<tool id="EMBOSS: newseq59" name="newseq" version="5.0.0">

  <description>Type in a short new sequence</description>

  <requirements><requirement type="package" version="5.0.0">emboss</requirement></requirements>

  <command>newseq -outseq $out_file1 -name "$seqname" -description "$description" -type $type -sequence "$sequence" -osformat5 $out_format1 -auto</command>

  <inputs>

    <param name="seqname" size="10" type="text" value="">

      <label>Name of of the sequence</label>

    </param>

    <param name="description" size="10" type="text" value="">

      <label>Description of the sequence</label>

    </param>

    <param name="type" type="select">

      <label>Type of sequence</label>

      <option value="N">Nucleic</option>

      <option value="P">Protein</option>

    </param>

    <param name="sequence" size="50" type="text" value="">

      <label>The sequence itself</label>

    </param>

    <param name="out_format1" type="select">

      <label>Output Sequence File Format</label>

      <option value="fasta">FASTA (m)</option>

      <option value="acedb">ACeDB (m)</option>

      <option value="asn1">ASN.1 (m)</option>

      <option value="clustal">Clustal (m)</option>

      <option value="codata">CODATA (m)</option>

      <option value="embl">EMBL (m)</option>

      <option value="fitch">Fitch (m)</option>

      <option value="gcg">Wisconsin Package GCG 9.x and 10.x (s)</option>

      <option value="genbank">GENBANK (m)</option>

      <option value="gff">GFF (m)</option>

      <option value="hennig86">Hennig86 (m)</option>

      <option value="ig">Intelligenetics (m)</option>

      <option value="jackknifer">Jackknifer (m)</option>

      <option value="jackknifernon">Jackknifernon (m)</option>

      <option value="mega">Mega (m)</option>

      <option value="meganon">Meganon (m)</option>

      <option value="msf">Wisconsin Package GCG's MSF (m)</option>

      <option value="pir">NBRF (PIR) (m)</option>

      <option value="ncbi">NCBI style FASTA (m)</option>

      <option value="nexus">Nexus/PAUP (m)</option>

      <option value="nexusnon">Nexusnon/PAUPnon (m)</option>

      <option value="phylip">PHYLIP interleaved (m)</option>

      <option value="phylipnon">PHYLIP non-interleaved (m)</option>

      <option value="selex">SELEX (m)</option>

      <option value="staden">Staden (s)</option>

      <option value="strider">DNA strider (m)</option>

      <option value="swiss">SwisProt entry (m)</option>

      <option value="text">Plain sequence (s)</option>

      <option value="treecon">Treecon (m)</option>

    </param>

  </inputs>

  <outputs>

    <data format="fasta" name="out_file1" />

  </outputs>
  <tests>
    <test>
      <param name="seqname" value="cytoc"/>
      <param name="description" value="fragment of cytochrome c"/>
      <param name="type" value="N"/>
      <param name="sequence" value="KKKEERADLIAY"/>
      <param name="out_format1" value="fasta"/>
      <output name="out_file1" file="emboss_newseq_out.fasta"/>
    </test>
  </tests>

  <code file="emboss_format_corrector.py" />

  <help>
    You can view the original documentation here_.
    
    .. _here: http://emboss.sourceforge.net/apps/release/5.0/emboss/apps/newseq.html



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**Citation**



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>