Last updated: 2026-03-20
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Knit directory: DXR_continue/
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library(tidyverse)
library(GenomicRanges)
library(plyranges)
library(genomation)
library(readr)
library(rtracklayer)
library(stringr)
library(ggrepel)
library(DT)
library(data.table)
library(circlize)
library(ComplexHeatmap)
repeatmasker <- read_delim("data/Other_paper_data/repeatmasker_20250911.txt",
delim = "\t", escape_double = FALSE,
trim_ws = TRUE)
colnames(repeatmasker)
[1] "#bin" "swScore" "milliDiv" "milliDel" "milliIns" "genoName"
[7] "genoStart" "genoEnd" "genoLeft" "strand" "repName" "repClass"
[13] "repFamily" "repStart" "repEnd" "repLeft" "id"
autosomes <- paste0("chr", 1:22)
repeatmasker_clean <- repeatmasker %>% mutate(
strand = ifelse(strand == "C", "-", "+")
) %>%
mutate(
start = genoStart + 1,
end = genoEnd)%>%
mutate(repFamily= str_remove(repFamily, "\\?$")) %>%
dplyr::filter(genoName %in% autosomes) %>%
mutate(RM_id=paste0(genoName,":",start,"-",end,":",id))
rpt_split <- split(repeatmasker_clean, repeatmasker_clean$repClass)
rpt_split_gr_list <- lapply(rpt_split, function(df) {
GRanges(
seqnames = df$genoName,
ranges = IRanges(start = df$start, end = df$end),
strand = df$strand,
repName = df$repName,
repClass = df$repClass,
repFamily = df$repFamily,
swScore = df$swScore,
milliDiv = df$milliDiv,
milliDel = df$milliDel,
milliIns = df$milliIns,
RM_id = df$RM_id
)
})
matrix_file <- "C:/Users/renee/Other_projects_data/DXR_data/computeMatrix_output/four_histone/matrix_MER61E_ERV1_LTR.gz"
cm <- fread(cmd = paste("gzip -dc", matrix_file), skip = 1)
dim(cm)
[1] 261 21606
head(cm[,1:10])
V1 V2 V3 V4 V5 V6 V7
<char> <int> <int> <char> <num> <char> <num>
1: chr1 63032707 63032840 chr1:63032708-63032840:1 0 + 0.000000
2: chr1 63033079 63033512 chr1:63033080-63033512:1 0 + 0.000000
3: chr1 69055251 69055817 chr1:69055252-69055817:1 0 + 0.000000
4: chr1 71345730 71345939 chr1:71345731-71345939:1 0 + 0.000000
5: chr1 72000824 72001353 chr1:72000825-72001353:1 0 + 0.000000
6: chr1 76040192 76040658 chr1:76040193-76040658:1 0 + 0.014045
V8 V9 V10
<num> <num> <num>
1: 0.000000 0.000000 0.000000
2: 0.000000 0.025281 0.028090
3: 0.000000 0.000000 0.000000
4: 0.000000 0.000000 0.000000
5: 0.000000 0.000000 0.000000
6: 0.014045 0.014045 0.014045
sample_names <- c(
"H3K27ac_DOX_144R_merged","H3K27ac_DOX_24R_merged","H3K27ac_DOX_24T_merged",
"H3K27ac_VEH_144R_merged","H3K27ac_VEH_24R_merged","H3K27ac_VEH_24T_merged",
"H3K27me3_DOX_144R_merged","H3K27me3_DOX_24R_merged","H3K27me3_DOX_24T_merged",
"H3K27me3_VEH_144R_merged","H3K27me3_VEH_24R_merged","H3K27me3_VEH_24T_merged",
"H3K36me3_DOX_144R_merged","H3K36me3_DOX_24R_merged","H3K36me3_DOX_24T_merged",
