Add new clusteriness score

clustering.R

@@ -2,6 +2,37 @@ library(data.table)
 library(progress)
 library(rlog)
 
+#' Perform a cluster analysis.
+#'
+#' This function will cluster the data using `hclust` and `cutree` (with the
+#' specified height). Every cluster with at least two members qualifies for
+#' further analysis. Clusters are then ranked based on their size in relation
+#' to the total number of values. The return value is a final score between
+#' zero and one. Lower ranking clusters contribute less to this score.
+clusteriness <- function(data, height = 1000000) {
+    # Cluster the data and compute the cluster sizes.
+
+    tree <- hclust(dist(data))
+    clusters <- cutree(tree, h = height)
+    cluster_sizes <- sort(tabulate(clusters), decreasing = TRUE)
+
+    # Compute the "cluteriness" score.
+
+    score <- 0.0
+    n <- length(data)
+
+    for (i in seq_along(cluster_sizes)) {
+        cluster_size <- cluster_sizes[i]
+
+        if (cluster_size >= 2) {
+            cluster_score <- cluster_size / n
+            score <- score + cluster_score / i
+        }
+    }
+
+    score
+}
+
 #' Process genes clustering their distance to telomeres.
 #'
 #' The return value will be a data.table with the following columns:
@@ -43,24 +74,11 @@ process_clustering <- function(distances, species_ids, gene_ids) {
             next
         }
 
-        clusters <- hclust(dist(data[, distance]))
+        score <- clusteriness(data[, distance])
-        clusters_cut <- cutree(clusters, h = 1000000)
-
-        # Find the largest cluster
-        cluster_indices <- unique(clusters_cut)
-        cluster_index <- cluster_indices[
-            which.max(tabulate(match(clusters_cut, cluster_indices)))
-        ]
-
-        cluster <- data[which(clusters_cut == cluster_index)]
 
         results[
             gene == gene_id,
-            `:=`(
+            clusteriness := score
-                cluster_length = cluster[, .N],
-                cluster_mean = mean(cluster[, distance]),
-                cluster_species = list(cluster[, species])
-            )
         ]
     }
 

init.R

@@ -90,8 +90,3 @@ results_replicative <- merge(
 
 setnames(results_all, "id", "gene")
 setnames(results_replicative, "id", "gene")
-
-# Order results by cluster length descendingly as a start.
-
-setorder(results_all, -cluster_length)
-setorder(results_replicative, -cluster_length)

scatter_plot.R

@@ -20,11 +20,6 @@ scatter_plot <- function(results, species, genes, distances) {
         by.x = "id", by.y = "gene"
     )
 
-    for (gene_id in genes[, id]) {
-        cluster_species <- unlist(results[gene == gene_id, cluster_species])
-        data[id == gene_id, in_cluster := species %in% cluster_species]
-    }
-
     ggplot(data) +
         scale_x_discrete(
             name = "Species",
@@ -42,17 +37,11 @@ scatter_plot <- function(results, species, genes, distances) {
             }
         ) +
         scale_color_discrete(name = "Gene") +
-        scale_shape_discrete(
-            name = "Part of cluster",
-            breaks = c(TRUE, FALSE),
-            labels = c("Yes", "No")
-        ) +
         geom_point(
             mapping = aes(
                 x = species,
                 y = distance / 1000000,
-                color = name,
+                color = name
-                shape = in_cluster
             ),
             size = 5
         ) +

server.R

@@ -17,36 +17,25 @@ server <- function(input, output) {
             results_replicative
         }
 
-        # Apply user defined filters.
-
-        results <- results[
-            cluster_length >= input$length &
-                cluster_mean >= input$range[1] * 1000000 &
-                cluster_mean <= input$range[2] * 1000000
-        ]
-
         # Compute scoring factors and the weighted score.
 
-        cluster_max <- results[, max(cluster_length)]
+        results[, score := input$clusteriness / 100 * clusteriness +
-        results[, cluster_score := cluster_length / cluster_max]
-
-        results[, score := input$clustering / 100 * cluster_score +
             input$correlation / 100 * r_mean]
 
         # Order the results based on their score. The resulting index will be
         # used as the "rank".
 
-        setorder(results, -score)
+        setorder(results, -score, na.last = TRUE)
     })
 
     output$genes <- renderDT({
         datatable(
-            results()[, .(.I, name, cluster_length, r_mean)],
+            results()[, .(.I, name, clusteriness, r_mean)],
             rownames = FALSE,
             colnames = c(
                 "Rank",
                 "Gene",
-                "Cluster length",
+                "Clusteriness",
                 "Correlation"
             ),
             style = "bootstrap"

ui.R

@@ -11,36 +11,21 @@ ui <- fluidPage(
                 "species",
                 "Species to include",
                 choices = list(
-                    "All qualified" = "all",
+                    "Replicatively aging" = "replicative",
-                    "Replicatively aging" = "replicative"
+                    "All qualified" = "all"
                 )
-            ),
-            sliderInput(
-                "range",
-                "Gene position (Mbp)",
-                min = 0,
-                max = 50,
-                value = c(0, 15),
-                step = 0.1
-            ),
-            sliderInput(
-                "length",
-                "Minimum cluster size",
-                min = 0,
-                max = 30,
-                value = 10
             )
         ),
         wellPanel(
             h3("Ranking"),
             sliderInput(
-                "clustering",
+                "clusteriness",
-                "Size of largest cluster",
+                "Clustering of genes",
                 post = "%",
                 min = 0,
                 max = 100,
                 step = 1,
-                value = 100
+                value = 50
             ),
             sliderInput(
                 "correlation",