Mercurial > repos > mvdbeek > mismatch_frequencies
diff mismatch_frequencies.xml @ 19:f7da7f3e2c98
planemo upload for repository https://bitbucket.org/drosofff/gedtools/
author | mvdbeek |
---|---|
date | Sun, 24 May 2015 11:12:24 -0400 |
parents | e3d950e52e38 |
children | 11a1dae1ab8e |
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--- a/mismatch_frequencies.xml Mon May 11 07:45:10 2015 -0400 +++ b/mismatch_frequencies.xml Sun May 24 11:12:24 2015 -0400 @@ -1,4 +1,4 @@ -<tool id="mismatch_frequencies" name="Mismatch Frequencies" version="0.0.7" hidden="false" > +<tool id="mismatch_frequencies" name="Mismatch Frequencies" version="0.0.8" hidden="false" > <description>Analyze mismatch frequencies in BAM/SAM alignments</description> <requirements> <requirement type="package" version="0.7.7">pysam</requirement> @@ -17,19 +17,31 @@ --n_mm $number_of_mismatches --five_p $five_p --three_p $three_p + --expanded_output_tab $expanded_tab + --possible_mismatches $possible_mismatches </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="possible_mismatches" label="Specify mismatches that should be counted" help="Ignores mismatches that are not listed" type="text" value="AC AG AT CA CG CT GA GC GT TA TC TG"> + <validator type="expression" message="Allowed values are AGCTN, seperated by space.">len([False for char in value if not char in " AGCTN"]) == 0</validator> + </param> <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"/> + <param help="Output expanded tabular format" label="Nucleotide mismatches per reference sequence" name="expanded" type="select"> + <option select="true" value="false">No</option> + <option value="expanded">Yes</option> + </param> </inputs> <outputs> <data format="tabular" name="output_tab" /> + <data format="fasta" name="expanded_tab"> + <filter> expanded == "expanded"</filter> + </data> <data format="pdf" name="output_pdf" /> </outputs> <tests> @@ -72,4 +84,6 @@ Written by Marius van den Beek, m.vandenbeek at gmail . com </help> + <citations> + </citations> </tool>