diff --git a/.Rbuildignore b/.Rbuildignore new file mode 100644 index 0000000..89b0d98 --- /dev/null +++ b/.Rbuildignore @@ -0,0 +1,4 @@ +^.*\.Rproj$ +^\.Rproj\.user$ +^\.github$ +^inst$ diff --git a/.github/.gitignore b/.github/.gitignore new file mode 100644 index 0000000..2d19fc7 --- /dev/null +++ b/.github/.gitignore @@ -0,0 +1 @@ +*.html diff --git a/.github/workflows/R-CMD-check.yaml b/.github/workflows/R-CMD-check.yaml new file mode 100644 index 0000000..f4b17a4 --- /dev/null +++ b/.github/workflows/R-CMD-check.yaml @@ -0,0 +1,29 @@ +# Workflow derived from https://github.com/r-lib/actions/tree/v2/examples +# Need help debugging build failures? Start at https://github.com/r-lib/actions#where-to-find-help +on: + push: + branches: [main, master] + pull_request: + branches: [main, master] + +name: R-CMD-check + +jobs: + R-CMD-check: + runs-on: ubuntu-latest + env: + GITHUB_PAT: ${{ secrets.GITHUB_TOKEN }} + R_KEEP_PKG_SOURCE: yes + steps: + - uses: actions/checkout@v3 + + - uses: r-lib/actions/setup-r@v2 + with: + use-public-rspm: true + + - uses: r-lib/actions/setup-r-dependencies@v2 + with: + extra-packages: any::rcmdcheck + needs: check + + - uses: r-lib/actions/check-r-package@v2 diff --git a/.gitignore b/.gitignore new file mode 100644 index 0000000..38f60e1 --- /dev/null +++ b/.gitignore @@ -0,0 +1,15 @@ +.Rproj.user +.Rhistory +.RData +.Ruserdata +*.Rproj +*.csv +*.pdf +inst/data/ +inst/ignore/ +mimic +*.Rout +*.bib +*.rds +*.sh + diff --git a/DESCRIPTION b/DESCRIPTION new file mode 100644 index 0000000..f6d5f87 --- /dev/null +++ b/DESCRIPTION @@ -0,0 +1,18 @@ +Package: comet +Type: Package +Title: Covariance Measure Tests for Conditional Independence +Version: 0.0-1 +Authors@R: person("Lucas", "Kook", email = "lucasheinrich.kook@gmail.com", + role = c("aut", "cre")) +Description: Covariance measure tests for conditional independence testing + against conditional covariance and nonlinear conditional mean alternatives. + Contains versions of the generalised covariance measure test (Shah and Peters, + 2020, ) and projected covariance measure test (Lundborg et al., 2023, + ). Applications can be found in Kook and Lundborg (2024, ). +Imports: mlt, sandwich, ranger, glmnet +License: GPL-3 +Encoding: UTF-8 +RoxygenNote: 7.2.3 +Suggests: + testthat (>= 3.0.0), tram, ggplot2, tidyr, ggpubr, dplyr +Config/testthat/edition: 3 diff --git a/LICENSE b/LICENSE deleted file mode 100644 index f288702..0000000 --- a/LICENSE +++ /dev/null @@ -1,674 +0,0 @@ - GNU GENERAL PUBLIC LICENSE - Version 3, 29 June 2007 - - Copyright (C) 2007 Free Software Foundation, Inc. - Everyone is permitted to copy and distribute verbatim copies - of this license document, but changing it is not allowed. - - Preamble - - The GNU General Public License is a free, copyleft license for -software and other kinds of works. - - The licenses for most software and other practical works are designed -to take away your freedom to share and change the works. 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If not, see . - -Also add information on how to contact you by electronic and paper mail. - - If the program does terminal interaction, make it output a short -notice like this when it starts in an interactive mode: - - Copyright (C) - This program comes with ABSOLUTELY NO WARRANTY; for details type `show w'. - This is free software, and you are welcome to redistribute it - under certain conditions; type `show c' for details. - -The hypothetical commands `show w' and `show c' should show the appropriate -parts of the General Public License. Of course, your program's commands -might be different; for a GUI interface, you would use an "about box". - - You should also get your employer (if you work as a programmer) or school, -if any, to sign a "copyright disclaimer" for the program, if necessary. -For more information on this, and how to apply and follow the GNU GPL, see -. - - The GNU General Public License does not permit incorporating your program -into proprietary programs. If your program is a subroutine library, you -may consider it more useful to permit linking proprietary applications with -the library. If this is what you want to do, use the GNU Lesser General -Public License instead of this License. But first, please read -. diff --git a/NAMESPACE b/NAMESPACE new file mode 100644 index 0000000..9e56258 --- /dev/null +++ b/NAMESPACE @@ -0,0 +1,13 @@ +# Generated by roxygen2: do not edit by hand + +S3method(plot,gcm) +S3method(plot,pcm) +export(gcm) +export(pcm) +importFrom(glmnet,cv.glmnet) +importFrom(ranger,ranger) +importFrom(stats,model.frame) +importFrom(stats,model.response) +importFrom(stats,pnorm) +importFrom(stats,predict) +importFrom(stats,terms) diff --git a/R/gcm.R b/R/gcm.R new file mode 100644 index 0000000..eeced97 --- /dev/null +++ b/R/gcm.R @@ -0,0 +1,166 @@ +#' GCM using random forests +#' +#' @param Y Response +#' @param X Covariates +#' @param Z Covariates +#' @param alternative Alternative +#' @param ... Additional arguments to ranger +#' +#' @return Object of class htest +#' @export +#' +#' @examples +#' X <- matrix(rnorm(2e3), ncol = 2) +#' colnames(X) <- c("X1", "X2") +#' Z <- matrix(rnorm(2e3), ncol = 2) +#' colnames(Z) <- c("Z1", "Z2") +#' Y <- rnorm(1e3) # X[, 2] + Z[, 2] + rnorm(1e3) +#' (gcm1 <- gcm(Y, X, Z)) +#' plot(gcm1) +#' +gcm <- function(Y, X, Z, alternative = c("two.sided", "less", "greater"), ...) { + alternative <- match.arg(alternative) + args <- if (length(list(...)) > 0) list(...) else NULL + YZ <- do.call("pcm_ranger", c(list(y = Y, x = Z), args)) + XZ <- apply(as.data.frame(X), 2, \(tX) { + do.call("pcm_ranger", c(list(y = tX, x = Z), args)) + }) + rY <- Y - predict(YZ, data = Z) + preds <- lapply(XZ, predict.pcm_ranger, data = Z) + rX <- X - do.call("cbind", preds) + stat <- .gcm(rY, rX) + pval <- .compute_normal_pval(stat, alternative) + + structure(list( + statistic = c("Z" = stat), p.value = pval, + hypothesis = c("E[cov(Y, X | Z)]" = "0"), + null.value = c("E[cov(Y, X | Z)]" = "0"), alternative = alternative, + method = paste0("Generalized covariance measure test"), + data.name = deparse(match.call(), width.cutoff = 80), + rY = rY, rX = rX), class = c("gcm", "htest")) + +} + +# Helpers ----------------------------------------------------------------- + +.gcm <- function (r, e) { + dR <- NCOL(r) + dE <- NCOL(e) + nn <- NROW(r) + if (dR > 1 || dE > 1) { + R_mat <- matrix(r, nrow = nn, ncol = dE) * e + sigma <- crossprod(R_mat)/nn - tcrossprod(colMeans(R_mat)) + eig <- eigen(sigma) + if (min(eig$values) < .Machine$double.eps) + warning("`vcov` of test statistic is not invertible") + siginvhalf <- eig$vectors %*% diag(eig$values^(-1/2)) %*% + t(eig$vectors) + tstat <- siginvhalf %*% colSums(R_mat)/sqrt(nn) + stat <- structure(sum(tstat^2), df = dR * dE) + } + else { + R <- r * e + R.sq <- R^2 + meanR <- mean(R) + stat <- sqrt(nn) * meanR/sqrt(mean(R.sq) - meanR^2) + } + stat +} + +#' @importFrom stats pnorm +.compute_normal_pval <- function(stat, alternative) { + if (!is.null(df <- attr(stat, "df"))) + return(stats::pchisq(stat, df = df, lower.tail = FALSE)) + switch( + alternative, + "two.sided" = 2 * stats::pnorm(-abs(stat)), + "greater" = stats::pnorm(-abs(stat)), + "less" = stats::pnorm(abs(stat)) + ) +} + +.rm_int <- function(x) { + if (all(x[, 1] == 1)) + return(x[, -1L, drop = FALSE]) + x +} + +#' @importFrom stats terms +.get_terms <- function(formula) { + if (is.null(formula)) + return(NULL) + atms <- stats::terms(formula) + tms <- attr(atms, "term.labels") + resp <- all.vars(formula)[1] + ridx <- grep("|", tms, fixed = TRUE) + tms[ridx] <- paste0("(", tms[ridx], ")") + ie <- grep(":", tms, value = TRUE) + me <- grep(":", tms, value = TRUE, invert = TRUE) + list(all = tms, me = me, ie = ie, response = resp, terms = atms, + fml = formula) +} + +# Ranger ------------------------------------------------------------------ + +#' @importFrom stats model.response model.frame +.ranger <- function(formula, data, ...) { + response <- stats::model.response(stats::model.frame(formula, data)) + is_factor <- is.factor(response) + tms <- .get_terms(formula) + resp <- if (is_factor) + .rm_int(stats::model.matrix(~ response, contrasts.arg = list( + "response" = "contr.treatment"))) + else response + tmp <- list(data = data, response = resp, is_factor = is_factor) + if (identical(tms$me, character(0))) { + if (is_factor) + return(structure(c(list(mean = base::colMeans(resp)), tmp), + class = "ranger")) + else return(structure(c(list(mean = mean(as.numeric(response))), + tmp), class = "ranger")) + } + ret <- ranger::ranger(formula, data, probability = is_factor, ...) + structure(c(ret, tmp), class = "ranger") +} + +#' @importFrom stats predict +residuals.ranger <- function(object, newdata = NULL, newy = NULL, ...) { + if (is.null(newdata)) + newdata <- object$data + if (!is.null(newy)) + newy <- if (object$is_factor) + .rm_int(stats::model.matrix(~ newy, contrasts.arg = list( + "newy" = "contr.treatment"))) + else newy + if (is.null(newy)) + newy <- object$response + if (!is.null(object$mean)) + return(newy - object$mean) + preds <- stats::predict(object, data = newdata)$predictions + if (object$is_factor) + preds <- preds[, -1] + unname(newy - preds) +} + +# Diagnostics ------------------------------------------------------------- + +#' @exportS3Method plot gcm +plot.gcm <- function(x, ...) { + .data <- NULL + pd <- tidyr::pivot_longer(data.frame(rY = x$rY, rX = unname(x$rX)), + dplyr::starts_with("rX")) + if (requireNamespace("ggplot2")) { + p1 <- ggplot2::ggplot(pd, ggplot2::aes(x = .data[["value"]] , + y = .data[["rY"]], + color = .data[["name"]])) + + ggplot2::geom_point(alpha = 0.3, show.legend = FALSE) + + ggplot2::geom_smooth(method = "lm", se = FALSE, show.legend = FALSE) + + ggplot2::theme_bw() + + ggplot2::labs(x = "Residuals X | Z", y = "Residuals Y | Z") + print(p1) + } + return(invisible(p1)) +} + +.mm <- function(preds, data) + .rm_int(stats::model.matrix(stats::reformulate(preds), data = data)) diff --git a/R/pcm.R b/R/pcm.R new file mode 100644 index 0000000..5422e01 --- /dev/null +++ b/R/pcm.R @@ -0,0 +1,213 @@ +#' Conditional mean independence test +#' +#' @param