library(DCFusion)
library(HMCGLMR)
##### Initialise example #####
seed <- 2022
set.seed(seed)
nsamples <- 10000
warmup <- 10000
time_choice <- 1
phi_rate <- 1
prior_means <- rep(0, 10)
prior_variances <- rep(10, 10)
ESS_threshold <- 0.5
CESS_0_threshold <- 0.2
CESS_j_threshold <- 0.05
diffusion_estimator <- 'NB'
n_cores <- parallel::detectCores()
##### Loading in Data #####
load_medical_demand_data <- function(seed = NULL) {
load('scripts/count_data_regression/medical_demand/DebTrivedi.rda')
med_demand <- data.frame(visits = DebTrivedi$ofp,
hosp_stays = DebTrivedi$hosp,
exc_health = as.numeric(DebTrivedi$health == "excellent"),
avg_health = as.numeric(DebTrivedi$health == "average"),
n_chron = DebTrivedi$numchron,
age = DebTrivedi$age,
black = as.numeric(DebTrivedi$black == "yes"),
gender = as.numeric(DebTrivedi$gender == "male"),
employed = as.numeric(DebTrivedi$employed == "yes"),
priv_ins = as.numeric(DebTrivedi$privins == "yes"))
med_demand <- med_demand[complete.cases(med_demand),]
if (!is.null(seed)) {
set.seed(seed)
med_demand <- med_demand[sample(1:nrow(med_demand)),]
}
X <- subset(med_demand, select = -c(visits))
design_mat <- as.matrix(cbind(rep(1, nrow(X)), X))
colnames(design_mat)[1] <- 'intercept'
return(list('data' = cbind(subset(design_mat, select = -c(intercept)),
'visits' = med_demand$visits),
'y' = med_demand$visits,
'X' = design_mat))
}
med_demand <- load_medical_demand_data()
##### Sampling from full posterior #####
full_posterior <- hmc_sample_GLMR(likelihood = 'NB',
y = med_demand$y,
X = med_demand$X,
C = 1,
phi = 1,
prior_means = prior_means,
prior_variances = prior_variances,
iterations = nsamples + 10000,
warmup = 10000,
chains = 1,
seed = seed,
output = T)
##### Sampling from sub-posterior C=32 #####
data_split_32 <- split_data(med_demand$data,
y_col_index = 10,
X_col_index = 1:9,
C = 32,
as_dataframe = F)
sub_posteriors_32 <- hmc_base_sampler_GLMR(likelihood = 'NB',
nsamples = nsamples,
warmup = 10000,
data_split = data_split_32,
C = 32,
phi = 1,
prior_means = prior_means,
prior_variances = prior_variances,
seed = seed,
output = T)
##### Applying other methodologies #####
print('Applying other methodologies')
consensus_mat_32 <- consensus_scott(S = 32, samples_to_combine = sub_posteriors_32, indep = F)
consensus_sca_32 <- consensus_scott(S = 32, samples_to_combine = sub_posteriors_32, indep = T)
neiswanger_true_32 <- neiswanger(S = 32,
samples_to_combine = sub_posteriors_32,
anneal = TRUE)
neiswanger_false_32 <- neiswanger(S = 32,
samples_to_combine = sub_posteriors_32,
anneal = FALSE)
weierstrass_importance_32 <- weierstrass(Samples = sub_posteriors_32,
method = 'importance')
weierstrass_rejection_32 <- weierstrass(Samples = sub_posteriors_32,
method = 'reject')
