rcellminer
rcellminer: R Package for NCI-60 Cancer Cell Line Data Integration and Analysis
rcellminer provides programmatic access to NCI-60 CellMiner datasets, integrating gene expression, protein expression, copy number variation, whole exome mutation, and drug activity data for approximately 21,000 compounds across 60 human cancer cell lines.
Key Features:
- Multi-Omics Data Access: Retrieves gene and protein expression profiles, copy number variations, whole exome mutations, and pharmacological activity data from the NCI-60 panel.
- Compound Annotation: Includes compound structure, mechanism of action, and repeat screening results linked to drug response data.
- Drug Response Analysis: Enables correlation of molecular features with compound activity patterns across cancer cell lines.
- Data Integration Functions: Supports computational extraction, manipulation, and integration of multi-platform NCI-60 datasets within R.
Scientific Applications:
- Drug Discovery: Identifies candidate compounds and repurposing opportunities through analysis of activity profiles and molecular correlates.
- Mechanistic Studies: Investigates relationships between genomic alterations, expression patterns, and compound mechanisms of action.
- Precision Oncology Research: Associates molecular characteristics of cancer cell lines with differential therapeutic response.
Methodology:
rcellminer integrates NCI-60 data from CellMiner into R, enabling structured retrieval and computational analysis of multi-omics and pharmacological datasets for cross-platform correlation and hypothesis testing.
Topics
Collections
Details
- License:
- GPL-3.0
- Tool Type:
- command-line tool, library
- Operating Systems:
- Linux, Windows, Mac
- Programming Languages:
- R
- Added:
- 1/17/2017
- Last Updated:
- 4/11/2022
Operations
Publications
Luna A, Rajapakse VN, Sousa FG, Gao J, Schultz N, Varma S, Reinhold W, Sander C, Pommier Y. rcellminer: exploring molecular profiles and drug response of the NCI-60 cell lines in R. Bioinformatics. 2015;32(8):1272-1274. doi:10.1093/bioinformatics/btv701. PMID:26635141. PMCID:PMC4907377.