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

Links