Mercurial > repos > peterjc > mira_assembler
view tools/sr_assembly/mira.xml @ 6:3e7eca1f5d04 draft
MIRA wrapper v0.0.5 with <version_command> support and check for MIRA V3.4
author | peterjc |
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date | Fri, 01 Feb 2013 10:34:21 -0500 |
parents | 216bf640baaf |
children | 4d3f94dfb857 |
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<tool id="mira_assembler" name="Assemble with MIRA" version="0.0.5"> <description>Takes Sanger, Roche, Illumina, and Ion Torrent data</description> <version_command interpreter="python">mira.py -v</version_command> <command interpreter="python">mira.py mira $out_fasta $out_qual $out_ace $out_caf $out_wig $out_log ##Give the wrapper script list of output filenames, then the mira command... mira --job=$job_method,$job_type,$job_quality ##Input files #if $condBackbone.use == "true": ## Can this be linked to job_method as well? If mapping we need the backbone... -SB:lb=1:bft=fasta -FN:bbin=${condBackbone.filename} #end if #if $condSanger.use == "true": SANGER_SETTINGS ## Not easy in Galaxy to add sanger to --job, so use load_sequence_data(lsd) instead ## I expect hard trimmed FASTQ files with no NCBI traceinfo XML file -LR:lsd=1:mxti=0:ft=fastq -FN:fqi=${condSanger.filename} #end if #if $condRoche.use == "true": 454_SETTINGS ## Not easy in Galaxy to add 454 to --job, so use load_sequence_data(lsd) instead ## I expect hard trimmed FASTQ files with no NCBI traceinfo XML file -LR:lsd=1:mxti=0:ft=fastq -FN:fqi=${condRoche.filename} #end if #if $condIllumina.use == "true": SOLEXA_SETTINGS ## Not easy in Galaxy to add solexa to --job, so use load_sequence_data(lsd) instead -LR:lsd=1:ft=fastq -FN:fqi=${condIllumina.filename} ##TODO - Look at -LR FASTQ qual offset (fqqo) #end if #if $condIonTorrent.use == "true": IONTOR_SETTINGS ## Not easy in Galaxy to add iontor to --job, so use load_sequence_data(lsd) instead ## I expect hard trimmed FASTQ files with no NCBI traceinfo XML file -LR:lsd=1:mxti=0:ft=fastq -FN:fqi=${condIonTorrent.filename} #end if ##Output files COMMON_SETTINGS ##Explicitly request the FASTA (+QUAL), CAF, ACE, WIG output ##Explicitly disable formats we won't use like MAF (reduce IO) -OUT:orf=1:orc=1:ora=1:orw=1:orm=0:org=0:ors=0 ##remove_rollover_tmps, remove_tmp_directory -OUT:rrot=1:rtd=1 </command> <inputs> <param name="job_method" type="select" label="Assembly method" help="Mapping mode requires backbone/reference sequence(s)"> <option value="denovo">De novo</option> <option value="mapping">Mapping</option> </param> <param name="job_type" type="select" label="Assembly type"> <option value="genome">Genome</option> <option value="est">EST (transcriptome)</option> </param> <param name="job_quality" type="select" label="Assembly quality grade"> <option value="accurate">Accurate</option> <option value="normal">Normal (deprecated)</option> <option value="draft">Draft</option> </param> <!-- Backbone --> <conditional name="condBackbone"> <param name="use" type="select" label="Backbones/reference chromosomes?" help="Required for mapping, optional for de novo assembly."> <option value="false">No</option> <option value="true">Yes</option> </param> <when value="false" /> <when value="true"> <!-- MIRA also allows CAF and GenBank, but Galaxy doesn't define those (yet) --> <param name="filename" type="data" format="fasta" label="Backbone/reference sequences" help="FASTA format" /> </when> </conditional> <!-- Sanger --> <conditional name="condSanger"> <param name="use" type="select" label="Sanger/Capillary reads?"> <option value="false">No</option> <option value="true">Yes</option> </param> <when value="false" /> <when value="true"> <param name="filename" type="data" format="fastq" label="Sanger/Capillary reads file" help="FASTQ format" /> </when> </conditional> <!-- Roche 454 --> <conditional name="condRoche"> <param name="use" type="select" label="454 reads?"> <option value="false">No</option> <option value="true">Yes</option> </param> <when value="false" /> <when value="true"> <!-- TODO? Support SFF files directly, e.g. with sff_extract, but will need linker sequences --> <param name="filename" type="data" format="fastq" label="Roche 454 reads file" help="FASTQ format" /> </when> </conditional> <!-- Illumina --> <conditional name="condIllumina"> <param name="use" type="select" label="Solexa/Illumina reads?"> <option value="false">No</option> <option value="true">Yes</option> </param> <when value="false" /> <when value="true"> <param name="filename" type="data" format="fastq" label="Solexa/Illumina reads file" help="FASTQ format" /> </when> </conditional> <!-- Ion Torrent --> <conditional name="condIonTorrent"> <param name="use" type="select" label="Ion Torrent reads?"> <option value="false">No</option> <option value="true">Yes</option> </param> <when value="false" /> <when value="true"> <!-- TODO? Support SFF files directly, e.g. with sff_extract --> <param name="filename" type="data" format="fastq" label="Ion Torrent reads file" help="FASTQ format" /> </when> </conditional> </inputs> <outputs> <data name="out_fasta" format="fasta" label="MIRA contigs (FASTA)" /> <data name="out_qual" format="qual454" label="MIRA contigs (QUAL)" /> <data name="out_caf" format="txt" label="MIRA contigs (CAF)" /> <data name="out_ace" format="txt" label="MIRA contigs (ACE)" /> <data name="out_wig" format="wig" label="MIRA coverage (Wiggle)" /> <data name="out_log" format="txt" label="MIRA log" /> </outputs> <tests> </tests> <requirements> <requirement type="python-module">Bio</requirement> </requirements> <help> **What it does** Runs MIRA v3, collects the output, and throws away all the temporary files. **Citation** This tool uses MIRA. If you use this tool in scientific work leading to a publication, please cite: Chevreux et al. (1999) Genome Sequence Assembly Using Trace Signals and Additional Sequence Information Computer Science and Biology: Proceedings of the German Conference on Bioinformatics (GCB) 99, pp. 45-56. </help> </tool>