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# ==================================================================== #
# TITLE #
# Antimicrobial Resistance (AMR) Analysis #
# #
# SOURCE #
# https://gitlab.com/msberends/AMR #
# #
# LICENCE #
# (c) 2019 Berends MS (m.s.berends@umcg.nl), Luz CF (c.f.luz@umcg.nl) #
# #
# 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. #
# #
# This R package was created for academic research and was publicly #
# released in the hope that it will be useful, but it comes WITHOUT #
# ANY WARRANTY OR LIABILITY. #
# Visit our website for more info: https://msberends.gitab.io/AMR. #
# ==================================================================== #
#' Transform to microorganism ID
#'
#' Use this function to determine a valid microorganism ID (\code{mo}). Determination is done using intelligent rules and the complete taxonomic kingdoms Bacteria, Chromista, Protozoa, Archaea, Viruses, and most microbial species from the kingdom Fungi (see Source). The input can be almost anything: a full name (like \code{"Staphylococcus aureus"}), an abbreviated name (like \code{"S. aureus"}), an abbreviation known in the field (like \code{"MRSA"}), or just a genus. Please see Examples.
#' @param x a character vector or a \code{data.frame} with one or two columns
#' @param Becker a logical to indicate whether \emph{Staphylococci} should be categorised into Coagulase Negative \emph{Staphylococci} ("CoNS") and Coagulase Positive \emph{Staphylococci} ("CoPS") instead of their own species, according to Karsten Becker \emph{et al.} [1].
#'
#' This excludes \emph{Staphylococcus aureus} at default, use \code{Becker = "all"} to also categorise \emph{S. aureus} as "CoPS".
#' @param Lancefield a logical to indicate whether beta-haemolytic \emph{Streptococci} should be categorised into Lancefield groups instead of their own species, according to Rebecca C. Lancefield [2]. These \emph{Streptococci} will be categorised in their first group, e.g. \emph{Streptococcus dysgalactiae} will be group C, although officially it was also categorised into groups G and L.
#'
#' This excludes \emph{Enterococci} at default (who are in group D), use \code{Lancefield = "all"} to also categorise all \emph{Enterococci} as group D.
#' @param allow_uncertain a logical (\code{TRUE} or \code{FALSE}) or a value between 0 and 3 to indicate whether the input should be checked for less possible results, see Details
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#' @param reference_df a \code{data.frame} to use for extra reference when translating \code{x} to a valid \code{mo}. See \code{\link{set_mo_source}} and \code{\link{get_mo_source}} to automate the usage of your own codes (e.g. used in your analysis or organisation).
#' @rdname as.mo
#' @aliases mo
#' @keywords mo Becker becker Lancefield lancefield guess
#' @details
#' A microbial ID from this package (class: \code{mo}) typically looks like these examples:\cr
#' \preformatted{
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#' Code Full name
#' --------------- --------------------------------------
#' B_KLBSL Klebsiella
#' B_KLBSL_PNE Klebsiella pneumoniae
#' B_KLBSL_PNE_RHI Klebsiella pneumoniae rhinoscleromatis
#' | | | |
#' | | | |
#' | | | ----> subspecies, a 3-4 letter acronym
#' | | ----> species, a 3-4 letter acronym
#' | ----> genus, a 5-7 letter acronym, mostly without vowels
#' ----> taxonomic kingdom: A (Archaea), AN (Animalia), B (Bacteria), C (Chromista),
#' F (Fungi), P (Protozoa), PL (Plantae) or V (Viruses)
#' }
#'
#' Values that cannot be coered will be considered 'unknown' and have an MO code \code{UNKNOWN}.
#'
#' Use the \code{\link{mo_property}} functions to get properties based on the returned code, see Examples.