Y Numeric; response +#' @param X Numeric; covariates +#' @param Z Numceric; covariates +#' @param rep Number of repetitions +#' @param est_vhat Estimate variance functional +#' @param ... Additional arguments passed to \code{reg} +#' @param reg Character; regression method +#' @param mtry Argument passed to \code{ranger} +#' @param ghat_args Arguments passed to reg +#' @param do.check Save check data +#' +#' @importFrom ranger ranger +#' +#' @return Object of class '\code{htest}' +#' @export +#' +#' @examples +#' X <- matrix(rnorm(2e3), ncol = 2) +#' colnames(X) <- c("X1", "X2") +#' Z <- matrix(rnorm(2e3), ncol = 2) +#' colnames(Z) <- c("Z1", "Z2") +#' Y <- rnorm(1e3) # X[, 2] + Z[, 2] + rnorm(1e3) +#' (pcm1 <- pcm(Y, X, Z, ghat_args = list(mtry = NULL, max.depth = NULL), +#' est_vhat = TRUE, do.check = TRUE)) +#' plot(pcm1) +#' +pcm <- function(Y, X, Z, rep = 1, est_vhat = TRUE, + reg = c("pcm_ranger", "pcm_lasso"), + ghat_args = NULL, mtry = identity, + do.check = FALSE, ...) { + reg <- match.arg(reg) + if (rep != 1) { + pcms <- lapply(seq_len(rep), \(iter) { + pcm(Y = Y, X = X, Z = Z, rep = 1, est_vhat = est_vhat, reg = reg, + ghat_args = ghat_args, mtry = mtry, do.check = FALSE, ... = ...) + }) + stat <- mean(unlist(lapply(pcms, \(tst) tst$statistic))) + pval <- pnorm(stat, lower.tail = FALSE) + return(structure(list( + statistic = c("Z" = stat), p.value = pval, + hypothesis = c("E[Y | X, Z]" = "E[Y | Z]"), + null.value = c("E[Y | X, Z]" = "E[Y | Z]"), alternative = "two.sided", + method = paste0("Projected covariance measure test (K = ", rep, " repetitions)"), + all_tests = pcms, data.name = deparse(match.call(), width.cutoff = 80)), + class = c("pcm", "htest"))) + } + ### Sample splitting + idx <- sample.int(NROW(Y), ceiling(NROW(Y) / 2)) + ### Split 1 + Ytr <- Y[idx] + Xtr <- data.frame(X)[idx, , drop = FALSE] + Ztr <- data.frame(Z)[idx, , drop = FALSE] + ### Split 2 + Yte <- Y[-idx] + Xte <- data.frame(X)[-idx, , drop = FALSE] + Zte <- data.frame(Z)[-idx, , drop = FALSE] + + ### Obtain hat{h} + ghat <- do.call(reg, c(list(y = Ytr, x = cbind(Xtr, Ztr)), ghat_args)) + mtilde <- ranger(x = Ztr, y = pghat <- predict(ghat, data = cbind(Xtr, Ztr)), + mtry = mtry, ...) + htilde <- \(X, Z) { + predict(ghat, data = cbind(X, Z)) - + predict(mtilde, data = Z)$predictions + } + rho <- mean((Ytr - mtilde$predictions) * predict(ghat, data = cbind(Xtr, Ztr))) + hhat <- \(X, Z) sign(rho) * htilde(X, Z) + + ### Obtain hat{v} + if (est_vhat) { + vtilde <- ranger(x = cbind(Xtr, Ztr), y = (sqr <- (Ytr - predict( + ghat, data = cbind(Xtr, Ztr)))^2), mtry = mtry, ...) + a <- function(c) mean(sqr / (pmax(vtilde$predictions, 0) + c)) + chat <- if (a(0) < 1) 0 else stats::uniroot(\(c) a(c) - 1, c(0, 10), extendInt = "yes")$root + vhat <- \(X, Z) pmax(predict(vtilde, data = cbind(X, Z))$predictions, 0) + chat + } + else + vhat <- \(X, Z) 1 + + ### Obtain residuals for test + fhat <- \(X, Z) hhat(X, Z) / vhat(X, Z) + mhatfhat <- ranger(x = Zte, y = (fhats <- fhat(Xte, Zte)), mtry = mtry, ...) + mhat <- do.call(reg, c(list(y = Yte, x = Zte), ghat_args)) + + ### Test + L <- (Yte - predict(mhat, data = Zte)) * (fhats - mhatfhat$predictions) + stat <- sqrt(length(idx)) * mean(L) / sqrt(mean(L^2) - mean(L)^2) + if (is.nan(stat)) stat <- -Inf + pval <- pnorm(stat, lower.tail = FALSE) + + dcheck <- if (do.check) { + pmtilde <- predict(mtilde, data = Ztr)$predictions + # pvtilde <- predict(vtilde, data = cbind(Xtr, Ztr))$predictions + pghat_test <- predict(ghat, data = cbind(Xte, Zte)) + mhats <- predict(mhat, data = Zte) + list( + train = data.frame( + id = idx, + fitted_ghat = pghat, + resid_ghat = Ytr - pghat, + fitted_mtilde = pmtilde, + resid_mtilde = pghat - pmtilde, + # fitted_vtilde = pvtilde, + # resid_vtilde = sqr - pvtilde, + hhat = hhat(Xtr, Ztr), + vhat = vhat(Xtr, Ztr), + MSE_YZ = (Ytr - predict(mhat, data = Ztr))^2, + MSE_YXZ = (Ytr - pghat)^2 + ), + test = data.frame( + id = setdiff(seq_len(NROW(Y)), idx), + fitted_ghat = pghat_test, + resid_ghat = Yte - pghat_test, + hhat = hhat(Xte, Zte), + vhat = vhat(Xte, Zte), + fhat = fhats, + resid_mhat = (Yte - mhats), + mhat = mhats, + resid_mhatfhat = (fhats - mhatfhat$predictions), + mhatfhat = mhats, + MSE_YXZ = (Yte - pghat_test)^2, + MSE_YZ = (Yte - mhats)^2 + ) + ) + } else NULL + + structure(list( + statistic = c("Z" = stat), p.value = pval, + hypothesis = c("E[Y | X, Z]" = "E[Y | Z]"), + null.value = c("E[Y | X, Z]" = "E[Y | Z]"), alternative = "two.sided", + method = paste0("Projected covariance measure test"), + data.name = deparse(match.call(), width.cutoff = 80), + check.data = dcheck), class = c("pcm", "htest")) +} + +# Regressions ------------------------------------------------------------- + +pcm_ranger <- function(y, x, ...) { + args <- list(...) + if (length(unique(y)) == 2) { + y <- as.factor(y) + args$probability <- TRUE + } + rf <- do.call("ranger", c(list(y = y, x = x), args)) + class(rf) <- c("pcm_ranger", class(rf)) + rf +} + +predict.pcm_ranger <- function(object, data = NULL, ...) { + class(object) <- class(object)[-1] + preds <- predict(object, data = data)$predictions + if (object$treetype == "Probability estimation") + preds <- preds[, 2] + preds +} + +#' @importFrom glmnet cv.glmnet +pcm_lasso <- function(y, x, ...) { + obj <- cv.glmnet(y = y, x = as.matrix(x), ...) + class(obj) <- c("pcm_lasso", class(obj)) + obj +} + +predict.pcm_lasso <- function(object, data = NULL, ...) { + class(object) <- class(object)[-1] + predict(object, newx = as.matrix(data), s = object$lambda.min)[, 1] +} + +# Diagnostics ------------------------------------------------------------- + +#' @exportS3Method plot pcm +plot.pcm <- function(x, ...) { + .data <- NULL + train <- x$check.data$train + test <- x$check.data$test + mse_train <- data.frame(MSE_YZ = train$MSE_YZ, MSE_YXZ = train$MSE_YXZ, set = "train") + mse_test <- data.frame(MSE_YZ = test$MSE_YZ, MSE_YXZ = test$MSE_YXZ, set = "test") + mses <- tidyr::pivot_longer(dplyr::bind_rows(mse_train, mse_test), + dplyr::starts_with("MSE")) + if (is.null(train)) + return("Nothing to plot. Consider running `pcm` with `do.check = TRUE`") + if (requireNamespace("ggplot2") && requireNamespace("tidyr") && requireNamespace("ggpubr")) { + mpl <- \(xx, yy, pdat, ...) { + ggplot2::ggplot(pdat, ggplot2::aes(y = .data[[yy]], x = .data[[xx]])) + + ggplot2::geom_point(alpha = 0.3) + + ggplot2::geom_smooth(se = FALSE, method = "lm") + + ggplot2::theme_bw() + } + # ptrain <- lapply(c("ghat", "mtilde", "vtilde"), \(tx) { + # mpl(paste0("fitted_", tx), paste0("resid_", tx), train, "direction") + # }) + # ptest <- apply(data.frame(y = c("resid_mhatfhat", "resid_mhat"), + # x = c("mhatfhat", "resid_mhatfhat")), 1, + # \(x) mpl(x[2], x[1], test), simplify = FALSE) + # p1 <- mpl("mhatfhat", "resid_mhatfhat", test) + + # ggplot2::labs(x = "f(X,Z)", y = "Residuals f(X,Z) | Z") + p2 <- mpl("resid_mhat", "resid_mhatfhat", test) + + ggplot2::labs(x = "Residuals f(X, Z) | Z", y = "Residuals Y | Z") + p3 <- ggplot2::ggplot(mses, ggplot2::aes(y = .data[["value"]], + x = .data[["name"]], + color = .data[["set"]])) + + ggplot2::geom_violin(width = 0.5, position = ggplot2::position_dodge(width = 0.7)) + + ggplot2::geom_boxplot(width = 0.3, outlier.shape = NA, position = ggplot2::position_dodge(width = 0.7)) + + ggplot2::geom_jitter(alpha = 0.1, position = ggplot2::position_dodge(width = 0.7)) + + ggplot2::theme_bw() + + ggplot2::scale_y_log10() + + ggplot2::labs(y = "MSE contributions", x = "Regression") + print(p2) + } + return(invisible(p2)) +} diff --git a/README.md b/README.md new file mode 100644 index 0000000..e486ad7 --- /dev/null +++ b/README.md @@ -0,0 +1,9 @@ + +[![R-CMD-check](https://github.com/LucasKook/comet/actions/workflows/R-CMD-check.yaml/badge.svg)](https://github.com/LucasKook/comet/actions/workflows/R-CMD-check.yaml) + + +# Covariance measure tests + + +# Replication materials + diff --git a/inst/Makefile b/inst/Makefile new file mode 100644 index 0000000..16fc0e4 --- /dev/null +++ b/inst/Makefile @@ -0,0 +1,23 @@ +dependencies: + (cd .. && Rscript --vanilla inst/dependencies.R > dependencies.out) + +mimic: + (cd .. && Rscript --vanilla inst/application/mimic.R > mimic.out) + +multiomics: + (cd .. && Rscript --vanilla inst/application/multiomics.R > multiomics.out) + +ccle: + (cd .. && Rscript --vanilla inst/application/ccle.R > ccle.out) + +dep: + bash dispatch.sh run-install.sh 1200 + +mim: + bash dispatch.sh run-mimic.sh 21600 + +mul: + bash dispatch.sh run-multiomics.sh 3600 + +sig: + bash dispatch.sh run-ccle.sh 3600 diff --git a/inst/code/ccle.R b/inst/code/ccle.R new file mode 100644 index 0000000..a54c8b8 --- /dev/null +++ b/inst/code/ccle.R @@ -0,0 +1,94 @@ +### Pre-process CCLE data +### LK 2024 + +bpath <- "inst/data/ccle" +set.seed(2410) + +# DEPs -------------------------------------------------------------------- + +library("tidyverse") +library("survival") +devtools::load_all() + +# Read -------------------------------------------------------------------- + +cmp <- "PLX4720" +nrep <- 10 + +# expression <- read_table("inst/data/ccle/expression.txt") +mutations <- read_table("inst/data/ccle/mutation.txt") |> + filter(Name %in% grep("_MUT$", Name, value = TRUE)) +response <- read_csv("inst/data/ccle/response.csv") |> + filter(Compound == cmp) + +idx <- match(response$`CCLE Cell Line Name`, colnames(mutations)) + +resp <- response |> filter(!is.na(idx)) +mut <- mutations[, c(1, idx[!is.na(idx)])] |> + column_to_rownames("Name") + +cors <- apply(mut, 1, \(muts) { + tc <- cor(resp$Amax, muts) + ifelse(!is.na(tc), tc, 0) +}) + +screen <- cors[abs(cors) > 0.05 & !is.na(cors)] +dat <- data.frame(Y = resp$Amax, t(mut[names(screen),])) + +# Run --------------------------------------------------------------------- + +response <- "Y" +tgt <- paste0(c("BRAF.V600E", "BRAF.MC", "HIP1", "FLT3", "CDC42BPA", + "THBS3", "DNMT1", "PRKD1", "PIP5K1A", "MAP3K5"), "_MUT") +muts <- setdiff(colnames(dat), c(response, tgt)) + +tmtry <- NULL +tmd <- NULL + +pb <- txtProgressBar(min = 0, max = length(tgt), style = 3) +out <- lapply(seq_along(tgt), \(tmut) { + setTxtProgressBar(pb, tmut) + pcm <- pcm(dat[, response], dat[, tgt[tmut]], dat[, c(tgt[-tmut], muts)], + mtry = tmtry, rep = nrep, est_vhat = TRUE, ghat_args = list( + mtry = tmtry, max.depth = tmd)) + gcm <- ranger_gcm(dat[, response], dat[, tgt[tmut]], dat[, c(tgt[-tmut], muts)], + mtry = identity, max.depth = tmd) + naive <- cor.test(x = dat[, tgt[tmut]], y = dat[, response]) + data.frame(gene = tgt[tmut], + pcm = pcm$p.value, + gcm = gcm$p.value, + naive = naive$p.value) +}) + +### Tabulate results +(res <- bind_rows(out)) +knitr::kable(t(res[, c("gcm", "pcm")]), col.names = res$gene, + format = "latex", booktabs = TRUE, digits = 3) + +# # Subsampling ------------------------------------------------------------- +# +# pb <- txtProgressBar(min = 0, max = length(tgt), style = 3) +# out <- lapply(seq_along(tgt), \(tmut) { +# setTxtProgressBar(pb, tmut) +# n <- NROW(dat) +# folds <- sample(rep(1:2, ceiling(n/2)), n) +# lapply(1:2, \(iter) { +# tidx <- which(folds == iter) +# pcm <- pcm(dat[tidx, response], dat[tidx, tgt[tmut]], dat[tidx, c(tgt[-tmut], muts)], +# mtry = tmtry, rep = nrep, est_vhat = TRUE, ghat_args = list( +# mtry = tmtry, max.depth = tmd)) +# gcm <- ranger_gcm(dat[tidx, response], dat[tidx, tgt[tmut]], dat[tidx, c(tgt[-tmut], muts)], +# mtry = identity, max.depth = tmd) +# naive <- cor.test(x = dat[tidx, tgt[tmut]], y = dat[tidx, response]) +# data.frame(gene = tgt[tmut], +# pcm = pcm$p.value, +# gcm = gcm$p.value, +# naive = naive$p.value, +# fold = iter) +# }) |> bind_rows() +# }) |> bind_rows() +# +# out |> pivot_wider(names_from = fold, values_from = pcm:naive) |> +# ggplot(aes(x = pcm_1, y = pcm_2)) + +# geom_point() + +# geom_abline(intercept = 0, slope = 1) diff --git a/inst/code/mimic.R b/inst/code/mimic.R new file mode 100644 index 0000000..3a6a285 --- /dev/null +++ b/inst/code/mimic.R @@ -0,0 +1,163 @@ +### MIMIC analysis GCM/PCM +### LK 2023 + +set.seed(2410) +nrep <- 5 +run_full <- TRUE +red <- 111 # 98% variance + +# Dependencies ------------------------------------------------------------ + +library("readr") +library("ranger") +library("ggplot2") +devtools::load_all() + +# Read data --------------------------------------------------------------- + +## Read meta data +bpath <- "inst/data/mimic/MIMIC" + +if (file.exists(temb <- file.path(bpath, "emb.csv"))) { + emb <- as.data.frame(read_csv(temb)) + emb$race <- as.factor(emb$race) + emb$sex <- as.factor(emb$sex) +} else { + library("reticulate") + np <-import("numpy") + meta <- read_csv(file.path(bpath, "mimic_cfm_train_meta.csv")) + meta_test <- read_csv(file.path(bpath, "mimic_cfm_test_meta.csv")) + meta$sex <- as.factor(meta$sex) + meta_test$sex <- as.factor(meta_test$sex) + ## race: Merge Asian, White, Black + meta$race <- as.factor(meta$race) + meta_test$race <- as.factor(meta_test$race) + + if(file.exists(file.path(bpath, "emb_svd.RDS"))) { + + emb <- np$load(file.path(bpath, "mimic_cfm_train_emb.npy")) + emb_svd <- readRDS(file.path(bpath, "emb_svd.RDS")) + + } else { + + emb <- np$load(file.path(bpath, "mimic_cfm_train_emb.npy")) + + ## SVD + emb_svd <- fast.svd(emb) + saveRDS(emb_svd, file = file.path(bpath, "emb_svd.RDS")) + plot(cumsum(emb_svd$d^2/sum(emb_svd$d^2)), type="b") + + } + + # create reduced embedding from SVD + emb <- emb %*% emb_svd$v[, 1:red] + emb_test <- tcrossprod( + np$load(file.path(bpath, "mimic_cfm_test_emb.npy")), emb_svd$v[1:red,]) + + ## Combine + emb <- cbind(as.data.frame(emb), meta) + emb_test <- cbind(as.data.frame(emb_test), meta_test) + rm(meta, meta_test); gc() + + ## Create response + name_resp <- "Pleural Effusion" + emb$resp <- emb[[name_resp]] + + write_csv(emb, temb) +} + +# Test -------------------------------------------------------------------- + +### Variables +nY <- "resp" +nX <- "race" +nC <- c("sex", "age") +nZ <- paste0("V", 1:red) + +### RF params +tmtry <- NULL # \(n) ceiling(sqrt(n)) +rargs <- list(mtry = NULL, max.depth = NULL) + +### Test function +run_tests <- function(splits = 20, max_size = 1e4, verbose = FALSE) { + pb <- txtProgressBar(min = 0, max = splits, style = 3) + n <- NROW(emb) + folds <- sample(rep(1:splits, ceiling(n/splits)), n) + lapply(seq_len(splits), \(iter) { + setTxtProgressBar(pb, iter) + idx <- which(folds == iter) + if (length(idx) > max_size) + idx <- idx[1:max_size] + nemb <- emb[idx, ] + + ### Test resp _||_ race | emb, age, sex ### GCM/PCM + gcm1 <- ranger_gcm(nemb[, nY], .mm(nX, nemb), .mm(c(nZ, nC), nemb), + mtry = rargs$mtry, max.depth = rargs$max.depth) + if (verbose) + cat("\nGCM1 done") + pcm1 <- pcm(nemb[, nY], .mm(nX, nemb), .mm(c(nZ, nC), nemb), rep = nrep, + mtry = tmtry, est_vhat = TRUE, ghat_args = c(rargs, list( + probability = TRUE)), do.check = FALSE) + if (verbose) + cat("\nPCM1 done") + ### Test resp _||_ emb | race, age, sex ### GCM/PCM + gcm2 <- ranger_gcm(nemb[, nY], .mm(nZ, nemb), .mm(c(nX, nC), nemb), + mtry = rargs$mtry, max.depth = rargs$max.depth) + if (verbose) + cat("\nGCM2 done") + pcm2 <- pcm(nemb[, nY], .mm(nZ, nemb), .mm(c(nX, nC), nemb), rep = nrep, + mtry = tmtry, est_vhat = TRUE, ghat_args = c(rargs, list( + probability = TRUE)), do.check = FALSE) + if (verbose) + cat("\nPCM2 