mirror of https://github.com/msberends/AMR.git
183 lines
7.8 KiB
R
Executable File
183 lines
7.8 KiB
R
Executable File
# ==================================================================== #
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# TITLE #
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# AMR: An R Package for Working with Antimicrobial Resistance Data #
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# #
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# SOURCE #
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# https://github.com/msberends/AMR #
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# #
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# CITE AS #
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# Berends MS, Luz CF, Friedrich AW, Sinha BNM, Albers CJ, Glasner C #
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# (2022). AMR: An R Package for Working with Antimicrobial Resistance #
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# Data. Journal of Statistical Software, 104(3), 1-31. #
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# https://doi.org/10.18637/jss.v104.i03 #
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# #
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# Developed at the University of Groningen and the University Medical #
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# Center Groningen in The Netherlands, in collaboration with many #
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# colleagues from around the world, see our website. #
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# #
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# This R package is free software; you can freely use and distribute #
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# it for both personal and commercial purposes under the terms of the #
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# GNU General Public License version 2.0 (GNU GPL-2), as published by #
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# the Free Software Foundation. #
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# We created this package for both routine data analysis and academic #
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# research and it was publicly released in the hope that it will be #
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# useful, but it comes WITHOUT ANY WARRANTY OR LIABILITY. #
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# #
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# Visit our website for the full manual and a complete tutorial about #
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# how to conduct AMR data analysis: https://msberends.github.io/AMR/ #
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# ==================================================================== #
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#' Principal Component Analysis (for AMR)
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#'
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#' Performs a principal component analysis (PCA) based on a data set with automatic determination for afterwards plotting the groups and labels, and automatic filtering on only suitable (i.e. non-empty and numeric) variables.
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#' @param x a [data.frame] containing [numeric] columns
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#' @param ... columns of `x` to be selected for PCA, can be unquoted since it supports quasiquotation.
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#' @inheritParams stats::prcomp
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#' @details The [pca()] function takes a [data.frame] as input and performs the actual PCA with the \R function [prcomp()].
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#'
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#' The result of the [pca()] function is a [prcomp] object, with an additional attribute `non_numeric_cols` which is a vector with the column names of all columns that do not contain [numeric] values. These are probably the groups and labels, and will be used by [ggplot_pca()].
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#' @return An object of classes [pca] and [prcomp]
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#' @importFrom stats prcomp
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#' @export
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#' @examples
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#' # `example_isolates` is a data set available in the AMR package.
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#' # See ?example_isolates.
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#'
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#' \donttest{
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#' if (require("dplyr")) {
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#' # calculate the resistance per group first
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#' resistance_data <- example_isolates %>%
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#' group_by(
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#' order = mo_order(mo), # group on anything, like order
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#' genus = mo_genus(mo)
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#' ) %>% # and genus as we do here;
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#' filter(n() >= 30) %>% # filter on only 30 results per group
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#' summarise_if(is.sir, resistance) # then get resistance of all drugs
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#'
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#' # now conduct PCA for certain antimicrobial drugs
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#' pca_result <- resistance_data %>%
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#' pca(AMC, CXM, CTX, CAZ, GEN, TOB, TMP, SXT)
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#'
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#' pca_result
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#' summary(pca_result)
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#'
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#' # old base R plotting method:
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#' biplot(pca_result)
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#' # new ggplot2 plotting method using this package:
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#' if (require("ggplot2")) {
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#' ggplot_pca(pca_result)
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#'
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#' ggplot_pca(pca_result) +
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#' scale_colour_viridis_d() +
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#' labs(title = "Title here")
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#' }
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#' }
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#' }
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pca <- function(x,
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...,
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retx = TRUE,
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center = TRUE,
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scale. = TRUE,
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tol = NULL,
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rank. = NULL) {
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meet_criteria(x, allow_class = "data.frame")
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meet_criteria(retx, allow_class = "logical", has_length = 1)
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meet_criteria(center, allow_class = "logical", has_length = 1)
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meet_criteria(scale., allow_class = "logical", has_length = 1)
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meet_criteria(tol, allow_class = "numeric", has_length = 1, allow_NULL = TRUE)
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meet_criteria(rank., allow_class = "numeric", has_length = 1, allow_NULL = TRUE)
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# unset data.table, tibble, etc.
