treedater fits a strict or relaxed molecular clock to a
phylogenetic tree and estimates evolutionary rates and times of common
ancestry. The calendar time of each sample must be specified (possibly
with bounds of uncertainty) and the length of the sequences used to
estimate the tree.
treedater uses heuristic search to optimise the TMRCAs
of a phylogeny and the substitution rate. An uncorrelated relaxed
molecular clock accounts for rate variation between lineages of the
phylogeny which is parameterised using a Gamma-Poisson mixture
model.
To cite: * E.M. Volz and Frost, S.D.W. (2017) Scalable relaxed clock phylogenetic dating. Virus Evolution.
You can install the latest development version from github using the
devtools package:
library(devtools)
install_github( 'emvolz/treedater')
dater( tre, sts, s, omega0)
where * tre is an ape::phylo phylogeny, *
sts is a named vector of sample times for each tip in
tre * s is the length of the genetic sequences
used to estimate tre * omega0 is an initial
guess of the substitution rate (can be omitted)
For a detailed introduction to features available in
treedater, see the vignette on analysis of Influenza H3N2:
vignette('h3n2').
You can also use treedater from the command line without starting R
using the tdcl script:
./tdcl -h
Usage: ./tdcl [-[-help|h] [<logical>]] [-[-treefn|t] <character>] [-[-samplefn|s] <character>] [-[-sequenceLength|l] <double>] [-[-output|o] [<character>]]
-t <file> : file name of tree in newick format
-s <file> : should be a comma-separated-value file with sample times in format <taxon-id,sample-time> and no header
-l <length> : the integer length of sequences in alignment used to construct the tree
-o <file>: name of file for saving output
Note that you may need to modify the first line of the
tdcl script with the correct path to Rscript
or littler.