00. Envirenment Settings

options(install.packages.compile.from.source = "always")
list.packages <- c(
  "readxl", "ggplot2", "ggpubr", "matrixStats", "ggrepel", "reshape2", "dplyr", "stringr",
  "grid", "tcltk", "parallel", "doParallel", "doSNOW", "data.table", "gplots",
  "randomcoloR", "factoextra", "RColorBrewer", "grDevices", "gmp", "xtable", "latex2exp",
  "httr", "jsonlite", "curl", "RCurl", "magrittr", "rlist", "pipeR", "plyr",
  "xml2", "rvest", "knn.covertree", "knitr", "rlang", "visNetwork", "hwriter", "htmltools"
)
bio.list.packages <- c(
  "limma", "ExperimentHub", "clusterProfiler", "GO.db",
  "org.Mm.eg.db", "pathview", "enrichplot", "org.Hs.eg.db"
)
new.packages <- list.packages[!list.packages %in% installed.packages()]
bio.new.packages <- bio.list.packages[!bio.list.packages %in% installed.packages()]
# Packages that does not install yet
if (!requireNamespace("BiocManager", quietly = TRUE)) {
  update.packages(ask = FALSE)
  install.packages("BiocManager", repos="https://cloud.r-project.org")
}
if (length(new.packages)) {
  install.packages(new.packages)
  devtools::install_github("grimbough/biomaRt", force = FALSE)
}
if (length(bio.new.packages)) {
  update.packages(ask = FALSE)
  BiocManager::install(bio.new.packages)
}
# Loading all packages & functions
invisible(lapply(c(list.packages, bio.list.packages, "biomaRt"), library, character.only = TRUE))

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    parCapply, parLapply, parRapply, parSapply, splitIndices, stopCluster

data.table 1.14.8 using 64 threads (see ?getDTthreads).  Latest news: r-datatable.com

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Welcome! Want to learn more? See two factoextra-related books at https://goo.gl/ve3WBa

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    %*%, apply, crossprod, matrix, tcrossprod

Using libcurl 7.81.0 with OpenSSL/3.0.2

Attaching package: ‘curl’

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----------------------------------------------------------------------------------------------------------------------------------------------
You have loaded plyr after dplyr - this is likely to cause problems.
If you need functions from both plyr and dplyr, please load plyr first, then dplyr:
library(plyr); library(dplyr)
----------------------------------------------------------------------------------------------------------------------------------------------

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Loading required package: BiocGenerics

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    IQR, mad, sd, var, xtabs

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    anyDuplicated, aperm, append, as.data.frame, basename, cbind, colnames, dirname, do.call, duplicated, eval, evalq, Filter,
    Find, get, grep, grepl, intersect, is.unsorted, lapply, Map, mapply, match, mget, order, paste, pmax, pmax.int, pmin,
    pmin.int, Position, rank, rbind, Reduce, rownames, sapply, setdiff, sort, table, tapply, union, unique, unsplit, which.max,
    which.min

Loading required package: AnnotationHub
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  print.tbl_lazy     
  print.tbl_sql      

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    ident, sql


clusterProfiler v4.6.2  For help: https://yulab-smu.top/biomedical-knowledge-mining-book/

If you use clusterProfiler in published research, please cite:
T Wu, E Hu, S Xu, M Chen, P Guo, Z Dai, T Feng, L Zhou, W Tang, L Zhan, X Fu, S Liu, X Bo, and G Yu. clusterProfiler 4.0: A universal enrichment tool for interpreting omics data. The Innovation. 2021, 2(3):100141

Attaching package: ‘clusterProfiler’

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Loading required package: AnnotationDbi
Loading required package: stats4
Loading required package: Biobase
Welcome to Bioconductor

    Vignettes contain introductory material; view with 'browseVignettes()'. To cite Bioconductor, see 'citation("Biobase")', and
    for packages 'citation("pkgname")'.


Attaching package: ‘Biobase’

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Loading required package: IRanges
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##############################################################################
Pathview is an open source software package distributed under GNU General
Public License version 3 (GPLv3). Details of GPLv3 is available at
http://www.gnu.org/licenses/gpl-3.0.html. Particullary, users are required to
formally cite the original Pathview paper (not just mention it) in publications
or products. For details, do citation("pathview") within R.

The pathview downloads and uses KEGG data. Non-academic uses may require a KEGG
license agreement (details at http://www.kegg.jp/kegg/legal.html).
##############################################################################

Attaching package: ‘enrichplot’

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options(rgl.useNULL = F, ggrepel.max.overlaps = Inf)

01. Check Results from GSE138783

01-01. Functional Enrichment Analysis (FEA) Results from GSE138783

Load the functional enrichment analysis (FEA) results from our re-analyzed GSE138783 Bulk RNA-seq

load(file.path(".", "01.HEK293_TMG_OSMI2", "00.Results", "DESeq2_Results.Rdata"))


Select the comparison with the most different treatment which is 6h TMG vs 6h OSMI-1

ORA_list <- DEGs_ls[["HEK293_TMG_6hBvsHEK293_OSMI2_6hA"]][["Over_Represent"]]


Keep the GO_BP terms that contains either “mitochondria” or “cytoskeleton”

for(i in c("All", "Up_regulated", "Down_regulated")){
  temp <- ORA_list[[i]]$GO_BP$Raw@result$Description %>%
    grep("(mitochondria(l){0,1}|cytoskele(ton|tal))", ., ignore.case = TRUE)
  ORA_list[[i]]$GO_BP$Raw@result <- ORA_list[[i]]$GO_BP$Raw@result[temp,]
  ORA_list[[i]]$GO_BP$Sig <- ORA_list[[i]]$GO_BP$Raw@result
}
names <- "TMG 6h vs OSMI-1 6h"
k <- "GO_BP"
temp <- ORA_list
mydf<-data.frame()
geneClusters<-list()
for(j in c("All","Up_regulated","Down_regulated")){
  if(is.null(nrow(temp[[j]][[k]][["Sig"]]))){next()}
  mydf<-rbind(
    mydf,
    cbind(
      group=rep(j,nrow(temp[[j]][[k]][["Sig"]])),
      temp[[j]][[k]][["Sig"]][,1:9]
    )
  )
  geneClusters[[j]]<-(temp[[j]][[k]][["Sig"]]$geneID)%>%
    str_split(.,"/")%>%unlist()%>%unique()
}

rownames(mydf)<-1:nrow(mydf)
mydf$group<-factor(mydf$group,levels=c("All","Up_regulated","Down_regulated"))
colnames(mydf)[1]<-"Cluster"
res <- new("compareClusterResult",
           compareClusterResult = mydf,
           geneClusters = geneClusters
)
.call<-match.call(compareCluster,call("compareCluster",
                                      ENSEMBL~group, data=mydf, fun="enrichGO",
                                      OrgDb         = org.Hs.eg.db,
                                      keyType       = "ENSEMBL",
                                      ont           = "BP",
                                      pAdjustMethod = "BH",
                                      pvalueCutoff  = 1,
                                      qvalueCutoff  = 1,
                                      readable      = TRUE))
.call$geneClusters<-as.symbol("geneClusters")
.call$OrgDb<-as.symbol("org.Hs.eg.db")
.call$data<-NULL
res@.call<-.call
res@fun<-"enrichGO"
res@keytype<-"UNKNOWN"
res@readable<-FALSE
if(!dir.exists(file.path(".","01.PlotOut"))){
  dir.create(file.path(".","01.PlotOut"))
}

01-02. Check FEA Results

Overlap

gp <- dotplot(
  res, showCategory=1000, label_format=85, color = "pvalue",
  title=paste0("ORA Summary of ", names, " for ", k," Terms.")
)
svg(filename = file.path(".", "01.PlotOut", "FEA_Overlap.svg"), width = 12, height = 17, pointsize = 12)
print(gp)
dev.off()
null device 
          1 
graphics.off()
knitr::opts_knit$set(global.device = TRUE)
print(gp)

knitr::opts_knit$set(global.device = FALSE)

All DEGs

j <- "GO_BP"
k <- "All"
Par_name <- "TMG 6h vs OSMI-1 6h"
FEA_title<-paste0(k, " ", nrow(ORA_list[[k]][[j]]$Raw)," significant GO_", j, " terms (", Par_name, "; the most descend terms)")
p1<-dotplot(ORA_list[[k]][[j]]$Raw, showCategory=1000, label_format=100, color = "pvalue", font.size = 18)
p2<-treeplot(
  pairwise_termsim(ORA_list[[k]][[j]]$Raw, method="JC"), showCategory=1000, color = "pvalue",
  cluster.params=list(hclust_method = "ward.D2", label_words_n = 5, n = 5, font.size = 18)
)
gp <- gridExtra::grid.arrange(
  p1, p2, nrow = 1, widths = c(1, 1),
  top=textGrob(paste0("GSEA: ",FEA_title," with similarity summary"), gp=gpar(fontsize=18, col="black"))
)
svg(filename = file.path(".", "01.PlotOut", "FEA_All.svg"), width = 26, height = 16, pointsize = 12)
plot(gp)
dev.off()
png 
  2 
graphics.off()
knitr::opts_knit$set(global.device = TRUE)
plot(gp)

knitr::opts_knit$set(global.device = FALSE)

Up-regulated DEGs

j <- "GO_BP"
k <- "Up_regulated"
Par_name <- "TMG 6h vs OSMI-1 6h"
FEA_title<-paste0(k, " ", nrow(ORA_list[[k]][[j]]$Raw)," significant GO_", j, " terms (", Par_name, "; the most descend terms)")
p1<-dotplot(ORA_list[[k]][[j]]$Raw, showCategory=1000, label_format=100, color = "pvalue", font.size = 18)
p2<-treeplot(
  pairwise_termsim(ORA_list[[k]][[j]]$Raw, method="JC"), showCategory=1000, color = "pvalue",
  cluster.params=list(hclust_method = "ward.D2", label_words_n = 5, n = 5, font.size = 18)
)
gp <- gridExtra::grid.arrange(
  p1, p2, nrow = 1, widths = c(1, 1),
  top=textGrob(paste0("GSEA: ",FEA_title," with similarity summary"), gp=gpar(fontsize=18, col="black"))
)
svg(filename = file.path(".", "01.PlotOut", "FEA_Up.svg"), width = 16, height = 9, pointsize = 12)
plot(gp)
dev.off()
png 
  2 
graphics.off()
knitr::opts_knit$set(global.device = TRUE)
plot(gp)

knitr::opts_knit$set(global.device = FALSE)

Down-regulated DEGs

j <- "GO_BP"
k <- "Down_regulated"
Par_name <- "TMG 6h vs OSMI-1 6h"
FEA_title<-paste0(k, " ", nrow(ORA_list[[k]][[j]]$Raw)," significant GO_", j, " terms (", Par_name, "; the most descend terms)")
p1<-dotplot(ORA_list[[k]][[j]]$Raw, showCategory=1000, label_format=70, color = "pvalue", font.size = 18)
p2<-treeplot(
  pairwise_termsim(ORA_list[[k]][[j]]$Raw, method="JC"), showCategory=1000, color = "pvalue",
  cluster.params=list(hclust_method = "ward.D2", label_words_n = 5, n = 5, font.size = 18), label_format=25
)
gp <- gridExtra::grid.arrange(
  p1, p2, nrow = 1, widths = c(1, 1),
  top=textGrob(paste0("GSEA: ",FEA_title," with similarity summary"), gp=gpar(fontsize=18, col="black"))
)
svg(filename = file.path(".", "01.PlotOut", "FEA_Down.svg"), width = 26, height = 15, pointsize = 12)
plot(gp)
dev.off()
png 
  2 
graphics.off()
knitr::opts_knit$set(global.device = TRUE)
plot(gp)

knitr::opts_knit$set(global.device = FALSE)

02. Retrieve up-stream transcription factors of interested GO_BP terms

In this section we will check the up-stream transcription factors that regulates the genes inside the Top5 overlapped mitochondrial/cytoskeletal GO_BP terms by using TFLink database.

The Top5 overlapped mitochondrial/cytoskeletal GO_BP terms are: 1. GO:0030705, cytoskeleton-dependent intracellular transport 2. GO:0061640, cytoskeleton-dependent cytokinesis 3. GO:0140053, mitochondrial gene expression 4. GO:0070507, regulation of microtubule cytoskeleton organization 5. GO:0006839, mitochondrial transport

02-01. Get up-stream Transcription factors list

Download TFLink database

TFLink <- fread(
  "https://cdn.netbiol.org/tflink/download_files/TFLink_Homo_sapiens_interactions_All_simpleFormat_v1.0.tsv.gz"
)

|==================================================|


Check the tables

head(res@compareClusterResult)
head(TFLink)


Get annotation of genes related to Mitochondrial/Cytoskeletal GO_BP terms.

TOP5 <- res@compareClusterResult[res@compareClusterResult$ID %in% c("GO:0030705", "GO:0061640", "GO:0140053", "GO:0070507", "GO:0006839"),]
GeneLs <- TOP5$geneID %>%
  str_split(., "/") %>%
  unlist() %>%
  unique()
Ann_0mart<-NULL
attempt<-1
attempt_max<-12
while(is.null(Ann_0mart)&&attempt<13){
  if(attempt%in%seq(from=1,to=attempt_max,3)){
    url<-"https://useast.ensembl.org"
  }else if(attempt%in%seq(from=2,to=attempt_max,3)){
    url<-"https://www.ensembl.org"
  }else if(attempt%in%seq(from=3,to=attempt_max,3)){
    url<-"https://useast.ensembl.org/"
  }else if(attempt%in%seq(from=4,to=attempt_max,3)){
    url<-"https://asia.ensembl.org/"
  }
  try({
    Ann_0mart <- useDataset(
      "hsapiens_gene_ensembl",
      useMart("ENSEMBL_MART_ENSEMBL", host = url)
    )
  }, silent = TRUE)
  attempt<-attempt+1
  if(is.null(Ann_0mart)){Sys.sleep(10)}
}
Anno_GeneLs <- getBM(
  mart = Ann_0mart,
  attributes = c("hgnc_symbol", "ensembl_gene_id", "external_gene_name"),
  filter = "ensembl_gene_id",
  values = GeneLs,
  uniqueRows = TRUE
)
rownames(Anno_GeneLs)<-Anno_GeneLs$ensembl_gene_id


Make functions based on the Uniport API and prepare the gene list.

library(httr)
isJobReady <- function(jobId) {
  pollingInterval <- 5
  nTries <- 20
  for (i in 1:nTries) {
    url <- paste("https://rest.uniprot.org/idmapping/status/", jobId, sep = "")
    r <- GET(url = url, accept_json())
    status <- httr::content(r, as = "parsed")
    if (!is.null(status[["results"]]) || !is.null(status[["failedIds"]])) {
      return(TRUE)
    }
    if (!is.null(status[["messages"]])) {
      print(status[["messages"]])
      return(FALSE)
    }
    Sys.sleep(pollingInterval)
  }
  return(FALSE)
}
get_next_link <- function(headers) {
  if (!is.null(headers[["Link"]])) {
    match <- str_match(
      headers[["Link"]],
      '^\\<\\s*(.*?)\\s*\\>\\; rel\\=\\"next\\"$'
    )
    if (!isEmpty(match)) {
      return(match[2])
    }
  } else {
    NULL
  }
}


Fetch UniprotID for the Mitochondrial/Cytoskeletal genes using Ensembl ID

temp <- Anno_GeneLs$ensembl_gene_id
files <- list(
  from = "Ensembl",
  to = "UniProtKB-Swiss-Prot",
  ids = paste0(temp, collapse = ",")
)
r <- POST(url = "https://rest.uniprot.org/idmapping/run", body = files, encode = "multipart", accept_json())
r <- POST(url = "https://rest.uniprot.org/idmapping/run", body = files, encode = "multipart", accept_json())
while (r$status_code != 200) {
  r <- POST(url = "https://rest.uniprot.org/idmapping/run", body = files, encode = "multipart", accept_json())
  Sys.sleep(5)
}
submission <- httr::content(r, as = "parsed")
if (isJobReady(submission[["jobId"]])) {
  url <- paste("https://rest.uniprot.org/idmapping/details/", submission[["jobId"]], sep = "")
  response <- GET(url = url, accept_json())
  details <- httr::content(response, as = "parsed")
  res_url <- paste0(
    details[["redirectURL"]],
    "?fields=accession%2Creviewed%2Cid%2Cprotein_name%2Clength%2Cgene_primary%2Cgo%2Cft_zn_fing%2Cft_repeat%2Cft_region%2Cft_domain%2Cft_motif%2Ccc_domain%2Cft_compbias%2Cft_coiled%2Cannotation_score%2Ckeyword%2Ccomment_count%2Ccc_subcellular_location%2Ccc_function%2Ccc_pathway%2Cprotein_families%2Cft_carbohyd%2Cft_peptide%2Cft_transit%2Cft_signal%2Cft_propep%2Ccc_ptm%2Cft_init_met%2Cft_lipid%2Cft_mod_res%2Cft_disulfid%2Cft_crosslnk%2Cft_chain%2Cxref_kegg&format=tsv&size=500"
  )
  response <- GET(url = res_url, accept_json())
  total <- response$headers$`x-total-results`
  temp2 <- data.table::fread(
    res_url,
    verbose = TRUE, showProgress = TRUE
  ) %>% as.data.frame()
  while (!is.null(res_url)) {
    response <- GET(url = res_url, accept_json())
    res_url <- get_next_link(headers(response))
    if (!is.null(res_url)) {
      temp2 <- rbind(
        temp2,
        data.table::fread(
          res_url,
          verbose = FALSE, showProgress = FALSE
        ) %>% as.data.frame()
      )
      print(
        paste0(
          nrow(temp2), "/", total
        )
      )
    }
  }
}
  OpenMP version (_OPENMP)       201511
  omp_get_num_procs()            128
  R_DATATABLE_NUM_PROCS_PERCENT  unset (default 50)
  R_DATATABLE_NUM_THREADS        unset
  R_DATATABLE_THROTTLE           unset (default 1024)
  omp_get_thread_limit()         2147483647
  omp_get_max_threads()          128
  OMP_THREAD_LIMIT               unset
  OMP_NUM_THREADS                unset
  RestoreAfterFork               true
  data.table is using 64 threads with throttle==1024. See ?setDTthreads.

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Input contains no \n. Taking this to be a filename to open
[01] Check arguments
  Using 64 threads (omp_get_max_threads()=128, nth=64)
  NAstrings = [<<NA>>]
  None of the NAstrings look like numbers.
  show progress = 1
  0/1 column will be read as integer
[02] Opening the file
  Opening file /tmp/RtmpXF8M4i/file14cae4651113d5.
  File opened, size = 1.736MB (1820314 bytes).
  Memory mapped ok
[03] Detect and skip BOM
[04] Arrange mmap to be \0 terminated
  \n has been found in the input and different lines can end with different line endings (e.g. mixed \n and \r\n in one file). This is common and ideal.
[05] Skipping initial rows if needed
  Positioned on line 1 starting: <<From Entry   Reviewed    Entry Name>>
[06] Detect separator, quoting rule, and ncolumns
  Detecting sep automatically ...
  sep=','  with 2 lines of 4 fields using quote rule 0
  sep='|'  with 2 lines of 18 fields using quote rule 0
  sep=0x9  with 100 lines of 36 fields using quote rule 0
  Detected 36 columns on line 1. This line is either column names or first data row. Line starts as: <<From Entry   Reviewed    Entry Name>>
  Quote rule picked = 0
  fill=false and the most number of columns found is 36
[07] Detect column types, good nrow estimate and whether first row is column names
  Number of sampling jump points = 1 because (1820313 bytes from row 1 to eof) / (2 * 478689 jump0size) == 1
  Type codes (jump 000)    : CCCCC5CCCCCCCCCC7CCCCCCC2CCCCCCCCCCC  Quote rule 0
  Type codes (jump 001)    : CCCCC5CCCCCCCCCC7CCCCCCC2CCCCCCCCCCC  Quote rule 0
  'header' determined to be true due to column 6 containing a string on row 1 and a lower type (int32) in the rest of the 170 sample rows
  =====
  Sampled 170 rows (handled \n inside quoted fields) at 2 jump points
  Bytes from first data row on line 2 to the end of last row: 1819858
  Line length: mean=4210.86 sd=3219.03 min=839 max=18007
  Estimated number of rows: 1819858 / 4210.86 = 433
  Initial alloc = 866 rows (433 + 100%) using bytes/max(mean-2*sd,min) clamped between [1.1*estn, 2.0*estn]
  =====
[08] Assign column names
[09] Apply user overrides on column types
  After 0 type and 0 drop user overrides : CCCCC5CCCCCCCCCC7CCCCCCC2CCCCCCCCCCC
[10] Allocate memory for the datatable
  Allocating 36 column slots (36 - 0 dropped) with 866 rows
[11] Read the data
  jumps=[0..1), chunk_size=4210858, total_size=1819858
  1 out-of-sample type bumps: CCCCC5CCCCCCCCCC7CCCCCCCCCCCCCCCCCCC
  jumps=[0..1), chunk_size=4210858, total_size=1819858
Read 428 rows x 36 columns from 1.736MB (1820314 bytes) file in 00:00.027 wall clock time
[12] Finalizing the datatable
  Type counts:
         1 : int32     '5'
         1 : float64   '7'
        34 : string    'C'
=============================
   0.001s (  4%) Memory map 0.002GB file
   0.016s ( 60%) sep='\t' ncol=36 and header detection
   0.000s (  1%) Column type detection using 170 sample rows
   0.000s (  1%) Allocation of 866 rows x 36 cols (0.000GB) of which 428 ( 49%) rows used
   0.009s ( 34%) Reading 1 chunks (0 swept) of 4.016MB (each chunk 428 rows) using 1 threads
   +    0.003s ( 11%) Parse to row-major thread buffers (grown 0 times)
   +    0.005s ( 21%) Transpose
   +    0.001s (  2%) Waiting
   0.001s (  5%) Rereading 1 columns due to out-of-sample type exceptions
   0.027s        Total
Column 25 ("Peptide") bumped from 'bool8' to 'string' due to <<PEPTIDE 688..713; /note="P3(42)"; /id="PRO_0000000095"; PEPTIDE 688..711; /note="P3(40)"; /id="PRO_0000000096">> on row 243
colnames(temp2)[1] <- "EnsemblID"
a <- str_split(temp2$EnsemblID, ",")
temp <- which((lengths(a) >= 2) == TRUE)
for (i in temp) {
  temp1 <- a[[i]]
  temp2$EnsemblID[i] <- temp1[1]
  for (j in 2:length(temp1)) {
    temp2 <- rbind(temp2, temp2[i, ])
    nrow <- nrow(temp2)
    temp2$EnsemblID[nrow] <- temp1[j]
  }
}
dup_ls <- temp2$EnsemblID[duplicated(temp2$EnsemblID)]
for(i in dup_ls){
  temp <- temp2[temp2$EnsemblID!=i,]
  dup_rows <- temp2[temp2$EnsemblID==i,]
  dup_rows <- dup_rows[dup_rows$Length == max(dup_rows$Length),]
  temp2 <-rbind(dup_rows, temp)
}
rownames(temp2) <- temp2$EnsemblID
Anno_GeneLs <- temp2


Get related Transcription Factors (TFs)

TFLink_related <- TFLink[TFLink$UniprotID.Target %in% Anno_GeneLs$Entry,]
#TF_ls <- unique(TFLink_related$UniprotID.TF)
#TFLink_related <- TFLink[(TFLink$UniprotID.TF %in% TF_ls | TFLink$UniprotID.Target %in% TF_ls),]
#TFLink_related <- TFLink_related[(TFLink_related$UniprotID.Target %in% c(TF_ls,Anno_GeneLs$Entry)),]
head(TFLink_related)


02-02. Get the O-GlcNAc info

Add the O-GlcNAc site information from the O-GlcNAcAtlas database.

