1 | /* |
---|
2 | |
---|
3 | PhyML: a program that computes maximum likelihood phylogenies from |
---|
4 | DNA or AA homologous sequences. |
---|
5 | |
---|
6 | Copyright (C) Stephane Guindon. Oct 2003 onward. |
---|
7 | |
---|
8 | All parts of the source except where indicated are distributed under |
---|
9 | the GNU public licence. See http://www.opensource.org for details. |
---|
10 | |
---|
11 | */ |
---|
12 | |
---|
13 | |
---|
14 | #include "help.h" |
---|
15 | |
---|
16 | |
---|
17 | /* int T_MAX_FILE; */ |
---|
18 | /* phydbl SMALL; */ |
---|
19 | /* phydbl UNLIKELY; */ |
---|
20 | |
---|
21 | ////////////////////////////////////////////////////////////// |
---|
22 | ////////////////////////////////////////////////////////////// |
---|
23 | |
---|
24 | |
---|
25 | void Usage() |
---|
26 | { |
---|
27 | |
---|
28 | char *BOLD=(char *)mCalloc(10,sizeof(char)); |
---|
29 | char *FLAT=(char *)mCalloc(10,sizeof(char)); |
---|
30 | char *LINE=(char *)mCalloc(10,sizeof(char)); |
---|
31 | char *cha; |
---|
32 | |
---|
33 | |
---|
34 | cha =getenv("OS"); |
---|
35 | |
---|
36 | if(cha!=NULL) |
---|
37 | { |
---|
38 | strcpy(BOLD, ""); |
---|
39 | strcpy(FLAT, ""); |
---|
40 | strcpy(LINE, ""); |
---|
41 | } |
---|
42 | else |
---|
43 | { |
---|
44 | strcpy(BOLD, "\033[00;01m"); |
---|
45 | strcpy(FLAT, "\033[00;00m"); |
---|
46 | strcpy(LINE, "\033[00;04m"); |
---|
47 | } |
---|
48 | |
---|
49 | #ifdef PHYML |
---|
50 | PhyML_Printf("%sNAME\n" |
---|
51 | "%s\t- PhyML %s - \n\n" |
---|
52 | "%s\t\''A simple, fast, and accurate algorithm to estimate\n" |
---|
53 | "%s\tlarge phylogenies by maximum likelihood\''\n\n" |
---|
54 | "%s\tStephane Guindon and Olivier Gascuel,\n" |
---|
55 | "%s\tSystematic Biology 52(5):696-704, 2003.\n\n" |
---|
56 | "%s\tPlease cite this paper if you use this software in your publications.\n",BOLD,FLAT,VERSION,FLAT,FLAT,FLAT,FLAT,FLAT); |
---|
57 | #endif |
---|
58 | |
---|
59 | #ifdef PHYTIME |
---|
60 | PhyML_Printf("%sNAME\n" |
---|
61 | "%s\t- PhyTime %s - \n\n" |
---|
62 | "%s\t'Bayesian estimation of divergence times from large sequence alignments.'\n" |
---|
63 | "%s\tStephane Guindon,\n" |
---|
64 | "%s\tMolecular Biology and Evolution 27(8):1768-81, 2010.\n\n" |
---|
65 | "%s\tPlease cite this paper if you use this software in your publications.\n",BOLD,FLAT,VERSION,FLAT,FLAT,FLAT,FLAT,FLAT); |
---|
66 | #endif |
---|
67 | |
---|
68 | |
---|
69 | |
---|
70 | #ifdef PHYML |
---|
71 | PhyML_Printf("%s\nSYNOPSIS:\n\n" |
---|
72 | "%s\tphyml %s[command args]\n",BOLD,BOLD,BOLD); |
---|
73 | #endif |
---|
74 | #ifdef PHYTIME |
---|
75 | PhyML_Printf("%s\nSYNOPSIS:\n\n" |
---|
76 | "%s\tphytime %s[command args]\n",BOLD,BOLD,BOLD); |
---|
77 | #endif |
