+ m->mothurOut("The phylo.diversity command can only be executed after a successful read.tree command.\n");
+ m->mothurOut("The phylo.diversity command parameters are groups, iters, freq, scale, rarefy, collect and summary. No parameters are required.\n");
+ m->mothurOut("The groups parameter allows you to specify which of the groups in your groupfile you would like analyzed. The group names are separated by dashes. By default all groups are used.\n");
+ m->mothurOut("The iters parameter allows you to specify the number of randomizations to preform, by default iters=1000, if you set rarefy to true.\n");
+ m->mothurOut("The freq parameter is used indicate when to output your data, by default it is set to 100. But you can set it to a percentage of the number of sequence. For example freq=0.10, means 10%. \n");
+ m->mothurOut("The scale parameter is used indicate that you want your ouptut scaled to the number of sequences sampled, default = false. \n");
+ m->mothurOut("The rarefy parameter allows you to create a rarefaction curve. The default is false.\n");
+ m->mothurOut("The collect parameter allows you to create a collectors curve. The default is false.\n");
+ m->mothurOut("The summary parameter allows you to create a .summary file. The default is true.\n");
+ m->mothurOut("The phylo.diversity command should be in the following format: phylo.diversity(groups=yourGroups, rarefy=yourRarefy, iters=yourIters).\n");
+ m->mothurOut("Example phylo.diversity(groups=A-B-C, rarefy=T, iters=500).\n");
+ m->mothurOut("The phylo.diversity command output two files: .phylo.diversity and if rarefy=T, .rarefaction.\n");
+ m->mothurOut("Note: No spaces between parameter labels (i.e. groups), '=' and parameters (i.e.yourGroups).\n\n");