First we have to retrieve the UniPort Accession number for each genes

library("httr") 
library("dplyr") 
library("jsonlite")
library("curl")
library("RCurl")
library("magrittr")
library("rlist")
library("pipeR")
library("plyr")
library("xml2")
library("rvest")
library("parallel")
library("doParallel")
library("doSNOW")
# Fetch O-GlcNAc records from https://www.oglcnac.org/atlas/search/
temp2 <- data.frame()
Uniportls <- unique(TFLink_related$UniprotID.TF)
Par_cl <- makeCluster(parallelly::freeCores()[1])
registerDoSNOW(Par_cl)
Par_pb <- txtProgressBar(min = 1, max = length(Uniportls), style = 3)
progress <- function(n) setTxtProgressBar(Par_pb, n)
Par_opts <- list(progress = progress)
temp2 <- foreach(
  i = 1:length(Uniportls), .combine = base::rbind, .errorhandling = "pass",
  .options.snow = Par_opts, .packages = c("tcltk", "dplyr", "utils")
) %dopar% {
  Query <- Uniportls[i]
  url <- c("https://www.oglcnac.org/atlas/search/")
  pg <- rvest::session(url)
  token <- xml2::xml_attrs(xml2::xml_find_all(xml2::read_html(pg), ".//input")[[1]])[["value"]]
  myheaders <- c(
  'accept' ='text/html,application/xhtml+xml,application/xml;q=0.9,image/avif,image/webp,image/apng,*/*;q=0.8,application/signed-exchange;v=b3;q=0.7',
  'accept-encoding' = 'gzip, deflate, br',
  'accept-language' = 'en-US,en;q=0.9,zh-CN;q=0.8,zh;q=0.7,zh-TW;q=0.6,ja;q=0.5',
  'cache-control' = 'max-age=0',
  'content-length' = as.character(nchar(Query) + 120),
  'content-type' = 'application/x-www-form-urlencoded',
  'cookie' = stringr::str_split(pg[["response"]][["headers"]][["set-cookie"]],";")[[1]][1],
  'dnt' = '1',
  'origin' = 'https://oglcnac.org',
  'referer' = 'https://oglcnac.org/atlas/search/',
  'sec-ch-ua' = '"Google Chrome";v="111", "Not(A:Brand";v="8", "Chromium";v="111"',
  'sec-ch-ua-mobile' = '?0',
  'sec-ch-ua-platform' = 'Linux',
  'sec-fetch-dest' = 'document',
  'sec-fetch-mode' = 'navigate',
  'sec-fetch-site' = 'same-origin',
  'sec-fetch-user' = '?1',
  'upgrade-insecure-requests' = '1',
  'user-agent' = 'Mozilla/5.0 (X11; Linux x86_64) AppleWebKit/537.36 (KHTML, like Gecko) Chrome/111.0.0.0 Safari/537.36'
  )
  response <- httr::POST(
    url = url,
    httr::add_headers(.headers = myheaders),
    body = list(
      "csrfmiddlewaretoken" = token,
      "search_term" = Query,
      "search_field" = "Accession"
    ),
    encode = "form"
  )
  if (httr::status_code(response) != 200) {
    out <- data.frame(
      Query = Query,
      Accession = "Failure",
      Entry_Name = "Failure",
      Protein_Name = "Failure",
      Gene_Name = "Failure",
      Position_in_Protein = "Failure",
      Status = httr::status_code(response),
      "O-GlcNAc" = "Unknown"
    )
  } else if (rvest::html_table(xml2::read_html(response))[[2]] %>% as.data.frame() %>% nrow() == 0) {
    out <- data.frame(
      Query = Query,
      Accession = "No_records",
      Entry_Name = "No_records",
      Protein_Name = "No_records",
      Gene_Name = "No_records",
      Position_in_Protein = "No_records",
      Status = httr::status_code(response),
      "O-GlcNAc" = "Non"
    )
  } else if (rvest::html_table(xml2::read_html(response))[[2]] %>% as.data.frame() %>% nrow() != 0) {
    out <- rvest::html_table(xml2::read_html(response))[[2]] %>% as.data.frame()
    out <- data.frame(
      Query = Query,
      Accession = out$Accession,
      Entry_Name = out$`Entry Name`,
      Protein_Name = out$`Protein Name`,
      Gene_Name = out$`Gene Name`,
      Position_in_Protein = out$`Position in Protein`,
      Status = httr::status_code(response),
      "O-GlcNAc" = "Yes"
    )
  }
  out
}


  |===================================================================================================================================== | 100%
  |======================================================================================================================================| 100%
stopCluster(Par_cl)
OGlcNAc_Anno <- temp2


Add O-GlcNAc info to TFs.

OGlcNAc <- rep("No", nrow(TFLink_related))
TFLink_related <- cbind(OGlcNAc, TFLink_related)
TFLink_related$OGlcNAc[TFLink_related$UniprotID.TF %in% OGlcNAc_Anno$Accession]<-"Yes"
head(TFLink_related)

02-03. Get signifciantly changed TFs

Add DEGs info to TFs.

DEGs <- DEGs_ls[["HEK293_TMG_6hBvsHEK293_OSMI2_6hA"]][["DEGs_raw"]]
DEGs <- DEGs[DEGs$Is.Sig.=="Yes",]
is.DEGs <- rep("No", nrow(TFLink_related))
TFLink_related <- cbind(is.DEGs, TFLink_related)
TFLink_related$is.DEGs[TFLink_related$UniprotID.TF %in% DEGs$UniProtKBID]<-"Yes"
head(TFLink_related)

02-04. Filtering & Visualization

1. Filtering

Filter out the TFs wihout both significantly changes and O-GlcNAc sites.

TFLink_related <- TFLink_related[(TFLink_related$is.DEGs == "Yes" | TFLink_related$OGlcNAc == "Yes"),]
TFLink_related <- TFLink_related[(TFLink_related$OGlcNAc == "Yes"),]
dim(TFLink_related)
[1] 105492     17
head(TFLink_related)


Remove the records that not related to both of Mitochondrial/Cytoskeletal genes and remained TFs.

ChkLs <- unique(c(TFLink_related$UniprotID.TF, Anno_GeneLs$Entry))
TFLink_related <- TFLink_related[TFLink_related$UniprotID.Target %in% ChkLs,]
dim(TFLink_related)
[1] 105492     17
head(TFLink_related)

2. Literature mining

Make functions

Make literature mining functions

#Load functions#
RetrieveEntrezID <- function(
    Homologues=FALSE,
    Homo_species=Homo_species,
    Par_species=Par_species,
    Par_species.Uniprot=Par_species.Uniprot,
    GenesLs=GenesLs,
    updateProgress = NULL
){
  #|----Set up Biomart parameters----|####
  Ann_0mart<-NULL
  attempt<-1
  attempt_max<-12
  while(is.null(Ann_0mart)&&attempt<13){
    if(attempt%in%seq(from=1,to=attempt_max,3)){
      url<-"https://useast.ensembl.org"
    }else if(attempt%in%seq(from=2,to=attempt_max,3)){
      url<-"https://www.ensembl.org"
    }else if(attempt%in%seq(from=3,to=attempt_max,3)){
      url<-"https://useast.ensembl.org/"
    }else if(attempt%in%seq(from=4,to=attempt_max,3)){
      url<-"https://asia.ensembl.org/"
    }
    try({
      Ann_0mart <- useMart("ENSEMBL_MART_ENSEMBL", host=url) %>%
        useDataset(Par_species, .)
    }, silent = TRUE)
    attempt<-attempt+1
    if(is.null(Ann_0mart)){Sys.sleep(10)}
  }
  
  if(Homologues){
    if (is.function(updateProgress)) {
      text <- paste0("Get Homologoeus Gene in ", Homo_species) 
      updateProgress(detail = text)
    }
    #listAttributes(Ann_0mart)%>%View()
    temp <- NULL
    attempt<-1
    attempt_max<-12
    while(is.null(temp)&&attempt<13){
      try({
        temp <- getBM(
          mart=Ann_0mart,
          attributes=c("ensembl_gene_id",
                       Homo_species),
          filter="ensembl_gene_id",
          values=GenesLs,
          uniqueRows = T)
      }, silent = TRUE)
      attempt<-attempt+1
      if(is.null(temp)){Sys.sleep(10)}
    }
    temp<-temp[!temp[,2]%in%"",]
    temp<-temp[!duplicated(temp[,2]),]
    NaMapping<-temp[,1]
    names(NaMapping)<-temp[,2]
    print(Homo_species)
    if(is_empty(temp)|nrow(temp)<1){
      return(NA)
    }
    #print("Set up Biomart parameters")
    #|----Set up Biomart parameters----|####
    if(Homo_species == "hsapiens_homolog_ensembl_gene"){
      Par_species <- "hsapiens_gene_ensembl"
    }else if(Homo_species == "mmusculus_homolog_ensembl_gene"){
      Par_species <- "mmusculus_gene_ensembl"
    }else if(Homo_species == "rnorvegicus_homolog_ensembl_gene"){
      Par_species <- "rnorvegicus_gene_ensembl"
    }else if(Homo_species == "sscrofa_homolog_ensembl_gene"){
      Par_species <- "sscrofa_gene_ensembl"
    }
    Ann_0mart<-NULL
    attempt<-1
    attempt_max<-12
    while(is.null(Ann_0mart)&&attempt<13){
      if(attempt%in%seq(from=1,to=attempt_max,3)){
        url<-"https://useast.ensembl.org"
      }else if(attempt%in%seq(from=2,to=attempt_max,3)){
        url<-"https://www.ensembl.org"
      }else if(attempt%in%seq(from=3,to=attempt_max,3)){
        url<-"https://useast.ensembl.org/"
      }else if(attempt%in%seq(from=4,to=attempt_max,3)){
        url<-"https://asia.ensembl.org/"
      }
      try({
        Ann_0mart <- useMart("ENSEMBL_MART_ENSEMBL", host=url) %>%
          useDataset(Par_species, .)
      }, silent = TRUE)
      attempt<-attempt+1
      if(is.null(Ann_0mart)){Sys.sleep(10)}
    }
    Anno_gene <- NULL
    attempt<-1
    attempt_max<-12
    while(is.null(Anno_gene)&&attempt<13){
      try({
        Anno_gene <- getBM(
          mart=Ann_0mart,
          attributes=c("ensembl_gene_id","entrezgene_id","gene_biotype",
                       "external_gene_name","description"),
          filter="ensembl_gene_id",
          values=temp[,2],
          uniqueRows = T)
      }, silent = TRUE)
      attempt<-attempt+1
      if(is.null(Anno_gene)){Sys.sleep(10)}
    }
    rm(temp)
  }else{
    print("getBM")
    if (is.function(updateProgress)) {
      text <- "Get PubMed Gene ID"
      updateProgress(detail = text)
    }
    Anno_gene <- NULL
    attempt<-1
    attempt_max<-12
    while(is.null(Anno_gene)&&attempt<13){
      try({
        Anno_gene <- getBM(
          mart=Ann_0mart,
          attributes=c("ensembl_gene_id","entrezgene_id","gene_biotype",
                       "external_gene_name","description"),
          filter="ensembl_gene_id",
          values=GenesLs,
          uniqueRows = T)
      }, silent = TRUE)
      attempt<-attempt+1
      if(is.null(Anno_gene)){Sys.sleep(10)}
    }
  }
  
  Anno<-Anno_gene[!duplicated(Anno_gene$ensembl_gene_id),]
  rownames(Anno)<-Anno$ensembl_gene_id
  Anno<-data.frame(
    ensembl_gene_id=Anno$ensembl_gene_id,
    entrezgene_id=Anno$entrezgene_id,
    external_gene_name=Anno$external_gene_name,
    gene_biotype=Anno$gene_biotype,
    row.names = rownames(Anno)
  )
  Anno2<-Anno[!is.na(Anno$entrezgene_id),] #For EntrezGeneID
  Anno2<-Anno2[!duplicated(Anno2[,'ensembl_gene_id']),] #For EntrezGeneID
  rownames(Anno2)<-Anno2$ensembl_gene_id
  temp<-Anno[is.na(Anno$entrezgene_id),"ensembl_gene_id"]
  print("Check EntrezGeneID again")
  #|----Check EntrezGeneID again----|####
  if(!is_empty(temp)){
    if(length(temp)<2){
      NCBIcheck<-read_html(
        paste0(
          "https://www.ncbi.nlm.nih.gov/gene/?term=",
          temp
        )
      )%>%xml_find_all(., ".//span")%>%xml_text()%>%
        grep("Gene ID",.,value = TRUE)
      if(!isEmpty(NCBIcheck)){
        NCBIcheck<-NCBIcheck%>%unlist()%>%
          str_extract_all(.,"(\\d)+")%>%.[[1]]%>%.[1]
      }else{
        NCBIcheck<-NA
      }
      out<-data.frame(
        ensembl_gene_id=temp,
        entrezgene_id=NCBIcheck
      )%>%as.data.frame()
      temp2<-out
    }else{
      Par_cl<-makeCluster(parallelly::freeConnections()-1)
      registerDoSNOW(Par_cl)
      Par_pb <- txtProgressBar(min=1, max=length(temp), style = 3)
      progress <- function(n) setTxtProgressBar(Par_pb, n)
      Par_opts<-list(progress = progress)
      #Refer here for all column names for Entrez API (https://www.ncbi.nlm.nih.gov/books/NBK25501/)
      temp2<-foreach(i=1:length(temp), .combine=rbind, .errorhandling = "pass", .inorder=FALSE,
                     .options.snow=Par_opts, .packages = c("dplyr","utils","xml2","S4Vectors","stringr","BiocGenerics")) %dopar% {
                       NCBIcheck<-read_html(
                         paste0(
                           "https://www.ncbi.nlm.nih.gov/gene/?term=",
                           temp[i]
                         )
                       )%>%xml_find_all(., ".//span")%>%xml_text()%>%
                         grep("Gene ID",.,value = TRUE)
                       if(!isEmpty(NCBIcheck)){
                         NCBIcheck<-NCBIcheck%>%unlist()%>%
                           str_extract_all(.,"(\\d)+")%>%.[[1]]%>%.[1]
                       }else{
                         NCBIcheck<-NA
                       }
                       out<-data.frame(
                         ensembl_gene_id=temp[i],
                         entrezgene_id=NCBIcheck
                       )%>%as.data.frame()
                       return(out)
                     }
      stopCluster(Par_cl)
    }
    temp2<-temp2[!is.na(temp2$entrezgene_id),]
    temp2<-temp2[!duplicated(temp2$ensembl_gene_id),]
    rownames(temp2)<-temp2$ensembl_gene_id
    temp2<-cbind(
      temp2,
      Anno[temp2$ensembl_gene_id,c(3:4)]
    )
    #sum(Anno2$ensembl_gene_id%in%temp2$ensembl_gene_id)==0
    Anno2<-rbind(
      Anno2,
      temp2
    )
  }
  if(Homologues){
    Anno2<-cbind(mapping=NaMapping[Anno2$ensembl_gene_id],Anno2)
    Anno2<-Anno2[!duplicated(Anno2$mapping),]
    rownames(Anno2) <- NaMapping[Anno2$ensembl_gene_id]
    Anno2<-Anno2[,-1]
  }
  print("end")
  if (is.function(updateProgress)) {
    text <- paste0("ID Convert Done ") 
    updateProgress(detail = text)
  }
  return(Anno2)
}

pseudoLog10 <- function(x){ asinh(x/2)/log(10) }

WZY_GetSummaryText<-function(p){
  pdata <- data.frame(name = p$data$label, color2 = p$data$group)
  pdata <- pdata[!is.na(pdata$name), ]
  cluster_color <- unique(pdata$color2)
  
  cluster_label <- sapply(
    cluster_color, enrichplot:::get_wordcloud,
    ggData = pdata, nWords = 4
  ) %>% paste0(.,collapse = " ") %>% str_split(., " ") %>% unlist()
  return(cluster_label)
}

WZY_literatureMining<-function(GenesLs=GenesLs, Mesh_term4Interesting=Mesh_term4Interesting, Species=Species, updateProgress = NULL){
  out<-list()
  N<-paste0(#To search for the total number of PubMed citations, enter all[sb] in the search box.(20210506)
    "https://pubmed.ncbi.nlm.nih.gov/?term=",
    URLencode('all[sb]'),
    "&sort=date"
  )%>%read_html()%>%html_nodes(".value")%>%html_text()%>%.[1]%>%gsub(",","",.)%>%as.numeric()
  K<-paste0(#the amounts of literature related to osteoblast differentiation #20210506# PubMed Query: 
    "https://pubmed.ncbi.nlm.nih.gov/?term=",
    URLencode(Mesh_term4Interesting),
    "&sort=date"
  )%>%read_html()%>%html_nodes(".value")%>%html_text()%>%.[1]%>%gsub(",","",.)%>%as.numeric()
  Thresh<-K/N*10
  
  ####|prepare gene-related articles|####
  # hsapiens_gene_ensembl; mmusculus_gene_ensembl; rnorvegicus_gene_ensembl; sscrofa_gene_ensembl
  # Homo sapiens (Human) [9606]; Mus musculus (Mouse) [10090]; Rattus norvegicus (rat) [10116]; Sus scrofa (pig) [9823]
  # (human) Homo sapiens (human) [hsa]; (mouse) Mus musculus (mouse) [mmu]; (rat) Rattus norvegicus [rno]; (pig) Sus scrofa [ssc]
  # hsapiens_homolog_ensembl_gene; mmusculus_homolog_ensembl_gene; rnorvegicus_homolog_ensembl_gene; sscrofa_homolog_ensembl_gene
  print(GenesLs)
  print(Mesh_term4Interesting)
  print(Species)
  if (is.function(updateProgress)) {
    text <- "Get All Homologoeus Genes"
    updateProgress(detail = text)
  }
  if(Species == "Hsa"){
    Par_species <- "hsapiens_gene_ensembl"
    Par_species.Uniprot <- "9606"
    Homo_species <- c(
      "mmusculus_homolog_ensembl_gene",
      "rnorvegicus_homolog_ensembl_gene",
      "sscrofa_homolog_ensembl_gene"
    )
  }else if(Species == "Mus"){
    Par_species <- "mmusculus_gene_ensembl"
    Par_species.Uniprot <- "10090"
    Homo_species <- c(
      "hsapiens_homolog_ensembl_gene",
      "rnorvegicus_homolog_ensembl_gene",
      "sscrofa_homolog_ensembl_gene"
    )
  }else if(Species == "Rno"){
    Par_species <- "rnorvegicus_gene_ensembl"
    Par_species.Uniprot <- "10116"
    Homo_species <- c(
      "mmusculus_homolog_ensembl_gene",
      "hsapiens_homolog_ensembl_gene",
      "sscrofa_homolog_ensembl_gene"
    )
  }else if(Species == "Ssc"){
    Par_species <- "sscrofa_gene_ensembl"
    Par_species.Uniprot <- "9823"
    Homo_species <- c(
      "mmusculus_homolog_ensembl_gene",
      "rnorvegicus_homolog_ensembl_gene",
      "hsapiens_homolog_ensembl_gene"
    )
  }
  print(Par_species)
  print(Par_species.Uniprot)
  query.res<-RetrieveEntrezID(Par_species=Par_species, Par_species.Uniprot=Par_species.Uniprot, GenesLs=GenesLs)
  homologeus1 <- RetrieveEntrezID(
    Homologues=TRUE, Homo_species=Homo_species[1], Par_species=Par_species,
    Par_species.Uniprot=Par_species.Uniprot, GenesLs=GenesLs, updateProgress = updateProgress
  )
  homologeus2 <- RetrieveEntrezID(
    Homologues=TRUE, Homo_species=Homo_species[2], Par_species=Par_species,
    Par_species.Uniprot=Par_species.Uniprot, GenesLs=GenesLs, updateProgress = updateProgress
  )
  homologeus3 <- RetrieveEntrezID(
    Homologues=TRUE, Homo_species=Homo_species[3], Par_species=Par_species,
    Par_species.Uniprot=Par_species.Uniprot, GenesLs=GenesLs, updateProgress = updateProgress
  )
  
