Mercurial > repos > iuc > gatk2
view variant_annotator.xml @ 4:f244b8209eb8 draft
bug fix release
author | iuc |
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date | Mon, 25 Aug 2014 17:43:11 -0400 |
parents | 8bcc13094767 |
children | 35c00763cb5c |
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<tool id="gatk2_variant_annotator" name="Variant Annotator" version="@VERSION@.0"> <description></description> <expand macro="requirements" /> <macros> <import>gatk2_macros.xml</import> </macros> <command interpreter="python"> gatk2_wrapper.py --stdout "${output_log}" #if str( $reference_source.input_bam ) != "None": -d "-I" "${reference_source.input_bam}" "${reference_source.input_bam.ext}" "gatk_input" #if str( $reference_source.input_bam.metadata.bam_index ) != "None": -d "" "${reference_source.input_bam.metadata.bam_index}" "bam_index" "gatk_input" ##hardcode galaxy ext type as bam_index #end if #end if -d "--variant" "${reference_source.input_variant}" "${reference_source.input_variant.ext}" "input_variant" -p ' @JAR_PATH@ -T "VariantAnnotator" \$GATK2_SITE_OPTIONS @THREADS@ #if $reference_source.reference_source_selector != "history": -R "${reference_source.ref_file.fields.path}" #end if -o "${output_vcf}" #if str( $annotations_type.annotations_type_selector ) == "use_all_annotations": --useAllAnnotations #else: #if $annotations_type.annotations: #for $annotation in str( $annotations_type.annotations.fields.gatk_value ).split( ',' ): --annotation "${annotation}" #end for #end if #end if #if $exclude_annotations: #for $annotation in str( $exclude_annotations.fields.gatk_value ).split( ',' ): --excludeAnnotation "${annotation}" #end for #end if #for $additional_annotation in $additional_annotations: --annotation "${additional_annotation.additional_annotation_name}" #end for ' #if $reference_source.input_variant_bti: -d "--intervals" "${reference_source.input_variant}" "${reference_source.input_variant.ext}" "input_variant_bti" #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}" #end for @DBSNP_OPTIONS@ #for $rod_binding in $resource_rod_bind: -d "--resource:${rod_binding.resource_rod_name},%(file_type)s" "${rod_binding.resource_input_rod}" "${rod_binding.resource_input_rod.ext}" "input_resource_${rod_binding.resource_rod_name}" #end for #if str( $snpEff_rod_bind_type.snpEff_rod_bind_type_selector ) == 'set_snpEff': -p '--annotation "SnpEff"' -d "--snpEffFile:${snpEff_rod_bind_type.snpEff_rod_name},%(file_type)s" "${snpEff_rod_bind_type.snpEff_input_rod}" "${snpEff_rod_bind_type.snpEff_input_rod.ext}" "input_snpEff_${snpEff_rod_bind_type.snpEff_rod_name}" #else: -p '--excludeAnnotation "SnpEff"' #end if #for $expression in $expressions: -p '--expression "${expression.expression}"' #end for #include source=$standard_gatk_options# -p ' #if str( $annotation_group ) != "None": #for $group in str( $annotation_group ).split( ',' ): --group "${group}" #end for #end if #if str( $family_string ) != "": --family_string "${family_string}" #end if --MendelViolationGenotypeQualityThreshold "${mendel_violation_genotype_quality_threshold}" ' </command> <inputs> <conditional name="reference_source"> <expand macro="reference_source_selector_param" /> <when value="cached"> <param name="input_variant" type="data" format="vcf" label="Variant file to annotate" help="-V,--variant &lt;variant&gt;"/> <param name="input_variant_bti" type="boolean" truevalue="-BTI variant" falsevalue="" label="Increase efficiency for small variant files." help="-BTI variant"/> <param name="input_bam" type="data" format="bam" label="BAM file" optional="True" help="Not needed for all annotations. (-I,--input_file &lt;input_file&gt;)" > <validator type="unspecified_build" /> <validator type="dataset_metadata_in_data_table" table_name="gatk2_picard_indexes" metadata_name="dbkey" metadata_column="dbkey" message="Sequences are not currently available for the specified build." /> <!