CNpare
CNpare compares genome-wide tumor DNA copy number profiles to identify cancer cell line models with similar DNA copy number variation patterns for use in cancer research.
Key Features:
- Genome-wide DNA copy number analysis: Performs comprehensive analysis across entire genomes focusing on DNA copy number profiles.
- Cell line model identification: Compares genome-wide DNA copy number profiles to identify cancer cell line models similar to tumor samples.
- R package implementation: Implemented as an R package to operate within R-based bioinformatics environments.
Scientific Applications:
- Cell line selection: Enables selection of cancer cell lines that closely match the DNA copy number landscapes of tumors.
- Tumor biology and translational studies: Supports comparative analyses of tumor genetics relevant to studies of tumor biology, drug response, and personalized medicine.
Methodology:
Analyzes genome-wide DNA copy number variations and compares copy number profiles between tumor samples and cell lines to identify similarities; implemented in R.
Topics
Details
- License:
- GPL-3.0
- Cost:
- Free of charge
- Tool Type:
- library
- Operating Systems:
- Mac, Linux, Windows
- Programming Languages:
- R
- Added:
- 9/9/2022
- Last Updated:
- 11/24/2024
Operations
Publications
Chaves-Urbano B, Hernando B, Garcia MJ, Macintyre G. CNpare: matching DNA copy number profiles. Bioinformatics. 2022;38(14):3638-3641. doi:10.1093/bioinformatics/btac371. PMID:35640971. PMCID:PMC9272807.
PMID: 35640971
PMCID: PMC9272807
Funding: - Spanish Ministry of Science and Innovation: MCIN/AEI/10.13039/501100011033, PID2019-111356RA-I00