view correctGCBias.xml @ 31:7889d260cc37 draft default tip

planemo upload for repository https://github.com/fidelram/deepTools/tree/master/galaxy/wrapper/ commit 3bc1d1c6f4e28ac7ff8df79fe4e3f00a195938e6-dirty

<tool id="deeptools_correctGCBias" name="correctGCBias" version="@WRAPPER_VERSION@.0">
    <description>uses the output from computeGCBias to generate corrected BAM files</description>
    <macros>
        <token name="@BINARY@">correctGCBias</token>
        <import>deepTools_macros.xml</import>
    </macros>
    <expand macro="requirements" />
    <command>
<![CDATA[
        ln -s $bamInput local_bamInput.bam;
        ln -s $bamInput.metadata.bam_index local_bamInput.bam.bai;

        correctGCBias
            @THREADS@
            --bamfile local_bamInput.bam
            --GCbiasFrequenciesFile $GCbiasFrequenciesFile

            @reference_genome_source@

            #if $effectiveGenomeSize.effectiveGenomeSize_opt == "specific":
                --effectiveGenomeSize $effectiveGenomeSize.effectiveGenomeSize
            #else:
                --effectiveGenomeSize $effectiveGenomeSize.effectiveGenomeSize_opt
            #end if

            #if str($region).strip() != '':
                --region '$region'
            #end if
            --correctedFile corrected.bam;

        mv corrected.bam $outFileName;
]]>
    </command>
    <inputs>
        <param name="GCbiasFrequenciesFile" type="data" format="tabular" label="Output of computeGCBias" />
        <param name="bamInput" format="bam" type="data"
            label="BAM file" help="This should be same file that was used for computeGCbias. The BAM file must be sorted. (--bamfile)" />
        <expand macro="reference_genome_source" />
        <expand macro="effectiveGenomeSize" />
        <expand macro="region_limit_operation" />
    </inputs>
    <outputs>
        <data format="bam" name="outFileName" />
    </outputs>
    <tests>
        <test>
            <param name="GCbiasFrequenciesFile" value="computeGCBias_result1.tabular" ftype="tabular" />
            <param name="bamInput" value="paired_chr2L.bam" ftype="bam" />
            <param name="ref_source" value="history" />
            <param name="input1" value="sequence.2bit" />
            <param name="effectiveGenomeSize_opt" value="specific" />
            <param name="effectiveGenomeSize" value="23011544" />
            <output name="outFileName" file="correctGCBias_result1.bam" ftype="bam" />
        </test>
    </tests>
    <help>
<![CDATA[
**What it does**

This tool requires the output from computeGCBias to correct a given BAM file according to the method proposed by
Benjamini and Speed (2012) Nucleic Acids Res.
The resulting BAM file can be used in any downstream analyses, but be aware that you should not filter out duplicates from here on.

You can find more details on the correctGCBias wiki page: https://github.com/fidelram/deepTools/wiki/QC#wiki-correctGCbias


**Output files**:

- GC-normalized BAM file

-----

@REFERENCES@
]]>
    </help>
    <expand macro="citations" />
</tool>