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#!/usr/bin/env Rscript
# b20. Estimation of several specifications from synchronized catalogs
#
# This example mirrors plot_b20_multiple_models.py. Catalogs are neutral R
# expression nodes until the complete likelihood is compiled. Native Biogeme
# then enumerates the synchronized catalog choices and performs every model
# estimation and result-processing operation.
library(rbiogeme)
# prepare_swissmetro_example() is defined in example_utils.R. It parses the
# command line, validates the data/Python paths, configures the bridge, reads
# the data, and creates the output directory. This shared helper is only data
# and run setup; the full b20 model specification is below.
script_path <- commandArgs(trailingOnly = FALSE)
script_path <- sub("^--file=", "", script_path[startsWith(script_path, "--file=")][[1L]])
source(file.path(dirname(normalizePath(script_path)), "example_utils.R"))
build_b20_multiple_models_model <- function(database) {
# These four names and starting values are exactly those in native b20.
asc_car <- biogeme_beta("asc_car", start = 0)
asc_train <- biogeme_beta("asc_train", start = 0)
b_time <- biogeme_beta("b_time", start = 0)
b_cost <- biogeme_beta("b_cost", start = 0)
# A catalog_controller() synchronizes selections across catalogs. Here the
# same ASC choice (unsegmented or MALE-segmented) is used for Train and Car.
gender <- biogeme_database_segmentation(
database,
variable = "MALE",
mapping = c(`0` = "female", `1` = "male")
)
asc_controller <- catalog_controller("asc", c("no_seg", "MALE"))
asc_train_catalog <- catalog(
"segmented_asc_train",
list(
no_seg = asc_train,
MALE = segment_beta(asc_train, list(gender))
),
controller = asc_controller
)
asc_car_catalog <- catalog(
"segmented_asc_car",
list(
no_seg = asc_car,
MALE = segment_beta(asc_car, list(gender))
),
controller = asc_controller
)
# A second shared controller forces Train and Swissmetro to use either a
# linear travel-time variable or its native log transformation together.
time_controller <- catalog_controller(
"train_tt_catalog",
c("linear", "log")
)
train_tt_catalog <- catalog(
"train_tt_catalog",
list(
linear = variable("TRAIN_TT_SCALED"),
log = log(variable("TRAIN_TT_SCALED"))
),
controller = time_controller
)
sm_tt_catalog <- catalog(
"sm_tt_catalog",
list(
linear = variable("SM_TT_SCALED"),
log = log(variable("SM_TT_SCALED"))
),
controller = time_controller
)
# Catalog objects participate in ordinary symbolic arithmetic. No R
# callback is evaluated when these utilities are estimated in Python.
utilities <- list(
`1` = asc_train_catalog + b_time * train_tt_catalog +
b_cost * variable("TRAIN_COST_SCALED"),
`2` = b_time * sm_tt_catalog + b_cost * variable("SM_COST_SCALED"),
`3` = asc_car_catalog + b_time * variable("CAR_TT_SCALED") +
b_cost * variable("CAR_CO_SCALED")
)
availability <- list(
`1` = variable("TRAIN_AV_SP"),
`2` = variable("SM_AV"),
`3` = variable("CAR_AV_SP")
)
# logit_log_probability() maps directly to native models.loglogit, the
# numerically stable log-likelihood constructor used by Python b20.
log_probability <- logit_log_probability(
utilities = utilities,
availability = availability,
alternative = variable("CHOICE")
)
biogeme_model(
database = database,
formula = log_probability,
control = biogeme_control(
output_directory = prepared$output,
model_name = "b20multiple_models",
generate_html = FALSE,
generate_yaml = FALSE,
save_iterations = FALSE
)
)
}
prepared <- prepare_swissmetro_example(
commandArgs(trailingOnly = TRUE),
default_model = "b20multiple_models"
)
database <- swissmetro_data(prepared$data)
model <- build_b20_multiple_models_model(database)
# force = TRUE makes every catalog configuration call native estimate(), so
# an old YAML or iteration file in this directory cannot be reused.
fit <- estimate_catalog(
model,
model_name = "b20multiple_models",
control = model$control,
force = TRUE
)
cat(sprintf("A total of %d models have been estimated:\n", length(fit$results)))
for (configuration in names(fit$results)) {
result <- fit$results[[configuration]]
cat(sprintf(
"%s: LL=%.2f K=%d\n",
configuration,
result$final_log_likelihood,
length(result$beta_names)
))
}
# These tables and the Pareto set are produced by native Biogeme result
# processing and returned as ordinary R tables/vectors for inspection.
print(fit$summary)
for (name in names(fit$description)) {
if (!identical(name, unname(fit$description[[name]]))) {
cat(sprintf("%s: %s\n", name, fit$description[[name]]))
}
}
cat(sprintf("Out of them, %d are non dominated.\n", length(fit$non_dominated)))
for (configuration in fit$non_dominated) cat(configuration, "\n", sep = "")
print(fit$non_dominated_summary)
cat(fit$latex, "\n")
invisible(fit)
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