#'
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#' \strong{Intelligent rules} \cr
#' This function uses intelligent rules to help getting fast and logical results. It tries to find matches in this order:
#' \itemize{
#' \item{Valid MO codes and full names: it first searches in already valid MO code and known genus/species combinations}
#' \item{Human pathogenic prevalence: it first searches in more prevalent microorganisms, then less prevalent ones (see \emph{Microbial prevalence of pathogens in humans} below)}
#' \item{Taxonomic kingdom: it first searches in Bacteria/Chromista, then Fungi, then Protozoa, then Viruses}
#' \item{Breakdown of input values: from here it starts to breakdown input values to find possible matches}
#' }
#'
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#' A couple of effects because of these rules:
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#' \itemize{
#' \item{\code{"E. coli"} will return the ID of \emph{Escherichia coli} and not \emph{Entamoeba coli}, although the latter would alphabetically come first}
#' \item{\code{"H. influenzae"} will return the ID of \emph{Haemophilus influenzae} and not \emph{Haematobacter influenzae} for the same reason}
#' \item{Something like \code{"stau"} or \code{"S aur"} will return the ID of \emph{Staphylococcus aureus} and not \emph{Staphylococcus auricularis}}
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#' }
#' This means that looking up human pathogenic microorganisms takes less time than looking up human non-pathogenic microorganisms.
#'
#' \strong{Uncertain results} \cr
#' The algorithm can additionally use three different levels of uncertainty to guess valid results. The default is \code{allow_uncertain = TRUE}, which is uqual to uncertainty level 2. Using \code{allow_uncertain = FALSE} will skip all of these additional rules:
#' \itemize{
#' \item{(uncertainty level 1): It tries to look for only matching genera}
#' \item{(uncertainty level 1): It tries to look for previously accepted (but now invalid) taxonomic names}
#' \item{(uncertainty level 1): It tries to look for some manual changes which are not (yet) published to the Catalogue of Life (like \emph{Propionibacterium} being \emph{Cutibacterium})}
#' \item{(uncertainty level 2): It strips off values between brackets and the brackets itself, and re-evaluates the input with all previous rules}
#' \item{(uncertainty level 2): It strips off words from the end one by one and re-evaluates the input with all previous rules}
#' \item{(uncertainty level 3): It strips off words from the start one by one and re-evaluates the input with all previous rules}
#' \item{(uncertainty level 3): It tries any part of the name}
#' }
#'
#' You can also use e.g. \code{as.mo(..., allow_uncertain = 1)} to only allow up to level 1 uncertainty.
#'
#' Examples:
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#' \itemize{
#' \item{\code{"Streptococcus group B (known as S. agalactiae)"}. The text between brackets will be removed and a warning will be thrown that the result \emph{Streptococcus group B} (\code{B_STRPT_GRB}) needs review.}
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#' \item{\code{"S. aureus - please mind: MRSA"}. The last word will be stripped, after which the function will try to find a match. If it does not, the second last word will be stripped, etc. Again, a warning will be thrown that the result \emph{Staphylococcus aureus} (\code{B_STPHY_AUR}) needs review.}
#' \item{\code{"Fluoroquinolone-resistant Neisseria gonorrhoeae"}. The first word will be stripped, after which the function will try to find a match. A warning will be thrown that the result \emph{Neisseria gonorrhoeae} (\code{B_NESSR_GON}) needs review.}
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#' }
#'
#' Use \code{mo_failures()} to get a vector with all values that could not be coerced to a valid value.
#'
#' Use \code{mo_uncertainties()} to get a data.frame with all values that were coerced to a valid value, but with uncertainty.
#'
#' Use \code{mo_renamed()} to get a vector with all values that could be coerced based on an old, previously accepted taxonomic name.
#'
#' \strong{Microbial prevalence of pathogens in humans} \cr
#' The intelligent rules takes into account microbial prevalence of pathogens in humans. It uses three groups and all (sub)species are in only one group. These groups are:
#' \itemize{
#' \item{1 (most prevalent): class is Gammaproteobacteria \strong{or} genus is one of: \emph{Enterococcus}, \emph{Staphylococcus}, \emph{Streptococcus}.}
#' \item{2: phylum is one of: Proteobacteria, Firmicutes, Actinobacteria, Sarcomastigophora \strong{or} genus is one of: \emph{Aspergillus}, \emph{Bacteroides}, \emph{Candida}, \emph{Capnocytophaga}, \emph{Chryseobacterium}, \emph{Cryptococcus}, \emph{Elisabethkingia}, \emph{Flavobacterium}, \emph{Fusobacterium}, \emph{Giardia}, \emph{Leptotrichia}, \emph{Mycoplasma}, \emph{Prevotella}, \emph{Rhodotorula}, \emph{Treponema}, \emph{Trichophyton}, \emph{Ureaplasma}.}
#' \item{3 (least prevalent): all others.}
#' }
#'
#' Group 1 contains all common Gram negatives, like all Enterobacteriaceae and e.g. \emph{Pseudomonas} and \emph{Legionella}.
