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# ==================================================================== #
# TITLE #
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# AMR: An R Package for Working with Antimicrobial Resistance Data #
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# #
# SOURCE #
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# https://github.com/msberends/AMR #
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# #
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# CITE AS #
# Berends MS, Luz CF, Friedrich AW, Sinha BNM, Albers CJ, Glasner C #
# (2022). AMR: An R Package for Working with Antimicrobial Resistance #
# Data. Journal of Statistical Software, 104(3), 1-31. #
# doi:10.18637/jss.v104.i03 #
# #
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# 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. #
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# #
# 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. #
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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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# ==================================================================== #
#' 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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#' \donttest{
#' if (require("dplyr")) {
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#' # calculate the resistance per group first
#' resistance_data <- example_isolates %>%
#' group_by(
#' order = mo_order(mo), # group on anything, like order
#' genus = mo_genus(mo)
#' ) %>% # and genus as we do here;
#' 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 %>%
#' pca(AMC, CXM, CTX, CAZ, GEN, TOB, TMP, SXT)
#'
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#' pca_result
#' 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:
#' if (require("ggplot2")) {
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#' ggplot_pca(pca_result)
#'
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#' ggplot_pca(pca_result) +
#' scale_colour_viridis_d() +
#' labs(title = "Title here")
#' }
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#' }
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#' }
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pca <- function ( x ,
... ,
retx = TRUE ,
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center = TRUE ,
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scale. = TRUE ,
tol = NULL ,
rank. = NULL ) {
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meet_criteria ( x , allow_class = " data.frame" )
meet_criteria ( retx , allow_class = " logical" , has_length = 1 )
meet_criteria ( center , allow_class = " logical" , has_length = 1 )
meet_criteria ( scale. , allow_class = " logical" , has_length = 1 )
meet_criteria ( tol , allow_class = " numeric" , has_length = 1 , allow_NULL = TRUE )
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
x <- as.data.frame ( x , stringsAsFactors = FALSE )
x.bak <- x
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# defuse R expressions, this replaces rlang::enquos()
dots <- substitute ( list ( ... ) )
if ( length ( dots ) > 1 ) {
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new_list <- list ( 0 )
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for ( i in seq_len ( length ( dots ) - 1 ) ) {
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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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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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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# 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_ (
" Columns selected for PCA: " , vector_and ( font_bold ( colnames ( pca_data ) , collapse = NULL ) , quotes = TRUE ) ,
" . Total observations available: " , nrow ( pca_data ) , " ."
)
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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
pca_model <- prcomp ( pca_data , retx = retx , center = center , scale. = scale. , tol = tol )
} else {
pca_model <- prcomp ( pca_data , retx = retx , center = center , scale. = scale. , tol = tol , rank. = rank. )
}
groups <- x [ , vapply ( FUN.VALUE = logical ( 1 ) , x , function ( y ) ! is.numeric ( y ) & ! all ( is.na ( y ) ) ) , drop = FALSE ]
rownames ( groups ) <- NULL
attr ( pca_model , " non_numeric_cols" ) <- groups
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class ( pca_model ) <- c ( " pca" , class ( pca_model ) )
pca_model
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}
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#' @method print pca
#' @export
#' @noRd
print.pca <- function ( x , ... ) {
a <- attributes ( x ) $ non_numeric_cols
if ( ! is.null ( a ) ) {
print_pca_group ( a )
class ( x ) <- class ( x ) [class ( x ) != " pca" ]
}
print ( x , ... )
}
#' @method summary pca
#' @export
#' @noRd
summary.pca <- function ( object , ... ) {
a <- attributes ( object ) $ non_numeric_cols
if ( ! is.null ( a ) ) {
print_pca_group ( a )
class ( object ) <- class ( object ) [class ( object ) != " pca" ]
}
summary ( object , ... )
}
print_pca_group <- function ( a ) {
grps <- sort ( unique ( a [ , 1 , drop = TRUE ] ) )
cat ( " Groups (n=" , length ( grps ) , " , named as '" , colnames ( a ) [1 ] , " '):\n" , sep = " " )
print ( grps )
cat ( " \n" )
}