Nothing
#' @title Bias-Corrected Meta-Analysis for Combining Studies of Different Types and Quality
#'
#' @description This function performers a Bayesian meta-analysis to jointly
#' combine different types of studies. The random-effects follows a finite
#' mixture of normals.
#'
#'
#'
#' @param data A data frame with at least two columns with the following names:
#' 1) TE = treatment effect,
#' 2) seTE = the standard error of the treatment effect.
#'
#' @param mean.mu Prior mean of the overall mean parameter mu, default value is 0.
#'
#' @param sd.mu Prior standard deviation of mu, the default value is 10.
#'
#' @param scale.sigma.between Prior scale parameter for scale gamma distribution for the
#' precision between studies. The default value is 0.5.
#'
#' @param df.scale.between Degrees of freedom of the scale gamma distribution for the precision between studies.
#' The default value is 1, which results in a Half Cauchy distribution for the standard
#' deviation between studies. Larger values e.g. 30 corresponds to a Half Normal distribution.
#'
#' @param B.lower Lower bound of the bias parameter B, the default value is 0.
#' @param B.upper Upper bound of the bias parameter B, the default value is 10.
#'
#' @param a.0 Parameter for the prior Beta distribution for the probability of bias. Default value is a0 = 1.
#' @param a.1 Parameter for the prior Beta distribution for the probability of bias. Default value is a1 = 1.
#'
#' @param nu Parameter for the Beta distribution for the quality weights. The default value is nu = 0.5.
#'
#' @param nu.estimate If TRUE, then we estimate nu from the data.
#'
#' @param b.0 If nu.estimate = TRUE, this parameter is the shape parameter of the prior Gamma distribution for nu.
#' @param b.1 If nu.estimate = TRUE, this parameter is the rate parameter of the prior Gamma distribution for nu.
#' Note that E(nu) = b.0/b.1 and we need to choose b.0 << b.1.
#'
#' @param nr.chains Number of chains for the MCMC computations, default 2.
#' @param nr.iterations Number of iterations after adapting the MCMC, default is 10000. Some models may need more iterations.
#' @param nr.adapt Number of iterations in the adaptation process, defualt is 1000. Some models may need more iterations during adptation.
#' @param nr.burnin Number of iteration discared for burnin period, default is 1000. Some models may need a longer burnin period.
#' @param nr.thin Thinning rate, it must be a positive integer, the default value 1.
#' @param be.quiet Do not print warning message if the model does not adapt. The default value is FALSE. If you are not sure about the adaptation period choose be.quiet=TRUE.
#' @param r2jags Which interface is used to link R to JAGS (rjags and R2jags), default value is R2Jags=TRUE.
#'
#' @return This function returns an object of the class "bcmeta". This object contains the MCMC
#' output of each parameter and hyper-parameter in the model and
#' the data frame used for fitting the model.
#'
#'
#' @details The results of the object of the class bcmeta can be extracted with R2jags or with rjags. In addition a summary, a print and a plot functions are
#' implemented for this type of object.
#'
#'
#' @references Verde, P. E. (2017) Two Examples of Bayesian Evidence Synthesis with the Hierarchical Meta-Regression Approach. Chap.9, pag 189-206. Bayesian Inference, ed. Tejedor, Javier Prieto. InTech.
#'
#' @references Verde, P.E. (2021) A Bias-Corrected Meta-Analysis Model for Combining Studies of Different Types and Quality. Biometrical Journal; 1–17.
#'
#'
#' @examples
#' \dontrun{
#' library(jarbes)
#'
#' # Example ppvipd data
#'
#' data(ppvipd)
#'
