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library(tidyverse)
library(GenomicRanges)
library(plyranges)
library(genomation)
library(readr)
library(rtracklayer)
library(stringr)
library(ggrepel)
library(DT)
library(ChIPseeker)
library(ggVennDiagram)
library(smplot2)
library(ggsignif)
First steps: breakdown repeatmasker into groups and pull out the ones by each class I am interested in.
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
)
})
SINE_gr <- rpt_split_gr_list$SINE
SINE_df <- SINE_gr %>%
as.data.frame()
SINE_split_df <- split(SINE_df, SINE_df$repFamily)
LINE_gr <- rpt_split_gr_list$LINE
LINE_df <- LINE_gr %>%
as.data.frame()
LINE_split_df <- split(LINE_df, LINE_df$repFamily)
LTR_gr <- rpt_split_gr_list$LTR
LTR_df <- LTR_gr %>%
as.data.frame()
LTR_split_df <- split(LTR_df, LTR_df$repFamily)
SVA_gr <- rpt_split_gr_list$Retroposon
SVA_df <- SVA_gr %>%
as.data.frame()
SVA_split_df <- split(SVA_df, SVA_df$repFamily)
DNA_gr <- rpt_split_gr_list$DNA
DNA_df <- DNA_gr %>%
as.data.frame()
DNA_split_df <- split(DNA_df, DNA_df$repFamily)
H3K27ac_summit_gr <- readRDS("data/RDS_files/H3K27ac_complete_summit_gr.RDS")
peakAnnoList_H3K27ac <- readRDS("data/motif_lists/H3K27ac_annotated_peaks.RDS")
peakAnnoList_H3K9me3 <- readRDS("data/motif_lists/H3K9me3_annotated_peaks.RDS")
H3K27ac_lookup <- imap_dfr(peakAnnoList_H3K27ac[1:3], ~
tibble(Peakid = .x@anno$Peakid, cluster = .y))
H3K9me3_lookup <- imap_dfr(peakAnnoList_H3K9me3[1:3], ~
tibble(Peakid = .x@anno$Peakid, cluster = .y))
H3K27ac_sets_gr <- lapply(peakAnnoList_H3K27ac, function(df) {
as_granges(df)
})
H3K9me3_sets_gr <- lapply(peakAnnoList_H3K9me3, function(df) {
as_granges(df)
})
##assigning Peakid as name of summit region
mcols(H3K27ac_summit_gr)$name <- mcols(H3K27ac_summit_gr)$Peakid
comparisons <- tibble(
cluster2 = c("Set_2", "Set_3"),
cluster1 = c("Set_1", "Set_1")
)
H3K9me3_toplist <- readRDS( "data/DER_data/H3K9me3_toplist_nooutlier.RDS")
H3K27ac_toplist <- readRDS( "data/DER_data/H3K27ac_toplist.RDS")
H3K27ac_toptable_list <- bind_rows(H3K27ac_toplist, .id = "group")
H3K9me3_toptable_list <- bind_rows(H3K9me3_toplist, .id = "group")
K9me3_lfctable <- H3K9me3_toptable_list %>%
dplyr::select(group,genes, logFC) %>%
pivot_wider(.,id_cols = genes, names_from = group, values_from = logFC) %>%
dplyr::left_join(H3K9me3_lookup, by =c("genes"="Peakid")) %>%
mutate(case= case_when(H3K9me3_24T > 0 & H3K9me3_24R >0 & H3K9me3_144R>0~"A",
H3K9me3_24T < 0 & H3K9me3_24R <0 & H3K9me3_144R<0~"B",
TRUE ~ "C")) %>%
mutate(set_case=paste0(cluster,"_",case))
K27ac_lfctable <- H3K27ac_toptable_list %>%
dplyr::select(group,genes, logFC) %>%
pivot_wider(.,id_cols = genes, names_from = group, values_from = logFC) %>%
dplyr::left_join(H3K27ac_lookup,by =c("genes"="Peakid")) %>%
mutate(case= case_when(H3K27ac_24T > 0 & H3K27ac_24R >0 & H3K27ac_144R>0~"A",
H3K27ac_24T < 0 & H3K27ac_24R <0 & H3K27ac_144R<0~"B",
TRUE ~ "C")) %>%
mutate(set_case=paste0(cluster,"_",case))
set_case_list_H3K27ac <- H3K27ac_toptable_list %>%
dplyr::select(group,genes, logFC) %>%
pivot_wider(.,id_cols = genes, names_from = group, values_from = logFC) %>%
dplyr::left_join(H3K27ac_lookup,by =c("genes"="Peakid")) %>%
mutate(case= case_when(H3K27ac_24T > 0 & H3K27ac_24R >0 & H3K27ac_144R>0~"A",
H3K27ac_24T < 0 & H3K27ac_24R <0 & H3K27ac_144R<0~"B",
TRUE ~ "C")) %>%
mutate(set_case=paste0(cluster,"_",case)) %>%
dplyr::select(genes, cluster,case,set_case)
cluster_colors <- c("Set_1" = "#d93e40","Set_2" = "#1c9f50","Set_3" = "#3570b3","NA" ="grey70")
# Generic pairwise Fisher test
test_pair_TE_generic <- function(df_long, te_name, cluster1, cluster2) {
sub_df <- df_long %>%
filter(TE_type == te_name) %>%
complete(
cluster = c(cluster1, cluster2),
status = c("TE", "not_TE"),
fill = list(count = 0))
# enforce fixed order
status_levels <- c("TE", "not_TE")
# assume "status" column has TE vs wnot_TE automatically
statuses <- unique(sub_df$status)
if(length(statuses) != 2) {
# ensure we have exactly two categories, fill missing with 0
sub_df <- sub_df %>%
complete(cluster, status, fill = list(count = 0))
statuses <- unique(sub_df$status)
}
# extract counts for cluster1
c1_counts <- sub_df %>%
filter(cluster == cluster1) %>%
arrange(factor(status, levels = status_levels)) %>% # ensure same order
pull(count)
# extract counts for cluster2
c2_counts <- sub_df %>%
filter(cluster == cluster2) %>%
arrange(factor(status, levels = status_levels)) %>%
pull(count)
# build 2x2 matrix
mat <- matrix(
c(c2_counts, c1_counts),
nrow = 2,
byrow = TRUE,
dimnames = list(
cluster = c(cluster2, cluster1),
category = status_levels
)
)
ft <- tryCatch(
fisher.test(mat, workspace = 2e8),
error = function(e) fisher.test(mat, simulate.p.value = TRUE, B = 1e5)
)
tibble(
TE_type = te_name,
comparison = paste(cluster2, "vs", cluster1),
odds_ratio = ft$estimate,
lower_CI = ft$conf.int[1],
upper_CI = ft$conf.int[2],
p_value = ft$p.value
)
}
Overlapping SINE family with ROIs
sine_hits <- findOverlaps(H3K27ac_sets_gr$all_H3K27ac, SINE_gr, ignore.strand = TRUE)
SINE_overlap_df <- tibble(
peak_row = queryHits(sine_hits),
Peakid = H3K27ac_sets_gr$all_H3K27ac$Peakid[queryHits(sine_hits)],
cluster = H3K27ac_sets_gr$all_H3K27ac$cluster[queryHits(sine_hits)],
repClass = SINE_gr$repClass[subjectHits(sine_hits)],
repName = SINE_gr$repName[subjectHits(sine_hits)],
TE_type = ifelse(
SINE_gr$repFamily[subjectHits(sine_hits)] == "SVA",
SINE_gr$repName[subjectHits(sine_hits)],
SINE_gr$repFamily[subjectHits(sine_hits)]
),
milliDiv = SINE_gr$milliDiv[subjectHits(sine_hits)],
milliDel = SINE_gr$milliDel[subjectHits(sine_hits)],
milliIns = SINE_gr$milliIns[subjectHits(sine_hits)]
)
SINE_overlap_df %>%
dplyr::left_join(H3K27ac_lookup) %>%
dplyr::filter(cluster %in% c("Set_1","Set_2","Set_3")) %>%
ggplot(., aes(x = TE_type, y = milliDiv)) +
geom_violin(trim = FALSE) +
geom_boxplot(width = 0.15, outlier.shape = NA) +
coord_flip() +
labs(
y = "Divergence from consensus (milliDiv)",
x = "TE family",
title = "Age distribution of SINE elements overlapping H3K27ac"
)+
facet_wrap(~cluster)

