@@ -4,7 +4,7 @@ Title: A framework for cross-validated classification problems, with

        applications to differential variability and differential

        distribution testing

 Version: 3.3.14

-Date: 2023-02-16

+Date: 2023-02-20

 Authors@R:

     c(

     person(given = "Dario", family = "Strbenac", email = "dario.strbenac@sydney.edu.au", role = c("aut", "cre")),

@@ -24,7 +24,7 @@ Imports: grid, genefilter, utils, dplyr, tidyr, rlang, ranger, ggplot2 (>= 3.0.0

 Suggests: limma, edgeR, car, Rmixmod, gridExtra (>= 2.0.0), cowplot,

         BiocStyle, pamr, PoiClaClu, parathyroidSE, knitr, htmltools, gtable,

         scales, e1071, rmarkdown, IRanges, robustbase, glmnet, class, randomForestSRC,

-        MatrixModels, xgboost

+        MatrixModels, xgboost, data.tree, ggnewscale

 Description: The software formalises a framework for classification and survival model evaluation

              in R. There are four stages; Data transformation, feature selection, model training,

              and prediction. The requirements of variable types and variable order are

@@ -1,6 +1,7 @@

 # Generated by roxygen2: do not edit by hand

 S3method(predict,trainedByClassifyR)

+S3method(summary,PrecisionPathways)

 S3method(train,DataFrame)

 S3method(train,MultiAssayExperiment)

 S3method(train,data.frame)

@@ -18,7 +19,9 @@ export(TransformParams)

 export(actualOutcome)

 export(allFeatureNames)

 export(available)

+export(bubblePlot.PrecisionPathways)

 export(calcCVperformance)

+export(calcCostsAndPerformance)

 export(calcExternalPerformance)

 export(chosenFeatureNames)

 export(colCoxTests)

@@ -29,6 +32,7 @@ export(distribution)

 export(edgesToHubNetworks)

 export(featureSetSummary)

 export(finalModel)

+export(flowchart.PrecisionPathways)

 export(interactorDifferences)

 export(models)

 export(performance)

@@ -42,6 +46,7 @@ export(runTests)

 export(sampleNames)

 export(samplesMetricMap)

 export(selectionPlot)

+export(strataPlot.PrecisionPathways)

 export(totalPredictions)

 export(tunedParameters)

 exportClasses(ClassifyResult)

@@ -8,6 +8,7 @@

 #

 ################################################################################

+setOldClass("PrecisionPathways")

 # Union of A Function and NULL

 setClassUnion("functionOrNULL", c("function", "NULL"))

@@ -26,7 +26,7 @@

 #' @param nFolds A numeric specifying the number of folds to use for cross-validation.

 #' @param nRepeats A numeric specifying the the number of repeats or permutations to use for cross-validation.

 #' @param nCores A numeric specifying the number of cores used if the user wants to use parallelisation.

-#' @param pathways A set of pathways created by \code{precisionPathwaysTrain} to be used for predicting on a new data set.

+#' @param pathways A set of pathways created by \code{precisionPathwaysTrain} which is an object of class \code{PrecisionPathways} to be used for predicting on a new data set.

 #' @rdname precisionPathways

 #' @return An object of class \code{PrecisionPathways} which is basically a named list that other plotting and

 #' tabulating functions can use.

@@ -57,7 +57,7 @@ setMethod("precisionPathwaysTrain", "MultiAssayExperimentOrList",

             measurementsAndClass <- do.call(prepareData, prepArgs)

             .precisionPathwaysTrain(measurementsAndClass[["measurements"]], measurementsAndClass[["outcome"]],

-                                   fixedAssays = fixedAssays, confidenceCutoff = confidenceCutoff,

+                                   clinicalPredictors = clinicalPredictors, fixedAssays = fixedAssays, confidenceCutoff = confidenceCutoff,

                                    minAssaySamples = minAssaySamples, nFeatures = nFeatures,

                                    selectionMethod = selectionMethod, classifier = classifier,

                                    nFolds = nFolds, nRepeats = nRepeats, nCores = nCores)

@@ -66,7 +66,7 @@ setMethod("precisionPathwaysTrain", "MultiAssayExperimentOrList",

 # Internal method which carries out all of the processing, obtaining reformatted data from the

 # MultiAssayExperiment and list (of basic rectangular tables) S4 methods.

 .precisionPathwaysTrain <- function(measurements, class, fixedAssays = "clinical",

