Please see http://wiki.g2.bx.psu.edu/Admin/Tools/Tool%20Config%20Syntax . There is a section for "<stdio>, <regex>, and <exit_code> tag sets". The documentation applies to the latest galaxy-dist, though most of what's mentioned (aside from updating stdout and stderr with warning messages) is supported in galaxy-central. (You can also use the fairly ugly URL http://wiki.g2.bx.psu.edu/Admin/Tools/Tool%20Config%20Syntax#A.3Cstdio.3E.2C... ). -Scott ----- Original Message -----
Hi
I'm writing a tools for an executable that writes results to stdout and reports success message to stderr, so it really need the improved error handling. Is there any sample code or documentation available?
Thanks
Birgit Crain, Ph.D. | Sr. Professional Services Scientist | Complete Genomics, Inc. (650) 428-6023 office | (408) 605-3938 mobile bcrain@completegenomics.com
From: Nicole Rockweiler < n.rockweiler@gmail.com > Date: Friday, July 20, 2012 10:53 AM To: Brian Haas < bhaas@broadinstitute.org > Cc: " galaxy-dev@bx.psu.edu " < galaxy-dev@bx.psu.edu > Subject: Re: [galaxy-dev] pipeline execution succeeds but galaxy shows failure
Hi Brian,
A couple of days ago, smcmanus pushed the following change to the repo:
Tools can now specify their own handling of stderr and stdout regular expressions as well as exit code ranges.
https://bitbucket.org/galaxy/galaxy-central/issue/325/allow-tool-authors-to-...
It looks like the documentation has yet to be written.
Hope this helps, Nicole
On Fri, Jul 20, 2012 at 12:46 PM, Brad Chapman < chapmanb@50mail.com
wrote:
Brian;
I wrote a pipeline (xml attached) that, from what I can gather,
succeeds, but galaxy shows it as an error and doesn't make the output
file accessible as a new data set.
Is it possible the software is writing to standard error? Galaxy doesn't
check status codes, but rather check for stderr and assumes that output
indicates a problem. You can wrap the problematic programs with a little
script to eat up stderr and check that everything is okay:
http://wiki.g2.bx.psu.edu/Future/Job%20Failure%20When%20stderr
Brad
From the server log, I can see that the command line is being
constructed correctly, and it even indicates that it's captured the
output, but in the display of the web browser, it just shows up in the
error state. The script being run exits (0) on success. Any ideas?
Here's what the output section of my xml file looks like:
<outputs>
<data format="bam" name="coordSortedBam" label="${ tool.name }
on ${on_string}: coord-sorted read alignments"
from_work_dir="alignment/alignment.coordSorted.bam"/>
</outputs>
and here's what the server log states:
galaxy.jobs.handler INFO 2012-07-20 09:52:05,240 (30) Job dispatched
galaxy.jobs.runners.local DEBUG 2012-07-20 09:52:05,453 executing:
alignReads.pl --target
/Users/bhaas/BioIfx/Galaxy/galaxy-dist/database/files/000/dataset_26.dat
-o alignment --aligner bowtie --single
/Users/bhaas/BioIfx/Galaxy/galaxy-dist/database/files/000/dataset_23.dat
--seqType fq
galaxy.jobs DEBUG 2012-07-20 09:52:16,673 finish(): Moved
/Users/bhaas/BioIfx/Galaxy/galaxy-dist/database/job_working_directory/000/30/alignment/alignment.coordSorted.bam
to /Users/bhaas/BioIfx/Galaxy/galaxy-dist/database/files/000/dataset_50.dat
as directed by from_work_dir
Again, as far as I can tell, everything worked - but the browser
doesn't think so.
I've run the exact command above on the command-line, and it exits(0)
indicating success.
Also, I've verified that when run through my galaxy instance, the
galaxy-relocated output file is as expected.