  #Calculate results and construct the literature mining table
  literature.mining<-data.frame(matrix(nrow = 0, ncol=14))
  colnames(literature.mining)<-c("ensembl_gene_id","entrezgene_id","GeneSymbol",
                                 "gene_biotype", "N", "K", "n", "k", "R", "10x Background of R","P.value",
                                 "Gene related PMID", "Overlapped PMID", "Overlapped Genes [Article No]")
  # Par_pb <- txtProgressBar(min=1, max=nrow(query.res), style = 3)
  print("StartLoop")
  list.packages <- c(
    "readxl", "ggplot2", "ggpubr", "matrixStats", "ggrepel", "reshape2", "dplyr", "stringr",
    "grid", "tcltk", "parallel", "doParallel", "doSNOW", "data.table", "gplots",
    "randomcoloR", "factoextra", "RColorBrewer", "grDevices", "gmp", "xtable", "latex2exp",
    "httr", "jsonlite", "curl", "RCurl", "magrittr", "rlist", "pipeR", "plyr",
    "xml2", "rvest", "knn.covertree", "knitr", "rlang", "visNetwork", "hwriter", "htmltools"
  )
  bio.list.packages <- c(
    "limma", "ExperimentHub", "clusterProfiler", "GO.db",
    "org.Mm.eg.db", "pathview", "enrichplot", "org.Hs.eg.db"
  )
  wzy_mainloop <- function(
    query.res = query.res, attempt_max = 3, Thresh = Thresh,
    K = K, N = N, i = i
  ){
    GeneID<-c(
      query.res$entrezgene_id[i],
      homologeus1[query.res$ensembl_gene_id[i],"entrezgene_id"],
      homologeus2[query.res$ensembl_gene_id[i],"entrezgene_id"],
      homologeus3[query.res$ensembl_gene_id[i],"entrezgene_id"]
    )
    #### Calculate n
    # Get UID number that within interested MeSH term
    uid.res<-c()
    for(a in GeneID){
      # Retrieve PMID of gene-related articles
      # https://www.ncbi.nlm.nih.gov/books/NBK25497/table/chapter2.T._entrez_unique_identifiers_ui/?report=objectonly
      # https://www.ncbi.nlm.nih.gov/books/NBK25499/
      # https://dataguide.nlm.nih.gov/eutilities/utilities.html
      # https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=gene&db=pubmed&id=68389&linkname=homologene_pubmed
      # https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=gene&db=pubmed&id=12393
      URL_temp<-NULL
      attempt<-1
      url <- paste0(
        "https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=gene&db=pubmed&id=",
        a
      )
      while(is.null(URL_temp)&&attempt<attempt_max){
        try({
          url <- url(url, "rb")
          if(class(url)[1]=="url"){
            URL_temp <- read_xml(
              url
            )%>%xml_find_all(., ".//Id")%>%xml_text()
            close(url)
          }
        }, silent = TRUE)
        attempt<-attempt+1
        if(is.null(URL_temp)){Sys.sleep(round(runif(1,10,180),1))}
      }
      uid.res<-c(
        uid.res,
        URL_temp
      )
    }
    uid.res<-unique(uid.res)
    n<-length(uid.res)
    #### Calculate k
    maxlimit<-125
    if(n>maxlimit){
      step<-n%/%maxlimit
      mod<-n%%maxlimit
      start<-seq(from=1, to=maxlimit*step, by=maxlimit)
      end<-seq(from=maxlimit, to=maxlimit*step, by=maxlimit)
      if(mod>0){
        start<-c(start, tail(end, 1)+1)
        end<-c(end, n)
      }
      step<-length(start)
    }else{
      step<-1
      start<-1
      end<-n
    }
    k<-0
    overlapped.uid<-c()
    for(a in 1:step){
      URL_temp<-NULL
      attempt<-1
      url <- URLencode(
        paste0(
          "https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esearch.fcgi?db=pubmed&term=",
          paste(uid.res[start[a]:end[a]],collapse=","),"[UID]+AND+(",URLencode(Mesh_term4Interesting),")",
          "&rettype=count"
        )
      )
      while(is.null(URL_temp)&&attempt<attempt_max){
        try({
          url <- url(url, "rb")
          if(class(url)[1]=="url"){
            URL_temp <- read_xml(#the amounts of articles of each gene on interested MeSH term:
              url
            )%>%xml_find_all(., ".//Count")%>%xml_text()%>%.[1]%>%as.numeric()
            close(url)
          }
        }, silent = TRUE)
        attempt<-attempt+1
        if(is.null(URL_temp)){Sys.sleep(round(runif(1,10,180),1))}
      }
      if(is.null(URL_temp)){URL_temp <- 0}
      k<-k+URL_temp
      URL_temp<-NULL
      attempt<-1
      url <- URLencode(
        paste0(
          "https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esearch.fcgi?db=pubmed&term=",
          paste(uid.res[start[a]:end[a]],collapse=","),"[UID]+AND+(",URLencode(Mesh_term4Interesting),")",
          "&rettype=unlist"
        )
      )
      while(is.null(URL_temp)&&attempt<attempt_max){
        try({
          url <- url(url, "rb")
          if(class(url)[1]=="url"){
            URL_temp <- read_xml(#the amounts of articles of each gene on interested MeSH term:
              url
            )%>%xml_find_all(., ".//Id")%>%xml_text()
            close(url)
          }
        }, silent = TRUE)
        attempt<-attempt+1
        if(is.null(URL_temp)){Sys.sleep(round(runif(1,10,180),1))}
      }
      overlapped.uid<-c(
        overlapped.uid,
        URL_temp
      )
    }
    if(is.na(k)){k<-0}
    #### Calculate P
    R<-k/n
    P<-0
    if(k<1){
      P<-0
    }else{
      for (a in 0:(k-1)) {
        P<-P+((chooseZ(K,a)*chooseZ(N-K,n-a))/chooseZ(N,n))
      }
    }
    P<-asNumeric(1-P)
    if(P==0){P<-1*10^-300}
    temp<-data.frame(
      ensembl_gene_id=query.res$ensembl_gene_id[i],
      entrezgene_id=query.res$entrezgene_id[i],
      GeneSymbol=query.res$external_gene_name[i],
      gene_biotype=query.res$gene_biotype[i],
      N=N,K=K,n=n,k=k,R=R,Thresh=Thresh,P=P,
      GenePMID=uid.res%>%paste(.,collapse = ","),
      OverlapPMID=overlapped.uid%>%paste(.,collapse = ",")
    )
    colnames(temp)<-c("ensembl_gene_id","entrezgene_id","GeneSymbol",
                      "gene_biotype", "N", "K", "n", "k", "R", "10x Background of R","P.value",
                      "Gene related PMID", "Overlapped PMID")
    return(temp)
  }
  Par_cl<-makeCluster(parallelly::freeConnections()-2)
  registerDoSNOW(Par_cl)
  Par_pb <- txtProgressBar(min=1, max=nrow(query.res), style = 3)
  progress <- function(n) setTxtProgressBar(Par_pb, n)
  Par_opts<-list(progress = progress)
  #Refer here for all column names for Entrez API (https://www.ncbi.nlm.nih.gov/books/NBK25501/)
  temp<-foreach(
    i=1:nrow(query.res), .combine=rbind, .errorhandling = "remove", .inorder=FALSE, .verbose = FALSE,
    .options.snow=Par_opts, .packages = c(list.packages, bio.list.packages)
  ) %dopar% {
    temp3 <- NULL
    temp3 <- wzy_mainloop(query.res = query.res, attempt_max = 5, Thresh = Thresh, K = K, N = N, i = i)
    if(is.null(temp3)){
      temp3<-data.frame(
        ensembl_gene_id=query.res$ensembl_gene_id[i],
        entrezgene_id=query.res$entrezgene_id[i],
        GeneSymbol=query.res$external_gene_name[i],
        gene_biotype=query.res$gene_biotype[i],
        N=NA,K=NA,n=NA,k=NA,R=NA,Thresh=NA,P=NA,
        GenePMID=NA,
        OverlapPMID=NA
      )
      colnames(temp3)<-c("ensembl_gene_id","entrezgene_id","GeneSymbol",
                         "gene_biotype", "N", "K", "n", "k", "R", "10x Background of R","P.value",
                         "Gene related PMID", "Overlapped PMID")
    }
    return(temp3)
  }
  stopCluster(Par_cl)
  literature.mining<-rbind(literature.mining,temp)
  rm(temp)
  gc()
  print("EndLoop")
  #Correcting P-value for multiple testing
  literature.mining<-cbind(literature.mining[,1:11], 
                           p.adj=p.adjust(as.numeric(literature.mining$P.value),method = "BH"),
                           literature.mining[,12:13])
  out<-list(
    literature.mining=literature.mining,
    query.res=query.res,
    homologeus1=homologeus1,
    homologeus2=homologeus2,
    homologeus3=homologeus3
  )
  print("end")
  return(out)
}

literatureMiningPlot<-function(
    literature.mining=out$literature.mining, Thresh.R=NULL,
    use.Padj = FALSE, Thresh.P=0.05, label=TRUE, label_n=5
){
  # print("Plotting")
  # Plotting Results
  literature.mining$n<-as.numeric(literature.mining$n)
  literature.mining$k<-as.numeric(literature.mining$k)
  literature.mining$R<-as.numeric(literature.mining$R)
  if(is.null(Thresh.R)){
    Thresh<-literature.mining$`10x Background of R`[1]
  }else{
    Thresh<-Thresh.R
  }
  df<-literature.mining[,1:12] 
  df$R<-df$R*1000
  df$n<-log10(df$n)
  df$R<-pseudoLog10(df$R)
  df$p.adj<-pseudoLog10(log(1/df$p.adj,2))
  df$P.value<-pseudoLog10(log(1/df$P.value,2))
  df <- df[order(df$P.value), ]
  maxR<-(max(df$R, na.rm=T)+0.3)%>%round(., digits = 1)
  maxP<-(max(df$p.adj, na.rm=T)+0.3)%>%round(., digits = 1)
  RepL_R<-length(rep(0:maxR, each = 9))%/%9
  RepL_P<-length(rep(0:maxP, each = 9))%/%9
  if(use.Padj){
    gplot<-ggplot(df,aes(x=p.adj, y=R, colour=n, size=k ))
  }else{
    gplot<-ggplot(df,aes(x=P.value, y=R, colour=n, size=k ))
  }
  gplot<-gplot +
    geom_point() +
    expand_limits(x=0) +
    scale_y_continuous(
      limits = c(0,maxR),
      breaks = 0:maxR,
      guide = "prism_offset_minor",
      minor_breaks = pseudoLog10(rep(1:9, RepL_R)*(10^rep(0:maxR, each = 9))),
      labels =  function(lab){
        do.call(
          expression,
          lapply(paste(lab), function(x) {
            if(x==0){bquote(bold("0"))}else{bquote(bold("10"^.(x)))}
          })
        )
      }
    )+
    scale_x_continuous(
      limits = c(0,maxP),
      breaks = 0:maxP,
      guide = "prism_offset_minor",
      minor_breaks = pseudoLog10(rep(1:9, RepL_P)*(10^rep(0:maxP, each = 9))),
      labels = function(lab){
        do.call(
          expression,
          lapply(paste(lab), function(x) {
            if(x==0){bquote(bold("0"))}else{bquote(bold("10"^.(x)))}
          })
        )
      }
    )+
    scale_size(range = c(0,20))+
    theme(
      axis.text=element_text(size=12),
      axis.title=element_text(size=14,face="bold"),
      axis.ticks.length = unit(5,"pt"),
      axis.ticks = element_line(linewidth = 0.7),
    )+
    coord_cartesian(clip = "off")+
    geom_hline(yintercept=pseudoLog10(Thresh*1000), linetype="dashed", 
               color = "red", size=0.4)+
    geom_vline(xintercept=pseudoLog10(log(1/Thresh.P,2)), linetype="dashed", 
               color = "red", size=0.4)+
    labs(x="log2(1/P.value)", 
         y="R (‰)", 
         title="",
         colour="log10(Gene Related Articles No.)", size="Topics\nRelated Articles No.")+
    annotation_custom(
      grob = grid::linesGrob(gp=gpar(lwd=2)),
      xmin = -Inf,
      xmax = -Inf,
      ymin = 0,
      ymax = maxR
    )+
    annotation_custom(
      grob = grid::linesGrob(gp=gpar(lwd=2)),
      xmin = 0,
      xmax = maxP,
      ymin = -Inf,
      ymax = -Inf
    )
  #print("PlottingEnd")
  if(label_n == "All"){
    label_n <- nrow(df) 
  }
  if(label){
    if(use.Padj){
      df <- df[df$R>=pseudoLog10(Thresh*1000) & df$p.adj>=pseudoLog10(log(1/Thresh.P,2)), ]
    }else{
      df <- df[df$R>=pseudoLog10(Thresh*1000) & df$P.value>=pseudoLog10(log(1/Thresh.P,2)), ]
    }
    df <- df[order(df$P.value, decreasing = TRUE), ]
    gplot <- gplot + geom_text_repel(
      data = df[1:label_n, ],
      aes(label=GeneSymbol),hjust=0, vjust=0, size=8, color="darkred"
    )
  }
  return(gplot)
}

literatureMiningOverlappedGenes<-function(out, updateProgress = NULL){
  
  literature.mining<-out$literature.mining
  query.res<-out$query.res
  homologeus1<-out$homologeus1
  homologeus2<-out$homologeus2
  homologeus3<-out$homologeus3
  
  outls<-c()
  
  for(i in 1:nrow(query.res)){
    print(paste0(i,"/",nrow(query.res)))
    if (is.function(updateProgress)) {
      text <- paste0(i," in ",nrow(query.res))
      updateProgress(message = text, detail = text)
    }
    GeneID<-c(
      query.res$entrezgene_id[i],
      homologeus1[query.res$ensembl_gene_id[i],"entrezgene_id"],
      homologeus2[query.res$ensembl_gene_id[i],"entrezgene_id"],
      homologeus3[query.res$ensembl_gene_id[i],"entrezgene_id"]
    )%>%.[!is.na(.)]
    
    overlapped.uid<-literature.mining$`Overlapped PMID`[i]%>%str_split(.,",")%>%unlist()
    
    overlapped.genes<-data.frame(matrix(nrow = 0, ncol=3))
    colnames(overlapped.genes)<-c("GeneSymbol","entrezgene_id","Overlapped_PMID")
    if(overlapped.uid[1]!=""){
      
      for(uid in overlapped.uid){
        
        print(paste0("PMID:", uid, " (", which(overlapped.uid==uid)," of ",length(overlapped.uid), ")"))
        temp.gene<-read_xml(
          paste0(
            "https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&db=gene&id=",
            uid
          )
        )%>%xml_find_all(., ".//Id")%>%xml_text()%>%.[-1]%>%unique()%>%.[!.%in%GeneID]
        
        if(is_empty(temp.gene)){next}
        if(length(temp.gene)>500){next}
        
        a.n<-length(temp.gene)
        maxlimit<-50
        if(a.n>maxlimit){
          step<-a.n%/%maxlimit
          mod<-a.n%%maxlimit
          start<-seq(from=1, to=maxlimit*step, by=maxlimit)
          end<-seq(from=maxlimit, to=maxlimit*step, by=maxlimit)
          if(mod>0){
            start<-c(start, tail(end, 1)+1)
            end<-c(end, a.n)
          }
          step<-length(start)
        }else{
          step<-1
          start<-1
          end<-a.n
        }
        
        if(step>1){
          pb <- txtProgressBar(min=1, max=step, style = 3)
        }
        
        removeIdx<-c()
        GeneSymbol<-c()
        for(a in 1:step){
          #print(paste0("b:",which(temp.gene==b),";",length(temp.gene)))
          GSB<-read_html(
            paste0(
              "https://eutils.ncbi.nlm.nih.gov/entrez/eutils/efetch.fcgi?db=gene&id=",
              temp.gene[start[a]:end[a]]%>%paste(.,collapse = ","),
              "&rettype=unlist"
            )
          )
          lh<-(end[a]-start[a]+1)
          if(lh==1){
            test<-xml_child(xml_child(xml_child(xml_child(xml_child(GSB, 1), 1), 1), 1), 2)%>%xml_text()%>%grep("Official Symbol:",.)
            if(!is_empty(test)){
              GeneSymbol<-c(
                GeneSymbol,
                xml_child(xml_child(xml_child(xml_child(xml_child(xml_child(xml_child(GSB, 1), 1), 1), 1), 2), 2), 2)%>%xml_text()
              )
            }else{
              removeIdx<-c(
                removeIdx,1
              )
            }
          }else{
            for(b in 1:lh){
              test<-xml_child(xml_child(xml_child(xml_child(xml_child(GSB, 1), 1), 1), b), 2)%>%xml_text()%>%grep("Official Symbol:",.)
              if(!is_empty(test)){
                GeneSymbol<-c(
                  GeneSymbol,
                  xml_child(xml_child(xml_child(xml_child(xml_child(xml_child(xml_child(xml_child(GSB, 1), 1), 1), b), 2), 2), 2), 2)%>%xml_text()
                )
              }else{
                removeIdx<-c(
                  removeIdx,(b+start[a]-1)
                )
              }
            }
          }
          
          if(step>1){
            setTxtProgressBar(pb, a)
          }
          if(is.function(updateProgress)) {
            text <- paste0(a," in ",step)
            updateProgress(message = paste0(i," in ",nrow(query.res)), detail = text)
          }
        }
        if(step>1){close(pb)}
        if(!is_empty(removeIdx)){
          temp.gene<-temp.gene[-removeIdx]
        }
        
        if(!is_empty(temp.gene)){
          temp<-data.frame(
            GeneSymbol=GeneSymbol%>%str_to_title(),
            entrezgene_id=temp.gene,
            Overlapped_PMID=rep(uid,length(temp.gene))
          )
          overlapped.genes<-rbind(
            overlapped.genes,
            temp
          )
        }
      }
    }
    
    temp<-c()
    OrderID<-c()
    for(a in overlapped.genes$GeneSymbol%>%unique()){
      temp2<-overlapped.genes[overlapped.genes$GeneSymbol==a,]
      OrderID<-c(
        OrderID,
        length(temp2$Overlapped_PMID%>%unique())
      )
      temp<-c(
        temp,
        paste0(
          temp2$GeneSymbol[1],
          " (EntrezID:", temp2$entrezgene_id[1], ";",
          "Overlapped_PMID[", tail(OrderID,1), "]:", paste(temp2$Overlapped_PMID%>%unique(),collapse = ","),")" 
        )
      )
    }
    OrderID<-as.numeric(OrderID)
    OrderID<-order(x=OrderID, decreasing=TRUE, na.last=T)
    overlapped.genes<-temp%>%.[OrderID]%>%paste(.,collapse = " ")
    outls<-c(
      outls,overlapped.genes
    )
  }
  
  overlapped.genes<-cbind(
    literature.mining[,1:4],
    overlapped.genes=outls
  )
  
  return(overlapped.genes)
  
}
library(rlang)
library(ggprism)

Results

Calcuate relativity of the TFs to the Mesh term “Osteoblasts”[Mesh] using a literature mining method.

TFs <- select(org.Hs.eg.db, keys = unique(TFLink_related$Name.TF), columns = c('ENSEMBL'), keytype = "SYMBOL")
'select()' returned 1:many mapping between keys and columns
Mesh_term4Interesting <- '"Osteoblasts"[Mesh]'
GenesLs <- TFs$ENSEMBL[!is.na(TFs$ENSEMBL)]
Species <- "Hsa" # Hsa Mus Rno Ssc
TFs.Mesh<-WZY_literatureMining(GenesLs=GenesLs, Mesh_term4Interesting=Mesh_term4Interesting, Species=Species, updateProgress = NULL)