done") + ### Return + list(GCM1 = gcm1, PCM1 = pcm1, GCM2 = gcm2, PCM2 = pcm2) + }) +} + +### RUN either on full data or with splits +if (run_full) { + + print(full <- run_tests(1, nrow(emb), verbose = TRUE)) + pvals <- c( + "GCM1" = -log10(full[[1]]$GCM1$p.value), + "PCM1" = -log10(full[[1]]$PCM1$p.value), + "GCM2" = -pchisq(unname(full[[1]]$GCM2$statistic), log.p = TRUE, + df = 111, lower.tail = FALSE) / log(10), + "PCM2" = -pnorm(unname(full[[1]]$PCM2$statistic), log.p = TRUE, + lower.tail = FALSE) / log(10) + ) + cat("Negative log10 p-values\n") + print(pvals) + saveRDS(full, "inst/results/mimic-full.rds") + +} else { + + ms <- 150 * 4^(0:2) + nsplit <- 75 + out <- dplyr::bind_rows(lapply(ms, \(nmax) { + res <- run_tests(splits = nsplit, max_size = nmax) + dplyr::bind_rows(lapply(res, \(x) unlist(lapply(x, \(y) y$p.value)))) |> + dplyr::mutate(n = nmax) + })) + + out |> tidyr::pivot_longer(-n) |> + dplyr::mutate(hypothesis = dplyr::case_when( + name %in% c("GCM1", "PCM1") ~ "PE~'_||_'~race~'|'~x*'-'*ray*','*~sex*','*~age", + name %in% c("GCM2", "PCM2") ~ "PE~'_||_'~x*'-'*ray~'|'~race*','*~sex*','*~age" + )) |> + ggplot(aes(x = ordered(n), color = stringr::str_remove(name, "[0-9]"), y = -log10(value))) + + geom_violin(width = 0.5, position = position_dodge(width = 0.5)) + + geom_boxplot(width = 0.3, position = position_dodge(width = 0.5), outlier.shape = NA) + + ggbeeswarm::geom_quasirandom(width = 0.1, dodge.width = 0.5, alpha = 0.3, size = 0.5) + + facet_wrap(~ hypothesis, labeller = label_parsed, scales = "free") + + labs(x = "Sample size", y = parse(text = "-log[10]~p*'-'*value"), color = "COMET") + + theme_bw() + + geom_hline(yintercept = -log10(0.05), color = "darkred", linetype = 3) + + scale_color_brewer(palette = "Dark2") + + theme(legend.position = "top") + + readr::write_csv(out, "inst/results/mimic-pvals.csv") + ggsave("inst/figures/mimic-pval.pdf", height = 3.5, width = 6, scale = 0.85) + +} diff --git a/inst/code/multiomics.R b/inst/code/multiomics.R new file mode 100644 index 0000000..94909e3 --- /dev/null +++ b/inst/code/multiomics.R @@ -0,0 +1,113 @@ +### Pre-process multiomics data +### LK 2024 + +bpath <- "inst/data/multiomics" +set.seed(2410) + +# DEPs -------------------------------------------------------------------- + +library("tidyverse") +library("survival") +devtools::load_all() + +# Read -------------------------------------------------------------------- + +rna <- read_tsv(file.path(bpath, "rna.tsv")) +meth <- read_tsv(file.path(bpath, "meth.tsv")) +mir <- read_tsv(file.path(bpath, "mir.tsv")) +surv <- read_tsv(file.path(bpath, "survival.tsv")) %>% + mutate(surv = Surv(days, event)) + +rna_idx <- match(rna$Samples, surv$Samples) +mir_idx <- match(mir$Samples, surv$Samples) +meth_idx <- match(meth$Samples, surv$Samples) + +stopifnot(all(rna_idx == mir_idx)) +stopifnot(all(meth_idx == mir_idx)) + +dat <- data.frame( + surv = surv$surv[rna_idx], + rna = scale(as.matrix(rna[, -1])), + mir = scale(as.matrix(mir[, -1])), + meth = scale(as.matrix(meth[, -1])) +) + +rm(list = c("mir", "rna", "surv", "meth")) + +# Run --------------------------------------------------------------------- + +response <- "surv" +names_mir <- grep("^mir", colnames(dat), value = TRUE) +names_rna <- grep("^rna", colnames(dat), value = TRUE) +names_meth <- grep("^meth", colnames(dat), value = TRUE) + +rargs <- list(mtry = NULL, max.depth = NULL, probability = TRUE) +tmtry <- NULL +nrep <- 10 + +(t1 <- pcm(dat[, response][, 2], dat[, names_rna], dat[, c(names_mir, names_meth)], + mtry = tmtry, rep = nrep, est_vhat = TRUE, ghat_args = rargs)) +(t2 <- pcm(dat[, response][, 2], dat[, names_mir], dat[, c(names_rna, names_meth)], + mtry = tmtry, rep = nrep, est_vhat = TRUE, ghat_args = rargs)) +(t3 <- pcm(dat[, response][, 2], dat[, names_meth], dat[, c(names_rna, names_mir)], + mtry = tmtry, rep = nrep, est_vhat = TRUE, ghat_args = rargs)) + +(t4 <- pcm(dat[, response][, 2], dat[, names_rna], dat[, c(names_mir, names_meth)], + mtry = tmtry, rep = nrep, est_vhat = TRUE, reg = "pcm_lasso")) +(t5 <- pcm(dat[, response][, 2], dat[, names_mir], dat[, c(names_rna, names_meth)], + mtry = tmtry, rep = nrep, est_vhat = TRUE, reg = "pcm_lasso")) +(t6 <- pcm(dat[, response][, 2], dat[, names_meth], dat[, c(names_rna, names_mir)], + mtry = tmtry, rep = nrep, est_vhat = TRUE, reg = "pcm_lasso")) + +### Don't run +# (g1 <- ranger_gcm(dat[, response][, 2], dat[, names_rna], dat[, c(names_mir, names_meth)], +# mtry = rargs$mtry, max.depth = rargs$max.depth)) +# (g2 <- ranger_gcm(dat[, response][, 2], dat[, names_mir], dat[, c(names_rna, names_meth)], +# mtry = rargs$mtry, max.depth = rargs$max.depth)) +# (g3 <- ranger_gcm(dat[, response][, 2], dat[, names_meth], dat[, c(names_rna, names_mir)], +# mtry = rargs$mtry, max.depth = rargs$max.depth)) + +# screen_rna <- names(which(sapply(names_rna, \(tx) cor(dat[, response][, 2], dat[, tx])) > 0.2)) +# screen_mir <- names(which(sapply(names_mir, \(tx) cor(dat[, response][, 2], dat[, tx])) > 0.2)) +# screen_meth <- names(which(sapply(names_meth, \(tx) cor(dat[, response][, 