Mercurial > repos > jjohnson > snpsift
view snpSift_annotate.xml @ 8:2f40467536cf draft
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tool_collections/snpsift/snpsift commit 93465571cf180554c3548338a68fa0f1604985dc-dirty
author | jjohnson |
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date | Sat, 09 Apr 2016 11:53:30 -0400 |
parents | 824f78c0d0df |
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<tool id="snpSift_annotate" name="SnpSift Annotate" version="@WRAPPER_VERSION@.0"> <description>SNPs from dbSnp</description> <!-- You can change the amount of memory used, just change the -Xmx parameter (e.g. use -Xmx2G for 2Gb of memory) --> <macros> <import>snpSift_macros.xml</import> </macros> <expand macro="requirements" /> <expand macro="stdio" /> <expand macro="version_command" /> <command><![CDATA[ java -Xmx6G -jar "\$SNPEFF_JAR_PATH/SnpSift.jar" $annotate_cmd #if $annotate.id : -id #elif str($annotate.info_ids).strip() != '' : -info "$annotate.info_ids" #end if -q "$dbSnp" "$input" > "$output" ]]> </command> <inputs> <param format="vcf" name="input" type="data" label="Variant input file in VCF format"/> <param format="vcf" name="dbSnp" type="data" label="VCF File with ID field annotated (e.g. dnSNP.vcf)" help="The ID field for a variant in input will be assigned from a matching variant in this file."/> <conditional name="annotate"> <param name="id" type="boolean" truevalue="id" falsevalue="info" checked="True" label="Only annotate ID field (do not add INFO field)" help=""/> <when value="id"/> <when value="info"> <param name="info_ids" type="text" value="" optional="true" label="Limit INFO annotation to these INFO IDs" help="list is a comma separated list of fields. When blank, all INFO fields are included"> <validator type="regex" message="IDs separted by commas">^(([a-zA-Z][a-zA-Z0-9_-]*)(,[a-zA-Z][a-zA-Z0-9_-]*)*)?$</validator> </param> </when> </conditional> <param name="annotate_cmd" type="boolean" truevalue="annMem" falsevalue="annotate" checked="false" label="Allow unsorted VCF files"> <help> This option will load the entire 'database' VCF file into memory (which may not be practical for large 'database' VCF files). Otherwise, both the database and the input VCF files should be sorted by position (Chromosome sort order can differ between files). </help> </param> </inputs> <outputs> <data format="vcf" name="output" /> </outputs> <tests> <test> <param name="input" ftype="vcf" value="annotate_1.vcf"/> <param name="dbSnp" ftype="vcf" value="db_test_1.vcf"/> <param name="annotate_cmd" value="False"/> <param name="id" value="True"/> <output name="output"> <assert_contents> <has_text text="rs76166080" /> </assert_contents> </output> </test> </tests> <help><![CDATA[ This is typically used to annotate IDs from dbSnp. Annotatating only the ID field from dbSnp137.vcf :: Input VCF: CHROM POS ID REF ALT QUAL FILTER INFO 22 16157571 . T G 0.0 FAIL NS=53 22 16346045 . T C 0.0 FAIL NS=244 22 16350245 . C A 0.0 FAIL NS=192 Annotated Output VCF: #CHROM POS ID REF ALT QUAL FILTER INFO 22 16157571 . T G 0.0 FAIL NS=53 22 16346045 rs56234788 T C 0.0 FAIL NS=244 22 16350245 rs2905295 C A 0.0 FAIL NS=192 Annotatating both the ID and INFO fields from dbSnp137.vcf :: Input VCF: #CHROM POS ID REF ALT QUAL FILTER INFO 22 16157571 . T G 0.0 FAIL NS=53 22 16346045 . T C 0.0 FAIL NS=244 22 16350245 . C A 0.0 FAIL NS=192 Annotated Output VCF: #CHROM POS ID REF ALT QUAL FILTER INFO 22 16157571 . T G 0.0 FAIL NS=53 22 16346045 rs56234788 T C 0.0 FAIL NS=244;RSPOS=16346045;GMAF=0.162248628884826;dbSNPBuildID=129;SSR=0;SAO=0;VP=050100000000000100000100;WGT=0;VC=SNV;SLO;GNO 22 16350245 rs2905295 C A 0.0 FAIL NS=192;RSPOS=16350245;GMAF=0.230804387568556;dbSNPBuildID=101;SSR=1;SAO=0;VP=050000000000000100000140;WGT=0;VC=SNV;GNO @EXTERNAL_DOCUMENTATION@ http://snpeff.sourceforge.net/SnpSift.html#annotate ]]> </help> <expand macro="citations" /> </tool>