# HG changeset patch # User ieguinoa # Date 1563898692 14400 # Node ID 9004217cddf4a880c415c1160ad062d1f1055bbc # Parent cbe62bd6e149b6eba83cf6abdc723ac04bb42303 Uploaded diff -r cbe62bd6e149 -r 9004217cddf4 data_manager_conf.xml --- a/data_manager_conf.xml Tue Jul 23 11:12:15 2019 -0400 +++ b/data_manager_conf.xml Tue Jul 23 12:18:12 2019 -0400 @@ -9,9 +9,9 @@ - ${dbkey}/salmon_index/${value} + ${dbkey}/salmon_index/${value}/${version} - ${GALAXY_DATA_MANAGER_DATA_PATH}/${dbkey}/salmon_index/${value}/${path} + ${GALAXY_DATA_MANAGER_DATA_PATH}/${dbkey}/salmon_index/${value}/${version} abspath diff -r cbe62bd6e149 -r 9004217cddf4 tool-data/all_fasta.loc.sample --- a/tool-data/all_fasta.loc.sample Tue Jul 23 11:12:15 2019 -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. -#