/*

PhyML:  a program that  computes maximum likelihood phylogenies from
DNA or AA homologous sequences.

Copyright (C) Stephane Guindon. Oct 2003 onward.

All parts of the source except where indicated are distributed under
the GNU public licence. See http://www.opensource.org for details.

*/


#include "help.h"


/* int  T_MAX_FILE; */
/* phydbl SMALL; */
/* phydbl UNLIKELY; */

//////////////////////////////////////////////////////////////
//////////////////////////////////////////////////////////////


void Usage()
{

  char *BOLD=(char *)mCalloc(10,sizeof(char));
  char *FLAT=(char *)mCalloc(10,sizeof(char));
  char *LINE=(char *)mCalloc(10,sizeof(char));
  char *cha;


  cha =getenv("OS");

  if(cha!=NULL) 
    {
      strcpy(BOLD, "");
      strcpy(FLAT, "");
      strcpy(LINE, "");
    } 
  else 
    {
      strcpy(BOLD, "\033[00;01m");
      strcpy(FLAT, "\033[00;00m");
      strcpy(LINE, "\033[00;04m");
    }

  #ifdef PHYML
  PhyML_Printf("%sNAME\n"
	 "%s\t- PhyML %s - \n\n"
	 "%s\t\''A simple, fast, and accurate algorithm to estimate\n"
	 "%s\tlarge phylogenies by maximum likelihood\''\n\n"
	 "%s\tStephane Guindon and Olivier Gascuel,\n"
	 "%s\tSystematic Biology 52(5):696-704, 2003.\n\n"
	 "%s\tPlease cite this paper if you use this software in your publications.\n",BOLD,FLAT,VERSION,FLAT,FLAT,FLAT,FLAT,FLAT);
  #endif

  #ifdef PHYTIME
  PhyML_Printf("%sNAME\n"
	 "%s\t- PhyTime %s - \n\n"
	 "%s\t'Bayesian estimation of divergence times from large sequence alignments.'\n"
	 "%s\tStephane Guindon,\n"
	 "%s\tMolecular Biology and Evolution 27(8):1768-81, 2010.\n\n"
	 "%s\tPlease cite this paper if you use this software in your publications.\n",BOLD,FLAT,VERSION,FLAT,FLAT,FLAT,FLAT,FLAT);
  #endif



  #ifdef PHYML
  PhyML_Printf("%s\nSYNOPSIS:\n\n"
	 "%s\tphyml %s[command args]\n",BOLD,BOLD,BOLD);
  #endif
  #ifdef PHYTIME
  PhyML_Printf("%s\nSYNOPSIS:\n\n"
	 "%s\tphytime %s[command args]\n",BOLD,BOLD,BOLD);
  #endif

  #ifdef PHYML
  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); 
  #endif

  #ifdef PHYTIME
  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); 
  #endif 

  PhyML_Printf("%s\nCommand options:\n%s",BOLD,FLAT);

  PhyML_Printf("\n\t%s-i (or --input) %sseq_file_name%s\n",BOLD,LINE,FLAT); 
  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);
  PhyML_Printf("\n");

  PhyML_Printf("%s\n\t-d (or --datatype) ""%sdata_type%s\n",BOLD,LINE,FLAT);
  PhyML_Printf("\t\t%sdata_type%s is 'nt' for nucleotide (default), 'aa' for amino-acid sequences, or 'generic',\n",LINE,FLAT); 
  PhyML_Printf("\t\t(use NEXUS file format and the 'symbols' parameter here).\n");
  PhyML_Printf("\n");

  
  PhyML_Printf("%s\n\t-q (or --sequential)\n",BOLD);
  PhyML_Printf("%s\t\tChanges interleaved format (default) to sequential format.\n",FLAT);
  PhyML_Printf("\n");


  #ifndef PHYTIME
  PhyML_Printf("%s\n\t-n (or --multiple) ""%snb_data_sets%s\n",BOLD,LINE,FLAT);
  PhyML_Printf("\t\t%snb_data_sets%s is an integer corresponding to the number of data sets to analyse.\n",LINE,FLAT);
  PhyML_Printf("\n");
  #endif


  #ifndef PHYTIME
  PhyML_Printf("%s\n\t-p (or --pars)%s\n",BOLD,FLAT);
  PhyML_Printf("%s\t\tUse a minimum parsimony starting tree. This option is taken into account when the '-u' option\n",FLAT);
  PhyML_Printf("%s\t\tis absent and when tree topology modifications are to be done.\n",FLAT);
  PhyML_Printf("\n");
  #endif