  [1] "ENSG00000136997" "ENSG00000118260" "ENSG00000177606" "ENSG00000141510" "ENSG00000141905" "ENSG00000173039" "ENSG00000126561"
  [8] "ENSG00000107485" "ENSG00000168610" "ENSG00000096717" "ENSG00000128573" "ENSG00000134323" "ENSG00000185591" "ENSG00000100811"
 [15] "ENSG00000187098" "ENSG00000105698" "ENSG00000115641" "ENSG00000109320" "ENSG00000185122" "ENSG00000284774" "ENSG00000118689"
 [22] "ENSG00000137203" "ENSG00000150907" "ENSG00000175592" "ENSG00000106459" "ENSG00000118058" "ENSG00000138385" "ENSG00000102878"
 [29] "ENSG00000102804" "ENSG00000001167" "ENSG00000134954" "ENSG00000102974" "ENSG00000143437" "ENSG00000123405" "ENSG00000275700"
 [36] "ENSG00000276072" "ENSG00000143162" "ENSG00000170345" "ENSG00000257923" "ENSG00000097007" "ENSG00000115415" "ENSG00000126767"
 [43] "ENSG00000091831" "ENSG00000066136" "ENSG00000129514" "ENSG00000112592" "ENSG00000130816" "ENSG00000130522" "ENSG00000071564"
 [50] "ENSG00000113580" "ENSG00000154727" "ENSG00000132170" "ENSG00000081189" "ENSG00000168214" "ENSG00000074047" "ENSG00000182979"
 [57] "ENSG00000077092" "ENSG00000065978" "ENSG00000136352" "ENSG00000007372" "ENSG00000134982" "ENSG00000120738" "ENSG00000149311"
 [64] "ENSG00000064393" "ENSG00000140464" "ENSG00000069667" "ENSG00000172845" "ENSG00000102554" "ENSG00000078403" "ENSG00000120837"
 [71] "ENSG00000132005" "ENSG00000288283" "ENSG00000141646" "ENSG00000162924" "ENSG00000144791" "ENSG00000143190" "ENSG00000020633"
 [78] "ENSG00000077150" "ENSG00000115966" "ENSG00000072310" "ENSG00000074319" "ENSG00000171843" "ENSG00000106462" "ENSG00000104964"
 [85] "ENSG00000178028" "ENSG00000121022" "ENSG00000121481" "ENSG00000074181" "ENSG00000125398" "ENSG00000172943" "ENSG00000072364"
 [92] "ENSG00000141867" "ENSG00000198026" "ENSG00000136807" "ENSG00000147140" "ENSG00000126457" "ENSG00000151702" "ENSG00000125686"
 [99] "ENSG00000111206" "ENSG00000099956" "ENSG00000275837" "ENSG00000183337" "ENSG00000108468" "ENSG00000075426" "ENSG00000164032"
[106] "ENSG00000072501" "ENSG00000117222" "ENSG00000136715" "ENSG00000164754" "ENSG00000185022" "ENSG00000108055" "ENSG00000185811"
[113] "ENSG00000066422" "ENSG00000100393" "ENSG00000272333" "ENSG00000108312" "ENSG00000067955" "ENSG00000136504" "ENSG00000173473"
[120] "ENSG00000177485" "ENSG00000088038" "ENSG00000276082" "ENSG00000273943" "ENSG00000275979" "ENSG00000274941" "ENSG00000274176"
[127] "ENSG00000274616" "ENSG00000277615" "ENSG00000277600" "ENSG00000277114" "ENSG00000113658" "ENSG00000159216" "ENSG00000029363"
[134] "ENSG00000180530" "ENSG00000101972" "ENSG00000188612" "ENSG00000170653" "ENSG00000100425" "ENSG00000121068" "ENSG00000130382"
[141] "ENSG00000141380" "ENSG00000133884" "ENSG00000100395" "ENSG00000030419" "ENSG00000204371" "ENSG00000238134" "ENSG00000232045"
[148] "ENSG00000224143" "ENSG00000236759" "ENSG00000227333" "ENSG00000206376" "ENSG00000160075" "ENSG00000111276" "ENSG00000196498"
[155] "ENSG00000108175" "ENSG00000171681" "ENSG00000116560" "ENSG00000084676" "ENSG00000129173" "ENSG00000100320" "ENSG00000277564"
[162] "ENSG00000185551" "ENSG00000011304" "ENSG00000169375" "ENSG00000147133" "ENSG00000136574" "ENSG00000285109" "ENSG00000143379"
[169] "ENSG00000142599" "ENSG00000067369" "ENSG00000167491" "ENSG00000147050" "ENSG00000157259" "ENSG00000276644" "ENSG00000105323"
[176] "ENSG00000028310" "ENSG00000103510" "ENSG00000167258" "ENSG00000120690" "ENSG00000198911" "ENSG00000149136" "ENSG00000055609"
[183] "ENSG00000140262" "ENSG00000179348" "ENSG00000126746" "ENSG00000143889" "ENSG00000124813" "ENSG00000134852" "ENSG00000111642"
[190] "ENSG00000137947" "ENSG00000100888" "ENSG00000196591" "ENSG00000089902" "ENSG00000171456" "ENSG00000122482" "ENSG00000164190"
[197] "ENSG00000004487" "ENSG00000173575" "ENSG00000143614" "ENSG00000261992" "ENSG00000033800" "ENSG00000270647" "ENSG00000276833"
[204] "ENSG00000140396" "ENSG00000107290" "ENSG00000196235" "ENSG00000149480" "ENSG00000123374" "ENSG00000137693" "ENSG00000160201"
[211] "ENSG00000068323" "ENSG00000073584" "ENSG00000187079" "ENSG00000123268" "ENSG00000170374" "ENSG00000184634" "ENSG00000104320"
[218] "ENSG00000064102" "ENSG00000129691" "ENSG00000138785" "ENSG00000168813" "ENSG00000272886" "ENSG00000163435" "ENSG00000163848"
[225] "ENSG00000166478" "ENSG00000116017" "ENSG00000169564" "ENSG00000168283" "ENSG00000163348" "ENSG00000137871" "ENSG00000285253"
[232] "ENSG00000178691" "ENSG00000119866" "ENSG00000122877" "ENSG00000172534" "ENSG00000114315" "ENSG00000175550" "ENSG00000100281"
[239] "ENSG00000197063" "ENSG00000171720" "ENSG00000063169" "ENSG00000204256" "ENSG00000234704" "ENSG00000235307" "ENSG00000230678"
[246] "ENSG00000234507" "ENSG00000236227" "ENSG00000215077" "ENSG00000165156" "ENSG00000118418" "ENSG00000086589" "ENSG00000103479"
[253] "ENSG00000133422" "ENSG00000105866" "ENSG00000102034" "ENSG00000111145" "ENSG00000111880" "ENSG00000104064" "ENSG00000095794"
[260] "ENSG00000128604" "ENSG00000132964" "ENSG00000198900" "ENSG00000141027" "ENSG00000177565" "ENSG00000168286" "ENSG00000158636"
[267] "ENSG00000177030" "ENSG00000282712" "ENSG00000101040" "ENSG00000025434" "ENSG00000171988" "ENSG00000137265" "ENSG00000186834"
[274] "ENSG00000253729" "ENSG00000160789" "ENSG00000164105" "ENSG00000204531" "ENSG00000206454" "ENSG00000230336" "ENSG00000237582"
[281] "ENSG00000229094" "ENSG00000235068" "ENSG00000233911" "ENSG00000132510" "ENSG00000136492" "ENSG00000156531" "ENSG00000187555"
[288] "ENSG00000102098" "ENSG00000117713" "ENSG00000164458" "ENSG00000198728" "ENSG00000125651" "ENSG00000121060" "ENSG00000171223"
[295] "ENSG00000119203" "ENSG00000101266" "ENSG00000134532" "ENSG00000196363" "ENSG00000112658" "ENSG00000007866" "ENSG00000169925"
[302] "ENSG00000122565" "ENSG00000204356" "ENSG00000206268" "ENSG00000233801" "ENSG00000231044" "ENSG00000229363" "ENSG00000206357"
[309] "ENSG00000198517" "ENSG00000169057" "ENSG00000171316" "ENSG00000118922" "ENSG00000197905" "ENSG00000168769" "ENSG00000169045"
[316] "ENSG00000284254" "ENSG00000099381" "ENSG00000101191" "ENSG00000119547" "ENSG00000130726" "ENSG00000104856" "ENSG00000148400"
[323] "ENSG00000114861" "ENSG00000183495" "ENSG00000127616" "ENSG00000181315" "ENSG00000120733" "ENSG00000171862" "ENSG00000284792"
[330] "ENSG00000122779" "ENSG00000105856" "ENSG00000283847" "ENSG00000165732" "ENSG00000096063" "ENSG00000121691" "ENSG00000147155"
[337] "ENSG00000167182" "ENSG00000139842" "ENSG00000239306" "ENSG00000088930" "ENSG00000005889" "ENSG00000102710" "ENSG00000145216"
[344] "ENSG00000141568" "ENSG00000166886" "ENSG00000120948" "ENSG00000112081" "ENSG00000083307" "ENSG00000197724" "ENSG00000129351"
[351] "ENSG00000079246" "ENSG00000131051" "ENSG00000189369" "ENSG00000204227" "ENSG00000228520" "ENSG00000235107" "ENSG00000226788"
[358] "ENSG00000206287" "ENSG00000231115" "ENSG00000070444" "ENSG00000166503" "ENSG00000063244" "ENSG00000123908" "ENSG00000153147"
[365] "ENSG00000124613" "ENSG00000115942" "ENSG00000178764" "ENSG00000136603" "ENSG00000138378" "ENSG00000173275" "ENSG00000165891"
[372] "ENSG00000174720" "ENSG00000170581" "ENSG00000165494" "ENSG00000104824" "ENSG00000282947" "ENSG00000118007" "ENSG00000157933"
[379] "ENSG00000100084" "ENSG00000136451" "ENSG00000120616" "ENSG00000125740" "ENSG00000166716" "ENSG00000136367" "ENSG00000010244"
[386] "ENSG00000101216" "ENSG00000140382" "ENSG00000164916" "ENSG00000064313" "ENSG00000162702" "ENSG00000143842" "ENSG00000204231"
[393] "ENSG00000231321" "ENSG00000235712" "ENSG00000227322" "ENSG00000228333" "ENSG00000206289" "ENSG00000049618" "ENSG00000159692"
[400] "ENSG00000168036" "ENSG00000005339" "ENSG00000186350" "ENSG00000159140" "ENSG00000124795" "ENSG00000058673" "ENSG00000089280"
[407] "ENSG00000109381" "ENSG00000110713" "ENSG00000166508" "ENSG00000108654" "ENSG00000135100" "ENSG00000119707" "ENSG00000137309"
[414] "ENSG00000186660" "ENSG00000163930" "ENSG00000101115" "ENSG00000073614" "ENSG00000181722" "ENSG00000057657" "ENSG00000124151"
[421] "ENSG00000170325" "ENSG00000101849" "ENSG00000143799" "ENSG00000105497" "ENSG00000204209" "ENSG00000231617" "ENSG00000229396"
[428] "ENSG00000227046" "ENSG00000206206" "ENSG00000206279" "ENSG00000181449" "ENSG00000140332" "ENSG00000180806" "ENSG00000130940"
[435] "ENSG00000060709" "ENSG00000090447" "ENSG00000139613" "ENSG00000175029" "ENSG00000185049" "ENSG00000104447" "ENSG00000128908"
[442] "ENSG00000143321" "ENSG00000171634" "ENSG00000125618" "ENSG00000106571" "ENSG00000162419" "ENSG00000135111" "ENSG00000189079"
[449] "ENSG00000187325" "ENSG00000197157" "ENSG00000182568" "ENSG00000077097" "ENSG00000116478" "ENSG00000174652" "ENSG00000170322"
[456] "ENSG00000147130" "ENSG00000174197" "ENSG00000189403" "ENSG00000160094" "ENSG00000136875" "ENSG00000144554" "ENSG00000149308"
[463] "ENSG00000175727" "ENSG00000281178" "ENSG00000060138" "ENSG00000173276" "ENSG00000100410" "ENSG00000118900" "ENSG00000112182"
[470] "ENSG00000165119" "ENSG00000141644" "ENSG00000102908" "ENSG00000131848" "ENSG00000173894" "ENSG00000160633" "ENSG00000180787"
[477] "ENSG00000158321" "ENSG00000171940" "ENSG00000134371" "ENSG00000143390" "ENSG00000166199" "ENSG00000187605" "ENSG00000162599"
[484] "ENSG00000080603" "ENSG00000113368" "ENSG00000113810" "ENSG00000143373" "ENSG00000204304" "ENSG00000236353" "ENSG00000225987"
[491] "ENSG00000232005" "ENSG00000224952" "ENSG00000206315" "ENSG00000237344" "ENSG00000106004" "ENSG00000118412" "ENSG00000288475"
[498] "ENSG00000110435" "ENSG00000085224" "ENSG00000157540" "ENSG00000159259" "ENSG00000165819" "ENSG00000118217" "ENSG00000068305"
[505] "ENSG00000140836" "ENSG00000138336" "ENSG00000182944" "ENSG00000186448" "ENSG00000281709" "ENSG00000129245" "ENSG00000054598"
[512] "ENSG00000124789" "ENSG00000166333" "ENSG00000083093" "ENSG00000093072" "ENSG00000071655" "ENSG00000101126" "ENSG00000120798"
[519] "ENSG00000171467" "ENSG00000112118" "ENSG00000243678" "ENSG00000124535" "ENSG00000147862" "ENSG00000124216" "ENSG00000116350"
[526] "ENSG00000142235" "ENSG00000117000" "ENSG00000143970" "ENSG00000277258" "ENSG00000278644" "ENSG00000116030" "ENSG00000198783"
[533] "ENSG00000168661" "ENSG00000197757" "ENSG00000163946" "ENSG00000100625" "ENSG00000140632" "ENSG00000145734" "ENSG00000274803"
[540] "ENSG00000273873" "ENSG00000087903" "ENSG00000179583" "ENSG00000109685" "ENSG00000198646" "ENSG00000178338" "ENSG00000167548"
[547] "ENSG00000069011" "ENSG00000181827" "ENSG00000163346" "ENSG00000079432" "ENSG00000116604" "ENSG00000126778" "ENSG00000115875"
[554] "ENSG00000095951" "ENSG00000114416" "ENSG00000094916" "ENSG00000172977" "ENSG00000104885" "ENSG00000176165" "ENSG00000133392"
[561] "ENSG00000276480" "ENSG00000245680" "ENSG00000104221" "ENSG00000266412" "ENSG00000164104" "ENSG00000169297" "ENSG00000197265"
[568] "ENSG00000092201" "ENSG00000100426" "ENSG00000197111" "ENSG00000147789" "ENSG00000117395" "ENSG00000096401" "ENSG00000121741"
[575] "ENSG00000068024" "ENSG00000182141" "ENSG00000170448" "ENSG00000158941" "ENSG00000198824" "ENSG00000135365" "ENSG00000243943"
[582] "ENSG00000104852" "ENSG00000164151" "ENSG00000177469" "ENSG00000126218" "ENSG00000152217" "ENSG00000130856" "ENSG00000101596"
[589] "ENSG00000162775" "ENSG00000108773" "ENSG00000198554" "ENSG00000092203" "ENSG00000164684" "ENSG00000196700" "ENSG00000175792"
[596] "ENSG00000284901" "ENSG00000161021" "ENSG00000283780" "ENSG00000215021" "ENSG00000132670" "ENSG00000146648" "ENSG00000183207"
[603] "ENSG00000135250" "ENSG00000111786" "ENSG00000187140" "ENSG00000052850" "ENSG00000176619" "ENSG00000179981" "ENSG00000169032"
[610] "ENSG00000100714" "ENSG00000132383" "ENSG00000071539" "ENSG00000073111" "ENSG00000165097" "ENSG00000149050" "ENSG00000011451"
[617] "ENSG00000074657" "ENSG00000188994"
[1] "\"Osteoblasts\"[Mesh]"
[1] "Hsa"
[1] "hsapiens_gene_ensembl"
[1] "9606"
[1] "getBM"
[1] "Check EntrezGeneID again"
[1] "end"
[1] "mmusculus_homolog_ensembl_gene"
[1] "Check EntrezGeneID again"
[1] "end"
[1] "rnorvegicus_homolog_ensembl_gene"
[1] "Check EntrezGeneID again"

  |======================================================================================================================================| 100%[1] "end"
[1] "sscrofa_homolog_ensembl_gene"
[1] "Check EntrezGeneID again"

  |======================================================================================================================================| 100%[1] "end"
[1] "StartLoop"

Calcuate relativity of the Mitochondrial/Cytoskeletal genes to the Mesh term “Osteoblasts”[Mesh] using a literature mining method.

Mesh_term4Interesting <- '"Osteoblasts"[Mesh]'
GenesLs <- Anno_GeneLs$EnsemblID[!is.na(Anno_GeneLs$EnsemblID)]
Species <- "Hsa" # Hsa Mus Rno Ssc
MitoCySk.Mesh<-WZY_literatureMining(GenesLs=GenesLs, Mesh_term4Interesting=Mesh_term4Interesting, Species=Species, updateProgress = NULL)
  [1] "ENSG00000105327" "ENSG00000001084" "ENSG00000002330" "ENSG00000004142" "ENSG00000005059" "ENSG00000006530" "ENSG00000007168"
  [8] "ENSG00000011295" "ENSG00000011426" "ENSG00000015475" "ENSG00000019144" "ENSG00000021574" "ENSG00000027001" "ENSG00000030110"
 [15] "ENSG00000032742" "ENSG00000041880" "ENSG00000043514" "ENSG00000044090" "ENSG00000044524" "ENSG00000047410" "ENSG00000055950"
 [22] "ENSG00000060762" "ENSG00000061794" "ENSG00000062582" "ENSG00000065000" "ENSG00000067606" "ENSG00000067704" "ENSG00000067900"
 [29] "ENSG00000068028" "ENSG00000069329" "ENSG00000070718" "ENSG00000070831" "ENSG00000072506" "ENSG00000072756" "ENSG00000072803"
 [36] "ENSG00000074071" "ENSG00000074695" "ENSG00000075336" "ENSG00000075945" "ENSG00000076826" "ENSG00000077380" "ENSG00000078674"
 [43] "ENSG00000080371" "ENSG00000080815" "ENSG00000080824" "ENSG00000083799" "ENSG00000083937" "ENSG00000084731" "ENSG00000084764"
 [50] "ENSG00000085491" "ENSG00000085760" "ENSG00000086065" "ENSG00000086758" "ENSG00000087088" "ENSG00000089060" "ENSG00000095066"
 [57] "ENSG00000096080" "ENSG00000096092" "ENSG00000096093" "ENSG00000096872" "ENSG00000097033" "ENSG00000099624" "ENSG00000099800"
 [64] "ENSG00000099821" "ENSG00000099849" "ENSG00000100075" "ENSG00000100242" "ENSG00000100300" "ENSG00000100360" "ENSG00000100503"
 [71] "ENSG00000100644" "ENSG00000100890" "ENSG00000101052" "ENSG00000101181" "ENSG00000101222" "ENSG00000101367" "ENSG00000101574"
 [78] "ENSG00000103254" "ENSG00000103723" "ENSG00000104164" "ENSG00000104381" "ENSG00000104765" "ENSG00000104833" "ENSG00000104892"
 [85] "ENSG00000105197" "ENSG00000105255" "ENSG00000105723" "ENSG00000105819" "ENSG00000105948" "ENSG00000105976" "ENSG00000106211"
 [92] "ENSG00000106299" "ENSG00000107186" "ENSG00000107282" "ENSG00000107643" "ENSG00000107816" "ENSG00000107819" "ENSG00000107863"
 [99] "ENSG00000108064" "ENSG00000108262" "ENSG00000108387" "ENSG00000108561" "ENSG00000108961" "ENSG00000109083" "ENSG00000109103"
[106] "ENSG00000109171" "ENSG00000109332" "ENSG00000109670" "ENSG00000109971" "ENSG00000110711" "ENSG00000111199" "ENSG00000111276"
[113] "ENSG00000111837" "ENSG00000111843" "ENSG00000112031" "ENSG00000112110" "ENSG00000112144" "ENSG00000112651" "ENSG00000112701"
[120] "ENSG00000114107" "ENSG00000114120" "ENSG00000114346" "ENSG00000114446" "ENSG00000114993" "ENSG00000115091" "ENSG00000115317"
[127] "ENSG00000115355" "ENSG00000115840" "ENSG00000115966" "ENSG00000115993" "ENSG00000116459" "ENSG00000116584" "ENSG00000116874"
[134] "ENSG00000117155" "ENSG00000117245" "ENSG00000117593" "ENSG00000118046" "ENSG00000118200" "ENSG00000118242" "ENSG00000118246"
[141] "ENSG00000118965" "ENSG00000119333" "ENSG00000119541" "ENSG00000120662" "ENSG00000120832" "ENSG00000121621" "ENSG00000121957"
[148] "ENSG00000122140" "ENSG00000122386" "ENSG00000122545" "ENSG00000122912" "ENSG00000122970" "ENSG00000123416" "ENSG00000123607"
[155] "ENSG00000124172" "ENSG00000124279" "ENSG00000124333" "ENSG00000124356" "ENSG00000124532" "ENSG00000125354" "ENSG00000125648"
[162] "ENSG00000125652" "ENSG00000125995" "ENSG00000126756" "ENSG00000126768" "ENSG00000126814" "ENSG00000126858" "ENSG00000127914"
[169] "ENSG00000127955" "ENSG00000127989" "ENSG00000128311" "ENSG00000128626" "ENSG00000128641" "ENSG00000128654" "ENSG00000128833"
[176] "ENSG00000128881" "ENSG00000129250" "ENSG00000129682" "ENSG00000130294" "ENSG00000130340" "ENSG00000130348" "ENSG00000130479"
[183] "ENSG00000130643" "ENSG00000130724" "ENSG00000130779" "ENSG00000131165" "ENSG00000131269" "ENSG00000131437" "ENSG00000131966"
[190] "ENSG00000132300" "ENSG00000132356" "ENSG00000132589" "ENSG00000132612" "ENSG00000132842" "ENSG00000132849" "ENSG00000134108"
[197] "ENSG00000134278" "ENSG00000134318" "ENSG00000134375" "ENSG00000134709" "ENSG00000134809" "ENSG00000134982" "ENSG00000135049"
[204] "ENSG00000135127" "ENSG00000135297" "ENSG00000135338" "ENSG00000135441" "ENSG00000135776" "ENSG00000135900" "ENSG00000136108"
[211] "ENSG00000136122" "ENSG00000136270" "ENSG00000136463" "ENSG00000136522" "ENSG00000137100" "ENSG00000137210" "ENSG00000137288"
[218] "ENSG00000137804" "ENSG00000137807" "ENSG00000137942" "ENSG00000138035" "ENSG00000138036" "ENSG00000138069" "ENSG00000138071"
[225] "ENSG00000138095" "ENSG00000138175" "ENSG00000138180" "ENSG00000138182" "ENSG00000138399" "ENSG00000138592" "ENSG00000138758"
[232] "ENSG00000138821" "ENSG00000139131" "ENSG00000139220" "ENSG00000139737" "ENSG00000140463" "ENSG00000140854" "ENSG00000141279"
[239] "ENSG00000141367" "ENSG00000141556" "ENSG00000141577" "ENSG00000141682" "ENSG00000142192" "ENSG00000142208" "ENSG00000142347"
[246] "ENSG00000142444" "ENSG00000143158" "ENSG00000143575" "ENSG00000143761" "ENSG00000143801" "ENSG00000143862" "ENSG00000144040"
[253] "ENSG00000144381" "ENSG00000144824" "ENSG00000144868" "ENSG00000145715" "ENSG00000146282" "ENSG00000146425" "ENSG00000147586"
[260] "ENSG00000149499" "ENSG00000149557" "ENSG00000150756" "ENSG00000150764" "ENSG00000151150" "ENSG00000151929" "ENSG00000152503"
[267] "ENSG00000154174" "ENSG00000154342" "ENSG00000154429" "ENSG00000154839" "ENSG00000155366" "ENSG00000155906" "ENSG00000155970"
[274] "ENSG00000156026" "ENSG00000156313" "ENSG00000156735" "ENSG00000156990" "ENSG00000157540" "ENSG00000157796" "ENSG00000158411"
[281] "ENSG00000158623" "ENSG00000158828" "ENSG00000158882" "ENSG00000160551" "ENSG00000160993" "ENSG00000161800" "ENSG00000162409"
[288] "ENSG00000162769" "ENSG00000162851" "ENSG00000162972" "ENSG00000163462" "ENSG00000163539" "ENSG00000163626" "ENSG00000163635"
[295] "ENSG00000163808" "ENSG00000163930" "ENSG00000164114" "ENSG00000164284" "ENSG00000164347" "ENSG00000164466" "ENSG00000164695"
[302] "ENSG00000164877" "ENSG00000164896" "ENSG00000164933" "ENSG00000164961" "ENSG00000165480" "ENSG00000165487" "ENSG00000165629"
[309] "ENSG00000165813" "ENSG00000166503" "ENSG00000166780" "ENSG00000166963" "ENSG00000167306" "ENSG00000167552" "ENSG00000167553"
[316] "ENSG00000167797" "ENSG00000167862" "ENSG00000168071" "ENSG00000168172" "ENSG00000168385" "ENSG00000168827" "ENSG00000169057"
[323] "ENSG00000169100" "ENSG00000170248" "ENSG00000170606" "ENSG00000170759" "ENSG00000170959" "ENSG00000171103" "ENSG00000171169"
[330] "ENSG00000171533" "ENSG00000171552" "ENSG00000171612" "ENSG00000172171" "ENSG00000172575" "ENSG00000172590" "ENSG00000173548"
[337] "ENSG00000173726" "ENSG00000173786" "ENSG00000173805" "ENSG00000174032" "ENSG00000174173" "ENSG00000174871" "ENSG00000175216"
[344] "ENSG00000175564" "ENSG00000175567" "ENSG00000175582" "ENSG00000175768" "ENSG00000176101" "ENSG00000176108" "ENSG00000176171"
[351] "ENSG00000176410" "ENSG00000176720" "ENSG00000177192" "ENSG00000177370" "ENSG00000177542" "ENSG00000177879" "ENSG00000178209"
[358] "ENSG00000178694" "ENSG00000178952" "ENSG00000178996" "ENSG00000180096" "ENSG00000180834" "ENSG00000181004" "ENSG00000181284"
[365] "ENSG00000181991" "ENSG00000182504" "ENSG00000182628" "ENSG00000183032" "ENSG00000183048" "ENSG00000183172" "ENSG00000183978"
[372] "ENSG00000184640" "ENSG00000184702" "ENSG00000185009" "ENSG00000185043" "ENSG00000185129" "ENSG00000185133" "ENSG00000185340"
[379] "ENSG00000185721" "ENSG00000185825" "ENSG00000185909" "ENSG00000186010" "ENSG00000186522" "ENSG00000187240" "ENSG00000188428"
[386] "ENSG00000188763" "ENSG00000188807" "ENSG00000188906" "ENSG00000189114" "ENSG00000196072" "ENSG00000196230" "ENSG00000196586"
[393] "ENSG00000196659" "ENSG00000197119" "ENSG00000197457" "ENSG00000197535" "ENSG00000197557" "ENSG00000197822" "ENSG00000197912"
[400] "ENSG00000198718" "ENSG00000198836" "ENSG00000198899" "ENSG00000198954" "ENSG00000204152" "ENSG00000204388" "ENSG00000204389"
[407] "ENSG00000204843" "ENSG00000205981" "ENSG00000213123" "ENSG00000213221" "ENSG00000213465" "ENSG00000213625" "ENSG00000214026"
[414] "ENSG00000214253" "ENSG00000215251" "ENSG00000217930" "ENSG00000230989" "ENSG00000238227" "ENSG00000241837" "ENSG00000250479"
[421] "ENSG00000254858" "ENSG00000255112" "ENSG00000262814" "ENSG00000267855" "ENSG00000274523" "ENSG00000288709" "ENSG00000288722"
[1] "\"Osteoblasts\"[Mesh]"
[1] "Hsa"
[1] "hsapiens_gene_ensembl"
[1] "9606"
[1] "getBM"
[1] "Check EntrezGeneID again"
[1] "end"

