diff variant_eval.xml @ 11:0d369d08ad6e draft

planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/gatk2 commit 344140b8df53b8b7024618bb04594607a045c03a
author iuc
date Mon, 04 May 2015 22:47:06 -0400
parents b80301676614
children 669a23f1f4b5
line wrap: on
line diff
--- a/variant_eval.xml	Tue Apr 28 22:56:25 2015 -0400
+++ b/variant_eval.xml	Mon May 04 22:47:06 2015 -0400
@@ -1,10 +1,10 @@
 <tool id="gatk2_variant_eval" name="Eval Variants" version="@VERSION@.0">
   <description></description>
-  <expand macro="requirements" />
-  <expand macro="version_command" />
   <macros>
     <import>gatk2_macros.xml</import>
   </macros>
+  <expand macro="requirements" />
+  <expand macro="version_command" />
   <command interpreter="python">
    #from binascii import hexlify
 
@@ -25,24 +25,23 @@
         -R "${reference_source.ref_file.fields.path}"
     #end if
    '
-   
+
     #for $rod_binding in $comp_rod_bind:
         -d "--comp:${rod_binding.comp_rod_name},%(file_type)s" "${rod_binding.comp_input_rod}" "${rod_binding.comp_input_rod.ext}" "input_comp_${rod_binding.comp_rod_name}"
         #if str( $rod_binding.comp_known_names ):
             -p '--known_names "${rod_binding.comp_rod_name}"'
         #end if
     #end for
-    
+
     #if $dbsnp_rod_bind_type.dbsnp_rod_bind_type_selector == 'set_dbsnp'
         -d "--dbsnp:${dbsnp_rod_bind_type.dbsnp_rod_name},%(file_type)s" "${dbsnp_rod_bind_type.dbsnp_input_rod}" "${dbsnp_rod_bind_type.dbsnp_input_rod.ext}" "input_dbsnp_${dbsnp_rod_bind_type.dbsnp_rod_name}"
         #if $dbsnp_rod_bind_type.dbsnp_known_names
             -p '--known_names "${dbsnp_rod_bind_type.dbsnp_rod_name}"'
         #end if
     #end if
-   
+
     #include source=$standard_gatk_options#
-    
-    
+
     ##start analysis specific options
     #if $analysis_param_type.analysis_param_type_selector == "advanced":
         #for $stratification in $analysis_param_type.stratifications:
@@ -50,39 +49,39 @@
             -o '${ hexlify( $select_string ) }'
         #end for
         -p '
-        
+
         #for $sample in $analysis_param_type.samples:
             --sample "${sample.sample}"
         #end for
-        
+
         #if str( $analysis_param_type.stratification_modules ) != "None":
             #for $stratification_module in str( $analysis_param_type.stratification_modules).split( ',' ):
                 --stratificationModule "${stratification_module}"
             #end for
         #end if
-        
+
         ${analysis_param_type.do_not_use_all_standard_stratifications}
-        
+
         #for $variant_type in $analysis_param_type.only_variants_of_type:
             --onlyVariantsOfType "${variant_type.variant_type}"
         #end for
-        
+
         #if str( $analysis_param_type.eval_modules ) != "None":
             #for $eval_module in str( $analysis_param_type.eval_modules).split( ',' ):
                 --evalModule "${eval_module}"
             #end for
         #end if
-        
+
         ${analysis_param_type.do_not_use_all_standard_modules}
-        
+
         #if str( $analysis_param_type.num_samples ) != "0":
             --numSamples "${analysis_param_type.num_samples}"
         #end if
-        
+
         --minPhaseQuality "${analysis_param_type.min_phase_quality}"
-        
+
         --mendelianViolationQualThreshold "${analysis_param_type.mendelian_violation_qual_threshold}"
-        
+
         #if str( $analysis_param_type.ancestral_alignments ) != "None":
             --ancestralAlignments "${analysis_param_type.ancestral_alignments}"
         #end if
@@ -90,14 +89,14 @@
         #if str( $analysis_param_type.known_cnvs ) != "None":
             -d "--knownCNVs" "${analysis_param_type.known_cnvs}" "${analysis_param_type.known_cnvs.ext}" "input_known_cnvs"
         #end if
-        
+
         #if str( $analysis_param_type.strat_intervals ) != "None":
             -d "--stratIntervals" "${analysis_param_type.strat_intervals}" "${analysis_param_type.strat_intervals.ext}" "input_strat_intervals"
         #end if
     #end if
   </command>
   <inputs>
-    
+
     <conditional name="reference_source">
       <expand macro="reference_source_selector_param" />
       <when value="cached">
@@ -118,7 +117,7 @@
         <param name="ref_file" type="data" format="fasta" label="Using reference file" help="-R,--reference_sequence &amp;lt;reference_sequence&amp;gt;" />
       </when>
     </conditional>
-    
+
     <repeat name="comp_rod_bind" title="Comparison Reference-Ordered Data (ROD) file" help="-comp,--comp &amp;lt;comp&amp;gt;">
       <param name="comp_input_rod" type="data" format="vcf" label="Comparison ROD file" />
       <param name="comp_rod_name" type="text" value="" label="Comparison ROD name">
@@ -140,10 +139,9 @@
         <param name="dbsnp_known_names" type="boolean" label="Use dbSNP ROD file as known_names" help="-knownName,--known_names &amp;lt;known_names&amp;gt;" />
       </when>
     </conditional>
-    
+
     <expand macro="gatk_param_type_conditional" />
-    
-    
+
     <expand macro="analysis_type_conditional">
