Mercurial > repos > gandres > fastme
comparison fastme.xml @ 4:aea74cec21e0 draft default tip
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date | Fri, 22 Apr 2016 08:04:53 -0400 |
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1 <tool id="sniplay_fastme" name="Fastme" version="1.1.0"> | 1 <tool id="fastme" name="FastME" version="2.1.4.2"> |
2 | 2 <description>Distance-based inference of phylogenetic trees</description> |
3 <!-- [REQUIRED] Tool description displayed after the tool name --> | |
4 <description> Calculate distance tree for an alignment file</description> | |
5 | |
6 <!-- [OPTIONAL] 3rd party tools, binaries, modules... required for the tool to work --> | |
7 <requirements> | 3 <requirements> |
8 <requirement type="binary">perl</requirement> | 4 <requirement type="package" version="2.1.4">fastme</requirement> |
9 <requirement type="package" version="2.1.4">fastme</requirement> | |
10 </requirements> | 5 </requirements> |
11 | 6 <version_command> |
12 <!-- [STRONGLY RECOMMANDED] Exit code rules --> | 7 <![CDATA[ fastme --version ]]> |
8 </version_command> | |
13 <stdio> | 9 <stdio> |
14 <!-- [HELP] If no exit code rule is defined, the tool will stop if anything is written to STDERR --> | |
15 <exit_code range="1:" level="fatal" /> | 10 <exit_code range="1:" level="fatal" /> |
16 </stdio> | 11 </stdio> |
17 | 12 <command>fastme --input_data=$input |
18 | 13 --output_tree=$outputTree |
19 <!-- [REQUIRED] The command to execute --> | 14 --output_matrix=$outputMatrix |
20 <command> | 15 --output_info=$outputLog |
21 fastme --input_data=$input_data --dna=$model --output_tree=$fileout | 16 --nb_threads=\${GALAXY_SLOTS:-1} |
22 #if str( $distance ) == "SPR": | 17 |
23 --spr | 18 #if $typeChoice.datatype =="d" |
24 #elif str( $distance )[:3] == "NNI" : | 19 --dna=$typeChoice.modeldna |
25 #if str( $distance ) == "NNI_B" : | 20 |
26 --nni=B | 21 #else if $typeChoice.datatype =="p" |
27 #else : | 22 --protein=$typeChoice.modelprot |
28 --nni=O | 23 |
29 #end if | 24 #else if $typeChoice.datatype =="cfg": |
30 | 25 ## Read information of sequence type |
31 #else : | 26 ## read an info file to choose which option set and set a model by default |
32 --method=$distance | 27 #set $info = open( str($input_info) ).read() |
33 #end if | 28 #if 'dna' in $info: |
34 > $fileout_log | 29 --dna=T |
30 #else if 'protein' in $info: | |
31 --protein=L | |
32 #end if | |
33 #end if | |
34 | |
35 #if $gammaChoice.gamma == "true" | |
36 --gamma=$gammaChoice.rate | |
37 #end if | |
38 | |
39 $distance | |
40 $equilibrium | |
41 $removeGap | |
42 $treeRefinement | |
43 | |
44 #if $bootChoice.boot == "true" | |
45 --output_boot=$outputBoostrap | |
46 --bootstrap=$bootChoice.replicates | |
47 #end if | |
48 | |
49 >> tmp_stdout; | |
50 cat tmp_stdout > $outputLog; | |
51 | |
35 </command> | 52 </command> |
36 | |
37 | |
38 | |
39 <!-- [REQUIRED] Input files and tool parameters --> | |
40 <inputs> | 53 <inputs> |
41 <param name="input_data" type="data" format="txt" optional="false" label="Phylip input" /> | 54 <param name="input" type="data" format="phylip, phy" label="Fastme input" help="Phylip Alignment or Matrix file"/> |
42 <param name="fileout_label" type="text" value="Newick tree" label="Output name" help="Output name for files" /> | 55 <param name="fileout_label" type="text" value="Newick tree" label="Output name" help="Output name for files" /> |
43 <param name="model" type="select" label="Evolutionary model" > | 56 <conditional name="typeChoice"> |
44 <option value="p">p-distance</option> | 57 <param name="datatype" type="select" display="radio" label="Data type" > |
45 <option value="Y">RY symetric</option> | 58 <option value="d">DNA</option> |
46 <option value="R">RY</option> | 59 <option value="p">Protein</option> |
