Nothing
## ---- echo = FALSE------------------------------------------------------------
# ###Start with a clean space
# rm(list = ls())
#
# ###Take care of some stuff that I don't want the user to see...
# path.package <- "/Users/sam/Documents/Postdoc/Software/spBFA/"
# suppressMessages(devtools::load_all(path.package)) #loads scripts
# suppressMessages(devtools::document(path.package)) #creates documentation
###Make sure to remove devtools from Suggests line in DESCRIPTION before submission
## -----------------------------------------------------------------------------
library(womblR)
library(spBFA)
## -----------------------------------------------------------------------------
head(VFSeries)
## ---- fig.align="center", fig.width = 5.5, fig.height = 5.5-------------------
PlotVfTimeSeries(Y = VFSeries$DLS,
Location = VFSeries$Location,
Time = VFSeries$Time,
main = "Visual field sensitivity time series \n at each location",
xlab = "Days from baseline visit",
ylab = "Differential light sensitivity (dB)",
line.col = 1, line.type = 1, line.reg = FALSE)
## -----------------------------------------------------------------------------
blind_spot <- c(26, 35) # define blind spot
VFSeries <- VFSeries[order(VFSeries$Location), ] # sort by location
VFSeries <- VFSeries[order(VFSeries$Visit), ] # sort by visit
VFSeries <- VFSeries[!VFSeries$Location %in% blind_spot, ] # remove blind spot locations
dat <- data.frame(Y = VFSeries$DLS / 10) # create data frame with scaled data
## -----------------------------------------------------------------------------
Time <- unique(VFSeries$Time) / 365 # years since baseline visit
print(Time)
## -----------------------------------------------------------------------------
W <- HFAII_Queen[-blind_spot, -blind_spot] # visual field adjacency matrix
M <- dim(W)[1] # number of locations
## -----------------------------------------------------------------------------
TimeDist <- as.matrix(dist(Time))
BPsi <- log(0.025) / -min(TimeDist[TimeDist > 0])
APsi <- log(0.975) / -max(TimeDist)
## -----------------------------------------------------------------------------
K <- 10
O <- 1
Hypers <- list(Sigma2 = list(A = 0.001, B = 0.001),
Kappa = list(SmallUpsilon = O + 1, BigTheta = diag(O)),
Delta = list(A1 = 1, A2 = 20),
Psi = list(APsi = APsi, BPsi = BPsi),
Upsilon = list(Zeta = K + 1, Omega = diag(K)))
## -----------------------------------------------------------------------------
Starting <- list(Sigma2 = 1,
Kappa = diag(O),
Delta = 2 * (1:K),
Psi = (APsi + BPsi) / 2,
Upsilon = diag(K))
## -----------------------------------------------------------------------------
Tuning <- list(Psi = 1)
## -----------------------------------------------------------------------------
MCMC <- list(NBurn = 1000, NSims = 1000, NThin = 2, NPilot = 5)
## ---- include = FALSE---------------------------------------------------------
data(reg.bfa_sp)
## ---- eval = FALSE------------------------------------------------------------
# reg.bfa_sp <- bfa_sp(Y ~ 0, data = dat, dist = W, time = Time, K = 10,
# starting = Starting, hypers = Hypers, tuning = Tuning, mcmc = MCMC,
# L = Inf,
# family = "tobit",
# trials = NULL,
# temporal.structure = "exponential",
# spatial.structure = "discrete",
# seed = 54,
# gamma.shrinkage = TRUE,
# include.space = TRUE,
# clustering = TRUE)
#
# ## Burn-in progress: |*************************************************|
# ## Sampler progress: 0%.. 10%.. 20%.. 30%.. 40%.. 50%.. 60%.. 70%.. 80%.. 90%.. 100%..
## -----------------------------------------------------------------------------
names(reg.bfa_sp)
## -----------------------------------------------------------------------------
library(coda)
## -----------------------------------------------------------------------------
Sigma2_1 <- as.mcmc(reg.bfa_sp$sigma2[, 1])
## ---- fig.width = 5.2, fig.height = 5.2, echo = FALSE-------------------------
par(mfrow = c(1, 1))
traceplot(Sigma2_1, ylab = expression(paste(sigma^2 ~ "(" ~ s[1]~ ")")), main = expression(paste("Posterior" ~ sigma^2 ~ "(" ~ s[1]~ ")")))
## ---- echo = FALSE------------------------------------------------------------
geweke.diag(Sigma2_1)$z
## -----------------------------------------------------------------------------
Diags <- spBFA::diagnostics(reg.bfa_sp, diags = c("dic", "dinf", "waic"), keepDeviance = TRUE)
## ---- fig.align = 'center', fig.width = 4, fig.height = 3.3-------------------
Deviance <- as.mcmc(Diags$deviance)
traceplot(Deviance, ylab = "Deviance", main = "Posterior Deviance")
## ---- eval = FALSE------------------------------------------------------------
# print(Diags)
## ---- echo = FALSE------------------------------------------------------------
unlist(Diags$dic)
unlist(Diags$dinf)
unlist(Diags$waic)
## -----------------------------------------------------------------------------
NewTimes <- 3
## -----------------------------------------------------------------------------
Predictions <- predict(reg.bfa_sp, NewTimes)
## -----------------------------------------------------------------------------
names(Predictions)
## ---- fig.align = 'center', fig.width = 4.5, fig.height = 4.5-----------------
PlotSensitivity(Y = apply(Predictions$Y$Y10, 2, mean) * 10,
main = "Posterior mean prediction\n at 3 years",
legend.lab = "Posterior Mean", legend.round = 2,
bins = 250, border = FALSE, zlim = c(0, 40))
## ---- fig.align = 'center', fig.width = 4.5, fig.height = 4.5-----------------
PlotSensitivity(Y = apply(Predictions$Y$Y10 * 10, 2, sd),
main = "Posterior standard deviation\n (SD) at 3 years",
legend.lab = "Posterior SD", legend.round = 2,
bins = 250, border = FALSE, zlim = c(0, 40))
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