Entering edit mode
7 months ago
sainavyav22
•
0
Hello, I am working on B cell lymphoma of dogs to identify the specific type of mutations related to this disease. I am performing NGS whole genome sequencing analysis. I have performed the variant annotation using ANNOVAR and received thousands of variants. I want to separate the cancer related variants among these, is there any online platforms that I can compare my variants with? OR how to proceed with this data? Could someone please help? Thanks.