47 <option value="J">JC69</option> | 60 <option value="m">Matrix</option> |
48 <option value="K">K2P</option> | 61 <option value="cfg">Config file</option> |
49 <option value="1">F81</option> | 62 </param> |
50 <option value="4" selected="true">F84</option> | 63 <when value="d"> |
51 <option value="T">TN93</option> | 64 <param name="modeldna" type="select" label="Evolutionary model"> |
52 <option value="L">LogDet</option> | 65 <option value="4">F84</option> |
66 <option value="R">RY</option> | |
67 <option value="1">F81</option> | |
68 <option value="J">JC69</option> | |
69 <option value="K">K2P</option> | |
70 <option value="T" selected="true">TN93</option> | |
71 <option value="p">p-distance</option> | |
72 </param> | |
73 </when> | |
74 <when value="p"> | |
75 <param name="modelprot" type="select" label="Evolutionary model"> | |
76 <option value="L">LG</option> | |
77 <option value="W">WAG</option> | |
78 <option value="J">JTT</option> | |
79 <option value="h">Day off</option> | |
80 <option value="C">CpRev</option> | |
81 <option value="D">DCMut</option> | |
82 <option value="b">HIVb</option> | |
83 <option value="I">HIVw</option> | |
84 <option value="M">MtREV</option> | |
85 <option value="R">RtREV</option> | |
86 <option value="p">p-distance</option> | |
87 </param> | |
88 </when> | |
89 <when value="m"/> | |
90 <when value="cfg"> | |
91 <param name="input_info" format="txt" type="data" multiple="false" label="Config file" help="Precompute file containning sequence description (dna or protein)"/> | |
92 </when> | |
93 </conditional> | |
94 <param name="equilibrium" type="boolean" label="Equilibrium frequencies" truevalue="--equilibrium" falsevalue="" help="By default, frequencies are globally counted from the nucleotides alignment or defined by the proteic substitution model. By checking the box, frequencies are pairwise estimated by counting the nucleotides or estimated by counting the amino-acids in the alignment."/> | |
95 <conditional name="gammaChoice"> | |
96 <param name="gamma" type="select" label="Gamma distributed rates across sites"> | |
97 <option value="true">Yes</option> | |
98 <option value="false">No</option> | |
99 </param> | |
100 <when value="true"> | |
101 <param name="rate" type="float" label="Gamma distribution parameter" value="1" min="0"/> | |
102 </when> | |
103 <when value="false" /> | |
104 </conditional> | |
105 <param name="removeGap" type="select" display="radio" label="Remove gap strategy"> | |
106 <option value="">Pairwise deletion of gaps</option> | |
107 <option value="--remove_gap">Remove all sites with gap</option> | |
53 </param> | 108 </param> |
54 <param name="distance" type="select" label="Distance methode" > | 109 <param name="distance" type="select" label="Distance algorithm"> |
55 <option value="B">TaxAdd_BalME</option> | 110 <option value="--method=I">BIONJ</option> |
56 <option value="O">TaxAdd_OLSME</option> | 111 <option value="--method=B --branch_length=B">TaxAdd BalME</option> |
57 <option value="I" selected="true">BIONJ</option> | 112 <option value="--method=O --branch_length=O">TaxAdd OLSME</option> |
58 <option value="N">NJ</option> | 113 <option value="--method=N">NJ</option> |
59 <option value="U">UNJ</option> | 114 <option value="--method=U">UNJ</option> |
60 <option value="NNI_B">NNI_BalME</option> | |
61 <option value="NNI_O">NNI_OLS</option> | |
62 <option value="SPR">SPR</option> | |
63 </param> | 115 </param> |
64 </inputs> | 116 <param name="treeRefinement" type="select" display="radio" label="Tree Refinement" help='(NNI) Nearest Neighbor Interchanges,(SPR) Subtree Pruning and Regrafting '> |
65 | 117 <option value="">None</option> |
66 <!-- [REQUIRED] Output files --> | 118 <option value="--nni=O">OLS NNI</option> |
119 <option value="--nni=B">BalME NNI</option> | |
