| tree.raxml | R Documentation | 
Performs tree inference under "RAxML" for aligned fasta sequences in
a given folder (default is "2.Alignments"). Note that you need at
least two gene regions to run a partitioned analysis.
tree.raxml(
  folder = "2.Alignments",
  FilePatterns = "Masked_",
  raxml_exec = "raxmlHPC",
  Bootstrap = 100,
  outgroup,
  partitioned = FALSE,
  ...
)
| folder | Name of the folder where the sequences to align are stored (character). | 
| FilePatterns | A string that is common to all the target files
in the relevant folder (character). Note that
this argument can be set to  | 
| raxml_exec | Where to find  | 
| Bootstrap | Number of bootstrap replicates (numeric). | 
| outgroup | A single string of comma-separated tip labels to be
used as outgroup in  | 
| partitioned | Whether analyses should be partitioned by gene (Logical). | 
| ... | Arguments passed to  | 
None
## Not run: 
sq.retrieve.direct(
  clades = c("Felis", "Vulpes", "Phoca"),
  species = "Manis_pentadactyla",
  genes = c("ADORA3", "CYTB")
)
sq.curate(
  filterTaxonomicCriteria = "Felis|Vulpes|Phoca|Manis",
  kingdom = "animals", folder = "0.Sequences"
)
sq.aln(folder = "1.CuratedSequences")
tree.raxml(
  folder = "2.Alignments", FilePatterns = "Masked",
  raxml_exec = "raxmlHPC", Bootstrap = 100,
  outgroup = "Manis_pentadactyla"
)
## End(Not run)
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.