Rdnaml(X, path=NULL, ...)
Rdnamlk(X, path=NULL, ...)
"phylo"
that is the optimized tree.quiet
suppress some output to R console (defaults to quiet = FALSE
); tree
object of class "phylo"
- if supplied, then the model will be optimized on a fixed input topology; kappa
transition:transversion ratio (defaults to kappa = 2.0
); bf
vector of base frequencies in alphabetical order (i.e., A, C, G, & T) - if not provided, then defaults to empirical frequencies; rates
vector of rates (defaults to single rate); rate.categories
vector of rate categories corresponding to the order of rates
; gamma
alpha shape parameter of a gamma model of rate heterogeneity among sites (defaults to no gamma rate heterogeneity); ncat
number of rate categories for the gamma model; inv
proportion of invariant sites for the invariant sites model (defaults to inv = 0
); weights
vector of weights of length equal to the number of columns in X
(defaults to unweighted); speedier
speedier but rougher analysis (defaults to speedier = FALSE
); global
perform global search (defaults to global = TRUE
); random.order
add taxa to tree in random order (defaults to random.order = TRUE
); random.addition
number of random addition replicates for random.order = TRUE
(defaults to random.addition = 10
); outgroup
outgroup if outgroup rooting of the estimated tree is desired; and cleanup
remove PHYLIP input & output files after the analysis is completed (defaults to cleanup = TRUE
).
Finally clock=TRUE
enforces a molecular clock. The argument clock
is only available for Rdnaml
. If clock=TRUE
then dnamlk is used internally. For Rdnamlk
a molecular clock is assumed, thus Rdnaml(...,clock=TRUE)
and Rdnamlk(...)
are equivalent.
More information about the dnaml and dnamlk programs in PHYLIP can be found here opt.Rdnaml
, Rcontml
, Rproml
data(primates)
tree<-Rdnaml(primates,kappa=10)
clockTree<-Rdnamlk(primates,kappa=10)
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