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planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/emboss_5 commit fc158bfe5f5927dc199321a2cf43310373cbc8ba
author | devteam |
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date | Fri, 12 Aug 2016 19:17:10 -0400 |
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children | 0e2484b6829b |
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<tool id="EMBOSS: oddcomp64" name="oddcomp" version="5.0.0"> <!-- output contains file location info, commented out functional tests --> <description>Find protein sequence regions with a biased composition</description> <requirements><requirement type="package" version="5.0.0">emboss</requirement></requirements> <command>oddcomp -sequence $input1 -infile $input2 -outfile $out_file1 -window $window -ignorebz $ignorebz -auto</command> <inputs> <param format="data" name="input1" type="data"> <label>Sequences</label> </param> <param format="data" name="input2" type="data"> <label>This is a file in the format of the output produced by 'compseq' that is used to set the minimum frequencies of words in this analysis</label> </param> <param name="window" type="text" value="30"> <label>This is the size of window in which to count. Thus if you want to count frequencies in a 40 aa stretch you should enter 40 here</label> </param> <param name="ignorebz" type="select"> <label>The amino acid code B represents Asparagine or Aspartic acid and the code Z represents Glutamine or Glutamic acid. These are not commonly used codes and you may wish not to count words containing them, just noting them in the count of 'Other' words</label> <option value="yes">Yes</option> <option value="no">No</option> </param> </inputs> <outputs> <data format="oddcomp" name="out_file1" /> </outputs> <!-- <tests> <test> <param name="input1" value="2.fasta"/> <param name="input2" value="emboss_compseq_out.compseq"/> <param name="window" value="30"/> <param name="ignorebz" value="yes"/> <output name="out_file1" file="emboss_oddcomp_out.oddcomp"/> </test> </tests> --> <help> You can view the original documentation here_. .. _here: http://emboss.sourceforge.net/apps/release/5.0/emboss/apps/oddcomp.html ------ **Citation** For the underlying tool, please cite `Rice P, Longden I, Bleasby A. EMBOSS: the European Molecular Biology Open Software Suite. Trends Genet. 2000 Jun;16(6):276-7. <http://www.ncbi.nlm.nih.gov/pubmed/10827456>`_ If you use this tool in Galaxy, please cite `Blankenberg D, Taylor J, Schenck I, He J, Zhang Y, Ghent M, Veeraraghavan N, Albert I, Miller W, Makova KD, Hardison RC, Nekrutenko A. A framework for collaborative analysis of ENCODE data: making large-scale analyses biologist-friendly. Genome Res. 2007 Jun;17(6):960-4. <http://www.ncbi.nlm.nih.gov/pubmed/17568012>`_ </help> </tool>