---|
78 | |
---|
79 | #ifdef PHYML |
---|
80 | PhyML_Printf("%s\n\tAll the options below are optional (except '%s-i%s' if you want to use the command-line interface).\n\n",FLAT,BOLD,FLAT); |
---|
81 | #endif |
---|
82 | |
---|
83 | #ifdef PHYTIME |
---|
84 | PhyML_Printf("%s\n\tAll the options below are optional except '%s-i%s','%s-u%s' and '%s--calibration%s'.\n\n",FLAT,BOLD,FLAT,BOLD,FLAT,BOLD,FLAT); |
---|
85 | #endif |
---|
86 | |
---|
87 | PhyML_Printf("%s\nCommand options:\n%s",BOLD,FLAT); |
---|
88 | |
---|
89 | PhyML_Printf("\n\t%s-i (or --input) %sseq_file_name%s\n",BOLD,LINE,FLAT); |
---|
90 | PhyML_Printf("\t\t%sseq_file_name%s is the name of the nucleotide or amino-acid sequence file in PHYLIP format.\n",LINE,FLAT); |
---|
91 | PhyML_Printf("\n"); |
---|
92 | |
---|
93 | PhyML_Printf("%s\n\t-d (or --datatype) ""%sdata_type%s\n",BOLD,LINE,FLAT); |
---|
94 | PhyML_Printf("\t\t%sdata_type%s is 'nt' for nucleotide (default), 'aa' for amino-acid sequences, or 'generic',\n",LINE,FLAT); |
---|
95 | PhyML_Printf("\t\t(use NEXUS file format and the 'symbols' parameter here).\n"); |
---|
96 | PhyML_Printf("\n"); |
---|
97 | |
---|
98 | |
---|
99 | PhyML_Printf("%s\n\t-q (or --sequential)\n",BOLD); |
---|
100 | PhyML_Printf("%s\t\tChanges interleaved format (default) to sequential format.\n",FLAT); |
---|
101 | PhyML_Printf("\n"); |
---|
102 | |
---|
103 | |
---|
104 | #ifndef PHYTIME |
---|
105 | PhyML_Printf("%s\n\t-n (or --multiple) ""%snb_data_sets%s\n",BOLD,LINE,FLAT); |
---|
106 | PhyML_Printf("\t\t%snb_data_sets%s is an integer corresponding to the number of data sets to analyse.\n",LINE,FLAT); |
---|
107 | PhyML_Printf("\n"); |
---|
108 | #endif |
---|
109 | |
---|
110 | |
---|
111 | #ifndef PHYTIME |
---|
112 | PhyML_Printf("%s\n\t-p (or --pars)%s\n",BOLD,FLAT); |
---|
113 | PhyML_Printf("%s\t\tUse a minimum parsimony starting tree. This option is taken into account when the '-u' option\n",FLAT); |
---|
114 | PhyML_Printf("%s\t\tis absent and when tree topology modifications are to be done.\n",FLAT); |
---|
115 | PhyML_Printf("\n"); |
---|
116 | #endif |
---|
117 | |
---|
118 | |
---|
119 | #ifndef PHYTIME |
---|
120 | PhyML_Printf("%s\n\t-b (or --bootstrap) %sint%s\n",BOLD,LINE,FLAT); |
---|
121 | PhyML_Printf("\t\t%sint%s > 0: %sint%s is the number of bootstrap replicates.\n",LINE,FLAT,LINE,FLAT); |
---|
122 | PhyML_Printf("\t\t%sint%s = 0: neither approximate likelihood ratio test nor bootstrap values are computed.\n",LINE,FLAT); |
---|
123 | PhyML_Printf("\t\t%sint%s = -1: approximate likelihood ratio test returning aLRT statistics.\n",LINE,FLAT); |
---|
124 | PhyML_Printf("\t\t%sint%s = -2: approximate likelihood ratio test returning Chi2-based parametric branch supports.\n",LINE,FLAT); |
