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