R/dimred_pca.R

Defines functions dimred_pca

Documented in dimred_pca

#' Dimensionality reduction through PCA
#'
#' @param MAE A multi-assay experiment object
#' @param tax_level The taxon level used for organisms
#' @param color A condition to color data points by e.g. "AGE"
#' @param shape A condition to shape data points by e.g. "SEX"
#' @param pcx Principal component on the x-axis e.g. 1
#' @param pcy Principal component on the y-axis e.g. 2
#' @param pcz Principal component on the z-axis e.g. 3
#' @param datatype Datatype to use e.g. c("logcpm", "relabu", "counts")
#' @return A list with a plotly object and summary table
#'
#' @examples
#' data_dir <- system.file("extdata/MAE.rds", package = "animalcules")
#' toy_data <- readRDS(data_dir)
#' result <- dimred_pca(toy_data,
#'   tax_level = "genus",
#'   color = "AGE",
#'   shape = "DISEASE",
#'   pcx = 1,
#'   pcy = 2,
#'   datatype = "logcpm"
#' )
#' result$plot
#' result$table
#'
#' @import dplyr
#' @import scales
#' @import plotly
#' @import magrittr
#' @import reshape2
#' @import MultiAssayExperiment
#'
#' @export
dimred_pca <- function(MAE,
    tax_level,
    color,
    shape = NULL,
    pcx = 1,
    pcy = 2,
    pcz = NULL,
    datatype = c("logcpm", "relabu", "counts")) {
    # Default variables
    datatype <- match.arg(datatype)
    
    # Extract data
    microbe <- MAE[["MicrobeGenetics"]]
    # host <- MultiAssayExperiment::experiments(MAE)[[2]]
    tax_table <- as.data.frame(rowData(microbe)) # organism x taxlev
    sam_table <- as.data.frame(colData(microbe)) # sample x condition
    counts_table <-
        as.data.frame(assays(microbe))[, rownames(sam_table)] #organism x sample
    
    df <- counts_table %>%
        # Sum counts by taxon level
        upsample_counts(tax_table, tax_level) %>%
        # Choose data type
        {
            if (datatype == "relabu") {
                counts_to_relabu(.)
            } else if (datatype == "logcpm") {
                counts_to_logcpm(.)
            } else {
                .
            }
        } %>%
        # Fix constant/zero row
        {
            if (sum(base::rowSums(as.matrix(.)) == 0) > 0) {
                . <- .[-which(base::rowSums(as.matrix(.)) == 0), ]
            } else {
                .
            }
        } %>%
        # Transpose
        t()
    
    # PCA
    df.prcomp <- stats::prcomp(df, scale = TRUE)
    # Principle Components
    df.pca <- df.prcomp$x
    # Importance
    df.imp <- t(summary(df.prcomp)$importance)
    
    # Merge in covariate information
    if (!is.null(shape)) {
        df.pca.m <- merge(df.pca,
            sam_table[, c(color, shape), drop = FALSE],
            by = 0, all = TRUE
        )
        # When shape is required
        # Bypass duplicate colnames if color == shape
        shape <- colnames(df.pca.m)[ncol(df.pca.m)]
        df.pca.m[[shape]] <- as.factor(df.pca.m[[shape]])
    } else {
        df.pca.m <-
            merge(df.pca, sam_table[, color, drop = FALSE], by = 0, all = TRUE)
        shape <- "shape" # Referenced by plotly later
        df.pca.m[[shape]] <- 1 # Constant results in omitting shape
    }
    
    # Plotly | Scatterplot
    if (is.null(pcz)) {
        # 2D Plot
        p <- plot_ly(df.pca.m,
            x = as.formula(paste("~PC", pcx, sep = "")),
            y = as.formula(paste("~PC", pcy, sep = "")),
            mode = "markers",
            color = as.formula(paste("~", color, sep = "")),
            symbol = as.formula(paste("~", shape, sep = "")),
            type = "scatter",
            text = df.pca.m$Row.names,
            marker = list(size = 10)
        )
    } else {
        # 3D Plot
        p <- plot_ly(df.pca.m,
            x = as.formula(paste("~PC", pcx, sep = "")),
            y = as.formula(paste("~PC", pcy, sep = "")),
            z = as.formula(paste("~PC", pcz, sep = "")),
            mode = "markers",
            color = as.formula(paste("~", color, sep = "")),
            symbol = as.formula(paste("~", shape, sep = "")),
            symbols = c(
                "circle",
                "square",
                "diamond",
                "cross",
                "square-open",
                "circle-open",
                "diamond-open",
                "x"
            ),
            type = "scatter3d",
            text = df.pca.m$Row.names,
            marker = list(size = 6)
        )
    }
    
    p$p <- NULL # To suppress a shiny warning
    
    # Formatting importance table
    colnames(df.imp) <- c(
        "Standard Deviation",
        "Variance Explained",
        "Cumulative Variance"
    )
    
    df.imp[, "Standard Deviation"] <- signif(df.imp[, "Standard Deviation"], 3)
    
    # Show variance as a percentage
    df.imp[, 2] <- scales::percent(as.numeric(df.imp[, 2]))
    df.imp[, 3] <- scales::percent(as.numeric(df.imp[, 3]))
    
    # Reorder
    df.imp <- as.data.frame(df.imp)
    df.imp$PC <- rownames(df.imp)
    df.imp <- df.imp[, c(4, 1, 2, 3)]
    
    return(list(plot = p, table = df.imp))
}
compbiomed/animalcules documentation built on Feb. 7, 2024, 12:13 p.m.