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galaxy/tools/emboss/emboss_marscan.xml
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<tool id="EMBOSS: marscan49" name="marscan">
<description>Finds MAR/SAR sites in nucleic sequences</description>
<command>marscan -sequence $input1 -outfile $out_file1 -rformat2 $out_format1 -auto</command>
<inputs>
<param format="data" name="input1" type="data">
<label>Sequence</label>
</param>
<param name="out_format1" type="select">
<label>Output Report File Format</label>
<option value="gff">GFF</option>
<option value="embl">EMBL</option>
<option value="genbank">GENBANK</option>
<option value="pir">PIR</option>
<option value="swiss">SwissProt</option>
<option value="dbmotif">DbMotif</option>
<option value="diffseq">Diffseq</option>
<option value="excel">Excel (tab delimited)</option>
<option value="feattable">FeatTable</option>
<option value="motif">Motif</option>
<option value="regions">Regions</option>
<option value="seqtable">SeqTable</option>
<option value="simple">SRS Simple</option>
<option value="srs">SRS</option>
<option value="table">Table</option>
<option value="tagseq">TagSeq</option>
</param>
</inputs>
<outputs>
<data format="gff" name="out_file1" />
</outputs>
<code file="emboss_format_corrector.py" />
<help>
You can view the original documentation here_.
.. _here: http://emboss.sourceforge.net/apps/release/4.0/emboss/apps/marscan.html
</help>
</tool>