1
0
mirror of https://github.com/msberends/AMR.git synced 2024-12-26 07:26:13 +01:00
AMR/R/random.R

168 lines
7.9 KiB
R
Executable File

# ==================================================================== #
# TITLE: #
# AMR: An R Package for Working with Antimicrobial Resistance Data #
# #
# SOURCE CODE: #
# https://github.com/msberends/AMR #
# #
# PLEASE CITE THIS SOFTWARE AS: #
# Berends MS, Luz CF, Friedrich AW, et al. (2022). #
# AMR: An R Package for Working with Antimicrobial Resistance Data. #
# Journal of Statistical Software, 104(3), 1-31. #
# https://doi.org/10.18637/jss.v104.i03 #
# #
# Developed at the University of Groningen and the University Medical #
# Center Groningen in The Netherlands, in collaboration with many #
# colleagues from around the world, see our website. #
# #
# This R package is free software; you can freely use and distribute #
# it for both personal and commercial purposes under the terms of the #
# GNU General Public License version 2.0 (GNU GPL-2), as published by #
# the Free Software Foundation. #
# We created this package for both routine data analysis and academic #
# research and it was publicly released in the hope that it will be #
# useful, but it comes WITHOUT ANY WARRANTY OR LIABILITY. #
# #
# Visit our website for the full manual and a complete tutorial about #
# how to conduct AMR data analysis: https://msberends.github.io/AMR/ #
# ==================================================================== #
#' Random MIC Values/Disk Zones/SIR Generation
#'
#' These functions can be used for generating random MIC values and disk diffusion diameters, for AMR data analysis practice. By providing a microorganism and antimicrobial drug, the generated results will reflect reality as much as possible.
#' @param size desired size of the returned vector. If used in a [data.frame] call or `dplyr` verb, will get the current (group) size if left blank.
#' @param mo any [character] that can be coerced to a valid microorganism code with [as.mo()]
#' @param ab any [character] that can be coerced to a valid antimicrobial drug code with [as.ab()]
#' @param prob_SIR a vector of length 3: the probabilities for "S" (1st value), "I" (2nd value) and "R" (3rd value)
#' @param ... ignored, only in place to allow future extensions
#' @details The base \R function [sample()] is used for generating values.
#'
#' Generated values are based on the EUCAST `r max(as.integer(gsub("[^0-9]", "", subset(clinical_breakpoints, guideline %like% "EUCAST")$guideline)))` guideline as implemented in the [clinical_breakpoints] data set. To create specific generated values per bug or drug, set the `mo` and/or `ab` argument.
#' @return class `mic` for [random_mic()] (see [as.mic()]) and class `disk` for [random_disk()] (see [as.disk()])
#' @name random
#' @rdname random
#' @export
#' @examples
#' random_mic(25)
#' random_disk(25)
#' random_sir(25)
#'
#' \donttest{
#' # make the random generation more realistic by setting a bug and/or drug:
#' random_mic(25, "Klebsiella pneumoniae") # range 0.0625-64
#' random_mic(25, "Klebsiella pneumoniae", "meropenem") # range 0.0625-16
#' random_mic(25, "Streptococcus pneumoniae", "meropenem") # range 0.0625-4
#'
#' random_disk(25, "Klebsiella pneumoniae") # range 8-50
#' random_disk(25, "Klebsiella pneumoniae", "ampicillin") # range 11-17
#' random_disk(25, "Streptococcus pneumoniae", "ampicillin") # range 12-27
#' }
random_mic <- function(size = NULL, mo = NULL, ab = NULL, ...) {
meet_criteria(size, allow_class = c("numeric", "integer"), has_length = 1, is_positive = TRUE, is_finite = TRUE, allow_NULL = TRUE)
