Mercurial > repos > rnateam > ribotaper
comparison ribotaper_part1_create_annotation_files.xml @ 0:bade631353d2 draft
planemo upload for repository https://github.com/bgruening/galaxytools/tree/master/tools/rna_tools/ribotaper/ commit 9a59864f0bfb9937309d2c18b8cf3715c8067808
author | rnateam |
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date | Wed, 30 Nov 2016 16:44:53 -0500 |
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children | 56ffbec351b3 |
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1 <tool id="ribotaper_create_annotation" name="ribotaper part 1: creation of annotation files" version="0.1.0"> | |
2 <requirements> | |
3 <requirement type="package" version="1.3.1a">ribotaper</requirement> | |
4 </requirements> | |
5 <stdio> | |
6 <exit_code range="1:" /> | |
7 </stdio> | |
8 | |
9 <command><![CDATA[ | |
10 create_annotations_files.bash | |
11 "$gtf" | |
12 "$fa" | |
13 "$ccdsid" | |
14 "$appris" | |
15 "annotation_path" | |
16 && | |
17 tar | |
18 "czvf" | |
19 "$output2" | |
20 "annotation_path" | |
21 | |
22 ]]></command> | |
23 <inputs> | |
24 <param name="gtf" type="data" format="GTF" label="GTF" | |
25 help="GTF should contain: | |
26 1) coding and non-coding genes, 2) a 'transcript_id' and a 'gene_id' field for each 'exon' and 'CDS' row. | |
27 "/> | |
28 <param name="fa" type="data" format="fasta" label="Genome fasta file" help="FASTA-format, indexed and not repeat masked."/> | |
29 <param name="ccdsid" type="boolean" falsevalue="false" truevalue="true" checked="true" label="Use ccdsid? (valid for Human Gencode 19 and Mouse Gencode M3 )" | |
30 help="If yes, only exons/transcripts with the CCDS tag will be used as CCDS exons/transcripts, otherwise all exons/transcripts with a CDS region are going to be annotated as CCDS. | |
31 "/> | |
32 <param name="appris" type="boolean" falsevalue="false" truevalue="true" checked="true" label="Use appris? (valid for Human Gencode 19 and Mouse Gencode M3 )" | |
33 help=" If yes, only exons/transcripts with the appris tag will be used, using only 1 transcript per appris gene (the appris_principal transcript or other appris transcript). If a gene does not have appris transcript, all the annotated transcript structures are used. | |
34 "/> | |
35 </inputs> | |
36 <outputs> | |
37 <data name="output1" format="bed" from_work_dir="annotation_path/start_stops_FAR.bed" label="start_stops_FAR"/> | |
38 <data name="output2" format="tar" label="annotation_path"/> | |
39 </outputs> | |
40 <tests> | |
41 <test> | |
42 <param name="gtf" value="test.gtf"/> | |
43 <param name="fa" value="test.fa"/> | |
44 <param name="ccdsid" value="true"/> | |
45 <param name="appris" value="true"/> | |
46 <output name="output1" file="annotation_path/start_stops_FAR.bed"/> | |
47 </test> | |
48 </tests> | |
49 <help><![CDATA[ | |
50 Overview | |
51 -------- | |
52 | |
53 RiboTaper is an analysis pipeline for Ribosome Profiling | |
54 (Ribo-seq) experiments, | |
55 which exploits the triplet periodicity of | |
56 ribosomal footprints to call translated regions. | |
57 See | |
58 https://ohlerlab.mdc-berlin.de/software/RiboTaper_126/ for details. | |
59 | |
60 | |
61 The Ribotaper Galaxy tool set consists of three tools: | |
62 | |
63 - ``ribotaper part 1``: creation of annotation files | |
64 - ``ribotaper part 2``: metagene analysis for P-sites definition | |
65 - ``ribotaper part 3``: ribosome profiling | |
66 | |
67 The order of execution should follow: | |
68 ``ribotaper part 1, part 2 and part 3``. | |
69 | |
70 The current tool is ``ribotaper part 1``, | |
71 creation of annotation files. | |
72 | |
73 Output | |
74 ------ | |
75 | |
76 ``Ribotaper part 1`` builds a list of exon coordinates, | |
77 exon sequences and transcript structures. | |
78 | |
79 ``Ribotaper part 1`` generates two files: | |
80 | |
81 - **start_stops_FAR** in BED format | |
82 - **annotation_path** in format of tar | |
83 | |
84 *Start_stops_FAR* | |
85 is used as an input for ``ribotaper part 2``. | |
86 *Annotation_path* | |
87 is used as an input for ``ribotaper part 3``. | |
88 | |
89 | |
90 ]]></help> | |
91 <citations> | |
92 <citation type="doi">10.1038/nmeth.3688</citation> | |
93 </citations> | |
94 </tool> |