Mercurial > repos > mheinzl > variant_analyzer2
diff read2mut.xml @ 27:5992e30ae50e draft
planemo upload for repository https://github.com/Single-Molecule-Genetics/VariantAnalyzerGalaxy/tree/master/tools/variant_analyzer commit ee4a8e6cf290e6c8a4d55f9cd2839d60ab3b11c8
author | mheinzl |
---|---|
date | Mon, 22 Feb 2021 16:56:05 +0000 |
parents | cf6f0fb05bad |
children | afda74e874ac |
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--- a/read2mut.xml Mon Feb 22 16:48:12 2021 +0000 +++ b/read2mut.xml Mon Feb 22 16:56:05 2021 +0000 @@ -1,5 +1,5 @@ <?xml version="1.0" encoding="UTF-8"?> -<tool id="read2mut" name="Call specific mutations in reads:" version="2.0.4" profile="17.01"> +<tool id="read2mut" name="Call specific mutations in reads:" version="2.0.1" profile="19.01"> <description>Looks for reads with mutation at known positions and calculates frequencies and stats.</description> <macros> <import>va_macros.xml</import> @@ -17,11 +17,9 @@ --sscsJson '$file4' --thresh '$thresh' --phred '$phred' - --trim5 '$trim5' - --trim3 '$trim3' + --trim '$trim' $chimera_correction --outputFile '$output_xlsx' - --outputFile_csv '$outputFile_csv' --outputFile2 '$output_xlsx2' --outputFile3 '$output_xlsx3' ]]> @@ -33,13 +31,11 @@ <param name="file4" type="data" format="json" label="JSON File with SSCS tag stats" optional="false" help="JSON file generated by DCS mutations to SSCS stats."/> <param name="thresh" type="integer" label="Tag count threshold" value="0" help="Integer threshold for displaying mutations. Only mutations occuring in DCS of less than thresh tags are displayed. Default of 0 displays all."/> <param name="phred" type="integer" label="Phred quality score threshold" min="0" max="41" value="20" help="Integer threshold for Phred quality score. Only reads higher than this threshold are considered. Default = 20."/> - <param name="trim5" type="integer" label="Trimming threshold at 5' end" value="10" help="Integer threshold for assigning mutations at the beginning of reads to lower tier. Default 10."/> - <param name="trim3" type="integer" label="Trimming threshold at 3' end" value="10" help="Integer threshold for assigning mutations at the end of reads to lower tier. Default 10."/> + <param name="trim" type="integer" label="Trimming threshold" value="10" help="Integer threshold for assigning mutations at start and end of reads to lower tier. Default 10."/> <param name="chimera_correction" type="boolean" label="Apply chimera correction?" truevalue="--chimera_correction" falsevalue="" checked="False" help="Count chimeric variants and correct the variant frequencies."/> </inputs> <outputs> <data name="output_xlsx" format="xlsx" label="${tool.name} on ${on_string}: XLSX summary"/> - <data name="outputFile_csv" format="csv" label="${tool.name} on ${on_string}: CSV summary"/> <data name="output_xlsx2" format="xlsx" label="${tool.name} on ${on_string}: XLSX allele frequencies"/> <data name="output_xlsx3" format="xlsx" label="${tool.name} on ${on_string}: XLSX tiers"/> </outputs> @@ -51,11 +47,9 @@ <param name="file4" value="SSCS_counts_test.json"/> <param name="thresh" value="0"/> <param name="phred" value="20"/> - <param name="trim5" value="10"/> - <param name="trim3" value="10"/> - <param name="delim_csv" value=","/> + <param name="trim" value="10"/> + <param name="chimera_correction" value="True"/> <output name="output_xlsx" file="Variant_Analyzer_summary_test.xlsx" decompress="true" lines_diff="10"/> - <output name="outputFile_csv" file="Variant_Analyzer_summary_test.csv" decompress="true" lines_diff="10"/> <output name="output_xlsx2" file="Variant_Analyzer_allele_frequencies_test.xlsx" decompress="true" lines_diff="10"/> <output name="output_xlsx3" file="Variant_Analyzer_tiers_test.xlsx" decompress="true" lines_diff="10"/> </test>