diff --git a/NAMESPACE b/NAMESPACE
index 2c28ab7..86a9935 100644
--- a/NAMESPACE
+++ b/NAMESPACE
@@ -8,6 +8,7 @@ export(optimal_weights)
 export(plot_boxplot)
 export(plot_chromosomes)
 export(plot_positions)
+export(plot_rankings)
 export(plot_scores)
 export(preset)
 export(ranking)
diff --git a/R/plots.R b/R/plots.R
index 5733f6f..e32e56f 100644
--- a/R/plots.R
+++ b/R/plots.R
@@ -63,6 +63,79 @@ plot_positions <- function(species_ids,
 }
 
 
+#' Plot a side-by-side comparison of multiple rankings.
+#'
+#' Each ranking's scores will be shown as a vertical violin plot without any
+#' additional markings. The gene sets will be shown as markers on top of the
+#' density visualization.
+#'
+#' This function requires the package `plotly`.
+#'
+#' @param rankings A named list of rankings to display. The names will be shown
+#'   as labels in the plot.
+#' @param gene_sets A named list of vectors of gene IDs to highlight. The names
+#'   will be used to distinguish the sets and in the legend.
+#'
+#' @export
+plot_rankings <- function(rankings, gene_sets) {
+    if (!requireNamespace("plotly", quietly = TRUE)) {
+        stop("Please install \"plotly\" to use this function.")
+    }
+
+    plot <- plotly::plot_ly(colors = "Set2") |>
+        plotly::layout(
+            xaxis = list(
+                title = "Ranking",
+                tickvals = names(rankings)
+            ),
+            yaxis = list(title = "Score")
+        )
+
+    is_first <- TRUE
+
+    for (ranking_name in names(rankings)) {
+        ranking <- rankings[[ranking_name]]
+
+        data <- merge(
+            ranking,
+            geposan::genes,
+            by.x = "gene",
+            by.y = "id"
+        )
+
+        plot <- plot |> plotly::add_trace(
+            data = ranking,
+            x = ranking_name,
+            y = ~score,
+            color = "All genes",
+            type = "violin",
+            spanmode = "hard",
+            points = FALSE,
+            showlegend = is_first,
+            hoverinfo = "skip"
+        )
+
+        for (gene_set_name in names(gene_sets)) {
+            gene_set <- gene_sets[[gene_set_name]]
+
+            plot <- plot |> plotly::add_markers(
+                data = data[gene %chin% gene_set],
+                x = ranking_name,
+                y = ~score,
+                text = ~name,
+                color = gene_set_name,
+                showlegend = is_first,
+                marker = list(size = 20, opacity = 0.66)
+            )
+        }
+
+        is_first <- FALSE
+    }
+
+    plot
+}
+
+
 #' Plot a ranking as a scatter plot of scores.
 #'
 #' This function requires the package `plotly`.
diff --git a/man/plot_rankings.Rd b/man/plot_rankings.Rd
new file mode 100644
index 0000000..dae97fb
--- /dev/null
+++ b/man/plot_rankings.Rd
@@ -0,0 +1,23 @@
+% Generated by roxygen2: do not edit by hand
+% Please edit documentation in R/plots.R
+\name{plot_rankings}
+\alias{plot_rankings}
+\title{Plot a side-by-side comparison of multiple rankings.}
+\usage{
+plot_rankings(rankings, gene_sets)
+}
+\arguments{
+\item{rankings}{A named list of rankings to display. The names will be shown
+as labels in the plot.}
+
+\item{gene_sets}{A named list of vectors of gene IDs to highlight. The names
+will be used to distinguish the sets and in the legend.}
+}
+\description{
+Each ranking's scores will be shown as a vertical violin plot without any
+additional markings. The gene sets will be shown as markers on top of the
+density visualization.
+}
+\details{
+This function requires the package \code{plotly}.
+}
diff --git a/man/preset.Rd b/man/preset.Rd
index 1b5d969..4d2c420 100644
--- a/man/preset.Rd
+++ b/man/preset.Rd
@@ -5,7 +5,7 @@
 \title{Create a new preset.}
 \usage{
 preset(
-  methods = c("clusteriness", "correlation", "neural", "proximity"),
+  methods = c("clusteriness", "correlation", "neural", "adjacency", "proximity"),
   species_ids = NULL,
   gene_ids = NULL,
   reference_gene_ids = NULL,
@@ -40,14 +40,10 @@ Available methods are:
 \itemize{
 \item \code{clusteriness} How much the gene distances to the nearest telomere
 cluster across species.
-\item \code{clusteriness_positions} The same as \code{clusteriness} but using absolute
-gene positions instead of distances.
 \item \code{correlation} The mean correlation of gene distances to the nearest
 telomere across species.
-\item \code{correlation_positions} Correlation using position data.
-\item \code{neural} Assessment by neural network trained using distances.
-\item \code{neural_positions} Assessment by neural network trained using absolute
-position data.
+\item \code{neural} Assessment by neural network trained on the reference genes.
+\item \code{adjacency} Proximity to reference genes.
 \item \code{proximity} Mean proximity to telomeres.
 }