library(data.table) #' 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 possible values (`n`). The return value is a final #' score between zero and one. Lower ranking clusters contribute less to this #' score. clusteriness <- function(data, n, height = 1000000) { # Return a score of 0.0 if there is just one or no value at all. if (length(data) < 2) { return(0.0) } # 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 "clusteriness" score. score <- 0.0 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: #' #' - `gene` Gene ID of the processed gene. #' - `clusteriness` Score quantidying the gene's clusters. #' #' @param distances Gene distance data to use. #' @param species_ids IDs of species to include in the analysis. #' @param gene_ids Genes to include in the computation. process_clustering <- function(distances, species_ids, gene_ids) { results <- data.table(gene = gene_ids) species_count <- length(species) # Prefilter the input data by species. distances <- distances[species %chin% species_ids] # Add an index for quickly accessing data per gene. setkey(distances, gene) #' Perform the cluster analysis for one gene. compute <- function(gene_id) { clusteriness(distances[gene_id, distance], species_count) } results[, clusteriness := compute(gene), by = 1:nrow(results)] }