Add new method adjacency

This commit is contained in:
Elias Projahn 2021-11-25 20:55:11 +01:00
parent b1eff374b3
commit 88b1a9ab6a
3 changed files with 85 additions and 6 deletions

81
R/adjacency.R Normal file
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@ -0,0 +1,81 @@
# Score genes based on their proximity to the reference genes.
#
# This method finds the distance value with the maximum density for each gene
# (i.e. the mode of its estimated distribution). Genes are scored by comparing
# those distance values with the values of the reference genes.
adjacency <- function(preset, progress = NULL) {
species_ids <- preset$species_ids
gene_ids <- preset$gene_ids
reference_gene_ids <- preset$reference_gene_ids
cached("adjacency", c(species_ids, gene_ids, reference_gene_ids), {
# Get the virtual distance value with the highest density.
compute_densest_distance <- function(distances) {
if (length(distances <= 2)) {
mean(distances)
} else {
d <- stats::density(distances)
d$x[which.max(d$y)]
}
}
# Filter distances by species and gene and find the distance with the
# highest density of values for each gene.
data <- geposan::distances[
species %chin% species_ids & gene %chin% gene_ids,
.(densest_distance = compute_densest_distance(distance)),
by = gene
]
# Compute the absolute value of the difference between the provided
# densest distance value in comparison to the mean of the densest
# distances of the comparison genes.
compute_difference <- function(densest_distance, comparison_ids) {
# Get the mean of the densest distances of the reference genes.
mean_densest_distance <- data[
gene %chin% comparison_ids,
mean(densest_distance)
]
abs(densest_distance - mean_densest_distance)
}
# Compute the differences to the reference genes.
data[
!gene %chin% reference_gene_ids,
difference := compute_difference(
densest_distance,
reference_gene_ids
)
]
if (!is.null(progress)) {
progress(0.5)
}
# Exclude the reference gene itself when computing its difference.
data[
gene %chin% reference_gene_ids,
difference := compute_difference(
densest_distance,
reference_gene_ids[reference_gene_ids != gene]
),
by = gene
]
# Compute the final score by normalizing the difference.
data[, score := 1 - difference / max(difference)]
if (!is.null(progress)) {
progress(1.0)
}
structure(
list(
results = data[, .(gene, score)],
details = data
),
class = "geposan_method_results"
)
})
}

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@ -34,6 +34,7 @@ analyze <- function(preset, progress = NULL) {
"clusteriness" = clusteriness,
"correlation" = correlation,
"neural" = neural,
"adjacency" = adjacency,
"proximity" = proximity
)

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@ -11,14 +11,10 @@
#'
#' - `clusteriness` How much the gene distances to the nearest telomere
#' cluster across species.
#' - `clusteriness_positions` The same as `clusteriness` but using absolute
#' gene positions instead of distances.
#' - `correlation` The mean correlation of gene distances to the nearest
#' telomere across species.
#' - `correlation_positions` Correlation using position data.
#' - `neural` Assessment by neural network trained using distances.
#' - `neural_positions` Assessment by neural network trained using absolute
#' position data.
#' - `neural` Assessment by neural network trained on the reference genes.
#' - `adjacency` Proximity to reference genes.
#' - `proximity` Mean proximity to telomeres.
#'
#' Available optimization targets are:
@ -42,6 +38,7 @@ preset <- function(methods = c(
"clusteriness",
"correlation",
"neural",
"adjacency",
"proximity"
),
species_ids = NULL,