#'
#' Group 2 probably contains all other microbial pathogens ever found in humans.
#' @inheritSection catalogue_of_life Catalogue of Life
# (source as a section, so it can be inherited by other man pages)
#' @section Source:
#' [1] Becker K \emph{et al.} \strong{Coagulase-Negative Staphylococci}. 2014. Clin Microbiol Rev. 27(4): 870–926. \url{https://dx.doi.org/10.1128/CMR.00109-13}
#'
#' [2] Lancefield RC \strong{A serological differentiation of human and other groups of hemolytic streptococci}. 1933. J Exp Med. 57(4): 571–95. \url{https://dx.doi.org/10.1084/jem.57.4.571}
#'
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#' [3] Catalogue of Life: Annual Checklist (public online taxonomic database), \url{www.catalogueoflife.org} (check included annual version with \code{\link{catalogue_of_life_version}()}).
#' @export
#' @return Character (vector) with class \code{"mo"}. Unknown values will return \code{NA}.
#' @seealso \code{\link{microorganisms}} for the \code{data.frame} that is being used to determine ID's. \cr
#' The \code{\link{mo_property}} functions (like \code{\link{mo_genus}}, \code{\link{mo_gramstain}}) to get properties based on the returned code.
#' @inheritSection AMR Read more on our website!
#' @importFrom dplyr %>% pull left_join
#' @examples
#' # These examples all return "B_STPHY_AUR", the ID of S. aureus:
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#' as.mo("sau") # WHONET code
#' as.mo("stau")
#' as.mo("STAU")
#' as.mo("staaur")
#' as.mo("S. aureus")
#' as.mo("S aureus")
#' as.mo("Staphylococcus aureus")
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#' as.mo("Staphylococcus aureus (MRSA)")
#' as.mo("Sthafilokkockus aaureuz") # handles incorrect spelling
#' as.mo("MRSA") # Methicillin Resistant S. aureus
#' as.mo("VISA") # Vancomycin Intermediate S. aureus
#' as.mo("VRSA") # Vancomycin Resistant S. aureus
#'
#' as.mo("Streptococcus group A")
#' as.mo("GAS") # Group A Streptococci
#' as.mo("GBS") # Group B Streptococci
#'
#' as.mo("S. epidermidis") # will remain species: B_STPHY_EPI
#' as.mo("S. epidermidis", Becker = TRUE) # will not remain species: B_STPHY_CNS
#'
#' as.mo("S. pyogenes") # will remain species: B_STRPT_PYO
#' as.mo("S. pyogenes", Lancefield = TRUE) # will not remain species: B_STRPT_GRA
#'
#' # Use mo_* functions to get a specific property based on `mo`
#' Ecoli <- as.mo("E. coli") # returns `B_ESCHR_COL`
#' mo_genus(Ecoli) # returns "Escherichia"
#' mo_gramstain(Ecoli) # returns "Gram negative"
#' # but it uses as.mo internally too, so you could also just use:
#' mo_genus("E. coli") # returns "Escherichia"
#'
#'
#' \dontrun{
#' df$mo <- as.mo(df$microorganism_name)
#'
#' # the select function of tidyverse is also supported:
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#' library(dplyr)
#' df$mo <- df %>%
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#' select(microorganism_name) %>%
#' as.mo()
#'
#' # and can even contain 2 columns, which is convenient for genus/species combinations:
#' df$mo <- df %>%
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#' select(genus, species) %>%
#' as.mo()
#' # although this works easier and does the same:
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#' df <- df %>%
#' mutate(mo = as.mo(paste(genus, species)))
#' }
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as.mo <- function(x, Becker = FALSE, Lancefield = FALSE, allow_uncertain = TRUE, reference_df = get_mo_source()) {
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if (!"AMR" %in% base::.packages()) {
library("AMR")
