Closed stroke1989 closed 2 years ago
The genes listed in the all_data_by_gene table are all of the genes in the reference genome used by the GISTIC analysis. The genes listed in the amp_genes and del_genes tables are limited to those that fall within the peak regions of significant copy number alterations. The cytoband of a gene is where the gene is located. The cytoband of a peak is the cytoband where the maximally significant part of the peak is located. In your case, the peak is wide enough that it spans several cytobands.
But it is confusing to identify the cytoband location of significant altered genes. Is there any parameter to improve the resolution of cytiband positions or I can only manually correct them? Thank you!
Hi, Thanks for this wonderful tool. I used GISTIC2 to analyze my WES data, and I got several file, including a file named "amp_genes.conf_95.txt", and a file named "all_data_by_genes.txt", I found the genes in wide peak in del_genes.conf_95.txt did not matched the genes in wide peak in all_data_by_genes.txt, details in below:
many genes were omitted in file amp_genes.conf_95.txt
additionally, the gene EGFR locats in 7p11.2, but in the file amp_genes.conf_95.txt, EGFR located in 7q36.1. Similarly, BRAF locates in 7q34, but in the amp_genes.conf_95.txt, BRAF located in 7q31.2. Hope your reponse! Appreciate