Mercurial > repos > devteam > rmap
comparison tool-data/faseq.loc.sample @ 0:ee49255302d8 draft
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author | devteam |
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date | Mon, 19 May 2014 12:33:09 -0400 |
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-1:000000000000 | 0:ee49255302d8 |
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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... |