comparison emboss_prettyseq.xml @ 10:9b98d3d903c6 draft

planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/emboss_5 commit fc158bfe5f5927dc199321a2cf43310373cbc8ba

10:9b98d3d903c6

<tool id="EMBOSS: prettyseq80" name="prettyseq" version="5.0.0">
  <description>Output sequence with translated ranges</description>
  <requirements><requirement type="package" version="5.0.0">emboss</requirement></requirements>
  <command>prettyseq -sequence $input1 -outfile $out_file1 -ruler $ruler -plabel $plabel -nlabel $nlabel -width $width -auto</command>
  <inputs>
    <param format="fasta" name="input1" type="data">
      <label>Sequence</label>
    </param>
    <param name="ruler" type="select">
      <label>Add a ruler</label>
      <option value="yes">Yes</option>
      <option value="no">No</option>
    </param>
    <param name="plabel" type="select">
      <label>Number translations</label>
      <option value="yes">Yes</option>
      <option value="no">No</option>
    </param>
    <param name="nlabel" type="select">
      <label>Number DNA sequence</label>
      <option value="yes">Yes</option>
      <option value="no">No</option>
    </param>
    <param name="width" type="text" value="60">
      <label>Width of screen</label>
    </param>
  </inputs>
  <outputs>
    <data format="prettyseq" name="out_file1" />
  </outputs>
  <tests>
    <test>
      <param name="input1" value="2.fasta"/>
      <param name="ruler" value="yes"/>
      <param name="plabel" value="yes"/>
      <param name="nlabel" value="yes"/>
      <param name="width" value="60"/>
      <output name="out_file1" file="emboss_prettyseq_out.prettyseq"/>
    </test>
  </tests>
  <help>

.. class:: warningmark

The input dataset needs to be sequences.

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    You can view the original documentation here_.
    
    .. _here: http://emboss.sourceforge.net/apps/release/5.0/emboss/apps/prettyseq.html

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**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. &lt;http://www.ncbi.nlm.nih.gov/pubmed/10827456&gt;`_

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. &lt;http://www.ncbi.nlm.nih.gov/pubmed/17568012&gt;`_
  </help>
</tool>