-                   confidenceCutoff = 0.8, minAssaySamples = 10,

+                   clinicalPredictors = clinicalPredictors, confidenceCutoff = 0.8, minAssaySamples = 10,

                    nFeatures = 20, selectionMethod = setNames(c(NULL, rep("t-test", length(measurements))), c("clinical", names(measurements))),

                    classifier = setNames(c("elasticNetGLM", rep("randomForest", length(measurements))), c("clinical", names(measurements))),

                    nFolds = 5, nRepeats = 20, nCores = 1)

@@ -101,6 +101,7 @@ setMethod("precisionPathwaysTrain", "MultiAssayExperimentOrList",

                 predictionsSamplesCounts <- table(allPredictions[, "sample"], allPredictions[, "class"])

                 confidences <- 2 * abs(predictionsSamplesCounts[, 1] / rowSums(predictionsSamplesCounts) - 0.5)

                 sampleIDsUse <- names(confidences)[confidences > confidenceCutoff]

+                sampleIDsUse <- setdiff(sampleIDsUse, samplesUsed)

                 # Check if too few samples left for next round. Include them in this round, if so.

                 remainingIDs <- setdiff(allSampleIDs, c(samplesUsed, sampleIDsUse))

@@ -134,14 +135,17 @@ setMethod("precisionPathwaysTrain", "MultiAssayExperimentOrList",

                 if(breakEarly == TRUE) break

               }

               pathwayString <- paste(assaysProcessed, collapse = '-')

-              parameters = list(confidenceCutoff = confidenceCutoff, minAssaySamples = minAssaySamples)

-              list(models = modelsList, parameters = parameters, pathway = pathwayString,

+              individualsTableAll[, "Tier"] <- factor(individualsTableAll[, "Tier"], levels = permutation)

+              list(pathway = pathwayString,

                   individuals = individualsTableAll, tiers = tierTableAll)

             })

-            

-            class(precisionPathways) <- "PrecisionPathways"

             names(precisionPathways) <- sapply(precisionPathways, "[[", "pathway")

-            precisionPathways

+            result <- list(models = modelsList, assaysPermutations = assaysPermutations,

+                           parameters = list(confidenceCutoff = confidenceCutoff, minAssaySamples = minAssaySamples),

+                           clinicalPredictors = clinicalPredictors, pathways = precisionPathways)

+            class(result) <- "PrecisionPathways"

+            

+            result

 }

 # A nice print method to avoid flooding the screen with lots of tables

@@ -150,7 +154,7 @@ print.PrecisionPathways <- function(x)

 {

   cat("An object of class 'PrecisionPathways'.\n")

   cat("Pathways:\n")

-  cat(paste(names(x), collapse = '\n'))

+  cat(paste(names(x[["pathways"]]), collapse = '\n'))

 }

 #' @usage NULL

@@ -159,7 +163,7 @@ setGeneric("precisionPathwaysPredict", function(pathways, measurements, class, .

 #' @rdname precisionPathways

 #' @export

-setMethod("precisionPathwaysPredict", "MultiAssayExperimentOrList", 

+setMethod("precisionPathwaysPredict", c("PrecisionPathways", "MultiAssayExperimentOrList"), 

           function(pathways, measurements, class)

           {

             if(is.list(measurements)) # Ensure plain list has clinical data.

@@ -168,7 +172,8 @@ setMethod("precisionPathwaysPredict", "MultiAssayExperimentOrList",

               if (!any(names(measurements) == "clinical"))

                 stop("One of the tables must be named \"clinical\".")

             }

-            prepArgs <- list(measurements, outcomeColumns = class)

+

+            prepArgs <- list(measurements, outcomeColumns = class, clinicalPredictors = pathways[["clinicalPredictors"]])

             measurementsAndClass <- do.call(prepareData, prepArgs)

             .precisionPathwaysPredict(pathways, measurementsAndClass[["measurements"]], measurementsAndClass[["outcome"]])

@@ -176,5 +181,259 @@ setMethod("precisionPathwaysPredict", "MultiAssayExperimentOrList",

 .precisionPathwaysPredict <- function(pathways, measurements, class)

 {

-  # To do.

+

+  # Step 1: Extract all of previously fitted models and permutations.

