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##################################################
## Project: DexStim Mouse Brain
## Date: 07.01.2020
## Author: Nathalie
##################################################
# GO plots single regions (Network analysis - nodebetweenness)
library(org.Mm.eg.db)
library(data.table)
library(ggplot2)
library(dplyr)
library(stringr)
library(anRichment)
library(anRichmentMethods)
basepath <- "~/Documents/ownCloud/DexStim_RNAseq_Mouse/"
regions <- c("AMY", "CER", "dCA1", "dDG", "PFC", "PVN", "vCA1", "vDG")
beta_cutoff <- 0.01
folder_plots <- paste0("figures")
folder_tables <- paste0("tables")
# 1. Read data from all regions ----------
list_reg <- list()
for (reg in regions){
res <- fread(paste0(basepath, "tables/coExpression_kimono/03_AnalysisFuncoup/04_",
reg,"_funcoup_differential_nodeBetweennessNorm_betacutoff",beta_cutoff,".csv"))
res <- res[res$nodebetweenness_norm>=0.5 & ! is.na(res$nodebetweenness_norm)]
res$entrez <- mapIds(org.Mm.eg.db, keys = res$ensembl_id,
keytype = "ENSEMBL", column="ENTREZID")
list_reg[[reg]] <- res
}
# 2. check uniqueness of DE genes ---------------
for (reg in regions){
index_reg <- which(regions == reg)
df <- bind_rows(list_reg[-index_reg], .id="region")
list_reg[[reg]]$regions_top <- sapply(list_reg[[reg]]$ensembl_id,
function(x) paste(df[df$ensembl_id == x,]$region, collapse = " "))
list_reg[[reg]]$unique_top <- sapply(list_reg[[reg]]$regions_top,
function(x) x == "")
}
# 3. GO enrichment for the genes of each region ------------------
go_enrichment_all <- function(df_reg, GOcoll, unique){
if (unique){
genes <- df_reg$entrez[df_reg$unique_top]
} else {
genes <- df_reg$entrez
}
background <- read.table(file = paste0(basepath, folder_tables, "/06_background_entrezID.txt"),
header = FALSE)
modules <- rep("not_significant", nrow(background))
modules[which(background$V1 %in% genes)] <- "significant"
# enrichment
GOenrichment <- enrichmentAnalysis(
classLabels = modules,
identifiers = background$V1,
refCollection = GOcoll,
useBackground = "given",
nBestDataSets = length(GOcoll$dataSets),
# threshold = 0.1,
# thresholdType = "Bonferroni",
getOverlapEntrez = TRUE,
getOverlapSymbols = TRUE,
ignoreLabels = "not_significant",
maxReportedOverlapGenes = 500
)
enrichmentTable <- GOenrichment$enrichmentTable
return(enrichmentTable)
}
GOcollection <- buildGOcollection(organism = "mouse")
list_GO <- list()
# GO.BPcollection = subsetCollection(GOcollection, tags = "GO.BP")
for (reg in regions){
go_enr_unique <- go_enrichment_all(list_reg[[reg]], GOcollection, TRUE)
# go_enr_all <- go_enrichment_all(list_reg[[reg]], GOcollection, FALSE)
list_GO[[reg]] <- go_enr_unique
}
# 4. Plot GO terms
df_all <- bind_rows(list_GO, .id="region")
for (reg in regions){
df_reg <- list_GO[[reg]] %>%
filter(nCommonGenes >= 10, pValue <= 0.1) %>%
group_by(inGroups) %>% slice_min(order_by = pValue, n = 10)
df <- df_all[df_all$dataSetName %in% df_reg$dataSetName,]
df$dataSetName <- sapply(df$dataSetName, function(x) str_trunc(x, 45, "right"))
df$dataSetName <- factor(df$dataSetName, levels = rev(reorder(df$dataSetName[df$region==reg], df$pValue[df$region==reg])))
df$region <- factor(df$region, levels = c("AMY", "CER", "PFC", "PVN", "vDG", "dDG", "vCA1", "dCA1"))
df$inGroups <- factor(df$inGroups)
levels(df$inGroups) <- c("Biological Process", "Cellular Components", "Molecular Function")
# Plot results (plotted pvalues are not adjusted for multiple testing)
df <- df %>%
arrange(desc(dataSetName))
print(ggplot(df, aes(x=dataSetName, y = -log10(pValue), fill = region)) +
geom_bar(position = position_dodge2(reverse=TRUE), stat="identity") +
geom_hline(yintercept = -log10(0.1),linetype="dashed", color = "red") +
coord_flip() +
xlab("GOterm") +
ggtitle(paste0("GO terms enriched for diff. co-expressed genes only in ",reg, " (Top 10 each)")) +
facet_wrap(~inGroups, scales="free") +
theme(axis.text.y = element_text(size = 10)))
ggsave(filename = paste0(basepath, folder_plots, "/02_CoExp_Kimono/03_AnalysisFuncoup/comparisonRegions/",
"06_",reg,"_GOterms_unique_nodebetweenness1.png"),
width = 13, height = 7)
}