## ----include = FALSE---------------------------------------------------------- knitr::opts_chunk$set( collapse = TRUE, comment = "#>" ) ## ----setup-------------------------------------------------------------------- library(nlmixr2targets) ## ----using-tar_nlmixr, eval = FALSE------------------------------------------- # library(targets) # library(tarchetypes) # library(nlmixr2targets) # # pheno <- function() { # ini({ # lcl <- log(0.008); label("Typical value of clearance") # lvc <- log(0.6); label("Typical value of volume of distribution") # etalcl + etalvc ~ c(1, # 0.01, 1) # cpaddSd <- 0.1; label("residual variability") # }) # model({ # cl <- exp(lcl + etalcl) # vc <- exp(lvc + etalvc) # kel <- cl / vc # d / dt(central) <- -kel * central # cp <- central / vc # cp ~ add(cpaddSd) # }) # } # # plan_model <- # tar_plan( # myData = nlmixr2data::pheno_sd, # tar_nlmixr( # model_pheno, # object = pheno, # data = myData, # est = "saem" # ) # ) # # list( # plan_model # ) ## ----using-tar_nlmixr_multimodel, eval = FALSE-------------------------------- # library(targets) # library(tarchetypes) # library(nlmixr2targets) # # pheno <- function() { # ini({ # lcl <- log(0.008); label("Typical value of clearance") # lvc <- log(0.6); label("Typical value of volume of distribution") # etalcl + etalvc ~ c(1, # 0.01, 1) # cpaddSd <- 0.1; label("residual variability") # }) # model({ # cl <- exp(lcl + etalcl) # vc <- exp(lvc + etalvc) # kel <- cl / vc # d / dt(central) <- -kel * central # cp <- central / vc # cp ~ add(cpaddSd) # }) # } # # pheno2 <- function() { # ini({ # lcl <- log(0.008); label("Typical value of clearance") # lvc <- log(0.6); label("Typical value of volume of distribution") # etalcl + etalvc ~ c(2, # 0.01, 2) # cpaddSd <- 3.0; label("residual variability") # }) # model({ # cl <- exp(lcl + etalcl) # vc <- exp(lvc + etalvc) # kel <- cl / vc # d / dt(central) <- -kel * central # cp <- central / vc # cp ~ add(cpaddSd) # }) # } # # plan_model <- # tar_nlmixr_multimodel( # all_models, # data = nlmixr2data::pheno_sd, # est = "saem", # "Base model; additive residual error = 1" = pheno, # "Base model; additive residual error = 3" = pheno2 # ) # # plan_report <- # tar_plan( # # Determine the AIC for all tested models # aic_list = sapply(X = all_models, FUN = AIC) # ) # # list( # plan_model, # plan_report # ) ## ----piping-tar_nlmixr_multimodel, eval = FALSE------------------------------- # library(targets) # library(tarchetypes) # library(nlmixr2targets) # library(nlmixr2) # # pheno <- function() { # ini({ # lcl <- log(0.008); label("Typical value of clearance") # lvc <- log(0.6); label("Typical value of volume of distribution") # etalcl + etalvc ~ c(1, # 0.01, 1) # cpaddSd <- 0.1; label("residual variability") # }) # model({ # cl <- exp(lcl + etalcl) # vc <- exp(lvc + etalvc) # kel <- cl / vc # d / dt(central) <- -kel * central # cp <- central / vc # cp ~ add(cpaddSd) # }) # } # # plan_model <- # tar_nlmixr_multimodel( # all_models, # data = nlmixr2data::pheno_sd, # est = "saem", # "Base model; additive residual error = 1" = pheno, # "Base model; additive residual error = 3" = # all_models[["Base model; additive residual error = 1"]] |> ini(cpaddSd = 3) # ) # # list( # plan_model # )