+  modelsList <- pathways[["models"]]

+  assayIDs <- lapply(PPT[["models"]], function(model) model@characteristics[model@characteristics[, 1] == "Assay Name", 2])

+  assaysPermutations <- pathways[["assaysPermutations"]]

+  confidenceCutoff <- pathways[["parameters"]][["confidenceCutoff"]]

+  minAssaySamples <- pathways[["parameters"]][["minAssaySamples"]]

+  

+  # Step 2: Loop over each pathway and each assay in order to determine which samples are used at that level

+  # and which are passed onwards.

+  precisionPathways <- lapply(as.data.frame(assaysPermutations), function(permutation)

+  {

+    assaysProcessed <- character()

+    samplesUsed <- character()

+    individualsTableAll <- S4Vectors::DataFrame()

+    tierTableAll <- S4Vectors::DataFrame()

+    breakEarly = FALSE

+    for(assay in permutation)

+    {

+      # Step 2a: Identify all samples which are consistently predicted.

+      modelIndex <- match(assay, assayIDs)

+      allPredictions <- predictions(modelsList[[modelIndex]])

+      allSampleIDs <- sampleNames(modelsList[[modelIndex]])

+      predictionsSamplesCounts <- table(allPredictions[, "sample"], allPredictions[, "class"])

+      confidences <- 2 * abs(predictionsSamplesCounts[, 1] / rowSums(predictionsSamplesCounts) - 0.5)

+      sampleIDsUse <- names(confidences)[confidences > confidenceCutoff]

+      sampleIDsUse <- setdiff(sampleIDsUse, samplesUsed)

+                

+      # Check if too few samples left for next round. Include them in this round, if so.

+      remainingIDs <- setdiff(allSampleIDs, c(samplesUsed, sampleIDsUse))

+      if(length(remainingIDs) < minAssaySamples)

+      {

+        sampleIDsUse <- c(sampleIDsUse, remainingIDs)

+        breakEarly = TRUE

+      } else { }

+                

+      predictionsSamplesCounts <- predictionsSamplesCounts[sampleIDsUse, ]

+                

+      # Step 2b: Individuals predictions and sample-wise accuracy, tier-wise error.

+      maxVotes <- apply(predictionsSamplesCounts, 1, function(sample) which.max(sample))

+      predictedClasses <- factor(colnames(predictionsSamplesCounts)[maxVotes],

+                                 levels = colnames(predictionsSamplesCounts))    

+      individualsTable <- S4Vectors::DataFrame(Tier = assay,

+                                               `Sample ID` = sampleIDsUse,

+                                               `Predicted` = predictedClasses,

+                                               `Accuracy` = performance(modelsList[[modelIndex]])[["Sample Accuracy"]][sampleIDsUse],

+                                                check.names = FALSE)

+      knownClasses <- actualOutcome(modelsList[[modelIndex]])[match(sampleIDsUse, allSampleIDs)]

+      balancedAccuracy <- calcExternalPerformance(knownClasses, predictedClasses)

+      tierTable <- S4Vectors::DataFrame(Tier = assay,

+                                        `Balanced Accuracy` = balancedAccuracy, check.names = FALSE)

+                

+      assaysProcessed <- c(assaysProcessed, assay)

+      individualsTableAll <- rbind(individualsTableAll, individualsTable)

+      tierTableAll <- rbind(tierTableAll, tierTable)

+      samplesUsed <- c(samplesUsed, sampleIDsUse)

+                

+      if(breakEarly == TRUE) break

+    }

+    pathwayString <- paste(assaysProcessed, collapse = '-')

+    individualsTableAll[, "Tier"] <- factor(individualsTableAll[, "Tier"], levels = permutation)

+    list(pathway = pathwayString,

+         individuals = individualsTableAll, tiers = tierTableAll)

+  })

+  names(precisionPathways) <- sapply(precisionPathways, "[[", "pathway")

+  result <- list(models = modelsList, assaysPermutations = assaysPermutations,

+                 parameters = list(confidenceCutoff = confidenceCutoff, minAssaySamples = minAssaySamples),

+                 clinicalPredictors = clinicalPredictors, pathways = precisionPathways)

+  class(result) <- "PrecisionPathways"

+            

+  result

+}

+

+# Calculate accuracy and costs of each pathway.

+

+#' Various Functions for Evaluating Precision Pathways

+#' 

+#' These functions tabulate or plot various aspects of precision pathways, such as accuracies and costs.

+#' 

+#' @param precisionPathways A pathway of class \code{PrecisionPathways}.

+#' @param costs A named vector of assays with the cost of each one.