# bcm1 = bcmeta(ppvipd, a.0 = 8, a.1 = 3) # 8 OS and 3 RCT...
# summary(bcm1)
# plot(bcm1)
#
# diagnostic(bcm1, study.names = ppvipd$name,
# post.p.value.cut = 0.1, shape.forest = 4, lwd.forest = 0.75)
#
#
# diagnostic(bcm1, post.p.value.cut = 0.1,
# shape.forest = 4, lwd.forest = 0.75,
# y.lim = c(0, 3),
# color.data.points = "blue",
# bias.plot = TRUE,
# S = 10000)
#
# # Example with stem cells
#
# data("stemcells")
# stemcells$TE = stemcells$effect.size
# stemcells$seTE = stemcells$se.effect
#
# bcm2 = bcmeta(stemcells, mean.mu = 0, sd.mu = 1000,
# nr.iterations = 50000,
# nr.adapt = 20000,
# nr.thin = 2)
#
# summary(bcm2)
#
# plot(bcm2, x.lim = c(-5, 15), y.lim = c(0, .8))
#
# diagnostic(bcm2, study.names = stemcells$trial,
# post.p.value.cut = 0.05,
# shape.forest = 4, lwd.forest = 0.75)
#
# # only bias plot
# diagnostic(bcm2, study.names = stemcells$trial,
# post.p.value.cut = 0.05,
# cross.val.plot = FALSE,
# shape.forest = 4, lwd.forest = 0.75)
#
# # only CV plot
# diagnostic(bcm2, study.names = stemcells$trial,
# post.p.value.cut = 0.05,
# cross.val.plot = TRUE,
# bias.plot = FALSE,
# shape.forest = 4, lwd.forest = 0.75)
#
#'
#' }
#'
#' @import R2jags
#' @import rjags
#'
#'
#' @export
bcmeta = function(
data,
# Hyperpriors parameters............................................
mean.mu = 0,
sd.mu = 10,
scale.sigma.between = 0.5,
df.scale.between = 1,
B.lower = 0,
B.upper = 10,
a.0 = 1,
a.1 = 1,
nu = 0.5,
nu.estimate = FALSE,
b.0 = 1,
b.1 = 2,
# MCMC setup........................................................
nr.chains = 2,
nr.iterations = 10000,
nr.adapt = 1000,
nr.burnin = 1000,
nr.thin = 1,
# Further options to link jags and R ...............................
be.quiet = FALSE,
r2jags = TRUE
)UseMethod("bcmeta")
#' @export
bcmeta.default = function(
data,
# Hyperpriors parameters............................................
mean.mu = 0,
sd.mu = 10,
scale.sigma.between = 0.5,
df.scale.between = 1,
B.lower = 0,
B.upper = 10,
a.0 = 1,
a.1 = 1,
nu = 0.5,
nu.estimate = FALSE,
b.0 = 1,
b.1 = 2,
# MCMC setup........................................................
nr.chains = 2,
nr.iterations = 10000,
nr.adapt = 1000,
nr.burnin = 1000,
nr.thin = 1,
# Further options to link jags and R ...............................
be.quiet = FALSE,
r2jags = TRUE
)
{
# Mixture of Normals Random effects meta-analysis
y = sort(data$TE)
se.y = data$seTE[order(data$TE)]
N = length(y)
# Note: prepare a regression equation ...
#x = data$design[order(data$TE)]
#x = as.numeric(x)
#T is the index that allocates each study to one of the two components
T = rep(NA, N)
T[1] = 1
T[N] = 2
# This list describes the data used by the BUGS script.
data.bcmeta <- list ("y", "se.y", "N", "T",
"mean.mu",
"sd.mu",
"scale.sigma.between",
"df.scale.between",
"B.lower",
"B.upper",
"a.0",
"a.1",
"nu")
if(nu.estimate==TRUE) {
data.bcmeta = data.bcmeta[-13] # Remove "nu"
data.bcmeta = c(data.bcmeta, "b.0", "b.1")} # Add hyper constants for "nu
# List of parameters
par.bcmeta <- c("theta.bc",
"theta",
"theta.bias",
"mu",
"mu.new", # BC component
"y.ghost", # Approx Cross-Validation
"tau",
"p.bias",
"I",
"w",
"w.diag", # Diagnostic weights
"B")
if(nu.estimate==TRUE) {par.bcmeta = c(par.bcmeta, "nu" )}
# Model in BUGS
model.bugs <-
"
model
{
for( i in 1 : N ) {
# Likelihood of theta[i] ..........................................
y[i] ~ dnorm(theta.bc[i], pre.y[i])
pre.y[i] <- pow(se.y[i], -2)
