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DBT.data <- function(data, ref, Multiarm_studies, method) {
##
# Find networks designs
##
nmades <- NMAdesigns(data, Multiarm_studies)
##
design <- nmades$designs # Network's designs
design_multi <- nmades$multi_design # Designs from multi-arm studies
studies_multi <- nmades$studies_multi # Multi-arm studies for each multi-arm design
##
# Calculate the number of inconsistency factors
##
n_nodes <- length(unique(c(data$treat1, data$treat2))) # Number of network's nodes
# List with the number of inconsistency factors for the Design-by-treatment methods
p_DBT <- numberIF.DBT(n_nodes, Multiarm_studies, design, design_multi, method)
##
p_Jackson <- p_DBT$Jackson # Number of inconsistency factor for the Jackson approach
p_Higgins <- p_DBT$Higgins # Number of inconsistency factor for the Higgins approach
IFmulti <- p_DBT$IFmulti # Number of inconsistency factors added for each multi-arm design
##
# Generate NMA MCMC data
##
p <- ifelse(method == "DBT", p_Higgins, p_Jackson)
# List with the NMA data and the treatment's effect
zy <- dbtdesign(data, ref, Multiarm_studies, studies_multi, design, IFmulti, p_Jackson, method, p_Higgins)
##
Z_MCMC <- zy$Z
y <- zy$y
##
Z <- as.matrix(Z_MCMC[, 4:dim(Z_MCMC)[2]])
colnames(Z) <- names(Z_MCMC)[4:dim(Z_MCMC)[2]]
##
# ZTZ <- solve(t(Z) %*% Z)
ZTZ <- t(Z) %*% Z
IF <- colnames(Z)
N <- dim(Z_MCMC)[1]
NHtH <- sum(table(Z_MCMC$studlab) == 1)
# Specify covariance matrices
cov_matrices <- hetmat(data, Z_MCMC, Multiarm_studies)
##
H <- cov_matrices$H
PREC <- cov_matrices$PREC
res <- list(
"Z_MCMC" = Z_MCMC,
"Z" = Z,
"ZTZ" = ZTZ,
"p" = p,
"H" = H,
"PREC" = PREC,
"y" = y,
"IF" = IF,
"N" = N,
"NHtH" = NHtH
)
res
}
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