Wei,

The pileup tool will help you find SNPs in your data; you'll want to read the 
documentation to understand how best to use it for your needs. You can also try 
the Unified Genotyper on our test server ( http://test.g2.bx.psu.edu/ ), but 
it's in alpha/beta status and we aren't providing any support for it yet.

Good luck,
J.


On Jan 9, 2012, at 1:28 AM, <ericliao...@gmail.com> <ericliao...@gmail.com> 
wrote:

> 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 do not know if anyone using RNA-seq data to find point 
> mutations, because there is whole Genome sequencing for reporting mutations 
> and SNPs). 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 main server? 
> Thanks!
>  
> Wei
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