---|
125 | /* PhyML_Printf("\t\t%sint%s = -3 : minimum of Chi2-based parametric and SH-like branch supports.\n",LINE,FLAT); */ |
---|
126 | PhyML_Printf("\t\t%sint%s = -4: SH-like branch supports alone.\n",LINE,FLAT); |
---|
127 | PhyML_Printf("\t\t%sint%s = -5: (default) approximate Bayes branch supports.\n",LINE,FLAT); |
---|
128 | PhyML_Printf("\n"); |
---|
129 | #endif |
---|
130 | |
---|
131 | |
---|
132 | PhyML_Printf("%s\n\t-m (or --model) %smodel%s\n",BOLD,LINE,FLAT); |
---|
133 | PhyML_Printf("\t\tmodel%s : substitution model name.\n",FLAT); |
---|
134 | PhyML_Printf("\t\t%s- %sNucleotide%s-based models : %sHKY85%s (default) | %sJC69%s | %sK80%s | %sF81%s | %sF84%s | %sTN93%s | %sGTR%s | %scustom (*)%s\n", |
---|
135 | FLAT,LINE,FLAT,LINE,FLAT,LINE,FLAT,LINE,FLAT,LINE,FLAT,LINE,FLAT,LINE,FLAT,LINE,FLAT,LINE,FLAT); |
---|
136 | PhyML_Printf("\t\t(*) : for the custom option, a string of six digits identifies the model. For instance, 000000\n"); |
---|
137 | PhyML_Printf("\t\t corresponds to F81 (or JC69 provided the distribution of nucleotide frequencies is uniform).\n"); |
---|
138 | PhyML_Printf("\t\t 012345 corresponds to GTR. This option can be used for encoding any model that is a nested within GTR.\n"); |
---|
139 | PhyML_Printf("\n"); |
---|
140 | PhyML_Printf("\t\t%s- %sAmino-acid%s based models : %sLG%s (default) | %sWAG%s | %sJTT%s | %sMtREV%s | %sDayhoff%s | %sDCMut%s | %sRtREV%s | %sCpREV%s | %sVT%s\n", |
---|
141 | FLAT,LINE,FLAT, |
---|
142 | LINE,FLAT, |
---|
143 | LINE,FLAT, |
---|
144 | LINE,FLAT, |
---|
145 | LINE,FLAT, |
---|
146 | LINE,FLAT, |
---|
147 | LINE,FLAT, |
---|
148 | LINE,FLAT, |
---|
149 | LINE,FLAT, |
---|
150 | LINE,FLAT); |
---|
151 | PhyML_Printf("\t\t %sBlosum62%s | %sMtMam%s | %sMtArt%s | %sHIVw%s | %sHIVb%s | %scustom%s\n", |
---|
152 | LINE,FLAT, |
---|
153 | LINE,FLAT, |
---|
154 | LINE,FLAT, |
---|
155 | LINE,FLAT, |
---|
156 | LINE,FLAT, |
---|
157 | LINE,FLAT); |
---|
158 | |
---|
159 | PhyML_Printf("\n"); |
---|
160 | |
---|
161 | PhyML_Printf("%s\n\t--aa_rate_file %sfilename%s\n",BOLD,LINE,FLAT); |
---|
162 | PhyML_Printf("\t\t%sfilename%s is the name of the file that provides the amino acid substitution rate matrix in PAML format.\n",LINE,FLAT); |
---|
163 | PhyML_Printf("\t\tIt is compulsory to use this option when analysing amino acid sequences with the `custom' model.\n"); |
---|
164 | PhyML_Printf("\n"); |
---|
165 | |
---|
166 | |
---|
167 | #ifndef PHYTIME |
---|
168 | PhyML_Printf("%s\n\t-f %se%s, %sm%s, or %sfA,fC,fG,fT%s\n",BOLD,LINE,BOLD,LINE,BOLD,LINE,FLAT); |
---|
169 | PhyML_Printf("\t\t%se%s : the character frequencies are determined as follows : \n",LINE,FLAT); |
---|
