comparison gemini_pathways.xml @ 0:14caa57eca63 draft

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author iuc
date Mon, 11 Aug 2014 07:44:30 -0400
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children e6512af21622
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-1:000000000000 0:14caa57eca63
1 <tool id="gemini_@BINARY@" name="GEMINI @BINARY@" version="@VERSION@.0">
2 <description>Map genes and variants to KEGG pathways</description>
3 <expand macro="requirements" />
4 <expand macro="version_command" />
5 <macros>
6 <import>gemini_macros.xml</import>
7 <token name="@BINARY@">pathways</token>
8 </macros>
9 <command>
10 <![CDATA[
11 gemini @BINARY@
12 -v $ensembl
13 $lof
14 "${ infile }"
15 > "${ outfile }"
16 ]]>
17 </command>
18 <expand macro="stdio" />
19 <inputs>
20 <param name="infile" type="data" format="sqlite" label="GEMINI database" />
21
22 <param name="ensemble" type="integer" value="68" size="5" label="Version of ensembl genes to use"
23 help="Supported versions: 66 to 71. use versions that match the VEP/snpEff versions of the annotated vcf for correctness. For e.g VEP v2.6 and snpEff v3.1 use Ensembl 68 version of the genomes. (-v)">
24 <validator type="in_range" min="66" max="71"/>
25 </param>
26
27 <param name="lof" type="boolean" truevalue="--lof" falsevalue="" checked="False"
28 label="Report only pathways with loss-of-function variants" help="(--lof)"/>
29
30 </inputs>
31 <outputs>
32 <data name="outfile" format="tabular" label="${tool.name} on ${on_string}" />
33 </outputs>
34 <tests>
35 <test>
36 </test>
37 </tests>
38 <help>
39 **What it does**
40
41 Mapping genes to biological pathways is useful in understanding the function/role played by a gene.
42 Likewise, genes involved in common pathways is helpful in understanding heterogeneous diseases.
43 We have integrated the KEGG pathway mapping for gene variants, to explain/annotate variation.
44
45 This requires your VCF be annotated with either snpEff/VEP.
46
47 @CITATION@
48 </help>
49 <expand macro="citations"/>
50 </tool>