| Version | Author | Date |
|---|---|---|
| 68a0095 | reneeisnowhere | 2026-02-02 |
SINE_overlap_df %>%
dplyr::left_join(H3K27ac_lookup) %>%
dplyr::filter(cluster %in% c("Set_1","Set_2","Set_3")) %>%
ggplot(., aes(x = cluster, y = milliDiv)) +
geom_violin(trim = FALSE) +
geom_boxplot(width = 0.15, outlier.shape = NA) +
coord_flip() +
labs(
y = "Divergence from consensus (milliDiv)",
x = "TE family",
title = "Age distribution of SINE elements overlapping H3K27ac"
)+
facet_wrap(~repName)

| Version | Author | Date |
|---|---|---|
| 68a0095 | reneeisnowhere | 2026-02-02 |
Overlapping LINE family with ROIs
LINE_hits <- findOverlaps(H3K27ac_sets_gr$all_H3K27ac, LINE_gr, ignore.strand = TRUE)
LINE_overlap_df <- tibble(
peak_row = queryHits(LINE_hits),
Peakid = H3K27ac_sets_gr$all_H3K27ac$Peakid[queryHits(LINE_hits)],
cluster = H3K27ac_sets_gr$all_H3K27ac$cluster[queryHits(LINE_hits)],
repClass = LINE_gr$repClass[subjectHits(LINE_hits)],
repName = LINE_gr$repName[subjectHits(LINE_hits)],
TE_type = ifelse(
LINE_gr$repFamily[subjectHits(LINE_hits)] == "SVA",
LINE_gr$repName[subjectHits(LINE_hits)],
LINE_gr$repFamily[subjectHits(LINE_hits)]
),
milliDiv = LINE_gr$milliDiv[subjectHits(LINE_hits)],
milliDel = LINE_gr$milliDel[subjectHits(LINE_hits)],
milliIns = LINE_gr$milliIns[subjectHits(LINE_hits)]
)
LINE_overlap_df %>%
dplyr::left_join(H3K27ac_lookup) %>%
dplyr::filter(cluster %in% c("Set_1","Set_2","Set_3")) %>%
ggplot(., aes(x = TE_type, y = milliDiv)) +
geom_violin(trim = FALSE) +
geom_boxplot(width = 0.15, outlier.shape = NA) +
coord_flip() +
labs(
y = "Divergence from consensus (milliDiv)",
x = "TE family",
title = "Age distribution of LINE elements overlapping H3K27ac"
)+
facet_wrap(~cluster)

| Version | Author | Date |
|---|---|---|
| 68a0095 | reneeisnowhere | 2026-02-02 |
Overlapping LTR family with ROIs
LTR_hits <- findOverlaps(H3K27ac_sets_gr$all_H3K27ac, LTR_gr, ignore.strand = TRUE)
LTR_overlap_df <- tibble(
peak_row = queryHits(LTR_hits),
Peakid = H3K27ac_sets_gr$all_H3K27ac$Peakid[queryHits(LTR_hits)],
cluster = H3K27ac_sets_gr$all_H3K27ac$cluster[queryHits(LTR_hits)],
repClass = LTR_gr$repClass[subjectHits(LTR_hits)],
repName = LTR_gr$repName[subjectHits(LTR_hits)],
RM_id = LTR_gr$RM_id[subjectHits(LTR_hits)],
TE_type = ifelse(
LTR_gr$repFamily[subjectHits(LTR_hits)] == "SVA",
LTR_gr$repName[subjectHits(LTR_hits)],
LTR_gr$repFamily[subjectHits(LTR_hits)]
),
milliDiv = LTR_gr$milliDiv[subjectHits(LTR_hits)],
milliDel = LTR_gr$milliDel[subjectHits(LTR_hits)],
milliIns = LTR_gr$milliIns[subjectHits(LTR_hits)]
)
LTR_overlap_df %>%
dplyr::left_join(H3K27ac_lookup) %>%
dplyr::filter(cluster %in% c("Set_1","Set_2","Set_3")) %>%
ggplot(., aes(x = cluster, y = milliDiv)) +
geom_violin(trim = FALSE) +
geom_boxplot(width = 0.15, outlier.shape = NA) +
coord_flip() +
labs(
y = "Divergence from consensus (milliDiv)",
x = "TE family",
title = "Age distribution of LTR elements overlapping H3K27ac"
)+
facet_wrap(~TE_type)

# saveRDS(LTR_overlap_df,"data/RDS_files/H3K27ac_Full_ROI_overlap_LTRs.RDS")
First test, within each TE family (ERVL, ERVK, etc…)do Set1,Set2 and Set3 differ?
age_kw <- LTR_overlap_df %>%
left_join(H3K27ac_lookup) %>%
filter(cluster %in% c("Set_1","Set_2","Set_3")) %>%
group_by(TE_type) %>%
summarise(
kw_p = kruskal.test(milliDiv ~ cluster)$p.value)
age_kw
# A tibble: 6 × 2
TE_type kw_p
<chr> <dbl>
1 ERV1 0.0681
2 ERVK 0.945
3 ERVL 0.0290
4 ERVL-MaLR 0.0223
5 Gypsy 0.211
6 LTR 0.0482
The answer shows for ERVL, ERVL-MaLR, and LTR, yes age difference differ between sets. now to look at ERVL,ERVL-MaLR and LTR individually
test_TE_age_pairs <- function(df,
TE_type_query,
sets = c("Set_1", "Set_2", "Set_3")) {
sub_df <- df %>%
dplyr::left_join(H3K27ac_lookup) %>%
dplyr::filter(
TE_type == TE_type_query,
cluster %in% sets,
!is.na(milliDiv)
)
# Medians first (ground truth)
med_df <- sub_df %>%
dplyr::group_by(cluster) %>%
dplyr::summarise(
median_age = median(milliDiv, na.rm = TRUE),
n = dplyr::n(),
.groups = "drop"
)
# Pairwise Wilcoxon
pw <- pairwise.wilcox.test(
x = sub_df$milliDiv,
g = sub_df$cluster,
p.adjust.method = "BH"
)
# Tidy + enforce symmetric pairs
pw_df <- as.data.frame(as.table(pw$p.value)) %>%
dplyr::filter(!is.na(Freq)) %>%
dplyr::rename(
set_A = Var1,
set_B = Var2,
p_adj = Freq
)
# Join medians *by value*, not position
pw_df %>%
dplyr::left_join(med_df, by = c("set_A" = "cluster")) %>%
dplyr::rename(median_A = median_age, n_A = n) %>%
dplyr::left_join(med_df, by = c("set_B" = "cluster")) %>%
dplyr::rename(median_B = median_age, n_B = n) %>%
dplyr::mutate(
older_set = dplyr::case_when(
median_A > median_B ~ set_A,
median_B > median_A ~ set_B,
TRUE ~ "equal"
),
TE_type = TE_type_query
)
}
test_TE_age_pairs(LTR_overlap_df, "ERV1")
set_A set_B p_adj median_A n_A median_B n_B older_set TE_type
1 Set_2 Set_1 0.09778575 165 107 157 6385 Set_2 ERV1
2 Set_3 Set_1 0.33055165 160 642 157 6385 Set_3 ERV1
3 Set_3 Set_2 0.14838385 160 642 165 107 Set_2 ERV1
test_TE_age_pairs(LTR_overlap_df, "ERVK")
set_A set_B p_adj median_A n_A median_B n_B older_set TE_type
1 Set_2 Set_1 1 77 4 90 537 Set_1 ERVK
2 Set_3 Set_1 1 93 25 90 537 Set_3 ERVK
3 Set_3 Set_2 1 93 25 77 4 Set_3 ERVK
test_TE_age_pairs(LTR_overlap_df, "ERVL")
set_A set_B p_adj median_A n_A median_B n_B older_set TE_type
1 Set_2 Set_1 0.42714314 251 91 242 6318 Set_2 ERVL
2 Set_3 Set_1 0.04056578 250 504 242 6318 Set_3 ERVL
3 Set_3 Set_2 0.99418468 250 504 251 91 Set_2 ERVL
test_TE_age_pairs(LTR_overlap_df, "ERVL-MaLR")
set_A set_B p_adj median_A n_A median_B n_B older_set TE_type
1 Set_2 Set_1 0.17332708 239 197 227 10698 Set_2 ERVL-MaLR
2 Set_3 Set_1 0.06074938 235 945 227 10698 Set_3 ERVL-MaLR
3 Set_3 Set_2 0.60549175 235 945 239 197 Set_2 ERVL-MaLR
test_TE_age_pairs(LTR_overlap_df, "LTR")
set_A set_B p_adj median_A n_A median_B n_B older_set TE_type
1 Set_2 Set_1 0.56351607 278.5 4 264.0 92 Set_2 LTR
2 Set_3 Set_1 0.04873491 282.0 13 264.0 92 Set_3 LTR
3 Set_3 Set_2 0.46137897 282.0 13 278.5 4 Set_3 LTR
Overlapping DNA family with ROIs
DNA_hits <- findOverlaps(H3K27ac_sets_gr$all_H3K27ac, DNA_gr, ignore.strand = TRUE)
DNA_overlap_df <- tibble(
peak_row = queryHits(DNA_hits),
Peakid = H3K27ac_sets_gr$all_H3K27ac$Peakid[queryHits(DNA_hits)],
cluster = H3K27ac_sets_gr$all_H3K27ac$cluster[queryHits(DNA_hits)],
repClass = DNA_gr$repClass[subjectHits(DNA_hits)],
repName = DNA_gr$repName[subjectHits(DNA_hits)],
TE_type = ifelse(
DNA_gr$repFamily[subjectHits(DNA_hits)] == "SVA",
DNA_gr$repName[subjectHits(DNA_hits)],
DNA_gr$repFamily[subjectHits(DNA_hits)]
),
milliDiv = DNA_gr$milliDiv[subjectHits(DNA_hits)],
milliDel = DNA_gr$milliDel[subjectHits(DNA_hits)],
milliIns = DNA_gr$milliIns[subjectHits(DNA_hits)]
)
DNA_overlap_df %>%
dplyr::left_join(H3K27ac_lookup) %>%
dplyr::filter(cluster %in% c("Set_1","Set_2","Set_3")) %>%
ggplot(., aes(x = TE_type, y = milliDiv)) +
geom_violin(trim = FALSE) +
geom_boxplot(width = 0.15, outlier.shape = NA) +
coord_flip() +
labs(
y = "Divergence from consensus (milliDiv)",
x = "TE family",
title = "Age distribution of DNA elements overlapping H3K27ac"
)+
facet_wrap(~cluster)

