<tool id="nanopolish_methylation" name="Nanopolish methylation" version="0.1.0">
    <description>- Classify nucleotides as methylated or not.</description>
    <macros>
        <import>macros.xml</import>
    </macros>
    <expand macro="requirements" />
    <command detect_errors="exit_code"><![CDATA[
        ln -s '$input_merged' reads.fasta && 
        
        #if $input_reads_raw.extension == 'fast5':
            mkdir fast5_files && ln -s '$input_reads_raw' fast5_files/read1.fast5 &&
        #else
            ln -s '$input_reads_raw' fast5_files.tar.gz &&
            mkdir fast5_files && tar -xzf fast5_files.tar.gz -C fast5_files &&
        #end if

        nanopolish index -d fast5_files/ reads.fasta &&
        ln -s '$b' reads.bam &&
        ln -s '${b.metadata.bam_index}' reads.bam.bai &&
        ln -s '$g' genome.fa &&
        
        nanopolish call-methylation
        -r reads.fasta
        -b reads.bam
        -g genome.fa
        #if $w and str($w).strip():
          -w "${w}"
        #end if  
        > methylation_calls.tsv
    ]]></command>
    <inputs>
      <!-- index inputs -->
        <param type="data" name="input_merged" format="fasta,fastq" label="Basecalled merged reads.fa"/>
        <param type="data" name="input_reads_raw" format="h5,fast5.tar.gz" label="Flat archive file of raw fast5 files"/>

        <!-- variants consensus inputs -->
        <param type="data" argument="-b" format="bam" label="Reads aligned to the reference genome" />
        <param type="data" argument="-g" format="fasta" label="The reference genome"/>

        <param argument="-w" type="text" optional="true"
            label="find variants in window of region chromsome:start-end" />

    </inputs>

    <outputs>
      <!-- variants consensus outputs -->
        <data name="output_methylation_calls" format="tabular" from_work_dir="methylation_calls.tsv" label="called methylation sites" />
    </outputs>
    <tests>
        <test>
      <!-- index test -->
            <param name="input_merged" ftype="fasta" value="reads.fasta" />
            <param name="input_reads_raw" ftype="fast5.tar.gz" value="fast5_files.tar.gz" />
            
      <!-- variants consensus test -->
            <param name="b" value="reads.sorted.bam" />
            <param name="g" value="draft.fa" />
            <param name="w" value="tig00000001:200000-202000" />
            
            <output name="output_methylation_calls" file="methylation_calls.tsv" />
        </test>
    </tests>
    <help><![CDATA[
        Usage: nanopolish call-methylation [OPTIONS] --reads reads.fa --bam alignments.bam --genome genome.fa
        Classify nucleotides as methylated or not.
        
        Quickstart tutorial and manual available at:
        http://nanopolish.readthedocs.io/en/latest/quickstart_call_methylation.html

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