<tool id="mismatch_frequencies" name="Mismatch Frequencies" version="0.0.3" hidden="false" >
	<description>Analyze mismatch frequencies in BAM/SAM alignments</description>
        <requirements>
    	    <requirement type="package" version="0.7.7">pysam</requirement>
    	    <requirement type="package" version="0.14">pandas</requirement>
    	    <requirement type="package" version="1.4">matplotlib</requirement>
        </requirements>
	<command interpreter="python">mismatch_frequencies.py --input 
		#for i in $rep
			"$i.input_file" 
		#end for
		--name 
		#for i in $rep
			"$i.input_file.name"
		#end for
		 --output_pdf $output_pdf --output_tab $output_tab --min $min_length --max $max_length
                 --n_mm $number_of_mismatches
                 --five_p $five_p
                 --three_p $three_p
        </command>
	<inputs>
            <repeat name="rep" title="alignment files">
        	<param name="input_file" type="data" format="bam,sam" label="Alignment file" help="The input alignment file(s) for which to analyze the mismatches."/>
            </repeat>
          <param name="number_of_mismatches" label="Maximum number of allowed mismatches per read" help="Discard reads with more than the chosen number of mismatches from the frequency calculation" type="integer" value="3"/>
          <param name="min_length" label="Minumum read length to analyse" type="integer" value="21"/>
	  <param name="max_length" label="Maximum read length to analyse" type="integer" value="21"/>
	  <param name="five_p" label="Ignore mismatches in the first N nucleotides of a read" type="integer" value="0"/>
	  <param name="three_p" label="Ignore mismatches in the last N nucleotides of a read" help="useful to discriminate between tailing events and editing events" type="integer" value="3"/>
	</inputs>
        <outputs>
                <data format="pdf" name="output_pdf" />
                <data format="tabular" name="output_tab" />
        </outputs>

</tool>