"H3K36me3_VEH_144R_merged","H3K36me3_VEH_24R_merged","H3K36me3_VEH_24T_merged",
"H3K9me3_DOX_144R_merged","H3K9me3_DOX_24R_merged","H3K9me3_DOX_24T_merged",
"H3K9me3_VEH_144R_merged","H3K9me3_VEH_24R_merged","H3K9me3_VEH_24T_merged"
)
meta <- meta <- cm[,1:6]
bins <- 900
signal_list <- lapply(1:length(sample_names), function(i) {
start <- 6 + (i-1)*bins + 1
end <- 6 + i*bins
as.matrix(cm[,start:end])
})
names(signal_list) <- sample_names
profiles <- lapply(signal_list, colMeans)
profiles_df <- do.call(cbind, profiles)
profiles_df <- as.data.frame(profiles_df)
profiles_df$bin <- 1:nrow(profiles_df)
long <- pivot_longer(
profiles_df,
-bin,
names_to="sample",
values_to="signal"
) %>%
separate(sample, into=c("mark","condition","time"), sep="_", remove = FALSE)
ggplot(long, aes(bin, signal, color=sample)) +
geom_line(size=1) +
theme_bw() +
labs(
x="Scaled TE region",
y="ChIP signal"
)+
facet_wrap(~time)

| Version | Author | Date |
|---|---|---|
| 8fe7ed0 | reneeisnowhere | 2026-03-19 |
long$condition <- ifelse(grepl("DOX", long$sample),"DOX","VEH")
long$mark <- sub("_.*","",long$sample)
ggplot(long, aes(bin, signal, color=time)) +
geom_line(size=1) +
facet_grid(mark ~ condition) +
theme_bw()+
geom_vline(xintercept=c(200,700), linetype="dashed")+
ggtitle("signal across all LTR:ERV1:MER61E")

| Version | Author | Date |
|---|---|---|
| 8fe7ed0 | reneeisnowhere | 2026-03-19 |
plot_deeptools_matrix <- function(matrix_file, bins = 900){
library(data.table)
library(dplyr)
library(tidyr)
library(ggplot2)
library(stringr)
message("Processing: ", matrix_file)
cm <- fread(cmd = paste("gzip -dc", matrix_file), skip = 1)
sample_names <- c(
"H3K27ac_DOX_144R_merged","H3K27ac_DOX_24R_merged","H3K27ac_DOX_24T_merged",
"H3K27ac_VEH_144R_merged","H3K27ac_VEH_24R_merged","H3K27ac_VEH_24T_merged",
"H3K27me3_DOX_144R_merged","H3K27me3_DOX_24R_merged","H3K27me3_DOX_24T_merged",
"H3K27me3_VEH_144R_merged","H3K27me3_VEH_24R_merged","H3K27me3_VEH_24T_merged",
"H3K36me3_DOX_144R_merged","H3K36me3_DOX_24R_merged","H3K36me3_DOX_24T_merged",
"H3K36me3_VEH_144R_merged","H3K36me3_VEH_24R_merged","H3K36me3_VEH_24T_merged",
"H3K9me3_DOX_144R_merged","H3K9me3_DOX_24R_merged","H3K9me3_DOX_24T_merged",
"H3K9me3_VEH_144R_merged","H3K9me3_VEH_24R_merged","H3K9me3_VEH_24T_merged"
)
signal_list <- lapply(seq_along(sample_names), function(i){
start <- 6 + (i-1)*bins + 1
end <- 6 + i*bins
as.matrix(cm[,start:end])
})
names(signal_list) <- sample_names
profiles <- lapply(signal_list, colMeans)
profiles_df <- do.call(cbind, profiles) |> as.data.frame()
profiles_df$bin <- 1:nrow(profiles_df)
long <- profiles_df |>
pivot_longer(-bin, names_to="sample", values_to="signal") |>