120 <option value="--spr" selected="true">BalME SPR</option> | |
121 <option value="--nni=B --spr">BalME NNI + SPR</option> | |
122 </param> | |
123 <conditional name="bootChoice"> | |
124 <param name="boot" type="select" label="Bootstrap"> | |
125 <option value="false">No</option> | |
126 <option value="true">Yes</option> | |
127 </param> | |
128 <when value="false"/> | |
129 <when value="true"> | |
130 <param name="replicates" type="integer" value="1000" label="Number of replicates"/> | |
131 </when> | |
132 </conditional> | |
133 </inputs> | |
67 <outputs> | 134 <outputs> |
68 <data name="fileout_log" type="data" format="txt" label="${fileout_label}.log" /> | 135 <data name="outputTree" format="nwk" label="${fileout_label}"/> |
69 <data name="fileout" type="data" format="txt" label="${fileout_label}" /> | 136 <data name="outputLog" format="txt" label="FastME Information"/> |
137 <data name="outputBoostrap" format="nwk" label="FastME Bootstrap trees"> | |
138 <filter>bootChoice['boot'] == "true"</filter> | |
139 </data> | |
140 <data name="outputMatrix" format="txt" label="FastME Distance matrix"/> | |
70 </outputs> | 141 </outputs> |
71 | |
72 <!-- [OPTIONAL] Tests to be run manually by the Galaxy admin --> | |
73 <tests> | 142 <tests> |
74 <!-- [HELP] Test files have to be in the ~/test-data directory --> | |
75 | |
76 <test> | 143 <test> |
77 <param name="input_data" value="phylip" /> | 144 <param name="input" value="phylip" /> |
78 <param name="model" value="4"/> | 145 <param name="modeldna" value="4"/> |
79 <param name="distance" value="I"/> | 146 <param name="gamma" value="false"/> |
80 <output name="fileout" file="newick" /> | 147 <param name="treeRefinement" value=""/> |
148 <param name="distance" value="--method=I"/> | |
149 <output name="outputTree" file="newick" /> | |
81 </test> | 150 </test> |
82 | |
83 <!-- [HELP] Multiple tests can be defined with different parameters --> | |
84 <!-- | |
85 <test> | 151 <test> |
152 <param name="input" value="phylip" /> | |
153 <param name="modeldna" value="T"/> | |
154 <param name="distance" value="--method=I"/> | |
155 <param name="treeRefinement" value="--nni=B --spr"/> | |
156 <param name="fileout_label" value="TreeTn93BionjSpr.nwk" /> | |
157 <output name="outputTree" file="TreeTn93BionjSpr.nwk" /> | |
86 </test> | 158 </test> |
87 --> | |
88 </tests> | 159 </tests> |
89 | |
90 <!-- [OPTIONAL] Help displayed in Galaxy --> | |
91 <help> | 160 <help> |
92 | 161 |
93 .. class:: infomark | 162 .. class:: infomark |
94 | 163 |
95 **Authors** | 164 |
96 | 165 **FastME version 2.1.4** |
97 | Richard Desper and Olivier Gascuel, | |
98 | Journal of Computational Biology 19(5), 687-705, 2002. | |
99 | Molecular Biology and Evolution 21(3), 587-598, 2004. | |
100 | Please cite these papers if you use this software in your publications. | |
101 | 166 |
102 | 167 |
103 .. class:: infomark | 168 .. class:: infomark |
104 | 169 |
105 **Galaxy integration** Andres Gwendoline, Institut Français de Bioinformatique. | 170 |
106 | 171 **Galaxy integration** Andres Gwendoline, Institut Français de Bioinformatique. Correia Damien, CNRS. |
107 .. class:: infomark | 172 **Support** For any questions about Galaxy integration, please send an e-mail to vincent.lefort@lirmm.fr |
108 | 173 |
109 **Support** For any questions about Galaxy integration, please send an e-mail to support.abims@sb-roscoff.fr | 174 |
110 | 175 ----- |
111 --------------------------------------------------- | 176 |
112 | 177 |
113 | 178 ############ |
114 ====== | 179 FastME 2.0 |
115 FastMe | 180 ############ |
116 ====== | 181 |
182 Comprehensive, accurate and fast distance-based phylogeny inference program | |
183 | |
117 | 184 |
118 ----------- | 185 ----------- |
119 Description | 186 Description |