+#' @rdname precisionPathwaysEvaluations

+#' @export

+calcCostsAndPerformance <- function(precisionPathways, costs = NULL)

+{

+  if(is.null(costs))

+    stop("'costs' of each assay must be specified.")      

+  pathwayIDs <- names(precisionPathways[["pathways"]])

+  accuraciesCosts <- do.call(rbind, lapply(precisionPathways[["pathways"]], function(pathway)

+  {

+    predictions <- pathway[["individuals"]][, "Predicted"]

+    knownClasses <- actualOutcome(precisionPathways$models[[1]])

+    allNames <- sampleNames(precisionPathways$models[[1]])

+    knownClasses <- knownClasses[match(pathway[["individuals"]][, "Sample ID"], allNames)]

+    balancedAccuracy <- calcExternalPerformance(knownClasses, predictions)

+    

+    costTotal <- sum(costs[match(pathway[["individuals"]][, "Tier"], names(costs))])

+    

+    data.frame(accuracy = round(balancedAccuracy, 2), cost = costTotal)

+  }))

+

+  precisionPathways$performance <- accuraciesCosts

+  precisionPathways

+}

+

+# Print a summary table, including accuracy and costs.

+

+#' @param object A set of pathways of class \code{PrecisionPathways}.

+#' @param weights A numeric vector of length two specifying how to weight the predictive accuracy

+#' and the cost during ranking. Must sum to 1.

+#' @rdname precisionPathwaysEvaluations

+#' @export

+summary.PrecisionPathways <- function(object, weights = c(accuracy = 0.5, cost = 0.5))

+{

+  summaryTable <- data.frame(Pathway = rownames(object[["performance"]]),

+                             `Balanced Accuracy` = object[["performance"]][, "accuracy"],

+                             `Total Cost` = object[["performance"]][, "cost"],

+                              check.names = FALSE)

+  rankingScores <- list(rank(object[["performance"]][, "accuracy"]), rank(-object[["performance"]][, "cost"]))

+  finalScores <- rowSums(mapply(function(scores, weight)

+               {

+                 scores * weight

+               }, rankingScores, as.list(weights)))

+  summaryTable <- cbind(summaryTable, Score = finalScores)

+  summaryTable

+}

+

+#' @param precisionPathways A pathway of class \code{PrecisionPathways}.

+#' @param pathwayColours A named vector of colours with names being the names of pathways. If none is specified,

+#' a default colour scheme will automatically be chosen.

+#' @rdname precisionPathwaysEvaluations

+#' @export

+bubblePlot.PrecisionPathways <- function(precisionPathways, pathwayColours = NULL)

+{

+  ggplot2::theme_set(ggplot2::theme_classic() + ggplot2::theme(panel.border = ggplot2::element_rect(fill = NA)))    

+  if(is.null(pathwayColours)) pathwayColours <- scales::hue_pal()(length(precisionPathways[["pathways"]]))

+  performance <- precisionPathways[["performance"]]

+  performance <- cbind(Sequence = rownames(performance), performance)

+  ggplot2::ggplot(performance, aes(x = accuracy, y = cost, colour = Sequence)) + geom_point() +

+    ggplot2::scale_color_manual(values = pathwayColours) + labs(x = "Balanced Accuracy", y = "Total Cost")

+}

+

+#' @param precisionPathways A pathway of class \code{PrecisionPathways}.

+#' @param pathway A chracter vector of length 1 specifying which pathway to plot, e.g. "clinical-mRNA".

+#' @param nodeColours A named vector of colours with names being \code{"assay"}, \code{"class1"},\code{"class2"}.

+#' a default colour scheme will automatically be chosen.

+#' @rdname precisionPathwaysEvaluations

+#' @export

+flowchart.PrecisionPathways <- function(precisionPathways, pathway, nodeColours = c(assay = "#86C57C", class1 = "#ACCEE0", class2 = "#F47F72"))

+{

+  if(!requireNamespace("data.tree", quietly = TRUE))

+    stop("The package 'data.tree' could not be found. Please install it.")