separate(sample, into=c("mark","condition","time","extra"), sep="_") |>
mutate(sample = paste(mark,condition,time,sep="_"))
# remove unwanted marks
long <- long |> filter(!mark %in% c("H3K27me3","H3K36me3"))
title <- tools::file_path_sans_ext(basename(matrix_file))
p <- ggplot(long, aes(bin, signal, color=time)) +
geom_line(linewidth=1) +
facet_grid(mark ~ condition) +
geom_vline(xintercept=c(200,700), linetype="dashed") +
theme_bw() +
ggtitle(title)
return(p)
}
plot_deeptools_matrix("C:/Users/renee/Other_projects_data/DXR_data/computeMatrix_output/four_histone/matrix_MER61E_ERV1_LTR.gz")

| Version | Author | Date |
|---|---|---|
| 8fe7ed0 | reneeisnowhere | 2026-03-19 |
matrix_dir <- "C:/Users/renee/Other_projects_data/DXR_data/computeMatrix_output/four_histone/"
matrix_files <- list.files(
matrix_dir,
pattern="matrix_.*gz$",
full.names=TRUE
)
plots <- lapply(matrix_files, plot_deeptools_matrix)
plots
[[1]]

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[[2]]

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meta <- cm[,1:6]
signal <- cm[,7:ncol(cm)]
bins <- 900
sample_index <- 2
start <- (sample_index - 1) * bins + 1
end <- sample_index * bins
mat <- as.matrix(signal[,start:end])
### sorting rows by signal
row_order <- order(rowMeans(mat), decreasing = TRUE)
mat <- mat[row_order,]
### Color scale
col_fun <- colorRamp2(
c(0, 0.5, 2),
c("white", "orange", "red")
)
#### color scale for centered data
# col_fun <- colorRamp2(
# c(-2, 0, 2),
# c("blue", "white", "red")
# )
region <- c(
rep("Upstream",200),
rep("TE",500),
rep("Downstream",200)
)
Heatmap(
mat,
col = col_fun,
name = "signal",
show_row_names = FALSE,
show_column_names = FALSE,
column_split = region,
cluster_columns = FALSE
)

| Version | Author | Date |
|---|---|---|
| 8fe7ed0 | reneeisnowhere | 2026-03-19 |
plot_2hist_deeptools_matrix <- function(matrix_file, bins = 400){
library(data.table)
library(dplyr)
library(tidyr)
library(ggplot2)
library(stringr)
message("Processing: ", matrix_file)
cm <- fread(cmd = paste("gzip -dc", matrix_file), skip = 1)
sample_names <- c(
"H3K27ac_DOX_144R_merged","H3K27ac_DOX_24R_merged","H3K27ac_DOX_24T_merged",
"H3K27ac_VEH_144R_merged","H3K27ac_VEH_24R_merged","H3K27ac_VEH_24T_merged",
"H3K9me3_DOX_144R_merged","H3K9me3_DOX_24R_merged","H3K9me3_DOX_24T_merged",
"H3K9me3_VEH_144R_merged","H3K9me3_VEH_24R_merged","H3K9me3_VEH_24T_merged"
)
signal_list <- lapply(seq_along(sample_names), function(i){
start <- 6 + (i-1)*bins + 1
end <- 6 + i*bins
as.matrix(cm[,start:end])
})
names(signal_list) <- sample_names
profiles <- lapply(signal_list, colMeans)
profiles_df <- do.call(cbind, profiles) |> as.data.frame()
profiles_df$pos_kb <- seq(-2, 2, length.out = nrow(profiles_df))
long <- profiles_df |>
