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analyze: Add optimization
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5 changed files with 63 additions and 32 deletions
22
R/analyze.R
22
R/analyze.R
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@ -9,9 +9,8 @@
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#' items:
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#' items:
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#' \describe{
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#' \describe{
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#' \item{`preset`}{The preset that was used.}
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#' \item{`preset`}{The preset that was used.}
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#' \item{`results`}{A [data.table] with one row for each gene identified by
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#' \item{`weights`}{The optimal weights for ranking the reference genes.}
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#' it's ID (`gene` column). The additional columns contain the resulting
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#' \item{`ranking`}{The optimal ranking created using the weights.}
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#' scores per method and are named after the method IDs.}
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#' }
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#' }
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#'
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#'
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#' @export
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#' @export
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@ -75,10 +74,25 @@ analyze <- function(preset, progress = NULL) {
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total_progress <- total_progress + 1 / method_count
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total_progress <- total_progress + 1 / method_count
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}
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}
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results <- structure(
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results,
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class = c("geposan_results", class(results))
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)
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weights <- optimal_weights(
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results,
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preset$methods,
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preset$reference_gene_ids,
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target = preset$optimization_target
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)
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ranking <- ranking(results, weights)
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structure(
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structure(
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list(
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list(
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preset = preset,
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preset = preset,
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results = results
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weights = weights,
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ranking = ranking
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),
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),
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class = "geposan_analysis"
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class = "geposan_analysis"
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)
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)
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21
R/preset.R
21
R/preset.R
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@ -21,10 +21,18 @@
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#' position data.
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#' position data.
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#' - `proximity` Mean proximity to telomeres.
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#' - `proximity` Mean proximity to telomeres.
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#'
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#'
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#' Available optimization targets are:
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#'
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#' - `mean` Mean rank of the reference genes.
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#' - `max` First rank of the reference genes.
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#' - `min` Last rank of the reference genes.
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#'
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#' @param methods Methods to apply.
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#' @param methods Methods to apply.
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#' @param species_ids IDs of species to include.
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#' @param species_ids IDs of species to include.
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#' @param gene_ids IDs of genes to screen.
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#' @param gene_ids IDs of genes to screen.
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#' @param reference_gene_ids IDs of reference genes to compare to.
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#' @param reference_gene_ids IDs of reference genes to compare to.
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#' @param optimization_target Parameter of the reference genes that the ranking
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#' should be optimized for.
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#'
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#'
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#' @return The preset to use with [analyze()].
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#' @return The preset to use with [analyze()].
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#'
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#'
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@ -40,7 +48,8 @@ preset <- function(methods = c(
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),
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),
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species_ids = NULL,
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species_ids = NULL,
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gene_ids = NULL,
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gene_ids = NULL,
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reference_gene_ids = NULL) {
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reference_gene_ids = NULL,
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optimization_target = "mean_rank") {
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# Count included species per gene.
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# Count included species per gene.
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genes_n_species <- geposan::distances[
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genes_n_species <- geposan::distances[
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species %chin% species_ids,
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species %chin% species_ids,
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@ -61,7 +70,8 @@ preset <- function(methods = c(
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methods = sort(methods),
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methods = sort(methods),
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species_ids = sort(species_ids),
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species_ids = sort(species_ids),
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gene_ids = sort(gene_ids_filtered),
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gene_ids = sort(gene_ids_filtered),
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reference_gene_ids = sort(reference_gene_ids)
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reference_gene_ids = sort(reference_gene_ids),
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optimization_target = optimization_target
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),
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),
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class = "geposan_preset"
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class = "geposan_preset"
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)
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)
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@ -87,9 +97,14 @@ print.geposan_preset <- function(x, ...) {
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))
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))
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cat(sprintf(
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cat(sprintf(
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"\n Comparison data: %i reference genes\n",
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"\n Comparison data: %i reference genes",
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length(x$reference_gene_ids)
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length(x$reference_gene_ids)
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))
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))
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cat(sprintf(
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"\n Optimization target: %s\n",
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x$optimization_target
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))
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invisible(x)
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invisible(x)
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}
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}
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34
R/ranking.R
34
R/ranking.R
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@ -13,11 +13,14 @@
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#'
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#'
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#' @export
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#' @export
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ranking <- function(analysis, weights) {
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ranking <- function(analysis, weights) {
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if (!"geposan_analysis" %chin% class(analysis)) {
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if ("geposan_analysis" %chin% class(analysis)) {
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ranking <- copy(analysis$ranking)
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} else if ("geposan_results" %chin% class(analysis)) {
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ranking <- copy(analysis)
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} else {
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stop("Invalid analyis. Use geposan::analyze().")
