root/galaxy-central/tools/solid_tools/maq_cs_wrapper.xml @ 3

<tool id="maq_cs_wrapper" name="MAQ for SOLiD" version="1.0.0">
    <description> </description>
    <command interpreter="python">
    maq_cs_wrapper.py 
    $output1 
    $output2 
    $ref 
    $library_type.f3_reads 
    $library_type.f3_qual 
    $library_type.is_paired
    #if $library_type.is_paired == "yes":  
     $library_type.r3_reads 
     $library_type.r3_qual 
    #else:
     "None"
     "None"
    #end if
    $min_mapqual
    $max_mismatch
    $output3
    
    </command>

    <inputs>
        <param name="ref" type="data" format="fasta" label="Target Genome"/> 
        <conditional name="library_type">
          <param name="is_paired" type="select" label="Is the library mate-paired?" multiple="false">
             <option value="no">No</option>
             <option value="yes">Yes</option>
         </param>
         <when value="no">
           <param name="f3_reads" type="data" format="csfasta" label="F3 reads file"/> 
           <param format="qualsolid" name="f3_qual" type="data" label="F3 quality file" help="If your dataset doesn't show up in the menu, click the pencil icon next to your dataset and set the datatype to 'qualsolid'" /> 
          </when>
          <when value="yes">
           <param name="f3_reads" type="data" format="csfasta" label="F3 reads file"/> 
           <param format="qualsolid" name="f3_qual" type="data" label="F3 quality file" help="If your dataset doesn't show up in the menu, click the pencil icon next to your dataset and set the datatype to 'qualsolid'" /> 
           <param name="r3_reads" type="data" format="csfasta" label="R3 reads file"/> 
           <param format="qualsolid" name="r3_qual" type="data" label="R3 quality file" help="If your dataset doesn't show up in the menu, click the pencil icon next to your dataset and set the datatype to 'qualsolid'" /> 
          </when>
      </conditional>
      <param name="min_mapqual" type="integer" size="3" value="0" label="Minimum mapping quality allowed for a read to be used" help="Reads below the specified mapping quality will not be considered in coverage and SNP analysis."/> 
      <param name="max_mismatch" type="integer" size="3" value="7" label="Maximum number of mismatches allowed for a read to be used" help="Reads above the specified threshold will not be considered in coverage and SNP analysis."/> 
    </inputs>
    <outputs>
        <data format="tabular" name="output1" metadata_source="ref" />
        <data format="tabular" name="output2" metadata_source="ref" />
        <data format="customtrack" name="output3" metadata_source="ref" />
    </outputs>
    
    <!--  "ToolTestCase does not deal with multiple outputs properly yet."
    <tests>
        
        <test>
            <param name="ref" value="phiX_mod.fasta" />
            <param name="is_paired" value="no" />
            <param name="f3_reads" value="phiX_solid.csfasta" />
            <param name="f3_qual" value="phiX_solid.qualsolid" />
            <param name="min_mapqual" value="0" />
            <param name="max_mismatch" value="7" />
            <output name="output1" file="phiX_solid_maq.map" />
            <output name="output2" file="phiX_solid_maq.pileup" />
            <output name="output3" file="phiX_solid_maq.ctrack" />
            
        </test>
    </tests>
    -->
<help>

.. class:: infomark

**What it does**

This tool maps SOLiD color-space reads against the target genome using MAQ. It produces three output datasets: 


**ALIGNMENT INFO** : contains the read alignment information, 

**PILEUP** : contains the coverage and SNP statistics for every nucleotide of the target genome,

**CUSTOM TRACK** : contains the coverage and SNP statistics as custom tracks displayable in the UCSC browser. 

-----

**The ALIGNMENT INFO dataset will contain the following fields:**

* column 1  = read name
* column 2  = chromosome
* column 3  = position
* column 4  = strand
* column 5  = insert size from the outer coorniates of a pair
* column 6  = paired flag
* column 7  = mapping quality
* column 8  = single-end mapping quality
* column 9  = alternative mapping quality
* column 10 = number of mismatches of the best hit
* column 11 = sum of qualities of mismatched bases of the best hit
* column 12 = number of 0-mismatch hits of the first 24bp
* column 13 = number of 1-mismatch hits of the first 24bp on the reference
* column 14 = length of the read
* column 15 = read sequence
* column 16 = read quality


**The PILEUP dataset will contain the following fields:**

* column 1  = chromosome
* column 2  = position
* column 3  = reference nucleotide
* column 4  = coverage (number of reads that cover this position)
* column 5  = number of SNPs
* column 6  = number of As
* column 7  = number of Ts
* column 8  = number of Gs
* column 9  = number of Cs

</help>
<code file="maq_cs_wrapper_code.py"/>

</tool>