pivot_longer(-pos_kb, names_to="sample", values_to="signal") |>
separate(sample, into=c("mark","condition","time","extra"), sep="_") |>
mutate(sample = paste(mark,condition,time,sep="_"))
# # remove unwanted marks
# long <- long |> filter(!mark %in% c("H3K27me3","H3K36me3"))
title <- tools::file_path_sans_ext(basename(matrix_file))
p <- ggplot(long, aes(pos_kb, signal, color=time)) +
geom_line(linewidth=1) +
facet_grid(mark ~ condition) +
geom_vline(xintercept = 0, linetype="dashed")+
# geom_smooth(se=FALSE, method = "loess")+
theme_bw() +
ggtitle(title)
return(p)
}
plot_2hist_deeptools_matrix("C:/Users/renee/Other_projects_data/DXR_data/computeMatrix_output_centered2histone/matcenter_MER61E_ERV1_LTR.gz", bins=400)

| Version | Author | Date |
|---|---|---|
| 8fe7ed0 | reneeisnowhere | 2026-03-19 |
matrix_dir_cent <- "C:/Users/renee/Other_projects_data/DXR_data/computeMatrix_output_centered2histone/"
matrix_files_cent <- list.files(
matrix_dir_cent,
pattern="matcenter_.*gz$",
full.names=TRUE
)
plots_cent <- lapply(matrix_files_cent, plot_2hist_deeptools_matrix)
for (p in plots_cent) {
print(p)
}

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col_fun <- colorRamp2(
c(-2, 0, 2),
c("blue", "white", "red")
)
bins=400
cm <- fread(cmd = paste("gzip -dc", "C:/Users/renee/Other_projects_data/DXR_data/computeMatrix_output_centered2histone/matcenter_MER61E_ERV1_LTR.gz"), skip = 1)
sample_names <- c(
"H3K27ac_DOX_144R_merged","H3K27ac_DOX_24R_merged","H3K27ac_DOX_24T_merged",
"H3K27ac_VEH_144R_merged","H3K27ac_VEH_24R_merged","H3K27ac_VEH_24T_merged",
"H3K9me3_DOX_144R_merged","H3K9me3_DOX_24R_merged","H3K9me3_DOX_24T_merged",
"H3K9me3_VEH_144R_merged","H3K9me3_VEH_24R_merged","H3K9me3_VEH_24T_merged"
)
##extract per-sample matrices
signal_list <- lapply(seq_along(sample_names), function(i){
start <- 6 + (i-1)*bins + 1
end <- 6 + i*bins
as.matrix(cm[,start:end])
})
ref_mat <-signal_list[[3]]
row_order <- order(rowMeans(ref_mat), decreasing = TRUE)
names(signal_list) <- sample_names
for (i in seq_along(signal_list)) {
#scaling
mat <- signal_list[[i]]
mat_scaled <- t(scale(t(mat)))
### sorting rows by signal
# row_order <- order(rowMeans(mat), decreasing = TRUE)
mat_scaled <- mat_scaled[row_order,]
mat_scaled[is.na(mat_scaled)] <- 0
region <- ifelse(seq_len(ncol(mat_scaled)) <= ncol(mat_scaled)/2, "Upstream", "Downstream")
Heatmap(
mat_scaled,
col = col_fun,
name = "signal",
show_row_names = FALSE,
show_column_names = FALSE,
cluster_rows = FALSE, # Important to preserve row_order
cluster_columns = FALSE,
column_split = region,
column_title = names(signal_list)[i])
}
plot_deeptools_heatmaps <- function(matrix_file,
sample_order_H3K27ac = c("H3K27ac_DOX_24T_merged",
"H3K27ac_DOX_24R_merged",
"H3K27ac_DOX_144R_merged",