# check onLoad() in R/zzz.R: data tables are created there.
}
if (mo_source_isvalid(reference_df)
& isFALSE(Becker)
& isFALSE(Lancefield)
& !is.null(reference_df)
& all(x %in% reference_df[,1][[1]])) {
# has valid own reference_df
# (data.table not faster here)
reference_df <- reference_df %>% filter(!is.na(mo))
# keep only first two columns, second must be mo
if (colnames(reference_df)[1] == "mo") {
reference_df <- reference_df[, c(2, 1)]
} else {
reference_df <- reference_df[, c(1, 2)]
}
colnames(reference_df)[1] <- "x"
# remove factors, just keep characters
suppressWarnings(
reference_df[] <- lapply(reference_df, as.character)
)
suppressWarnings(
y <- data.frame(x = x, stringsAsFactors = FALSE) %>%
left_join(reference_df, by = "x") %>%
pull("mo")
)
} else if (all(x %in% AMR::microorganisms$mo)
& isFALSE(Becker)
& isFALSE(Lancefield)) {
y <- x
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} else if (all(tolower(x) %in% microorganismsDT$fullname_lower)
& isFALSE(Becker)
& isFALSE(Lancefield)) {
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# we need special treatment for very prevalent full names, they are likely! (case insensitive)
# e.g. as.mo("Staphylococcus aureus")
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y <- microorganismsDT[prevalence == 1][data.table(fullname_lower = tolower(x)),
on = "fullname_lower",
"mo"][[1]]
if (any(is.na(y))) {
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y[is.na(y)] <- microorganismsDT[prevalence == 2][data.table(fullname_lower = tolower(x[is.na(y)])),
on = "fullname_lower",
"mo"][[1]]
}
if (any(is.na(y))) {
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y[is.na(y)] <- microorganismsDT[prevalence == 3][data.table(fullname_lower = tolower(x[is.na(y)])),
on = "fullname_lower",
"mo"][[1]]
}
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} else {
# will be checked for mo class in validation and uses exec_as.mo internally if necessary
y <- mo_validate(x = x, property = "mo",
Becker = Becker, Lancefield = Lancefield,
allow_uncertain = allow_uncertain, reference_df = reference_df)
}
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structure(.Data = y, class = "mo")
}
#' @rdname as.mo
#' @export
is.mo <- function(x) {
identical(class(x), "mo")
}
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#' @importFrom dplyr %>% pull left_join n_distinct progress_estimated filter distinct
#' @importFrom data.table data.table as.data.table setkey
#' @importFrom crayon magenta red blue silver italic has_color
exec_as.mo <- function(x, Becker = FALSE, Lancefield = FALSE,
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allow_uncertain = TRUE, reference_df = get_mo_source(),
property = "mo", clear_options = TRUE) {
if (!"AMR" %in% base::.packages()) {
library("AMR")
# check onLoad() in R/zzz.R: data tables are created there.
}
if (clear_options == TRUE) {
options(mo_failures = NULL)
options(mo_uncertainties = NULL)
options(mo_renamed = NULL)
}
if (NCOL(x) == 2) {
# support tidyverse selection like: df %>% select(colA, colB)
# paste these columns together
x_vector <- vector("character", NROW(x))
for (i in 1:NROW(x)) {
x_vector[i] <- paste(pull(x[i,], 1), pull(x[i,], 2), sep = " ")
}
x <- x_vector
} else {
if (NCOL(x) > 2) {
stop('`x` can be 2 columns at most', call. = FALSE)
}
x[is.null(x)] <- NA
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# support tidyverse selection like: df %>% select(colA)
if (!is.vector(x) & !is.null(dim(x))) {
x <- pull(x, 1)
}
}
notes <- character(0)