170 | PhyML_Printf("%s\t\t- %sNucleotide%s sequences: (Empirical) the equilibrium base frequencies are estimated by counting\n" |
---|
171 | "\t\t the occurence of the different bases in the alignment.\n",FLAT,LINE,FLAT); |
---|
172 | PhyML_Printf("%s\t\t- %sAmino-acid%s sequences: (Empirical) the equilibrium amino-acid frequencies are estimated by counting\n" |
---|
173 | "\t\t the occurence of the different amino-acids in the alignment.\n",FLAT,LINE,FLAT); |
---|
174 | PhyML_Printf("\n"); |
---|
175 | PhyML_Printf("\t\t%sm%s : the character frequencies are determined as follows : \n",LINE,FLAT); |
---|
176 | PhyML_Printf("%s\t\t- %sNucleotide%s sequences: (ML) the equilibrium base frequencies are estimated using maximum likelihood \n",FLAT,LINE,FLAT); |
---|
177 | PhyML_Printf("%s\t\t- %sAmino-acid%s sequences: (Model) the equilibrium amino-acid frequencies are estimated using\n" |
---|
178 | "\t\t the frequencies defined by the substitution model.\n",FLAT,LINE,FLAT); |
---|
179 | PhyML_Printf("\n"); |
---|
180 | PhyML_Printf("\t\t%s\"fA,fC,fG,fT\"%s : only valid for nucleotide-based models. fA, fC, fG and fT are floating numbers that \n",LINE,FLAT); |
---|
181 | PhyML_Printf("\t\t correspond to the frequencies of A, C, G and T respectively (WARNING: do not use any blank space between\n"); |
---|
182 | PhyML_Printf("\t\t your values of nucleotide frequencies, only commas!)\n"); |
---|
183 | PhyML_Printf("\n"); |
---|
184 | #endif |
---|
185 | |
---|
186 | #ifdef PHYTIME |
---|
187 | PhyML_Printf("%s\n\t--calibration %sfilename%s\n",BOLD,LINE,FLAT); |
---|
188 | PhyML_Printf("\t\t%sfilename%s is the name of the calibration file that provides a priori defined boundaries for node ages.\n",LINE,FLAT); |
---|
189 | PhyML_Printf("\t\tPlease read the manual for more information about the format of this file.\n"); |
---|
190 | PhyML_Printf("\n"); |
---|
191 | #endif |
---|
192 | |
---|
193 | |
---|
194 | |
---|
195 | |
---|
196 | PhyML_Printf("%s\n\t-t (or --ts/tv) %sts/tv_ratio%s\n",BOLD,LINE,FLAT); |
---|
197 | PhyML_Printf("\t\tts/tv_ratio%s : transition/transversion ratio. DNA sequences only.\n",FLAT); |
---|
198 | PhyML_Printf("\t\tCan be a fixed positive value (ex:4.0) or %se%s to get the maximum likelihood estimate.\n",LINE,FLAT); |
---|
199 | PhyML_Printf("\n"); |
---|
200 | |
---|
201 | PhyML_Printf("%s\n\t-v (or --pinv) %sprop_invar%s\n",BOLD,LINE,FLAT); |
---|
202 | PhyML_Printf("\t\tprop_invar%s : proportion of invariable sites.\n",FLAT); |
---|
203 | PhyML_Printf("\t\tCan be a fixed value in the [0,1] range or %se%s to get the maximum likelihood estimate.\n",LINE,FLAT); |
---|
204 | PhyML_Printf("\n"); |
---|
205 | |
---|
206 | PhyML_Printf("%s\n\t-c (or --nclasses) %snb_subst_cat%s\n",BOLD,LINE,FLAT); |
