The groomer was recently migrated to the tool shed - this has not been released as part of a galaxy-dist though so I assume you are still running a version of the fastq groomer bundled with Galaxy? If yes, what version of Galaxy are you running (i.e. can you attach the output of "hg summary")?
On Mon, Feb 10, 2014 at 7:00 AM, graham etherington (TSL) email@example.com wrote:
Hi Philippe, I’m unable to suggest a reason as to why this has happened, other than some sort of corruption whilst the job was running, but I would point out two things to you.
- I don’t think you need to run the fastq groomer on your data anyway as
it’s in Illumina 1.8+ format, which should already be in fastqsanger format. 2. It appears that the fastq groomer hasn’t worked as the quality scores haven’t changed format. (A general question to anyone here – will fastq groomer change the quality format of reads that are already in fastqsanger format?)
Dr. Graham Etherington Bioinformatics Support Officer, The Sainsbury Laboratory, Norwich Research Park, Norwich NR4 7UH. UK Tel: +44 (0)1603 450601
From: Philippe Moncuquet firstname.lastname@example.org Date: Monday, 10 February 2014 03:50 To: Galaxy Dev email@example.com Subject: [galaxy-dev] Error introduced with Fastq Groomer
Some unexpected symbols were introduced while grooming my fastq file
@DJTPB5M1:327:C3PC4ACXX:6:1104:9355:84986 1:N:0:GTCCGC GAGCCTTGCTAGGAGAGGGAAGGTGGAAGATCATCATTTCCAGGAGAGCACTGCTAGCAGGAAGCCACGTCTGCATTACACGCTTCATTAGGGACTTCCC
@DJTPB5M1:327:C3PC4ACXX:6:1104:9355:84986 1:N:0:GTCCGC GAGCCTTGCTAGGAGAGGGAAGGTGGAAGATCATCATTTCCAGGAGAGCACTGCTAGCAGGAAGCCACG+1�CATTACACGCTTCATTAGGGACTTCCC
I relaunch this step without being able to reproduce the bug. Any ideas about this problem ? Have you guys came across the same problem before ?
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