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<tool id="metaspades" name="metaspades" version="1.0"> <description>genome assembler for metagenomics datasets</description> <requirements> <requirement type="package" version="3.9.0">spades</requirement> </requirements> <command interpreter="perl">spades.pl $out_contigs $out_contig_stats $out_scaffolds $out_scaffold_stats $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 --careful -1 Y.fastq.gz -2 X.fastq.gz -t 24 -o output spades.py ## Forces unzipped output, faster --disable-gzip-output --meta $onlyassembler -t \${GALAXY_SLOTS:-16} #if not $kmer_choice.auto_kmer_choice: -k "$kmer_choice.kmers" #end if ## 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)" /> <conditional name="kmer_choice"> <param name="auto_kmer_choice" type="boolean" checked="False" truevalue="true" falsevalue="false" label="Automatically choose k-mer values" help="k-mer choices can be chosen by SPAdes instead of being entered manually" /> <when value="false"> <param name="kmers" type="text" label="K-mers to use, separated by commas" value="21,33,55" help="Comma-separated list of k-mer sizes to be used (all values must be odd, less than 128, listed in ascending order, and smaller than the read length). The default value is 21,33,55." /> </when> <when value="true"> </when> </conditional> <!-- 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">-> <- (fr)</option> <option value="rf"><- -> (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="SPAdes contigs (fasta)" /> <data name="out_contig_stats" format="tabular" label="SPAdes contig stats" /> <data name="out_scaffolds" format="fasta" label="SPAdes scaffolds (fasta)" /> <data name="out_scaffold_stats" format="tabular" label="SPAdes scaffold stats" /> <data name="out_log" format="txt" label="SPAdes log" /> </outputs> <tests> <test> <param name="sc" value="false" /> <param name="careful" value="false" /> <param name="kmers" value="33,55" /> <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="reference_1K.fa" ftype="fasta" 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 tab file with contig names, length and coverage. **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>