Plots

gp <- literatureMiningPlot(
  literature.mining=TFs.Mesh$literature.mining, Thresh.R=0.002,
  use.Padj = FALSE, Thresh.P=0.05, label=TRUE, label_n = 10
)
Warning: Using `size` aesthetic for lines was deprecated in ggplot2 3.4.0.
Please use `linewidth` instead.
svg(filename = file.path(".", "01.PlotOut", "LiteratureMiningRes_01.svg"), width = 12, height = 8, pointsize = 12)
print(gp)
dev.off()
null device 
          1 
graphics.off()
knitr::opts_knit$set(global.device = TRUE)
print(gp)

knitr::opts_knit$set(global.device = FALSE)
gp <- literatureMiningPlot(
  literature.mining=MitoCySk.Mesh$literature.mining, Thresh.R=0.001,
  use.Padj = FALSE, Thresh.P=0.15, label=TRUE, label_n = 10
)
svg(filename = file.path(".", "01.PlotOut", "LiteratureMiningRes_02.svg"), width = 12, height = 8, pointsize = 12)
print(gp)
dev.off()
null device 
          1 
graphics.off()
knitr::opts_knit$set(global.device = TRUE)
print(gp)

knitr::opts_knit$set(global.device = FALSE)

02-06. Retrieve SNP records of TFs

Retrieve SNP records on the O-GlcNAc sites of TFs. If the a O-GlcNAc site of a TF really have a profound influences on the function of this TF, the misssense SNP on this site should be associated with some clincial pathogenic phenotype.

# Setup BioMart for SNP
Ann_Mart.Loc<-NULL
attempt<-1
attempt_max<-12
while(is.null(Ann_Mart.Loc)&&attempt<13){
  if(attempt%in%seq(from=1,to=attempt_max,3)){
    url<-"https://useast.ensembl.org"
  }else if(attempt%in%seq(from=2,to=attempt_max,3)){
    url<-"https://www.ensembl.org"
  }else if(attempt%in%seq(from=3,to=attempt_max,3)){
    url<-"https://useast.ensembl.org/"
  }else if(attempt%in%seq(from=4,to=attempt_max,3)){
    url<-"https://asia.ensembl.org/"
  }
  try({
    Ann_Mart.Loc <- useDataset(
      "hsapiens_gene_ensembl",
      useMart("ENSEMBL_MART_ENSEMBL", host = url)
    )
  }, silent = TRUE)
  attempt<-attempt+1
  if(is.null(Ann_Mart.Loc)){Sys.sleep(10)}
}
# Setup BioMart for Gene ID
Ann_Mart.snp<-NULL
attempt<-1
attempt_max<-12
while(is.null(Ann_Mart.snp)&&attempt<13){
  if(attempt%in%seq(from=1,to=attempt_max,3)){
    url<-"https://useast.ensembl.org"
  }else if(attempt%in%seq(from=2,to=attempt_max,3)){
    url<-"https://www.ensembl.org"
  }else if(attempt%in%seq(from=3,to=attempt_max,3)){
    url<-"https://useast.ensembl.org/"
  }else if(attempt%in%seq(from=4,to=attempt_max,3)){
    url<-"https://asia.ensembl.org/"
  }
  try({
    Ann_Mart.snp <- useDataset(
      "hsapiens_snp",
      useMart("ENSEMBL_MART_SNP", host = url)
    )
  }, silent = TRUE)
  attempt<-attempt+1
  if(is.null(Ann_Mart.snp)){Sys.sleep(10)}
}
# Get SNP results
UniPort.rs.OGlcNAc <- data.frame()
TFs.UniPort <- nodes$title[nodes$group=="TF"]
Par_pb <- txtProgressBar(min = 1, max = length(TFs.UniPort), style = 3)
n <- 1
for(i in TFs.UniPort){
  n<-n+0.49
  setTxtProgressBar(Par_pb, n)
  UniPort.Loc <- getBM(
    mart=Ann_Mart.Loc,
    attributes=c(
      "uniprotswissprot", "ensembl_gene_id", "ensembl_transcript_id", "strand",
      "chromosome_name", "transcript_start", "transcript_end", "cds_length"
    ),
    filter=c(
      "uniprotswissprot"
    ),
    values=i,
    uniqueRows = T
  )
  n<-n+0.49
  setTxtProgressBar(Par_pb, n)
  UniPort.Loc <- UniPort.Loc[order(UniPort.Loc$cds_length, decreasing = TRUE),][1,]
  UniPort.rs<-NULL
  rm(UniPort.rs)
  try({
    UniPort.rs <- UniPort.Loc %>%
      {
        paste(
          .[]$chromosome_name,
          min(c(.[]$transcript_start, .[]$transcript_end)),
          max(c(.[]$transcript_start, .[]$transcript_end)),
          sep = ":"
        )
      } %>%
      getBM(
        mart=Ann_Mart.snp,
        attributes=c(
          "refsnp_id", "consequence_type_tv", "consequence_allele_string",
          "ensembl_peptide_allele", "translation_start",
          "translation_end",  "ensembl_transcript_stable_id",
          "chr_name",  "chrom_start",  "chrom_end"
        ),
        filter="chromosomal_region",
        values=.,
        uniqueRows = TRUE,
        verbose = FALSE
      )
  }, silent = TRUE)
  if(!exists("UniPort.rs")) next
  UniPort.rs <- UniPort.rs[UniPort.rs$ensembl_transcript_stable_id == UniPort.Loc$ensembl_transcript_id,]
  UniPort.rs <- UniPort.rs[UniPort.rs$consequence_type_tv == "missense_variant",]
  UniPort.rs <- UniPort.rs[UniPort.rs$translation_start == UniPort.rs$translation_end,]
  temp <- OGlcNAc_Anno[OGlcNAc_Anno$Accession==i,]$Position_in_Protein %>% 
    {UniPort.rs[UniPort.rs$translation_start%in%.[],]}
  if(nrow(temp)){
    temp <-  cbind(
      UniPort_ID = i, temp
    )
    UniPort.rs.OGlcNAc <- rbind(
      UniPort.rs.OGlcNAc, temp
    )
  }
  n<-n+0.02
  setTxtProgressBar(Par_pb, n)
}


  |======================================================================================================================================| 100%
cat("\n")
close(Par_pb)
SNP.Phenotype <- getBM(
  mart=Ann_Mart.snp,
  attributes=c(
    "refsnp_id", "clinical_significance", "p_value",
    "phenotype_name", "phenotype_description", "variation_names"
  ),
  filter="snp_filter",
  values=UniPort.rs.OGlcNAc$refsnp_id%>%unique(),
  uniqueRows = TRUE
)
SNP.Phenotype<-SNP.Phenotype[SNP.Phenotype$phenotype_description!="",]
UniPort.rs.OGlcNAc.Clinc <- UniPort.rs.OGlcNAc[UniPort.rs.OGlcNAc$refsnp_id%in%unique(SNP.Phenotype$refsnp_id),]
UniPort.rs.OGlcNAc.Clinc <- merge(UniPort.rs.OGlcNAc.Clinc, SNP.Phenotype, by="refsnp_id")

02-07. Visualization of the gene regulatory network

Code

Filter out the TFs that doesn’t have pathogenic SNP on O-GlcNAc sites.

temp <- nodes[nodes$group=="TF",]
temp <- temp[temp$title%in%unique(UniPort.rs.OGlcNAc.Clinc$UniPort_ID),]
nodes <- rbind(
  nodes[nodes$group!="TF",],
  temp
)
edges <- edges[edges$from%in%nodes$id & edges$to%in%nodes$id,]
nodes<-nodes[nodes$id%in%unique(c(edges$from,edges$to)),]


Add url link to nodes.

for(i in nodes$title[nodes$group=="TF"]){
  OGlcNAc.site <- OGlcNAc_Anno[OGlcNAc_Anno$Query==i,]$Position_in_Protein %>%
    unique() %>% paste(., collapse = ";")
  temp <- UniPort.rs.OGlcNAc.Clinc[UniPort.rs.OGlcNAc.Clinc$UniPort_ID==i, ]
  temp <- temp[!duplicated(temp$refsnp_id), ]
  SNP.list <- c()
  for (k in temp$refsnp_id) {
    SNP.list <- c(
      SNP.list,
      paste0(
        "<br><a href='https://www.ensembl.org/Homo_sapiens/Variation/Phenotype?db=core;r=",
        paste0(temp$chr_name[temp$refsnp_id==k],":",temp$chrom_start[temp$refsnp_id==k],"-",temp$chrom_end[temp$refsnp_id==k]),
        ";v=", k, ";vdb=variation' target='_blank'>SNP: ",
        k, "; on AA site: ", temp$translation_start[temp$refsnp_id==k],
        " of ", temp$ensembl_transcript_stable_id[temp$refsnp_id==k], "</a>"
      )
    )
  }
  nodes$title[nodes$title==i] <- HTML(
    paste0(
      '<a href="https://www.uniprot.org/uniprotkb/',i,'/entry" target="_blank">', i, '</a><br>',
      '<a href="https://oglcnac.org/atlas/detail/', i, '" target="_blank">O-GlcNAc Site: ', OGlcNAc.site, '</a><br>',
      'O-GlcNAc site with pathogenic SNP:'
    ), HTML(SNP.list)
  )
}
for(i in nodes$title[nodes$group!="TF"]){
  nodes$title[nodes$title==i] <- HTML(
    paste0(
      '<a href="https://www.uniprot.org/uniprotkb/',i,'/entry" target="_blank">', i, '</a>'
    )
  )
}
TFs.Mesh.keep <- TFs.Mesh$literature.mining[TFs.Mesh$literature.mining$GeneSymbol%in%nodes$label[nodes$group=="TF"],]
MitoCySk.Mesh.keep <- MitoCySk.Mesh$literature.mining[MitoCySk.Mesh$literature.mining$GeneSymbol%in%nodes$label[nodes$group!="TF"],]
Mesh.keep <- rbind(
  TFs.Mesh.keep, MitoCySk.Mesh.keep
)
R.max <- max(Mesh.keep$R)
R.min <- min(Mesh.keep$R)
for(i in nodes$label){
  nodes$value[nodes$label==i]<-1+(((Mesh.keep$R[Mesh.keep$GeneSymbol==i]-R.min)/R.max)*100)
}
TF_ls <- TFLink$Name.TF %>% unique()
for(i in nodes$label[nodes$group!="TF"]){
  if(i %in% TF_ls){
    nodes$shape[nodes$label==i] <- "dot"
  }
}


Add url link to edge.

edges <- cbind(
  edges, title = 1, width = 1, color="lightblue", highlight = "red"
)
for(i in 1:nrow(edges)){
  from <- edges[i,]$from
  to <- edges[i,]$to
  from <- nodes$label[nodes$id==from]
  to <- nodes$label[nodes$id==to]
  temp <- TFLink_related_filter[TFLink_related_filter$Name.TF==from & TFLink_related_filter$Name.Target==to,]
  PubMed.ls <- temp$PubmedID %>%
    str_split(.,";") %>% unlist() %>%
    paste0(
      "<a href='https://pubmed.ncbi.nlm.nih.gov/", ., "/' target='_blank'>",
      ., "</a><br>"
    )
  edges$title[i] <- paste0(
    "Has Small-scale Evidence: ", temp$`Small-scale.evidence`, "<br>", HTML(PubMed.ls)
  ) %>% HTML()
  edges$width[i] <- length(PubMed.ls)
  if(temp$`Small-scale.evidence`=="Yes"){
    edges$color[i] <- "#9999FF"
  }
}
e.Max <- max(edges$width)
e.Min <- min(edges$width)
edges$width <- round(log(edges$width - e.Min + 1, base = 2) + 1)


Add legends

# nodes data.frame for legend
lnodes <- data.frame(
  label = c(
    "TFs related to cytoskeleton\nwithout O-GlcNAc site records\nand is not DEGs in GSE138783",
    "TFs related to cytoskeleton\nwith O-GlcNAc site records\nand is DEGs in GSE138783",
    "TFs with O-GlcNAc site records\nand is not DEGs in GSE138783",
    "TFs with O-GlcNAc site records\nand is DEGs in GSE138783",
    "Targets related to cytoskeleton", "Targets related to mitochondria",
    "Targets related to\nboth of cytoskeleton and mitochondria",
    "Size of node indicates the amount\nof articles related to osteoblast",
    "Width of edge indicates\nthe amount of articles"
  ),
  shape = c(
    "dot", "star", "square", "star", "triangle", "triangle", "diamond", "text", "text"
  ),
  color = c(
    "red", "red", "blue", "blue", "red", "orange", "black", "#FFFFFF", "#FFFFFF"
  ),
  title = "Legends",
  id = 1:9
)
# edges data.frame for legend
ledges <- data.frame(
  color = c("#9999FF", "lightblue"),
  label = c("Has small-scale\nevidence", "No small-scale\nevidence"),
  arrows =c("to", "to"), width = 10
)


Make interactive network

network <- visNetwork(nodes, edges, height = "800px", width = "100%") %>%
  visNodes(physics = TRUE) %>%
  visPhysics(stabilization = TRUE, solver = "repulsion", maxVelocity = 1) %>%
  visEdges(
    smooth = TRUE, shadow = FALSE,
    arrows =list(to = list(enabled = TRUE, scaleFactor = 0.5))
  ) %>%
  visOptions(
    nodesIdSelection = TRUE, selectedBy = "group", manipulation = FALSE,
    highlightNearest = list(enabled = TRUE, degree = 9999, algorithm = "hierarchical")
  ) %>%
  visLegend(addEdges = ledges, addNodes = lnodes, useGroups = FALSE)
network %>% visSave(file = "network.html")

Result

print(network)
NULL

03. Supplementary

save.image("./CheckPoint.RData")
---
title: "O-GlcNAc Regulated Mitochondrial Genes"
author: "WZY"
date: "2023-04-01"
output:
  html_notebook:
    toc: yes
    toc_float: yes
    toc_depth: 3
    css: ./HTML_source/style.css
---

# 00. Envirenment Settings

```{r 01-01.Envirenment Settings}
options(install.packages.compile.from.source = "always")
list.packages <- c(
  "readxl", "ggplot2", "ggpubr", "matrixStats", "ggrepel", "reshape2", "dplyr", "stringr",
  "grid", "tcltk", "parallel", "doParallel", "doSNOW", "data.table", "gplots",
  "randomcoloR", "factoextra", "RColorBrewer", "grDevices", "gmp", "xtable", "latex2exp",
  "httr", "jsonlite", "curl", "RCurl", "magrittr", "rlist", "pipeR", "plyr",
  "xml2", "rvest", "knn.covertree", "knitr", "rlang", "visNetwork", "hwriter", "htmltools"
)
bio.list.packages <- c(
  "limma", "ExperimentHub", "clusterProfiler", "GO.db",
  "org.Mm.eg.db", "pathview", "enrichplot", "org.Hs.eg.db"
)
new.packages <- list.packages[!list.packages %in% installed.packages()]
bio.new.packages <- bio.list.packages[!bio.list.packages %in% installed.packages()]
# Packages that does not install yet
if (!requireNamespace("BiocManager", quietly = TRUE)) {
  update.packages(ask = FALSE)
  install.packages("BiocManager", repos="https://cloud.r-project.org")
}
if (length(new.packages)) {
  install.packages(new.packages)
  devtools::install_github("grimbough/biomaRt", force = FALSE)
}
if (length(bio.new.packages)) {
  update.packages(ask = FALSE)
  BiocManager::install(bio.new.packages)
}
# Loading all packages & functions
invisible(lapply(c(list.packages, bio.list.packages, "biomaRt"), library, character.only = TRUE))
options(rgl.useNULL = F, ggrepel.max.overlaps = Inf)
```

# 01. Check Results from GSE138783

## 01-01. Functional Enrichment Analysis (FEA) Results from GSE138783

Load the functional enrichment analysis (FEA) results from our re-analyzed GSE138783 Bulk RNA-seq
```{r 01-01.1}
load(file.path(".", "01.HEK293_TMG_OSMI2", "00.Results", "DESeq2_Results.Rdata"))
```
<br>

Select the comparison with the most different treatment which is 6h TMG vs 6h OSMI-1
```{r 01-01.2}
ORA_list <- DEGs_ls[["HEK293_TMG_6hBvsHEK293_OSMI2_6hA"]][["Over_Represent"]]
```
<br>

Keep the GO_BP terms that contains either "mitochondria" or "cytoskeleton"
```{r 01-01.3}
for(i in c("All", "Up_regulated", "Down_regulated")){
  temp <- ORA_list[[i]]$GO_BP$Raw@result$Description %>%
    grep("(mitochondria(l){0,1}|cytoskele(ton|tal))", ., ignore.case = TRUE)
  ORA_list[[i]]$GO_BP$Raw@result <- ORA_list[[i]]$GO_BP$Raw@result[temp,]
  ORA_list[[i]]$GO_BP$Sig <- ORA_list[[i]]$GO_BP$Raw@result
}
names <- "TMG 6h vs OSMI-1 6h"
k <- "GO_BP"
temp <- ORA_list
mydf<-data.frame()
geneClusters<-list()
for(j in c("All","Up_regulated","Down_regulated")){
  if(is.null(nrow(temp[[j]][[k]][["Sig"]]))){next()}
  mydf<-rbind(
    mydf,
    cbind(
      group=rep(j,nrow(temp[[j]][[k]][["Sig"]])),
      temp[[j]][[k]][["Sig"]][,1:9]
    )
  )
  geneClusters[[j]]<-(temp[[j]][[k]][["Sig"]]$geneID)%>%
    str_split(.,"/")%>%unlist()%>%unique()
}

rownames(mydf)<-1:nrow(mydf)
mydf$group<-factor(mydf$group,levels=c("All","Up_regulated","Down_regulated"))
colnames(mydf)[1]<-"Cluster"
res <- new("compareClusterResult",
           compareClusterResult = mydf,
           geneClusters = geneClusters
)
.call<-match.call(compareCluster,call("compareCluster",
                                      ENSEMBL~group, data=mydf, fun="enrichGO",
                                      OrgDb         = org.Hs.eg.db,
                                      keyType       = "ENSEMBL",
                                      ont           = "BP",
                                      pAdjustMethod = "BH",
                                      pvalueCutoff  = 1,
                                      qvalueCutoff  = 1,
                                      readable      = TRUE))
.call$geneClusters<-as.symbol("geneClusters")
.call$OrgDb<-as.symbol("org.Hs.eg.db")
.call$data<-NULL
res@.call<-.call
res@fun<-"enrichGO"
res@keytype<-"UNKNOWN"
res@readable<-FALSE
if(!dir.exists(file.path(".","01.PlotOut"))){
  dir.create(file.path(".","01.PlotOut"))
}
```

## 01-02. Check FEA Results {.tabset .tabset-fade }

### Overlap {.tabset .tabset-fade}

```{r 01-02.a, fig.width=12, fig.height=17, out.width="100%"}
gp <- dotplot(
  res, showCategory=1000, label_format=85, color = "pvalue",
  title=paste0("ORA Summary of ", names, " for ", k," Terms.")
)
svg(filename = file.path(".", "01.PlotOut", "FEA_Overlap.svg"), width = 12, height = 17, pointsize = 12)
print(gp)
dev.off()
graphics.off()
knitr::opts_knit$set(global.device = TRUE)
print(gp)
knitr::opts_knit$set(global.device = FALSE)
```

