Mercurial > repos > iuc > delly_merge
comparison macros.xml @ 0:6331d804f983 draft
"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/delly commit 86ada42b811af0262618636f2d8d1788274f9884"
author | iuc |
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date | Mon, 28 Sep 2020 07:45:03 +0000 |
parents | |
children | 97c7441aed0d |
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-1:000000000000 | 0:6331d804f983 |
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1 <?xml version="1.0"?> | |
2 <macros> | |
3 <token name="@TOOL_VERSION@">0.8.3</token> | |
4 <token name="@DESCRIPTION@"></token> | |
5 <xml name="requirements"> | |
6 <requirements> | |
7 <requirement type="package" version="@TOOL_VERSION@">delly</requirement> | |
8 <requirement type="package" version="1.10.2">bcftools</requirement> | |
9 </requirements> | |
10 </xml> | |
11 <xml name="version_command"> | |
12 <version_command><![CDATA[delly -v 2>&1 | grep 'Delly version' | cut -f 3 -d ' ']]></version_command> | |
13 </xml> | |
14 <xml name="citations"> | |
15 <citations> | |
16 <citation type="doi">10.1093/bioinformatics/bts378</citation> | |
17 </citations> | |
18 </xml> | |
19 | |
20 <!-- | |
21 input | |
22 --> | |
23 | |
24 <xml name="exclude"> | |
25 <param argument="--exclude" type="data" format="tabular" optional="true" label="Select file with regions to exclude"/> | |
26 </xml> | |
27 <xml name="genome"> | |
28 <param argument="--genome" type="data" format="fasta" label="Select genome"/> | |
29 </xml> | |
30 <xml name="genoqual"> | |
31 <param name="genoqual" type="integer" value="5" label="Set minimum mapping quality for genotyping" help="(--geno-qual)"/> | |
32 </xml> | |
33 <xml name="minclip"> | |
34 <param argument="--minclip" type="integer" value="25" label="Set minimum clipping length"/> | |
35 </xml> | |
36 <xml name="maxreadsep"> | |
37 <param argument="--maxreadsep" type="integer" value="40" label="Set maximum read separation"/> | |
38 </xml> | |
39 <xml name="minrefsep"> | |
40 <param argument="--minrefsep" type="integer" value="25" label="Set minimum reference separation"/> | |
41 </xml> | |
42 <xml name="samples" token_format="bam" token_multiple="true" token_label="Select sample file(s)"> | |
43 <param name="samples" type="data" format="@FORMAT@" multiple="@MULTIPLE@" label="@LABEL@"/> | |
44 </xml> | |
45 <xml name="svtype"> | |
46 <param argument="--svtype" type="select" label="Select type(s) of structural variants to detect"> | |
47 <option value="ALL" selected="true">All types (ALL)</option> | |
48 <option value="DEL">Deletion (DEL)</option> | |
49 <option value="INS">Insertion (INS)</option> | |
50 <option value="DUP">Duplication (DUP)</option> | |
51 <option value="INV">Inversion (INV)</option> | |
52 <option value="BND">Translocation (BND)</option> | |
53 </param> | |
54 </xml> | |
55 <xml name="vcffile"> | |
56 <param argument="--vcffile" type="data" format="vcf,bcf" optional="true" label="Select genotyping file"/> | |
57 </xml> | |
58 | |
59 <!-- | |
60 output | |
61 --> | |
62 | |
63 <xml name="vcf"> | |
64 <data name="out_vcf" format="vcf" from_work_dir="result.vcf" label="${tool.name} on ${on_string}: Result (VCF)"> | |
65 <filter>'vcf' in oo['out']</filter> | |
66 </data> | |
67 </xml> | |
68 <xml name="bcf"> | |
69 <data name="out_bcf" format="bcf" from_work_dir="result.bcf" label="${tool.name} on ${on_string}: Result (BCF)"> | |
70 <filter>'bcf' in oo['out']</filter> | |
71 </data> | |
72 </xml> | |
73 <xml name="dump"> | |
74 <data name="out_dump" format="tabular" from_work_dir="dump.tsv" label="${tool.name} on ${on_string}: SV-reads"> | |
75 <filter>'dump' in oo['out']</filter> | |
76 </data> | |
77 </xml> | |
78 <xml name="log"> | |
79 <data name="out_log" format="txt" from_work_dir="log.txt" label="${tool.name} on ${on_string}: Log"> | |
80 <filter>'log' in oo['out']</filter> | |
81 </data> | |
82 </xml> | |
83 | |
84 <!-- | |
85 Help | |
86 --> | |
87 | |
88 <token name="@WID@"><![CDATA[ | |
89 Delly is an integrated structural variant (SV) prediction method that can discover, genotype and visualize deletions, tandem duplications, inversions and translocations at single-nucleotide resolution in short-read massively parallel sequencing data. It uses paired-ends, split-reads and read-depth to sensitively and accurately delineate genomic rearrangements throughout the genome. | |
90 ]]></token> | |
91 <token name="@REFERENCES@"><![CDATA[ | |
92 More information are available on `github <https://github.com/dellytools/delly>`_. | |
93 ]]></token> | |
94 </macros> |