CNA2Subpathway
CNA2Subpathway identifies subpathways dysregulated by copy number alterations (CNAs) in cancer by integrating multi-omics data and pathway topology in a network-based analysis.
Key Features:
- Integration of Multi-Omics Data: Utilizes high-throughput sequencing–derived multi-omics datasets to link CNAs with subpathway dysfunction.
- Pathway Topology Information: Incorporates pathway topology to evaluate the positional and interaction effects of altered genes within pathways.
- Subpathway Crosstalk Analysis: Accounts for interactions between subpathways to capture network-level crosstalk in dysregulation.
- Network-Based Approach: Applies a network-based computational framework to integrate topology, multi-omics signals, and subpathway crosstalk.
- Validation and Comparative Evaluation: Validated on breast cancer and head and neck cancer datasets and compared with five other pathway or subpathway analysis methods.
- Implementation: Implemented as an R package.
Scientific Applications:
- Subpathway discovery in cancer: Identification of dysfunctional subpathways associated with cancer development and progression.
- Immune-related pathway analysis: Detection of subpathways linked to cancer immune response.
- Prognostic association: Association of dysregulated subpathways with patient prognosis for potential prognostic assessment.
- Tumor-type validation: Application and validation in breast cancer and head and neck cancer datasets.
Methodology:
Uses a network-based method that integrates pathway topology, multi-omics data, and subpathway (SP) crosstalk to identify subpathways dysregulated by CNAs.
Topics
Details
- License:
- Apache-2.0
- Tool Type:
- library
- Programming Languages:
- R
- Added:
- 3/19/2021
- Last Updated:
- 4/26/2021
Operations
Data Inputs & Outputs
Copy number variation detection
Inputs
Outputs
Publications
Sheng Y, Jiang Y, Yang Y, Li X, Qiu J, Wu J, Cheng L, Han J. CNA2Subpathway: identification of dysregulated subpathway driven by copy number alterations in cancer. Briefings in Bioinformatics. 2021;22(5). doi:10.1093/bib/bbaa413. PMID:33423051.
DOI: 10.1093/BIB/BBAA413
PMID: 33423051
Funding: - National Natural Science Foundation of China: 62072145, 81804158
- Natural Science Foundation of Heilongjiang Province: LH2019C042
- China Postdoctoral Science Foundation: 2016M591566