Mercurial > repos > yufei-luo > s_mart
comparison SMART/galaxy/coordinatesToSequence.xml @ 31:0ab839023fe4
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author | m-zytnicki |
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date | Tue, 30 Apr 2013 14:33:21 -0400 |
parents | 94ab73e8a190 |
children |
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30:5677346472b5 | 31:0ab839023fe4 |
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1 <tool id="coordinatesToSequence" name="coordinates to sequence"> | 1 <tool id="coordinatesToSequence" name="coordinates to sequence"> |
2 <description>Coordinates to Sequences: Extract the sequences from a list of coordinates.</description> | 2 <description>Coordinates to Sequences: Extract the sequences from a list of coordinates.</description> |
3 <requirements> | |
4 <requirement type="set_environment">PYTHONPATH</requirement> | |
5 </requirements> | |
6 <command interpreter="python"> | 3 <command interpreter="python"> |
7 ../Java/Python/coordinatesToSequence.py -i $formatType.inputFileName1 | 4 ../Java/Python/coordinatesToSequence.py -i $formatType.inputFileName1 |
8 #if $formatType.FormatInputFileName1 == 'bed': | 5 #if $formatType.FormatInputFileName1 == 'bed': |
9 -f bed | 6 -f bed |
10 #elif $formatType.FormatInputFileName1 == 'gff': | 7 #elif $formatType.FormatInputFileName1 == 'gff': |
60 | 57 |
61 <outputs> | 58 <outputs> |
62 <data name="outputFileFasta" format="fasta" label="coordinates to sequences output"/> | 59 <data name="outputFileFasta" format="fasta" label="coordinates to sequences output"/> |
63 </outputs> | 60 </outputs> |
64 | 61 |
65 <help> | |
66 You can use this tool, if you just want to convert your mapping data to genomic coordinates, without any filtering. It requires a genomic coordinates file together with its format, an output format (GFF3, BED, etc...), the genome, and prints you the corresponding file. | |
67 </help> | |
68 </tool> | 62 </tool> |