view tools/sr_assembly/mira.xml @ 4:117cce3296af

Uploaded wrapper v0.0.3, which is for MIRA v3.4.x which includes support for Ion Torrent. The Galaxy wrapper will no longer work with MIRA v3.2.x - if you are still using the old version of MIRA, please continue to use v0.0.2 of the wrapper.

<tool id="mira_assembler" name="Assemble with MIRA" version="0.0.3">
    <description>Takes Sanger, Roche, Illumina, and Ion Torrent data</description>
	<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 $condBackbone.use == "true":
    ## Can this be linked to job_method as well? If mapping we need the backbone...
    -SB:lb=1:bft=1 -FN:bbin=${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>