P281424/AMR
1
0
Fork 0
mirror of https://github.com/msberends/AMR.git synced 2025-07-08 22:41:52 +02:00
Code Releases Activity

speed improvement eucast_rules(), support more old MO codes

Browse Source
This commit is contained in:
dr. M.S. (Matthijs) Berends
2019-05-20 12:00:18 +02:00
parent b0033dae1b
commit 4ca00e1868
35 changed files with 590 additions and 683 deletions
Download Patch File Download Diff File Expand all files Collapse all files

21
R/mo.R
View File

@ -111,18 +111,18 @@
#' 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:
#' The intelligent rules take 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 1 contains all common Gram positives and 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.
#' Group 2 probably contains less microbial pathogens; all other members of phyla that were found in humans in the Northern Netherlands between 2001 and 2018.
#' @inheritSection catalogue_of_life Catalogue of Life
# (source as a section, so it can be inherited by other man pages)
# (source as a section here, 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}
#'
@ -349,13 +349,24 @@ exec_as.mo <- function(x,
# 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$mo)) {
x <- gsub("^F_CANDD_GLB$", "F_CANDD_GLA", x) # specific old code for C. glabrata
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)])
}
# now check if some are still old
still_old <- x[x %in% names(mo_codes_v0.5.0)]
if (length(still_old) > 0) {
x[x %in% names(mo_codes_v0.5.0)] <- data.frame(old = still_old, stringsAsFactors = FALSE) %>%
left_join(data.frame(old = names(mo_codes_v0.5.0),
new = mo_codes_v0.5.0,
stringsAsFactors = FALSE), by = "old") %>%
# if they couldn't be found, replace them with the old ones again,
# so they will throw a warning in the end
mutate(new = ifelse(is.na(new), old, new)) %>%
pull(new)
}
}
# defined df to check for