Here’s a simple exome analysis pipeline using VarScan for variant calling and ANNOVAR for annotation:

https://usegalaxy.org/u/jeremy/w/exome-analysis

You may want to tweak some aspects of it, such as using FreeBayes rather than VarScan and/or using a different set of annotations from ANNOVAR.

Best,
J.

--
Jeremy Goecks
Assistant Professor, Computational Biology Institute
George Washington University



On Mar 14, 2014, at 9:01 PM, Björn Grüning <bjoern.gruening@gmail.com> wrote:

Hi,

we are currently working on one pipeline. I can share if you are interested, but its not yet finished, parameter wise, but all tools should be there.

We tried to stick to the GATK2 best-practise guide and are using snpeff for annotation.

Cheers,
Bjoern

Am 15.03.2014 01:55, schrieb Mathew Bunj:
No I have not received any feedback as yet.

Thanks



On Friday, March 14, 2014 7:42 AM, Kristin Kernohan <kristinkernohan@gmail.com> wrote:

Hi

did anyone answer this? Id be curious to know as well

thanks

Kristin



On Thu, Mar 13, 2014 at 10:22 PM, Mathew Bunj <mathewbunj@yahoo.com> wrote:

I was wondering if Galaxy has any work flow for calling mutations in Exome seq and then annotating. Alignment can be done by BWA.


Thanks


Mathew
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___________________________________________________________
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
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