condition-specific biological networks.
Key Features:
- Integration of Genomic Data Types: Integrates gene expression profiles, gene networks, and mutation data for combined analysis.
- Two-stage process: Constructs condition-specific networks and then identifies potential coding and miRNA cancer drivers.
- BRCA benchmarking: Demonstrated superior effectiveness in detecting coding cancer drivers on BRCA datasets compared to existing methods.
- Prediction of miRNA drivers: Predicts non-coding miRNA drivers and identified 17 miRNA drivers in breast cancer, with several supported by literature.
- Subtype-specific driver detection: Detects subtype-specific cancer drivers in breast cancer cohorts.
- EMT drivers discovery: Identifies epithelial–mesenchymal transition (EMT) coding and miRNA drivers relevant to metastasis and progression.
Scientific Applications:
- Coding and non-coding driver discovery: Identification of coding genes and miRNA drivers from integrated genomic datasets.
- Breast cancer research: Discovery and prioritization of breast cancer drivers, including application to BRCA datasets and miRNA driver prediction.
- Subtype-specific analysis: Characterization of genetic drivers specific to breast cancer subtypes for stratified studies.
- EMT and metastasis studies: Identification of EMT-associated drivers to investigate mechanisms of metastasis and progression.
Methodology:
Integrates gene expression profiles, gene networks, and mutation data; constructs condition-specific biological networks; and performs driver identification to detect coding genes and miRNAs.
Topics
Details
- Tool Type:
- command-line tool
- Programming Languages:
- R
- Added:
- 1/14/2020
- Last Updated:
- 1/14/2021
Operations
Publications
Pham VVH, Liu L, Bracken CP, Goodall GJ, Long Q, Li J, Le TD. CBNA: A control theory based method for identifying coding and non-coding cancer drivers. PLOS Computational Biology. 2019;15(12):e1007538. doi:10.1371/journal.pcbi.1007538. PMID:31790386. PMCID:PMC6907873.
PMID: 31790386
PMCID: PMC6907873
Funding: - The NHMRC Grant: 1123042
- The Australian Research Council Discovery Grant: DP170101306