Mercurial > repos > devteam > rmapq
comparison tool-data/faseq.loc.sample @ 0:f6e5bb5aa2f5 draft
Imported from capsule None
| author | devteam |
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| date | Mon, 19 May 2014 12:34:22 -0400 |
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| -1:000000000000 | 0:f6e5bb5aa2f5 |
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| 1 #This is a sample file distributed with Galaxy that enables tools | |
| 2 #to use genome fasta sequence files. The faseq.loc file has this format | |
| 3 #(white space characters are TAB characters): | |
| 4 # | |
| 5 # <GenomeBuild> <dir> | |
| 6 # | |
| 7 # In the dir, each file is fasta format and contains only one sequence. So, | |
| 8 #for example, if you had hg18 fasta sequences stored in /depot/data2/galaxy/faseq/hg18, | |
| 9 #then your faseq.loc entry would look like this: | |
| 10 # | |
| 11 #hg18 /depot/data2/galaxy/faseq/hg18 | |
| 12 # | |
| 13 #and your /depot/data2/galaxy/faseq/hg18 directory would contain all of | |
| 14 #your fasta sequence files (e.g.): | |
| 15 # | |
| 16 #-rw-r--r-- 1 wychung galaxy 138082251 2008-04-16 11:57 chr10.fa | |
| 17 #-rw-r--r-- 1 wychung galaxy 115564 2008-04-16 11:57 chr10_random.fa | |
| 18 #-rw-r--r-- 1 wychung galaxy 137141451 2008-04-16 11:58 chr11.fa | |
| 19 #...etc... | |
| 20 #Your faseq.loc file should include an entry per line for each set of fasta | |
| 21 #sequence files you have stored. For example: | |
| 22 # | |
| 23 #hg18 /depot/data2/galaxy/faseq/hg18 | |
| 24 #mm9 /depot/data2/galaxy/faseq/mm9 | |
| 25 #Arabidopsis /depot/data2/galaxy/faseq/Arabidopsis | |
| 26 #...etc... |
