view test-data/fasta_indexes.loc @ 0:e46944a59b31 draft

"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/freec commit bec4fb59dc4776d33c2ce8c0bd614c90e5d4ecb2"

#This is a sample file distributed with Galaxy that enables tools
#to use a directory of Samtools indexed sequences data files.  You will need
#to create these data files and then create a fasta_indexes.loc file
#similar to this one (store it in this directory) that points to
#the directories in which those files are stored. The fasta_indexes.loc
#file has this format (white space characters are TAB characters):
#
# <unique_build_id>	<dbkey>	<display_name>	<file_base_path>
#
#So, for example, if you had hg19 Canonical indexed stored in
#
# /depot/data2/galaxy/hg19/sam/,
#
#then the fasta_indexes.loc entry would look like this:
#
#hg19canon	hg19	Human (Homo sapiens): hg19 Canonical	/depot/data2/galaxy/hg19/sam/hg19canon.fa
#
#and your /depot/data2/galaxy/hg19/sam/ directory
#would contain hg19canon.fa and hg19canon.fa.fai files.
#
#Your fasta_indexes.loc file should include an entry per line for
#each index set you have stored.  The file in the path does actually
#exist, but it should never be directly used. Instead, the name serves
#as a prefix for the index file.  For example:
#
test_buildid	hg17	test_displayname	${__HERE__}/genome.fasta