# Mixture heterocedastic random effects ..........................
theta.bc[i] <- theta[i]*(1-I[i]) + theta.bias[i]*I[i]
I[i] <- T[i] - 1
theta[i] ~ dnorm(mu[1], prec.tau[i])
theta.bias[i] ~ dnorm(mu[2], prec.tau[i])
T[i] ~ dcat(p.bias[1:2])
prec.tau[i] <- inv.var[T[i]] * w[T[i],i] #Slash parametrization
w[1,i] <- 1
# Slash distribution ...
w[2,i] ~ dbeta(nu, 1)
# Diagnostic weights
w.diag[i] <- 1/w[T[i],i]
}
# Posterior predictive based on the Bias Corrected component...
mu.new.1 ~ dnorm(mu[1], inv.var[1])
#mu.new.2 ~ dnorm(mu[2], inv.var[2])
#y.bias.new ~ dbern(p.bias[1])
#mu.new <- (1-y.bias.new)*mu.new.1 + y.bias.new*mu.new.2
#inv.var.new <- (1-y.bias.new)*inv.var[1] + y.bias.new*inv.var[2]
mu.new <- mu.new.1
inv.var.new <- inv.var[1]
# Approximate Bayesian Cross-Validation ......................
theta.ghost ~ dnorm(mu.new, inv.var.new)
for(i in 1:N)
{
y.ghost[i] ~ dnorm(theta.ghost, pre.y[i])
}
# Priors for hyper-parameters .................................
# Prior of probability classes
p.bias[2] ~ dbeta(a.0, a.1)
p.bias[1] <- 1 - p.bias[2]
# Variance components ...
tau <- 1/sqrt(inv.var[1])
inv.var[1] ~ dscaled.gamma(scale.sigma.between,
df.scale.between)
inv.var[2] <- inv.var[1]
# Prior for mu
inv.var.mu <- pow(sd.mu, -2)
mu[1] ~ dnorm(mean.mu, inv.var.mu)
B ~ dunif(B.lower, B.upper)
mu[2] <- mu[1] + B
}
"
model.bugs.connection <- textConnection(model.bugs)
if(r2jags == TRUE){
# Use R2jags as interface for JAGS ...
results <- jags( data = data.bcmeta,
parameters.to.save = par.bcmeta,
model.file = model.bugs.connection,
n.chains = nr.chains,
n.iter = nr.iterations,
n.burnin = nr.burnin,
n.thin = nr.thin)
}
else {
# Use rjags as interface for JAGS ...
# Send the model to JAGS, check syntax, run ...
jm <- jags.model(file = model.bugs.connection,
data = data.bcmeta,
# inits = inits.model,
n.chains = nr.chains,
n.adapt = nr.adapt,
quiet = be.quiet)
results <- coda.samples(jm,
variable.names = par.bcmeta,
n.iter = nr.iterations)
}
if(r2jags == FALSE)
{cat("You are using the package rjags as interface to JAGS.", "\n")
cat("The plot functions for output analysis are not implemented in this jarbes version", "\n")
}
# Close text connection
close(model.bugs.connection)
# Extra outputs that are linked with other functions ...
results$data = data
# Hyperpriors parameters............................................
results$prior$mean.mu = mean.mu
results$prior$sd.mu = sd.mu
results$prior$scale.sigma.between = scale.sigma.between
results$prior$df.scale.between = df.scale.between
results$prior$B.lower = B.lower
results$prior$B.upper = B.upper
results$prior$a.0 = a.0
results$prior$a.1 = a.1
results$prior$nu = nu
results$prior$nu.estimate = nu.estimate
results$prior$b.0 = b.0
results$prior$b.1 = b.1
class(results) = c("bcmeta")
return(results)
}
#' Generic print function for bcmeta object in jarbes.
#'
#' @param x The object generated by the function bcmeta.
#'
#' @param digits The number of significant digits printed. The default value is 3.
#'
#' @param ... \dots
#'
#' @export
print.bcmeta <- function(x, digits, ...)
{
print(x$BUGSoutput,...)
}
Any scripts or data that you put into this service are public.
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.