-- fixme!!! this needs to be a select --> </param> <param name="ref_file" type="select" label="Using reference genome" help="-R,--reference_sequence &lt;reference_sequence&gt;"> <options from_data_table="gatk2_picard_indexes"> <filter type="data_meta" key="dbkey" ref="input_variant" column="dbkey"/> </options> <validator type="no_options" message="A built-in reference genome is not available for the build associated with the selected input file"/> </param> </when> <when value="history"> <!-- FIX ME!!!! --> <param name="input_variant" type="data" format="vcf" label="Variant file to annotate" help="-V,--variant &lt;variant&gt;"/> <param name="input_variant_bti" type="boolean" truevalue="-BTI variant" falsevalue="" label="Increase efficiency for small variant files." help="-BTI variant"/> <param name="input_bam" type="data" format="bam" label="BAM file" optional="True" help="Not needed for all annotations. (-I,--input_file &lt;input_file&gt;)" /> <param name="ref_file" type="data" format="fasta" label="Using reference file" help="-R,--reference_sequence &lt;reference_sequence&gt;" /> </when> </conditional> <conditional name="annotations_type"> <param name="annotations_type_selector" type="select" label="Use all possible annotations"> <option value="use_all_annotations">Use all</option> <option value="choose" selected="True">Use selected</option> </param> <when value="use_all_annotations"> <!-- no extra options here --> </when> <when value="choose"> <param name="annotations" type="select" multiple="True" display="checkboxes" label="Annotations to apply" help="-A,--annotation &lt;annotation&gt;" > <!-- load the available annotations from an external configuration file, since additional ones can be added to local installs --> <options from_data_table="gatk2_annotations"> <filter type="multiple_splitter" column="tools_valid_for" separator=","/> <filter type="static_value" value="VariantAnnotator" column="tools_valid_for"/> </options> </param> </when> </conditional> <repeat name="additional_annotations" title="Additional annotation" help="-A,--annotation &lt;annotation&gt;"> <param name="additional_annotation_name" type="text" value="" label="Annotation name" /> </repeat> <repeat name="comp_rod_bind" title="Binding for reference-ordered comparison data" help="-comp,--comp &lt;comp&gt;"> <param name="comp_input_rod" type="data" format="vcf" label="ROD file" /> <param name="comp_rod_name" type="text" value="Unnamed" label="ROD Name"/> </repeat> <expand macro="dbsnp_param" /> <repeat name="resource_rod_bind" title="Binding for reference-ordered resource data" help="-resource,--resource &lt;resource&gt;"> <param name="resource_input_rod" type="data" format="vcf" label="ROD file" /> <param name="resource_rod_name" type="text" value="Unnamed" label="ROD Name"/> </repeat> <conditional name="snpEff_rod_bind_type"> <param name="snpEff_rod_bind_type_selector" type="select" label="Provide a snpEff reference-ordered data file (VCF)" help="-snpEffFile,--snpEffFile &lt;snpEffFile&gt;"> <option value="set_snpEff">Set snpEff</option> <option value="exclude_snpEff" selected="True">Don't set snpEff</option> </param> <when value="exclude_snpEff"> <!-- Do nothing here --> </when> <when value="set_snpEff"> <param name="snpEff_input_rod" type="data" format="vcf" label="ROD file" /> <param name="snpEff_rod_name" type="hidden" value="snpEff" label="ROD Name"/> </when> </conditional> <repeat name="expressions" title="Expression" help="-E,--expression &lt;expression&gt;"> <param name="expression" type="text" value="" label="Expression"/> </repeat> <expand macro="gatk_param_type_conditional" /> <param name="annotation_group" type="select" multiple="True" display="checkboxes" label="annotation interfaces/groups to apply to variant calls" help="-G,--group &lt;group&gt;"> <option value="RodRequiringAnnotation">RodRequiringAnnotation</option> <option value="Standard">Standard</option> <option value="Experimental">Experimental</option> <option value="WorkInProgress">WorkInProgress</option> <option