| Version | Author | Date |
|---|---|---|
| 68a0095 | reneeisnowhere | 2026-02-02 |
Overlapping SVA family with ROIs
SVA_hits <- findOverlaps(H3K27ac_sets_gr$all_H3K27ac, SVA_gr, ignore.strand = TRUE)
SVA_overlap_df <- tibble(
peak_row = queryHits(SVA_hits),
Peakid = H3K27ac_sets_gr$all_H3K27ac$Peakid[queryHits(SVA_hits)],
cluster = H3K27ac_sets_gr$all_H3K27ac$cluster[queryHits(SVA_hits)],
repClass = SVA_gr$repClass[subjectHits(SVA_hits)],
repName = SVA_gr$repName[subjectHits(SVA_hits)],
TE_type = ifelse(
SVA_gr$repFamily[subjectHits(SVA_hits)] == "SVA",
SVA_gr$repName[subjectHits(SVA_hits)],
SVA_gr$repFamily[subjectHits(SVA_hits)]
),
milliDiv = SVA_gr$milliDiv[subjectHits(SVA_hits)],
milliDel = SVA_gr$milliDel[subjectHits(SVA_hits)],
milliIns = SVA_gr$milliIns[subjectHits(SVA_hits)]
)
SVA_overlap_df %>%
dplyr::left_join(H3K27ac_lookup) %>%
dplyr::filter(cluster %in% c("Set_1","Set_2","Set_3")) %>%
ggplot(., aes(x = TE_type, y = milliDiv)) +
geom_violin(trim = FALSE) +
geom_boxplot(width = 0.15, outlier.shape = NA) +
coord_flip() +
labs(
y = "Divergence from consensus (milliDiv)",
x = "TE family",
title = "Age distribution of SVA elements overlapping H3K27ac"
)+
facet_wrap(~cluster)

| Version | Author | Date |
|---|---|---|
| 68a0095 | reneeisnowhere | 2026-02-02 |
Here I am exploring H3K27ac ROIs which overlap LTRs and also overlap H3K9me3 ROIs, then exploring LFC of the H3K27ac ROI sets across families of LTRs. First I wanted to know how many H3K27ac ROIs overlap LTRs, and how many of those LTRs overlap more than one ROI:
LTR_overlap_df %>%
count(Peakid, name = "n_peaks") %>%
count(n_peaks)
# A tibble: 12 × 2
n_peaks n
<int> <int>
1 1 18389
2 2 4997
3 3 1468
4 4 432
5 5 144
6 6 56
7 7 26
8 8 8
9 9 8
10 10 3
11 11 1
12 12 1
LTR_only_K27ac_peakids <- LTR_overlap_df %>% distinct(Peakid)
I then overlapped ROIs with H3K9me3 ROIs to see how many H3K9me3 ROIs overlap H3K27ac ROIs. (interpret with n_peaks being how many H3K27ac ROIs and n being number of H3K9me3 ROIS, So 33,567 K9me3 rOIs overlap 1 H3K27me3
K9me3_hits <- findOverlaps(H3K27ac_sets_gr$all_H3K27ac, H3K9me3_sets_gr$all_H3K9me3_regions, ignore.strand = TRUE)
K9me3_overlap_df <- tibble(
peak_row = queryHits(K9me3_hits),
Peakid = H3K27ac_sets_gr$all_H3K27ac$Peakid[queryHits(K9me3_hits)],
cluster = H3K27ac_sets_gr$all_H3K27ac$cluster[queryHits(K9me3_hits)],
ROI_K9me3 = H3K9me3_sets_gr$all_H3K9me3_regions$Peakid[subjectHits(K9me3_hits)])
K9me3_overlap_df %>%
count(Peakid, name = "n_peaks") %>%
count(n_peaks)
# A tibble: 17 × 2
n_peaks n
<int> <int>
1 1 33567
2 2 5184
3 3 1072
4 4 303
5 5 161
6 6 59
7 7 38
8 8 20
9 9 11
10 10 8
11 11 12
12 12 3
13 13 4
14 14 1
15 15 4
16 16 3
17 17 2
K9me3_only_K27ac_peakids <- K9me3_overlap_df %>% distinct(Peakid)
Now to filter and connect H3K27ac ROIs, that overlap LTRs and at least one H3K9me3
LTR_overlap_df %>%
dplyr::filter(Peakid %in% K9me3_only_K27ac_peakids$Peakid) %>% distinct(RM_id)
# A tibble: 12,645 × 1
RM_id
<chr>
1 chr1:1003379-1003425:1
2 chr1:1003500-1003623:1
3 chr1:1005447-1005607:1
4 chr1:1017170-1018876:1
5 chr1:1214911-1215005:1
6 chr1:1235837-1235999:1
7 chr1:1259547-1259908:1
8 chr1:1357233-1357526:1
9 chr1:1357817-1357890:1
10 chr1:1382090-1382288:1
# ℹ 12,635 more rows
LTR_overlap_df %>%
dplyr::filter(Peakid %in% K9me3_only_K27ac_peakids$Peakid) %>%
left_join(., K27ac_lfctable, by = c("Peakid"="genes")) %>%
group_by(TE_type) %>%
tally() %>%
ungroup() %>%
DT::datatable(
rownames = FALSE,
caption = htmltools::tags$caption(
style = "caption-side: top; text-align: left;",
"H3K27ac LTR specific overlap counts by TE familiy which also overlap H3K9me3"),
options = list(pageLength = 10,
autoWidth = TRUE,
dom = "tip"))
LTR_overlap_df %>%
dplyr::left_join(H3K27ac_lookup) %>%
dplyr::filter(Peakid %in% K9me3_only_K27ac_peakids$Peakid) %>%
dplyr::filter(cluster %in% c("Set_1","Set_2","Set_3")) %>%
ggplot(., aes(x = TE_type, y = milliDiv)) +
geom_violin(trim = FALSE) +
geom_boxplot(width = 0.15, outlier.shape = NA) +
coord_flip() +
labs(
y = "Divergence from consensus (milliDiv)",
x = "TE family",
title = "Age distribution of LTR elements overlapping H3K27ac and H3K9me3"
)+
facet_wrap(~cluster)

