<tool id="tb_profiler_profile" name="TB-Profiler Profile" version="2.1.0">
    <description>Infer strain types and drug resistance markers from sequences</description>	
    <requirements>
        <requirement type="package" version="2.1.0">tb-profiler</requirement>
    </requirements>
    <command detect_errors="exit_code"><![CDATA[
        #if str($fastq_or_bam.input_select.value) in ("paired_fastq", "paired_collection_fastq", "single_fastq")
            #if str($fastq_or_bam.input_select.value) == "paired_fastq"
                #set r1_ext = $fastq_or_bam.read1.extension
                #set r2_ext = $fastq_or_bam.read2.extension
                ln -s '$fastq_or_bam.read1' fastq_r1.'$r1_ext' &&
                ln -s '$fastq_or_bam.read2' fastq_r2.'$r2_ext' &&
            #else if str($fastq_or_bam.input_select.value) == "single_fastq"
                #set r1_ext = $fastq_or_bam.fastq.extension
                ln -s '$fastq_or_bam.fastq' fastq_r1.'$r1_ext' &&
            #else if str($fastq_or_bam.input_select.value) == "paired_collection_fastq"
                #set r1_ext = $fastq_or_bam.fastq_collection.forward.extension
                #set r2_ext = $fastq_or_bam.fastq_collection.reverse.extension
                ln -s '$fastq_or_bam.fastq_collection.forward' fastq_r1.'$r1_ext' &&
                ln -s '$fastq_or_bam.fastq_collection.reverse' fastq_r2.'$r2_ext' &&
            #end if
        #else if str($fastq_or_bam.input_select.value) == "bam"
            ln -s '$fastq_or_bam.bam_input' input.bam &&
        #end if

        tb-profiler profile
            
            --platform '${platform.value}'

        #if str($fastq_or_bam.input_select.value) in ("paired_fastq", "paired_collection_fastq", "single_fastq")
            -1 fastq_r1.'$r1_ext'
        #end if
        #if str($fastq_or_bam.input_select.value) in ("paired_fastq", "paired_collection_fastq")
            -2 fastq_r2.'$r1_ext'
        #else if str($fastq_or_bam.input_select.value) == "bam"
            --bam input.bam
        #end if

            --threads "\${GALAXY_SLOTS:-1}"
        #if $advanced.options == 'yes'
            --call_method '${advanced.call_method}'
            --min_gene_frac '${advanced.min_gene_frac}'
            --mapper '${advanced.mapper}'
            --min_depth '${advanced.min_depth}'
        #end if

        #if $output_format == "pdf"
            --pdf
        #else if $output_format == "txt"
            --txt
        #end if
        && mv results/tbprofiler.results.json $results_json
        #if str($fastq_or_bam.input_select) != "bam"
            && mv bam/tbprofiler.bam '${output_bam}'
        #end if
        && bcftools view -Ov -o'${output_vcf}' vcf/tbprofiler.targets.csq.bcf
        #if $output_format == "pdf"
            && mv results/tbprofiler.results.pdf '${output_pdf}'
        #else if $output_format == "txt"
            && mv results/tbprofiler.results.txt '${output_txt}'
        #end if 

    ]]></command>
    <inputs>
        <param name="platform" type="select" label="Platform">
            <option value="Illumina" selected="true">Illumina</option>
            <option value="minION">MinION</option>
        </param>
        <conditional name="fastq_or_bam">
            <param name="input_select" type="select" label="Input File Type">
                <option value="paired_fastq">Paired Fastq</option>
                <option value="paired_collection_fastq">Paired Collection Fastq</option>
                <option value="single_fastq">Single Fastq</option>
                <option value="bam">BAM</option>
            </param>
            <when value="paired_fastq">
                <param name="read1" type="data" format="fastq" label="Read1" help="First read file (default: None)"/>
                <param name="read2" type="data" format="fastq" optional="true" label="Read2" help="Second read file (default: None)"/>
            </when>
            <when value="paired_collection_fastq">
                <param label="Reads (collection)" name="fastq_collection" type="data_collection" collection_type="paired" format="fastq,fastq.gz,fastqsanger,fastqsanger.gz" />
            </when>
            <when value="single_fastq">
                <param label="Reads" name="fastq" type="data" format="fastq,fastq.gz,fastqsanger,fastqsanger.gz" />
            </when>            
            <when value="bam">
                <param name="bam_input" type="data" format="bam" label="Bam" help="Warning!!!: The BAM files must have been created using the ensembl version of the genome."/>
            </when>
        </conditional>
        <param name="output_format" label="Output format" type="select">
            <option value="txt">Text</option>
            <option value="pdf">PDF</option>
        </param>
        <conditional name="advanced">
            <param label="Select advanced options" type="select" name="options">
                <option value="yes">Yes</option>
                <option value="no" selected="true">No</option>
            </param>
            <when value="no">
            </when>
            <when value="yes">
                <param label="Quality required for calls to be accepted" type="select" argument="--call_method">
                    <option value="low" selected="true">Low</option>
                    <option value="high">High</option>
                    <option value="optimise">Optimise</option>
                </param>
                <param label="Minimum coverage fraction to infer deletion" type="float"
                        help="Used to infer a deletion if the fraction of a gene covered falls below this value."
                        argument="--min_gene_frac" value="0.9" />

