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Update auto-generated Rd files after documentation rebuild
https://claude.ai/code/session_01FC43syPbzhGmKgrrVNHjnF
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@@ -25,7 +25,8 @@ antibiogram(x, antimicrobials = where(is.sir), mo_transform = "shortname",
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ifelse(wisca, 14, 18)), col_mo = NULL, language = get_AMR_locale(),
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minimum = 30, combine_SI = TRUE, sep = " + ", sort_columns = TRUE,
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wisca = FALSE, simulations = 1000, conf_interval = 0.95,
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interval_side = "two-tailed", info = interactive(), ...)
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interval_side = "two-tailed", info = interactive(), parallel = FALSE,
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...)
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wisca(x, antimicrobials = where(is.sir), ab_transform = "name",
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syndromic_group = NULL, only_all_tested = FALSE, digits = 1,
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@@ -33,7 +34,7 @@ wisca(x, antimicrobials = where(is.sir), ab_transform = "name",
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col_mo = NULL, language = get_AMR_locale(), combine_SI = TRUE,
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sep = " + ", sort_columns = TRUE, simulations = 1000,
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conf_interval = 0.95, interval_side = "two-tailed",
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info = interactive(), ...)
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info = interactive(), parallel = FALSE, ...)
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retrieve_wisca_parameters(wisca_model, ...)
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@@ -80,7 +81,7 @@ retrieve_wisca_parameters(wisca_model, ...)
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\item{digits}{Number of digits to use for rounding the antimicrobial coverage, defaults to 1 for WISCA and 0 otherwise.}
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\item{formatting_type}{Numeric value (1–22 for WISCA, 1-12 for non-WISCA) indicating how the 'cells' of the antibiogram table should be formatted. See \emph{Details} > \emph{Formatting Type} for a list of options.}
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\item{formatting_type}{Numeric value (1-22 for WISCA, 1-12 for non-WISCA) indicating how the 'cells' of the antibiogram table should be formatted. See \emph{Details} > \emph{Formatting Type} for a list of options.}
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\item{col_mo}{Column name of the names or codes of the microorganisms (see \code{\link[=as.mo]{as.mo()}}) - the default is the first column of class \code{\link{mo}}. Values will be coerced using \code{\link[=as.mo]{as.mo()}}.}
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@@ -104,6 +105,8 @@ retrieve_wisca_parameters(wisca_model, ...)
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\item{info}{A \link{logical} to indicate info should be printed - the default is \code{TRUE} only in interactive mode.}
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\item{parallel}{A \link{logical} to indicate if parallel computing must be used, defaults to \code{FALSE}. Requires the \code{\link[future.apply:future_lapply]{future.apply}} package. For WISCA, Monte Carlo simulations are distributed across workers; for grouped antibiograms, each group is processed by a separate worker. \strong{A non-sequential \code{\link[future:plan]{future::plan()}} must already be active before setting \code{parallel = TRUE}} -- for example, \code{future::plan(future::multisession)}. An error is thrown if \code{parallel = TRUE} is used without a plan set by the user.}
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\item{...}{When used in \link[knitr:kable]{R Markdown or Quarto}: arguments passed on to \code{\link[knitr:kable]{knitr::kable()}} (otherwise, has no use).}
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\item{wisca_model}{The outcome of \code{\link[=wisca]{wisca()}} or \code{\link[=antibiogram]{antibiogram(..., wisca = TRUE)}}.}
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@@ -45,9 +45,8 @@ A list with class \code{"htest"} containing the following
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\item{residuals}{the Pearson residuals,
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\code{(observed - expected) / sqrt(expected)}.}
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\item{stdres}{standardized residuals,
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\code{(observed - expected) / sqrt(V)}, where \code{V} is the
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residual cell variance (Agresti, 2007, section 2.4.5
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for the case where \code{x} is a matrix, \code{n * p * (1 - p)} otherwise).}
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\code{(observed - expected) / sqrt(V)}, where \code{V} is the residual cell variance (Agresti, 2007,
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section 2.4.5 for the case where \code{x} is a matrix, \code{n * p * (1 - p)} otherwise).}
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}
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\description{
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\code{\link[=g.test]{g.test()}} performs chi-squared contingency table tests and goodness-of-fit tests, just like \code{\link[=chisq.test]{chisq.test()}} but is more reliable (1). A \emph{G}-test can be used to see whether the number of observations in each category fits a theoretical expectation (called a \strong{\emph{G}-test of goodness-of-fit}), or to see whether the proportions of one variable are different for different values of the other variable (called a \strong{\emph{G}-test of independence}).
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@@ -32,7 +32,7 @@ pca(x, ..., retx = TRUE, center = TRUE, scale. = TRUE, tol = NULL,
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standard deviations are less than or equal to \code{tol} times the
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standard deviation of the first component.) With the default null
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setting, no components are omitted (unless \code{rank.} is specified
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less than \code{min(dim(x))}.). Other settings for \code{tol} could be
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less than \code{min(dim(x))}.). Other settings for tol could be
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\code{tol = 0} or \code{tol = sqrt(.Machine$double.eps)}, which
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would omit essentially constant components.}
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