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Reproduce clinical breakpoints from latest WHONET/AMRIE data
- Ran reproduction_of_microorganisms.groups.R and reproduction_of_clinical_breakpoints.R against the latest WHONET/AMRIE source (includes EUCAST 2026, CLSI 2025) - Updated data/clinical_breakpoints.rda, microorganisms.codes.rda, microorganisms.groups.rda, and data-raw/organisms.rds - Fixed reproduction_of_microorganisms.groups.R: replaced base ifelse() with dplyr::if_else() to preserve the <mo> S3 class; base ifelse() strips class attributes, causing bind_rows() to fail with strict vctrs type checking in dplyr >= 1.1.0 - Added data-raw/_run_reproduction.R: non-interactive wrapper that overrides View(), sets UTF-8 locale, and sources both scripts in the correct order https://claude.ai/code/session_01S5vMqfsiJb59RN2Gyz1tDY
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Package: AMR
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Version: 3.0.1.9040
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Date: 2026-03-24
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Version: 3.0.1.9041
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Date: 2026-03-26
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Title: Antimicrobial Resistance Data Analysis
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Description: Functions to simplify and standardise antimicrobial resistance (AMR)
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data analysis and to work with microbial and antimicrobial properties by
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3
NEWS.md
3
NEWS.md
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# AMR 3.0.1.9040
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# AMR 3.0.1.9041
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### New
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* Integration with the **tidymodels** framework to allow seamless use of SIR, MIC and disk data in modelling pipelines via `recipes`
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* Fixed SIR and MIC coercion of combined values, e.g. `as.sir("<= 0.002; S") ` or `as.mic("S; 0.002")` (#252)
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### Updates
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* Reproduced `clinical_breakpoints`, `microorganisms.codes`, and `microorganisms.groups` from the latest WHONET/AMRIE source data (EUCAST 2026 and CLSI 2025 included); fixed `reproduction_of_microorganisms.groups.R` to use `dplyr::if_else()` instead of base `ifelse()` to preserve the `<mo>` class in `bind_rows()`
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* Extensive `cli` integration for better message handling and clickable links in messages and warnings (#191, #265)
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* `mdro()` now infers resistance for a _missing_ base drug column from an _available_ corresponding drug+inhibitor combination showing resistance (e.g., piperacillin is absent but required, while piperacillin/tazobactam available and resistant). Can be set with the new argument `infer_from_combinations`, which defaults to `TRUE` (#209). Note that this can yield a higher MDRO detection (which is a good thing as it has become more reliable).
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* `susceptibility()` and `resistance()` gained the argument `guideline`, which defaults to EUCAST, for interpreting the 'I' category correctly.
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@@ -85,9 +85,9 @@ microorganisms.groups <- whonet_organisms %>%
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"Mycobacterium canetti")) %>%
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filter(!is.na(SPECIES_GROUP), SPECIES_GROUP != ORGANISM_CODE) %>%
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transmute(mo_group = as.mo(SPECIES_GROUP),
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mo = ifelse(is.na(mo),
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as.character(as.mo(ORGANISM, keep_synonyms = TRUE, minimum_matching_score = 0)),
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mo)) %>%
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mo = if_else(is.na(mo),
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as.mo(ORGANISM, keep_synonyms = TRUE, minimum_matching_score = 0),
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mo)) %>%
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# add our own CoNS and CoPS, WHONET does not strictly follow Becker et al. (2014, 2019, 2020)
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filter(mo_group != as.mo("CoNS")) %>%
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bind_rows(tibble(mo_group = as.mo("CoNS"), mo = MO_CONS)) %>%
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27
data-raw/_run_reproduction.R
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data-raw/_run_reproduction.R
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# Wrapper to run clinical breakpoints reproduction non-interactively
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# Set UTF-8 locale so gsub() can handle Unicode patterns
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Sys.setlocale("LC_CTYPE", "C.utf8")
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Sys.setlocale("LC_ALL", "C.utf8")
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# Overrides View() to just print a summary instead
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View <- function(x, title = NULL) {
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if (is.data.frame(x) || is.matrix(x)) {
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cat("=== View() called:", if (!is.null(title)) title else deparse(substitute(x)), "===\n")
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cat("Dimensions:", nrow(x), "rows x", ncol(x), "cols\n")
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print(head(x, 10))
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cat("...\n\n")
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} else {
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print(x)
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}
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invisible(x)
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}
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setwd("/home/user/AMR")
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cat("=== Step 1: Running reproduction_of_microorganisms.groups.R ===\n")
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source("data-raw/_reproduction_scripts/reproduction_of_microorganisms.groups.R")
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cat("\n=== Step 2: Running reproduction_of_clinical_breakpoints.R ===\n")
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source("data-raw/_reproduction_scripts/reproduction_of_clinical_breakpoints.R")
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cat("\n=== Done! ===\n")
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