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uncertainties <- data.frame(input = character(0),
fullname = character(0),
mo = character(0))
failures <- character(0)
if (isTRUE(allow_uncertain)) {
# default to uncertainty level 2
allow_uncertain <- 2
} else {
allow_uncertain <- as.integer(allow_uncertain)
if (!allow_uncertain %in% c(0:3)) {
stop("`allow_uncertain` must be a number between 0 (none) and 3 (all), or TRUE (= 2) or FALSE (= 0).", call. = FALSE)
}
}
x_input <- x
# already strip leading and trailing spaces
x <- trimws(x, which = "both")
# only check the uniques, which is way faster
x <- unique(x)
# remove empty values (to later fill them in again with NAs)
# ("xxx" is WHONET code for 'no growth' and "con" is WHONET code for 'contamination')
x <- x[!is.na(x)
& !is.null(x)
& !identical(x, "")
& !identical(x, "xxx")
& !identical(x, "con")]
# conversion of old MO codes from v0.5.0 (ITIS) to later versions (Catalogue of Life)
if (any(x %like% "^[BFP]_[A-Z]{3,7}") & !all(x %in% microorganisms$mo)) {
leftpart <- gsub("^([BFP]_[A-Z]{3,7}).*", "\\1", x)
if (any(leftpart %in% names(mo_codes_v0.5.0))) {
rightpart <- gsub("^[BFP]_[A-Z]{3,7}(.*)", "\\1", x)
leftpart <- mo_codes_v0.5.0[leftpart]
x[!is.na(leftpart)] <- paste0(leftpart[!is.na(leftpart)], rightpart[!is.na(leftpart)])
}
}
# defined df to check for
if (!is.null(reference_df)) {
if (!mo_source_isvalid(reference_df)) {
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stop("`reference_df` must contain a column `mo` with values from the 'microorganisms' data set.", call. = FALSE)
}
reference_df <- reference_df %>% filter(!is.na(mo))
# keep only first two columns, second must be mo
if (colnames(reference_df)[1] == "mo") {
reference_df <- reference_df[, c(2, 1)]
} else {
reference_df <- reference_df[, c(1, 2)]
}
colnames(reference_df)[1] <- "x"
# remove factors, just keep characters
suppressWarnings(
reference_df[] <- lapply(reference_df, as.character)
)
}
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# all empty
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if (all(identical(trimws(x_input), "") | is.na(x_input) | length(x) == 0)) {
if (property == "mo") {
return(structure(rep(NA_character_, length(x_input)),
class = "mo"))
} else {
return(rep(NA_character_, length(x_input)))
}
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} else if (all(x %in% reference_df[, 1][[1]])) {
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# all in reference df
colnames(reference_df)[1] <- "x"
suppressWarnings(
x <- data.frame(x = x, stringsAsFactors = FALSE) %>%
left_join(reference_df, by = "x") %>%
left_join(AMR::microorganisms, by = "mo") %>%
pull(property)
)
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} else if (all(x %in% AMR::microorganisms$mo)) {
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# existing mo codes when not looking for property "mo", like mo_genus("B_ESCHR_COL")
y <- microorganismsDT[prevalence == 1][data.table(mo = x), on = "mo", ..property][[1]]
if (any(is.na(y))) {
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y[is.na(y)] <- microorganismsDT[prevalence == 2][data.table(mo = x[is.na(y)]),
on = "mo",
..property][[1]]
}
if (any(is.na(y))) {
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y[is.na(y)] <- microorganismsDT[prevalence == 3][data.table(mo = x[is.na(y)]),
on = "mo",
..property][[1]]
}
x <- y
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} else if (all(tolower(x) %in% microorganismsDT$fullname_lower)) {