---|
207 | PhyML_Printf("\t\tnb_subst_cat%s : number of relative substitution rate categories. Default : %snb_subst_cat%s=4.\n", |
---|
208 | FLAT,LINE,FLAT); |
---|
209 | PhyML_Printf("\t\tMust be a positive integer.\n"); |
---|
210 | PhyML_Printf("\n"); |
---|
211 | |
---|
212 | PhyML_Printf("%s\n\t-a (or --alpha) %sgamma%s\n",BOLD,LINE,FLAT); |
---|
213 | PhyML_Printf("\t\tgamma%s : distribution of the gamma distribution shape parameter.\n",FLAT); |
---|
214 | PhyML_Printf("\t\tCan be a fixed positive value or %se%s to get the maximum likelihood estimate.\n",LINE,FLAT); |
---|
215 | PhyML_Printf("\n"); |
---|
216 | |
---|
217 | #ifndef PHYTIME |
---|
218 | PhyML_Printf("%s\n\t-s (or --search) %smove%s\n",BOLD,LINE,FLAT); |
---|
219 | PhyML_Printf("\t\tTree topology search operation option.\n"); |
---|
220 | PhyML_Printf("\t\tCan be either %sNNI%s (default, fast) or %sSPR%s (a bit slower than NNI) or %sBEST%s (best of NNI and SPR search).\n",LINE,FLAT,LINE,FLAT,LINE,FLAT); |
---|
221 | PhyML_Printf("\n"); |
---|
222 | #endif |
---|
223 | |
---|
224 | |
---|
225 | PhyML_Printf("%s\n\t-u (or --inputtree) %suser_tree_file%s\n",BOLD,LINE,FLAT); |
---|
226 | PhyML_Printf("\t\tuser_tree_file%s : starting tree filename. The tree must be in Newick format.\n",FLAT); |
---|
227 | PhyML_Printf("\n"); |
---|
228 | |
---|
229 | |
---|
230 | #ifndef PHYTIME |
---|
231 | PhyML_Printf("%s\n\t-o %sparams%s\n",BOLD,LINE,FLAT); |
---|
232 | PhyML_Printf("\t\tThis option focuses on specific parameter optimisation.\n"); |
---|
233 | PhyML_Printf("\t\t%sparams%s=tlr : tree topology (t), branch length (l) and rate parameters (r) are optimised.\n",LINE,FLAT); |
---|
234 | PhyML_Printf("\t\t%sparams%s=tl : tree topology and branch length are optimised.\n",LINE,FLAT); |
---|
235 | PhyML_Printf("\t\t%sparams%s=lr : branch length and rate parameters are optimised.\n",LINE,FLAT); |
---|
236 | PhyML_Printf("\t\t%sparams%s=l : branch length are optimised.\n",LINE,FLAT); |
---|
237 | PhyML_Printf("\t\t%sparams%s=r : rate parameters are optimised.\n",LINE,FLAT); |
---|
238 | PhyML_Printf("\t\t%sparams%s=n : no parameter is optimised.\n",LINE,FLAT); |
---|
239 | PhyML_Printf("\n"); |
---|
240 | #endif |
---|
241 | |
---|
242 | |
---|
243 | #ifndef PHYTIME |
---|
244 | PhyML_Printf("%s\n\t--rand_start%s\n",BOLD,FLAT); |
---|
245 | PhyML_Printf("\t\tThis option sets the initial tree to random.\n"); |
---|
246 | PhyML_Printf("\t\tIt is only valid if SPR searches are to be performed.\n"); |
---|
247 | PhyML_Printf("\n"); |
---|
248 | #endif |
---|
249 | |
---|
250 | #ifndef PHYTIME |
---|
251 | PhyML_Printf("%s\n\t--n_rand_starts %snum%s\n",BOLD,LINE,FLAT); |
---|
252 | PhyML_Printf("\t\tnum%s is the number of initial random trees to be used.\n",FLAT); |