120 ----------- | 187 ----------- |
121 | 188 |
122 | 189 FastME provides distance algorithms to infer phylogenies. It's based on balanced minimum evolution, which is the very principle of NJ. |
123 FastME - A distance based phylogeny reconstruction algorithm. | 190 |
124 | 191 FastME included Nearest Neighbor Interchange (NNI) and also Subtree Pruning and Regrafting (SPR), while remaining as fast as NJ and providing a number of facilities: distance estimation for DNA and proteins with various models and options, bootstrapping, and parallel computations. |
125 FastME showed better topological accuracy than NJ, | |
126 BIONJ, WEIGHBOR and FITCH, in all evolutionary | |
127 conditions we tested, which include large range | |
128 deviations from molecular clock and substitution rates. | |
129 | |
130 | |
131 | |
132 ----------------- | |
133 Workflow position | |
134 ----------------- | |
135 | |
136 **Upstream tools** | |
137 | |
138 =========== ========================== ======= | |
139 Name output file(s) format | |
140 =========== ========================== ======= | |
141 Readseq phylip conversion phylip | |
142 =========== ========================== ======= | |
143 | |
144 | |
145 **Downstream tools** | |
146 | |
147 =========== ========================== ======= | |
148 Name output file(s) format | |
149 =========== ========================== ======= | |
150 Rooting out tree Newick | |
151 =========== ========================== ======= | |
152 | |
153 | |
154 ---------- | |
155 Input file | |
156 ---------- | |
157 | |
158 Phylip file | |
159 Phylip file with sequence alignments | |
160 | |
161 | |
162 ---------- | |
163 Parameters | |
164 ---------- | |
165 | |
166 Output name | |
167 Output base name for the ouput files | |
168 | |
169 Evolutionary model | |
170 Indicate the evolutionary [model] which can be choosen from:p-distance, RY symmetric, RY, JC69, K2P, F81, F84 (default), TN93, LogDet. | |
171 | |
172 Distance methode | |
173 FastME computes a tree using a distance algorithm. You may choose this method/topologie from: TaxAdd_BalME, TaxAdd_OLSME, BIONJ (default), NJ, UNJ, NNI_BalME, NNI_OLS or SPR | |
174 | |
175 ------------ | |
176 Output files | |
177 ------------ | |
178 | |
179 Output_name | |
180 Resulting tree at Newick format | |
181 | |
182 Output_name.log | |
183 Log file | |
184 | 192 |
185 ------------ | 193 ------------ |
186 Dependencies | 194 Dependencies |
187 ------------ | 195 ------------ |
188 FastME | 196 FastME |
189 http://www.atgc-montpellier.fr/fastme | 197 http://www.atgc-montpellier.fr/fastme |
190 | 198 |
191 | 199 |
192 | 200 |
193 --------------------------------------------------- | 201 --------------------------------------------------- |
194 | 202 |
195 --------------- | 203 --------------- |
197 --------------- | 205 --------------- |
198 | 206 |
199 Input files | 207 Input files |
200 =========== | 208 =========== |
201 | 209 |
202 Philip file | 210 **Phylip file**:: |
203 ----------- | 211 |
204 | 212 |
205 :: | 213 4 120 |
206 | 214 Orangutan CCAAACGACA TTTCATATGC TGTCATTTCT GAAGATATGA GACAAGTGAG CTGTCCGGAA |
207 168 5125 | 215 Gorilla CCAAACAACA TTTCATGTGC TGTCATTTCT GAAGATATGA GACAAGTGAG CTCTCCGAAA |
208 IRAT112 GAGAACCGTC CTGTAAGTAC TCTTGCTTTA AGTAATAAAG TAATACTAAT | 216 Human CCAAACAACA TTTCATGTGC TGTCATTTCT GAAGATAAGA GACAAGTGAG CTCTCCGAAA |
209 KARASUKARA GAGAACCGTC CTGTAAGTAC TCTTGCTTTA AATACGAAAG TAATACTAAT | 217 Chimp CCAAACAACA TTTCATGTGC TGTCATTTCT GAAGATATGA GACAAGTGAG CTCTCCGAAA |
218 | |
219 CCAACATATC AGACATATGT GAATTTCAAT TATTGTACGG GCATCCTGGG CTCTCAAAGT | |
220 CCAAGATATC AGACATTTAT GAATTTCAAT TATTGTACGG GCATCCTGGG CTCTCAAAGT | |
221 CCAAGATACC AGACATTTGT GAATTTCAAT TATTGTACTG GCATCCTGGG CTCTCAAAGT | |
222 CCAAGATATC AGACATTTAT GAATTTCAAT TATTGTACTG GCATCCTGGG CTCTCAAAGT | |