# we need special treatment for very prevalent full names, they are likely!
# e.g. as.mo("Staphylococcus aureus")
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y <- microorganismsDT[prevalence == 1][data.table(fullname_lower = tolower(x)), on = "fullname_lower", ..property][[1]]
if (any(is.na(y))) {
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y[is.na(y)] <- microorganismsDT[prevalence == 2][data.table(fullname_lower = tolower(x[is.na(y)])),
on = "fullname_lower",
..property][[1]]
}
if (any(is.na(y))) {
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y[is.na(y)] <- microorganismsDT[prevalence == 3][data.table(fullname_lower = tolower(x[is.na(y)])),
on = "fullname_lower",
..property][[1]]
}
x <- y
} else if (all(toupper(x) %in% AMR::microorganisms.codes$code)) {
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# commonly used MO codes
y <- as.data.table(AMR::microorganisms.codes)[data.table(code = toupper(x)), on = "code", ]
x <- microorganismsDT[data.table(mo = y[["mo"]]), on = "mo", ..property][[1]]
} else if (!all(x %in% AMR::microorganisms[, property])) {
x_backup <- x
# remove spp and species
x <- trimws(gsub(" +(spp.?|ssp.?|sp.? |ss ?.?|subsp.?|subspecies|biovar |serovar |species)", " ", x_backup, ignore.case = TRUE), which = "both")
x_backup_without_spp <- x
x_species <- paste(x, "species")
# translate to English for supported languages of mo_property
x <- gsub("(Gruppe|gruppe|groep|grupo|gruppo|groupe)", "group", x, ignore.case = TRUE)
# remove non-text in case of "E. coli" except dots and spaces
x <- gsub("[^.a-zA-Z0-9/ \\-]+", "", x)
# replace minus by a space
x <- gsub("-+", " ", x)
# replace hemolytic by haemolytic
x <- gsub("ha?emoly", "haemoly", x)
# place minus back in streptococci
x <- gsub("(alpha|beta|gamma) ha?emoly", "\\1-haemoly", x)
# remove genus as first word
x <- gsub("^Genus ", "", x)
# allow characters that resemble others
x <- gsub("[iy]+", "[iy]+", x, ignore.case = TRUE)
x <- gsub("[sz]+", "[sz]+", x, ignore.case = TRUE)
x <- gsub("(c|k|q|qu)+", "(c|k|q|qu)+", x, ignore.case = TRUE)
x <- gsub("(ph|f|v)+", "(ph|f|v)+", x, ignore.case = TRUE)
x <- gsub("(th|t)+", "(th|t)+", x, ignore.case = TRUE)
x <- gsub("a+", "a+", x, ignore.case = TRUE)
x <- gsub("e+", "e+", x, ignore.case = TRUE)
x <- gsub("o+", "o+", x, ignore.case = TRUE)
# but spaces before and after should be omitted
x <- trimws(x, which = "both")
x_trimmed <- x
x_trimmed_species <- paste(x_trimmed, "species")
x_trimmed_without_group <- gsub(" gro.u.p$", "", x_trimmed, ignore.case = TRUE)
# remove last part from "-" or "/"
x_trimmed_without_group <- gsub("(.*)[-/].*", "\\1", x_trimmed_without_group)
# replace space and dot by regex sign
x_withspaces <- gsub("[ .]+", ".* ", x)
x <- gsub("[ .]+", ".*", x)
# add start en stop regex
x <- paste0('^', x, '$')
x_withspaces_start_only <- paste0('^', x_withspaces)
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x_withspaces_end_only <- paste0(x_withspaces, '$')
x_withspaces_start_end <- paste0('^', x_withspaces, '$')
# cat(paste0('x "', x, '"\n'))
# cat(paste0('x_species "', x_species, '"\n'))
# cat(paste0('x_withspaces_start_only "', x_withspaces_start_only, '"\n'))
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# cat(paste0('x_withspaces_end_only "', x_withspaces_end_only, '"\n'))
# cat(paste0('x_withspaces_start_end "', x_withspaces_start_end, '"\n'))
# cat(paste0('x_backup "', x_backup, '"\n'))
# cat(paste0('x_backup_without_spp "', x_backup_without_spp, '"\n'))
# cat(paste0('x_trimmed "', x_trimmed, '"\n'))
# cat(paste0('x_trimmed_species "', x_trimmed_species, '"\n'))
# cat(paste0('x_trimmed_without_group "', x_trimmed_without_group, '"\n'))
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progress <- progress_estimated(n = length(x), min_time = 3)
for (i in 1:length(x)) {
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progress$tick()$print()
found <- microorganismsDT[mo == toupper(x_backup[i]), ..property][[1]]
# is a valid MO code
if (length(found) > 0) {
x[i] <- found[1L]
next
}
found <- microorganismsDT[fullname_lower %in% tolower(c(x_backup[i], x_backup_without_spp[i])), ..property][[1]]
# most probable: is exact match in fullname
if (length(found) > 0) {
x[i] <- found[1L]
next
}
if (any(x_backup_without_spp[i] %in% c(NA, "", "xxx", "con"))) {
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x[i] <- NA_character_
next
}
if (tolower(x_backup_without_spp[i]) %in% c("other", "none", "unknown")) {
# empty and nonsense values, ignore without warning
x[i] <- microorganismsDT[mo == "UNKNOWN", ..property][[1]]
next
}
if (nchar(gsub("[^a-zA-Z]", "", x_trimmed[i])) < 3) {
# check if search term was like "A. species", then return first genus found with ^A
if (x_backup[i] %like% "[a-z]+ species" | x_backup[i] %like% "[a-z] spp[.]?") {
# get mo code of first hit
found <- microorganismsDT[fullname %like% x_withspaces_start_only[i], mo]
if (length(found) > 0) {
mo_code <- found[1L] %>% strsplit("_") %>% unlist() %>% .[1:2] %>% paste(collapse = "_")
found <- microorganismsDT[mo == mo_code, ..property][[1]]