| Version | Author | Date |
|---|---|---|
| 81af285 | reneeisnowhere | 2026-02-04 |
LTR_K9me3_H3K27ac_lfc <- LTR_overlap_df %>%
left_join(., K27ac_lfctable, by = c("Peakid"="genes")) %>%
dplyr::filter(Peakid %in% K9me3_only_K27ac_peakids$Peakid)
plot_K27_family <- function(lfc_df,
grp="H3K27ac",
repFamily,
fam_name){
lfc_df %>%
dplyr::filter(Peakid %in% K9me3_only_K27ac_peakids$Peakid) %>%
dplyr::filter(.data$TE_type %in% fam_name) %>%
dplyr::filter(cluster != "NA") %>%
pivot_longer(.,cols=c(starts_with(grp)), names_to="group", values_to = "LFC") %>%
group_by(cluster, group) %>%
summarise(median_abs_LFC = median(abs(LFC), na.rm = TRUE),
.groups = "drop")%>%
mutate(time=str_remove(group,grp))%>%
mutate(time=factor(time, levels=c("_24T","_24R","_144R"))) %>%
ggplot(., aes(x=time, y=median_abs_LFC, group=cluster, color=cluster))+
geom_point(size=4)+
geom_line(aes(alpha = 0.8, linewidth = 4))+
theme_bw()+
ggtitle(paste0(grp," absolute LFC overlapping ",repFamily,":",fam_name))
}
plot_K27_family(LTR_K9me3_H3K27ac_lfc,"H3K27ac","LTR","ERV1")+
scale_color_manual(values = cluster_colors, drop = FALSE)

| Version | Author | Date |
|---|---|---|
| 68a0095 | reneeisnowhere | 2026-02-02 |
plot_K27_family(LTR_K9me3_H3K27ac_lfc,"H3K27ac","LTR","ERVK")+
scale_color_manual(values = cluster_colors, drop = FALSE)

| Version | Author | Date |
|---|---|---|
| 68a0095 | reneeisnowhere | 2026-02-02 |
plot_K27_family(LTR_K9me3_H3K27ac_lfc,"H3K27ac","LTR","ERVL")+
scale_color_manual(values = cluster_colors, drop = FALSE)

| Version | Author | Date |
|---|---|---|
| 68a0095 | reneeisnowhere | 2026-02-02 |
plot_K27_family(LTR_K9me3_H3K27ac_lfc,"H3K27ac","LTR","Gypsy")+
scale_color_manual(values = cluster_colors, drop = FALSE)

| Version | Author | Date |
|---|---|---|
| 68a0095 | reneeisnowhere | 2026-02-02 |
plot_K27_family(LTR_K9me3_H3K27ac_lfc,"H3K27ac","LTR","ERVL-MaLR")+
scale_color_manual(values = cluster_colors, drop = FALSE)

| Version | Author | Date |
|---|---|---|
| 68a0095 | reneeisnowhere | 2026-02-02 |
plot_K27_family(LTR_K9me3_H3K27ac_lfc,"H3K27ac","LTR","LTR")+
scale_color_manual(values = cluster_colors, drop = FALSE)

| Version | Author | Date |
|---|---|---|
| 68a0095 | reneeisnowhere | 2026-02-02 |
This will look at Raw LFC for all H3K27ac ROIs that overlap an LTR
LTR_overlap_df %>%
left_join(., K27ac_lfctable, by = c("Peakid"="genes")) %>%
pivot_longer(.,cols=c(starts_with("H3K27ac")), names_to="group", values_to = "LFC") %>%
group_by(cluster, group) %>%
# summarise(median_LFC = median(LFC), na.rm = TRUE),
# .groups = "drop")%>%
dplyr::filter(cluster=="Set_2") %>%
mutate(time=str_remove(group,"H3K27ac"))%>%
mutate(time=factor(time, levels=c("_24T","_24R","_144R"))) %>%
ggplot(., aes(x=time, y = LFC, group=Peakid))+
geom_line(alpha = 0.3) +
geom_point(size = 1) +
theme_classic() +
labs(
x = "Time point",
y = "Log2 Fold Change",
title = "H3K27ac LFC for Set_2 LTR-overlapping regions")

| Version | Author | Date |
|---|---|---|
| 81af285 | reneeisnowhere | 2026-02-04 |
LTR_overlap_df %>%
left_join(., K27ac_lfctable, by = c("Peakid"="genes")) %>%
pivot_longer(.,cols=c(starts_with("H3K27ac")), names_to="group", values_to = "LFC") %>%
group_by(cluster, group) %>%
# summarise(median_LFC = median(LFC), na.rm = TRUE),
# .groups = "drop")%>%
# dplyr::filter(cluster=="Set_3") %>%
mutate(time=str_remove(group,"H3K27ac"))%>%
mutate(time=factor(time, levels=c("_24T","_24R","_144R"))) %>%
ggplot(., aes(x=time, y = LFC, group=Peakid, color=case))+
geom_line(alpha = 0.3) +
geom_point(size = 1) +
theme_classic() +
facet_wrap(~cluster)+
labs(
x = "Time point",
y = "Log2 Fold Change",
title = "H3K27ac LFC for all LTR-overlapping regions")

| Version | Author | Date |
|---|---|---|
| 81af285 | reneeisnowhere | 2026-02-04 |
Getting some number about how many, etc…
LTR_overlap_df %>%
dplyr::left_join(H3K27ac_lookup) %>%
group_by(TE_type,cluster) %>%
tally() %>%
pivot_wider(id_cols = TE_type, names_from = cluster, values_from = n) %>%
ungroup() %>%
DT::datatable(
rownames = FALSE,
caption = htmltools::tags$caption(
style = "caption-side: top; text-align: left;",
"H3K27ac LTR specific overlap counts by TE familiy"),
options = list(pageLength = 10,
autoWidth = TRUE,
dom = "tip"))
now breaking out by family
LTR_overlap_df %>%
left_join(., K27ac_lfctable, by = c("Peakid"="genes")) %>%
pivot_longer(.,cols=c(starts_with("H3K27ac")), names_to="group", values_to = "LFC") %>%
group_by(cluster, group) %>%
# summarise(median_LFC = median(LFC), na.rm = TRUE),
# .groups = "drop")%>%
dplyr::filter(cluster=="Set_2") %>%
mutate(time=str_remove(group,"H3K27ac"))%>%
mutate(time=factor(time, levels=c("_24T","_24R","_144R"))) %>%
ggplot(., aes(x=time, y = LFC, group=Peakid, color=case))+
geom_line(alpha = 0.3) +
geom_point(size = 1) +
theme_classic() +
facet_wrap(~TE_type)+
labs(
x = "Time point",
y = "Log2 Fold Change",
title = "H3K27ac LFC for Set_2 LTR-overlapping regions")

| Version | Author | Date |
|---|---|---|
| 81af285 | reneeisnowhere | 2026-02-04 |
LTR_overlap_df %>%
left_join(., K27ac_lfctable, by = c("Peakid"="genes")) %>%
pivot_longer(.,cols=c(starts_with("H3K27ac")), names_to="group", values_to = "LFC") %>%
group_by(cluster, group) %>%
# summarise(median_LFC = median(LFC), na.rm = TRUE),
# .groups = "drop")%>%
dplyr::filter(cluster=="Set_3") %>%
mutate(time=str_remove(group,"H3K27ac"))%>%
mutate(time=factor(time, levels=c("_24T","_24R","_144R"))) %>%
ggplot(., aes(x=time, y = LFC, group=Peakid, color=case))+
geom_line(alpha = 0.3) +
geom_point(size = 1) +
theme_classic() +
facet_wrap(~TE_type)+
labs(
x = "Time point",
y = "Log2 Fold Change",
title = "H3K27ac LFC for Set_3 LTR-overlapping regions")