223 | |
224 | |
210 | 225 |
211 Parameters | 226 Parameters |
212 ========== | 227 ========== |
213 | 228 |
214 Output name -> Newick tree | 229 :: |
215 | 230 |
216 Evolutionary model -> F84 | 231 Output name: Newick tree |
217 | 232 Evolutionary model : TN93 |
218 Distance methode -> BIONJ | 233 Distance method : BIONJ |
234 | |
219 | 235 |
220 Output files | 236 Output files |
221 ============ | 237 ============ |
222 | 238 |
223 Newick tree | 239 **Newick tree**:: |
224 ----------- | 240 |
225 | 241 ((Gorilla:0.005755,Orangutan:0.020680):0.001063,Human:0.006655,Chimp:0.002132); |
226 :: | 242 |
227 | 243 ----- |
228 (((((((((((((((((((((((((GOGOLEMPUK:0.001198,GOGOLEMPAK:0.002128):0.030378,TREMBESE:0.013258):0.055246,(((JIMBRUKJOL:0.045219,KETANKONIR:0.035298):0.006267, ... | 244 |
229 | 245 OPTIONS |
246 ======= | |
247 | |
248 | |
249 -i file, --input_data=file | |
250 The input data file contains sequence alignment(s) or a distance matrix(ces). | |
251 | |
252 -u input_tree_file, --user_tree=input_tree_file | |
253 FastME may use an existing topology available in the input user tree file which corresponds to the input dataset. | |
254 | |
255 -o output_tree_file, --output_tree=output_tree_file | |
256 FastME will write the infered tree into the output tree file. | |
257 | |
258 -O output_matrix_file, --output_matrix=output_matrix_file | |
259 Use output matrix file option if you want FastME to write the distances | |
260 matrix computed from the input alignment in the output matrix file. | |
261 | |
262 -I output_information_file, --output_info=output_information_file | |
263 Use this option if you want FastME to write information | |
264 about its execution in the output information file. | |
265 | |
266 -B output_bootstrap_trees_file, --output_boot=output_bootstrap_trees_file | |
267 Use this option if you want FastME to write bootstrap trees | |
268 in the bootstrap trees file. | |
269 | |
270 -a, --append | |
271 Use this option to append results to existing output files (if any). | |
272 By default output files will be overwritten. | |
273 | |
274 -m method, --method=method | |
275 FastME computes a tree using a distance algorithm. | |
276 You may choose this method from: | |
277 TaxAdd_(B)alME, TaxAdd_(O)LSME, B(I)ONJ (default), | |
278 (N)J or (U)NJ. | |
279 | |
280 -d model, --dna=model | |
281 Use this option if your input data file contains DNA sequences alignment(s). | |
282 You may also indicate the evolutionary [model] which can be choosen from: | |
283 (p)-distance, R(Y) symmetric, (R)Y, (J)C69, (K)2P, F8(1), F8(4) (default), (T)N93, (L)ogDet. | |
284 | |
285 -p model, --protein=model | |
286 Use this option if your input data file contains protein sequences alignment(s). | |
287 You may also indicate the evolutionary [model] which can be choosen from: | |
288 (p)-distance, (F)81 like, (L)G (default), (W)AG, (J)TT, Day(h)off, (D)CMut, (C)pRev, | |
289 (M)tREV, (R)tREV, HIV(b), H(I)Vw or FL(U). | |
290 | |
291 -r, --remove_gap | |
292 Use this option to completely remove any site which has a gap in | |
293 any sequence. By default, FastME is doing pairwise deletion of gaps. | |
294 | |
295 -e, --equilibrium | |
296 The equilibrium frequencies for DNA are always estimated by counting | |
297 the occurence of the nucleotides in the input alignment. | |
298 For amino-acid sequences, the equilibrium frequencies are estimated | |
299 using the frequencies defined by the substitution model. | |
300 Use this option if you whish to estimate the amino-acid frequencies | |
301 by counting their occurence in the input alignment. | |
302 | |
303 -g alpha, --gamma=alpha | |
304 Use this option if you wish to have gamma distributed rates across sites. | |
305 By default, FastME runs with no gamma variation. | |
