# 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.
-#