comparison artic_guppyplex.xml @ 0:7a82006f7c05 draft

"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/artic commit dacdfa7ecfbdd1c1a12494cf7d0450185c122c84"

0:7a82006f7c05

<tool id="artic_guppyplex" name="ARTIC guppyplex" version="@PACKAGE_VERSION@+galaxy0" profile="20.09">
    <description>Filter Nanopore reads by read length and (optionally) quality</description>
    <macros>
        <import>macros.xml</import>
    </macros>
    <requirements>
        <requirement type="package" version="@PACKAGE_VERSION@">artic</requirement>
    </requirements>
    <command detect_errors="exit_code">
    <![CDATA[
        mkdir inputs &&
        #for $i, $elem in enumerate($input)
            ln -fs '$elem' inputs/fastq${i}.fastq &&
        #end for
        artic guppyplex --min-length $min_length --max-length $max_length
            --directory inputs/
            --prefix artic_guppyplex --output '$output1'
    ]]>
    </command>
    <inputs>
        <param name="input" multiple="true" type="data" format="fastq" label="Nanopore reads (FASTQ format" />
        <param name="max_length" type="integer" label="Remove reads longer than" value="700" help="remove reads greater than this number of base pairs" />
        <param name="min_length" type="integer" label="Remove reads shorter than" value="400" help="remove reads less than this number of base pairs" />
        <param name="skip_quality_check" argument="--skip-quality-check" type="boolean" truevalue="--skip-quality-check" falsevalue="" checked="False" label="Do not filter on quality score (speeds up processing)" />
    </inputs>
    <outputs>
        <data name="output1" format="fastq" from_work_dir="run_name_.fastq" />
    </outputs>
    <tests>
        <test>
            <param name="input" value="test.fastq" />
            <output name="output1" file="gupplyplex_output.fastq"/>
        </test>
    </tests>
    <help><![CDATA[
        The ARTIC_ guppyplex tool filters reads by length and (optionally) quality.
        This filter is typically used as a pre-processing step in the processing
        of amplicon sequencing Nanopore reads, where a size-based filter can
        be used to remove possibly-chimeric reads.
        
        The default paramters of the tool (minimum length of 400 and maximum of 700)
        are based on the ARTIC amplicon scheme. If used with a different amplicon
        scheme they should be adjusted to use the minimum length of an amplicon as
        the minimum length and the maximum length of an amplicon plus 200 as the
        maximum length.

        .. _ARTIC: https://artic.readthedocs.io/en/latest/
    ]]></help>
    <expand macro="citations" />
</tool>