306 If running FastME with gamma distributed rates across sites, the [alpha] default value is 1.0. | |
307 Only helpful when the input data file contains sequences alignment(s). | |
308 | |
309 -n NNI, --nni=NNI | |
310 Use this option to do [NNI] tree topology improvement. | |
311 You may choose the [NNI] type from: | |
312 NNI_(B)alME (default) or NNI_(O)LS. | |
313 | |
314 -s, --spr | |
315 Use this option to do SPR tree topology improvement. | |
316 | |
317 -w branch, --branch_length=branch | |
318 Use this option to indicate the branch length to assign to the tree. | |
319 Only helpful when not improving the tree topology (no NNI nor SPR). | |
320 You may choose the branch length from: | |
321 (B)alLS (default), (O)LS or (n)one. (n)one is only available with BIONJ, NJ or UNJ. | |
322 | |
323 -D datasets, --datasets=datasets | |
324 Use this option to indicate the number of datasets in your input | |
325 data file. Default value is 1. | |
326 | |
327 -b replicates, --bootstrap=replicates | |
328 Use this option to indicate the number of replicates FastME will | |
329 do for bootstrapping. Default value is 0. | |
330 Only helpful when the input data file contains sequences alignment(s). | |
331 | |
332 -z seed, --seed=seed | |
333 Use this option to initialize randomization with seed value. Only helpful when bootstrapping. | |
334 | |
335 -c Use this option if you want FastME only to compute distance matrix. | |
336 Only helpful when the input data file contains sequences alignment(s). | |
337 | |
338 -T number_of_threads, --nb_threads=number_of_threads | |
339 Use this option to set the number of threads to use. | |
340 Default number of threads is 4. | |
341 | |
342 -v value, --verbose=value | |
343 Sets the verbose level to value [0-3]. Default value is 0 | |
344 | |
345 -V, --version | |
346 Prints the FastME version. | |
347 | |
348 -h, --help Display this usage. | |
349 | |
350 | |
351 For further informations, please visite FastME_ | |
352 | |
353 .. _FastME: http://www.atgc-montpellier.fr/fastme/usersguide.php | |
230 | 354 |
231 </help> | 355 </help> |
232 | |
233 <citations> | 356 <citations> |
234 <!-- [HELP] As DOI or BibTex entry --> | 357 <citation type="doi">10.1093/molbev/msv150</citation> |
235 <citation type="bibtex"> | 358 <citation type="doi">10.1089/106652702761034136</citation> |
236 @article{Lefort30062015, | |
237 author = {Lefort, Vincent and Desper, Richard and Gascuel, Olivier}, | |
238 title = {FastME 2.0: A Comprehensive, Accurate, and Fast Distance-Based Phylogeny Inference Program}, | |
239 year = {2015}, | |
240 doi = {10.1093/molbev/msv150}, | |
241 abstract ={FastME provides distance algorithms to infer phylogenies. FastME is based on balanced minimum evolution, which is the very principle of Neighbor Joining (NJ). FastME improves over NJ by performing topological moves using fast, sophisticated algorithms. The first version of FastME only included Nearest Neighbor Interchange. The new 2.0 version also includes Subtree Pruning and Regrafting, while remaining as fast as NJ and providing a number of facilities: Distance estimation for DNA and proteins with various models and options, bootstrapping, and parallel computations. FastME is available using several interfaces: Command-line (to be integrated in pipelines), PHYLIP-like, and a Web server (http://www.atgc-montpellier.fr/fastme/).}, | |
242 URL = {http://mbe.oxfordjournals.org/content/early/2015/07/25/molbev.msv150.abstract}, | |
243 eprint = {http://mbe.oxfordjournals.org/content/early/2015/07/25/molbev.msv150.full.pdf+html}, | |
244 journal = {Molecular Biology and Evolution} | |
245 } | |
246 | |
247 </citation> | |
248 | |
249 </citations> | 359 </citations> |
250 | |
251 | |
252 </tool> | 360 </tool> |