Mercurial > repos > yufei-luo > s_mart
annotate SMART/galaxy/CollapseReads.xml @ 71:d96f6c9a39e0 draft default tip
Removed pyc files.
author | m-zytnicki |
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date | Thu, 07 Apr 2016 09:25:18 -0400 |
parents | 1473ab954708 |
children |
rev | line source |
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38 | 1 <tool id="collapseReads" name="collapse reads"> |
2 <description>Merges two genomic features if they have exactly the same genomic coordinates.</description> | |
3 <requirements> | |
4 <requirement type="set_environment">PYTHONPATH</requirement> | |
5 </requirements> | |
6 <command interpreter="python"> | |
7 ../Java/Python/CollapseReads.py -i $formatType.inputFileName | |
8 #if $formatType.FormatInputFileName == 'bed': | |
9 -f bed | |
10 #elif $formatType.FormatInputFileName == 'gff': | |
11 -f gff | |
12 #elif $formatType.FormatInputFileName == 'gff2': | |
13 -f gff2 | |
14 #elif $formatType.FormatInputFileName == 'gff3': | |
15 -f gff3 | |
16 #elif $formatType.FormatInputFileName == 'sam': | |
17 -f sam | |
56 | 18 #elif $formatType.FormatInputFileName == 'bam': |
19 -f bam | |
38 | 20 #elif $formatType.FormatInputFileName == 'gtf': |
21 -f gtf | |
22 #end if | |
69
1473ab954708
Corrected bug in "CollapsedReads" XML file.
m-zytnicki
parents:
56
diff
changeset
|
23 $strand |
38 | 24 -o $outputFileGff |
25 </command> | |
26 | |
27 <inputs> | |
28 <conditional name="formatType"> | |
29 <param name="FormatInputFileName" type="select" label="Input File Format"> | |
30 <option value="bed">bed</option> | |
31 <option value="gff">gff</option> | |
32 <option value="gff2">gff2</option> | |
33 <option value="gff3">gff3</option> | |
34 <option value="sam">sam</option> | |
56 | 35 <option value="bam">bam</option> |
38 | 36 <option value="gtf">gtf</option> |
37 </param> | |
38 <when value="bed"> | |
39 <param name="inputFileName" format="bed" type="data" label="Input File"/> | |
40 </when> | |
41 <when value="gff"> | |
42 <param name="inputFileName" format="gff" type="data" label="Input File"/> | |
43 </when> | |
44 <when value="gff2"> | |
45 <param name="inputFileName" format="gff2" type="data" label="Input File"/> | |
46 </when> | |
47 <when value="gff3"> | |
48 <param name="inputFileName" format="gff3" type="data" label="Input File"/> | |
49 </when> | |
50 <when value="sam"> | |
51 <param name="inputFileName" format="sam" type="data" label="Input File"/> | |
52 </when> | |
56 | 53 <when value="bam"> |
54 <param name="inputFileName" format="bam" type="data" label="Input File"/> | |
55 </when> | |
38 | 56 <when value="gtf"> |
57 <param name="inputFileName" format="gtf" type="data" label="Input File"/> | |
58 </when> | |
59 </conditional> | |
60 | |
61 <param name="strand" type="boolean" truevalue="-s" falsevalue="" checked="false" label="Merges features even if they are on different strands."/> | |
62 </inputs> | |
63 | |
64 <outputs> | |
65 <data name="outputFileGff" format="gff3"/> | |
66 </outputs> | |
67 | |
68 <help> | |
69 Merge two input genomic coordinates iff they are exactly the same. If two or more genomic coordinates are merged, the tag **nbElements** is updated accordingly. As a consequence, all the reads which are exactly the same appear as one genomic coordinate. | |
70 | |
71 This is especially useful for short RNA sequencing (where you want to count the number of read per miRNA, siRNA, etc.) or 5' capped short reads. | |
72 </help> | |
73 </tool> |