Mercurial > repos > bcrain-completegenomics > testing1
changeset 0:8caa26b33983 draft
Uploaded
author | bcrain-completegenomics |
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date | Thu, 24 May 2012 15:05:55 -0400 |
parents | |
children | fec197eb2f00 |
files | listvariants.xml |
diffstat | 1 files changed, 118 insertions(+), 0 deletions(-) [+] |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/listvariants.xml Thu May 24 15:05:55 2012 -0400 @@ -0,0 +1,118 @@ +<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>