Thanks Jen,
I am also intrested in this. Has any one used FreeBayes in Galaxy or out side
Gaaxy to detect CNV from a ilumina sequencing data. Is their a tutorial for
running this tools.
Thanks.
From: Jennifer Jackson <j...@bx.psu.edu>
To: shamsher jagat <kanwar...@gmail.com>
Cc: galaxy-user@lists.bx.psu.edu
Sent: Thursday, August 16, 2012 12:48 AM
Subject: Re: [galaxy-user] copy number variation detcetion in Glaxay
Hello,
The tool "FreeBayes" may be of interest. Please see the tool form for
links to the primary tool documentation to see if the functionality will
meet your needs.
Best,
Jen
Galaxy team
On 8/15/12 4:46 AM, shamsher jagat wrote:
> Is there any tool/ combination of tools with in galaxy which can detect
> CNV. I have 100X paired sequencing data between cancer and normal.
> Thanks
>
>
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--
Jennifer Jackson
http://galaxyproject.org
___________________________________________________________
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:
http://lists.bx.psu.edu/listinfo/galaxy-dev
To manage your subscriptions to this and other Galaxy lists,
please use the interface at:
http://lists.bx.psu.edu/
___________________________________________________________
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:
http://lists.bx.psu.edu/listinfo/galaxy-dev
To manage your subscriptions to this and other Galaxy lists,
please use the interface at:
http://lists.bx.psu.edu/