annotate snpSift_vartype.xml @ 4:b04635ebfab0 draft

planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tool_collections/snpsift/snpsift commit 9d2052269bfbca81a5f9cd10c3153e611358a329

<tool id="snpsift_vartype" name="SnpSift Variant Type" version="@WRAPPER_VERSION@.1">
    <description>Annotate with variant type</description>
    <macros>
        <import>snpSift_macros.xml</import>
    </macros>
    <expand macro="requirements" />
    <expand macro="stdio" />
    <expand macro="version_command" />
    <command><![CDATA[
SnpSift varType
'$input'
2> '$log'
> '$output'
    ]]></command>
    <inputs>
        <param name="input" type="data" format="vcf" label="Variant file (VCF)"/>
    </inputs>
    <outputs>
        <data name="output" format="vcf" label="${tool.name} on ${on_string}: VCF" />
        <data name="log" format="txt" label="${tool.name} on ${on_string}: log" />
    </outputs>
    <tests>
    </tests>
    <help><![CDATA[
**What it does**

This tool uses `SnpSift Variant type`_ to add the variant type (SNP/MNP/INS/DEL/MIXED) in the INFO field. It also adds "HOM/HET", but this last one works if there is only one sample (otherwise it doesn't make any sense).

.. _SnpSift Variant type: http://snpeff.sourceforge.net/SnpSift.html#VariantType

------

**License**

This Galaxy tool is Copyright © 2013-2014 `CRS4 Srl.`_ and is released under the `MIT license`_.

.. _CRS4 Srl.: http://www.crs4.it/
.. _MIT license: https://opensource.org/licenses/MIT
    ]]></help>
    <expand macro="citations" />
</tool>