Mercurial > repos > bcrain-completegenomics > testing1
changeset 3:a2b8590be75e draft
Deleted selected files
author | bcrain-completegenomics |
---|---|
date | Thu, 24 May 2012 15:17:00 -0400 |
parents | 3a4894be7df2 |
children | cd57fc5f9ca0 |
files | listvariants.xml |
diffstat | 1 files changed, 0 insertions(+), 118 deletions(-) [+] |
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--- a/listvariants.xml Thu May 24 15:16:40 2012 -0400 +++ /dev/null Thu Jan 01 00:00:00 1970 +0000 @@ -1,118 +0,0 @@ -<tool id="cga_listvariant" name="listvariants" version="0.0.1"> - - <description>lists all called variants</description> <!--adds description in toolbar--> - - <command> <!--run executable--> - cgatools listvariants - --beta - --reference ${crr.fields.path} - --output $output - --variants - #for $v in $varfiles <!--get each var file--> - ${v.input} - #end for - #if $include_list.listing == "yes" <!--only added when yes--> - --variant-listing $include_list.list - #end if - $longvar - </command> - - <inputs> - <!--form field to select crr file--> - <param name="crr" type="select" label="Genome build"> - <options from_data_table="cgatools" /> - </param> - - <!--form field to select long variants option--> - <param name="longvar" type="select" label="List long variants?"> - <option value="" selected="true">no</option> - <option value="--list-long-variants">yes</option> - </param> - - <!--form fields to include existing variant list--> - <conditional name="include_list"> - <param name="listing" type="select" label="Include variant listing?"> - <option value="no" selected="true">no</option> - <option value="yes">yes</option> - </param> - <when value="yes"> - <param name="list" type="data" format="tabular" label="Variant listing"/> - </when> - </conditional> - - <!--form field to select all variant files--> - <repeat name="varfiles" title="Var file"> - <param name="input" type="data" format="tabular" label="Dataset"> - <validator type="unspecified_build" /> - <validator type="dataset_metadata_in_file" filename="cgatools.loc" - metadata_name="dbkey" metadata_column="0" - message="cgatools is not currently available for this build."/> - </param> - </repeat> - </inputs> - - <outputs> - <data format="tabular" name="output" /> - </outputs> - - <help> - -**What it does** - -This tool uses the cgatools listvariants to list all called variants present in the var or mastervar files. - -cgatools: http://sourceforge.net/projects/cgatools/files/ - ------ - -**cgatools Manual**:: - - COMMAND NAME - listvariants - Lists the variants present in a variant file. - - DESCRIPTION - Lists all called variants present in the specified variant files, in a - format suitable for processing by the testvariants command. The output is a - tab-delimited file consisting of the following columns: - - variantId Sequential id assigned to each variant. - chromosome The chromosome of the variant. - begin 0-based reference offset of the beginning of the variant. - end 0-based reference offset of the end of the variant. - varType The varType as extracted from the variant file. - reference The reference sequence. - alleleSeq The variant allele sequence as extracted from the variant - file. - xRef The xRef as extrated from the variant file. - - OPTIONS - -h [ --help ] - Print this help message. - - --beta - This is a beta command. To run this command, you must pass the --beta - flag. - - --reference arg - The reference crr file. - - --output arg (=STDOUT) - The output file (may be omitted for stdout). - - --variants arg - The input variant files (may be positional args). - - --variant-listing arg - The output of another listvariants run, to be merged in to produce the - output of this run. - - --list-long-variants - In addition to listing short variants, list longer variants as well - (10's of bases) by concatenating nearby calls. - - - - SUPPORTED FORMAT_VERSION - 0.3 or later - </help> -</tool>