I have 10 normal-tumor paired genomes of mice suffering from pancreatic cancer. I have started doing the usual NGS analysis of checking the quality of bam reads, calling variants and annotating them. Now I want to find driver mutations and subsequently driver genes from the samples. Now, most of the driver identification tools are based on human genomes. Can you suggest a tool that works for non-human (esp. mice) genomes as well?SIFT driver mutation