Joshua and Philipe thanks for the input. I was able to run the GATK in another 
pipeline but does not serve my purpose. It was FASTQ groomer followed by BWA 
alignment with human_g1k_v37 with the read groups. It produced a SAM file which 
I put into GATK pipeline with option "use as BAM(SAM file)". Once it started 
running, it kept going. But several issues with it. GATK best practices 
recommend removing the duplicates with Picard before this but after using 
Picard this output wont work in galaxy GATK. The second issue is if I align 
with Hg 19 because this is what I have been working with, even if I provide the 
reference H19 from history (uploaded) GATK does not work. 

All I needed was base recalibration and indel realignment so I decided to do 
these before running the picard duplicate removal tool and run everything with 
human_g1k_v37. It worked from base recalibration then indel realignment band 
then Picard duplicate removal. But I needed to run mpileup on this output. A 
very interesting thing I found that even though everything in this pipeline was 
with human_g1k_v37 but the mpileup will run only with Hg19. As I cannot rely on 
such a twisted pipeline so essentially cannot use GATK in galaxy. 


________________________________________
From: Joshua Orvis [jor...@gmail.com]
Sent: Tuesday, December 11, 2012 5:34 PM
To: Philipe Moncuquet
Cc: Farooq,Umar (res); galaxy-user@lists.bx.psu.edu
Subject: Re: [galaxy-user] GATK Not running

I'm having some problems with GATK as well, but do have a functional pipeline 
that uses the following GATK tools in Galaxy:

- Realigner Target Creator
- Indel Realigner
- Unified Genotyper
- Variant Filtration

The main problem I'm having with them is that it seems I need to run the 
fasta/fastq groomer on all inputs before starting, and if I attempt to use the 
'advanced' options on either of the last two steps above it fails immediately 
every time with a command-line option parsing error.  I plan on digging into 
the wrapper script in the coming days in an attempt to correct this, which is 
currently attributed to Dan Blankenberg.  I'm relatively new to Galaxy 
development though and don't know where to submit my updates though should I 
fix any of these problems.

Joshua




On Tue, Dec 11, 2012 at 4:26 PM, Philipe Moncuquet 
<philippe.m...@gmail.com<mailto:philippe.m...@gmail.com>> wrote:
Hi,

I have encountered the same kind of errors. When I update the loc files link to 
GATK, some of the tools display the reference genomes I added and some not. It 
seems that the galaxy wrapper for GATK 1.6 is not very functional. GATK don't 
really care because they are not supporting it any more, even documentation has 
disappeared. And I understand that galaxy developers have other stuff to do 
than supporting a tool that will disappear because it's not open source any 
more. I don't know what tool could replace the recalibration process done by 
GATK and don't know how to correct bugs neither. Any suggestions ?

Philippe



2012/12/12 Farooq,Umar (res) 
<ufar...@resident.uchc.edu<mailto:ufar...@resident.uchc.edu>>
Hi,

I am trying to incorporate GATK in my pipeline but not been able to make it 
work. I aligned my data with Hg 19 and then ran sam tool filter and then picard 
duplicate removal. I uploaded dbSNP and the reference FASTA file for Hg 19 in 
galaxy to run this pipeline. But for some reason GATK tool for base 
recalibration will not accept this output file. I wonder if there is sorting or 
indexing issue but how to fix this in galaxy.


An error occurred running this job: Picked up _JAVA_OPTIONS: 
-Djava.io.tmpdir=/space/g2main [Mon Dec 10 10:30:42 EST 2012] 
net.sf.picard.sam.CreateSequenceDictionary 
REFERENCE=/space/g2main/tmp-gatk-tKp41A/gatk_input.fasta 
OUTPUT=/space/g2main/tmp-gatk-tKp41A/dict3503196447953523717.tmp

Thanks,
Umar

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