### All DEGs {.tabset .tabset-fade}

```{r 01-02.b, fig.width=26, fig.height=16, out.width="100%"}
j <- "GO_BP"
k <- "All"
Par_name <- "TMG 6h vs OSMI-1 6h"
FEA_title<-paste0(k, " ", nrow(ORA_list[[k]][[j]]$Raw)," significant GO_", j, " terms (", Par_name, "; the most descend terms)")
p1<-dotplot(ORA_list[[k]][[j]]$Raw, showCategory=1000, label_format=100, color = "pvalue", font.size = 18)
p2<-treeplot(
  pairwise_termsim(ORA_list[[k]][[j]]$Raw, method="JC"), showCategory=1000, color = "pvalue",
  cluster.params=list(hclust_method = "ward.D2", label_words_n = 5, n = 5, font.size = 18)
)
gp <- gridExtra::grid.arrange(
  p1, p2, nrow = 1, widths = c(1, 1),
  top=textGrob(paste0("GSEA: ",FEA_title," with similarity summary"), gp=gpar(fontsize=18, col="black"))
)
svg(filename = file.path(".", "01.PlotOut", "FEA_All.svg"), width = 26, height = 16, pointsize = 12)
plot(gp)
dev.off()
graphics.off()
knitr::opts_knit$set(global.device = TRUE)
plot(gp)
knitr::opts_knit$set(global.device = FALSE)
```

### Up-regulated DEGs {.tabset .tabset-fade}

```{r 01-02.c, fig.width=26, fig.height=9, out.width="100%"}
j <- "GO_BP"
k <- "Up_regulated"
Par_name <- "TMG 6h vs OSMI-1 6h"
FEA_title<-paste0(k, " ", nrow(ORA_list[[k]][[j]]$Raw)," significant GO_", j, " terms (", Par_name, "; the most descend terms)")
p1<-dotplot(ORA_list[[k]][[j]]$Raw, showCategory=1000, label_format=100, color = "pvalue", font.size = 18)
p2<-treeplot(
  pairwise_termsim(ORA_list[[k]][[j]]$Raw, method="JC"), showCategory=1000, color = "pvalue",
  cluster.params=list(hclust_method = "ward.D2", label_words_n = 5, n = 5, font.size = 18)
)
gp <- gridExtra::grid.arrange(
  p1, p2, nrow = 1, widths = c(1, 1),
  top=textGrob(paste0("GSEA: ",FEA_title," with similarity summary"), gp=gpar(fontsize=18, col="black"))
)
svg(filename = file.path(".", "01.PlotOut", "FEA_Up.svg"), width = 16, height = 9, pointsize = 12)
plot(gp)
dev.off()
graphics.off()
knitr::opts_knit$set(global.device = TRUE)
plot(gp)
knitr::opts_knit$set(global.device = FALSE)
```

### Down-regulated DEGs {.tabset .tabset-fade}

```{r 01-02.d, fig.width=26, fig.height=15, out.width="100%"}
j <- "GO_BP"
k <- "Down_regulated"
Par_name <- "TMG 6h vs OSMI-1 6h"
FEA_title<-paste0(k, " ", nrow(ORA_list[[k]][[j]]$Raw)," significant GO_", j, " terms (", Par_name, "; the most descend terms)")
p1<-dotplot(ORA_list[[k]][[j]]$Raw, showCategory=1000, label_format=70, color = "pvalue", font.size = 18)
p2<-treeplot(
  pairwise_termsim(ORA_list[[k]][[j]]$Raw, method="JC"), showCategory=1000, color = "pvalue",
  cluster.params=list(hclust_method = "ward.D2", label_words_n = 5, n = 5, font.size = 18), label_format=25
)
gp <- gridExtra::grid.arrange(
  p1, p2, nrow = 1, widths = c(1, 1),
  top=textGrob(paste0("GSEA: ",FEA_title," with similarity summary"), gp=gpar(fontsize=18, col="black"))
)
svg(filename = file.path(".", "01.PlotOut", "FEA_Down.svg"), width = 26, height = 15, pointsize = 12)
plot(gp)
dev.off()
graphics.off()
knitr::opts_knit$set(global.device = TRUE)
plot(gp)
knitr::opts_knit$set(global.device = FALSE)
```

# 02. Retrieve up-stream transcription factors of interested GO_BP terms

In this section we will check the up-stream transcription factors that regulates the genes inside the Top5 overlapped mitochondrial/cytoskeletal GO_BP terms by using [TFLink database](https://tflink.net/).

The Top5 overlapped mitochondrial/cytoskeletal GO_BP terms are:
1. GO:0030705, cytoskeleton-dependent intracellular transport
2. GO:0061640, cytoskeleton-dependent cytokinesis
3. GO:0140053, mitochondrial gene expression
4. GO:0070507, regulation of microtubule cytoskeleton organization
5. GO:0006839, mitochondrial transport

## 02-01. Get up-stream Transcription factors list

Download TFLink database
```{r 02-01.a}
TFLink <- fread(
  "https://cdn.netbiol.org/tflink/download_files/TFLink_Homo_sapiens_interactions_All_simpleFormat_v1.0.tsv.gz"
)
```
<br>

Check the tables
```{r 02-01.b}
head(res@compareClusterResult)
head(TFLink)
```
<br>

Get annotation of genes related to Mitochondrial/Cytoskeletal GO_BP terms.
```{r 02-01.c}
TOP5 <- res@compareClusterResult[res@compareClusterResult$ID %in% c("GO:0030705", "GO:0061640", "GO:0140053", "GO:0070507", "GO:0006839"),]
GeneLs <- TOP5$geneID %>%
  str_split(., "/") %>%
  unlist() %>%
  unique()
Ann_0mart<-NULL
attempt<-1
attempt_max<-12
while(is.null(Ann_0mart)&&attempt<13){
  if(attempt%in%seq(from=1,to=attempt_max,3)){
    url<-"https://useast.ensembl.org"
  }else if(attempt%in%seq(from=2,to=attempt_max,3)){
    url<-"https://www.ensembl.org"
  }else if(attempt%in%seq(from=3,to=attempt_max,3)){
    url<-"https://useast.ensembl.org/"
  }else if(attempt%in%seq(from=4,to=attempt_max,3)){
    url<-"https://asia.ensembl.org/"
  }
  try({
    Ann_0mart <- useDataset(
      "hsapiens_gene_ensembl",
      useMart("ENSEMBL_MART_ENSEMBL", host = url)
    )
  }, silent = TRUE)
  attempt<-attempt+1
  if(is.null(Ann_0mart)){Sys.sleep(10)}
}
Anno_GeneLs <- getBM(
  mart = Ann_0mart,
  attributes = c("hgnc_symbol", "ensembl_gene_id", "external_gene_name"),
  filter = "ensembl_gene_id",
  values = GeneLs,
  uniqueRows = TRUE
)
rownames(Anno_GeneLs)<-Anno_GeneLs$ensembl_gene_id
```
<br>

Make functions based on the [Uniport API](https://www.uniprot.org/help/api_queries) and prepare the gene list.
```{r 02-01.d}
library(httr)
isJobReady <- function(jobId) {
  pollingInterval <- 5
  nTries <- 20
  for (i in 1:nTries) {
    url <- paste("https://rest.uniprot.org/idmapping/status/", jobId, sep = "")
    r <- GET(url = url, accept_json())
    status <- httr::content(r, as = "parsed")
    if (!is.null(status[["results"]]) || !is.null(status[["failedIds"]])) {
      return(TRUE)
    }
    if (!is.null(status[["messages"]])) {
      print(status[["messages"]])
      return(FALSE)
    }
    Sys.sleep(pollingInterval)
  }
  return(FALSE)
}
get_next_link <- function(headers) {
  if (!is.null(headers[["Link"]])) {
    match <- str_match(
      headers[["Link"]],
      '^\\<\\s*(.*?)\\s*\\>\\; rel\\=\\"next\\"$'
    )
    if (!isEmpty(match)) {
      return(match[2])
    }
  } else {
    NULL
  }
}
```
<br>

Fetch UniprotID for the Mitochondrial/Cytoskeletal genes using Ensembl ID
```{r 02-01.e}
temp <- Anno_GeneLs$ensembl_gene_id
files <- list(
  from = "Ensembl",
  to = "UniProtKB-Swiss-Prot",
  ids = paste0(temp, collapse = ",")
)
r <- POST(url = "https://rest.uniprot.org/idmapping/run", body = files, encode = "multipart", accept_json())
r <- POST(url = "https://rest.uniprot.org/idmapping/run", body = files, encode = "multipart", accept_json())
while (r$status_code != 200) {
  r <- POST(url = "https://rest.uniprot.org/idmapping/run", body = files, encode = "multipart", accept_json())
  Sys.sleep(5)
}
submission <- httr::content(r, as = "parsed")
if (isJobReady(submission[["jobId"]])) {
  url <- paste("https://rest.uniprot.org/idmapping/details/", submission[["jobId"]], sep = "")
  response <- GET(url = url, accept_json())
  details <- httr::content(response, as = "parsed")
  res_url <- paste0(
    details[["redirectURL"]],
    "?fields=accession%2Creviewed%2Cid%2Cprotein_name%2Clength%2Cgene_primary%2Cgo%2Cft_zn_fing%2Cft_repeat%2Cft_region%2Cft_domain%2Cft_motif%2Ccc_domain%2Cft_compbias%2Cft_coiled%2Cannotation_score%2Ckeyword%2Ccomment_count%2Ccc_subcellular_location%2Ccc_function%2Ccc_pathway%2Cprotein_families%2Cft_carbohyd%2Cft_peptide%2Cft_transit%2Cft_signal%2Cft_propep%2Ccc_ptm%2Cft_init_met%2Cft_lipid%2Cft_mod_res%2Cft_disulfid%2Cft_crosslnk%2Cft_chain%2Cxref_kegg&format=tsv&size=500"
  )
  response <- GET(url = res_url, accept_json())
  total <- response$headers$`x-total-results`
  temp2 <- data.table::fread(
    res_url,
    verbose = TRUE, showProgress = TRUE
  ) %>% as.data.frame()
  while (!is.null(res_url)) {
    response <- GET(url = res_url, accept_json())
    res_url <- get_next_link(headers(response))
    if (!is.null(res_url)) {
      temp2 <- rbind(
        temp2,
        data.table::fread(
          res_url,
          verbose = FALSE, showProgress = FALSE
        ) %>% as.data.frame()
      )
      print(
        paste0(
          nrow(temp2), "/", total
        )
      )
    }
  }
}
colnames(temp2)[1] <- "EnsemblID"
a <- str_split(temp2$EnsemblID, ",")
temp <- which((lengths(a) >= 2) == TRUE)
for (i in temp) {
  temp1 <- a[[i]]
  temp2$EnsemblID[i] <- temp1[1]
  for (j in 2:length(temp1)) {
    temp2 <- rbind(temp2, temp2[i, ])
    nrow <- nrow(temp2)
    temp2$EnsemblID[nrow] <- temp1[j]
  }
}
dup_ls <- temp2$EnsemblID[duplicated(temp2$EnsemblID)]
for(i in dup_ls){
  temp <- temp2[temp2$EnsemblID!=i,]
  dup_rows <- temp2[temp2$EnsemblID==i,]
  dup_rows <- dup_rows[dup_rows$Length == max(dup_rows$Length),]
  temp2 <-rbind(dup_rows, temp)
}
rownames(temp2) <- temp2$EnsemblID
Anno_GeneLs <- temp2
```
<br>

Get related Transcription Factors (TFs)
```{r 02-01.f}
TFLink_related <- TFLink[TFLink$UniprotID.Target %in% Anno_GeneLs$Entry,]
#TF_ls <- unique(TFLink_related$UniprotID.TF)
#TFLink_related <- TFLink[(TFLink$UniprotID.TF %in% TF_ls | TFLink$UniprotID.Target %in% TF_ls),]
#TFLink_related <- TFLink_related[(TFLink_related$UniprotID.Target %in% c(TF_ls,Anno_GeneLs$Entry)),]
head(TFLink_related)
```
<br>

## 02-02. Get the O-GlcNAc info

Add the O-GlcNAc site information from the [O-GlcNAcAtlas](https://oglcnac.org/atlas/search/) database.

First we have to retrieve the UniPort Accession number for each genes
```{r 02-02.a}
library("httr") 
library("dplyr") 
library("jsonlite")
library("curl")
library("RCurl")
library("magrittr")
library("rlist")
library("pipeR")
library("plyr")
library("xml2")
library("rvest")
library("parallel")
library("doParallel")
library("doSNOW")
# Fetch O-GlcNAc records from https://www.oglcnac.org/atlas/search/
temp2 <- data.frame()
Uniportls <- unique(TFLink_related$UniprotID.TF)
Par_cl <- makeCluster(parallelly::freeCores()[1])
registerDoSNOW(Par_cl)
Par_pb <- txtProgressBar(min = 1, max = length(Uniportls), style = 3)
progress <- function(n) setTxtProgressBar(Par_pb, n)
Par_opts <- list(progress = progress)
temp2 <- foreach(
  i = 1:length(Uniportls), .combine = base::rbind, .errorhandling = "pass",
  .options.snow = Par_opts, .packages = c("tcltk", "dplyr", "utils")
) %dopar% {
  Query <- Uniportls[i]
  url <- c("https://www.oglcnac.org/atlas/search/")
  pg <- rvest::session(url)
  token <- xml2::xml_attrs(xml2::xml_find_all(xml2::read_html(pg), ".//input")[[1]])[["value"]]
  myheaders <- c(
  'accept' ='text/html,application/xhtml+xml,application/xml;q=0.9,image/avif,image/webp,image/apng,*/*;q=0.8,application/signed-exchange;v=b3;q=0.7',
  'accept-encoding' = 'gzip, deflate, br',
  'accept-language' = 'en-US,en;q=0.9,zh-CN;q=0.8,zh;q=0.7,zh-TW;q=0.6,ja;q=0.5',
  'cache-control' = 'max-age=0',
  'content-length' = as.character(nchar(Query) + 120),
  'content-type' = 'application/x-www-form-urlencoded',
  'cookie' = stringr::str_split(pg[["response"]][["headers"]][["set-cookie"]],";")[[1]][1],
  'dnt' = '1',
  'origin' = 'https://oglcnac.org',
  'referer' = 'https://oglcnac.org/atlas/search/',
  'sec-ch-ua' = '"Google Chrome";v="111", "Not(A:Brand";v="8", "Chromium";v="111"',
  'sec-ch-ua-mobile' = '?0',
  'sec-ch-ua-platform' = 'Linux',
  'sec-fetch-dest' = 'document',
  'sec-fetch-mode' = 'navigate',
  'sec-fetch-site' = 'same-origin',
  'sec-fetch-user' = '?1',
  'upgrade-insecure-requests' = '1',
  'user-agent' = 'Mozilla/5.0 (X11; Linux x86_64) AppleWebKit/537.36 (KHTML, like Gecko) Chrome/111.0.0.0 Safari/537.36'
  )
  response <- httr::POST(
    url = url,
    httr::add_headers(.headers = myheaders),
    body = list(
      "csrfmiddlewaretoken" = token,
      "search_term" = Query,
      "search_field" = "Accession"
    ),
    encode = "form"
  )
  if (httr::status_code(response) != 200) {
    out <- data.frame(
      Query = Query,
      Accession = "Failure",
      Entry_Name = "Failure",
      Protein_Name = "Failure",
      Gene_Name = "Failure",
      Position_in_Protein = "Failure",
      Status = httr::status_code(response),
      "O-GlcNAc" = "Unknown"
    )
  } else if (rvest::html_table(xml2::read_html(response))[[2]] %>% as.data.frame() %>% nrow() == 0) {
    out <- data.frame(
      Query = Query,
      Accession = "No_records",
      Entry_Name = "No_records",
      Protein_Name = "No_records",
      Gene_Name = "No_records",
      Position_in_Protein = "No_records",
      Status = httr::status_code(response),
      "O-GlcNAc" = "Non"
    )
  } else if (rvest::html_table(xml2::read_html(response))[[2]] %>% as.data.frame() %>% nrow() != 0) {
    out <- rvest::html_table(xml2::read_html(response))[[2]] %>% as.data.frame()
    out <- data.frame(
      Query = Query,
      Accession = out$Accession,
      Entry_Name = out$`Entry Name`,
      Protein_Name = out$`Protein Name`,
      Gene_Name = out$`Gene Name`,
      Position_in_Protein = out$`Position in Protein`,
      Status = httr::status_code(response),
      "O-GlcNAc" = "Yes"
    )
  }
  out
}
stopCluster(Par_cl)
OGlcNAc_Anno <- temp2
```
<br>

Add O-GlcNAc info to TFs.
```{r 02-02.b}
OGlcNAc <- rep("No", nrow(TFLink_related))
TFLink_related <- cbind(OGlcNAc, TFLink_related)
TFLink_related$OGlcNAc[TFLink_related$UniprotID.TF %in% OGlcNAc_Anno$Accession]<-"Yes"
head(TFLink_related)
```

## 02-03. Get signifciantly changed TFs

Add DEGs info to TFs.
```{r 02-03}
DEGs <- DEGs_ls[["HEK293_TMG_6hBvsHEK293_OSMI2_6hA"]][["DEGs_raw"]]
DEGs <- DEGs[DEGs$Is.Sig.=="Yes",]
is.DEGs <- rep("No", nrow(TFLink_related))
TFLink_related <- cbind(is.DEGs, TFLink_related)
TFLink_related$is.DEGs[TFLink_related$UniprotID.TF %in% DEGs$UniProtKBID]<-"Yes"
head(TFLink_related)
```

## 02-04. Filtering & Visualization

### 1. Filtering

Filter out the TFs wihout both significantly changes and O-GlcNAc sites.
```{r 02-04.1.a}
TFLink_related <- TFLink_related[(TFLink_related$is.DEGs == "Yes" | TFLink_related$OGlcNAc == "Yes"),]
TFLink_related <- TFLink_related[(TFLink_related$OGlcNAc == "Yes"),]
dim(TFLink_related)
head(TFLink_related)
```
<br>

Remove the records that not related to both of Mitochondrial/Cytoskeletal genes and remained TFs.
```{r 02-04.1.b}
ChkLs <- unique(c(TFLink_related$UniprotID.TF, Anno_GeneLs$Entry))
TFLink_related <- TFLink_related[TFLink_related$UniprotID.Target %in% ChkLs,]
dim(TFLink_related)
head(TFLink_related)
```