Many thanks for your help. I'm still getting my feet wet with
galaxy, reading through all the documentation and searching the
mailing list for additional help.
best regards,
-brian
--
--
Brian J. Haas
Manager, Genome Annotation and Analysis, Research and Development
The Broad Institute
<tool id="alignreads" name="alignReads" version="0.0.1">
<description>alignReads: short read alignment tool wrapper</description>
<requirements>
<requirement type="package">trinity</requirement>
</requirements>
<command>
alignReads.pl --target $target -o alignment --aligner $aligner_selection.aligner
## Inputs.
#if str($inputs.paired_or_single) == "paired":
--left $inputs.left_input --right $inputs.right_input
#if $inputs.left_input.ext == 'fa':
--seqType fa
#else:
--seqType fq
#end if
#if str($inputs.library_type) != "None":
--SS_lib_type $inputs.library_type
#end if
--max_dist_between_pairs $inputs.max_dist_between_pairs
#else:
--single $inputs.input
#if str($inputs.input.ext) == 'fa':
--seqType fa
#else:
--seqType fq
#end if
#if str($inputs.library_type) != "None":
--SS_lib_type $inputs.library_type
#end if
#end if
## Additional parameters.
##if str($inputs.use_additional) == "yes":
## -- $inputs.additional_params
##end if
## direct to output
## > $trinity_log 2>&1
</command>
<inputs>
<param format="fasta" name="target" type="data" label="target" help="Fasta sequences targeted for short-read alignment" />
<conditional name="inputs">
<param name="paired_or_single" type="select" label="Paired or Single-end data?">
<option value="paired">Paired</option>
<option value="single">Single</option>
</param>
<when value="paired">
<param format="fasta,fastq" name="left_input" type="data" label="Left/Forward strand reads" help=""/>
<param format="fasta,fastq" name="right_input" type="data" label="Right/Reverse strand reads" help=""/>
<param name="library_type" type="select" label="Strand-specific Library Type">
<option value="None">None</option>
<option value="FR">FR</option>
<option value="RF">RF</option>
</param>
<param name="max_dist_between_pairs" type="integer" value="2000" min="1" label="max_dist_between_pairs" help="Maximum length expected between fragment pairs as aligned to the target, including introns where relevant."/>
</when>
<when value="single">
<param format="fasta,fastq" name="input" type="data" label="Single-end reads" help=""/>
<param name="library_type" type="select" label="Strand-specific Library Type">
<option value="None">None</option>
<option value="F">F</option>
<option value="R">R</option>
</param>
</when>
</conditional>
<conditional name="aligner_selection">
<param name="aligner" type="select" label="Select alignment tool to run">
<option value="bowtie">bowtie</option>
<option value="bwa">bwa</option>
<option value="blat">blat</option>
</param>
<when value="blat">
<param name="max_intron_length" type="integer" value="10000" min = "1" label="maximum intron length" help="" />
<param name="min_percent_identity" type="integer" value="95" min="1" label="minimum percent identity" help="" />
</when>
<when value="bwa">
</when>
<when value="bowtie">
</when>
</conditional>
<!--
<conditional name="use_additional_params">
<param name="use_additional" type="select" label="Use Additional Params?">
<option value="no">No</option>
<option value="yes">Yes</option>
</param>
<when value="no">
</when>
<when value="yes">
<param name="additional_params" type="text" value="" label="Additional command-line parameters to aligner" help="" />
</when>
</conditional>
-->
</inputs>
<outputs>
<data format="bam" name="coordSortedBam" label="${ tool.name } on ${on_string}: coord-sorted read alignments" from_work_dir="alignment/alignment.coordSorted.bam"/>
<!-- <data format="bam" name="nameSortedBam" label="${ tool.name } on ${on_string}: name-sorted read alignments" from_work_dir="alignment/alignment.nameSorted.bam"/> -->
</outputs>
<tests>
</tests>
<help>
.. _Trinity: http://trinityrnaseq.sourceforge.net
</help>
</tool>
___________________________________________________________
Please keep all replies on the list by using "reply all"
in your mail client. To manage your subscriptions to this
and other Galaxy lists, please use the interface at:
___________________________________________________________
Please keep all replies on the list by using "reply all"
in your mail client. To manage your subscriptions to this
and other Galaxy lists, please use the interface at:
-- Nicole Rockweiler Genome Technology Access Center Washington University in St. Louis Campus Box 8510 4444 Forest Park Avenue Saint Louis, MO 63108
The contents of this e-mail and any attachments are confidential and only for use by the intended recipient. Any unauthorized use, distribution or copying of this message is strictly prohibited. If you are not the intended recipient please inform the sender immediately by reply e-mail and delete this message from your system. Thank you for your co-operation. ___________________________________________________________ Please keep all replies on the list by using "reply all" in your mail client. To manage your subscriptions to this and other Galaxy lists, please use the interface at: