comparison rg_rnaStar.xml @ 0:b2326241bb09 draft

planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/rgrnastar commit 13522d2ad2efbb8dab405723f491bd1a6591e3ef

0:b2326241bb09

<tool id="rna_star" name="rnastar" version="2.4.0d">
    <description>Gapped-read mapper for RNA-seq data</description>
    <requirements>
        <requirement type="package" version="2.4.0d">rnastar</requirement>
        <requirement type="package" version="0.1.19">samtools</requirement>
    </requirements>
    <stdio>
        <regex match=".*" source="both" level="warning" description="Some stderr/stdout text"/>
    </stdio>

    <command>
    ##
    ## Run STAR.
    ##
    #if str($refGenomeSource.genomeSource) == 'history':
       mkdir -p tempstargenomedir; STAR --runMode genomeGenerate --genomeDir "tempstargenomedir" --genomeFastaFiles "$refGenomeSource.ownFile" --runThreadN 2
        #if str($refGenomeSource.geneModel) != 'None':
          --sjdbOverhang "100" --sjdbGTFfile "$refGenomeSource.geneModel"
          #if str($refGenomeSource.geneModel.ext) == 'gff3':
            --sjdbGTFtagExonParentTranscript Parent
          #end if
        #end if
        ;
    #end if
    STAR
    ## Can adjust this as appropriate for the system.
    --genomeLoad NoSharedMemory
    #if str($refGenomeSource.genomeSource) == 'history':
        --genomeDir "tempstargenomedir"
    #else
        --genomeDir "$refGenomeSource.index.fields.path"
    #end if
    --readFilesIn $singlePaired.input1
    #if str($singlePaired.sPaired) == "paired"
            $singlePaired.input2
    #end if
        --runThreadN 4
    #if str($params.settingsType) == "full":
        --chimSegmentMin $params.chim_segment_min
        --chimScoreMin $params.chim_score_min
    #end if

    ## may or may not need to generate SAM tags and handle non-canonicals for Cufflinks tools.
    $outSAMstrandField $outFilterIntronMotifs $outSAMattributes

    ;
    ##
    ## BAM conversion.
    ##

    ## Convert aligned reads.
    samtools view -Shb Aligned.out.sam | samtools sort - AlignedSorted 2&gt;/dev/null

    ## Convert chimeric reads.
    #if str($params.settingsType) == "full" and $params.chim_segment_min > 0:
        ; samtools view -Shb Chimeric.out.sam | samtools sort - ChimericSorted 2&gt;/dev/null
    #end if
    </command>

    <inputs>
        <param name="jobName" type="text" size="120" value="rna-star run" label="Job narrative (added to output names)"
          help="Only letters, numbers and underscores (_) will be retained in this field">
           <sanitizer invalid_char="">
              <valid initial="string.letters,string.digits"><add value="_" /> </valid>
           </sanitizer>
        </param>
        <!-- FASTQ input(s) and options specifically for paired-end data. -->
        <conditional name="singlePaired">
            <param name="sPaired" type="select" label="Single ended or mate-pair ended reads in this library?">
              <option value="single" selected="true">Single-end</option>
              <option value="paired">Paired-end</option>
            </param>
            <when value="single">
                <param format="fastqsanger,fastq,fasta" name="input1" type="data" label="RNA-Seq FASTQ file" help="Nucleotide-space: Must have Sanger-scaled quality values with ASCII offset 33"/>
            </when>
            <when value="paired">
                <param format="fastqsanger,fastq,fasta" name="input1" type="data" label="RNA-Seq FASTQ file, forward reads"
            help="Nucleotide-space: Must have Sanger-scaled quality values with ASCII offset 33" />
                <param format="fastqsanger,fastq,fasta" name="input2" type="data" label="RNA-Seq FASTQ file, reverse reads"
            help="Nucleotide-space: Must have Sanger-scaled quality values with ASCII offset 33" />
            </when>
        </conditional>

