HI,
I am new to the RNA-seq, and the only available sources for me to do analysis is the Galaxy server. I want find out SNP and point mutations in RNA-Seq data using Galaxy. I have been searching in the forum for a step-by-step protocols for doing it, but could not find it.
I have one normal sample and two cancer samples, a TopHat produced "accepted Hits.bam" file for each one.
I want to find out SNP and point mutations in the cancer samples, so How do I go from here? Can anyone show me how to do it in Galaxy?
Thanks!
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