Mercurial > repos > iuc > crossmap_vcf
diff crossmap_vcf.xml @ 1:a40d9af7d058 draft
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/crossmap commit e365f2835488e73b870c73502c24ff23d28b76a5
author | iuc |
---|---|
date | Fri, 20 Oct 2017 02:51:15 -0400 |
parents | 734eedede47c |
children | 7a3c34157901 |
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--- a/crossmap_vcf.xml Tue Sep 26 05:45:41 2017 -0400 +++ b/crossmap_vcf.xml Fri Oct 20 02:51:15 2017 -0400 @@ -8,70 +8,65 @@ <expand macro="version_command"/> <command><![CDATA[ - #set $input_file = str($seq_source.input) +#set $input_file = str($seq_source.input) - CrossMap.py - vcf +CrossMap.py vcf - #if $seq_source.index_source == "cached" - <!-- This is the 2nd dbkey, and the corresponding value has to be looked up --> - "${filter(lambda x: str( x[1] ) == str($chain_source.input_chain ), $__app__.tool_data_tables['liftOver'].get_fields())[0][2] }" - #else - "$chain_source.input_chain" - #end if +#if $seq_source.index_source_s == "cached" + ## This is the 2nd dbkey, and the corresponding value has to be looked up + "${filter(lambda x: str( x[1] ) == str($chain_source.input_chain ), $__app__.tool_data_tables['liftOver'].get_fields())[0][2] }" +#else + '${chain_source.input_chain}' +#end if - '${input_file}' - '${seq_source.input_fasta}' +'${input_file}' +'${seq_source.input_fasta}' - '${output}' +'${output}' - && mv "${output}.unmap" "$output_unmapped" +&& mv '${output}.unmap' '$output_unmapped' ]]></command> <inputs> <conditional name="seq_source"> - <expand macro="source" /> - + <param name="index_source_s" type="select" label="Source for Input Data"> + <option value="cached">Local data (in galaxy)</option> + <option value="history">From History</option> + </param> <when value="cached"> - <param type="data" format="vcf" name="input" label="VCF file"> + <param name="input" type="data" format="vcf" label="VCF file"> + <!-- <validator type="unspecified_build"/> + --> <!-- Gives error in tests <validator type="dataset_metadata_in_file" filename="liftOver.loc" metadata_name="dbkey" metadata_column="0" message="LiftOver mapping (chain file) is not available for the specified build."/> --> </param> - <!-- automatically fetch a FASTA file from the same DBKEY as the chain file --> <param name="input_fasta" type="select" label="Lift Over To (FASTA file)" help="The FASTA file must be on the same build (dbkey) as the LiftOver chain file"> - <options from_file="all_fasta.loc"> - <column name="name" index="2"/> - <column name="value" index="3"/> - <column name="dbkey" index="1"/> - <filter type="param_value" ref="input_chain" column="1"/> - </options> + <options from_data_table="all_fasta"/> </param> </when> <when value="history"> - <param type="data" format="vcf" name="input" label="VCF file"/> - <param type="data" format="fasta" name="input_fasta" multiple="false" label="Full genome FASTA file"/> + <param name="input" type="data" format="vcf" label="VCF file"/> + <param name="input_fasta" type="data" format="fasta" label="Full genome FASTA file"/> </when> </conditional> <expand macro="chain" /> - </inputs> <outputs> - <data format="vcf" name="output" label="${tool.name} on ${on_string}" /> - <data format="vcf" name="output_unmapped" label="${tool.name} (unmapped) on ${on_string}" /> + <data name="output" format="vcf" label="${tool.name} on ${on_string}" /> + <data name="output_unmapped" format="vcf" label="${tool.name} (unmapped) on ${on_string}" /> </outputs> <tests> - <!-- VCF --> <test> - <param name="index_source" value="history_all"/> + <param name="index_source_s" value="history"/> <param name="input" value="test_vcf_01_input.vcf" ftype="vcf"/> - <param name="input_chain" value="test_vcf_01.over.chain" ftype="csv"/> + <param name="index_source" value="history"/> <param name="input_fasta" value="test_vcf_01.fasta" ftype="fasta"/> - <param name="include_fails" value="False"/> + <param name="input_chain" value="test_vcf_01.over.chain" ftype="csv"/> <output name="output"> <assert_contents> @@ -93,25 +88,24 @@ VCF --- - VCF (variant call format) is a flexible and extendable line-oriented - text format developed by the 1000 Genome Project. It is useful for - representing single nucleotide variants, indels, copy number - variants, and structural variants. Chromosomes, coordinates, and - reference alleles are updated to a new assembly, and all the other - fields are not changed. +VCF (variant call format) is a flexible and extendable line-oriented +text format developed by the 1000 Genome Project. It is useful for +representing single nucleotide variants, indels, copy number +variants, and structural variants. Chromosomes, coordinates, and +reference alleles are updated to a new assembly, and all the other +fields are not changed. - NOTE: +Notes: - - Genome coordinates and reference allele will be updated to target assembly. - - Reference genome is genome sequence of target assembly. - - If the reference genome sequence file (../database/genome/hg18.fa) was - not indexed, CrossMap will automatically indexed it (only the first time - you run CrossMap). - - In the output VCF file, whether the chromosome IDs contain “chr” or not - depends on the format of the input VCF file. +- Genome coordinates and reference allele will be updated to target assembly. +- Reference genome is genome sequence of target assembly. +- If the reference genome sequence file (../database/genome/hg18.fa) was + not indexed, CrossMap will automatically indexed it (only the first time + you run CrossMap). +- In the output VCF file, whether the chromosome IDs contain “chr” or not + depends on the format of the input VCF file. -Please see `the manual <http://crossmap.sourceforge.net/#convert-vcf-format-files>`__ for more details -]]></help> + ]]></help> <citations> <citation type="doi">10.1093/bioinformatics/btt730</citation>