        <!-- Genome source. -->
        <conditional name="refGenomeSource">
            <param name="genomeSource" type="select" label="Will you select a reference genome from your history or use a built-in index?" help="Built-ins were indexed using default options">
                <option value="indexed" selected="True">Use a built-in index</option>
                <option value="history">Index and use a genome fasta file from my current history</option>
            </param>
            <when value="indexed">
            <param name="index" type="select" label="Select a reference genome">
                <options from_data_table="rnastar_index">
                    <filter type="sort_by" column="2"/>
                    <validator type="no_options" message="No indexes are available for the selected input dataset"/>
                </options>
            </param>
            </when>
            <when value="history">
                <param name="ownFile" type="data" format="fasta" metadata_name="dbkey" label="Select the reference genome" />
                <param name="geneModel" type="data" format="gff3,gtf" label="Gene model (gff3,gtf) file for splice junctions. Leave blank for none"
                optional="true" help="Optional. If supplied, the index file will retain exon junction information for mapping splices" />
            </when>
        </conditional>
            <param name="outSAMattributes" type="select" label="Include extra sam attributes for downstream processing">
              <option value="--outSAMattributes Standard">Standard - eg for old Samtools downstream</option>
              <option value="--outSAMattributes All" selected="true">All modern Samtools attributes - see below</option>
            </param>
            <param name="outSAMstrandField" type="select" label="Include extra sam attributes for downstream processing">
              <option value="--outSAMstrandField intronMotif" selected="true">Add XS for cufflinks</option>
              <option value="">No XS added to sam output</option>
            </param>
            <param name="outFilterIntronMotifs" type="select" label="Canonical junction preparation for unstranded data">
              <option value="">No special handling - all non-canonical junctions passed through</option>
              <option value="--outFilterIntronMotifs RemoveNoncanonical" selected="true">Remove all non-canonical junctions for eg cufflinks</option>
              <option value="--outFilterIntronMotifs RemoveNoncanonicalUnannotated">Remove only unannotated non-canonical junctions for eg cufflinks</option>
            </param>
        <!-- Parameter settings. -->
        <conditional name="params">
            <param name="settingsType" type="select" label="Settings to use" help="You can use the default settings or set custom values for any STAR parameter.">
                <option value="preSet" selected="true">Use Defaults</option>
                <option value="full">Full parameter list</option>
            </param>
            <when value="preSet" />
            <!-- Full/advanced params. -->
            <when value="full">
            <param name="chim_segment_min" type="integer" min="0" value="0" label="Minimum chimeric segment length" />
            <param name="chim_score_min" type="integer" min="0" value="0" label="Minimum total (summed) score of the chimeric segments" />

            </when>
        </conditional>
    </inputs>

    <outputs>
       <data format="txt" name="output_log" label="${jobName}.log" from_work_dir="Log.final.out"/>
       <data format="interval" name="chimeric_junctions" label="${jobName}_starchimjunc.bed" from_work_dir="Chimeric.out.junction">
          <filter>(params['settingsType'] == 'full' and params['chim_segment_min'] > 0)</filter>
          <actions>
             <conditional name="refGenomeSource.genomeSource">
             <when value="indexed">
               <action type="metadata" name="dbkey">
                <option type="from_data_table" name="rnastar_index" column="1" offset="0">
                 <filter type="param_value" column="0" value="#" compare="startswith" keep="False"/>
                  <filter type="param_value" ref="refGenomeSource.index" column="0"/>
                </option>
               </action>
             </when>
             <when value="history">
               <action type="metadata" name="dbkey">
                 <option type="from_param" name="refGenomeSource.ownFile" param_attribute="dbkey" />
               </action>
             </when>
             </conditional>
          </actions>
       </data>
       <data format="bam" name="chimeric_reads" label="${jobName}_starmappedchim.bam"
                    from_work_dir="ChimericSorted.bam">
         <filter>(params['settingsType'] == 'full' and params['chim_segment_min'] > 0)</filter>
          <actions>
             <conditional name="refGenomeSource.genomeSource">
             <when value="indexed">
               <action type="metadata" name="dbkey">
                <option type="from_data_table" name="rnastar_index" column="1" offset="0">
                 <filter type="param_value" column="0" value="#" compare="startswith" keep="False"/>
                  <filter type="param_value" ref="refGenomeSource.index" column="0"/>
                </option>
               </action>
             </when>
             <when value="history">
               <action type="metadata" name="dbkey">
                 <option type="from_param" name="refGenomeSource.ownFile" param_attribute="dbkey" />
               </action>
             </when>
             </conditional>
          </actions>
        </data>
        <data format="interval" name="splice_junctions" label="${jobName}_starsplicejunct.bed"
                   from_work_dir="SJ.out.tab">
          <actions>
             <conditional name="refGenomeSource.genomeSource">
             <when value="indexed">
               <action type="metadata" name="dbkey">
                <option type="from_data_table" name="rnastar_index" column="1" offset="0">
                 <filter type="param_value" column="0" value="#" compare="startswith" keep="False"/>
                  <filter type="param_value" ref="refGenomeSource.index" column="0"/>
                </option>
               </action>
             </when>
             <when value="history">
               <action type="metadata" name="dbkey">
                 <option type="from_param" name="refGenomeSource.ownFile" param_attribute="dbkey" />
               </action>
             </when>
             </conditional>
          </actions>
        </data>
        <data format="bam" name="mapped_reads" label="${jobName}_starmapped.bam"
                    from_work_dir="AlignedSorted.bam">
          <actions>
             <conditional name="refGenomeSource.genomeSource">
             <when value="indexed">
               <action type="metadata" name="dbkey">
                <option type="from_data_table" name="rnastar_index" column="1" offset="0">
                 <filter type="param_value" column="0" value="#" compare="startswith" keep="False"/>
                  <filter type="param_value" ref="refGenomeSource.index" column="0"/>
                </option>
               </action>
             </when>
             <when value="history">
               <action type="metadata" name="dbkey">
                 <option type="from_param" name="refGenomeSource.ownFile" param_attribute="dbkey" />
               </action>
             </when>
             </conditional>
          </actions>
        </data>
    </outputs>
    <tests>
        <test>
 <param name='input1' value='tophat_in2.fastqsanger' ftype='fastqsanger' />
 <param name='jobName' value='rnastar_test' />
 <param name='genomeSource' value='history' />
 <param name='ownFile' value='tophat_test.fa' />
 <param name='sPaired' value='single' />
 <param name='outSAMattributes' value='--outSAMattributes All' />
 <param name='outSAMstrandField' value='--outSAMstrandField intronMotif' />
 <param name='outFilterIntronMotifs' value='--outFilterIntronMotifs RemoveNoncanonical' />
 <output name='output_log' file='rnastar_test.log' compare='diff' lines_diff = '10'/>
 <output name='splice_junctions' file="rnastar_test_splicejunctions.bed" compare="sim_size" delta="200"/>
 <output name='mapped_reads' file="rnastar_test_mapped_reads.bam" compare="sim_size" delta="200" />
        </test>
    </tests>
<help>