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# also removes groups made by dplyr::group_by
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x <- as.data.frame(x, stringsAsFactors = FALSE)
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x.bak <- x
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# defuse R expressions, this replaces rlang::enquos()
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dots <- substitute(list(...))
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if (length(dots) > 1) {
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new_list <- list(0)
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for (i in seq_len(length(dots) - 1)) {
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new_list[[i]] <- tryCatch(eval(dots[[i + 1]], envir = x),
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error = function(e) stop(e$message, call. = FALSE)
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)
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if (length(new_list[[i]]) == 1) {
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if (is.character(new_list[[i]]) && new_list[[i]] %in% colnames(x)) {
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# this is to support quoted variables: df %pm>% pca("mycol1", "mycol2")
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new_list[[i]] <- x[, new_list[[i]]]
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} else {
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# remove item - it's an argument like `center`
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new_list[[i]] <- NULL
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}
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}
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}
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x <- as.data.frame(new_list, stringsAsFactors = FALSE)
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if (any(vapply(FUN.VALUE = logical(1), x, function(y) !is.numeric(y)))) {
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warning_("in `pca()`: be sure to first calculate the resistance (or susceptibility) of variables with antimicrobial test results, since PCA works with numeric variables only. See Examples in ?pca.", call = FALSE)
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}
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# set column names
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tryCatch(colnames(x) <- as.character(dots)[2:length(dots)],
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error = function(e) warning("column names could not be set")
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)
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# keep only numeric columns
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x <- x[, vapply(FUN.VALUE = logical(1), x, function(y) is.numeric(y)), drop = FALSE]
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# bind the data set with the non-numeric columns
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x <- cbind(x.bak[, vapply(FUN.VALUE = logical(1), x.bak, function(y) !is.numeric(y) & !all(is.na(y))), drop = FALSE], x)
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}
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x <- pm_ungroup(x) # would otherwise select the grouping vars
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x <- x[rowSums(is.na(x)) == 0, ] # remove columns containing NAs
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pca_data <- x[, which(vapply(FUN.VALUE = logical(1), x, function(x) is.numeric(x))), drop = FALSE]
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message_(
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"Columns selected for PCA: ", vector_and(font_bold(colnames(pca_data), collapse = NULL), quotes = TRUE),
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". Total observations available: ", nrow(pca_data), "."
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)
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if (getRversion() < "3.4.0") {
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# stats::prcomp prior to 3.4.0 does not have the 'rank.' argument
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pca_model <- prcomp(pca_data, retx = retx, center = center, scale. = scale., tol = tol)
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} else {
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pca_model <- prcomp(pca_data, retx = retx, center = center, scale. = scale., tol = tol, rank. = rank.)
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}
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groups <- x[, vapply(FUN.VALUE = logical(1), x, function(y) !is.numeric(y) & !all(is.na(y))), drop = FALSE]
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rownames(groups) <- NULL
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attr(pca_model, "non_numeric_cols") <- groups
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class(pca_model) <- c("pca", class(pca_model))
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pca_model
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}
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#' @method print pca
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#' @export
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#' @noRd
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print.pca <- function(x, ...) {
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a <- attributes(x)$non_numeric_cols
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if (!is.null(a)) {
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print_pca_group(a)
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class(x) <- class(x)[class(x) != "pca"]
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}
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print(x, ...)
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}
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#' @method summary pca
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#' @export
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#' @noRd
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summary.pca <- function(object, ...) {
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a <- attributes(object)$non_numeric_cols
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if (!is.null(a)) {
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print_pca_group(a)
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class(object) <- class(object)[class(object) != "pca"]
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}
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summary(object, ...)
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}
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print_pca_group <- function(a) {
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grps <- sort(unique(a[, 1, drop = TRUE]))
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cat("Groups (n=", length(grps), ", named as '", colnames(a)[1], "'):\n", sep = "")
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print(grps)
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cat("\n")
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}
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