  #ifndef PHYTIME
  PhyML_Printf("%s\n\t-b (or --bootstrap) %sint%s\n",BOLD,LINE,FLAT);
  PhyML_Printf("\t\t%sint%s >  0: %sint%s is the number of bootstrap replicates.\n",LINE,FLAT,LINE,FLAT);
  PhyML_Printf("\t\t%sint%s =  0: neither approximate likelihood ratio test nor bootstrap values are computed.\n",LINE,FLAT);
  PhyML_Printf("\t\t%sint%s = -1: approximate likelihood ratio test returning aLRT statistics.\n",LINE,FLAT);
  PhyML_Printf("\t\t%sint%s = -2: approximate likelihood ratio test returning Chi2-based parametric branch supports.\n",LINE,FLAT);
/*   PhyML_Printf("\t\t%sint%s = -3 : minimum of Chi2-based parametric and SH-like branch supports.\n",LINE,FLAT); */
  PhyML_Printf("\t\t%sint%s = -4: SH-like branch supports alone.\n",LINE,FLAT);
  PhyML_Printf("\t\t%sint%s = -5: (default) approximate Bayes branch supports.\n",LINE,FLAT);
  PhyML_Printf("\n");
  #endif


  PhyML_Printf("%s\n\t-m (or --model) %smodel%s\n",BOLD,LINE,FLAT);
  PhyML_Printf("\t\tmodel%s : substitution model name.\n",FLAT);
  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",
	 FLAT,LINE,FLAT,LINE,FLAT,LINE,FLAT,LINE,FLAT,LINE,FLAT,LINE,FLAT,LINE,FLAT,LINE,FLAT,LINE,FLAT);
  PhyML_Printf("\t\t(*) : for the custom option, a string of six digits identifies the model. For instance, 000000\n");
  PhyML_Printf("\t\t corresponds to F81 (or JC69 provided the distribution of nucleotide frequencies is uniform).\n");
  PhyML_Printf("\t\t 012345 corresponds to GTR. This option can be used for encoding any model that is a nested within GTR.\n");
  PhyML_Printf("\n");
  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",	 
	 FLAT,LINE,FLAT,
	 LINE,FLAT,
	 LINE,FLAT,
	 LINE,FLAT,
	 LINE,FLAT,
	 LINE,FLAT,
	 LINE,FLAT,
	 LINE,FLAT,
	 LINE,FLAT,
	 LINE,FLAT);
  PhyML_Printf("\t\t %sBlosum62%s | %sMtMam%s | %sMtArt%s | %sHIVw%s |  %sHIVb%s | %scustom%s\n",
	 LINE,FLAT,
	 LINE,FLAT,
	 LINE,FLAT,
	 LINE,FLAT,
	 LINE,FLAT,
	 LINE,FLAT);

  PhyML_Printf("\n");

  PhyML_Printf("%s\n\t--aa_rate_file %sfilename%s\n",BOLD,LINE,FLAT);
  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);
  PhyML_Printf("\t\tIt is compulsory to use this option when analysing amino acid sequences with the `custom' model.\n");
  PhyML_Printf("\n");


  #ifndef PHYTIME
  PhyML_Printf("%s\n\t-f %se%s, %sm%s, or %sfA,fC,fG,fT%s\n",BOLD,LINE,BOLD,LINE,BOLD,LINE,FLAT);
  PhyML_Printf("\t\t%se%s : the character frequencies are determined as follows : \n",LINE,FLAT);
  PhyML_Printf("%s\t\t- %sNucleotide%s sequences: (Empirical) the equilibrium base frequencies are estimated by counting\n"
	 "\t\t the occurence of the different bases in the alignment.\n",FLAT,LINE,FLAT);
  PhyML_Printf("%s\t\t- %sAmino-acid%s sequences: (Empirical) the equilibrium amino-acid frequencies are estimated by counting\n"
"\t\t the occurence of the different amino-acids in the alignment.\n",FLAT,LINE,FLAT);
  PhyML_Printf("\n");
  PhyML_Printf("\t\t%sm%s : the character frequencies are determined as follows : \n",LINE,FLAT);
  PhyML_Printf("%s\t\t- %sNucleotide%s sequences: (ML) the equilibrium base frequencies are estimated using maximum likelihood \n",FLAT,LINE,FLAT);
  PhyML_Printf("%s\t\t- %sAmino-acid%s sequences: (Model) the equilibrium amino-acid frequencies are estimated using\n"
"\t\t the frequencies defined by the substitution model.\n",FLAT,LINE,FLAT);
  PhyML_Printf("\n");
  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);
  PhyML_Printf("\t\t correspond to the frequencies of A, C, G and T respectively (WARNING: do not use any blank space between\n");
  PhyML_Printf("\t\t your values of nucleotide frequencies, only commas!)\n");
  PhyML_Printf("\n");
  #endif

