This repository contains code and resources for visualizing different types of genome data, focussed on copy number variants (CNV). The software is mostly used for the progenetix.org visualizations; however, users can just download the package & use with their own data (though documentatuion is ... sparse).
Current implementations (in bin
):
- example implementations
- example implementations
- CNVsegfilePlotter.pl
- for progenetix and TCGA style segmentation & probe files
- download
PGX
to whichever location (___my_path___
) - run as in example below, replacing the segment and label files with your own
cd ___my_path___/PGX/bin/
perl CNVsegfilePlotter.pl -outdir ./out -f ./data/testfile_segments.tab -sf ./data/testfile_labels.tab -min_group_no 1
- installation as above
- for more about Progenetix see
cd ___my_path___/PGX/bin/
perl CNVdbPlotter.pl -query icdom-81 -randno 500