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author | bcrain-completegenomics |
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date | Thu, 07 Jun 2012 14:50:45 -0400 |
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<tool id="cga_testvariants" name="testvariants(beta)" version="0.0.1"> <!-- This tool creates a GUI for cgatools testvariants from Complete Genomics, Inc. written 5-29-2012 by bcrain@completegenomics.com --> <description>test for the presence of variants</description> <!--adds description in toolbar--> <requirements> <requirement type="binary">cgatools</requirement> </requirements> <command> <!--run executable--> cgatools testvariants --beta --reference ${crr.fields.path} --output $output --input $listing --variants #if $file_types.data_sources.data_source == "in" #for $v in $file_types.data_sources.varfiles <!--get each var/mastervar file--> ${v.input} #end for #else `cat $file_types.data_sources.varlist` #end if </command> <outputs> <data format="tabular" name="output" /> </outputs> <inputs> <!--form field to select crr file--> <param name="crr" type="select" label="Genome build"> <options from_data_table="cg_crr_files" /> </param> <!--form fields to select variant list--> <param name="listing" type="data" format="tabular" label="Select variant list"> <validator type="unspecified_build" /> <validator type="dataset_metadata_in_file" filename="cg_crr_files.loc" metadata_name="dbkey" metadata_column="1" message="cgatools is not currently available for this build."/> </param> <!--conditional to select input file type--> <conditional name="file_types"> <param name="file_type" type="select" label="Select the input file type"> <option value="var" selected="true">var files</option> <option value="mastervar">mastervar files</option> </param> <when value="var"> <!--conditional to select variant file input--> <conditional name="data_sources"> <param name="data_source" type="select" label="Where are the input var files?"> <option value="in" selected="true">imported into Galaxy</option> <option value="out">located outside Galaxy (available only for local Galaxy instances)</option> </param> <when value="in"> <!--form field to select variant files--> <repeat name="varfiles" title="Variant files"> <param name="input" type="data" format="cg_var" label="Dataset"> <validator type="unspecified_build" /> <validator type="dataset_metadata_in_file" filename="cg_crr_files.loc" metadata_name="dbkey" metadata_column="1" message="cgatools is not currently available for this build."/> </param> </repeat> </when> <when value="out"> <!--form field to select crr file--> <param name="varlist" type="text" label="List of variant files (/path/file)" size="200" help="file with list of var files (/path/varfile), var files can be compressed (gz, bz2)."/> </when> </conditional> </when> <when value="mastervar"> <!--conditional to select variant file input--> <conditional name="data_sources"> <param name="data_source" type="select" label="Where are the input mastervar files?"> <option value="in" selected="true">imported into Galaxy</option> <option value="out">located outside Galaxy (available only for local Galaxy instances)</option> </param> <when value="in"> <!--form field to select variant files--> <repeat name="varfiles" title="Variant files"> <param name="input" type="data" format="cg_mastervar" label="Dataset"> <validator type="unspecified_build" /> <validator type="dataset_metadata_in_file" filename="cg_crr_files.loc" metadata_name="dbkey" metadata_column="1" message="cgatools is not currently available for this build."/> </param> </repeat> </when> <when value="out"> <!--form field to select crr file--> <param name="varlist" type="text" label="List of mastervar files (/path/file)" size="200" help="file with list of mastervar files (/path/varfile), mastervar files can be compressed (gz, bz2)."/> </when> </conditional> </when> </conditional> </inputs> <help> **What it does** This tool uses the cgatools testvariants to test variant or mastervar files for the presence of variants. cgatools: http://sourceforge.net/projects/cgatools/files/ ----- **cgatools Manual**:: COMMAND NAME testvariants - Tests variant files for presence of variants. DESCRIPTION Tests variant files for presence of variants. The output is a tab-delimited file consisting of the columns of the input variants file, plus a column for each assembly results file that contains a character code for each allele. The character codes have meaning as follows: 0 This allele of this genome is consistent with the reference at this locus but inconsistent with the variant. 1 This allele of this genome has the input variant at this locus. N This allele of this genome has no-calls but is consistent with the input variant. 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. --input arg (=STDIN) The input variants to test for. --output arg (=STDOUT) The output file (may be omitted for stdout). --variants arg The input variant files (may be passed in as arguments at the end of the command). SUPPORTED FORMAT_VERSION 0.3 or later </help> </tool>