Mercurial > repos > nml > spades
view spades.xml @ 5:909c315b656d draft
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/spades commit 9d484642914b581ce35f254466b849d3c4c2c06c-dirty
author | iuc |
---|---|
date | Wed, 01 Mar 2017 15:33:26 -0500 |
parents | 35cb17bd8bf9 |
children | 65c2d63fcbe6 |
line wrap: on
line source
<tool id="spades" name="SPAdes" version="3.9.0"> <description>genome assembler for regular and single-cell projects</description> <requirements> <requirement type="package" version="3.9.0">spades</requirement> </requirements> <stdio> <exit_code range="1:" /> </stdio> <command> <![CDATA[ ## 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 -o . --disable-gzip-output $sc $onlyassembler $careful -t \${GALAXY_SLOTS:-16} #if not $kmer_choice.auto_kmer_choice: -k "$kmer_choice.kmers" #end if #if $cov.state == "auto": --cov-cutoff 'auto' #elif $cov.state == "value": --cov-cutoff '$cov.cutoff' #end if $iontorrent ## Sequence files, libraries #for $i, $library in enumerate( $libraries, start=1 ) #if str( $library.lib_type ) == "paired_end": #set prefix = 'pe' #elif str( $library.lib_type ) == "mate_paired": #set prefix = 'mp' #elif str( $library.lib_type ) == "nxmate_paired": #set prefix = 'nxmate' #else: #set prefix = 'hqmp' #end if --$prefix$i-$library.orientation #for $file in $library.files #if $file.file_type.type == "separate" --$prefix$i-1 fastq:$file.file_type.fwd_reads --$prefix$i-2 fastq:$file.file_type.rev_reads #elif $file.file_type.type == "interleaved" --$prefix$i-12 fastq:$file.file_type.interleaved_reads #elif $file.file_type.type == "unpaired" --$prefix$i-s fastq:$file.file_type.unpaired_reads #elif $file.file_type.type == "paired-collection" --$prefix$i-1 fastq:$file.file_type.fastq_collection.forward --$prefix$i-2 fastq:$file.file_type.fastq_collection.reverse #end if #end for #end for #for $read in $pacbio_reads: #if $read: --pacbio fastq:$read #end if #end for #for $read in $nanopore_reads: #if $read: --nanopore fastq:$read #end if #end for #for $read in $sanger_reads: #if $read: --sanger $read.extension:$read #end if #end for #for $contig in $trusted_contigs: #if $contig: --trusted-contigs $contig.extension:$contig #end if #end for #for $contig in $untrusted_contigs: #if $contig: --untrusted-contigs $contig.extension:$contig #end if #end for ]]> </command> <inputs> <param argument="--sc" falsevalue="" help="This option is required for MDA (single-cell) data." label="Single-cell?" name="sc" truevalue="--sc" type="boolean"> <option value="false">No</option> <option value="true">Yes</option> </param> <param argument="--only-assembler" checked="False" falsevalue="" label="Run only assembly? (without read error correction)" name="onlyassembler" truevalue="--only-assembler" type="boolean" /> <param argument="----careful" checked="True" falsevalue="" help="Tries to reduce number of mismatches and short indels. Also runs MismatchCorrector – a post processing tool, which uses BWA tool (comes with SPAdes)." label="Careful correction?" name="careful" truevalue="--careful" type="boolean" /> <conditional name="kmer_choice"> <param checked="False" falsevalue="false" help="k-mer choices can be chosen by SPAdes instead of being entered manually" label="Automatically choose k-mer values" name="auto_kmer_choice" truevalue="true" type="boolean" /> <when value="false"> <param 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." label="K-mers to use, separated by commas" name="kmers" type="text" value="21,33,55" /> </when> <when value="true" /> </conditional> <conditional name="cov"> <param label="Coverage Cutoff" name="state" type="select"> <option value="off">Off</option> <option value="value">User Specific</option> <option value="auto">Auto</option> </param> <when value="off" /> <when value="value"> <param help="coverage cutoff value (a positive float number, or 'auto', or 'off') [default: 'off']" label="Coverage cutoff value" name="cutoff" type="float" value="" /> </when> <when value="auto" /> </conditional> <param checked="False" falsevalue="" label="Libraries are IonTorrent reads?" name="iontorrent" truevalue="--iontorrent" type="boolean" /> <repeat