| Version | Author | Date |
|---|---|---|
| 81af285 | reneeisnowhere | 2026-02-04 |
There appears to be a lot of variation on LFC. Direction is obscuring information. I am now attempting to create a list of ROIs by set where LFC across time is always >0 (The up group), another set where LFC across time is always <0 (The down group), and the catch all mixed group.
### already added to the K27ac_lfctable
# LTR_overlap_df %>%
# dplyr::left_join(H3K27ac_lookup) %>%
# left_join(., K27ac_lfctable, by = c("Peakid"="genes")) %>%
# mutate(case= case_when(H3K27ac_24T > 0 & H3K27ac_24R >0 & H3K27ac_144R>0~"A",
# H3K27ac_24T < 0 & H3K27ac_24R <0 & H3K27ac_144R<0~"B",
# TRUE ~ "C")) %>%
# mutate(set_case=paste0(cluster,"_",case))
median_df <- K27ac_lfctable %>%
pivot_longer(.,cols=c(starts_with("H3K27ac")), names_to="group", values_to = "LFC") %>%
mutate(
time = stringr::str_remove(group, "H3K27ac"),
time = factor(time, levels = c("_24T", "_24R", "_144R"))
) %>%
group_by(cluster, time) %>%
summarise(
median_LFC = median(LFC, na.rm = TRUE),
n_peaks = dplyr::n(),
.groups = "drop")
K27ac_lfctable %>%
pivot_longer(.,cols=c(starts_with("H3K27ac")), names_to="group", values_to = "LFC") %>%
mutate(time=str_remove(group,"H3K27ac"))%>%
mutate(time=factor(time, levels=c("_24T","_24R","_144R"))) %>%
ggplot(., aes(x=time, y = LFC, group=genes, color=case))+
ggrastr::rasterise(geom_line(alpha = 0.15)) +
ggrastr::geom_point_rast(size = 1) +
geom_line(data=median_df, aes(x=time, y=median_LFC, group = cluster),inherit.aes = FALSE, linewidth =2)+
theme_classic() +
facet_wrap(~cluster)+
labs(
x = "Time point",
y = "Log2 Fold Change",
title = "H3K27ac LFC for all H3K27ac regions")

| Version | Author | Date |
|---|---|---|
| 3fa291d | reneeisnowhere | 2026-02-03 |
K27ac_lfctable %>%
pivot_longer(.,cols=c(starts_with("H3K27ac")), names_to="group", values_to = "LFC") %>%
mutate(time=str_remove(group,"H3K27ac"))%>%
mutate(time=factor(time, levels=c("_24T","_24R","_144R"))) %>%
ggplot(., aes(x=time, y = LFC, group=genes))+
ggrastr::rasterise(geom_line(alpha = 0.15,color="darkgray")) +
ggrastr::geom_point_rast(size = 1) +
geom_line(data=median_df, aes(x=time, y=median_LFC, group = cluster),inherit.aes = FALSE, linewidth =2)+
theme_classic() +
facet_wrap(~cluster)+
labs(
x = "Time point",
y = "Log2 Fold Change",
title = "H3K27ac LFC for all H3K27ac regions")

K27ac_lfctable %>%
group_by(cluster,case) %>%
tally() %>% pivot_wider(id_cols=case, names_from = cluster, values_from = n) %>%
mutate(type=case_when(case=="A"~"All LFC > 0",
case=="B" ~ "All LFC < 0",
case=="C"~"Mixed up and down LFC")) %>%
DT::datatable(
rownames = FALSE,
caption = htmltools::tags$caption(
style = "caption-side: top; text-align: left;",
"H3K27ac ROI counts stratified by LFC case"),
options = list(pageLength = 10,
autoWidth = TRUE,
dom = "tip"))
H3K27ac_Sets <- K27ac_lfctable %>%
dplyr::rename("Peakid"=genes)
H3K27ac_set_case_lfc <- split(H3K27ac_Sets, H3K27ac_Sets$set_case)
# saveRDS(H3K27ac_set_case_lfc, "data/RDS_files/H3K27ac_set_case_lfc.RDS")
unique(rpt_split$`LTR`$repFamily)
Zooming back in on summits,
What do LFCs of ROIs whose summits cross LTRs?
toss <- findOverlaps(H3K27ac_summit_gr, LTR_gr)
# toss %>%
# as.data.frame() %>%
# distinct(Peakid)
LTR_summits_overlap_df <- tibble(
peak_row = queryHits(toss),
Peakid = H3K27ac_summit_gr$Peakid[queryHits(toss)],
cluster = H3K27ac_sets_gr$cluster[queryHits(toss)],
repClass = LTR_gr$repClass[subjectHits(toss)],
repName = LTR_gr$repName[subjectHits(toss)],
RM_id = LTR_gr$RM_id[subjectHits(toss)],
TE_type = ifelse(
LTR_gr$repFamily[subjectHits(toss)] == "SVA",
LTR_gr$repName[subjectHits(toss)],
LTR_gr$repFamily[subjectHits(toss)]
),
milliDiv = LTR_gr$milliDiv[subjectHits(toss)],
milliDel = LTR_gr$milliDel[subjectHits(toss)],
milliIns = LTR_gr$milliIns[subjectHits(toss)]
)
summit_LTR_peakids <- LTR_summits_overlap_df %>% distinct(Peakid)
split_summit_LTR_peakids <- split(LTR_summits_overlap_df, LTR_summits_overlap_df$TE_type)
saveRDS(LTR_summits_overlap_df,"data/RDS_files/H3K27ac_summit_LTR_overlaps.RDS")
med_LTR_LFC <- K27ac_lfctable %>%
dplyr::filter(genes %in% summit_LTR_peakids$Peakid) %>%
pivot_longer(.,cols=c(starts_with("H3K27ac")), names_to="group", values_to = "LFC") %>%
mutate(
time = stringr::str_remove(group, "H3K27ac"),
time = factor(time, levels = c("_24T", "_24R", "_144R"))
) %>%
group_by(cluster, time) %>%
summarise(
median_LFC = median(LFC, na.rm = TRUE),
n_peaks = dplyr::n(),
.groups = "drop")
K27ac_lfctable %>%
dplyr::filter(genes %in% summit_LTR_peakids$Peakid) %>%
pivot_longer(.,cols=c(starts_with("H3K27ac")), names_to="group", values_to = "LFC") %>%
mutate(time=str_remove(group,"H3K27ac"))%>%
mutate(time=factor(time, levels=c("_24T","_24R","_144R"))) %>%
ggplot(., aes(x=time, y = LFC, group=genes, color=case))+
ggrastr::rasterise(geom_line(alpha = 0.15)) +
ggrastr::geom_point_rast(size = 1) +
geom_line(data=med_LTR_LFC, aes(x=time, y=median_LFC, group = cluster),inherit.aes = FALSE, linewidth =2)+
theme_classic() +
facet_wrap(~cluster)+
labs(
x = "Time point",
y = "Log2 Fold Change",
title = "H3K27ac LFC for all H3K27ac regions whose summits cross an LTR")

| Version | Author | Date |
|---|---|---|
| 81af285 | reneeisnowhere | 2026-02-04 |
median_LFC_H3K27ac_group_plot <- function(lfc_df,repFam){
pid_df <- split_summit_LTR_peakids[[repFam]]
med_df <- lfc_df %>%
dplyr::filter(genes %in% pid_df$Peakid) %>%
pivot_longer(.,cols=c(starts_with("H3K27ac")), names_to="group", values_to = "LFC") %>%
mutate(
time = stringr::str_remove(group, "H3K27ac"),
time = factor(time, levels = c("_24T", "_24R", "_144R"))
) %>%
group_by(cluster, time) %>%
summarise(
median_LFC = median(LFC, na.rm = TRUE),
n_peaks = dplyr::n(),
.groups = "drop")
label_df <- med_df %>%
group_by(cluster) %>%
summarise(n_peaks = unique(n_peaks), # same for all times within a cluster
.groups = "drop") %>%
mutate(label = paste0("n = ", n_peaks),
time = "_144R", # anchor text at first x position
y = Inf ) ##place at top of panel
lfc_df %>%
dplyr::filter(genes %in% pid_df$Peakid) %>%
pivot_longer(.,cols=c(starts_with("H3K27ac")), names_to="group", values_to = "LFC") %>%
mutate(time=str_remove(group,"H3K27ac"))%>%
mutate(time=factor(time, levels=c("_24T","_24R","_144R"))) %>%
ggplot(., aes(x=time, y = LFC, group=genes, color=case))+
ggrastr::rasterise(geom_line(alpha = 0.15)) +
ggrastr::geom_point_rast(size = 1) +
geom_line(data=med_df, aes(x=time, y=median_LFC, group = cluster),inherit.aes = FALSE, linewidth =2)+
geom_text(data = label_df, aes(x = time, y = y, label = label), inherit.aes = FALSE, vjust = 1.2, hjust = .2, size = 4)+
theme_classic() +
facet_wrap(~cluster)+
labs(
x = "Time point",
y = "Log2 Fold Change",
title = paste0("H3K27ac LFC, ROI summits cross an LTR:",repFam))
}
median_LFC_H3K27ac_group_plot(K27ac_lfctable,"ERVL-MaLR")

| Version | Author | Date |
|---|---|---|
| 81af285 | reneeisnowhere | 2026-02-04 |
median_LFC_H3K27ac_group_plot(K27ac_lfctable,"ERV1")

