Mercurial > repos > rnateam > gotohscan
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planemo upload for repository https://github.com/bgruening/galaxytools/tree/master/tools/gotohscan commit d18a08287799b0aa6ca50242ebcc218820923fb2-dirty
author | rnateam |
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date | Thu, 02 Jul 2015 12:06:30 -0400 |
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children | c172fed9eb75 |
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<tool id="rbc_gotohscan" name="GotohScan" version="1.3.0"> <description>Find subsequences in db</description> <requirements> <requirement type="package" version="1.3">gotohscan</requirement> </requirements> <stdio> <exit_code range="1:" level="fatal" description="Error occurred. Please check Tool Standard Error"/> <exit_code range=":-1" level="fatal" description="Error occurred. Please check Tool Standard Error"/> </stdio> <version_command><![CDATA[GotohScan --version | sed -n -e 2p]]></version_command> <command><![CDATA[ GotohScan -d $dbase -q $query #if $split and $split is not None --split $split #end if #if $e and $e is not None -e $e #end if #if $p and $p is not None -p $p #end if $s -o $o > #if $o.value == '0' $output0 #elif $o.value == '1' $output1 #elif $o.value == '2' $output2 #elif $o.value == '3' $output3 #elif $o.value == '4' $output4 #elif $o.value == '5' $output5 #end if ]]></command> <inputs> <param argument="-d" name="dbase" type="data" format="fasta" label="Input Database"/> <param argument="-q" name="query" type="data" format="fasta" label="Input Query"/> <param argument="--split" name="split" type="integer" optional="true" label="Database is split into subsequences of size:" help="default: 10000"/> <param argument="-e" name="e" type="float" optional="true" label="E-value" help="Value should be < 10. default: 1e-3"/> <param argument="-p" name="p" type="float" optional="true" label="Percent identity of aligned sequences" help="Value should be in [0.0,100.00]"/> <param argument="-s" name="s" type="boolean" checked="false" truevalue="-s" falsevalue="" label="Print score distribution data for each query to a file"/> <param argument="-o" name="o" type="select" label="Output Format"> <option value="0" selected="true">Blast tabular output</option> <option value="1">Blast tabular output + aligned sequences</option> <option value="2">FASTA format. NOTE: Hit sequence only, without gaps !</option> <option value="3">MAF format. NOTE: Header truncated to 30 characters!</option> <option value="4">BED + aligned sequences</option> <option value="5">GFF + aligned sequences</option> </param> </inputs> <outputs> <data name="output0" format="tabular" label="${tool.name} on ${on_string}"> <filter>o == '0'</filter> </data> <data name="output1" format="tabular" label="${tool.name} on ${on_string}"> <filter>o == '1'</filter> </data> <data name="output2" format="fasta" label="${tool.name} on ${on_string}"> <filter>o == '2'</filter> </data> <data name="output3" format="maf" label="${tool.name} on ${on_string}"> <filter>o == '3'</filter> </data> <data name="output4" format="bed" label="${tool.name} on ${on_string}"> <filter>o == '4'</filter> </data> <data name="output5" format="gff" label="${tool.name} on ${on_string}"> <filter>o == '5'</filter> </data> </outputs> <tests> <test> <param name="dbase" value="NC_000913.fna"/> <param name="query" value="C0299.fa"/> <param name="o" value="2"/> <output name="" ftype="fasta" file="gotohscan.result1"/> </test> </tests> <help> <![CDATA[ **GotohScan** is a search tool that finds shorter sequences (usually genes) in large database sequences (chromosomes, genomes, ..) by computing all semi-global alignments. Thus, the query sequence is never truncated or split into subsequences, but always mapped to the database over its complete length. The alignment is computed via the Gotoh-alignment algorithm using affine gap costs. ]]></help> <citations> <citation type="doi">10.1093/nar/gkn1084</citation> </citations> </tool>