help="It is not possible to specify only mate-pair libraries. Scaffolds are not produced if neither a paired-end nor a mate-pair library is provided." min="1" name="libraries" title="Libraries"> <param label="Library type" name="lib_type" type="select"> <option value="paired_end">Paired-end / Single reads</option> <option value="mate_paired">Mate pairs</option> <option value="high_mate_paired">High Quality Mate pairs</option> <option value="nxmate_paired">Lucigen NxMate pairs</option> </param> <param label="Orientation" name="orientation" type="select"> <option selected="true" value="fr"><![CDATA[-> <- (fr)]]></option> <option value="rf"><![CDATA[<- -> (rf)]]></option> <option value="ff"><![CDATA[-> -> (ff)]]></option> </param> <repeat min="1" name="files" title="Files"> <conditional name="file_type"> <param label="Select file format" name="type" type="select"> <option value="separate">Separate input files</option> <option value="interleaved">Interleaved files</option> <option value="unpaired">Unpaired/Single reads</option> <option value="paired-collection">Paired List Collection</option> </param> <when value="separate"> <param format="fastq" help="FASTQ format" label="Forward reads" name="fwd_reads" type="data" /> <param format="fastq" help="FASTQ format" label="Reverse reads" name="rev_reads" type="data" /> </when> <when value="interleaved"> <param format="fastq" help="FASTQ format" label="Interleaved paired reads" name="interleaved_reads" type="data" /> </when> <when value="unpaired"> <param format="fastq" help="FASTQ format" label="Unpaired reads" name="unpaired_reads" type="data" /> </when> <when value="paired-collection"> <param collection_type="paired" format="fastq" help="FASTQ format" label="Paired-end reads collection" name="fastq_collection" optional="false" type="data_collection" /> </when> </conditional> </repeat> </repeat> <param optional="true" format="fastq" label="PacBio CLR reads" multiple="true" name="pacbio_reads" type="data" /> <param optional="true" format="fastq" label="Nanopore reads" multiple="true" name="nanopore_reads" type="data" /> <param optional="true" format="fasta,fastq" label="Sanger reads" multiple="true" name="sanger_reads" type="data" /> <param optional="true" format="fasta,fastq" label="Trusted contigs" multiple="true" name="trusted_contigs" type="data" /> <param optional="true" format="fasta,fastq" label="Untrusted contigs" multiple="true" name="untrusted_contigs" type="data" /> </inputs> <outputs> <data format="fasta" from_work_dir="contigs.fasta" label="SPAdes contigs (fasta)" name="out_contigs" /> <data format="fasta" from_work_dir="scaffolds.fasta" label="SPAdes scaffolds (fasta)" name="out_scaffolds" /> <data format="txt" from_work_dir="spades.log" label="SPAdes log" name="out_log" /> </outputs> <tests> <test> <param name="sc" value="false" /> <param name="careful" value="false" /> <param name="kmers" value="33" /> <param name="lib_type" value="paired_end" /> <param ftype="fastq" name="fwd_reads" value="ecoli_1K_1.fq" /> <param ftype="fastq" name="rev_reads" value="ecoli_1K_2.fq" /> <output compare="re_match" file="kmer_33_output.fa" ftype="fasta" lines_diff="1" name="out_contigs" /> </test> <test> <param name="sc" value="false" /> <param name="careful" value="false" /> <param name="auto_kmer_choice" value="true" /> <param name="lib_type" value="paired_end" /> <param ftype="fastq" name="fwd_reads" value="ecoli_1K_1.fq" /> <param ftype="fastq" name="rev_reads" value="ecoli_1K_2.fq" /> <output compare="re_match" file="auto_kmer_output.fa" ftype="fasta" lines_diff="1" name="out_contigs" /> </test> <test> <param name="sc" value="false" /> <param name="careful" value="false" /> <param name="kmers" value="77" /> <param name="lib_type" value="paired_end" /> <param ftype="fastq" name="fwd_reads" value="ecoli_1K_1.fq" /> <param ftype="fastq" name="rev_reads" value="ecoli_1K_2.fq" /> <output compare="re_match" file="kmer_77_output.fa" ftype="fasta" lines_diff="1" name="out_contigs" /> </test> </tests> <help> <![CDATA[ **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>