                <param name="min_depth" label="Min Depth" type="integer" value="10" help="Minimum depth required to call variant. Bases with depth below this cutoff will be marked as missing (default: 10)"/>
                <param name="mapper" label="Mapper" type="select" help="Mapping tools to use (default: bwa)">
                    <option value="bwa" selected="true">bwa</option>
                    <option value="minimap2">minimap2</option>
                    <option value="bowtie2">bowtie2</option>
                </param>
                <param name="min_gene_frac" label="Minimum Gene Fraction" type="float" value="0.9" help="Used to infer a deletion if the fraction of a gene covered falls below this value. Also used to see if sample is high quality to continue by checking the fraction for rpoB (where deletion should not occur). (default: 0.9)" />
            </when>
        </conditional>
    </inputs>
    <outputs>
        <data name="results_json" format="json" from_work_dir="results/tbprofiler.results.json" label="${tool.name} on ${on_string}: Results.json"/>
        <data format="vcf" name="output_vcf" label="${tool.name} VCF on ${on_string}" />
        <data format="bam" name="output_bam" label="${tool.name} BAM on ${on_string}">
            <filter>fastq_or_bam['input_select'] != 'bam'</filter>
        </data>
        <data format="pdf" name="output_pdf" label="${tool.name} PDF report on ${on_string}">
            <filter>output_format == 'pdf'</filter>
        </data>
        <data format="txt" name="output_txt" label="${tool.name} report on ${on_string}">
            <filter>output_format == 'txt'</filter>
        </data>

    </outputs>
    <tests>
        <test>
            <param name="input_select" value="single_fastq"/>
            <param name="fastq" ftype="fastq.gz" value="rif_resistant.fastq.gz" />
            <param name="output_format" value="txt" />
            <param name="platform" value="Illumina" />
            <param name="options" value="no" />
            <output name="output_txt">
                <assert_contents>
                    <has_line line="Drug-resistance: Drug-resistant" />
		    <has_line line="lineage2.2.2&#009;1.000&#009;East-Asian (Beijing)&#009;Beijing-RD105/RD207&#009;RD105;RD207" />
                    <has_line line="rifampicin&#009;R&#009;rpoB p.Asp435Val (1.00)" />
                    <has_line line="763031&#009;Rv0667&#009;c.3225T>C&#009;1.000" />
                </assert_contents>
            </output>
        </test>
        <test>
            <param name="input_select" value="bam"/>
            <param name="bam_input" ftype="bam" value="rif_resistant.bam" />
            <param name="output_format" value="txt" />
            <param name="platform" value="Illumina" />
            <param name="options" value="no" />
            <output name="output_txt">
                <assert_contents>
                    <has_line line="Drug-resistance: Drug-resistant" />
		    <has_line line="lineage2.2.2&#009;1.000&#009;East-Asian (Beijing)&#009;Beijing-RD105/RD207&#009;RD105;RD207" />
                    <has_line line="rifampicin&#009;R&#009;rpoB p.Asp435Val (1.00)" />
                    <has_line line="763031&#009;Rv0667&#009;c.3225T>C&#009;1.000" />
                </assert_contents>
            </output>
        </test>
    </tests>
    <help><![CDATA[    
Summary
=======

The pipeline aligns reads to the H37Rv reference using bowtie2, BWA or minimap2 and then calls variants using SAMtools. These variants are then compared to a drug-resistance database. We also predict the number of reads supporting drug resistance variants as an insight into hetero-resistance (not applicable for minION data).

Produces a JSON output file by default.

    ]]></help>
    <citations>
        <citation type="bibtex">
@UNPUBLISHED{Phelan2016,
    author = {Phelan, Jody},
    title = {TBProfiler},
    year = {2016},
    url = {https://github.com/jodyphelan/TBProfiler},
}
        </citation>
    </citations>
</tool>