## Not run:
# ## Examples below (except for m3) should take 3-4 minutes.
#
# ## ------ (use simul1) ------
# # load simulated data set 'simul1'
# data(simul1)
# y <- simul1$y
# E <- simul1$E
# X <- as.matrix(simul1[, -c(1,2,8,9)]) # W = X
# validation <- simul1[, c("m", "v"), drop = FALSE]
#
# # function call (with specific MCMC settings)
# m1 <- pogitBvs(y = y, E = E, X = X, validation = validation,
# mcmc = list(M = 4000, thin = 5, verbose = 1000))
#
# # print, summarize and plot results
# print(m1)
# summary(m1)
# plot(m1)
#
# # show traceplots disregarding burn-in and thinning
# plot(m1, burnin = FALSE, thin = FALSE)
# # show density plot of MCMC draws
# plot(m1, type = "density")
#
# # informative prior instead of validation data (change prior settings)
# # e.g. available prior information on reporting probabilities
# p.a0 <- 0.9
# p.a <- c(0.125, 0.5, 0.5, 0.5)
# m0a_inf <- log(p.a0/(1 - p.a0)) # prior information for alpha_0
# aj0_inf <- log(p.a/(1 - p.a)) # prior information for alpha
#
# prior.set <- list(m0a = m0a_inf, aj0 = aj0_inf, VL = 0.005, slabL = "Normal")
# m2 <- pogitBvs(y = y, E = E, X = X, method = "infprior", prior = prior.set,
# mcmc = list(M = 4000, burnin = 2000, thin = 2), BVS = FALSE)
# print(m2)
# summary(m2)
# plot(m2)
# plot(m2, type = "acf", lag.max = 30)
#
# ## ------ (use simul2) ------
# # complex model (with a long (!) runtime)
#
# # load simulated data set 'simul2'
# data(simul2)
# y <- simul2$y
# E <- simul2$E
# cID <- simul2$cID
# X <- as.matrix(simul2[, -c(1:3,9,10)])
# validation <- simul2[, c("v", "m"), drop = FALSE]
#
# # function call (with random intercept in both sub-models)
# model <- list(riBeta = 1, riAlpha = 1, clBetaID = cID, clAlphaID = cID)
# m3 <- pogitBvs(y = y, E = E, X = X, validation = validation, model = model,
# mcmc = list(M = 6000, burnin = 200, thin = 10), BVS = TRUE)
# print(m3)
# summary(m3)
# plot(m3)
#
# ## ------ (use cervical cancer data) ------
# # load cervical cancer data
# data(cervical)
# data(cervical_validation)
# y <- cervical$y
# E <- cervical$E
# X <- as.matrix(cervical[, -c(1:4)])
# validation <- cervical_validation[, c(1, 2), drop = FALSE]
# W <- as.matrix(cervical_validation[, -c(1:3)])
# subcat <- factor(as.numeric(cervical$country))
#
# # function call
# m4 <- pogitBvs(y = y, E = E, X = X, W = W, validation = validation,
# model = list(subcat = subcat), mcmc = list(M = 10000,
# burnin = 2000, thin = 10), start = list(firth = TRUE),
# BVS = TRUE)
# print(m4)
# # additionally compute estimated risks and reporting probabilities
# summary(m4, printRes = TRUE)
# plot(m4, burnin = FALSE, thin = FALSE)
# plot(m4, type = "acf", lag.max = 50)
#
# # informative prior instead of validation data (change prior settings)
# # e.g. prior information on country-specific reporting probabilities
# p.a0 <- 0.85
# p.a <- c(0.99, 0.70, 0.85)
# m0a_inf <- log(p.a0/(1 - p.a0)) # prior information for alpha_0
# aj0_inf <- log(p.a/(1 - p.a)) # prior information for alpha
#
# prior.set <- list(m0a = m0a_inf, aj0 = aj0_inf, VL = 0.005, slabL = "Normal")
# m5 <- pogitBvs(y = y, X = X, W = W, E = E, method = "infprior",
# model = list(subcat = subcat), prior = prior.set,
# mcmc = list(M = 10000, burnin = 2000, thin = 10))
# print(m5)
# summary(m5, printRes = TRUE)
# plot(m5, burnin = FALSE, thin = FALSE)
# plot(m5, type = "acf", lag.max = 50)
# ## End(Not run)
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