| Version | Author | Date |
|---|---|---|
| 81af285 | reneeisnowhere | 2026-02-04 |
median_LFC_H3K27ac_group_plot(K27ac_lfctable,"ERVL")

| Version | Author | Date |
|---|---|---|
| 81af285 | reneeisnowhere | 2026-02-04 |
median_LFC_H3K27ac_group_plot(K27ac_lfctable,"ERVK")

| Version | Author | Date |
|---|---|---|
| 81af285 | reneeisnowhere | 2026-02-04 |
median_LFC_H3K27ac_group_plot(K27ac_lfctable,"Gypsy")

| Version | Author | Date |
|---|---|---|
| 81af285 | reneeisnowhere | 2026-02-04 |
median_LFC_H3K27ac_group_plot(K27ac_lfctable,"LTR")

| Version | Author | Date |
|---|---|---|
| 81af285 | reneeisnowhere | 2026-02-04 |
I had a question about age and LTRs:
age_summit_kw <- LTR_summits_overlap_df %>%
left_join(H3K27ac_lookup) %>%
filter(cluster %in% c("Set_1","Set_2","Set_3")) %>%
group_by(TE_type) %>%
summarise(
kw_p = kruskal.test(milliDiv ~ cluster)$p.value)
age_summit_kw
# A tibble: 6 × 2
TE_type kw_p
<chr> <dbl>
1 ERV1 0.177
2 ERVK 0.681
3 ERVL 0.0257
4 ERVL-MaLR 0.0299
5 Gypsy 0.0835
6 LTR 0.306
test_TE_age_pairs_summits <- function(df,
TE_type_query,
sets = c("Set_1", "Set_2", "Set_3")) {
pid_df <- split_summit_LTR_peakids[[TE_type_query]]
sub_df <- pid_df %>%
dplyr::left_join(H3K27ac_lookup) %>%
dplyr::filter(
TE_type == TE_type_query,
cluster %in% sets,
!is.na(milliDiv)
)
# Medians first (ground truth)
med_df <- sub_df %>%
dplyr::group_by(cluster) %>%
dplyr::summarise(
median_age = median(milliDiv, na.rm = TRUE),
n = dplyr::n(),
.groups = "drop"
)
# Pairwise Wilcoxon
pw <- pairwise.wilcox.test(
x = sub_df$milliDiv,
g = sub_df$cluster,
p.adjust.method = "BH"
)
# Tidy + enforce symmetric pairs
pw_df <- as.data.frame(as.table(pw$p.value)) %>%
dplyr::filter(!is.na(Freq)) %>%
dplyr::rename(
set_A = Var1,
set_B = Var2,
p_adj = Freq
)
# Join medians *by value*, not position
pw_df %>%
dplyr::left_join(med_df, by = c("set_A" = "cluster")) %>%
dplyr::rename(median_A = median_age, n_A = n) %>%
dplyr::left_join(med_df, by = c("set_B" = "cluster")) %>%
dplyr::rename(median_B = median_age, n_B = n) %>%
dplyr::mutate(
older_set = dplyr::case_when(
median_A > median_B ~ set_A,
median_B > median_A ~ set_B,
TRUE ~ "equal"
),
TE_type = TE_type_query
)
}
testing age pairs between ROI summits
test_TE_age_pairs_summits(LTR_summits_overlap_df, "ERVL")
set_A set_B p_adj median_A n_A median_B n_B older_set TE_type
1 Set_2 Set_1 0.55190415 254 33 244 2137 Set_2 ERVL
2 Set_3 Set_1 0.02482948 256 136 244 2137 Set_3 ERVL
3 Set_3 Set_2 0.55190415 256 136 254 33 Set_3 ERVL
test_TE_age_pairs_summits(LTR_summits_overlap_df, "ERV1")
set_A set_B p_adj median_A n_A median_B n_B older_set TE_type
1 Set_2 Set_1 0.8642775 150 33 156 1837 Set_1 ERV1
2 Set_3 Set_1 0.1945868 150 203 156 1837 Set_1 ERV1
3 Set_3 Set_2 0.6037261 150 203 150 33 equal ERV1
test_TE_age_pairs_summits(LTR_summits_overlap_df, "ERVL-MaLR")
set_A set_B p_adj median_A n_A median_B n_B older_set TE_type
1 Set_2 Set_1 0.1007233 247 53 235 2699 Set_2 ERVL-MaLR
2 Set_3 Set_1 0.1455446 246 201 235 2699 Set_3 ERVL-MaLR
3 Set_3 Set_2 0.2753333 246 201 247 53 Set_2 ERVL-MaLR
compare_case_age <- function(df,
TE_family,
set_case_1,
set_case_2) {
sub_df <- df %>%
dplyr::left_join(set_case_list_H3K27ac, by=c("Peakid"="genes")) %>%
dplyr::filter(
TE_type == TE_family,
set_case %in% c(set_case_1, set_case_2),
!is.na(milliDiv)
)
med_df <- sub_df %>%
dplyr::group_by(set_case) %>%
dplyr::summarise(
median_age = median(milliDiv),
n = dplyr::n(),
.groups = "drop"
)
test <- wilcox.test(milliDiv ~ set_case, data = sub_df)
tibble::tibble(
TE_type = TE_family,
group_1 = set_case_1,
group_2 = set_case_2,
median_1 = med_df$median_age[med_df$set_case == set_case_1],
median_2 = med_df$median_age[med_df$set_case == set_case_2],
n_1 = med_df$n[med_df$set_case == set_case_1],
n_2 = med_df$n[med_df$set_case == set_case_2],
p_value = test$p.value,
older_group = dplyr::case_when(
median_1 > median_2 ~ set_case_1,
median_2 > median_1 ~ set_case_2,
TRUE ~ "equal"
)
)
}
LTR_summits_overlap_df %>%
dplyr::left_join(set_case_list_H3K27ac, by=c("Peakid"="genes")) %>%
dplyr::filter(
TE_type == "ERV1",
set_case %in% c("Set_1_A", "Set_2_A")
) %>%
ggplot(aes(x = set_case, y = milliDiv, fill = set_case)) +
geom_violin(trim = FALSE) +
geom_boxplot(width = 0.15, outlier.shape = NA) +
theme_classic() +
labs(
y = "Divergence from consensus (milliDiv)",
x = NULL,
title = "ERV1 age comparison by set_case"
)

| Version | Author | Date |
|---|---|---|
| 81af285 | reneeisnowhere | 2026-02-04 |
compare_case_age(LTR_summits_overlap_df,"ERV1","Set_1_A","Set_3_A")
# A tibble: 1 × 9
TE_type group_1 group_2 median_1 median_2 n_1 n_2 p_value older_group
<chr> <chr> <chr> <dbl> <dbl> <int> <int> <dbl> <chr>
1 ERV1 Set_1_A Set_3_A 152. 150 292 115 0.308 Set_1_A
compare_case_age(LTR_summits_overlap_df,"ERVL","Set_1_A","Set_3_A")
# A tibble: 1 × 9
TE_type group_1 group_2 median_1 median_2 n_1 n_2 p_value older_group
<chr> <chr> <chr> <dbl> <dbl> <int> <int> <dbl> <chr>
1 ERVL Set_1_A Set_3_A 242 221 339 33 0.311 Set_1_A
compare_case_age(LTR_summits_overlap_df,"ERVK","Set_1_A","Set_3_A")
# A tibble: 1 × 9
TE_type group_1 group_2 median_1 median_2 n_1 n_2 p_value older_group
<chr> <chr> <chr> <dbl> <dbl> <int> <int> <dbl> <chr>
1 ERVK Set_1_A Set_3_A 87.5 82 60 2 0.780 Set_1_A
compare_case_age(LTR_summits_overlap_df,"ERVL-MaLR","Set_1_A","Set_3_A")
# A tibble: 1 × 9
TE_type group_1 group_2 median_1 median_2 n_1 n_2 p_value older_group
<chr> <chr> <chr> <dbl> <dbl> <int> <int> <dbl> <chr>
1 ERVL-MaLR Set_1_A Set_3_A 237 244 477 71 0.548 Set_3_A
compare_case_age(LTR_summits_overlap_df,"ERV1","Set_1_A","Set_3_A")
# A tibble: 1 × 9
TE_type group_1 group_2 median_1 median_2 n_1 n_2 p_value older_group
<chr> <chr> <chr> <dbl> <dbl> <int> <int> <dbl> <chr>
1 ERV1 Set_1_A Set_3_A 152. 150 292 115 0.308 Set_1_A
compare_case_age(LTR_summits_overlap_df,"ERV1","Set_1_A","Set_3_A")
# A tibble: 1 × 9
TE_type group_1 group_2 median_1 median_2 n_1 n_2 p_value older_group
<chr> <chr> <chr> <dbl> <dbl> <int> <int> <dbl> <chr>
1 ERV1 Set_1_A Set_3_A 152. 150 292 115 0.308 Set_1_A
ERV1_summit_df <- split_summit_LTR_peakids$ERV1 %>%
left_join(., set_case_list_H3K27ac, by = c("Peakid"="genes")) %>%
dplyr::filter(cluster %in% c("Set_1","Set_2","Set_3"))
cluster_pairs <- list(c("Set_1","Set_2"),
c("Set_1", "Set_3"),
c("Set_2","Set_3"))
ERV1_pval_df <- ERV1_summit_df %>%
group_by(case) %>%
group_modify(~ {
map_dfr(cluster_pairs, function(pair) {
x <- .x %>% filter(cluster == pair[1]) %>% pull(milliDiv)
y <- .x %>% filter(cluster == pair[2]) %>% pull(milliDiv)
tibble(
cluster1 = pair[1],
cluster2 = pair[2],
p_value = wilcox.test(x, y)$p.value)
})
})
ggplot(ERV1_summit_df, aes(x = cluster, y = milliDiv, fill = cluster)) +
geom_violin(trim = FALSE) +
geom_boxplot(width = 0.15, outlier.shape = NA) +
facet_wrap(~case) +
theme_classic() +
labs(
y = "Divergence from consensus (milliDiv)",
x = "Set",
title = "ERV1 age comparisons across sets within each case"
) +
geom_signif(
comparisons = cluster_pairs,
test = "wilcox.test",
map_signif_level = TRUE,
textsize = 3,
step_increase = 0.1
)