"H3K27ac_VEH_24T_merged",
"H3K27ac_VEH_24R_merged",
"H3K27ac_VEH_144R_merged"),
sample_order_H3K9me3 = c("H3K9me3_DOX_24T_merged",
"H3K9me3_DOX_24R_merged",
"H3K9me3_DOX_144R_merged",
"H3K9me3_VEH_24T_merged",
"H3K9me3_VEH_24R_merged",
"H3K9me3_VEH_144R_merged"),
bins = 400,
reference_sample = "H3K27ac_DOX_24T_merged") {
# Read the matrix
cm <- fread(cmd = paste("gzip -dc", matrix_file), skip = 1)
# Full list of samples
sample_names <- c(
"H3K27ac_DOX_144R_merged","H3K27ac_DOX_24R_merged","H3K27ac_DOX_24T_merged",
"H3K27ac_VEH_144R_merged","H3K27ac_VEH_24R_merged","H3K27ac_VEH_24T_merged",
"H3K9me3_DOX_144R_merged","H3K9me3_DOX_24R_merged","H3K9me3_DOX_24T_merged",
"H3K9me3_VEH_144R_merged","H3K9me3_VEH_24R_merged","H3K9me3_VEH_24T_merged"
)
# Extract per-sample matrices
signal_list <- lapply(seq_along(sample_names), function(i){
start <- 6 + (i-1)*bins + 1
end <- 6 + i*bins
as.matrix(cm[, start:end])
})
names(signal_list) <- sample_names
file_part <- str_extract(basename(matrix_file), "(?<=matcenter_).*?(?=_ERV1_LTR)")
# Determine row order from reference sample
ref_mat <- signal_list[[which(names(signal_list) == reference_sample)]]
row_order <- order(rowMeans(ref_mat), decreasing = TRUE)
# Color function
col_fun <- colorRamp2(c(-2, 0, 2), c("blue", "white", "red"))
## Helper function to scale and reorder matrix
prepare_mat <- function(mat) {
mat_scaled <- t(scale(t(mat))) # row scaling
mat_scaled[is.na(mat_scaled)] <- 0
mat_scaled[row_order, , drop = FALSE] # apply reference row order
}
# Function to create heatmaps for a given sample vector
plot_heatmap_group <- function(sample_vector, group_name) {
ht_list <- NULL
for (s in sample_vector) {
mat <- prepare_mat(signal_list[[s]])
region <- ifelse(seq_len(ncol(mat)) <= ncol(mat)/2, "Upstream", "Downstream")
# Shorten the column title
short_title <- str_extract(s, "(DOX|VEH)_\\d+[RT]") # keeps "DOX_24T" etc.
short_title <- str_replace(short_title, "_merged", "")
ht <- Heatmap(mat,
col = col_fun,
name = "signal",
show_row_names = FALSE,
show_column_names = FALSE,
cluster_rows = FALSE,
cluster_columns = FALSE,
# column_split = region,
column_title = short_title)
if (is.null(ht_list)) {
ht_list <- ht
} else {
ht_list <- ht_list + ht
}
}
# Draw all heatmaps with a master title
draw(ht_list, heatmap_legend_side = "right", column_title = paste0(group_name," - ",file_part))
}
# Plot H3K27ac group
plot_heatmap_group(sample_order_H3K27ac, "H3K27ac")
# Plot H3K9me3 group
plot_heatmap_group(sample_order_H3K9me3, "H3K9me3")
}
plot_deeptools_heatmaps("C:/Users/renee/Other_projects_data/DXR_data/computeMatrix_output_centered2histone/matcenter_MER61E_ERV1_LTR.gz")

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for (f in matrix_files_cent) {
