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 <jen@bx.psu.edu> To: shamsher jagat <kanwarjag@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/