Mercurial > repos > dereeper > sniplay
annotate SNP_density/calculateSlidingWindowsSNPdensitiesFromVCF_wrapper.xml @ 12:88748d846a20 draft
planemo upload commit 11382afe87364aaafb19973470d5066229a6e34f
author | dereeper |
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date | Tue, 14 Aug 2018 08:21:55 -0400 |
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9 | 1 <tool id="sniplay_density" name="SNP density" version="2.0.0"> |
2 | |
3 <!-- [REQUIRED] Tool description displayed after the tool name --> | |
4 <description> Calculate SNP densities along chromosome from a VCF input</description> | |
5 | |
6 <!-- [OPTIONAL] 3rd party tools, binaries, modules... required for the tool to work --> | |
7 <requirements> | |
8 <requirement type="binary">perl</requirement> | |
9 <requirement type="package" version="1.6.924">perl-bioperl</requirement> | |
10 <requirement type="package" version="0.1.14">vcftools</requirement> | |
11 <requirement type="package" version="0.1.14">perl-vcftools-vcf</requirement> | |
12 </requirements> | |
13 | |
14 <!-- [STRONGLY RECOMMANDED] Exit code rules --> | |
15 <stdio> | |
16 <!-- [HELP] If no exit code rule is defined, the tool will stop if anything is written to STDERR --> | |
17 <exit_code range="1:" level="fatal" /> | |
18 </stdio> | |
19 | |
20 <!-- [OPTIONAL] Command to be executed to get the tool's version string --> | |
21 <version_command> | |
22 <!-- | |
23 tool_binary -v | |
24 --> | |
25 </version_command> | |
26 | |
27 <!-- [REQUIRED] The command to execute --> | |
28 <command interpreter="bash"> | |
29 calculateSlidingWindowsSNPdensitiesFromVCF.sh $filein $fileout $fileout_bysample $step | |
30 </command> | |
31 | |
32 <!-- [REQUIRED] Input files and tool parameters --> | |
33 <inputs> | |
34 <param name="filein" type="data" format="vcf" optional="false" label="VCF input" /> | |
35 <param name="step" type="integer" value="200000" label="Step" help="Step in bp"/> | |
36 <param name="fileout_label" type="text" value="densities" label="Output name" help="Output name for tabular files" /> | |
37 </inputs> | |
38 | |
39 <!-- [REQUIRED] Output files --> | |
40 <outputs> | |
41 <data name="fileout" format="txt" label="${fileout_label}" /> | |
42 <data name="fileout_bysample" format="txt" label="${fileout_label}.by_sample" /> | |
43 </outputs> | |
44 | |
45 <tests> | |
46 <test> | |
47 <param name="filein" value="vcf2fastaAndHapmap-sample.vcf" /> | |
48 <param name="step" value="20000" /> | |
49 <output name="fileout" file="SNPden-result.txt" /> | |
50 <output name="fileout_bysample" file="SNPden-result_bysample.txt" /> | |
51 </test> | |
52 <!-- [HELP] Multiple tests can be defined with different parameters --> | |
53 <!-- | |
54 <test> | |
55 </test> | |
56 --> | |
57 </tests> | |
58 | |
59 <!-- [OPTIONAL] Help displayed in Galaxy --> | |
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60 <help><![CDATA[ |
9 | 61 |
62 .. class:: infomark | |
63 | |
64 **Authors** Dereeper Alexis (alexis.dereeper@ird.fr), IRD, South Green platform | |
65 | |
66 | **Please cite** "SNiPlay3: a web-based application for exploration and large scale analyses of genomic variations", **Dereeper A. et al.**, Nucl. Acids Res. (1 july 2015) 43 (W1). | |
67 | |
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68 .. class:: infomark |
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69 |
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70 **Galaxy integration** Provided by Southgreen & Andres Gwendoline (Institut Français de Bioinformatique) & Marcon Valentin (IFB & INRA) |
9 | 71 |
72 .. class:: infomark | |
73 | |
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74 **Support** For any questions about Galaxy integration, please send an e-mail to alexis.dereeper@ird.fr |
9 | 75 |
76 --------------------------------------------------- | |
77 | |
78 ============= | |
79 SNP densities | |
80 ============= | |
81 | |
82 ----------- | |
83 Description | |
84 ----------- | |
85 | |
86 Calculate SNP densities along chromosome from a VCF file | |
87 | |
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88 ------------ |
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89 Dependencies |
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90 ------------ |
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91 VCFtools |
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92 vcftools_ 0.1.14, Conda version |
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93 VCFtools Perl libraries |
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94 perl-vcftools-vcf_ 0.1.14, Conda version |
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95 Bioperl |
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96 perl-bioperl_ 1.6.924, Conda version |