plot_deeptools_heatmaps(f) # plots automatically
}

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plot_switching_TEs <- function(matrix_file,
bins = 400,
fc_threshold_ac = 0.01,
fc_threshold_me3 = -0.5) {
# -----------------------------
# 1️⃣ Load matrix
# -----------------------------
cm <- fread(cmd = paste("gzip -dc", matrix_file), skip = 1)
sample_names <- c(
"H3K27ac_DOX_144R_merged","H3K27ac_DOX_24R_merged","H3K27ac_DOX_24T_merged",
"H3K27ac_VEH_144R_merged","H3K27ac_VEH_24R_merged","H3K27ac_VEH_24T_merged",
"H3K9me3_DOX_144R_merged","H3K9me3_DOX_24R_merged","H3K9me3_DOX_24T_merged",
"H3K9me3_VEH_144R_merged","H3K9me3_VEH_24R_merged","H3K9me3_VEH_24T_merged"
)
# -----------------------------
# 2️⃣ Extract matrices
# -----------------------------
signal_list <- lapply(seq_along(sample_names), function(i){
start <- 6 + (i-1)*bins + 1
end <- 6 + i*bins
as.matrix(cm[, start:end])
})
names(signal_list) <- sample_names
# -----------------------------
# 3️⃣ Compute average signal across bins for each mark & condition
# -----------------------------
avg_signal <- function(mark, cond) {
rows <- grep(paste0(mark,"_",cond), names(signal_list))
# Average across replicates
Reduce("+", signal_list[rows]) / length(rows)
}
H3K27ac_DOX_avg <- avg_signal("H3K27ac", "DOX")
H3K27ac_VEH_avg <- avg_signal("H3K27ac", "VEH")
H3K9me3_DOX_avg <- avg_signal("H3K9me3", "DOX")
H3K9me3_VEH_avg <- avg_signal("H3K9me3", "VEH")
# -----------------------------
# 4️⃣ Compute log2 fold-changes
# -----------------------------
H3K27ac_log2fc <- log2((H3K27ac_DOX_avg + 1) / (H3K27ac_VEH_avg + 1))
H3K9me3_log2fc <- log2((H3K9me3_DOX_avg + 1) / (H3K9me3_VEH_avg + 1))
# -----------------------------
# 5️⃣ Identify switching TEs
# -----------------------------
switching_rows <- which(H3K27ac_log2fc > fc_threshold_ac &
H3K9me3_log2fc < fc_threshold_me3)
if(length(switching_rows) == 0) {
message("No switching TEs found with these thresholds.")
return(NULL)
}
# -----------------------------
# 6️⃣ Prepare matrices for plotting
# -----------------------------
prepare_mat <- function(mat, rows) {
mat_sub <- mat[rows, , drop = FALSE]
mat_scaled <- t(scale(t(mat_sub)))
mat_scaled[is.na(mat_scaled)] <- 0
mat_scaled
}
# Reference row order: H3K27ac DOX 24T
ref_mat <- signal_list[["H3K27ac_DOX_24T_merged"]][switching_rows, ]
row_order <- order(rowMeans(ref_mat), decreasing = TRUE)
# Function to make heatmaps for a given mark
make_heatmap <- function(mark, samples) {
ht_list <- NULL
for(s in samples) {
mat_scaled <- prepare_mat(signal_list[[s]], switching_rows)
mat_scaled <- mat_scaled[row_order, ]
short_title <- str_extract(s, "(DOX|VEH)_\\d+[RT]")
ht <- Heatmap(mat_scaled,
col = colorRamp2(c(-2,0,2), c("blue","white","red")),