value="RankSumTest">RankSumTest</option> </param> <param name="family_string" type="text" value="" label="Family String" help="--family_string"/> <param name="mendel_violation_genotype_quality_threshold" type="float" value="0.0" label="genotype quality treshold in order to annotate mendelian violation ratio." help="-mvq,--MendelViolationGenotypeQualityThreshold &lt;MendelViolationGenotypeQualityThreshold&gt;"/> <param name="exclude_annotations" type="select" multiple="True" display="checkboxes" label="Annotations to exclude" help="-XA,--excludeAnnotation &lt;excludeAnnotation&gt;" > <!-- load the available annotations from an external configuration file, since additional ones can be added to local installs --> <options from_data_table="gatk2_annotations"> <filter type="multiple_splitter" column="tools_valid_for" separator=","/> <filter type="static_value" value="VariantAnnotator" column="tools_valid_for"/> </options> </param> </inputs> <outputs> <data format="vcf" name="output_vcf" label="${tool.name} on ${on_string} (Variant File)" /> <data format="txt" name="output_log" label="${tool.name} on ${on_string} (log)" /> </outputs> <tests> <test> <param name="reference_source_selector" value="history" /> <param name="ref_file" value="phiX.fasta" ftype="fasta" /> <param name="input_bam" value="gatk/gatk_table_recalibration/gatk_table_recalibration_out_1.bam" ftype="bam" /> <param name="input_variant" value="gatk/gatk_unified_genotyper/gatk_unified_genotyper_out_1.vcf" ftype="vcf" /> <param name="input_variant_bti" /> <param name="annotations_type_selector" value="choose" /> <param name="annotations" value="AlleleBalance,BaseQualityRankSumTest,DepthOfCoverage,HomopolymerRun,MappingQualityRankSumTest,MappingQualityZero,QualByDepth,RMSMappingQuality,SpanningDeletions,HaplotypeScore" /> <param name="additional_annotations" value="0" /> <param name="dbsnp_rod_bind_type_selector" value="set_dbsnp" /> <param name="dbsnp_input_rod" value="gatk/fake_phiX_variant_locations.vcf" ftype="vcf" /> <param name="dbsnp_rod_name" value="dbsnp" /> <param name="snpEff_rod_bind_type_selector" value="exclude_snpEff" /> <param name="gatk_param_type_selector" value="basic" /> <output name="output_vcf" file="gatk/gatk_variant_annotator/gatk_variant_annotator_out_1.vcf" lines_diff="4" /> <output name="output_log" file="gatk/gatk_variant_annotator/gatk_variant_annotator_out_1.log.contains" compare="contains" /> <param name="comp_rod_bind" value="0" /> <param name="resource_rod_bind" value="0" /> <param name="expressions" value="0" /> <!-- <param name="annotation_group" /> --> </test> </tests> <help> **What it does** Annotates variant calls with context information. Users can specify which of the available annotations to use. For more information on using the VariantAnnotator, see this `tool specific page <http://www.broadinstitute.org/gatk/gatkdocs/org_broadinstitute_sting_gatk_walkers_annotator_VariantAnnotator.html>`_. To learn about best practices for variant detection using GATK, see this `overview <http://www.broadinstitute.org/gatk/guide/topic?name=best-practices>`_. If you encounter errors, please view the `GATK FAQ <http://www.broadinstitute.org/gatk/guide/topic?name=faqs>`_. ------ **Inputs** GenomeAnalysisTK: VariantAnnotator accepts a variant input file. **Outputs** The output is in VCF format. Go `here <http://www.broadinstitute.org/gatk/guide/topic?name=intro>`_ for details on GATK file formats. ------- **Settings**:: sampleName The sample (NA-ID) corresponding to the variant input (for non-VCF input only) annotation One or more specific annotations to apply to variant calls group One or more classes/groups of annotations to apply to variant calls expression One or more specific expressions to apply to variant calls; see documentation for more details useAllAnnotations Use all possible annotations (not for the faint of heart) @CITATION_SECTION@ </help> <expand macro="citations" /> </tool>