| Version | Author | Date |
|---|---|---|
| 81af285 | reneeisnowhere | 2026-02-04 |
ERVL_summit_df <- split_summit_LTR_peakids$ERVL %>%
left_join(., set_case_list_H3K27ac, by = c("Peakid"="genes")) %>%
dplyr::filter(cluster %in% c("Set_1","Set_2","Set_3"))
cluster_pairs <- list(c("Set_1","Set_2"),
c("Set_1", "Set_3"),
c("Set_2","Set_3"))
ERVL_pval_df <- ERVL_summit_df %>%
group_by(case) %>%
group_modify(~ {
map_dfr(cluster_pairs, function(pair) {
x <- .x %>% filter(cluster == pair[1]) %>% pull(milliDiv)
y <- .x %>% filter(cluster == pair[2]) %>% pull(milliDiv)
tibble(
cluster1 = pair[1],
cluster2 = pair[2],
p_value = wilcox.test(x, y)$p.value)
})
})
ggplot(ERVL_summit_df, aes(x = cluster, y = milliDiv, fill = cluster)) +
geom_violin(trim = FALSE) +
geom_boxplot(width = 0.15, outlier.shape = NA) +
facet_wrap(~case) +
theme_classic() +
labs(
y = "Divergence from consensus (milliDiv)",
x = "Set",
title = "ERVL age comparisons across sets within each case"
) +
geom_signif(
comparisons = cluster_pairs,
test = "wilcox.test",
map_signif_level = TRUE,
textsize = 3,
step_increase = 0.1
)

| Version | Author | Date |
|---|---|---|
| 81af285 | reneeisnowhere | 2026-02-04 |
split_summit_LTR_peakids$ERV1 %>%
left_join(., set_case_list_H3K27ac, by = c("Peakid"="genes")) %>%
dplyr::filter(cluster %in% c("Set_1","Set_2","Set_3")) %>%
ggplot(., aes(x = cluster, y = milliDiv)) +
geom_violin(trim = FALSE) +
geom_boxplot(width = 0.15, outlier.shape = NA) +
facet_wrap(~case)

| Version | Author | Date |
|---|---|---|
| 81af285 | reneeisnowhere | 2026-02-04 |
ERV1_case_df <- split_summit_LTR_peakids$ERV1 %>%
left_join(set_case_list_H3K27ac, by = c("Peakid" = "genes")) %>%
filter(cluster %in% c("Set_1", "Set_2", "Set_3"),
case %in% c("A", "B")) # only compare A vs B
ggplot(ERV1_case_df, aes(x = case, y = milliDiv, fill = case)) +
geom_violin(trim = FALSE) +
geom_boxplot(width = 0.15, outlier.shape = NA) +
facet_wrap(~cluster) +
theme_classic() +
labs(
y = "Divergence from consensus (milliDiv)",
x = "Case",
title = "ERV1 age comparison: A vs B within each cluster"
) +
geom_signif(
comparisons = list(c("A", "B")),
test = "wilcox.test",
map_signif_level = TRUE,
textsize = 3,
step_increase = .1)

| Version | Author | Date |
|---|---|---|
| 81af285 | reneeisnowhere | 2026-02-04 |
ERVL_case_df <- split_summit_LTR_peakids$ERVL %>%
left_join(set_case_list_H3K27ac, by = c("Peakid" = "genes")) %>%
filter(cluster %in% c("Set_1", "Set_2", "Set_3"),
case %in% c("A", "B")) # only compare A vs B
ggplot(ERVL_case_df, aes(x = case, y = milliDiv, fill = case)) +
geom_violin(trim = FALSE) +
geom_boxplot(width = 0.15, outlier.shape = NA) +
facet_wrap(~cluster) +
theme_classic() +
labs(
y = "Divergence from consensus (milliDiv)",
x = "Case",
title = "ERVL age comparison: A vs B within each cluster"
) +
geom_signif(
comparisons = list(c("A", "B")),
test = "wilcox.test",
map_signif_level = TRUE,
textsize = 3,
step_increase = .1)

| Version | Author | Date |
|---|---|---|
| 81af285 | reneeisnowhere | 2026-02-04 |
ERVK_case_df <- split_summit_LTR_peakids$ERVK %>%
left_join(set_case_list_H3K27ac, by = c("Peakid" = "genes")) %>%
filter(cluster %in% c("Set_1", "Set_2", "Set_3"),
case %in% c("A", "B")) # only compare A vs B
ggplot(ERVK_case_df, aes(x = case, y = milliDiv, fill = case)) +
geom_violin(trim = FALSE) +
geom_boxplot(width = 0.15, outlier.shape = NA) +
facet_wrap(~cluster) +
theme_classic() +
labs(
y = "Divergence from consensus (milliDiv)",
x = "Case",
title = "ERVK age comparison: A vs B within each cluster"
) +
geom_signif(
comparisons = list(c("A", "B")),
test = "wilcox.test",
map_signif_level = TRUE,
textsize = 3,
step_increase = .1)

| Version | Author | Date |
|---|---|---|
| 81af285 | reneeisnowhere | 2026-02-04 |
ERVL_MaLR_case_df <- split_summit_LTR_peakids$`ERVL-MaLR` %>%
left_join(set_case_list_H3K27ac, by = c("Peakid" = "genes")) %>%
filter(cluster %in% c("Set_1", "Set_2", "Set_3"),
case %in% c("A", "B")) # only compare A vs B
ggplot(ERVL_MaLR_case_df, aes(x = case, y = milliDiv, fill = case)) +
geom_violin(trim = FALSE) +
geom_boxplot(width = 0.15, outlier.shape = NA) +
facet_wrap(~cluster) +
theme_classic() +
labs(
y = "Divergence from consensus (milliDiv)",
x = "Case",
title = "ERVL-MaLR age comparison: A vs B within each cluster"
) +
geom_signif(
comparisons = list(c("A", "B")),
test = "wilcox.test",
map_signif_level = TRUE,
textsize = 3,
step_increase = .1)

| Version | Author | Date |
|---|---|---|
| 81af285 | reneeisnowhere | 2026-02-04 |
Gypsy_case_df <- split_summit_LTR_peakids$Gypsy %>%
left_join(set_case_list_H3K27ac, by = c("Peakid" = "genes")) %>%
filter(cluster %in% c("Set_1", "Set_2", "Set_3"),
case %in% c("A", "B")) # only compare A vs B
ggplot(Gypsy_case_df, aes(x = case, y = milliDiv, fill = case)) +
geom_violin(trim = FALSE) +
geom_boxplot(width = 0.15, outlier.shape = NA) +
facet_wrap(~cluster) +
theme_classic() +
labs(
y = "Divergence from consensus (milliDiv)",
x = "Case",
title = "Gypsy age comparison: A vs B within each cluster"
) +
geom_signif(
comparisons = list(c("A", "B")),
test = "wilcox.test",
map_signif_level = TRUE,
textsize = 3,
step_increase = .1)

