Mercurial > repos > iuc > medaka_variant
view variant.xml @ 14:cc36773a3681 draft
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/medaka commit 8051b858e0f5c6d7c1092754df02ed8303a53054
author | iuc |
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date | Mon, 27 Jun 2022 17:29:38 +0000 |
parents | 222669c4afb6 |
children | ec699520444c |
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<tool id="medaka_variant" name="medaka variant tool" version="@TOOL_VERSION@+galaxy@VERSION_SUFFIX@" profile="@PROFILE@"> <description>decodes variant calls from medaka consensus output</description> <macros> <import>macros.xml</import> </macros> <expand macro="requirements"/> <expand macro="version_command"/> <command detect_errors="exit_code"><![CDATA[ ## initialize @REF_FASTA@ #if $pool.pool_mode == "Yes": ## run medaka variant ## optional --debug #if $regions --regions '${regions}' #end if $verbose ${ambig_ref} ${gvcf} ## required reference.fa #for $current in $pool.inputs '$current' #end for #elif $pool.pool_mode == "No": ## run medaka variant ## optional --debug #if $regions --regions '${regions}' #end if $verbose ${ambig_ref} ${gvcf} ## required reference.fa '$pool.input' #end if #if str($output_annotated.output_annotated_select) == 'false': '$out_variants' ##output 2>&1 | tee '$out_log' #else raw.vcf ##output of medaka variant 2>&1 | tee '$out_log' && ln -s '$output_annotated.in_bam' in.bam && ln -s '$output_annotated.in_bam.metadata.bam_index' in.bai && medaka tools annotate --dpsp --pad $output_annotated.pad raw.vcf reference.fa in.bam tmp.vcf && python '$__tool_directory__/convert_VCF_info_fields.py' tmp.vcf '$out_variants' #end if ]]></command> <inputs> <conditional name="pool"> <param name="pool_mode" type="select" label="Are you pooling HDF5 datasets?"> <option value="No" selected="true">No</option> <option value="Yes">Yes</option> </param> <when value="Yes"> <param name="inputs" type="data" format="h5" multiple="true" label="Select consensus file(s)"/> </when> <when value="No"> <param name="input" type="data" format="h5" label="Select consensus file(s)"/> </when> </conditional> <expand macro="reference"/> <param argument="--regions" type="text" value="" optional="true" label="Set reference names to limit variant calling" help="Separated by ','."> <sanitizer invalid_char=""> <valid initial="string.ascii_letters,string.digits"> <add value="_"/> <add value=","/> <add value="."/> </valid> </sanitizer> </param> <param argument="--verbose" type="boolean" truevalue="--verbose" falsevalue="" label="Populate VCF info fields?"/> <param argument="--ambig_ref" type="boolean" truevalue="--ambig_ref" falsevalue="" label="Decode variants at ambiguous reference positions?" checked="false"/> <param argument="--gvcf" type="boolean" truevalue="--gvcf" falsevalue="" label="Output VCF records for reference loci predicted to be non-variant?" checked="false"/> <conditional name="output_annotated"> <param name="output_annotated_select" type="select" label="Type of VCF to generate" help="Variant INFO fields in the VCF can be extended to include allele frequency, depth of coverage, etc., but this requires a BAM dataset to calculate those values from."> <option value="true" selected="true">Write annotated VCF with extended INFO</option> <option value="false">Write original decoded VCF with minimal INFO field</option> </param> <when value="true"> <param name="in_bam" type="data" format="bam" optional="false" label="BAM to caclulate additional INFO fields from"/> <param name="pad" type="integer" min="1" value="25" label="Padding width on either side of variant for realignment" help="To calculate the additional INFO fields the tool will run medaka tools anntotate, which performs local realignment of the region +- this width around each variant. All calculated new fields will depend on the width chosen, so only change this value if you know what you are doing." /> </when> <when value="false"/> </conditional> <param name="output_log_bool" type="boolean" label="Output log file?" checked="true"/> </inputs> <outputs> <data name="out_variants" format="vcf" label="${tool.name} on ${on_string}: called variants"/> <data name="out_log" format="tabular" label="${tool.name} on ${on_string}: Log"> <filter>output_log_bool</filter> </data> </outputs> <tests> <!-- #1 default --> <test expect_num_outputs="2"> <conditional name="pool"> <param name="pool_mode" value="Yes"/> <param name="inputs" value="medaka_test.hdf,medaka_test.hdf"/> </conditional> <conditional name="reference_source"> <param name="reference_source_selector" value="history"/> <param name="ref_file" value="ref.fasta"/> </conditional> <param name="ambig_ref" value="true"/> <conditional name="output_annotated"> <param name="output_annotated_select" value="true"/> <param name="in_bam" value="medaka_test.bam"/> </conditional> <param name="output_log_bool" value="true"/> <output name="out_variants"> <assert_contents> <has_n_lines n="18"/> <has_line line="##fileformat=VCFv4.1" /> <has_line_matching expression="##medaka_version=[0-9]+\.[0-9]+\.[0-9]+" /> <has_line_matching expression="##convert_VCF_info_fields=[0-9]+\.[0-9]+" /> </assert_contents> </output> <output name="out_log"> <assert_contents> <has_n_lines n="10" /> </assert_contents> </output> </test> <!--No pooling--> <test expect_num_outputs="2"> <conditional name="pool"> <param name="pool_mode" value="No"/> <param name="input" value="medaka_test.hdf"/> </conditional> <conditional name="reference_source"> <param name="reference_source_selector" value="history"/> <param name="ref_file" value="ref.fasta.gz" ftype="fasta.gz"/> </conditional> <param name="ambig_ref" value="true"/> <conditional name="output_annotated"> <param name="output_annotated_select" value="true"/> <param name="in_bam" value="medaka_test.bam"/> </conditional> <param name="output_log_bool" value="true"/> <output name="out_variants"> <assert_contents> <has_n_lines n="18"/> <has_line line="##fileformat=VCFv4.1" /> <has_line_matching expression="##medaka_version=[0-9]+\.[0-9]+\.[0-9]+" /> <has_line_matching expression="##convert_VCF_info_fields=[0-9]+\.[0-9]+" /> </assert_contents> </output> <output name="out_log"> <assert_contents> <has_n_lines n="8" /> </assert_contents> </output> </test> <!--No annotation or log--> <test expect_num_outputs="1"> <conditional name="pool"> <param name="pool_mode" value="No"/> <param name="input" value="medaka_test.hdf"/> </conditional> <conditional name="reference_source"> <param name="reference_source_selector" value="history"/> <param name="ref_file" value="ref.fasta"/> </conditional> <conditional name="output_annotated"> <param name="output_annotated_select" value="false"/> </conditional> <param name="output_log_bool" value="false"/> <output name="out_variants"> <assert_contents> <has_n_lines n="9"/> <has_line line="##fileformat=VCFv4.1" /> <has_line_matching expression="##medaka_version=[0-9]+\.[0-9]+\.[0-9]+" /> </assert_contents> </output> </test> </tests> <help><![CDATA[ .. class:: infomark **What it does** @WID@ The module *variant* decodes probabilities. ---- .. class:: infomark **Input** - reference sequence (FASTA) - (several) consensus files (H5/HDF) ---- .. class:: infomark **Output** - decoded probabilities (VCF) ---- .. class:: infomark **References** @REFERENCES@ ]]></help> <expand macro="citations"/> </tool>