| PGOcc {spOccupancy} | R Documentation |
Function for Fitting Single-Species Occupancy Models Using Polya-Gamma Latent Variables
Description
Function for fitting single-species occupancy models using Polya-Gamma latent variables.
Usage
PGOcc(occ.formula, det.formula, data, inits, priors, n.samples,
n.omp.threads = 1, verbose = TRUE, n.report = 100,
n.burn = round(.10 * n.samples), n.thin = 1, n.chains = 1,
k.fold, k.fold.threads = 1, k.fold.seed, k.fold.only = FALSE, ...)
Arguments
occ.formula |
a symbolic description of the model to be fit for the occurrence portion of the model using R's model syntax. Only right-hand side of formula is specified. See example below. Random intercepts are allowed using lme4 syntax (Bates et al. 2015). |
det.formula |
a symbolic description of the model to be fit for the detection portion of the model using R's model syntax. Only right-hand side of formula is specified. See example below. Random intercepts are allowed using lme4 syntax (Bates et al. 2015). |
data |
a list containing data necessary for model fitting.
Valid tags are |
inits |
a list with each tag corresponding to a parameter name.
Valid tags are |
priors |
a list with each tag corresponding to a parameter name.
Valid tags are |
n.samples |
the number of posterior samples to collect in each chain. |
n.omp.threads |
a positive integer indicating the number of threads
to use for SMP parallel processing. The package must be compiled for
OpenMP support. For most Intel-based machines, we recommend setting
|
verbose |
if |
n.report |
the interval to report MCMC progress. |
n.burn |
the number of samples out of the total |
n.thin |
the thinning interval for collection of MCMC samples. The
thinning occurs after the |
n.chains |
the number of chains to run in sequence. |
k.fold |
specifies the number of k folds for cross-validation.
If not specified as an argument, then cross-validation is not performed
and |
k.fold.threads |
number of threads to use for cross-validation. If
|
k.fold.seed |
seed used to split data set into |
k.fold.only |
a logical value indicating whether to only perform
cross-validation ( |
... |
currently no additional arguments |
Value
An object of class PGOcc that is a list comprised of:
beta.samples |
a |
alpha.samples |
a |
z.samples |
a |
psi.samples |
a |
sigma.sq.psi.samples |
a |
sigma.sq.p.samples |
a |
beta.star.samples |
a |
alpha.star.samples |
a |
like.samples |
a |
rhat |
a list of Gelman-Rubin diagnostic values for some of the model parameters. |
ESS |
a list of effective sample sizes for some of the model parameters. |
run.time |
execution time reported using |
k.fold.deviance |
scoring rule (deviance) from k-fold cross-validation.
Only included if |
The return object will include additional objects used for
subsequent prediction and/or model fit evaluation. Note that detection
probability estimated values are not included in the model object, but can be
extracted using fitted().
Note
Some of the underlying code used for generating random numbers from the Polya-Gamma distribution is taken from the pgdraw package written by Daniel F. Schmidt and Enes Makalic. Their code implements Algorithm 6 in PhD thesis of Jesse Bennett Windle (2013) https://repositories.lib.utexas.edu/handle/2152/21842.
Author(s)
Jeffrey W. Doser doserjef@msu.edu,
Andrew O. Finley finleya@msu.edu
References
Polson, N.G., J.G. Scott, and J. Windle. (2013) Bayesian Inference for Logistic Models Using Polya-Gamma Latent Variables. Journal of the American Statistical Association, 108:1339-1349.
Bates, Douglas, Martin Maechler, Ben Bolker, Steve Walker (2015). Fitting Linear Mixed-Effects Models Using lme4. Journal of Statistical Software, 67(1), 1-48. doi:10.18637/jss.v067.i01.
Hooten, M. B., and Hobbs, N. T. (2015). A guide to Bayesian model selection for ecologists. Ecological monographs, 85(1), 3-28.
MacKenzie, D. I., J. D. Nichols, G. B. Lachman, S. Droege, J. Andrew Royle, and C. A. Langtimm. 2002. Estimating Site Occupancy Rates When Detection Probabilities Are Less Than One. Ecology 83: 2248-2255.
Examples
set.seed(400)
J.x <- 10
J.y <- 10
J <- J.x * J.y
n.rep <- sample(2:4, J, replace = TRUE)
beta <- c(0.5, -0.15)
p.occ <- length(beta)
alpha <- c(0.7, 0.4)
p.det <- length(alpha)
dat <- simOcc(J.x = J.x, J.y = J.y, n.rep = n.rep, beta = beta, alpha = alpha,
sp = FALSE)
occ.covs <- dat$X[, 2, drop = FALSE]
colnames(occ.covs) <- c('occ.cov')
det.covs <- list(det.cov = dat$X.p[, , 2])
# Data bundle
data.list <- list(y = dat$y,
occ.covs = occ.covs,
det.covs = det.covs)
# Priors
prior.list <- list(beta.normal = list(mean = 0, var = 2.72),
alpha.normal = list(mean = 0, var = 2.72))
# Initial values
inits.list <- list(alpha = 0, beta = 0,
z = apply(data.list$y, 1, max, na.rm = TRUE))
n.samples <- 5000
n.report <- 1000
out <- PGOcc(occ.formula = ~ occ.cov,
det.formula = ~ det.cov,
data = data.list,
inits = inits.list,
n.samples = n.samples,
priors = prior.list,
n.omp.threads = 1,
verbose = TRUE,
n.report = n.report,
n.burn = 1000,
n.thin = 1,
n.chains = 1)
summary(out)