--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/rnaspades.xml	Tue Aug 09 10:52:40 2016 -0400
@@ -0,0 +1,128 @@
+<tool id="rnaspades" name="rnaspades" version="1.0">
+  <description>pipeline for de novo transcriptome assembly from RNA-Seq</description>
+  <requirements>
+    <requirement type="package" version="3.9.0">spades</requirement>
+  </requirements>
+  <command interpreter="perl">spades.pl 
+    $out_contigs 
+    $out_paths 
+    $out_log
+
+    ## if the first fileset is a paired-collection, use the key as the name
+    #if $files[0].file_type.type == "paired-collection":
+        $files[0].file_type.fastq_collection.name
+    #else:
+        NODE
+    #end if
+    ## A real command looks like: spades.py -k 21,33,55,77,99,127  -1 Y.fastq.gz -2 X.fastq.gz -t 24 -o output
+    spades.py
+    ## Forces unzipped output, faster
+    --disable-gzip-output
+    --rna
+    $onlyassembler
+
+    -t \${GALAXY_SLOTS:-16}
+
+    -k "$kmers"    
+
+
+    ## Sequence files
+      #set num=1
+      #if str( $lib_type ) == "paired_end":
+        #set prefix = 'pe'
+      #end if
+      --$prefix$num-$orientation    
+      #for $file in $files
+	#if $file.file_type.type == "separate"
+          --$prefix$num-1 fastq:$file.file_type.fwd_reads
+          --$prefix$num-2 fastq:$file.file_type.rev_reads
+        #elif $file.file_type.type == "interleaved"
+          --$prefix$num-12 fastq:$file.file_type.interleaved_reads
+        #elif $file.file_type.type == "paired-collection"
+        --$prefix$num-1 fastq:$file.file_type.fastq_collection.forward
+        --$prefix$num-2 fastq:$file.file_type.fastq_collection.reverse
+        #end if
+      #end for
+
+
+  </command>
+  <inputs>
+    <param name="onlyassembler" type="boolean" truevalue="--only-assembler" falsevalue="" checked="False" label="Run only assembly? (without read error correction)" />
+
+        <param name="kmers" type="text" label="K-mers to use, separated by commas" value="55" help="Recommended to use default of k-mer size of 55. In case your RNA-Seq data set contains long Illumina reads (150 bp and longer) you may try to use longer k-mer size (approximately half of the read length)" />
+    <!-- Reads -->
+
+      <param name="lib_type" type="select" label="Library type">
+	<option value="paired_end">Paired-end</option>
+      </param>
+      <param name="orientation" type="select" label="Orientation">
+	<option value="fr" selected="true">-> &lt;- (fr)</option>
+	<option value="rf">&lt;- -> (rf)</option>
+	<option value="ff">-> -> (ff)</option>
+      </param>
+      <repeat name="files" title="Files" min="1">
+	<conditional name="file_type">
+	  <param name="type" type="select" label="Select file format">
+	    <option value="separate">Separate input files</option>
+	    <option value="interleaved">Interleaved files</option>
+            <option value="paired-collection">Paired List Collection</option>
+	  </param>
+	  <when value="separate">
+	    <param name="fwd_reads" type="data" format="fastq" label="Forward reads" help="FASTQ format" />
+	    <param name="rev_reads" type="data" format="fastq" label="Reverse reads" help="FASTQ format" />
+	  </when>
+	  <when value="interleaved">
+	    <param name="interleaved_reads" type="data" format="fastq" label="Interleaved paired reads" help="FASTQ format" />
+	  </when>
+          <when value="paired-collection">
+            <param name="fastq_collection" type="data_collection" label="Paired-end reads collection" optional="false" format="fastq" collection_type="paired" help="FASTQ format" /> 
+          </when>
+	</conditional>
+      </repeat>
+
+
+  </inputs>
+  <outputs>
+    <data name="out_contigs" format="fasta" label="rnaSPAdes fasta" />
+    <data name="out_paths" format="txt" label="rnaSPAdes fastg" />
+    <data name="out_log" format="txt" label="SPAdes log" />
+  </outputs>
+  <tests>
+    <test>
+      <param name="kmers" value="55" />
+      <param name="lib_type" value="paired_end" />
+      <param name="fwd_reads" value="ecoli_1K_1.fq" ftype="fastq" />
+      <param name="rev_reads" value="ecoli_1K_2.fq" ftype="fastq" />
+      <output name="out_contigs" file="transcripts.fasta" ftype="fasta" compare="re_match" lines_diff="1" />
+      <output name="out_paths" file="transcripts.paths" ftype="txt" compare="re_match" lines_diff="1" />
+    </test> 
+ </tests>
+  <help>
+**What it does**
+
+SPAdes – St. Petersburg genome assembler – is intended for both standard isolates and single-cell MDA bacteria assemblies. See http://bioinf.spbau.ru/en/spades for more details on SPAdes.
+
+This wrapper runs SPAdes 3.9, collects the output, and throws away all the temporary files. It also produces a single Fasta file with a corresponding file assembly_graph.fastg.
+
+**License**
+
+SPAdes is developed by and copyrighted to Saint-Petersburg Academic University, and is released under GPLv2.
+
+This wrapper is copyrighted by Philip Mabon and is free software: you can redistribute it and/or modify it under the terms of the GNU General Public License as published by the Free Software Foundation, either version 3 of the License, or (at your option) any later version.
+
+This program is distributed in the hope that it will be useful, but WITHOUT ANY WARRANTY; without even the implied warranty of MERCHANTABILITY or FITNESS FOR A PARTICULAR PURPOSE. See the GNU General Public License for more details.
+
+You should have received a copy of the GNU General Public License along with this program.  If not, see http://www.gnu.org/licenses/.
+
+** Acknowledgments **
+
+Original wrapper developed by Lionel Guy.
+
+Anton Korobeynikov greatlty helped understanding how SPAdes work, and integrated handy features into SPAdes.
+
+Nicola Soranzo fixed various bugs.
+  </help>
+    <citations>
+        <citation type="doi">10.1089/cmb.2012.0021</citation>
+    </citations>
+</tool>