  #ifdef PHYTIME
  PhyML_Printf("%s\n\t--calibration %sfilename%s\n",BOLD,LINE,FLAT);
  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);
  PhyML_Printf("\t\tPlease read the manual for more information about the format of this file.\n");
  PhyML_Printf("\n");
  #endif




  PhyML_Printf("%s\n\t-t (or --ts/tv) %sts/tv_ratio%s\n",BOLD,LINE,FLAT);
  PhyML_Printf("\t\tts/tv_ratio%s : transition/transversion ratio. DNA sequences only.\n",FLAT);
  PhyML_Printf("\t\tCan be a fixed positive value (ex:4.0) or %se%s to get the maximum likelihood estimate.\n",LINE,FLAT);
  PhyML_Printf("\n");

  PhyML_Printf("%s\n\t-v (or --pinv) %sprop_invar%s\n",BOLD,LINE,FLAT);
  PhyML_Printf("\t\tprop_invar%s : proportion of invariable sites.\n",FLAT);
  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);
  PhyML_Printf("\n");

  PhyML_Printf("%s\n\t-c (or --nclasses) %snb_subst_cat%s\n",BOLD,LINE,FLAT);
  PhyML_Printf("\t\tnb_subst_cat%s : number of relative substitution rate categories. Default : %snb_subst_cat%s=4.\n",
	 FLAT,LINE,FLAT);
  PhyML_Printf("\t\tMust be a positive integer.\n");
  PhyML_Printf("\n");
  
  PhyML_Printf("%s\n\t-a (or --alpha) %sgamma%s\n",BOLD,LINE,FLAT);
  PhyML_Printf("\t\tgamma%s : distribution of the gamma distribution shape parameter.\n",FLAT);
  PhyML_Printf("\t\tCan be a fixed positive value or %se%s to get the maximum likelihood estimate.\n",LINE,FLAT);
  PhyML_Printf("\n");

  #ifndef PHYTIME
  PhyML_Printf("%s\n\t-s (or --search) %smove%s\n",BOLD,LINE,FLAT);
  PhyML_Printf("\t\tTree topology search operation option.\n");
  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);
  PhyML_Printf("\n");
  #endif


  PhyML_Printf("%s\n\t-u (or --inputtree) %suser_tree_file%s\n",BOLD,LINE,FLAT);
  PhyML_Printf("\t\tuser_tree_file%s : starting tree filename. The tree must be in Newick format.\n",FLAT);
  PhyML_Printf("\n");


  #ifndef PHYTIME
  PhyML_Printf("%s\n\t-o %sparams%s\n",BOLD,LINE,FLAT);
  PhyML_Printf("\t\tThis option focuses on specific parameter optimisation.\n");
  PhyML_Printf("\t\t%sparams%s=tlr : tree topology (t), branch length (l) and rate parameters (r) are optimised.\n",LINE,FLAT);
  PhyML_Printf("\t\t%sparams%s=tl  : tree topology and branch length are optimised.\n",LINE,FLAT);
  PhyML_Printf("\t\t%sparams%s=lr  : branch length and rate parameters are optimised.\n",LINE,FLAT);
  PhyML_Printf("\t\t%sparams%s=l   : branch length are optimised.\n",LINE,FLAT);
  PhyML_Printf("\t\t%sparams%s=r   : rate parameters are optimised.\n",LINE,FLAT);
  PhyML_Printf("\t\t%sparams%s=n   : no parameter is optimised.\n",LINE,FLAT);  
  PhyML_Printf("\n");
  #endif


  #ifndef PHYTIME
  PhyML_Printf("%s\n\t--rand_start%s\n",BOLD,FLAT);
  PhyML_Printf("\t\tThis option sets the initial tree to random.\n");
  PhyML_Printf("\t\tIt is only valid if SPR searches are to be performed.\n");
  PhyML_Printf("\n");
  #endif

  #ifndef PHYTIME
  PhyML_Printf("%s\n\t--n_rand_starts %snum%s\n",BOLD,LINE,FLAT);
  PhyML_Printf("\t\tnum%s is the number of initial random trees to be used.\n",FLAT);
  PhyML_Printf("\t\tIt is only valid if SPR searches are to be performed.\n");
  PhyML_Printf("\n");
  #endif

  PhyML_Printf("%s\n\t--r_seed %snum%s\n",BOLD,LINE,FLAT);
  PhyML_Printf("\t\tnum%s is the seed used to initiate the random number generator.\n",FLAT);
  PhyML_Printf("\t\tMust be an integer.\n");
  PhyML_Printf("\n");