+

+  pathwayUse <- precisionPathways[["pathways"]][[pathway]]

+  assayIDs <- pathwayUse[["tiers"]][, 1]

+  possibleClasses <- levels(precisionPathways$models[[1]]@actualOutcome)

+  samplesTiers <- pathwayUse$individuals

+      

+  pathwayTree <- Node$new(assayIDs[1])

+  currentNode <- pathwayTree

+  for(assay in assayIDs)

+  {

+    toDo <- nrow(samplesTiers) - max(which(samplesTiers[, "Tier"] == assay))

+    class1Predictions <- currentNode$AddChild(possibleClasses[1], counter = nrow(subset(samplesTiers, Predicted == possibleClasses[1] & Tier == assay)), nodeType = "Class1")

+    uncertain <- currentNode$AddChild("Uncertain", counter = toDo, nodeType = "Uncertain")

+    class2Predictions = currentNode$AddChild(possibleClasses[2], counter = nrow(subset(samplesTiers, Predicted == possibleClasses[2] & Tier == assay)), nodeType = "Class2")

+    

+    if(toDo == 0) {break} else {

+      currentNode <- uncertain

+      currentNode <- currentNode$AddChild(assayIDs[match(assay, assayIDs) + 1], nodeType = "Platform")

+    }

+  }

+          

+  SetGraphStyle(pathwayTree, rankdir = "LR")

+  SetEdgeStyle(pathwayTree, fontname = 'helvetica', label = .getEdgeLabel)

+  SetNodeStyle(pathwayTree, style = "filled", shape = .getNodeShape, fontcolor = "black", fillcolor = .getFillColour, fontname = 'helvetica')

+  plot(pathwayTree)

+}

+

+.getEdgeLabel <- function(node)

+{

+  nSamples <<- nrow(samplesTiers)

+  if(node$isRoot || node$nodeType == "Platform")

+  {

+    label <- NULL

+  } else {

+    value <- round((node$counter / nSamples) * 100)

+    label <- paste(value,  "% (", node$counter, ")", sep = '')

+  }

+  return(label)

+}

+

+.getNodeShape <- function(node){

+  if(node$isRoot || node$nodeType == "Platform"){

+    shape = "oval"

+  } else {

+    shape = "box"

+  }

+}

+

+.getFillColour <- function(node) {

+  if(node$isRoot || node$nodeType == "Platform"){

+    colour <<- nodeColours[["assay"]]

+  } else if(node$nodeType == "Class1"){

+    colour <<- nodeColours[["class1"]]

+  } else if(node$nodeType == "Class2"){

+    colour <<- nodeColours[["class2"]]

+  } else {

+    colour = "snow3"

+  }

+  return(colour)

+}

+

+

+#' @param classColours A named vector of colours with names being \code{"class1"},\code{"class2"}, and \code{"accuracy"}.

+#' a default colour scheme will automatically be chosen.

+#' @rdname precisionPathwaysEvaluations

+#' @export

+strataPlot.PrecisionPathways <- function(precisionPathways, pathway, classColours = c(class1 = "#4DAF4A", class2 = "#984EA3"))

+{

+  pathwayUse <- precisionPathways[["pathways"]][[pathway]]

+  assayIDs <- pathwayUse[["tiers"]][, 1]

+  possibleClasses <- levels(precisionPathways$models[[1]]@actualOutcome)

+  samplesTiers <- pathwayUse$individuals

+  samplesTiers$trueClass <- actualOutcome(precisionPathways$models[[1]])[match(samplesTiers[, "Sample ID"], sampleNames(precisionPathways$models[[1]]))]

+  samplesTiers <- dplyr::arrange(as.data.frame(samplesTiers), Tier, trueClass, Accuracy)

+  samplesTiers$ID = 1:nrow(samplesTiers)

+  samplesTiers$colour = ifelse(samplesTiers$trueClass == levels(samplesTiers[, "Predicted"])[1], classColours["class1"], classColours["class2"])

+

+  strataPlot <- ggplot(mapping = aes(x = ID, y = Tier), data = samplesTiers) +

+                geom_tile(aes(fill = trueClass)) +

+    scale_fill_manual(values = unname(classColours))  +

+    labs(title = paste("Pathway:", pathway), fill = "True Class", x = "", y = "") +

+    guides(fill = guide_legend(title.position = "top")) +

+    ggnewscale::new_scale_fill() +

+    geom_tile(aes(fill = Accuracy)) +

+    scale_fill_gradient(low = "#377EB8", high = "#E41A1C") +

+    labs(fill = "Accuracy") +

+    guides(fill = guide_colorbar(title.position = "top")) +

+    theme(panel.background = element_blank(),

+          axis.text.x = element_blank(),

+          aspect.ratio = 1/4, 

+          plot.title = element_text(face = "bold", size = 20),

+          legend.title = element_text(face = "bold", size = 12),

+          legend.text = element_text(size = 10),

+          legend.position = "bottom",

+          axis.text = element_text(size = 15)) +

+    annotate("tile",

+               x = samplesTiers$ID,

+               y = length(levels(samplesTiers[, "Tier"])) + 0.8,

+               height = 0.6,

+               fill = samplesTiers$colour)  +

+    coord_cartesian(expand = FALSE) 

