The function haploGen
implements simulations of genealogies of
haplotypes. This forward-time, individual-based simulation tool allows
haplotypes to replicate and mutate according to specified parameters,
and keeps track of their genealogy.
Simulations can be spatially explicit or not (see geo.sim
argument). In the first case, haplotypes are assigned to locations on
a regular grip. New haplotypes disperse from their ancestor's location
according to a random Poisson diffusion, or alternatively according to
a pre-specified migration scheme. This tool does not allow for
simulating selection or linkage disequilibrium.
Produced objects are lists with the class haploGen
; see 'value'
section for more information on this class. Other functions are
available to print, plot, subset, sample or convert haploGen
objects. A seqTrack method is also provided for analysing
haploGen
objects.
Note that for simulation of outbreaks, the new tool simOutbreak
in the outbreaker
package should be used.
haploGen(seq.length=1e4, mu.transi=1e-4, mu.transv=mu.transi/2, t.max=20,
gen.time=function(){1+rpois(1,0.5)},
repro=function(){rpois(1,1.5)}, max.nb.haplo=200,
geo.sim=FALSE, grid.size=10, lambda.xy=0.5,
mat.connect=NULL,
ini.n=1, ini.xy=NULL)
# S3 method for haploGen
print(x, ...)
# S3 method for haploGen
as.igraph(x, col.pal=redpal, ...)
# S3 method for haploGen
plot(x, y=NULL, col.pal=redpal, ...)
# S3 method for haploGen
[(x, i, j, drop=FALSE)
# S3 method for haploGen
labels(object, ...)
# S3 method for haploGen
as.POSIXct(x, tz="", origin=as.POSIXct("2000/01/01"), ...)
# S3 method for haploGen
seqTrack(x, best=c("min","max"), prox.mat=NULL, ...)
as.seqTrack.haploGen(x)
plotHaploGen(x, annot=FALSE, date.range=NULL, col=NULL, bg="grey", add=FALSE, ...)
sample.haploGen(x, n)
=== haploGen class ===
haploGen
objects are lists containing the following slots:
- seq: DNA sequences in the DNAbin matrix format
- dates: dates of appearance of the haplotypes
- ances: a vector of integers giving the index of each haplotype's
ancestor
- id: a vector of integers giving the index of each haplotype
- xy: (optional) a matrix of spatial coordinates of haplotypes
- call: the matched call
=== misc functions ===
- as.POSIXct: returns a vector of dates with POSIXct format
- labels: returns the labels of the haplotypes
- as.seqTrack: returns a seqTrack object. Note that this object is not a
proper seqTrack analysis, but just a format conversion convenient for
plotting haploGen
objects.
an integer indicating the length of the simulated haplotypes, in number of nucleotides.
the rate of transitions, in number of mutation per site and per time unit.
the rate of transversions, in number of mutation per site and per time unit.
an integer indicating the maximum number of time units to run the simulation for.
an integer indicating the generation time, in number of time units. Can be a (fixed) number or a function returning a number (then called for each reproduction event).
an integer indicating the number of descendents per haplotype. Can be a (fixed) number or a function returning a number (then called for each reproduction event).
an integer indicating the maximum number of haplotypes handled at any time of the simulation, used to control the size of the produced object. Larger number will lead to slower simulations. If this number is exceeded, the genealogy is prunded to as to keep this number of haplotypes.
a logical stating whether simulations should be spatially explicit (TRUE) or not (FALSE, default). Spatially-explicit simulations are slightly slower than their non-spatial counterpart.
the size of the square grid of possible locations for spatial simulations. The total number of locations will be this number squared.
the parameter of the Poisson distribution used to determine dispersion in x and y axes.
a matrix of connectivity describing migration
amongts all pairs of locations. mat.connect[i,j]
indicates the
probability, being in 'i', to migrate to 'j'. The rows of this matrix
thus sum to 1. It has as many rows and columns as there are locations,
with row 'i' / column 'j' corresponding to locations number 'i' and 'j'.
Locations are numbered as in a matrix in which rows and columns are
respectively x and y coordinates. For instance, in a 5x5 grid, locations
are numbered as in matrix(1:25,5,5)
.
an integer specifying the number of (identical) haplotypes to initiate the simulation
a vector of two integers giving the x/y coordinates of the initial haplotype.
haploGen
objects.
unused argument, for compatibility with 'plot'.
a color palette to be used to represent weights using
colors on the edges of the graph. See ?num2col
. Note that the
palette is inversed by default.
i
is a vector used for subsetting the object. For
instance, i=1:3
will retain only the first three haplotypes of the
genealogy. j
and drop
are only provided for compatibility,
but not used.
arguments to be passed to the
seqTrack
function. See documentation of
seqTrack
for more information.
arguments to be passed to plotSeqTrack
.
an integer indicating the number of haplotypes to be retained in the sample
aguments to be passed to as.POSIXct
(see ?as.POSIXct)
further arguments to be passed to other methods; for
'plot', arguments are passed to plot.igraph
.
Thibaut Jombart t.jombart@imperial.ac.uk
=== Dependencies with other packages ===
- ape package is required as it implements efficient handling of DNA
sequences used in haploGen
objects. To install this package,
simply type:
install.packages("ape")
- for various purposes including plotting, converting genealogies to
graphs can be useful. From adegenet version 1.3-5 onwards, this is
achieved using the package igraph
. See below.
=== Converting haploGen objects to graphs ===
haploGen
objects can be converted to igraph
objects (package igraph
), which can in turn be plotted and manipulated using classical
graph tools. Simply use 'as.igraph(x)' where 'x' is a
haploGen
object. This functionality requires the igraph
package. Graphs are time oriented (top=old, bottom=recent).
Jombart T, Eggo R, Dodd P, Balloux F (2010) Reconstructing disease outbreaks from genetic data: a graph approach. Heredity. doi: 10.1038/hdy.2010.78.
simOutbreak
in the package 'outbreaker' for simulating disease
outbreaks under a realistic epidemiological model.
if (FALSE) {
if(require(ape) && require(igraph)){
## PERFORM SIMULATIONS
x <- haploGen(geo.sim=TRUE)
x
## PLOT DATA
plot(x)
## PLOT SPATIAL SPREAD
plotHaploGen(x, bg="white")
title("Spatial dispersion")
## USE SEQTRACK RECONSTRUCTION
x.recons <- seqTrack(x)
mean(x.recons$ances==x$ances, na.rm=TRUE) # proportion of correct reconstructions
g <- as.igraph(x)
g
plot(g)
plot(g, vertex.size=0)
}
}
Run the code above in your browser using DataLab