# return first genus that begins with x_trimmed, e.g. when "E. spp."
if (length(found) > 0) {
x[i] <- found[1L]
next
}
}
}
# fewer than 3 chars and not looked for species, add as failure
x[i] <- microorganismsDT[mo == "UNKNOWN", ..property][[1]]
failures <- c(failures, x_backup[i])
next
}
if (x_backup_without_spp[i] %like% "virus") {
# there is no fullname like virus, so don't try to coerce it
x[i] <- microorganismsDT[mo == "UNKNOWN", ..property][[1]]
4 years ago
failures <- c(failures, x_backup[i])
next
}
# translate known trivial abbreviations to genus + species ----
if (!is.na(x_trimmed[i])) {
if (toupper(x_backup_without_spp[i]) %in% c('MRSA', 'MSSA', 'VISA', 'VRSA')) {
x[i] <- microorganismsDT[mo == 'B_STPHY_AUR', ..property][[1]][1L]
next
}
if (toupper(x_backup_without_spp[i]) %in% c('MRSE', 'MSSE')) {
x[i] <- microorganismsDT[mo == 'B_STPHY_EPI', ..property][[1]][1L]
next
}
if (toupper(x_backup_without_spp[i]) == "VRE"
| x_backup_without_spp[i] %like% '(enterococci|enterokok|enterococo)[a-z]*?$') {
x[i] <- microorganismsDT[mo == 'B_ENTRC', ..property][[1]][1L]
next
}
if (toupper(x_backup_without_spp[i]) %in% c("EHEC", "EPEC", "EIEC", "STEC", "ATEC")) {
x[i] <- microorganismsDT[mo == 'B_ESCHR_COL', ..property][[1]][1L]
next
}
if (toupper(x_backup_without_spp[i]) == 'MRPA') {
# multi resistant P. aeruginosa
x[i] <- microorganismsDT[mo == 'B_PSDMN_AER', ..property][[1]][1L]
next
}
if (toupper(x_backup_without_spp[i]) == 'CRS'
| toupper(x_backup_without_spp[i]) == 'CRSM') {
# co-trim resistant S. maltophilia
x[i] <- microorganismsDT[mo == 'B_STNTR_MAL', ..property][[1]][1L]
next
}
if (toupper(x_backup_without_spp[i]) %in% c('PISP', 'PRSP', 'VISP', 'VRSP')) {
# peni I, peni R, vanco I, vanco R: S. pneumoniae
x[i] <- microorganismsDT[mo == 'B_STRPT_PNE', ..property][[1]][1L]
next
}
if (x_backup_without_spp[i] %like% '^G[ABCDFGHK]S$') {
# Streptococci, like GBS = Group B Streptococci (B_STRPT_GRB)
x[i] <- microorganismsDT[mo == gsub("G([ABCDFGHK])S", "B_STRPT_GR\\1", x_backup_without_spp[i], ignore.case = TRUE), ..property][[1]][1L]
next
}
if (x_backup_without_spp[i] %like% '(streptococ|streptokok).* [ABCDFGHK]$') {
# Streptococci in different languages, like "estreptococos grupo B"
x[i] <- microorganismsDT[mo == gsub(".*(streptococ|streptokok|estreptococ).* ([ABCDFGHK])$", "B_STRPT_GR\\2", x_backup_without_spp[i], ignore.case = TRUE), ..property][[1]][1L]
next
}
if (x_backup_without_spp[i] %like% 'group [ABCDFGHK] (streptococ|streptokok|estreptococ)') {
# Streptococci in different languages, like "Group A Streptococci"
x[i] <- microorganismsDT[mo == gsub(".*group ([ABCDFGHK]) (streptococ|streptokok|estreptococ).*", "B_STRPT_GR\\1", x_backup_without_spp[i], ignore.case = TRUE), ..property][[1]][1L]
next
}
# CoNS/CoPS in different languages (support for German, Dutch, Spanish, Portuguese) ----
if (x_backup_without_spp[i] %like% '[ck]oagulas[ea] negatie?[vf]'
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| x_trimmed[i] %like% '[ck]oagulas[ea] negatie?[vf]'
| x_backup_without_spp[i] %like% '[ck]o?ns[^a-z]?$') {
