rCGH

rCGH: Analysis and Visualization of aCGH Data

rCGH processes array Comparative Genomic Hybridization (aCGH) data to perform automated genomic profile segmentation, gene annotation, and visualization for the identification of copy number alterations.


Key Features:

  • aCGH Platform Compatibility: Supports commercial and custom aCGH arrays for genomic profiling.
  • Automated Segmentation: Performs segmentation of genomic copy number profiles to detect genomic alterations.
  • Gene Annotation Integration: Integrates gene annotations to contextualize copy number changes.
  • Traceable Analysis Pipeline: Ensures full traceability of analytical steps for reproducibility.
  • Interactive Genomic Visualization: Generates interactive visualizations for exploration of genomic profiles.

Scientific Applications:

  • Copy Number Alteration Analysis: Identifies clinically and biologically relevant genomic alterations from aCGH data.
  • Precision Medicine: Supports interpretation of genomic profiles for individualized therapeutic strategies.

Methodology:

rCGH reads aCGH data from multiple platforms, performs automated segmentation of genomic copy number profiles, integrates gene annotations to annotate segmented regions, and generates interactive visualizations to support interpretation of genomic alterations.

Topics

Collections

Details

License:
Artistic-2.0
Tool Type:
command-line tool, library
Operating Systems:
Linux, Windows, Mac
Programming Languages:
R
Added:
1/17/2017
Last Updated:
11/25/2024

Operations

Data Inputs & Outputs

Publications

Commo F, Guinney J, Ferté C, Bot B, Lefebvre C, Soria J, André F. rCGH: a comprehensive array-based genomic profile platform for precision medicine. Bioinformatics. 2015;32(9):1402-1404. doi:10.1093/bioinformatics/btv718. PMID:26708336. PMCID:PMC4848396.

Documentation

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