+    

+  strataPlot

 }

\ No newline at end of file

@@ -3,7 +3,7 @@

 \name{precisionPathwaysTrain}

 \alias{precisionPathwaysTrain}

 \alias{precisionPathwaysTrain,MultiAssayExperimentOrList-method}

-\alias{precisionPathwaysPredict,MultiAssayExperimentOrList-method}

+\alias{precisionPathwaysPredict,PrecisionPathways,MultiAssayExperimentOrList-method}

 \title{Precision Pathways for Sample Prediction Based on Prediction Confidence.}

 \usage{

 \S4method{precisionPathwaysTrain}{MultiAssayExperimentOrList}(

@@ -25,7 +25,7 @@

   nCores = 1

 )

-\S4method{precisionPathwaysPredict}{MultiAssayExperimentOrList}(pathways, measurements, class)

+\S4method{precisionPathwaysPredict}{PrecisionPathways,MultiAssayExperimentOrList}(pathways, measurements, class)

 }

 \arguments{

 \item{measurements}{Either a \code{\link{MultiAssayExperiment}} or a list of the basic tabular objects containing the data.}

@@ -63,7 +63,7 @@ would have less than this number of samples, the samples are incorporated into t

 \item{nCores}{A numeric specifying the number of cores used if the user wants to use parallelisation.}

-\item{pathways}{A set of pathways created by \code{precisionPathwaysTrain} to be used for predicting on a new data set.}

+\item{pathways}{A set of pathways created by \code{precisionPathwaysTrain} which is an object of class \code{PrecisionPathways} to be used for predicting on a new data set.}

 }

 \value{

 An object of class \code{PrecisionPathways} which is basically a named list that other plotting and

new file mode 100644

@@ -0,0 +1,52 @@

+% Generated by roxygen2: do not edit by hand

+% Please edit documentation in R/precisionPathways.R

+\name{calcCostsAndPerformance}

+\alias{calcCostsAndPerformance}

+\alias{summary.PrecisionPathways}

+\alias{bubblePlot.PrecisionPathways}

+\alias{flowchart.PrecisionPathways}

+\alias{strataPlot.PrecisionPathways}

+\title{Various Functions for Evaluating Precision Pathways}

+\usage{

+calcCostsAndPerformance(precisionPathways, costs = NULL)

+

+\method{summary}{PrecisionPathways}(object, weights = c(accuracy = 0.5, cost = 0.5))

+

+bubblePlot.PrecisionPathways(precisionPathways, pathwayColours = NULL)

+

+flowchart.PrecisionPathways(

+  precisionPathways,

+  pathway,

+  nodeColours = c(assay = "#86C57C", class1 = "#ACCEE0", class2 = "#F47F72")

+)

+

+strataPlot.PrecisionPathways(

+  precisionPathways,

+  pathway,

+  classColours = c(class1 = "#4DAF4A", class2 = "#984EA3")

+)

+}

+\arguments{

+\item{precisionPathways}{A pathway of class \code{PrecisionPathways}.}

+

+\item{costs}{A named vector of assays with the cost of each one.}

+

+\item{object}{A set of pathways of class \code{PrecisionPathways}.}

+

+\item{weights}{A numeric vector of length two specifying how to weight the predictive accuracy

+and the cost during ranking. Must sum to 1.}

+

+\item{pathwayColours}{A named vector of colours with names being the names of pathways. If none is specified,

+a default colour scheme will automatically be chosen.}

+

+\item{pathway}{A chracter vector of length 1 specifying which pathway to plot, e.g. "clinical-mRNA".}

+

+\item{nodeColours}{A named vector of colours with names being \code{"assay"}, \code{"class1"},\code{"class2"}.

+a default colour scheme will automatically be chosen.}

+

+\item{classColours}{A named vector of colours with names being \code{"class1"},\code{"class2"}, and \code{"accuracy"}.

+a default colour scheme will automatically be chosen.}

+}

+\description{

+These functions tabulate or plot various aspects of precision pathways, such as accuracies and costs.

+}