         <repeat name="stratifications" title="Stratification">
           <param name="select_exps" value="" type="text" label="Stratification Expression" help="-select,--select_exps &amp;lt;select_exps&amp;gt;">
@@ -156,11 +154,11 @@
           </param>
           <param name="select_name" value="" type="text" label="Name" help="-selectName,--select_names &amp;lt;select_names&amp;gt;"/>
         </repeat>
-        
+
         <repeat name="samples" title="Sample" help="-sn,--sample &amp;lt;sample&amp;gt;">
           <param name="sample" value="" type="text" label="Derive eval and comp contexts using only these sample genotypes, when genotypes are available in the original context"/>
         </repeat>
-        
+
         <param name="stratification_modules" type="select" multiple="True" display="checkboxes" label="Stratification modules to apply to the eval track(s)" help="-ST,--stratificationModule &amp;lt;stratificationModule&amp;gt;" >
           <option value="AlleleCount" />
           <option value="AlleleFrequency" />
@@ -182,11 +180,11 @@
           <option value="VariantType" />
         </param>
         <param name="do_not_use_all_standard_stratifications" checked="false" type="boolean" truevalue="--doNotUseAllStandardStratifications" falsevalue="" label="Do not use the standard stratification modules by default" help="-noST,--doNotUseAllStandardStratifications" />
-        
+
         <repeat name="only_variants_of_type" title="only Variants Of Type" help="--onlyVariantsOfType">
           <param name="variant_type" type="text" value="" label="only variants of these types will be considered during the evaluation"/>
         </repeat>
-        
+
         <param name="eval_modules" type="select" multiple="True" display="checkboxes" label="Eval modules to apply to the eval track(s)" help="-EV,--evalModule &amp;lt;evalModule&amp;gt;" >
           <option value="CompOverlap" />
           <option value="CountVariants" />
@@ -201,17 +199,15 @@
           <option value="VariantSummary" />
         </param>
         <param name="do_not_use_all_standard_modules" checked="false" type="boolean" truevalue="--doNotUseAllStandardModules" falsevalue="" label="Do not use the standard eval modules by default" help="-noEV,--doNotUseAllStandardModules" />
-        
+
         <param name="num_samples" type="integer" label="Number of samples (used if no samples are available in the VCF file" value="0" help="-ns,--numSamples &amp;lt;numSamples&amp;gt;"/>
         <param name="min_phase_quality" type="float" label="Minimum phasing quality " value="10.0" help="-mpq,--minPhaseQuality &amp;lt;minPhaseQuality&amp;gt;"/>
         <param name="mendelian_violation_qual_threshold" type="integer" label="Minimum genotype QUAL score for each trio member required to accept a site as a violation" value="50" help="-mvq,--mendelianViolationQualThreshold &amp;lt;mendelianViolationQualThreshold&amp;gt;"/>
         <param name="ancestral_alignments" type="data" format="fasta" optional="True" label="Fasta file with ancestral alleles" help="-aa,--ancestralAlignments &amp;lt;ancestralAlignments&amp;gt;" />
         <param name="known_cnvs" type="data" format="bed,gatk_interval,picard_interval_list" optional="True" label="File containing tribble-readable features describing a known list of copy number variants" help="-knownCNVs,--knownCNVs &amp;lt;knownCNVs&amp;gt;" />
         <param name="strat_intervals" type="data" format="bed,gatk_interval,picard_interval_list" optional="True" label="File containing tribble-readable features for the IntervalStratificiation" help="-stratIntervals,--stratIntervals &amp;lt;stratIntervals&amp;gt;" />
-        
     </expand>
-    
-    
+
   </inputs>
   <outputs>
     <data format="gatk_report" name="output_report" label="${tool.name} on ${on_string} (report)" />
@@ -270,7 +266,7 @@
  known_names                           Name of ROD bindings containing variant sites that should be treated as known when splitting eval rods into known and novel subsets
  stratificationModule                  One or more specific stratification modules to apply to the eval track(s) (in addition to the standard stratifications, unless -noS is specified)
  doNotUseAllStandardStratifications    Do not use the standard stratification modules by default (instead, only those that are specified with the -S option)
- onlyVariantsOfType                    If provided, only variants of these types will be considered during the evaluation, in 
+ onlyVariantsOfType                    If provided, only variants of these types will be considered during the evaluation, in
  evalModule                            One or more specific eval modules to apply to the eval track(s) (in addition to the standard modules, unless -noE is specified)
  doNotUseAllStandardModules            Do not use the standard modules by default (instead, only those that are specified with the -E option)
  numSamples                            Number of samples (used if no samples are available in the VCF file