<tool id="stringtie_merge" name="StringTie merge" version="@TOOL_VERSION@+galaxy@VERSION_SUFFIX@">
    <description>transcripts</description>
    <macros>
        <import>macros.xml</import>
    </macros>
    <xrefs>
        <xref type="bio.tools">stringtie</xref>
    </xrefs>
    <expand macro="requirements" />
    <expand macro="stdio" />
    <expand macro="version_command" />
    <command><![CDATA[
        stringtie --merge
        -p \${GALAXY_SLOTS:-1}
        #if $guide_gff:
            -G '$guide_gff'
        #end if
        -m $min_len
        -c $min_cov
        -F $min_fpkm
        -T $min_tpm
        -f $min_iso
        -g $gap_len
        $keep_introns
        #set inputs = "' '".join(str($input_gtf).split(','))
        -o '$out_gtf' '$inputs'
    ]]></command>
    <inputs>
        <param name="input_gtf" type="data" format="gtf,gff3" multiple="true" label="Transcripts" help="In GTF or GFF3 format"/>
        <param name="guide_gff" argument="-G" type="data" format="gtf,gff3" optional="true" label="Reference annotation to include in the merging"/>
        <param name="min_len" argument="-m" type="integer" min="0" value="50" label="Minimum input transcript length to include in the merge"/>
        <param name="min_cov" argument="-c" type="integer" min="0" value="0" label="Minimum input transcript coverage to include in the merge"/>
        <param name="min_fpkm" argument="-F" type="float" min="0" value="1" label="Minimum input transcript FPKM to include in the merge"/>
        <param name="min_tpm" argument="-T" type="float" min="0" value="1" label="Minimum input transcript TPM to include in the merge"/>
        <param name="min_iso" argument="-f" type="float" value="0.01" label="Minimum isoform fraction"/>
        <param name="gap_len" argument="-g" type="integer" value="250" label="Gap between transcripts to merge together"/>
        <param name="keep_introns" argument="-i" type="boolean" truevalue="-i" falsevalue="" checked="false" label="Keep merged transcripts with retained introns" help="By default these are not kept unless there is strong evidence for them"/>
    </inputs>
    <outputs>
        <data name="out_gtf" format="gtf"/>
    </outputs>
    <tests>
        <test>
            <param name="input_gtf" ftype="gtf" value="stringtie_out1.gtf,stringtie_out2.gtf,stringtie_out3.gtf,stringtie_out4.gtf"/>
            <param name="guide_gff" ftype="gtf" value="stringtie_in.gtf"/>
            <output name="out_gtf" file="stringtie_merge_out1.gtf" ftype="gtf" lines_diff="2"/>
        </test>
        <test>
            <param name="input_gtf" ftype="gtf" value="stringtie_merge_in1.gtf,stringtie_merge_in2.gtf"/>
            <param name="guide_gff" ftype="gtf" value="stringtie_merge_in3.gtf" />
            <output name="out_gtf" file="stringtie_merge_out2.gtf" ftype="gtf" lines_diff="4"/>
        </test>
        <test>
            <param name="input_gtf" ftype="gtf" value="stringtie_merge_in1.gtf,stringtie_merge_in2.gtf"/>
            <output name="out_gtf" ftype="gtf">
                <assert_contents>
                    <has_text text="stringtie --merge"/>
                </assert_contents>
            </output>
        </test>
    </tests>
    <help><![CDATA[
**What it does?**

This is a special usage mode of StringTie_, distinct from the assembly usage mode. In the merge mode, StringTie takes as input a list of GTF/GFF files and merges/assembles these transcripts into a non-redundant set of transcripts. This mode is used in the new differential analysis pipeline to generate a global, unified set of transcripts (isoforms) across multiple RNA-Seq samples.

If a reference annotation is provided, StringTie will assemble the transfrags from the input GTF files with the reference transcripts.

.. _StringTie: http://ccb.jhu.edu/software/stringtie/
    ]]></help>
    <expand macro="citations" />
</tool>