name = "signal",
show_row_names = FALSE,
show_column_names = FALSE,
cluster_rows = FALSE,
cluster_columns = FALSE,
column_title = short_title)
ht_list <- if(is.null(ht_list)) ht else ht_list + ht
}
ht_list
}
# Define sample order for plotting
H3K27ac_samples <- c("H3K27ac_DOX_24T_merged","H3K27ac_DOX_24R_merged","H3K27ac_DOX_144R_merged",
"H3K27ac_VEH_24T_merged","H3K27ac_VEH_24R_merged","H3K27ac_VEH_144R_merged")
H3K9me3_samples <- c("H3K9me3_DOX_24T_merged","H3K9me3_DOX_24R_merged","H3K9me3_DOX_144R_merged",
"H3K9me3_VEH_24T_merged","H3K9me3_VEH_24R_merged","H3K9me3_VEH_144R_merged")
ht_H3K27ac <- make_heatmap("H3K27ac", H3K27ac_samples)
ht_H3K9me3 <- make_heatmap("H3K9me3", H3K9me3_samples)
# -----------------------------
# 7️⃣ Extract file part for master title
# -----------------------------
file_part <- str_extract(basename(matrix_file), "(?<=matcenter_).*?(?=_ERV1_LTR)")
draw(ht_H3K27ac, heatmap_legend_side = "right", column_title = paste0("H3K27ac - ", file_part))
draw(ht_H3K9me3, heatmap_legend_side = "right", column_title = paste0("H3K9me3 - ", file_part))
return(list(H3K27ac = ht_H3K27ac, H3K9me3 = ht_H3K9me3, switching_rows = switching_rows))
}
result <- plot_switching_TEs(
"C:/Users/renee/Other_projects_data/DXR_data/computeMatrix_output_centered2histone/matcenter_MER61E_ERV1_LTR.gz")
#
##debug
matrix_file <- ("C:/Users/renee/Other_projects_data/DXR_data/computeMatrix_output_centered2histone/matcenter_MER61E_ERV1_LTR.gz")
bins <- 400
H3K27ac_DOX_24T <- rowMeans(signal_list[["H3K27ac_DOX_24T_merged"]])
H3K27ac_VEH_24T <- rowMeans(signal_list[["H3K27ac_VEH_24T_merged"]])
H3K9me3_DOX_24T <- rowMeans(signal_list[["H3K9me3_DOX_24T_merged"]])
H3K9me3_VEH_24T <- rowMeans(signal_list[["H3K9me3_VEH_24T_merged"]])
summary(H3K27ac_DOX_24T)
summary(H3K27ac_VEH_24T)
summary(H3K9me3_DOX_24T)
summary(H3K9me3_H3K9me3_VEH_24TVEH_144R)
H3K27ac_log2fc_24T <- log2((H3K27ac_DOX_24T + 1) / (H3K27ac_VEH_24T + 1))
H3K9me3_log2fc_24T <- log2((H3K9me3_DOX_24T + 1) / (H3K9me3_VEH_24T + 1))
summary(H3K27ac_log2fc_24T)
summary(H3K9me3_log2fc_24T)
fc_threshold_ac <- 0.01
fc_threshold_me3 <- 0
switching_rows <- which(
H3K27ac_log2fc_24T > fc_threshold_ac &
H3K9me3_log2fc_24T <= fc_threshold_me3)
mat_H3K27ac_24T <- signal_list[["H3K27ac_DOX_24T_merged"]][switching_rows, ]
mat_H3K9me3_24T <- signal_list[["H3K9me3_DOX_24T_merged"]][switching_rows, ]
row_order <- order(rowMeans(mat_H3K27ac_24T), decreasing = TRUE)
mat_H3K27ac_24T <- mat_H3K27ac_24T[row_order, ]
mat_H3K9me3_24T <- mat_H3K9me3_24T[row_order, ]
bed_names <- cm[switching_rows, 4] # column 4 = name
test <- rpt_split$LTR
test %>%
dplyr::filter(RM_id %in% bed_names$V4)
H3K27ac_summit_ols %>% dplyr::filter(ID %in%bed_names$V4)
sessionInfo()
