view gemini_de_novo.xml @ 2:4aabe53ecfe0 draft

planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/gemini commit 11ee7ac206d41894c0b6a11f2439aaea490824f0
author iuc
date Thu, 09 Nov 2017 13:15:51 -0500
parents 285f519dab87
children 9db3e299b1c8
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<tool id="gemini_@BINARY@" name="GEMINI @BINARY@" version="@VERSION@.0">
    <description>Identifying potential de novo mutations</description>
    <macros>
        <import>gemini_macros.xml</import>
        <token name="@BINARY@">de_novo</token>
    </macros>
    <expand macro="requirements" />
    <expand macro="stdio" />
    <expand macro="version_command" />
    <command>
<![CDATA[
        gemini @BINARY@

            @COLUMN_SELECT@

            @CMDLN_SQL_FILTER_FILTER_OPTION@

            #if int($min_kindreds) > 0:
                --min-kindreds $min_kindreds
            #end if

            #if str($families).strip():
                --families "$families"
            #end if

            $lenient
            $allow_unaffected


            -d $d

            #if int($min_gq) > 0:
                --min-gq $min_gq
            #end if

            #if int($gt_pl_max) > -1:
                --gt-pl-max $gt_pl_max
            #end if


            "${ infile }"
            > "${ outfile }"
]]>
    </command>
    <inputs>
        <expand macro="infile" />
        <expand macro="column_filter" />
        <expand macro="filter" />
        <expand macro="min_kindreds" />
        <expand macro="family" />
        <expand macro="lenient" />
        <expand macro="unaffected" />
        <expand macro="min_sequence_depth" />
        <expand macro="min_gq" />
        <expand macro="gt_pl_max" />
    </inputs>
    <outputs>
        <data name="outfile" format="tabular" />
    </outputs>
    <tests>
        <test>
            <param name="infile" value="gemini_de_novo_input.db" ftype="gemini.sqlite" />
            <param name="columns" value="gene,ref,alt,impact" />
            <output name="outfile" file="gemini_de_novo_result.tabular" />
        </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.

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