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stop("Invalid analyis. Use geposan::analyze().")
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}
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}
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ranking <- copy(analysis$results)
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ranking[, score := 0.0]
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ranking[, score := 0.0]
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for (method in names(weights)) {
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for (method in names(weights)) {
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@ -36,7 +39,7 @@ ranking <- function(analysis, weights) {
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structure(
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structure(
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ranking,
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ranking,
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class = c("geposan_ranking", "geposan_analysis", class(ranking))
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class = c("geposan_ranking", "geposan_results", class(ranking))
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)
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)
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}
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}
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@ -57,24 +60,13 @@ ranking <- function(analysis, weights) {
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#' @export
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#' @export
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optimal_weights <- function(analysis, methods, reference_gene_ids,
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optimal_weights <- function(analysis, methods, reference_gene_ids,
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target = "mean") {
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target = "mean") {
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if (!"geposan_analysis" %chin% class(analysis)) {
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if (!any(c("geposan_analysis", "geposan_results") %chin% class(analysis))) {
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stop("Invalid analyis. Use geposan::analyze().")
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stop("Invalid analyis. Use geposan::analyze().")
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}
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}
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# Create the named list from the factors vector.
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weights <- function(factors) {
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result <- NULL
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mapply(function(method, factor) {
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result[[method]] <<- factor
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}, methods, factors)
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result
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}
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# Compute the target rank of the reference genes when applying the weights.
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# Compute the target rank of the reference genes when applying the weights.
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target_rank <- function(factors) {
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target_rank <- function(factors) {
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data <- ranking(analysis, weights(factors))
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data <- ranking(analysis, as.list(factors))
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result <- data[gene %chin% reference_gene_ids, if (target == "min") {
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result <- data[gene %chin% reference_gene_ids, if (target == "min") {
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min(rank)
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min(rank)
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@ -91,10 +83,10 @@ optimal_weights <- function(analysis, methods, reference_gene_ids,
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}
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}
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}
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}
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factors <- stats::optim(
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initial_factors <- rep(1.0, length(methods))
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rep(0.0, length(methods)),
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names(initial_factors) <- methods
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target_rank
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)$par
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weights(factors / max(abs(factors)))
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optimal_factors <- stats::optim(initial_factors, target_rank)$par
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as.list(optimal_factors / max(abs(optimal_factors)))
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}
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}
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@ -18,9 +18,8 @@ An object containing the results of the analysis with the following
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items:
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items:
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\describe{
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\describe{
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\item{\code{preset}}{The preset that was used.}
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\item{\code{preset}}{The preset that was used.}
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\item{\code{results}}{A \link{data.table} with one row for each gene identified by
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\item{\code{weights}}{The optimal weights for ranking the reference genes.}
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it's ID (\code{gene} column). The additional columns contain the resulting
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\item{\code{ranking}}{The optimal ranking created using the weights.}
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scores per method and are named after the method IDs.}
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}
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}
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}
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}
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\description{
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\description{
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@ -9,7 +9,8 @@ preset(
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"correlation_positions", "neural", "neural_positions", "proximity"),
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"correlation_positions", "neural", "neural_positions", "proximity"),
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species_ids = NULL,
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species_ids = NULL,
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gene_ids = NULL,
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gene_ids = NULL,
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reference_gene_ids = NULL
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reference_gene_ids = NULL,
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optimization_target = "mean_rank"
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)
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)
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}
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}
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\arguments{
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\arguments{
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@ -20,6 +21,9 @@ preset(
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\item{gene_ids}{IDs of genes to screen.}
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\item{gene_ids}{IDs of genes to screen.}
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\item{reference_gene_ids}{IDs of reference genes to compare to.}
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\item{reference_gene_ids}{IDs of reference genes to compare to.}
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\item{optimization_target}{Parameter of the reference genes that the ranking
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should be optimized for.}
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}
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}
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\value{
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\value{
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The preset to use with \code{\link[=analyze]{analyze()}}.
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The preset to use with \code{\link[=analyze]{analyze()}}.
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@ -47,4 +51,11 @@ telomere across species.
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position data.
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position data.
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\item \code{proximity} Mean proximity to telomeres.
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\item \code{proximity} Mean proximity to telomeres.
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}
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}
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Available optimization targets are:
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\itemize{
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\item \code{mean} Mean rank of the reference genes.
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\item \code{max} First rank of the reference genes.
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\item \code{min} Last rank of the reference genes.
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}
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}
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}
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