view test-data/fasta_indexes.loc @ 4:d09254e37c68 draft

"planemo upload for repository https://github.com/ARTbio/tools-artbio/tree/master/tools/manta commit 61062db986142ec4ba86757a724bcb9b94d9f838"
author artbio
date Mon, 08 Jun 2020 03:11:56 -0400
parents 6a69e5d7c21f
children
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#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	/path/to/genome/hg19/sam_indexes/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:
#
#hg18canon	hg18	Human (Homo sapiens): hg18 Canonical	/path/to/genome/hg18/sam_indexes/hg18canon.fa
#hg18full	hg18	Human (Homo sapiens): hg18 Full	/path/to/genome/sam_indexes/hg18full.fa
#hg19canon	hg19	Human (Homo sapiens): hg19 Canonical	/path/to/genome/hg19/sam_indexes/hg19canon.fa
#hg19full	hg19	Human (Homo sapiens): hg19 Full	/path/to/genome/hg19/sam_indexes/hg19full.fa

hg19	hg19	Human hg19	${__HERE__}/cached_locally/cached_region.fa