2], dat[, tx])) > 0.2)) +# +# (t1 <- pcm(dat[, response][, 2], dat[, screen_rna], dat[, c(screen_mir, screen_meth)], +# mtry = tmtry, rep = nrep, est_vhat = TRUE, ghat_args = rargs)) +# (t2 <- pcm(dat[, response][, 2], dat[, screen_mir], dat[, c(screen_rna, screen_meth)], +# mtry = tmtry, rep = nrep, est_vhat = TRUE, ghat_args = rargs)) +# (t3 <- pcm(dat[, response][, 2], dat[, screen_meth], dat[, c(screen_rna, screen_mir)], +# mtry = tmtry, rep = nrep, est_vhat = TRUE, ghat_args = rargs)) +# (g1 <- ranger_gcm(dat[, response][, 2], as.matrix(dat[, screen_rna]), +# as.matrix(dat[, c(screen_mir, screen_meth)]), +# mtry = rargs$mtry, max.depth = rargs$max.depth)) +# (g2 <- ranger_gcm(dat[, response][, 2], as.matrix(dat[, screen_mir]), +# as.matrix(dat[, c(screen_rna, screen_meth)]), +# mtry = rargs$mtry, max.depth = rargs$max.depth)) +# (g3 <- ranger_gcm(dat[, response][, 2], as.matrix(dat[, screen_meth]), +# as.matrix(dat[, c(screen_rna, screen_mir)]), +# mtry = rargs$mtry, max.depth = rargs$max.depth)) + +# SurvGCM ----------------------------------------------------------------- + +# dmeth <- dat[, c(response, screen_meth)] +# pb <- txtProgressBar(0, length(screen_meth), style = 3) +# out <- lapply(seq_along(screen_meth), \(tmeth) { +# setTxtProgressBar(pb, tmeth) +# fm <- reformulate(screen_meth[-tmeth], response) +# mY <- survforest(fm, dmeth) +# tst <- gcm(mY, reformulate(screen_meth[-tmeth], screen_meth[tmeth]), data = dmeth) +# mY2 <- .ranger(reformulate(screen_meth[-tmeth], "surv[, 2]"), dmeth) +# tst2 <- gcm(mY2, reformulate(screen_meth[-tmeth], screen_meth[tmeth]), data = dmeth) +# # mY2 <- coxph(fm, dmeth) +# # tst2 <- gcm(mY2, reformulate(screen_meth[-tmeth], screen_meth[tmeth]), data = dmeth) +# data.frame(meth = screen_meth[tmeth], survgcm = tst$p.value, gcm = tst2$p.value) +# }) +# bind_rows(out) +# +# ggplot(bind_rows(out), aes(x = gcm, y = coxph, color = gcm < 0.05 & coxph < 0.05)) + +# geom_point(show.legend = FALSE) + +# theme_bw() + +# scale_x_log10() + +# scale_y_log10() + +# geom_abline(slope = 1, intercept = 0) + +# labs(x = "Survival GCM", y = "Binary GCM") diff --git a/inst/dependencies.R b/inst/dependencies.R new file mode 100644 index 0000000..ba05f81 --- /dev/null +++ b/inst/dependencies.R @@ -0,0 +1,15 @@ +# Install all dependencies for reproducing the results in the paper +# LK 2024 + +.libPaths(c("~/tutu/lib", .libPaths())) + +### Install remotes for installing all other packages +install.packages("remotes", repos = "https://cloud.r-project.org") + +### Install all other packages from CRAN +pkgs <- c("tidyverse", "ranger", "mlt", "sandwich", "glmnet", "tram", + "reticulate", "mgcv", "survival") +remotes::install_cran(pkgs) + +### Install comet +remotes::install_local(force = TRUE) diff --git a/inst/figures/components-overview.R b/inst/figures/components-overview.R new file mode 100644 index 0000000..54839f3 --- /dev/null +++ b/inst/figures/components-overview.R @@ -0,0 +1,103 @@ +### Figure 1 +### LK 2024 + +set.seed(2410) + +# DEPs -------------------------------------------------------------------- + +library("tidyverse") +library("mgcv") +devtools::load_all() +theme_set(theme_bw() + theme(text = element_text(size = 13.5))) + +pd1 <- data.frame(id = seq_len(1e3), pvalue = -log10(p.adjust(runif(1e3)^2))) + +ggplot(pd1, aes(x = id, y = pvalue, col = pvalue)) + + geom_col(show.legend = FALSE) + + geom_hline(yintercept = -log10(0.05), color = "darkred", linetype = 2) + + labs(x = element_blank(), y = parse(text = "-log[10]~p*'-'*value"), + color = parse(text = "-log[10]~p*'-'*value")) + + scale_color_viridis_c(begin = 0.1, end = 0.9, option = "C") + + theme(legend.position = "top", axis.text.x = element_blank(), + axis.ticks.x = element_blank()) + +ggsave("inst/figures/manhatten.pdf", height = 2, width = 3) + +# GCM v PCM --------------------------------------------------------------- + +f <- \(x) 1 + sin(3 * X^2) +g <- \(z) 1 + z^3 +mu <- \(x, z) f(x) * g(z) + +X <- runif(n <- 3e2, -1, 1) +Z <- runif(n, -1, 1) +Y <- mu(X, Z) + rnorm(n, sd = 0.05) +pd2 <- data.frame(Y = Y, X = X, Z = Z) + +mY <- .ranger(Y ~ Z, data = pd2) +pd2$RY <- residuals.ranger(mY) +mX <- .ranger(X ~ Z, data = pd2) +pd2$RX <- residuals.ranger(mX) +pd2$TX <- (f(X) - mean(f(X))) * g(Z) +mTX <- .ranger(TX ~ Z, data = pd2) +pd2$RTX <- residuals.ranger(mTX) + +ggplot(pd2 |> mutate(id = 1:n) |> pivot_longer(X:Z, names_to = "Predictor", + values_to = "value"), + aes(y = Y, x = value, color = Predictor, group = Predictor)) + + geom_point(alpha = 0.5) + + geom_smooth(method = "gam", se = FALSE) + + scale_color_brewer(palette = "Dark2") + + theme(legend.position = "bottom", legend.box.spacing = unit(-0.3, "cm")) + + labs(y = "Response Y", subtitle = "Y depends on X given Z", + x = element_blank()) + +ggsave("inst/figures/pcmgcmdata.pdf", height = 3.3, width = 3.3) + +ggplot(pd2, aes(x = X, y = RY)) + + geom_point(alpha = 0.5) + + geom_smooth(method = "lm", se = FALSE, col = "gray80") + + geom_smooth(method = "gam", se = FALSE, col = "#1E88E5", linetype = 2, linewidth = 1.8) + + labs(x = "X", y = "Residual Y on