**What it does**
Runs the rna star gapped aligner. Suited to paired or single end rna-seq.

8.2: SAM alignments

The number of loci Nmap a read maps to (multi-mapping) is given by NH:i: field.
The mapping quality MAPQ (column 5) is 255 for uniquely mapping reads, and int(-10*log10(1-1/Nmap)) for
multi-mapping reads. This scheme is same as the one used by Tophat and is compatible with Cufflinks.

For multi-mappers, all alignments except one are marked with 0x100 (secondary alignment) in the FLAG
column 2. The un-marked alignment is either the best one (i.e. highest scoring), or is randomly selected from
the alignments of equal quality.

8.2.1: Standard SAM attributes
With default --outSAMattributes Standard option the following SAM attributes will be generated:

Column 12: NH: number of loci a read (pair) maps to
Column 13: IH: alignment index for all alignments of a read
Column 14: aS: alignment score
Column 15: nM: number of mismatches (does not include indels)

8.2.2: Extra SAM attrbiutes
If --outSAMattributes All option is used, the following additional attributes will be output:

Column 16: jM:B:c,M1,M2,... Intron motifs for all junctions (i.e. N in CIGAR):
0: non-canonical; 1:GT/AG, 2: CT/AC, 3: GC/AG, 4: CT/GC, 5: AT/AC, 6: GT/AT.

If splice junctions database is used, and a junction is annotated, 20 is added to its motif value.
Column 17: jI:B:I,Start1,End1,Start2,End2,... Start and End of introns for all junctions (1-based)

Note, that samtools 0.1.18 or later have to be used with these extra attributes.


8.2.3: XS SAM strand attribute for Cufflinks/Cuffdiff

If you have un-stranded RNA-seq data, and wish to run Cufflinks/Cuffdiff on STAR alignments, you will
need to run STAR with --outSAMstrandField intronMotif option, which will generate the XS
strand attribute for all alignments that contain splice junctions. The spliced alignments that have undefined
strand (i.e. containing only non-canonical junctions) will be suppressed.

If you have stranded RNA-seq data, you do not need to use any specific STAR options. Instead, you need
to run Cufflinks with the library option --library-type options. For example, cufflinks with
library-type fr-firststrand should be used for the b

It is recommended to remove the non-canonical junctions for Cufflinks runs using b


--outFilterIntronMotifs RemoveNoncanonical
filter out alignments that contain non-canonical junctions

OR

--outFilterIntronMotifs RemoveNoncanonicalUnannotated
filter out alignments that contain non-canonical unannotated junctions
when using annotated splice junctions database. The annotated non-
canonical junctions will be kept.


**Attributions**

Note that each component has its own license. Good luck with figuring out your obligations.

rna_star - see the web site at rna_star_

For details, please see the rna_starMS_
"STAR: ultrafast universal RNA-seq aligner"
A. Dobin et al, Bioinformatics 2012; doi: 10.1093/bioinformatics/bts635

Galaxy_ (that's what you are using right now!) for gluing everything together

Most of the work for this wrapper XML is Jeremy Goecks' original STAR_ wrapper

Minor tweaks to output names to suit our downstream purposes, toolshed automated dependencies
and odds and ends of other code and documentation comprising this tool was
written by Ross Lazarus and that part is licensed_ the same way as other rgenetics artefacts

.. _STAR: https://bitbucket.org/jgoecks/jeremys-code/raw/fa1930a689b8e2f6b59cc1706e5ba0ed8ad357be/galaxy/tool-wrappers/star.xml
.. _licensed: http://creativecommons.org/licenses/by-nc-nd/3.0/
.. _rna_star: http://code.google.com/p/rna-star/
.. _rna_starMS: http://bioinformatics.oxfordjournals.org/content/29/1/15.full
.. _Galaxy: http://getgalaxy.org

</help>
<citations>
    <citation type="doi">doi: 10.1093/bioinformatics/bts635</citation>
</citations>
</tool>