Mercurial > repos > drosofff > msp_sr_bowtie_parser
annotate sRbowtieParser.xml @ 4:2c7f42686440 draft
planemo upload for repository https://bitbucket.org/drosofff/gedtools/
author | mvdbeek |
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date | Thu, 11 Jun 2015 12:35:45 -0400 |
parents | 3fcc752a7101 |
children | aa3620d405b1 |
rev | line source |
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4
2c7f42686440
planemo upload for repository https://bitbucket.org/drosofff/gedtools/
mvdbeek
parents:
3
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changeset
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1 <tool id="sRbowtieParser" name="Parse items in sRbowtie alignment" version="1.0.3"> |
0 | 2 <description></description> |
3 <requirements> | |
4 <requirement type="package" version="0.12.7">bowtie</requirement> | |
3
3fcc752a7101
planemo upload for repository https://bitbucket.org/drosofff/gedtools/
mvdbeek
parents:
2
diff
changeset
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5 <requirement type="package" version="1.2">samtools</requirement> |
0 | 6 <requirement type="package" version="0.7.7">pysam</requirement> |
4
2c7f42686440
planemo upload for repository https://bitbucket.org/drosofff/gedtools/
mvdbeek
parents:
3
diff
changeset
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7 <requirement type="package" version="2.7">python</requirement> |
2c7f42686440
planemo upload for repository https://bitbucket.org/drosofff/gedtools/
mvdbeek
parents:
3
diff
changeset
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8 <requirement type="package" version="0.14">scipy</requirement> |
0 | 9 </requirements> |
10 <command interpreter="python"> | |
11 sRbowtieParser.py | |
12 #if $refGenomeSource.genomeSource == "history": | |
13 --IndexSource $refGenomeSource.ownFile | |
14 --ExtractDirective fastaSource | |
15 #else: | |
16 #silent reference= filter( lambda x: str( x[0] ) == str( $input_list.dbkey ), $__app__.tool_data_tables[ 'bowtie_indexes' ].get_fields() )[0][-1] | |
17 --IndexSource $reference | |
18 --ExtractDirective bowtieIndex | |
19 #end if | |
20 --output $output | |
21 --polarity $polarity | |
22 --alignmentSource | |
23 #for $i in $refGenomeSource.input_list | |
24 $i | |
25 #end for | |
26 --alignmentFormat | |
27 #for $i in $refGenomeSource.input_list | |
28 $i.ext | |
29 #end for | |
30 --alignmentLabel | |
31 #for $i in $refGenomeSource.input_list | |
32 "$i.name" | |
33 #end for | |
34 | |
35 </command> | |
36 <inputs> | |
37 <conditional name="refGenomeSource"> | |
38 <param name="genomeSource" type="select" label="Will you select a reference genome from your history or use a built-in index?" help="Built-ins were indexed using default options"> | |
39 <option value="indexed">Use a built-in index</option> | |
40 <option value="history">Use one from the history</option> | |
41 </param> | |
42 <when value="indexed"> | |
43 <param name="input_list" type="data" label="Select multiple alignments to parse" multiple="true"> | |
44 <validator type="dataset_metadata_in_data_table" table_name="bowtie_indexes" metadata_name="dbkey" metadata_column="0" message="database not set for this bowtie output. Select the database(=genome used for matching) manually, or select a reference fasta from your history."/> | |
45 </param> | |
46 </when> | |
47 <when value="history"> | |
48 <param name="ownFile" type="data" format="fasta" label="Select the fasta reference" /> | |
49 <param name="input_list" type="data" label="Select multiple alignments to parse" multiple="true"/> | |
50 </when> | |
51 </conditional> <!-- refGenomeSource --> | |
52 <param name="polarity" type="select" label="how to count sense and antisense reads"> | |
53 <option value="both">count both sense and antisense reads</option> | |
54 <option value="forward">count only sense reads</option> | |
55 <option value="reverse">count only antisense reads</option> | |
56 </param> | |
57 </inputs> | |
58 <outputs> | |
59 <data format="tabular" name="output" label="Read Count Lists"/> | |
60 </outputs> | |
61 <help> | |
62 | |
63 **What it does** | |
64 | |
65 Parses read counts from one or several sRBowtie alignments (in tabular, Sam or Bam format). | |
66 Here a bowtie match done against an index composed of a set of items is parsed and expressed as a hit list of the corresponding items | |
67 | |
68 Sense, antisense or both sense and antisense alignments can be counted | |
69 | |
70 The library labels are infered from the input dataset names in the galaxy history. | |
71 | |
72 **It is thus essential that input datasets are appropriately renamed** | |
73 | |
74 **it is preferable that you do not put any space in this input dataset names. You may edit these names in the history** | |
75 | |
76 </help> | |
1 | 77 <tests> |
78 <test> | |
0 | 79 <param name="genomeSource" value="history" /> |
80 <param name="ownFile" value ="dme-mir-v20" ftype="fasta" /> | |
1 | 81 <param name="input_list" value="matchedSample_1,matchedSample_2" ftype="tabular" /> |
0 | 82 <param name="polarity" value="forward" /> |
1 | 83 <output name="output" ftype="tabular" file="Read_Count_Lists.tab" /> |
84 </test> | |
85 </tests> | |
0 | 86 </tool> |
87 |