In order to run GISTIC(2.0), you need at least:
- Segmented copy numbers (.seg file, e.g. CBS output)
- Gene annotation file in GISTIC format (refgene file)
- A markers file that gives the genomic position of probes/windows that was used (before segmentation)
I wonder what GISTIC does with the markers file does and why it is required. To me it seems that all relevant information is already contained within the seg file?
I have the same question? Do you know how to run GISTIC from BIC-seq cnv output?