  #ifndef PHYTIME
  PhyML_Printf("%s\n\t--print_site_lnl%s\n",BOLD,FLAT);
  PhyML_Printf("\t\t%sPrint the likelihood for each site in file *_phyml_lk.txt.\n",FLAT);
  PhyML_Printf("\n");
  #endif

  #ifndef PHYTIME
  PhyML_Printf("%s\n\t--print_trace%s\n",BOLD,FLAT);
  PhyML_Printf("\t\t%sPrint each phylogeny explored during the tree search process\n",FLAT);
  PhyML_Printf("\t\t%sin file *_phyml_trace.txt.\n",FLAT);
  PhyML_Printf("\n");
  #endif


  PhyML_Printf("%s\n\t--run_id %sID_string%s\n",BOLD,LINE,FLAT);
  PhyML_Printf("\t\t%sAppend the string %sID_string%s at the end of each PhyML output file.\n",FLAT,LINE,FLAT);
  PhyML_Printf("\t\t%sThis option may be useful when running simulations involving PhyML.\n",FLAT);
  PhyML_Printf("\n");
  
  PhyML_Printf("%s\n\t--quiet%s\n",BOLD,FLAT);
  PhyML_Printf("\t\t%sNo interactive question (for running in batch mode) and quiet output.\n",FLAT);
  PhyML_Printf("\n");


  PhyML_Printf("%s\n\t--no_memory_check%s\n",BOLD,FLAT);
  PhyML_Printf("\t\t%sNo interactive question for memory usage (for running in batch mode). Normal ouput otherwise.\n",FLAT);
  PhyML_Printf("\n");

  #ifndef PHYTIME
  PhyML_Printf("%s\n\t--alias_subpatt%s\n",BOLD,FLAT);
  PhyML_Printf("\t\t%sSite aliasing is generalized at the subtree level. Sometimes lead to faster calculations.\n",FLAT);
  PhyML_Printf("\t\t%sSee Kosakovsky Pond SL, Muse SV, Sytematic Biology (2004) for an example.\n",FLAT);
  PhyML_Printf("\n");
  #endif

  #ifndef PHYTIME
  PhyML_Printf("%s\n\t--boot_progress_display %snum%s (default=20)\n",BOLD,LINE,FLAT);
  PhyML_Printf("\t\t%snum%s is the frequency at which the bootstrap progress bar will be updated.\n",LINE,FLAT);
  PhyML_Printf("\t\tMust be an integer.\n");
  PhyML_Printf("\n");
  #endif


  #ifdef PHYTIME
  PhyML_Printf("%s\n\t--chain_len %snum%s\n",BOLD,LINE,FLAT);
  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);
  PhyML_Printf("\t\tMust be an integer.\n");
  PhyML_Printf("\n");  
  #endif

/*   #ifdef PHYTIME */
/*   PhyML_Printf("%s\n\t--burnin %snum%s\n",BOLD,LINE,FLAT); */
/*   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); */
/*   PhyML_Printf("\t\t%sSet to 1E+5 by default. Must be an integer. \n",FLAT); */
/*   PhyML_Printf("\n");   */
/*   #endif */

  #ifdef PHYTIME
  PhyML_Printf("%s\n\t--sample_freq %snum%s\n",BOLD,LINE,FLAT);
  PhyML_Printf("\t\tThe chain is sampled every %snum%s generations. Set to 1E+3 by default. \n",LINE,FLAT);
  PhyML_Printf("\t\tMust be an integer.\n");
  PhyML_Printf("\n");  
  #endif


  #ifdef PHYTIME
  PhyML_Printf("%s\n\t--no_sequences%s\n",BOLD,FLAT);
  PhyML_Printf("\t\tUse this option to run the sampler without sequence data.\n");
  PhyML_Printf("\n");  
  #endif


  #ifdef PHYTIME
  PhyML_Printf("%s\n\t--fastlk%s\n",BOLD,FLAT);
  PhyML_Printf("\t\tUse the multivariate normal approximation to the likelihood and speed up calculations\n");
  PhyML_Printf("\n");  
  #endif


  #ifdef PHYML
  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);
  PhyML_Printf("%s\ta parameter by typing its corresponding character as shown on screen.\n\n",FLAT);
  #endif

  #ifdef PHYML
  PhyML_Printf("%sEXAMPLES\n\n"
	 "%s\tDNA interleaved sequence file, default parameters : ""%s  ./phyml -i seqs1"
	 "%s\n\tAA interleaved sequence file, default parameters :  ""%s  ./phyml -i seqs2 -d aa"
	 "%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);
  #endif

  Exit("");
}

//////////////////////////////////////////////////////////////
//////////////////////////////////////////////////////////////