Mercurial > repos > devteam > emboss_5
view emboss_etandem.xml @ 10:9b98d3d903c6 draft
planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/emboss_5 commit fc158bfe5f5927dc199321a2cf43310373cbc8ba
author | devteam |
---|---|
date | Fri, 12 Aug 2016 19:17:10 -0400 |
parents | |
children | 0e2484b6829b |
line wrap: on
line source
<tool id="EMBOSS: etandem33" name="etandem" version="5.0.0"> <description>Looks for tandem repeats in a nucleotide sequence</description> <requirements><requirement type="package" version="5.0.0">emboss</requirement></requirements> <command>etandem -sequence $input1 -outfile $out_file1 -origfile $ofile2 -minrepeat $minrepeat -maxrepeat $maxrepeat -threshold $threshold -mismatch $mismatch -uniform $uniform -rformat2 $out_format1 -auto</command> <inputs> <param format="fasta" name="input1" type="data"> <label>Sequence</label> </param> <param name="minrepeat" type="text" value="10"> <label>Minimum repeat size</label> </param> <param name="maxrepeat" type="text" value="10"> <label>Maximum repeat size</label> </param> <param name="threshold" type="text" value="20"> <label>Threshold score</label> </param> <param name="mismatch" type="select"> <label>Allow N as a mismatch</label> <option value="no">No</option> <option value="yes">Yes</option> </param> <param name="uniform" type="select"> <label>Allow uniform consensus</label> <option value="no">No</option> <option value="yes">Yes</option> </param> <param name="out_format1" type="select"> <label>Output Report File Format</label> <option value="table">Table</option> <option value="embl">EMBL</option> <option value="genbank">GENBANK</option> <option value="gff">GFF</option> <option value="pir">PIR</option> <option value="swiss">SwissProt</option> <option value="dbmotif">DbMotif</option> <option value="diffseq">Diffseq</option> <option value="excel">Excel (tab delimited)</option> <option value="feattable">FeatTable</option> <option value="motif">Motif</option> <option value="regions">Regions</option> <option value="seqtable">SeqTable</option> <option value="simple">SRS Simple</option> <option value="srs">SRS</option> <option value="tagseq">TagSeq</option> </param> </inputs> <outputs> <data format="etandem" name="out_file1" /> <data format="table" name="ofile2" /> </outputs> <tests> <test> <param name="input1" value="1.fasta"/> <param name="minrepeat" value="10"/> <param name="maxrepeat" value="10"/> <param name="threshold" value="20"/> <param name="mismatch" value="no"/> <param name="uniform" value="no"/> <param name="out_format1" value="table"/> <output name="ofile2" file="emboss_etandem_out.table"/> </test> </tests> <code file="emboss_format_corrector.py" /> <help> .. class:: warningmark The input dataset needs to be sequences. ----- You can view the original documentation here_. .. _here: http://emboss.sourceforge.net/apps/release/5.0/emboss/apps/etandem.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>