view gemini_de_novo.xml @ 1:d3c4d0208bb2 draft

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<tool id="gemini_@BINARY@" name="GEMINI @BINARY@" version="@VERSION@.0">
    <description>Identifying potential de novo mutations</description>
    <expand macro="requirements" />
    <expand macro="version_command" />
    <macros>
        <import>gemini_macros.xml</import>
        <token name="@BINARY@">de_novo</token>
    </macros>
    <command>
<![CDATA[
        gemini @BINARY@

            #if $report.report_selector != 'all':
                --columns "${report.columns}"
            #end if

            #if $filter.filter_selector == 'yes':
                --filter "${filter.filter}"
            #end if
            -d $d
            "${ infile }"
            > "${ outfile }"
]]>
    </command>
    <expand macro="stdio" />
    <inputs>
        <param name="infile" type="data" format="sqlite" label="GEMINI database" />

        <expand macro="column_filter" />
        <expand macro="filter" />
        <expand macro="min_sequence_depth" />
    </inputs>
    <outputs>
        <data name="outfile" format="tabular" label="${tool.name} on ${on_string}" />
    </outputs>
    <tests>
        <test>
        </test>
    </tests>
    <help>
**What it does**

Assuming you have defined the familial relationships between samples when loading your VCF into GEMINI, 
you can use this tool for identifying de novo (a.k.a spontaneous) mutations that arise in offspring.

@CITATION@
    </help>
    <expand macro="citations"/>
</tool>