Mercurial > repos > drosofff > msp_sr_bowtie_cascade
annotate sRbowtieCascade.xml @ 3:0052d1dd31df draft default tip
planemo upload for repository https://bitbucket.org/drosofff/gedtools/
author | drosofff |
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date | Mon, 29 Jun 2015 05:54:27 -0400 |
parents | 0dfcb397699e |
children |
rev | line source |
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1 | 1 <tool id="sRbowtie_cascade" name="Annotate smRNA datasets" version="1.0.1"> |
0 | 2 <description>Using iterative sRbowtie Alignments</description> |
3 <requirements> | |
4 <requirement type="package" version="0.12.7">bowtie</requirement> | |
5 </requirements> | |
6 <command interpreter="python"> sRbowtieCascade.py --output $output | |
7 --num-threads \${GALAXY_SLOTS:-4} ## number of processors to be handled by bowtie | |
8 --mismatch $mismatches | |
9 --input | |
10 #for $i in $input: | |
11 $i | |
12 #end for | |
13 --label | |
14 #for $i in $input: | |
15 "$i.name" | |
16 #end for | |
17 --index | |
18 #if $refGenomeSource1.genomeSource == "history": | |
19 $refGenomeSource1.ownFile | |
20 #else: | |
21 $refGenomeSource1.index.fields.path | |
22 #end if | |
23 #for $i in $AdditionalQueries: | |
24 #if $i.refGenomeSource.genomeSource == "history": | |
25 $i.refGenomeSource.ownFile | |
26 #else: | |
27 $i.refGenomeSource.index.fields.path | |
28 #end if | |
29 #end for | |
30 --indexing-flags | |
31 $refGenomeSource1.genomeSource | |
32 #for $i in $AdditionalQueries: | |
33 $i.refGenomeSource.genomeSource | |
34 #end for | |
35 --indexName | |
36 #if $refGenomeSource1.genomeSource == "history": | |
37 "$refGenomeSource1.ownFile.name" | |
38 #else: | |
39 "$refGenomeSource1.index.fields.name" | |
40 #end if | |
41 #for $i in $AdditionalQueries: | |
42 #if $i.refGenomeSource.genomeSource == "history": | |
43 "$i.refGenomeSource.ownFile.name" | |
44 #else: | |
45 "$i.refGenomeSource.index.fields.name" | |
46 #end if | |
47 #end for | |
48 </command> | |
49 <inputs> | |
50 <param name="input" type="data" format="fasta" label="Input fasta file: reads clipped from their adapter" help="Only with clipped, raw fasta files" multiple="true"/> | |
51 <param name="mismatches" type="select" label="Number of mismatches allowed" help="specify the number of mismatches allowed during alignments"> | |
52 <option value="0">0</option> | |
53 <option value="1" selected="true">1</option> | |
54 <option value="2">2</option> | |
55 <option value="3">3</option> | |
56 </param> | |
57 <!-- First bowtie index selection --> | |
58 <conditional name="refGenomeSource1"> | |
59 <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"> | |
60 <option value="indexed">Use a built-in index</option> | |
61 <option value="history">Use one from the history</option> | |
62 </param> | |
63 <when value="indexed"> | |
3
0052d1dd31df
planemo upload for repository https://bitbucket.org/drosofff/gedtools/
drosofff
parents:
1
diff
changeset
|
64 <param name="index" type="select" label="Select a DNA reference index" help="if your genome of interest is not listed - contact instance administrator"> |
0 | 65 <options from_data_table="bowtie_indexes"/> |
66 </param> | |
67 </when> | |
68 <when value="history"> | |
69 <param name="ownFile" type="data" format="fasta" label="Select a fasta file, to serve as index reference" /> | |
70 </when> | |
71 </conditional> | |
72 <!-- End of first bowtie index selection --> | |
73 <!-- other bowtie index selections --> | |
74 <repeat name="AdditionalQueries" title="Additional Alignment Step"> | |
75 <conditional name="refGenomeSource"> | |
76 <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"> | |
77 <option value="indexed">Use a built-in index</option> | |
78 <option value="history">Use one from the history</option> | |
79 </param> | |
80 <when value="indexed"> | |
3
0052d1dd31df
planemo upload for repository https://bitbucket.org/drosofff/gedtools/
drosofff
parents:
1
diff
changeset
|
81 <param name="index" type="select" label="Select a DNA reference index" help="if your genome of interest is not listed - contact instance administrator"> |
0 | 82 <options from_data_table="bowtie_indexes"/> |
83 </param> | |
84 </when> | |
85 <when value="history"> | |
86 <param name="ownFile" type="data" format="fasta" label="Select a fasta file, to serve as index reference" /> | |
87 </when> | |
88 </conditional> | |
89 </repeat> | |
90 <!-- End of other bowtie index selections --> | |
91 </inputs> | |
92 <outputs> | |
93 <data format="tabular" name="output" label="Cascade Annotation Analysis"/> | |
94 </outputs> | |
95 | |
96 | |
1 | 97 <tests> |
98 <test> | |
99 <param name="input" value ="sample1.fa,sample2.fa,sample3.fa" ftype="fasta" /> | |
100 <param name="genomeSource" value="history" /> | |
101 <param name="ownFile" value ="dmel-2L-r6.04.fasta" ftype="fasta" /> | |
102 <param name="AdditionalQueries_0|refGenomeSource|genomeSource" value="history"/> | |
103 <param name="AdditionalQueries_0|refGenomeSource|ownFile" value="dme_miR21_hairpin.fa" ftype="fasta" /> | |
104 <param name="AdditionalQueries_1|refGenomeSource|genomeSource" value="history"/> | |
105 <param name="AdditionalQueries_1|refGenomeSource|ownFile" value="Ensembl_transposon_set.fa" ftype="fasta" /> | |
106 <output name="output" ftype="tabular" file="Cascade_Annotation_Analysis.tab" /> | |
107 </test> | |
108 </tests> | |
0 | 109 <help> |
110 | |
111 **Intro** | |
112 | |
113 Bowtie_ is a short read aligner designed to be ultrafast and memory-efficient. | |
114 A generic "Map with Bowtie for Illumina" Galaxy tool is available in the main Galaxy distribution. | |
115 However, this Bowtie wrapper tool only takes FASTQ files as inputs. | |
116 | |
117 Here The sRbowtie wrapper specifically works with short reads FASTA inputs (-v bowtie mode, with -k 1) | |
118 | |
119 .. _Bowtie: http://bowtie-bio.sourceforge.net/index.shtml | |
120 | |
121 | |
122 ------ | |
123 | |
124 **What it does** | |
125 | |
126 .. class:: infomark | |
127 | |
128 This script uses the sRbowtie wrapper to iteratively match reads on a reference indexes. | |
129 | |
130 Reads are Matched on DNA references as fast as possible, without taking care of mapping issues | |
131 | |
132 *-v [0,1,2,3] -k 1 --best -p 12 --suppress 6,7,8* | |
133 | |
134 unaligned reads at step N are used as input for sRbowtie at step N+1 | |
135 | |
136 ----- | |
137 | |
138 **Input formats** | |
139 | |
140 .. class:: warningmark | |
141 | |
142 *The only accepted format for the script is a raw fasta list of reads, clipped from their adapter* | |
143 | |
144 ----- | |
145 | |
146 **OUTPUTS** | |
147 | |
148 **Annotation table** | |
149 | |
150 </help> | |
151 </tool> |