---|
253 | PhyML_Printf("\t\tIt is only valid if SPR searches are to be performed.\n"); |
---|
254 | PhyML_Printf("\n"); |
---|
255 | #endif |
---|
256 | |
---|
257 | PhyML_Printf("%s\n\t--r_seed %snum%s\n",BOLD,LINE,FLAT); |
---|
258 | PhyML_Printf("\t\tnum%s is the seed used to initiate the random number generator.\n",FLAT); |
---|
259 | PhyML_Printf("\t\tMust be an integer.\n"); |
---|
260 | PhyML_Printf("\n"); |
---|
261 | |
---|
262 | #ifndef PHYTIME |
---|
263 | PhyML_Printf("%s\n\t--print_site_lnl%s\n",BOLD,FLAT); |
---|
264 | PhyML_Printf("\t\t%sPrint the likelihood for each site in file *_phyml_lk.txt.\n",FLAT); |
---|
265 | PhyML_Printf("\n"); |
---|
266 | #endif |
---|
267 | |
---|
268 | #ifndef PHYTIME |
---|
269 | PhyML_Printf("%s\n\t--print_trace%s\n",BOLD,FLAT); |
---|
270 | PhyML_Printf("\t\t%sPrint each phylogeny explored during the tree search process\n",FLAT); |
---|
271 | PhyML_Printf("\t\t%sin file *_phyml_trace.txt.\n",FLAT); |
---|
272 | PhyML_Printf("\n"); |
---|
273 | #endif |
---|
274 | |
---|
275 | |
---|
276 | PhyML_Printf("%s\n\t--run_id %sID_string%s\n",BOLD,LINE,FLAT); |
---|
277 | PhyML_Printf("\t\t%sAppend the string %sID_string%s at the end of each PhyML output file.\n",FLAT,LINE,FLAT); |
---|
278 | PhyML_Printf("\t\t%sThis option may be useful when running simulations involving PhyML.\n",FLAT); |
---|
279 | PhyML_Printf("\n"); |
---|
280 | |
---|
281 | PhyML_Printf("%s\n\t--quiet%s\n",BOLD,FLAT); |
---|
282 | PhyML_Printf("\t\t%sNo interactive question (for running in batch mode) and quiet output.\n",FLAT); |
---|
283 | PhyML_Printf("\n"); |
---|
284 | |
---|
285 | |
---|
286 | PhyML_Printf("%s\n\t--no_memory_check%s\n",BOLD,FLAT); |
---|
287 | PhyML_Printf("\t\t%sNo interactive question for memory usage (for running in batch mode). Normal ouput otherwise.\n",FLAT); |
---|
288 | PhyML_Printf("\n"); |
---|
289 | |
---|
290 | #ifndef PHYTIME |
---|
291 | PhyML_Printf("%s\n\t--alias_subpatt%s\n",BOLD,FLAT); |
---|
292 | PhyML_Printf("\t\t%sSite aliasing is generalized at the subtree level. Sometimes lead to faster calculations.\n",FLAT); |
---|
293 | PhyML_Printf("\t\t%sSee Kosakovsky Pond SL, Muse SV, Sytematic Biology (2004) for an example.\n",FLAT); |
---|
294 | PhyML_Printf("\n"); |
---|
295 | #endif |
---|
296 | |
---|
297 | #ifndef PHYTIME |
---|
298 | PhyML_Printf("%s\n\t--boot_progress_display %snum%s (default=20)\n",BOLD,LINE,FLAT); |
---|
299 | PhyML_Printf("\t\t%snum%s is the frequency at which the bootstrap progress bar will be updated.\n",LINE,FLAT); |
---|
300 | PhyML_Printf("\t\tMust be an integer.\n"); |
---|
301 | PhyML_Printf("\n"); |
---|
302 | #endif |
---|
303 | |
---|
304 | |
---|
305 | #ifdef PHYTIME |