9 | 97 |
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98 .. _vcftools: https://anaconda.org/bioconda/vcftools |
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99 .. _perl-vcftools-vcf: https://anaconda.org/bioconda/perl-vcftools-vcf |
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100 .. _perl-bioperl: https://anaconda.org/bioconda/perl-bioperl |
9 | 101 |
102 ---------- | |
103 Input file | |
104 ---------- | |
105 | |
106 VCF file | |
107 File with SNPs | |
108 | |
109 ---------- | |
110 Parameters | |
111 ---------- | |
112 | |
113 Step | |
114 Step in bp for the window to calculate SNP density | |
115 | |
116 Output name | |
117 Output base name for the two ouput files | |
118 | |
119 ------------ | |
120 Output files | |
121 ------------ | |
122 | |
123 Output_name | |
124 Tabular file with SNP density in each postion | |
125 | |
126 Output_name.by_sample | |
127 Tabular file with SNP density for each sample | |
128 | |
129 --------------------------------------------------- | |
130 | |
131 --------------- | |
132 Working example | |
133 --------------- | |
134 | |
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135 Input file |
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136 ========== |
9 | 137 |
138 vcf file | |
139 ----------- | |
140 | |
141 :: | |
142 | |
143 #fileformat=VCFv4.1 | |
144 #FILTER=<ID=LowQual,Description="Low quality"> | |
145 #FORMAT=<ID=AD,Number=.,Type=Integer,Description="Allelic depths for the ref and alt alleles in the order listed"> | |
146 [...] | |
147 CHROM POS ID REF ALT QUAL FILTER INFO FORMAT CATB1 | |
148 chr1 2209 . G T 213.84 . AC=2;AF=1.00;AN=2;DP=7;Dels=0.00;FS=0.000;HaplotypeScore=0.0000;MLEAC=2;MLEAF=1.00;MQ=41.50;MQ0=0;QD=30.55;EFF=DOWNSTREAM(MODIFIER||||Cc01g00020|mRNA||GSCOCT00012438001|),UPSTREAM(MODIFIER||||Cc01g00010|mRNA||GSCOCT00012439001|) GT:AD:DP:GQ:PL 1/1:0,7:7:18:242,18,0 | |
149 | |
150 Parameters | |
151 ========== | |
152 | |
153 Step -> 200000 | |
154 | |
155 Output name -> densities | |
156 | |
157 | |
158 Output files | |
159 ============ | |
160 | |
161 densities | |
162 --------- | |
163 | |
164 :: | |
165 | |
166 Chromosome Position SNPs | |
167 chr1 200000 355 | |
168 chr1 400000 228 | |
169 chr1 600000 63 | |
170 chr1 800000 191 | |
171 | |
172 | |
173 densities.by_sample | |
174 ------------------- | |
175 | |
176 :: | |
177 | |
178 Chromosome BA58 BA59 BD54 | |
179 chr1 220 197 225 | |
180 chr1 130 119 133 | |
181 chr1 43 43 40 | |
182 chr1 139 167 141 | |
183 | |
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184 ]]></help> |
9 | 185 <citations> |
186 <!-- [HELP] As DOI or BibTex entry --> | |
187 <citation type="bibtex">@article{Dereeper03062015, | |
188 author = {Dereeper, Alexis and Homa, Felix and Andres, Gwendoline and Sempere, Guilhem and Sarah, Gautier and Hueber, Yann and Dufayard, Jean-François and Ruiz, Manuel}, | |
189 title = {SNiPlay3: a web-based application for exploration and large scale analyses of genomic variations}, | |
190 year = {2015}, | |
191 doi = {10.1093/nar/gkv351}, | |
192 abstract ={SNiPlay is a web-based tool for detection, management and analysis of genetic variants including both single nucleotide polymorphisms (SNPs) and InDels. Version 3 now extends functionalities in order to easily manage and exploit SNPs derived from next generation sequencing technologies, such as GBS (genotyping by sequencing), WGRS (whole gre-sequencing) and RNA-Seq technologies. Based on the standard VCF (variant call format) format, the application offers an intuitive interface for filtering and comparing polymorphisms using user-defined sets of individuals and then establishing a reliable genotyping data matrix for further analyses. Namely, in addition to the various scaled-up analyses allowed by the application (genomic annotation of SNP, diversity analysis, haplotype reconstruction and network, linkage disequilibrium), SNiPlay3 proposes new modules for GWAS (genome-wide association studies), population stratification, distance tree analysis and visualization of SNP density. Additionally, we developed a suite of Galaxy wrappers for each step of the SNiPlay3 process, so that the complete pipeline can also be deployed on a Galaxy instance using the Galaxy ToolShed procedure and then be computed as a Galaxy workflow. SNiPlay is accessible at http://sniplay.southgreen.fr.}, | |
193 URL = {http://nar.oxfordjournals.org/content/early/2015/06/03/nar.gkv351.abstract}, | |
194 eprint = {http://nar.oxfordjournals.org/content/early/2015/06/03/nar.gkv351.full.pdf+html}, | |
195 journal = {Nucleic Acids Research} | |
196 } | |
197 | |
198 </citation> | |
199 | |
200 </citations> | |
201 </tool> |