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#' Compute ranking of biomarkers by sorting effect sizes
#'
#' Computes ranking of biomarkers based effect sizes, which are computed by
#' Targeted Minimum Loss-Based Estimation. This function is designed to be
#' called inside \code{adaptest}; it should not be run by itself outside of that
#' context.
#'
#' @param Y (numeric vector) - continuous or binary biomarkers outcome variables
#' @param A (numeric vector) - binary treatment indicator: \code{1} = treatment,
#' \code{0} = control
#' @param W (numeric vector, numeric matrix, or numeric data.frame) - matrix of
#' baseline covariates where each column corrspond to one baseline covariate.
#' Each row correspond to one observation
#' @param absolute (logical) - whether or not to test for absolute effect size.
#' If \code{FALSE}, test for directional effect. This overrides argument
#' \code{negative}.
#' @param negative (logical) - whether or not to test for negative effect size.
#' If \code{FALSE} = test for positive effect size. This is effective only when
#' \code{absolute = FALSE}.
#' @param learning_library (character vector) - library of learning algorithms
#' to be used in fitting the "Q" and "g" step of the standard TMLE procedure.
#'
#' @return an \code{integer vector} containing ranks of biomarkers.
#'
#' @importFrom tmle tmle
#' @importFrom stats lm as.formula coef
#'
#' @export
#' @examples
#' set.seed(1234)
#' data(simpleArray)
#' simulated_array <- simulated_array
#' simulated_treatment <- simulated_treatment
#' rank_DE(Y = simulated_array,
#' A = simulated_treatment,
#' W = rep(1, length(simulated_treatment)),
#' absolute = FALSE,
#' negative = FALSE)
rank_DE <- function(Y,
A,
W,
absolute = FALSE,
negative = FALSE,
learning_library = c(
"SL.glm", "SL.step",
"SL.glm.interaction", "SL.gam"
)) {
n_here <- nrow(Y)
p_all <- ncol(Y)
B1_fitted <- rep(0, p_all)
for (it in seq_len(p_all)) {
A_fit <- A
Y_fit <- Y[, it]
W_fit <- as.matrix(W)
# CASE 1: TMLE for DE effect size
if (sum(W - as.matrix(rep(1, n_here))) != 0) {
# if there are W
tmle_fit <- tmle(
Y = Y_fit, A = A_fit, W = W,
Q.SL.library = learning_library, g.SL.library = learning_library
)
B1_fitted[it] <- tmle_fit$estimates$ATE$psi
} else {
# CASE 2: OLS for faster effect size
lm_fit <- stats::lm(Y_fit ~ A_fit)
B1_fitted[it] <- lm_fit$coefficients[2]
}
}
# rank by absolute differential expression
if (absolute == TRUE) {
B1_fitted_abs <- abs(B1_fitted)
} else {
B1_fitted_abs <- B1_fitted
}
# calculate rank of each covariate
if (negative) {
rank_out <- rank(B1_fitted_abs)
} else {
rank_out <- rank(-B1_fitted_abs)
}
# final object to be exported by this function
return(rank_out)
}
#' Compute ranking of biomarkers by sorting t-test p-values
#'
#' @param Y (numeric vector) - continuous or binary biomarkers outcome variables
#' @param A (numeric vector) - binary treatment indicator: \code{1} = treatment,
#' \code{0} = control
#' @param W (numeric vector, numeric matrix, or numeric data.frame) - matrix of
#' baseline covariates where each column corrspond to one baseline covariate
#' and each row correspond to one observation.
#'
#' @return an \code{integer vector} containing ranks of biomarkers.
#'
#' @importFrom stats lm coef
#'
#' @export
#'
#' @examples
#' set.seed(1234)
#' data(simpleArray)
#' rank_ttest(Y = simulated_array,
#' A = simulated_treatment,
#' W = rep(1, length(A)))
#
rank_ttest <- function(Y,
A,
W) {
n_here <- nrow(Y)
p_all <- ncol(Y)
lm_out <- stats::lm(Y ~ A)
lm_summary <- summary(lm_out)
pval_lm <- lapply(lm_summary, function(x) x$coefficients[2, 4])
pval_lm_out <- do.call(rbind, pval_lm)
rank_out <- rank(pval_lm_out)
# final object to be exported by this function
return(rank_out)
}
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