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annotate check_gwas_inputs/CheckGWASInputs.xml @ 15:31c23d943c29 draft default tip
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author | dereeper |
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date | Tue, 08 Jan 2019 08:47:56 -0500 |
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1 <tool id="check_GWAS_inputs" name="Check GWAS Inputs" version="2.0.0"> |
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2 <description>Checks concordance between input files for GWAS analysis</description> |
9 | 3 |
4 <!-- [OPTIONAL] 3rd party tools, binaries, modules... required for the tool to work --> | |
5 <requirements> | |
6 <requirement type="binary">perl</requirement> | |
7 </requirements> | |
8 | |
9 <!-- [STRONGLY RECOMMANDED] Exit code rules --> | |
10 <stdio> | |
11 <!-- [HELP] If no exit code rule is defined, the tool will stop if anything is written to STDERR --> | |
12 <exit_code range="1:" level="fatal" /> | |
13 </stdio> | |
14 | |
15 <command interpreter="bash">./CheckGWASInputs.sh $hapmap $trait $out_hapmap $out_trait $stats | |
16 </command> | |
17 <inputs> | |
18 <param format="txt" name="hapmap" type="data" label="Allelic file in Hapmap format" help="Allelic file in Hapmap format"/> | |
19 <param format="txt" name="trait" type="data" label="Trait file" help="Phenotypic file"/> | |
20 </inputs> | |
21 <outputs> | |
22 <data format="txt" name="out_hapmap" label="Hapmap output"/> | |
23 <data format="txt" name="out_trait" label="Trait output"/> | |
24 <data format="txt" name="stats" label="Logfile and statistics"/> | |
25 </outputs> | |
26 | |
27 <!-- [OPTIONAL] Tests to be run manually by the Galaxy admin --> | |
28 <tests> | |
29 <!-- [HELP] Test files have to be in the ~/test-data directory --> | |
30 <!-- [HELP] Multiple tests can be defined with different parameters --> | |
31 <test> | |
32 <param name="hapmap" value="gwas-hapmap" /> | |
33 <param name="trait" value="gwas-trait" /> | |
34 <output name="out_hapmap" file="gwas-result.hapmap" /> | |
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35 <output name="out_trait" file="gwas-result.trait" compare="sim_size" delta="0"/> |
9 | 36 <output name="stats" file="gwas-result.stats" /> |
37 </test> | |
38 </tests> | |
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39 <help><![CDATA[ |
9 | 40 |
41 .. class:: infomark | |
42 | |
43 **Authors** South Green | |
44 | |
45 | **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). | |
46 | |
47 .. class:: infomark | |
48 | |
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49 **Galaxy integration** Provided by Southgreen & Dereeper Alexis (IRD) & Marcon Valentin (IFB & INRA) |
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50 |
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51 .. class:: infomark |
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52 |
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53 **Support** For any questions about Galaxy integration, please send an e-mail to alexis.dereeper@ird.fr |
9 | 54 |
55 --------------------------------------------------- | |
56 | |
57 =============== | |
58 CheckGWASInputs | |
59 =============== | |
60 | |
61 ----------- | |
62 Description | |
63 ----------- | |
64 | |
65 | CheckGWASInputs checks concordance between input files for GWAS analysis. | |
66 | |
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67 ----------- |
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68 Input files |
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69 ----------- |
9 | 70 |
71 Hapmap file | |
72 Allelic file in Hapmap format | |
73 | |
74 Trait file | |
75 Phenotypic file | |
76 | |
77 ------------ | |
78 Output files | |
79 ------------ | |
80 | |
81 Hapmap output | |
82 | |
83 Trait output | |
84 | |
85 Logfile and statistics | |
86 | |
87 --------------------------------------------------- | |
88 | |
89 --------------- | |
90 Working example | |
91 --------------- | |
92 | |
93 Input files | |
94 =========== | |
95 | |
96 Hapmap file | |
97 ----------- | |
98 | |
99 :: | |
100 | |
101 rs# alleles chrom pos strand assembly# center protLSID assayLSID panel QCcode Ind1 Ind2 | |
102 SNP1 A/T 1 3102 + assembly NA NA NA speciesname NA AA AA AA | |
103 SNP2 A/T 1 4648 + assembly NA NA NA speciesname NA AA AA AA | |
104 | |
105 Trait file | |
106 ---------- | |
107 | |
108 :: | |
109 | |
110 <Trait> Test | |
111 Ind1 -2.9985936006411 | |
112 Ind2 -2.68669426456267 | |
113 | |
114 Output files | |
115 ============ | |
116 | |
117 Hapmap output | |
118 ------------- | |
119 | |
120 :: | |
121 | |
122 rs# alleles chrom pos strand assembly# center protLSID assayLSID panel QCcode Ind1 Ind2 Ind3 Ind4 | |
123 SNP1 A/T 1 3102 + assembly NA NA NA speciesname NA AA AA AA AA AA | |
124 SNP2 A/T 1 4648 + assembly NA NA NA speciesname NA AA AA AA AA TT | |
125 | |
126 | |
127 Trait output | |
128 ------------ | |
129 | |
130 :: | |
131 | |
132 <Trait> Test | |
133 Ind429 -26.2142525264157 | |
134 Ind373 12.0306115988504 | |
135 Ind81 1.98118654229534 | |
136 | |
137 Logfile and statistics | |
138 ---------------------- | |
139 | |
140 :: | |
141 | |
142 | |
143 ============================================== | |
144 Individuals | |
145 ============================================== | |
146 Individuals in hapmap file: 500 | |
147 Individuals in trait file: 500 | |
148 Individuals found in both files: 500 | |
149 ============================================== | |
150 Markers | |
151 ============================================== | |
152 Discarded markers: | |
153 Monomorphic: 0 | |
154 Not biallelic: 0 | |
155 Modified markers: | |
156 Difference in variation: 0 | |
157 | |
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158 ]]></help> |
9 | 159 <citations> |
160 <!-- [HELP] As DOI or BibTex entry --> | |
161 <citation type="bibtex">@article{Dereeper03062015, | |
162 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}, | |
163 title = {SNiPlay3: a web-based application for exploration and large scale analyses of genomic variations}, | |
164 year = {2015}, | |
165 doi = {10.1093/nar/gkv351}, | |
166 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.}, | |
167 URL = {http://nar.oxfordjournals.org/content/early/2015/06/03/nar.gkv351.abstract}, | |
168 eprint = {http://nar.oxfordjournals.org/content/early/2015/06/03/nar.gkv351.full.pdf+html}, | |
169 journal = {Nucleic Acids Research} | |
170 } | |
171 | |
172 </citation> | |
173 | |
174 </citations> | |
175 </tool> |