R version 4.4.2 (2024-10-31 ucrt)
Platform: x86_64-w64-mingw32/x64
Running under: Windows 11 x64 (build 26200)
Matrix products: default
locale:
[1] LC_COLLATE=English_United States.utf8
[2] LC_CTYPE=English_United States.utf8
[3] LC_MONETARY=English_United States.utf8
[4] LC_NUMERIC=C
[5] LC_TIME=English_United States.utf8
time zone: America/Chicago
tzcode source: internal
attached base packages:
[1] grid stats4 stats graphics grDevices utils datasets
[8] methods base
other attached packages:
[1] ComplexHeatmap_2.22.0 circlize_0.4.16 data.table_1.17.8
[4] DT_0.33 ggrepel_0.9.6 rtracklayer_1.66.0
[7] genomation_1.38.0 plyranges_1.26.0 GenomicRanges_1.58.0
[10] GenomeInfoDb_1.42.3 IRanges_2.40.1 S4Vectors_0.44.0
[13] BiocGenerics_0.52.0 lubridate_1.9.4 forcats_1.0.0
[16] stringr_1.5.1 dplyr_1.1.4 purrr_1.1.0
[19] readr_2.1.5 tidyr_1.3.1 tibble_3.3.0
[22] ggplot2_3.5.2 tidyverse_2.0.0 workflowr_1.7.1
loaded via a namespace (and not attached):
[1] bitops_1.0-9 rlang_1.1.6
[3] magrittr_2.0.3 clue_0.3-66
[5] GetoptLong_1.0.5 git2r_0.36.2
[7] gridBase_0.4-7 matrixStats_1.5.0
[9] compiler_4.4.2 getPass_0.2-4
[11] png_0.1-8 callr_3.7.6
[13] vctrs_0.6.5 reshape2_1.4.4
[15] shape_1.4.6.1 pkgconfig_2.0.3
[17] crayon_1.5.3 fastmap_1.2.0
[19] magick_2.8.7 XVector_0.46.0
[21] labeling_0.4.3 Rsamtools_2.22.0
[23] promises_1.3.3 rmarkdown_2.29
[25] tzdb_0.5.0 UCSC.utils_1.2.0
[27] ps_1.9.1 bit_4.6.0
[29] xfun_0.52 zlibbioc_1.52.0
[31] cachem_1.1.0 jsonlite_2.0.0
[33] later_1.4.2 DelayedArray_0.32.0
[35] BiocParallel_1.40.2 cluster_2.1.8.1
[37] parallel_4.4.2 R6_2.6.1
[39] bslib_0.9.0 stringi_1.8.7
[41] RColorBrewer_1.1-3 jquerylib_0.1.4
[43] iterators_1.0.14 Rcpp_1.1.0
[45] SummarizedExperiment_1.36.0 knitr_1.50
[47] httpuv_1.6.16 Matrix_1.7-3
[49] timechange_0.3.0 tidyselect_1.2.1
[51] rstudioapi_0.17.1 dichromat_2.0-0.1
[53] abind_1.4-8 yaml_2.3.10
[55] seqPattern_1.38.0 doParallel_1.0.17
[57] codetools_0.2-20 curl_7.0.0
[59] processx_3.8.6 lattice_0.22-7
[61] plyr_1.8.9 Biobase_2.66.0
[63] withr_3.0.2 evaluate_1.0.5
[65] Biostrings_2.74.1 pillar_1.11.0
[67] MatrixGenerics_1.18.1 whisker_0.4.1
[69] KernSmooth_2.23-26 foreach_1.5.2
[71] generics_0.1.4 vroom_1.6.5
[73] rprojroot_2.1.1 RCurl_1.98-1.17
[75] hms_1.1.3 scales_1.4.0
[77] glue_1.8.0 tools_4.4.2
[79] BiocIO_1.16.0 BSgenome_1.74.0
[81] GenomicAlignments_1.42.0 fs_1.6.6
[83] XML_3.99-0.18 Cairo_1.6-5
[85] impute_1.80.0 plotrix_3.8-4
[87] colorspace_2.1-1 GenomeInfoDbData_1.2.13
[89] restfulr_0.0.16 cli_3.6.5
[91] S4Arrays_1.6.0 gtable_0.3.6
[93] sass_0.4.10 digest_0.6.37
[95] SparseArray_1.6.2 htmlwidgets_1.6.4
[97] rjson_0.2.23 farver_2.1.2
[99] htmltools_0.5.8.1 lifecycle_1.0.4
[101] httr_1.4.7 GlobalOptions_0.1.2
[103] bit64_4.6.0-1