### 2. Literature mining {.tabset .tabset-fade}

#### Make functions {.tabset .tabset-fade}

Make literature mining functions
```{r 02-04.2.a}
#Load functions#
RetrieveEntrezID <- function(
    Homologues=FALSE,
    Homo_species=Homo_species,
    Par_species=Par_species,
    Par_species.Uniprot=Par_species.Uniprot,
    GenesLs=GenesLs,
    updateProgress = NULL
){
  #|----Set up Biomart parameters----|####
  Ann_0mart<-NULL
  attempt<-1
  attempt_max<-12
  while(is.null(Ann_0mart)&&attempt<13){
    if(attempt%in%seq(from=1,to=attempt_max,3)){
      url<-"https://useast.ensembl.org"
    }else if(attempt%in%seq(from=2,to=attempt_max,3)){
      url<-"https://www.ensembl.org"
    }else if(attempt%in%seq(from=3,to=attempt_max,3)){
      url<-"https://useast.ensembl.org/"
    }else if(attempt%in%seq(from=4,to=attempt_max,3)){
      url<-"https://asia.ensembl.org/"
    }
    try({
      Ann_0mart <- useMart("ENSEMBL_MART_ENSEMBL", host=url) %>%
        useDataset(Par_species, .)
    }, silent = TRUE)
    attempt<-attempt+1
    if(is.null(Ann_0mart)){Sys.sleep(10)}
  }
  
  if(Homologues){
    if (is.function(updateProgress)) {
      text <- paste0("Get Homologoeus Gene in ", Homo_species) 
      updateProgress(detail = text)
    }
    #listAttributes(Ann_0mart)%>%View()
    temp <- NULL
    attempt<-1
    attempt_max<-12
    while(is.null(temp)&&attempt<13){
      try({
        temp <- getBM(
          mart=Ann_0mart,
          attributes=c("ensembl_gene_id",
                       Homo_species),
          filter="ensembl_gene_id",
          values=GenesLs,
          uniqueRows = T)
      }, silent = TRUE)
      attempt<-attempt+1
      if(is.null(temp)){Sys.sleep(10)}
    }
    temp<-temp[!temp[,2]%in%"",]
    temp<-temp[!duplicated(temp[,2]),]
    NaMapping<-temp[,1]
    names(NaMapping)<-temp[,2]
    print(Homo_species)
    if(is_empty(temp)|nrow(temp)<1){
      return(NA)
    }
    #print("Set up Biomart parameters")
    #|----Set up Biomart parameters----|####
    if(Homo_species == "hsapiens_homolog_ensembl_gene"){
      Par_species <- "hsapiens_gene_ensembl"
    }else if(Homo_species == "mmusculus_homolog_ensembl_gene"){
      Par_species <- "mmusculus_gene_ensembl"
    }else if(Homo_species == "rnorvegicus_homolog_ensembl_gene"){
      Par_species <- "rnorvegicus_gene_ensembl"
    }else if(Homo_species == "sscrofa_homolog_ensembl_gene"){
      Par_species <- "sscrofa_gene_ensembl"
    }
    Ann_0mart<-NULL
    attempt<-1
    attempt_max<-12
    while(is.null(Ann_0mart)&&attempt<13){
      if(attempt%in%seq(from=1,to=attempt_max,3)){
        url<-"https://useast.ensembl.org"
      }else if(attempt%in%seq(from=2,to=attempt_max,3)){
        url<-"https://www.ensembl.org"
      }else if(attempt%in%seq(from=3,to=attempt_max,3)){
        url<-"https://useast.ensembl.org/"
      }else if(attempt%in%seq(from=4,to=attempt_max,3)){
        url<-"https://asia.ensembl.org/"
      }
      try({
        Ann_0mart <- useMart("ENSEMBL_MART_ENSEMBL", host=url) %>%
          useDataset(Par_species, .)
      }, silent = TRUE)
      attempt<-attempt+1
      if(is.null(Ann_0mart)){Sys.sleep(10)}
    }
    Anno_gene <- NULL
    attempt<-1
    attempt_max<-12
    while(is.null(Anno_gene)&&attempt<13){
      try({
        Anno_gene <- getBM(
          mart=Ann_0mart,
          attributes=c("ensembl_gene_id","entrezgene_id","gene_biotype",
                       "external_gene_name","description"),
          filter="ensembl_gene_id",
          values=temp[,2],
          uniqueRows = T)
      }, silent = TRUE)
      attempt<-attempt+1
      if(is.null(Anno_gene)){Sys.sleep(10)}
    }
    rm(temp)
  }else{
    print("getBM")
    if (is.function(updateProgress)) {
      text <- "Get PubMed Gene ID"
      updateProgress(detail = text)
    }
    Anno_gene <- NULL
    attempt<-1
    attempt_max<-12
    while(is.null(Anno_gene)&&attempt<13){
      try({
        Anno_gene <- getBM(
          mart=Ann_0mart,
          attributes=c("ensembl_gene_id","entrezgene_id","gene_biotype",
                       "external_gene_name","description"),
          filter="ensembl_gene_id",
          values=GenesLs,
          uniqueRows = T)
      }, silent = TRUE)
      attempt<-attempt+1
      if(is.null(Anno_gene)){Sys.sleep(10)}
    }
  }
  
  Anno<-Anno_gene[!duplicated(Anno_gene$ensembl_gene_id),]
  rownames(Anno)<-Anno$ensembl_gene_id
  Anno<-data.frame(
    ensembl_gene_id=Anno$ensembl_gene_id,
    entrezgene_id=Anno$entrezgene_id,
    external_gene_name=Anno$external_gene_name,
    gene_biotype=Anno$gene_biotype,
    row.names = rownames(Anno)
  )
  Anno2<-Anno[!is.na(Anno$entrezgene_id),] #For EntrezGeneID
  Anno2<-Anno2[!duplicated(Anno2[,'ensembl_gene_id']),] #For EntrezGeneID
  rownames(Anno2)<-Anno2$ensembl_gene_id
  temp<-Anno[is.na(Anno$entrezgene_id),"ensembl_gene_id"]
  print("Check EntrezGeneID again")
  #|----Check EntrezGeneID again----|####
  if(!is_empty(temp)){
    if(length(temp)<2){
      NCBIcheck<-read_html(
        paste0(
          "https://www.ncbi.nlm.nih.gov/gene/?term=",
          temp
        )
      )%>%xml_find_all(., ".//span")%>%xml_text()%>%
        grep("Gene ID",.,value = TRUE)
      if(!isEmpty(NCBIcheck)){
        NCBIcheck<-NCBIcheck%>%unlist()%>%
          str_extract_all(.,"(\\d)+")%>%.[[1]]%>%.[1]
      }else{
        NCBIcheck<-NA
      }
      out<-data.frame(
        ensembl_gene_id=temp,
        entrezgene_id=NCBIcheck
      )%>%as.data.frame()
      temp2<-out
    }else{
      Par_cl<-makeCluster(parallelly::freeConnections()-1)
      registerDoSNOW(Par_cl)
      Par_pb <- txtProgressBar(min=1, max=length(temp), style = 3)
      progress <- function(n) setTxtProgressBar(Par_pb, n)
      Par_opts<-list(progress = progress)
      #Refer here for all column names for Entrez API (https://www.ncbi.nlm.nih.gov/books/NBK25501/)
      temp2<-foreach(i=1:length(temp), .combine=rbind, .errorhandling = "pass", .inorder=FALSE,
                     .options.snow=Par_opts, .packages = c("dplyr","utils","xml2","S4Vectors","stringr","BiocGenerics")) %dopar% {
                       NCBIcheck<-read_html(
                         paste0(
                           "https://www.ncbi.nlm.nih.gov/gene/?term=",
                           temp[i]
                         )
                       )%>%xml_find_all(., ".//span")%>%xml_text()%>%
                         grep("Gene ID",.,value = TRUE)
                       if(!isEmpty(NCBIcheck)){
                         NCBIcheck<-NCBIcheck%>%unlist()%>%
                           str_extract_all(.,"(\\d)+")%>%.[[1]]%>%.[1]
                       }else{
                         NCBIcheck<-NA
                       }
                       out<-data.frame(
                         ensembl_gene_id=temp[i],
                         entrezgene_id=NCBIcheck
                       )%>%as.data.frame()
                       return(out)
                     }
      stopCluster(Par_cl)
    }
    temp2<-temp2[!is.na(temp2$entrezgene_id),]
    temp2<-temp2[!duplicated(temp2$ensembl_gene_id),]
    rownames(temp2)<-temp2$ensembl_gene_id
    temp2<-cbind(
      temp2,
      Anno[temp2$ensembl_gene_id,c(3:4)]
    )
    #sum(Anno2$ensembl_gene_id%in%temp2$ensembl_gene_id)==0
    Anno2<-rbind(
      Anno2,
      temp2
    )
  }
  if(Homologues){
    Anno2<-cbind(mapping=NaMapping[Anno2$ensembl_gene_id],Anno2)
    Anno2<-Anno2[!duplicated(Anno2$mapping),]
    rownames(Anno2) <- NaMapping[Anno2$ensembl_gene_id]
    Anno2<-Anno2[,-1]
  }
  print("end")
  if (is.function(updateProgress)) {
    text <- paste0("ID Convert Done ") 
    updateProgress(detail = text)
  }
  return(Anno2)
}

pseudoLog10 <- function(x){ asinh(x/2)/log(10) }

WZY_GetSummaryText<-function(p){
  pdata <- data.frame(name = p$data$label, color2 = p$data$group)
  pdata <- pdata[!is.na(pdata$name), ]
  cluster_color <- unique(pdata$color2)
  
  cluster_label <- sapply(
    cluster_color, enrichplot:::get_wordcloud,
    ggData = pdata, nWords = 4
  ) %>% paste0(.,collapse = " ") %>% str_split(., " ") %>% unlist()
  return(cluster_label)
}

WZY_literatureMining<-function(GenesLs=GenesLs, Mesh_term4Interesting=Mesh_term4Interesting, Species=Species, updateProgress = NULL){
  out<-list()
  N<-paste0(#To search for the total number of PubMed citations, enter all[sb] in the search box.(20210506)
    "https://pubmed.ncbi.nlm.nih.gov/?term=",
    URLencode('all[sb]'),
    "&sort=date"
  )%>%read_html()%>%html_nodes(".value")%>%html_text()%>%.[1]%>%gsub(",","",.)%>%as.numeric()
  K<-paste0(#the amounts of literature related to osteoblast differentiation #20210506# PubMed Query: 
    "https://pubmed.ncbi.nlm.nih.gov/?term=",
    URLencode(Mesh_term4Interesting),
    "&sort=date"
  )%>%read_html()%>%html_nodes(".value")%>%html_text()%>%.[1]%>%gsub(",","",.)%>%as.numeric()
  Thresh<-K/N*10
  
  ####|prepare gene-related articles|####
  # hsapiens_gene_ensembl; mmusculus_gene_ensembl; rnorvegicus_gene_ensembl; sscrofa_gene_ensembl
  # Homo sapiens (Human) [9606]; Mus musculus (Mouse) [10090]; Rattus norvegicus (rat) [10116]; Sus scrofa (pig) [9823]
  # (human) Homo sapiens (human) [hsa]; (mouse) Mus musculus (mouse) [mmu]; (rat) Rattus norvegicus [rno]; (pig) Sus scrofa [ssc]
  # hsapiens_homolog_ensembl_gene; mmusculus_homolog_ensembl_gene; rnorvegicus_homolog_ensembl_gene; sscrofa_homolog_ensembl_gene
  print(GenesLs)
  print(Mesh_term4Interesting)
  print(Species)
  if (is.function(updateProgress)) {
    text <- "Get All Homologoeus Genes"
    updateProgress(detail = text)
  }
  if(Species == "Hsa"){
    Par_species <- "hsapiens_gene_ensembl"
    Par_species.Uniprot <- "9606"
    Homo_species <- c(
      "mmusculus_homolog_ensembl_gene",
      "rnorvegicus_homolog_ensembl_gene",
      "sscrofa_homolog_ensembl_gene"
    )
  }else if(Species == "Mus"){
    Par_species <- "mmusculus_gene_ensembl"
    Par_species.Uniprot <- "10090"
    Homo_species <- c(
      "hsapiens_homolog_ensembl_gene",
      "rnorvegicus_homolog_ensembl_gene",
      "sscrofa_homolog_ensembl_gene"
    )
  }else if(Species == "Rno"){
    Par_species <- "rnorvegicus_gene_ensembl"
    Par_species.Uniprot <- "10116"
    Homo_species <- c(
      "mmusculus_homolog_ensembl_gene",
      "hsapiens_homolog_ensembl_gene",
      "sscrofa_homolog_ensembl_gene"
    )
  }else if(Species == "Ssc"){
    Par_species <- "sscrofa_gene_ensembl"
    Par_species.Uniprot <- "9823"
    Homo_species <- c(
      "mmusculus_homolog_ensembl_gene",
      "rnorvegicus_homolog_ensembl_gene",
      "hsapiens_homolog_ensembl_gene"
    )
  }
  print(Par_species)
  print(Par_species.Uniprot)
  query.res<-RetrieveEntrezID(Par_species=Par_species, Par_species.Uniprot=Par_species.Uniprot, GenesLs=GenesLs)
  homologeus1 <- RetrieveEntrezID(
    Homologues=TRUE, Homo_species=Homo_species[1], Par_species=Par_species,
    Par_species.Uniprot=Par_species.Uniprot, GenesLs=GenesLs, updateProgress = updateProgress
  )
  homologeus2 <- RetrieveEntrezID(
    Homologues=TRUE, Homo_species=Homo_species[2], Par_species=Par_species,
    Par_species.Uniprot=Par_species.Uniprot, GenesLs=GenesLs, updateProgress = updateProgress
  )
  homologeus3 <- RetrieveEntrezID(
    Homologues=TRUE, Homo_species=Homo_species[3], Par_species=Par_species,
    Par_species.Uniprot=Par_species.Uniprot, GenesLs=GenesLs, updateProgress = updateProgress
  )
  
  #Calculate results and construct the literature mining table
  literature.mining<-data.frame(matrix(nrow = 0, ncol=14))
  colnames(literature.mining)<-c("ensembl_gene_id","entrezgene_id","GeneSymbol",
                                 "gene_biotype", "N", "K", "n", "k", "R", "10x Background of R","P.value",
                                 "Gene related PMID", "Overlapped PMID", "Overlapped Genes [Article No]")
  # Par_pb <- txtProgressBar(min=1, max=nrow(query.res), style = 3)
  print("StartLoop")
  list.packages <- c(
    "readxl", "ggplot2", "ggpubr", "matrixStats", "ggrepel", "reshape2", "dplyr", "stringr",
    "grid", "tcltk", "parallel", "doParallel", "doSNOW", "data.table", "gplots",
    "randomcoloR", "factoextra", "RColorBrewer", "grDevices", "gmp", "xtable", "latex2exp",
    "httr", "jsonlite", "curl", "RCurl", "magrittr", "rlist", "pipeR", "plyr",
    "xml2", "rvest", "knn.covertree", "knitr", "rlang", "visNetwork", "hwriter", "htmltools"
  )
  bio.list.packages <- c(
    "limma", "ExperimentHub", "clusterProfiler", "GO.db",
    "org.Mm.eg.db", "pathview", "enrichplot", "org.Hs.eg.db"
  )
  wzy_mainloop <- function(
    query.res = query.res, attempt_max = 3, Thresh = Thresh,
    K = K, N = N, i = i
  ){
    GeneID<-c(
      query.res$entrezgene_id[i],
      homologeus1[query.res$ensembl_gene_id[i],"entrezgene_id"],
      homologeus2[query.res$ensembl_gene_id[i],"entrezgene_id"],
      homologeus3[query.res$ensembl_gene_id[i],"entrezgene_id"]
    )
    #### Calculate n
    # Get UID number that within interested MeSH term
    uid.res<-c()
    for(a in GeneID){
      # Retrieve PMID of gene-related articles
      # https://www.ncbi.nlm.nih.gov/books/NBK25497/table/chapter2.T._entrez_unique_identifiers_ui/?report=objectonly
      # https://www.ncbi.nlm.nih.gov/books/NBK25499/
      # https://dataguide.nlm.nih.gov/eutilities/utilities.html
      # https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=gene&db=pubmed&id=68389&linkname=homologene_pubmed
      # https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=gene&db=pubmed&id=12393
      URL_temp<-NULL
      attempt<-1
      url <- paste0(
        "https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=gene&db=pubmed&id=",
        a
      )
      while(is.null(URL_temp)&&attempt<attempt_max){
        try({
          url <- url(url, "rb")
          if(class(url)[1]=="url"){
            URL_temp <- read_xml(
              url
            )%>%xml_find_all(., ".//Id")%>%xml_text()
            close(url)
          }
        }, silent = TRUE)
        attempt<-attempt+1
        if(is.null(URL_temp)){Sys.sleep(round(runif(1,10,180),1))}
      }
      uid.res<-c(
        uid.res,
        URL_temp
      )
    }
    uid.res<-unique(uid.res)
    n<-length(uid.res)
    #### Calculate k
    maxlimit<-125
    if(n>maxlimit){
      step<-n%/%maxlimit
      mod<-n%%maxlimit
      start<-seq(from=1, to=maxlimit*step, by=maxlimit)
      end<-seq(from=maxlimit, to=maxlimit*step, by=maxlimit)
      if(mod>0){
        start<-c(start, tail(end, 1)+1)
        end<-c(end, n)
      }
      step<-length(start)
    }else{
      step<-1
      start<-1
      end<-n
    }
    k<-0
    overlapped.uid<-c()
    for(a in 1:step){
      URL_temp<-NULL
      attempt<-1
      url <- URLencode(
        paste0(
          "https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esearch.fcgi?db=pubmed&term=",
          paste(uid.res[start[a]:end[a]],collapse=","),"[UID]+AND+(",URLencode(Mesh_term4Interesting),")",
          "&rettype=count"
        )
      )
      while(is.null(URL_temp)&&attempt<attempt_max){
        try({
          url <- url(url, "rb")
          if(class(url)[1]=="url"){
            URL_temp <- read_xml(#the amounts of articles of each gene on interested MeSH term:
              url
            )%>%xml_find_all(., ".//Count")%>%xml_text()%>%.[1]%>%as.numeric()
            close(url)
          }
        }, silent = TRUE)
        attempt<-attempt+1
        if(is.null(URL_temp)){Sys.sleep(round(runif(1,10,180),1))}
      }
      if(is.null(URL_temp)){URL_temp <- 0}
      k<-k+URL_temp
      URL_temp<-NULL
      attempt<-1
      url <- URLencode(
        paste0(
          "https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esearch.fcgi?db=pubmed&term=",
          paste(uid.res[start[a]:end[a]],collapse=","),"[UID]+AND+(",URLencode(Mesh_term4Interesting),")",
          "&rettype=unlist"
        )
      )
      while(is.null(URL_temp)&&attempt<attempt_max){
        try({
          url <- url(url, "rb")
          if(class(url)[1]=="url"){
            URL_temp <- read_xml(#the amounts of articles of each gene on interested MeSH term:
              url
            )%>%xml_find_all(., ".//Id")%>%xml_text()
            close(url)
          }
        }, silent = TRUE)
        attempt<-attempt+1
        if(is.null(URL_temp)){Sys.sleep(round(runif(1,10,180),1))}
      }
      overlapped.uid<-c(
        overlapped.uid,
        URL_temp
      )
    }
    if(is.na(k)){k<-0}
    #### Calculate P
    R<-k/n
    P<-0
    if(k<1){
      P<-0
    }else{
      for (a in 0:(k-1)) {
        P<-P+((chooseZ(K,a)*chooseZ(N-K,n-a))/chooseZ(N,n))
      }
    }
    P<-asNumeric(1-P)
    if(P==0){P<-1*10^-300}
    temp<-data.frame(
      ensembl_gene_id=query.res$ensembl_gene_id[i],
      entrezgene_id=query.res$entrezgene_id[i],
      GeneSymbol=query.res$external_gene_name[i],
      gene_biotype=query.res$gene_biotype[i],
      N=N,K=K,n=n,k=k,R=R,Thresh=Thresh,P=P,
      GenePMID=uid.res%>%paste(.,collapse = ","),
      OverlapPMID=overlapped.uid%>%paste(.,collapse = ",")
    )
    colnames(temp)<-c("ensembl_gene_id","entrezgene_id","GeneSymbol",
                      "gene_biotype", "N", "K", "n", "k", "R", "10x Background of R","P.value",
                      "Gene related PMID", "Overlapped PMID")
    return(temp)
  }
  Par_cl<-makeCluster(parallelly::freeConnections()-2)
  registerDoSNOW(Par_cl)
  Par_pb <- txtProgressBar(min=1, max=nrow(query.res), style = 3)
  progress <- function(n) setTxtProgressBar(Par_pb, n)
  Par_opts<-list(progress = progress)
  #Refer here for all column names for Entrez API (https://www.ncbi.nlm.nih.gov/books/NBK25501/)
  temp<-foreach(
    i=1:nrow(query.res), .combine=rbind, .errorhandling = "remove", .inorder=FALSE, .verbose = FALSE,
    .options.snow=Par_opts, .packages = c(list.packages, bio.list.packages)
  ) %dopar% {
    temp3 <- NULL
    temp3 <- wzy_mainloop(query.res = query.res, attempt_max = 5, Thresh = Thresh, K = K, N = N, i = i)
    if(is.null(temp3)){
      temp3<-data.frame(
        ensembl_gene_id=query.res$ensembl_gene_id[i],
        entrezgene_id=query.res$entrezgene_id[i],
        GeneSymbol=query.res$external_gene_name[i],
        gene_biotype=query.res$gene_biotype[i],
        N=NA,K=NA,n=NA,k=NA,R=NA,Thresh=NA,P=NA,
        GenePMID=NA,
        OverlapPMID=NA
      )
      colnames(temp3)<-c("ensembl_gene_id","entrezgene_id","GeneSymbol",
                         "gene_biotype", "N", "K", "n", "k", "R", "10x Background of R","P.value",
                         "Gene related PMID", "Overlapped PMID")
    }
    return(temp3)
  }
  stopCluster(Par_cl)
  literature.mining<-rbind(literature.mining,temp)
  rm(temp)
  gc()
  print("EndLoop")
  #Correcting P-value for multiple testing
  literature.mining<-cbind(literature.mining[,1:11], 
                           p.adj=p.adjust(as.numeric(literature.mining$P.value),method = "BH"),
                           literature.mining[,12:13])
  out<-list(
    literature.mining=literature.mining,
    query.res=query.res,
    homologeus1=homologeus1,
    homologeus2=homologeus2,
    homologeus3=homologeus3
  )
  print("end")
  return(out)
}

literatureMiningPlot<-function(
    literature.mining=out$literature.mining, Thresh.R=NULL,
    use.Padj = FALSE, Thresh.P=0.05, label=TRUE, label_n=5
){
  # print("Plotting")
  # Plotting Results
  literature.mining$n<-as.numeric(literature.mining$n)
  literature.mining$k<-as.numeric(literature.mining$k)
  literature.mining$R<-as.numeric(literature.mining$R)
  if(is.null(Thresh.R)){
    Thresh<-literature.mining$`10x Background of R`[1]
  }else{
    Thresh<-Thresh.R
  }
  df<-literature.mining[,1:12] 
  df$R<-df$R*1000
  df$n<-log10(df$n)
  df$R<-pseudoLog10(df$R)
  df$p.adj<-pseudoLog10(log(1/df$p.adj,2))
  df$P.value<-pseudoLog10(log(1/df$P.value,2))
  df <- df[order(df$P.value), ]
  maxR<-(max(df$R, na.rm=T)+0.3)%>%round(., digits = 1)
  maxP<-(max(df$p.adj, na.rm=T)+0.3)%>%round(., digits = 1)
  RepL_R<-length(rep(0:maxR, each = 9))%/%9
  RepL_P<-length(rep(0:maxP, each = 9))%/%9
  if(use.Padj){
    gplot<-ggplot(df,aes(x=p.adj, y=R, colour=n, size=k ))
  }else{
    gplot<-ggplot(df,aes(x=P.value, y=R, colour=n, size=k ))
  }
  gplot<-gplot +
    geom_point() +
    expand_limits(x=0) +
    scale_y_continuous(
      limits = c(0,maxR),
      breaks = 0:maxR,
      guide = "prism_offset_minor",
      minor_breaks = pseudoLog10(rep(1:9, RepL_R)*(10^rep(0:maxR, each = 9))),
      labels =  function(lab){
        do.call(
          expression,
          lapply(paste(lab), function(x) {
            if(x==0){bquote(bold("0"))}else{bquote(bold("10"^.(x)))}
          })
        )
      }
    )+
    scale_x_continuous(
      limits = c(0,maxP),
      breaks = 0:maxP,
      guide = "prism_offset_minor",
      minor_breaks = pseudoLog10(rep(1:9, RepL_P)*(10^rep(0:maxP, each = 9))),
      labels = function(lab){
        do.call(
          expression,
          lapply(paste(lab), function(x) {
            if(x==0){bquote(bold("0"))}else{bquote(bold("10"^.(x)))}
          })
        )
      }
    )+
    scale_size(range = c(0,20))+
    theme(
      axis.text=element_text(size=12),
      axis.title=element_text(size=14,face="bold"),
      axis.ticks.length = unit(5,"pt"),
      axis.ticks = element_line(linewidth = 0.7),
    )+
    coord_cartesian(clip = "off")+
    geom_hline(yintercept=pseudoLog10(Thresh*1000), linetype="dashed", 
               color = "red", size=0.4)+
    geom_vline(xintercept=pseudoLog10(log(1/Thresh.P,2)), linetype="dashed", 
               color = "red", size=0.4)+
    labs(x="log2(1/P.value)", 
         y="R (‰)", 
         title="",
         colour="log10(Gene Related Articles No.)", size="Topics\nRelated Articles No.")+
    annotation_custom(
      grob = grid::linesGrob(gp=gpar(lwd=2)),
      xmin = -Inf,
      xmax = -Inf,
      ymin = 0,
      ymax = maxR
    )+
    annotation_custom(
      grob = grid::linesGrob(gp=gpar(lwd=2)),
      xmin = 0,
      xmax = maxP,
      ymin = -Inf,
      ymax = -Inf
    )
  #print("PlottingEnd")
  if(label_n == "All"){
    label_n <- nrow(df) 
  }
  if(label){
    if(use.Padj){
      df <- df[df$R>=pseudoLog10(Thresh*1000) & df$p.adj>=pseudoLog10(log(1/Thresh.P,2)), ]
    }else{
      df <- df[df$R>=pseudoLog10(Thresh*1000) & df$P.value>=pseudoLog10(log(1/Thresh.P,2)), ]
    }
    df <- df[order(df$P.value, decreasing = TRUE), ]
    gplot <- gplot + geom_text_repel(
      data = df[1:label_n, ],
      aes(label=GeneSymbol),hjust=0, vjust=0, size=8, color="darkred"
    )
  }
  return(gplot)
}

literatureMiningOverlappedGenes<-function(out, updateProgress = NULL){
  
  literature.mining<-out$literature.mining
  query.res<-out$query.res
  homologeus1<-out$homologeus1
  homologeus2<-out$homologeus2
  homologeus3<-out$homologeus3
  
  outls<-c()
  
  for(i in 1:nrow(query.res)){
    print(paste0(i,"/",nrow(query.res)))
    if (is.function(updateProgress)) {
      text <- paste0(i," in ",nrow(query.res))
      updateProgress(message = text, detail = text)
    }
    GeneID<-c(
      query.res$entrezgene_id[i],
      homologeus1[query.res$ensembl_gene_id[i],"entrezgene_id"],
      homologeus2[query.res$ensembl_gene_id[i],"entrezgene_id"],
      homologeus3[query.res$ensembl_gene_id[i],"entrezgene_id"]
    )%>%.[!is.na(.)]
    
    overlapped.uid<-literature.mining$`Overlapped PMID`[i]%>%str_split(.,",")%>%unlist()
    
    overlapped.genes<-data.frame(matrix(nrow = 0, ncol=3))
    colnames(overlapped.genes)<-c("GeneSymbol","entrezgene_id","Overlapped_PMID")
    if(overlapped.uid[1]!=""){
      
      for(uid in overlapped.uid){
        
        print(paste0("PMID:", uid, " (", which(overlapped.uid==uid)," of ",length(overlapped.uid), ")"))
        temp.gene<-read_xml(
          paste0(
            "https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&db=gene&id=",
            uid
          )
        )%>%xml_find_all(., ".//Id")%>%xml_text()%>%.[-1]%>%unique()%>%.[!.%in%GeneID]
        
        if(is_empty(temp.gene)){next}
        if(length(temp.gene)>500){next}
        
        a.n<-length(temp.gene)
        maxlimit<-50
        if(a.n>maxlimit){
          step<-a.n%/%maxlimit
          mod<-a.n%%maxlimit
          start<-seq(from=1, to=maxlimit*step, by=maxlimit)
          end<-seq(from=maxlimit, to=maxlimit*step, by=maxlimit)
          if(mod>0){
            start<-c(start, tail(end, 1)+1)
            end<-c(end, a.n)
          }
          step<-length(start)
        }else{
          step<-1
          start<-1
          end<-a.n
        }
        
        if(step>1){
          pb <- txtProgressBar(min=1, max=step, style = 3)
        }
        
        removeIdx<-c()
        GeneSymbol<-c()
        for(a in 1:step){
          #print(paste0("b:",which(temp.gene==b),";",length(temp.gene)))
          GSB<-read_html(
            paste0(
              "https://eutils.ncbi.nlm.nih.gov/entrez/eutils/efetch.fcgi?db=gene&id=",
              temp.gene[start[a]:end[a]]%>%paste(.,collapse = ","),
              "&rettype=unlist"
            )
          )
          lh<-(end[a]-start[a]+1)
          if(lh==1){
            test<-xml_child(xml_child(xml_child(xml_child(xml_child(GSB, 1), 1), 1), 1), 2)%>%xml_text()%>%grep("Official Symbol:",.)
            if(!is_empty(test)){
              GeneSymbol<-c(
                GeneSymbol,
                xml_child(xml_child(xml_child(xml_child(xml_child(xml_child(xml_child(GSB, 1), 1), 1), 1), 2), 2), 2)%>%xml_text()
              )
            }else{
              removeIdx<-c(
                removeIdx,1
              )
            }
          }else{
            for(b in 1:lh){
              test<-xml_child(xml_child(xml_child(xml_child(xml_child(GSB, 1), 1), 1), b), 2)%>%xml_text()%>%grep("Official Symbol:",.)
              if(!is_empty(test)){
                GeneSymbol<-c(
                  GeneSymbol,
                  xml_child(xml_child(xml_child(xml_child(xml_child(xml_child(xml_child(xml_child(GSB, 1), 1), 1), b), 2), 2), 2), 2)%>%xml_text()
                )
              }else{
                removeIdx<-c(
                  removeIdx,(b+start[a]-1)
                )
              }
            }
          }
          
          if(step>1){
            setTxtProgressBar(pb, a)
          }
          if(is.function(updateProgress)) {
            text <- paste0(a," in ",step)
            updateProgress(message = paste0(i," in ",nrow(query.res)), detail = text)
          }
        }
        if(step>1){close(pb)}
        if(!is_empty(removeIdx)){
          temp.gene<-temp.gene[-removeIdx]
        }
        
        if(!is_empty(temp.gene)){
          temp<-data.frame(
            GeneSymbol=GeneSymbol%>%str_to_title(),
            entrezgene_id=temp.gene,
            Overlapped_PMID=rep(uid,length(temp.gene))
          )
          overlapped.genes<-rbind(
            overlapped.genes,
            temp
          )
        }
      }
    }
    
    temp<-c()
    OrderID<-c()
    for(a in overlapped.genes$GeneSymbol%>%unique()){
      temp2<-overlapped.genes[overlapped.genes$GeneSymbol==a,]
      OrderID<-c(
        OrderID,
        length(temp2$Overlapped_PMID%>%unique())
      )
      temp<-c(
        temp,
        paste0(
          temp2$GeneSymbol[1],
          " (EntrezID:", temp2$entrezgene_id[1], ";",
          "Overlapped_PMID[", tail(OrderID,1), "]:", paste(temp2$Overlapped_PMID%>%unique(),collapse = ","),")" 
        )
      )
    }
    OrderID<-as.numeric(OrderID)
    OrderID<-order(x=OrderID, decreasing=TRUE, na.last=T)
    overlapped.genes<-temp%>%.[OrderID]%>%paste(.,collapse = " ")
    outls<-c(
      outls,overlapped.genes
    )
  }
  
  overlapped.genes<-cbind(
    literature.mining[,1:4],
    overlapped.genes=outls
  )
  
  return(overlapped.genes)
  
}
library(rlang)
library(ggprism)
```