# coerce S. coagulase negative
x[i] <- microorganismsDT[mo == 'B_STPHY_CNS', ..property][[1]][1L]
next
}
if (x_backup_without_spp[i] %like% '[ck]oagulas[ea] positie?[vf]'
4 years ago
| x_trimmed[i] %like% '[ck]oagulas[ea] positie?[vf]'
| x_backup_without_spp[i] %like% '[ck]o?ps[^a-z]?$') {
# coerce S. coagulase positive
x[i] <- microorganismsDT[mo == 'B_STPHY_CPS', ..property][[1]][1L]
next
}
if (x_backup_without_spp[i] %like% 'gram[ -]?neg.*'
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| x_trimmed[i] %like% 'gram[ -]?neg.*') {
# coerce Gram negatives
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x[i] <- microorganismsDT[mo == 'B_GRAMN', ..property][[1]][1L]
next
}
if (x_backup_without_spp[i] %like% 'gram[ -]?pos.*'
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| x_trimmed[i] %like% 'gram[ -]?pos.*') {
# coerce Gram positives
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x[i] <- microorganismsDT[mo == 'B_GRAMP', ..property][[1]][1L]
next
}
if (grepl("[sS]almonella [A-Z][a-z]+ ?.*", x_backup_without_spp[i], ignore.case = FALSE)) {
if (x_backup_without_spp[i] %like% "Salmonella group") {
# Salmonella Group A to Z, just return S. species for now
x[i] <- microorganismsDT[mo == 'B_SLMNL', ..property][[1]][1L]
options(mo_renamed = c(getOption("mo_renamed"),
magenta(paste0("Note: ",
italic("Salmonella"), " ", trimws(gsub("Salmonella", "", x_backup_without_spp[i])),
" was considered ",
italic("Salmonella species"),
" (B_SLMNL)"))))
} else {
# Salmonella with capital letter species like "Salmonella Goettingen" - they're all S. enterica
x[i] <- microorganismsDT[mo == 'B_SLMNL_ENT', ..property][[1]][1L]
options(mo_renamed = c(getOption("mo_renamed"),
magenta(paste0("Note: ",
italic("Salmonella"), " ", trimws(gsub("Salmonella", "", x_backup_without_spp[i])),
" was considered a subspecies of ",
italic("Salmonella enterica"),
" (B_SLMNL_ENT)"))))
}
next
}
}
# FIRST TRY FULLNAMES AND CODES
# if only genus is available, return only genus
if (all(!c(x[i], x_trimmed[i]) %like% " ")) {
4 years ago
found <- microorganismsDT[fullname_lower %in% tolower(c(x_species[i], x_trimmed_species[i])), ..property][[1]]
if (length(found) > 0) {
x[i] <- found[1L]
next
}
if (nchar(x_backup_without_spp[i]) >= 6) {
found <- microorganismsDT[fullname_lower %like% paste0("^", x_backup_without_spp[i], "[a-z]+"), ..property][[1]]
if (length(found) > 0) {
x[i] <- found[1L]
next
}
}
# rest of genus only is in allow_uncertain part.
}
# TRY OTHER SOURCES ----
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# WHONET and other common LIS codes
if (toupper(x_backup[i]) %in% AMR::microorganisms.codes[, 1]) {
mo_found <- AMR::microorganisms.codes[toupper(x_backup[i]) == AMR::microorganisms.codes[, 1], "mo"][1L]
if (length(mo_found) > 0) {
x[i] <- microorganismsDT[mo == mo_found, ..property][[1]][1L]
next
}
}
if (!is.null(reference_df)) {
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# self-defined reference
if (x_backup[i] %in% reference_df[, 1]) {
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