I posted this question in Dev- list so re-posting to correct list with some
additional information.
I have paired end  sequencing files on which I would like to call SNPs
compared to databases well check sequence variation among samples. I dont
have access to any local galaxy instance. My question are-
1. Is there a way that I can upload these large files to galaxy and analyze
them then delete?
2. Is there a work flow to call SNPs and analyze and annotate SNPS in
Galaxy, If some one know about a work flow summarized  by some one in
addition to  Galaxy list that will be bonus.


The Galaxy User list should be used for the discussion of
Galaxy analysis and other features on the public server
at usegalaxy.org.  Please keep all replies on the list by
using "reply all" in your mail client.  For discussion of
local Galaxy instances and the Galaxy source code, please
use the Galaxy Development list:


To manage your subscriptions to this and other Galaxy lists,
please use the interface at:


Reply via email to