comparison PoorGeneCoverage.xml @ 0:7cdd13ff182a default tip

initial commit
author Yusuf Ali <ali@yusuf.email>
date Wed, 25 Mar 2015 15:49:28 -0600
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-1:000000000000 0:7cdd13ff182a
1 <?xml version="1.0"?>
2
3 <tool id="poor_gene_coverage" name="Report Poor Coverage">
4 <description>regions for a set of genes</description>
5 <version_string>echo 1.0.0</version_string>
6 <command interpreter="perl">annotate_low_coverage $__tool_data_path__ ${captureKitRegions} $poorCaptureRegions $outputTable
7 #if $targetGenes.dataset and str($targetGenes) > '':
8 $targetGenes
9 #else:
10 /dev/null
11 #end if
12 NM_
13 </command>
14 <inputs>
15 <param name="sampleName" type="text" label="Biological sample name" help="Will be used to name the output files"/>
16 <param name="captureKitRegions" type="select" display="radio" dynamic_options="kit_fileOptions()" label="The enrichment (capture) kit used for the sequencing experiment"/>
17 <param format="bed" name="poorCaptureRegions" type="data" label="BED file of low coverage regions"/>
18 <param format="text" name="targetGenes" type="data" optional="true" label="List of genes to report, one per line"/>
19 </inputs>
20 <outputs>
21 <data format="tabular" name="outputTable"/>
22 </outputs>
23
24 <!-- the following code populates the selection from the public capture kit BED datasets available in the local Galaxy installation -->
25 <code file="capture_kits.py"/>
26 <tests/>
27
28 <help>This tools summarized low coverage regions on a per gene basis, including information on clinically relevant variants (according to ClinVar) that might have been missed</help>
29
30 </tool>