---|
306 | PhyML_Printf("%s\n\t--chain_len %snum%s\n",BOLD,LINE,FLAT); |
---|
307 | PhyML_Printf("\t\t%snum%s is the number of generations or runs of the Markov Chain Monte Carlo. Set to 1E+6 by default. \n",LINE,FLAT); |
---|
308 | PhyML_Printf("\t\tMust be an integer.\n"); |
---|
309 | PhyML_Printf("\n"); |
---|
310 | #endif |
---|
311 | |
---|
312 | /* #ifdef PHYTIME */ |
---|
313 | /* PhyML_Printf("%s\n\t--burnin %snum%s\n",BOLD,LINE,FLAT); */ |
---|
314 | /* PhyML_Printf("\t\t%snum%s is the number of generations of runs of the Markov Chain Monte Carlo during the 'burnin' period.\n",LINE,FLAT); */ |
---|
315 | /* PhyML_Printf("\t\t%sSet to 1E+5 by default. Must be an integer. \n",FLAT); */ |
---|
316 | /* PhyML_Printf("\n"); */ |
---|
317 | /* #endif */ |
---|
318 | |
---|
319 | #ifdef PHYTIME |
---|
320 | PhyML_Printf("%s\n\t--sample_freq %snum%s\n",BOLD,LINE,FLAT); |
---|
321 | PhyML_Printf("\t\tThe chain is sampled every %snum%s generations. Set to 1E+3 by default. \n",LINE,FLAT); |
---|
322 | PhyML_Printf("\t\tMust be an integer.\n"); |
---|
323 | PhyML_Printf("\n"); |
---|
324 | #endif |
---|
325 | |
---|
326 | |
---|
327 | #ifdef PHYTIME |
---|
328 | PhyML_Printf("%s\n\t--no_sequences%s\n",BOLD,FLAT); |
---|
329 | PhyML_Printf("\t\tUse this option to run the sampler without sequence data.\n"); |
---|
330 | PhyML_Printf("\n"); |
---|
331 | #endif |
---|
332 | |
---|
333 | |
---|
334 | #ifdef PHYTIME |
---|
335 | PhyML_Printf("%s\n\t--fastlk%s\n",BOLD,FLAT); |
---|
336 | PhyML_Printf("\t\tUse the multivariate normal approximation to the likelihood and speed up calculations\n"); |
---|
337 | PhyML_Printf("\n"); |
---|
338 | #endif |
---|
339 | |
---|
340 | |
---|
341 | #ifdef PHYML |
---|
342 | PhyML_Printf("%sPHYLIP-LIKE INTERFACE\n""%s\n\tYou can also use PhyML with no argument, in this case change the value of\n",BOLD,FLAT); |
---|
343 | PhyML_Printf("%s\ta parameter by typing its corresponding character as shown on screen.\n\n",FLAT); |
---|
344 | #endif |
---|
345 | |
---|
346 | #ifdef PHYML |
---|
347 | PhyML_Printf("%sEXAMPLES\n\n" |
---|
348 | "%s\tDNA interleaved sequence file, default parameters : ""%s ./phyml -i seqs1" |
---|
349 | "%s\n\tAA interleaved sequence file, default parameters : ""%s ./phyml -i seqs2 -d aa" |
---|
350 | "%s\n\tAA sequential sequence file, with customization : ""%s ./phyml -i seqs3 -q -d aa -m JTT -c 4 -a e%s\n",BOLD,FLAT,BOLD,FLAT,BOLD,FLAT,BOLD,FLAT); |
---|
351 | #endif |
---|
352 | |
---|
353 | Exit(""); |
---|
354 | } |
---|
355 | |
---|
356 | ////////////////////////////////////////////////////////////// |
---|
357 | ////////////////////////////////////////////////////////////// |
---|
358 | |
---|
359 | |
---|
360 | |
---|