<tool id="EMBOSS: transeq101" name="transeq" version="5.0.0">
  <description>Translate nucleic acid sequences</description>
  <macros>
    <import>macros.xml</import>
  </macros>
  <expand macro="requirements" />
  <code file="emboss_format_corrector.py" />
  <command><![CDATA[
    transeq 
      -sequence '$input1' 
      -outseq '$out_file1' 
      -frame $frame 
      -table $table
      #if str($regions).strip():
        -regions '$regions'
      #end if
      -trim $trim 
      -clean $clean 
      -alternative $alternative 
      -osformat2 '$out_format1' 
      -auto
  ]]>
  </command>
  <inputs>
    <param name="input1" type="data" format="fasta" label="Sequences" />
    <param name="frame" type="select" label="Frame(s) to translate">
      <option value="1">Frame 1</option>
      <option value="2">Frame 2</option>
      <option value="3">Frame 3</option>
      <option value="F">Forward three frames</option>
      <option value="-1">Frame -1</option>
      <option value="-2">Frame -2</option>
      <option value="-3">Frame -3</option>
      <option value="R">Reverse three frames</option>
      <option value="6">All six frames</option>
    </param>
    <param name="table" type="select" label="Code to use">
      <option value="0">Standard</option>
      <option value="1">Standard (with alternative initiation codons)</option>
      <option value="2">Vertebrate Mitochondrial</option>
      <option value="3">Yeast Mitochondrial</option>
      <option value="4">Mold, Protozoan, Coelenterate Mitochondrial and Mycoplasma/Spiroplasma</option>
      <option value="5">Invertebrate Mitochondrial</option>
      <option value="6">Ciliate Macronuclear and Dasycladacean</option>
      <option value="9">Echinoderm Mitochondrial</option>
      <option value="10">Euplotid Nuclear</option>
      <option value="11">Bacterial</option>
      <option value="12">Alternative Yeast Nuclear</option>
      <option value="13">Ascidian Mitochondrial</option>
      <option value="14">Flatworm Mitochondrial</option>
      <option value="15">Blepharisma Macronuclear</option>
      <option value="16">Chlorophycean Mitochondrial</option>
      <option value="21">Trematode Mitochondrial</option>
      <option value="22">Scenedesmus obliquus</option>
      <option value="23">Thraustochytrium Mitochondrial</option>
    </param>
    <param name="regions" type="text" value="" label="Regions to translate" />
    <param name="trim" type="select" label="Remove all 'X' and '*' characters from the right end of the translation">
      <option value="no">No</option>
      <option value="yes">Yes</option>
    </param>
    <param name="clean" type="select" label="Change all STOP codon positions from the '*' character to 'X'">
      <option value="no">No</option>
      <option value="yes">Yes</option>
    </param>
    <param name="alternative" type="select" label="Define frame '-1' as using the set of codons starting with the last codon of the sequence">
      <option value="no">No</option>
      <option value="yes">Yes</option>
    </param>
    <param name="out_format1" type="select" label="Output sequence file format">
      <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 name="out_file1" format="fasta" />
  </outputs>
  <tests>
    <test>
      <param name="input1" value="2.fasta"/>
      <param name="frame" value="1"/>
      <param name="table" value="0"/>
      <param name="regions" value=""/>
      <param name="trim" value="no"/>
      <param name="clean" value="no"/>
      <param name="alternative" value="no"/>
      <param name="out_format1" value="fasta"/>
      <output name="out_file1" file="emboss_transeq_out.fasta"/>
    </test>
  </tests>
  <help>
.. class:: warningmark

The input dataset needs to be sequences.

-----

    You can view the original documentation here_.

    .. _here: http://galaxy-iuc.github.io/emboss-5.0-docs/transeq.html
  </help>
  <expand macro="citations" />
</tool>