meet_criteria(mo, allow_class = "character", has_length = 1, allow_NULL = TRUE)
meet_criteria(ab, allow_class = "character", has_length = 1, allow_NULL = TRUE)
if (is.null(size)) {
size <- NROW(get_current_data(arg_name = "size", call = -3))
}
random_exec("MIC", size = size, mo = mo, ab = ab)
}
#' @rdname random
#' @export
random_disk <- function(size = NULL, mo = NULL, ab = NULL, ...) {
meet_criteria(size, allow_class = c("numeric", "integer"), has_length = 1, is_positive = TRUE, is_finite = TRUE, allow_NULL = TRUE)
meet_criteria(mo, allow_class = "character", has_length = 1, allow_NULL = TRUE)
meet_criteria(ab, allow_class = "character", has_length = 1, allow_NULL = TRUE)
if (is.null(size)) {
size <- NROW(get_current_data(arg_name = "size", call = -3))
}
random_exec("DISK", size = size, mo = mo, ab = ab)
}
#' @rdname random
#' @export
random_sir <- function(size = NULL, prob_SIR = c(0.33, 0.33, 0.33), ...) {
meet_criteria(size, allow_class = c("numeric", "integer"), has_length = 1, is_positive = TRUE, is_finite = TRUE, allow_NULL = TRUE)
meet_criteria(prob_SIR, allow_class = c("numeric", "integer"), has_length = 3)
if (is.null(size)) {
size <- NROW(get_current_data(arg_name = "size", call = -3))
}
sample(as.sir(c("S", "I", "R")), size = size, replace = TRUE, prob = prob_SIR)
}
random_exec <- function(method_type, size, mo = NULL, ab = NULL) {
df <- AMR::clinical_breakpoints %pm>%
pm_filter(guideline %like% "EUCAST") %pm>%
pm_arrange(pm_desc(guideline)) %pm>%
subset(guideline == max(guideline) &
method == method_type &
type == "human")
if (!is.null(mo)) {
mo_coerced <- as.mo(mo)
mo_include <- c(
mo_coerced,
as.mo(mo_genus(mo_coerced)),
as.mo(mo_family(mo_coerced)),
as.mo(mo_order(mo_coerced))
)
df_new <- df %pm>%
subset(mo %in% mo_include)
if (nrow(df_new) > 0) {
df <- df_new
} else {
warning_("in `random_", tolower(method_type), "()`: no rows found that match mo '", mo, "', ignoring argument `mo`")
}
}
if (!is.null(ab)) {
ab_coerced <- as.ab(ab)
df_new <- df %pm>%
subset(ab %in% ab_coerced)
if (nrow(df_new) > 0) {
df <- df_new
} else {
warning_("in `random_", tolower(method_type), "()`: no rows found that match ab '", ab, "' (", ab_name(ab_coerced, tolower = TRUE, language = NULL), "), ignoring argument `ab`")
}
}
if (method_type == "MIC") {
# set range
mic_range <- c(0.001, 0.002, 0.005, 0.010, 0.025, 0.0625, 0.125, 0.250, 0.5, 1, 2, 4, 8, 16, 32, 64, 128, 256)
# get highest/lowest +/- random 1 to 3 higher factors of two
max_range <- mic_range[min(
length(mic_range),
which(mic_range == max(df$breakpoint_R, na.rm = TRUE)) + sample(c(1:3), 1)
)]
min_range <- mic_range[max(
1,
which(mic_range == min(df$breakpoint_S, na.rm = TRUE)) - sample(c(1:3), 1)
)]
mic_range_new <- mic_range[mic_range <= max_range & mic_range >= min_range]
if (length(mic_range_new) == 0) {
mic_range_new <- mic_range
}
out <- as.mic(sample(mic_range_new, size = size, replace = TRUE))
# 50% chance that lowest will get <= and highest will get >=
if (stats::runif(1) > 0.5) {
out[out == min(out)] <- paste0("<=", out[out == min(out)])
}
if (stats::runif(1) > 0.5) {
out[out == max(out)] <- paste0(">=", out[out == max(out)])
}
return(out)
} else if (method_type == "DISK") {
set_range <- seq(
from = as.integer(min(df$breakpoint_R, na.rm = TRUE) / 1.25),
to = as.integer(max(df$breakpoint_S, na.rm = TRUE) * 1.25),
by = 1
)
out <- sample(set_range, size = size, replace = TRUE)
out[out < 6] <- sample(c(6:10), length(out[out < 6]), replace = TRUE)
out[out > 50] <- sample(c(40:50), length(out[out > 50]), replace = TRUE)
return(as.disk(out))
}
}