view samtools_rmdup.xml @ 4:9129584416e2 draft

planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tool_collections/samtools/samtools_rmdup commit 411130b45dc30f7f24f41cdeec5e148c5d8faf40
author iuc
date Tue, 09 May 2017 11:18:58 -0400
parents bb40e4252392
children
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<tool id="samtools_rmdup" name="RmDup" version="2.0.1">
    <description>remove PCR duplicates</description>
    <macros>
        <import>macros.xml</import>
    </macros>

    <expand macro="requirements" />
    <expand macro="stdio"/>
    <expand macro="version_command"/>

    <command><![CDATA[
    samtools rmdup
        #if str( $bam_paired_end_type.bam_paired_end_type_selector ) == "PE"
            ${bam_paired_end_type.force_se}
        #else:
            -s
        #end if
        '$input1'
        '$output1'
    ]]></command>

    <inputs>
        <param name="input1" type="data" format="bam" label="BAM File" />

        <conditional name="bam_paired_end_type">
            <param name="bam_paired_end_type_selector" type="select" label="Is this paired-end or single end data">
                <option value="PE" selected="True">BAM is paired-end</option>
                <option value="SE">BAM is single-end (-s)</option>
            </param>
            <when value="PE">
                <param name="force_se" argument="-S" type="boolean" truevalue="-S" falsevalue="" checked="False" label="Treat as single-end"/>
            </when>
            <when value="SE" /> <!-- No extra parameters here -->
        </conditional>
    </inputs>

    <outputs>
        <data name="output1" format="bam" />
    </outputs>

    <tests>
        <test>
            <param name="input1" value="samtools-rmdup-input1.bam" ftype="bam" />
            <param name="bam_paired_end_type_selector" value="PE" />
            <param name="force_se" />

            <output name="output1" file="samtools-rmdup-test1.bam" ftype="bam" sort="True" />
        </test>
    </tests>
    <help>
**What it does**

Remove potential PCR duplicates: if multiple read pairs have identical external coordinates, only retain the pair with highest mapping quality. In the paired-end mode, this command ONLY works with FR orientation and requires ISIZE is correctly set. It does not work for unpaired reads (e.g. two ends mapped to different chromosomes or orphan reads).
    </help>
    <expand macro="citations"/>
</tool>