Last updated: 2026-03-20

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Knit directory: DXR_continue/

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Rmd e77cb37 reneeisnowhere 2026-03-19 first commit

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)

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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")

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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")

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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
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Heatmap plotting

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
)

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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)

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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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finding switches

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