# HG changeset patch # User yhoogstrate # Date 1472201135 14400 # Node ID c53938d8a6dafbb660276c709393585de33f8021 # Parent f36e648ed12a25b294ec1be59096c8548f2b202d planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/star_fusion commit 38b164ccb9b3cdfb58d83cdc1f05063a40123bab-dirty diff -r f36e648ed12a -r c53938d8a6da all_fasta.loc.sample --- a/all_fasta.loc.sample Wed Aug 24 07:18:07 2016 -0400 +++ /dev/null Thu Jan 01 00:00:00 1970 +0000 @@ -1,18 +0,0 @@ -#This file lists the locations and dbkeys of all the fasta files -#under the "genome" directory (a directory that contains a directory -#for each build). The script extract_fasta.py will generate the file -#all_fasta.loc. This file has the format (white space characters are -#TAB characters): -# -# -# -#So, all_fasta.loc could look something like this: -# -#apiMel3 apiMel3 Honeybee (Apis mellifera): apiMel3 /path/to/genome/apiMel3/apiMel3.fa -#hg19canon hg19 Human (Homo sapiens): hg19 Canonical /path/to/genome/hg19/hg19canon.fa -#hg19full hg19 Human (Homo sapiens): hg19 Full /path/to/genome/hg19/hg19full.fa -# -#Your all_fasta.loc file should contain an entry for each individual -#fasta file. So there will be multiple fasta files for each build, -#such as with hg19 above. -# diff -r f36e648ed12a -r c53938d8a6da star_fusion.xml --- a/star_fusion.xml Wed Aug 24 07:18:07 2016 -0400 +++ b/star_fusion.xml Fri Aug 26 04:45:35 2016 -0400 @@ -1,4 +1,4 @@ - + detect fusion genes in RNA-Seq data @@ -6,6 +6,10 @@ + + + + @@ -106,7 +110,10 @@ - + + + + diff -r f36e648ed12a -r c53938d8a6da tool_data_table_conf.xml.sample --- a/tool_data_table_conf.xml.sample Wed Aug 24 07:18:07 2016 -0400 +++ /dev/null Thu Jan 01 00:00:00 1970 +0000 @@ -1,7 +0,0 @@ - - - - value, dbkey, name, path - -
-