# HG changeset patch # User yhoogstrate # Date 1447231865 18000 # Node ID 64017ce705b6c730636e9cbe9934995fb4735c18 # Parent 418343b53afd8584fae5dd70f90e9fe4de2a02f1 planemo upload for repository https://bitbucket.org/EMCbioinf/galaxy-tool-shed-tools commit c475b4222a15cdadc6085865f4d13426249fec25-dirty diff -r 418343b53afd -r 64017ce705b6 datatypes_conf.xml --- a/datatypes_conf.xml Tue Nov 10 11:18:20 2015 -0500 +++ b/datatypes_conf.xml Wed Nov 11 03:51:05 2015 -0500 @@ -12,6 +12,7 @@ + diff -r 418343b53afd -r 64017ce705b6 lib/galaxy/datatypes/completegenomics.py --- a/lib/galaxy/datatypes/completegenomics.py Tue Nov 10 11:18:20 2015 -0500 +++ b/lib/galaxy/datatypes/completegenomics.py Wed Nov 11 03:51:05 2015 -0500 @@ -14,6 +14,7 @@ from galaxy.datatypes import tabular from galaxy.datatypes.metadata import MetadataElement from galaxy.datatypes.tabular import Tabular +from galaxy.datatypes.binary import Binary import galaxy_utils.sequence.vcf from galaxy.datatypes.sniff import * @@ -69,3 +70,15 @@ def display_peek( self, dataset ): """Returns formated html of peek""" return Tabular.make_html_table( self, dataset, column_names=self.column_names ) + +class CRR( Binary ): + file_ext = "crr" + + def sniff( self, filename ): + try: + header = open( filename ).read(4) + if binascii.b2a_hex( header ) == binascii.hexlify( 'CRR\n' ): + return True + return False + except: + return False diff -r 418343b53afd -r 64017ce705b6 lib/galaxy/datatypes/completegenomics.pyc Binary file lib/galaxy/datatypes/completegenomics.pyc has changed diff -r 418343b53afd -r 64017ce705b6 tools/cgatools17/listvariants_v17.xml --- a/tools/cgatools17/listvariants_v17.xml Tue Nov 10 11:18:20 2015 -0500 +++ b/tools/cgatools17/listvariants_v17.xml Wed Nov 11 03:51:05 2015 -0500 @@ -1,75 +1,92 @@ - Lists all variants present in CG var or masterVar file + Lists all variants present in CG var or masterVar file + + + cgatools17 + - - cgatools17 - + cgatools | head -1 + + + cgatools + listvariants + --beta - - echo \$PATH; - cgatools | head -1; - cgatools listvariants - --beta - --reference ${crr.fields.crr_path} - --output $output - #if $include_list.listing == "yes" - --variant-listing $include_list.list - #end if - $longvar - --variants - #for $v in $file_types.varfiles - ${v.input} - #end for + #if $reference_gene_sets_source.source_select == "indexed_filtered" + ${reference_gene_sets_source.crr.fields.crr_path} + #else if $reference_gene_sets_source.source_select == "history" + ${reference_gene_sets_source.crr} + #end if + + --output $output + #if $include_list.listing == "yes" + --variant-listing $include_list.list + #end if + $longvar + --variants + #for $v in $file_types.varfiles + ${v.input} + #end for - - - - - - - - + - - - - - - - - - - - - - - - - + + + + + + + + + + + + + + + + - - - - + + + + + + + + + + + + + + + + - - - - - - - - - - - + + + + + + + + + + + + + + + + - - - + + + - + **What it does** This tool uses the cgatools listvariants to list all called variants present in the var or mastervar files. @@ -82,50 +99,50 @@ **Command line reference**:: - COMMAND NAME - listvariants - Lists the variants present in a variant file. + 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. + 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. + OPTIONS + -h [ --help ] + Print this help message. - --beta - This is a beta command. To run this command, you must pass the --beta - flag. + --beta + This is a beta command. To run this command, you must pass the --beta + flag. - --reference arg - The reference crr file. + --reference arg + The reference crr file. - --output arg (=STDOUT) - The output file (may be omitted for stdout). + --output arg (=STDOUT) + The output file (may be omitted for stdout). - --variants arg - The input variant files (may be positional args). + --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. + --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. + --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 - + SUPPORTED FORMAT_VERSION + 0.3 or later + diff -r 418343b53afd -r 64017ce705b6 tools/cgatools17/testvariants_v17.xml --- a/tools/cgatools17/testvariants_v17.xml Tue Nov 10 11:18:20 2015 -0500 +++ b/tools/cgatools17/testvariants_v17.xml Wed Nov 11 03:51:05 2015 -0500 @@ -11,7 +11,7 @@ cgatools testvariants --beta --reference - + #if $reference_gene_sets_source.source_select == "indexed_filtered" ${reference_gene_sets_source.crr.fields.crr_path} #else if $reference_gene_sets_source.source_select == "history" @@ -30,7 +30,7 @@ - +