Z", + subtitle = "GCM (fails to reject)") + + geom_label(aes(x = -0.5, y = 0.05, + label = paste0("R==", round(cor(RX, RY), 2))), + inherit.aes = FALSE, parse = TRUE) + +ggsave("inst/figures/gcm.pdf", height = 3.3, width = 3.3) + +ggplot(pd2, aes(x = TX, y = RY)) + + geom_point(alpha = 0.5) + + geom_smooth(method = "lm", se = FALSE, col = "gray80") + + labs(x = "Transformed X", y = "Residual Y on Z", + subtitle = "PCM (correctly rejects)") + + geom_label(aes(x = 0.3, y = 0.1, + label = paste0("R==", round(cor(TX, RY), 2))), + inherit.aes = FALSE, parse = TRUE) + +ggsave("inst/figures/pcm.pdf", height = 3.3, width = 3.3) + +# Modality selection ------------------------------------------------------ + +pd3 <- data.frame(MSE1 = runif(3e1, min = 1, max = 3), + MSE2 = runif(3e1, min = 0.3, max = 2.5)) +ggplot(pivot_longer(pd3, MSE1:MSE2), aes(x = name, y = value)) + + geom_violin(width = 0.5) + + geom_boxplot(width = 0.3) + + ggbeeswarm::geom_quasirandom(alpha = 0.3, width = 0.2) + + labs(x = element_blank(), y = "MSPE") + + scale_x_discrete(labels = c("MSE1" = "Y | X", "MSE2" = "Y | X, Z")) + +ggsave("inst/figures/modsec.pdf", height = 2, width = 3) + +# GCM --------------------------------------------------------------------- + +X <- matrix(runif(3e2), ncol = 1) +colnames(X) <- c("X1") +Z <- matrix(runif(6e2), ncol = 2) +colnames(Z) <- c("Z1", "Z2") +Y <- exp(X[, 1]) + Z[, 2]^3 + exp(Z[, 1]) + rnorm(3e2) +(gcm1 <- ranger_gcm(Y, X, Z)) +plot(gcm1) + labs(x = "Transformation of X and Z") + +ggsave("inst/figures/simple-gcm.pdf", height = 2, width = 2.5) diff --git a/man/gcm.Rd b/man/gcm.Rd new file mode 100644 index 0000000..8037965 --- /dev/null +++ b/man/gcm.Rd @@ -0,0 +1,35 @@ +% Generated by roxygen2: do not edit by hand +% Please edit documentation in R/gcm.R +\name{gcm} +\alias{gcm} +\title{GCM using random forests} +\usage{ +gcm(Y, X, Z, alternative = c("two.sided", "less", "greater"), ...) +} +\arguments{ +\item{Y}{Response} + +\item{X}{Covariates} + +\item{Z}{Covariates} + +\item{alternative}{Alternative} + +\item{...}{Additional arguments to ranger} +} +\value{ +Object of class htest +} +\description{ +GCM using random forests +} +\examples{ +X <- matrix(rnorm(2e3), ncol = 2) +colnames(X) <- c("X1", "X2") +Z <- matrix(rnorm(2e3), ncol = 2) +colnames(Z) <- c("Z1", "Z2") +Y <- rnorm(1e3) # X[, 2] + Z[, 2] + rnorm(1e3) +(gcm1 <- gcm(Y, X, Z)) +plot(gcm1) + +} diff --git a/man/pcm.Rd b/man/pcm.Rd new file mode 100644 index 0000000..240c2ca --- /dev/null +++ b/man/pcm.Rd @@ -0,0 +1,57 @@ +% Generated by roxygen2: do not edit by hand +% Please edit documentation in R/pcm.R +\name{pcm} +\alias{pcm} +\title{Conditional mean independence test} +\usage{ +pcm( + Y, + X, + Z, + rep = 1, + est_vhat = TRUE, + reg = c("pcm_ranger", "pcm_lasso"), + ghat_args = NULL, + mtry = identity, + do.check = FALSE, + ... +) +} +\arguments{ +\item{Y}{Numeric; response} + +\item{X}{Numeric; covariates} + +\item{Z}{Numceric; covariates} + +\item{rep}{Number of repetitions} + +\item{est_vhat}{Estimate variance functional} + +\item{reg}{Character; regression method} + +\item{ghat_args}{Arguments passed to reg} + +\item{mtry}{Argument passed to \code{ranger}} + +\item{do.check}{Save check data} + +\item{...}{Additional arguments passed to \code{reg}} +} +\value{ +Object of class '\code{htest}' +} +\description{ +Conditional mean independence test +} +\examples{ +X <- matrix(rnorm(2e3), ncol = 2) +colnames(X) <- c("X1", "X2") +Z <- matrix(rnorm(2e3), ncol = 2) +colnames(Z) <- c("Z1", "Z2") +Y <- rnorm(1e3) # X[, 2] + Z[, 2] + rnorm(1e3) +(pcm1 <- pcm(Y, X, Z, ghat_args = list(mtry = NULL, max.depth = NULL), + est_vhat = TRUE, do.check = TRUE)) +plot(pcm1) + +} diff --git a/tests/testthat.R b/tests/testthat.R new file mode 100644 index 0000000..6ef959c --- /dev/null +++ b/tests/testthat.R @@ -0,0 +1,12 @@ +# This file is part of the standard setup for testthat. +# It is recommended that you do not modify it. +# +# Where should you do additional test configuration? +# Learn more about the roles of various files in: +# * https://r-pkgs.org/tests.html +# * https://testthat.r-lib.org/reference/test_package.html#special-files + +library("testthat") +library("comet") + +test_check("comet") diff --git a/tests/testthat/test_main.R b/tests/testthat/test_main.R new file mode 100644 index 0000000..81edfc3 --- /dev/null +++ b/tests/testthat/test_main.R @@ -0,0 +1,28 @@ + +test_that(".ranger works", { + set.seed(12) + dat <- data.frame(bin = factor(sample(0:1, 1e3, TRUE)), + ord = ordered(sample(7:10, 1e3, TRUE)), + mcc = factor(sample(11:15, 1e3, TRUE)), + num = rnorm(1e3), + x = rnorm(1e3)) + lapply(colnames(dat)[-ncol(dat)], \(resp) { + fm <- reformulate("x", resp) + rf <- .ranger(fm, data = dat) + rr <- residuals.ranger(rf) + expect_lt(abs(mean(rr)), 0.005) + }) +}) + +test_that("gcm and pcm work", { + expect_no_error({ + set.seed(12) + X <- matrix(rnorm(2e3), ncol = 2) + colnames(X) <- c("X1", "X2") + Z <- matrix(rnorm(2e3), ncol = 2) + colnames(Z) <- c("Z1", "Z2") + Y <- rnorm(1e3) + gcm1 <- gcm(Y, X, Z) + pcm1 <- pcm(Y, X, Z) + }) +})