| Version | Author | Date |
|---|---|---|
| 81af285 | reneeisnowhere | 2026-02-04 |
LTR_case_df <- split_summit_LTR_peakids$LTR %>%
left_join(set_case_list_H3K27ac, by = c("Peakid" = "genes")) %>%
filter(cluster %in% c("Set_1", "Set_2", "Set_3"),
case %in% c("A", "B")) # only compare A vs B
ggplot(LTR_case_df, aes(x = case, y = milliDiv, fill = case)) +
geom_violin(trim = FALSE) +
geom_boxplot(width = 0.15, outlier.shape = NA) +
facet_wrap(~cluster) +
theme_classic() +
labs(
y = "Divergence from consensus (milliDiv)",
x = "Case",
title = "LTR age comparison: A vs B within each cluster"
) +
geom_signif(
comparisons = list(c("A", "B")),
test = "wilcox.test",
map_signif_level = TRUE,
textsize = 3,
step_increase = .1)

| Version | Author | Date |
|---|---|---|
| 81af285 | reneeisnowhere | 2026-02-04 |
listit <- data.frame(x=width(H3K9me3_sets_gr$all_H3K9me3_regions))
ggplot(listit, aes(x=x))+
geom_density()+ggtitle("H3K9me3 ROI widths")

listit_k27ac <- data.frame(x=width(H3K27ac_sets_gr$all_H3K27ac))
listit %>%
summary()
x
Min. : 85.0
1st Qu.: 264.0
Median : 394.0
Mean : 519.2
3rd Qu.: 634.0
Max. :41434.0
ggplot(listit_k27ac, aes(x=x))+
geom_density()+ggtitle("H3K27ac ROI widths")

listit_k27ac %>%
summary()
x
Min. : 87
1st Qu.: 581
Median : 869
Mean : 1299
3rd Qu.: 1469
Max. :97107
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] ggsignif_0.6.4 smplot2_0.2.5 ggVennDiagram_1.5.4
[4] ChIPseeker_1.42.1 DT_0.33 ggrepel_0.9.6
[7] rtracklayer_1.66.0 genomation_1.38.0 plyranges_1.26.0
[10] GenomicRanges_1.58.0 GenomeInfoDb_1.42.3 IRanges_2.40.1
[13] S4Vectors_0.44.0 BiocGenerics_0.52.0 lubridate_1.9.4
[16] forcats_1.0.0 stringr_1.5.1 dplyr_1.1.4
[19] purrr_1.1.0 readr_2.1.5 tidyr_1.3.1
[22] tibble_3.3.0 ggplot2_3.5.2 tidyverse_2.0.0
[25] workflowr_1.7.1
loaded via a namespace (and not attached):
[1] splines_4.4.2
[2] later_1.4.2
[3] BiocIO_1.16.0
[4] bitops_1.0-9
[5] ggplotify_0.1.2
[6] R.oo_1.27.1
[7] XML_3.99-0.18
[8] rpart_4.1.24
[9] lifecycle_1.0.4
[10] rstatix_0.7.2
[11] rprojroot_2.1.1
[12] vroom_1.6.5
[13] processx_3.8.6
[14] lattice_0.22-7
[15] crosstalk_1.2.2
[16] backports_1.5.0
[17] magrittr_2.0.3
[18] Hmisc_5.2-3
[19] sass_0.4.10
[20] rmarkdown_2.29
[21] jquerylib_0.1.4
[22] yaml_2.3.10
[23] plotrix_3.8-4
[24] httpuv_1.6.16
[25] ggtangle_0.0.7
[26] cowplot_1.2.0
[27] DBI_1.2.3
[28] RColorBrewer_1.1-3
[29] abind_1.4-8
[30] zlibbioc_1.52.0
[31] R.utils_2.13.0
[32] RCurl_1.98-1.17
[33] yulab.utils_0.2.1
[34] nnet_7.3-20
[35] rappdirs_0.3.3
[36] git2r_0.36.2
[37] GenomeInfoDbData_1.2.13
[38] enrichplot_1.26.6
[39] tidytree_0.4.6
[40] codetools_0.2-20
[41] DelayedArray_0.32.0
[42] DOSE_4.0.1
[43] tidyselect_1.2.1
[44] aplot_0.2.8
[45] UCSC.utils_1.2.0
[46] farver_2.1.2
[47] matrixStats_1.5.0
[48] base64enc_0.1-3
[49] GenomicAlignments_1.42.0
[50] jsonlite_2.0.0
[51] Formula_1.2-5
[52] tools_4.4.2
[53] treeio_1.30.0
[54] TxDb.Hsapiens.UCSC.hg19.knownGene_3.2.2
[55] Rcpp_1.1.0
[56] glue_1.8.0
[57] gridExtra_2.3
[58] SparseArray_1.6.2
[59] xfun_0.52
[60] qvalue_2.38.0
[61] MatrixGenerics_1.18.1
[62] withr_3.0.2
[63] fastmap_1.2.0
[64] boot_1.3-32
[65] callr_3.7.6
[66] caTools_1.18.3
[67] digest_0.6.37
[68] timechange_0.3.0
[69] R6_2.6.1
[70] gridGraphics_0.5-1
[71] seqPattern_1.38.0
[72] colorspace_2.1-1
[73] Cairo_1.6-5
[74] GO.db_3.20.0
[75] gtools_3.9.5
[76] dichromat_2.0-0.1
[77] RSQLite_2.4.3
[78] R.methodsS3_1.8.2
[79] utf8_1.2.6
[80] generics_0.1.4
[81] data.table_1.17.8
[82] httr_1.4.7
[83] htmlwidgets_1.6.4
[84] S4Arrays_1.6.0
[85] whisker_0.4.1
[86] pkgconfig_2.0.3
[87] gtable_0.3.6
[88] blob_1.2.4
[89] impute_1.80.0
[90] XVector_0.46.0
[91] htmltools_0.5.8.1
[92] carData_3.0-5
[93] pwr_1.3-0
[94] fgsea_1.32.4
[95] scales_1.4.0
[96] Biobase_2.66.0
[97] png_0.1-8
[98] ggfun_0.2.0
[99] knitr_1.50
[100] rstudioapi_0.17.1
[101] tzdb_0.5.0
[102] reshape2_1.4.4
[103] rjson_0.2.23
[104] checkmate_2.3.3
[105] nlme_3.1-168
[106] curl_7.0.0
[107] zoo_1.8-14
[108] cachem_1.1.0
[109] KernSmooth_2.23-26
[110] vipor_0.4.7
[111] parallel_4.4.2
[112] foreign_0.8-90
[113] AnnotationDbi_1.68.0
[114] ggrastr_1.0.2
[115] restfulr_0.0.16
[116] pillar_1.11.0
[117] vctrs_0.6.5
[118] gplots_3.2.0
[119] ggpubr_0.6.1
[120] promises_1.3.3
[121] car_3.1-3
[122] cluster_2.1.8.1
[123] beeswarm_0.4.0
[124] htmlTable_2.4.3
[125] evaluate_1.0.5
[126] GenomicFeatures_1.58.0
[127] cli_3.6.5
[128] compiler_4.4.2
[129] Rsamtools_2.22.0
[130] rlang_1.1.6
[131] crayon_1.5.3
[132] labeling_0.4.3
[133] ps_1.9.1
[134] ggbeeswarm_0.7.2
[135] getPass_0.2-4
[136] plyr_1.8.9
[137] fs_1.6.6
[138] stringi_1.8.7
[139] gridBase_0.4-7
[140] BiocParallel_1.40.2
[141] Biostrings_2.74.1
[142] lazyeval_0.2.2
[143] GOSemSim_2.32.0
[144] Matrix_1.7-3
[145] BSgenome_1.74.0
[146] hms_1.1.3
[147] patchwork_1.3.2
[148] bit64_4.6.0-1
[149] KEGGREST_1.46.0
[150] SummarizedExperiment_1.36.0
[151] broom_1.0.9
[152] igraph_2.1.4
[153] memoise_2.0.1
[154] bslib_0.9.0
[155] ggtree_3.14.0
[156] fastmatch_1.1-6
[157] bit_4.6.0
[158] ape_5.8-1