# ##### NB (Hypercube Centre) #####
# print('NB Fusion (hypercube centre)')
# NB_hc_32 <- bal_binary_fusion_SMC_BNBR(N_schedule = rep(nsamples, 5),
# m_schedule = rep(2, 5),
# time_schedule = rep(time_choice, 5),
# base_samples = sub_posteriors_32,
# L = 6,
# dim = 10,
# phi_rate = phi_rate,
# data_split = data_split_32,
# prior_means = prior_means,
# prior_variances = prior_variances,
# C = 32,
# precondition = TRUE,
# resampling_method = 'resid',
# ESS_threshold = ESS_threshold,
# diffusion_estimator = diffusion_estimator,
# seed = seed,
# n_cores = n_cores)
# NB_hc_32$particles <- resample_particle_y_samples(particle_set = NB_hc_32$particles[[1]],
# multivariate = TRUE,
# resampling_method = 'resid',
# seed = seed)
# NB_hc_32$proposed_samples <- NB_hc_32$proposed_samples[[1]]
# print(integrated_abs_distance(full_posterior, NB_hc_32$particles$y_samples))
# ##### Generalised Bayesian Fusion #####
##### bal binary combining two sub-posteriors at a time #####
# regular mesh
balanced_C32 <- list('reg' = bal_binary_GBF_BNBR(N_schedule = rep(nsamples, 5),
m_schedule = rep(2, 5),
time_mesh = NULL,
base_samples = sub_posteriors_32,
L = 6,
dim = 10,
phi_rate = phi_rate,
data_split = data_split_32,
prior_means = prior_means,
prior_variances = prior_variances,
C = 32,
precondition = TRUE,
resampling_method = 'resid',
ESS_threshold = ESS_threshold,
adaptive_mesh = FALSE,
mesh_parameters = list('condition' = 'SH',
'CESS_0_threshold' = CESS_0_threshold,
'CESS_j_threshold' = CESS_j_threshold,
'vanilla' = FALSE),
diffusion_estimator = diffusion_estimator,
seed = seed))
balanced_C32$reg$particles <- resample_particle_y_samples(particle_set = balanced_C32$reg$particles[[1]],
multivariate = TRUE,
resampling_method = 'resid',
seed = seed)
balanced_C32$reg$proposed_samples <- balanced_C32$reg$proposed_samples[[1]]
print(integrated_abs_distance(full_posterior, balanced_C32$reg$particles$y_samples))
# adaptive mesh
balanced_C32$adaptive <- bal_binary_GBF_BNBR(N_schedule = rep(nsamples, 5),
m_schedule = rep(2, 5),
time_mesh = NULL,
base_samples = sub_posteriors_32,
L = 6,
dim = 10,
phi_rate = phi_rate,
data_split = data_split_32,
prior_means = prior_means,
prior_variances = prior_variances,
C = 32,
precondition = TRUE,
resampling_method = 'resid',
ESS_threshold = ESS_threshold,
adaptive_mesh = TRUE,
mesh_parameters = list('condition' = 'SH',
'CESS_0_threshold' = CESS_0_threshold,
'CESS_j_threshold' = CESS_j_threshold,
'vanilla' = FALSE),
diffusion_estimator = diffusion_estimator,
seed = seed)
balanced_C32$adaptive$particles <- resample_particle_y_samples(particle_set = balanced_C32$adaptive$particles[[1]],
multivariate = TRUE,
resampling_method = 'resid',
seed = seed)
balanced_C32$adaptive$proposed_samples <- balanced_C32$adaptive$proposed_samples[[1]]
print(integrated_abs_distance(full_posterior, balanced_C32$adaptive$particles$y_samples))
##### IAD #####
integrated_abs_distance(full_posterior, balanced_C32$reg$particles$y_samples)
integrated_abs_distance(full_posterior, balanced_C32$adaptive$particles$y_samples)
# integrated_abs_distance(full_posterior, NB_hc_32$particles$y_samples)
integrated_abs_distance(full_posterior, consensus_mat_32$samples)
integrated_abs_distance(full_posterior, consensus_sca_32$samples)
integrated_abs_distance(full_posterior, neiswanger_true_32$samples)
integrated_abs_distance(full_posterior, neiswanger_false_32$samples)
integrated_abs_distance(full_posterior, weierstrass_importance_32$samples)
integrated_abs_distance(full_posterior, weierstrass_rejection_32$samples)
save.image('DB32.RData')
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