#### Results {.tabset .tabset-fade}

Calcuate relativity of the TFs to the Mesh term "Osteoblasts"[Mesh] using a literature mining method.
```{r 02-04.2.b}
TFs <- select(org.Hs.eg.db, keys = unique(TFLink_related$Name.TF), columns = c('ENSEMBL'), keytype = "SYMBOL")
Mesh_term4Interesting <- '"Osteoblasts"[Mesh]'
GenesLs <- TFs$ENSEMBL[!is.na(TFs$ENSEMBL)]
Species <- "Hsa" # Hsa Mus Rno Ssc
TFs.Mesh<-WZY_literatureMining(GenesLs=GenesLs, Mesh_term4Interesting=Mesh_term4Interesting, Species=Species, updateProgress = NULL)
```

Calcuate relativity of the Mitochondrial/Cytoskeletal genes to the Mesh term "Osteoblasts"[Mesh] using a literature mining method.
```{r 02-04.2.c}
Mesh_term4Interesting <- '"Osteoblasts"[Mesh]'
GenesLs <- Anno_GeneLs$EnsemblID[!is.na(Anno_GeneLs$EnsemblID)]
Species <- "Hsa" # Hsa Mus Rno Ssc
MitoCySk.Mesh<-WZY_literatureMining(GenesLs=GenesLs, Mesh_term4Interesting=Mesh_term4Interesting, Species=Species, updateProgress = NULL)
```

#### Plots {.tabset .tabset-fade}

```{r 02-04.2.d, fig.width=12, fig.height=8, out.width="100%"}
gp <- literatureMiningPlot(
  literature.mining=TFs.Mesh$literature.mining, Thresh.R=0.002,
  use.Padj = FALSE, Thresh.P=0.05, label=TRUE, label_n = 10
)
svg(filename = file.path(".", "01.PlotOut", "LiteratureMiningRes_01.svg"), width = 12, height = 8, pointsize = 12)
print(gp)
dev.off()
graphics.off()
knitr::opts_knit$set(global.device = TRUE)
print(gp)
knitr::opts_knit$set(global.device = FALSE)
```

```{r 02-04.2.e, fig.width=12, fig.height=8, out.width="100%"}
gp <- literatureMiningPlot(
  literature.mining=MitoCySk.Mesh$literature.mining, Thresh.R=0.001,
  use.Padj = FALSE, Thresh.P=0.15, label=TRUE, label_n = 10
)
svg(filename = file.path(".", "01.PlotOut", "LiteratureMiningRes_02.svg"), width = 12, height = 8, pointsize = 12)
print(gp)
dev.off()
graphics.off()
knitr::opts_knit$set(global.device = TRUE)
print(gp)
knitr::opts_knit$set(global.device = FALSE)
```

## 02-05. Filter for osteoblast-related genes

```{r 02-05}
TFs.Correlated <- TFs.Mesh$literature.mining[TFs.Mesh$literature.mining$P.value<0.05,]
TFs.Correlated <- TFs.Correlated[TFs.Correlated$R > 0.002,]
GeneLs.Correlated <- MitoCySk.Mesh$literature.mining[MitoCySk.Mesh$literature.mining$P.value<0.15,]
GeneLs.Correlated <- GeneLs.Correlated[GeneLs.Correlated$R > 0.001,]
Gene.keep <- TFLink_related$Name.TF %>% unique()
Gene.keep <- Gene.keep[Gene.keep %in% TFs.Correlated$GeneSymbol]
Gene.keep <- c(
  Gene.keep,
  GeneLs.Correlated$GeneSymbol %>% unique()
)%>%unique()
TFLink_related_filter <- TFLink_related[TFLink_related$Name.Target%in%Gene.keep,]
TFLink_related_filter <- TFLink_related_filter[TFLink_related_filter$Name.TF%in%Gene.keep,]
for (i in unique(GeneLs.Correlated$GeneSymbol)) {
  temp<-TFLink_related_filter[TFLink_related_filter$Name.Target==i,]
  if(!nrow(temp)) next
  if(sum(temp$`Small-scale.evidence`=="Yes")){
    temp <- temp[temp$`Small-scale.evidence`=="Yes",]
  }else{
    PubMed.No <- temp$PubmedID%>%str_split(.,";")%>%sapply(.,length)
    temp <- temp[PubMed.No>1,]
  }
  TFLink_related_filter <- rbind(
    temp, TFLink_related_filter[TFLink_related_filter$Name.Target!=i,]
  )
}
for (i in unique(TFLink_related$Name.TF)) {
  temp<-TFLink_related_filter[TFLink_related_filter$Name.Target==i,]
  if(!nrow(temp)) next
  if(sum(temp$`Small-scale.evidence`=="Yes")){
    temp <- temp[temp$`Small-scale.evidence`=="Yes",]
  }else{
    PubMed.No <- temp$PubmedID%>%str_split(.,";")%>%sapply(.,length)
    temp <- temp[PubMed.No>1,]
  }
  TFLink_related_filter <- rbind(
    temp, TFLink_related_filter[TFLink_related_filter$Name.Target!=i,]
  )
}
# Prepare nodes table
# Add TFs
TF_ls <- TFLink_related_filter$UniprotID.TF %>% unique()
nodes <- data.frame(
  label = NULL,
  group = NULL,
  value = NULL,          
  shape = NULL,
  title = NULL,
  color = NULL,
  shadow = NULL
)
# Legend:
# Sig TF: blue dot
# O-GlcNAc TF: blue square
# Sig and O-GlcNAc TF: blue star
for (i in TF_ls) {
  label <- TFLink_related$Name.TF[TFLink_related$UniprotID.TF==i] %>% unique() %>% as.character()
  group <- "TF"
  value <- 3
  title <- i
  shadow <- FALSE
  color <- "blue"
  is.DEGs <- TFLink_related[TFLink_related$UniprotID.TF==i, "is.DEGs"] %>% unique() %>% as.character()
  OGlcNAc <- TFLink_related[TFLink_related$UniprotID.TF==i, "OGlcNAc"] %>% unique() %>% as.character()
  if(is.DEGs == "Yes" & OGlcNAc == "Yes"){
    shape <- "star"
  }else if (is.DEGs == "Yes") {
    shape <- "dot"
  }else if (OGlcNAc == "Yes") {
    shape <- "square"
  }
  ENSEMBL <- Anno_GeneLs$EnsemblID[Anno_GeneLs$Entry==i][1]
  if(!is.na(ENSEMBL)){
    FEA_Related <- res@compareClusterResult[grepl(ENSEMBL, res@compareClusterResult$geneID),]
    Mito <- grepl("mitochondria(l){0,1}", FEA_Related$Description, ignore.case = TRUE) %>% sum() %>% as.logical()
    CySk <- grepl("cytoskele(ton|tal)", FEA_Related$Description, ignore.case = TRUE) %>% sum() %>% as.logical()
    if(Mito & CySk){
      color <- "black"
      value <- 10
    }else if(Mito){
      color <- "orange"
      value <- 10
    }else if(CySk){
      color <- "red"
      value <- 10
    }
  }
  nodes <- rbind(
    nodes,
    data.frame(
      label = label,
      group = group,
      value = value,          
      shape = shape,
      title = title,
      color = color,
      shadow = shadow
    )
  )
}
# Add Mitochondrial/Cytoskeletal genes
GeneLs <- TFLink_related_filter$UniprotID.Target[!TFLink_related_filter$UniprotID.Target %in% TF_ls] %>% unique() %>% as.character()
GeneLs <- GeneLs[!GeneLs%in%TFLink_related_filter$UniprotID.TF]
# Legend:
# Mito Gene: orange triangle
# Cytoskeletal Gene: red triangle
# both Mito and Cytoskeletal gene: black diamond
for (i in GeneLs) {
  label <- Anno_GeneLs$`Gene Names (primary)`[Anno_GeneLs$Entry==i][1]
  title <- i
  ENSEMBL <- Anno_GeneLs$EnsemblID[Anno_GeneLs$Entry==i][1]
  if(is.na(ENSEMBL)){next}
  if(is.na(label)){
    label <- ENSEMBL
  }
  FEA_Related <- res@compareClusterResult[grepl(ENSEMBL,res@compareClusterResult$geneID),]
  Mito <- grepl("mitochondria(l){0,1}", FEA_Related$Description, ignore.case = TRUE) %>% sum() %>% as.logical()
  CySk <- grepl("cytoskele(ton|tal)", FEA_Related$Description, ignore.case = TRUE) %>% sum() %>% as.logical()
  if(Mito & CySk){
    shadow <- TRUE
    group <- "Mito/CySk"
    value <- 10
    color <- "black"
    shape <- "diamond"
  }else if(Mito){
    shadow <- FALSE
    group <- "Mito"
    value <- 6
    color <- "orange"
    shape <- "triangle"
  }else if(CySk){
    shadow <- FALSE
    group <- "CySk"
    value <- 6
    color <- "red"
    shape <- "triangle"
  }
  nodes <- rbind(
    nodes,
    data.frame(
      label = label,
      group = group,
      value = value,          
      shape = shape,
      title = title,
      color = color,
      shadow = shadow
    )
  )
}
nodes <- cbind(
  id = 1:nrow(nodes),
  nodes
)
# Prepare edge table
edges <- data.frame(
  from = NULL,
  to = NULL
)
NodesLs <- nodes$title
Par_cl <- makeCluster(parallelly::freeCores()[1])
registerDoSNOW(Par_cl)
Par_pb <- txtProgressBar(min = 1, max = length(NodesLs), style = 3)
progress <- function(n) setTxtProgressBar(Par_pb, n)
Par_opts <- list(progress = progress)
edges <- foreach(
  i = 1:length(NodesLs), .combine = base::rbind, .errorhandling = "pass",
  .options.snow = Par_opts, .packages = c("tcltk", "dplyr", "utils")
) %dopar% {
  temp <- TFLink_related_filter[(TFLink_related_filter$UniprotID.TF %in% NodesLs[i] | TFLink_related_filter$UniprotID.Target %in% NodesLs[i]),]
  temp <- temp[(temp$UniprotID.TF %in% NodesLs | temp$UniprotID.Target %in% NodesLs),]
  from <- temp$UniprotID.TF
  to <- temp$UniprotID.Target
  for (k in 1:length(from)) {
    from[k] <- which(nodes$title == from[k])
    to[k] <- which(nodes$title == to[k])
  }
  out <- data.frame(
    from = from,
    to = to
  )
  out
}
stopCluster(Par_cl)
dupLs <- paste0(edges$from, "-", edges$to)
edges <- edges[!duplicated(dupLs),]
edges <- edges[edges$from != edges$to,]
```

## 02-06. Retrieve SNP records of TFs

Retrieve SNP records on the O-GlcNAc sites of TFs. If the a O-GlcNAc site of a TF really have a profound influences on the function of this TF, the misssense SNP on this site should be associated with some clincial pathogenic phenotype.
```{r 02-06}
# Setup BioMart for SNP
Ann_Mart.Loc<-NULL
attempt<-1
attempt_max<-12
while(is.null(Ann_Mart.Loc)&&attempt<13){
  if(attempt%in%seq(from=1,to=attempt_max,3)){
    url<-"https://useast.ensembl.org"
  }else if(attempt%in%seq(from=2,to=attempt_max,3)){
    url<-"https://www.ensembl.org"
  }else if(attempt%in%seq(from=3,to=attempt_max,3)){
    url<-"https://useast.ensembl.org/"
  }else if(attempt%in%seq(from=4,to=attempt_max,3)){
    url<-"https://asia.ensembl.org/"
  }
  try({
    Ann_Mart.Loc <- useDataset(
      "hsapiens_gene_ensembl",
      useMart("ENSEMBL_MART_ENSEMBL", host = url)
    )
  }, silent = TRUE)
  attempt<-attempt+1
  if(is.null(Ann_Mart.Loc)){Sys.sleep(10)}
}
# Setup BioMart for Gene ID
Ann_Mart.snp<-NULL
attempt<-1
attempt_max<-12
while(is.null(Ann_Mart.snp)&&attempt<13){
  if(attempt%in%seq(from=1,to=attempt_max,3)){
    url<-"https://useast.ensembl.org"
  }else if(attempt%in%seq(from=2,to=attempt_max,3)){
    url<-"https://www.ensembl.org"
  }else if(attempt%in%seq(from=3,to=attempt_max,3)){
    url<-"https://useast.ensembl.org/"
  }else if(attempt%in%seq(from=4,to=attempt_max,3)){
    url<-"https://asia.ensembl.org/"
  }
  try({
    Ann_Mart.snp <- useDataset(
      "hsapiens_snp",
      useMart("ENSEMBL_MART_SNP", host = url)
    )
  }, silent = TRUE)
  attempt<-attempt+1
  if(is.null(Ann_Mart.snp)){Sys.sleep(10)}
}
# Get SNP results
UniPort.rs.OGlcNAc <- data.frame()
TFs.UniPort <- nodes$title[nodes$group=="TF"]
Par_pb <- txtProgressBar(min = 1, max = length(TFs.UniPort), style = 3)
n <- 1
for(i in TFs.UniPort){
  n<-n+0.49
  setTxtProgressBar(Par_pb, n)
  UniPort.Loc <- getBM(
    mart=Ann_Mart.Loc,
    attributes=c(
      "uniprotswissprot", "ensembl_gene_id", "ensembl_transcript_id", "strand",
      "chromosome_name", "transcript_start", "transcript_end", "cds_length"
    ),
    filter=c(
      "uniprotswissprot"
    ),
    values=i,
    uniqueRows = T
  )
  n<-n+0.49
  setTxtProgressBar(Par_pb, n)
  UniPort.Loc <- UniPort.Loc[order(UniPort.Loc$cds_length, decreasing = TRUE),][1,]
  UniPort.rs<-NULL
  rm(UniPort.rs)
  try({
    UniPort.rs <- UniPort.Loc %>%
      {
        paste(
          .[]$chromosome_name,
          min(c(.[]$transcript_start, .[]$transcript_end)),
          max(c(.[]$transcript_start, .[]$transcript_end)),
          sep = ":"
        )
      } %>%
      getBM(
        mart=Ann_Mart.snp,
        attributes=c(
          "refsnp_id", "consequence_type_tv", "consequence_allele_string",
          "ensembl_peptide_allele", "translation_start",
          "translation_end",  "ensembl_transcript_stable_id",
          "chr_name",  "chrom_start",  "chrom_end"
        ),
        filter="chromosomal_region",
        values=.,
        uniqueRows = TRUE,
        verbose = FALSE
      )
  }, silent = TRUE)
  if(!exists("UniPort.rs")) next
  UniPort.rs <- UniPort.rs[UniPort.rs$ensembl_transcript_stable_id == UniPort.Loc$ensembl_transcript_id,]
  UniPort.rs <- UniPort.rs[UniPort.rs$consequence_type_tv == "missense_variant",]
  UniPort.rs <- UniPort.rs[UniPort.rs$translation_start == UniPort.rs$translation_end,]
  temp <- OGlcNAc_Anno[OGlcNAc_Anno$Accession==i,]$Position_in_Protein %>% 
    {UniPort.rs[UniPort.rs$translation_start%in%.[],]}
  if(nrow(temp)){
    temp <-  cbind(
      UniPort_ID = i, temp
    )
    UniPort.rs.OGlcNAc <- rbind(
      UniPort.rs.OGlcNAc, temp
    )
  }
  n<-n+0.02
  setTxtProgressBar(Par_pb, n)
}
cat("\n")
close(Par_pb)
SNP.Phenotype <- getBM(
  mart=Ann_Mart.snp,
  attributes=c(
    "refsnp_id", "clinical_significance", "p_value",
    "phenotype_name", "phenotype_description", "variation_names"
  ),
  filter="snp_filter",
  values=UniPort.rs.OGlcNAc$refsnp_id%>%unique(),
  uniqueRows = TRUE
)
SNP.Phenotype<-SNP.Phenotype[SNP.Phenotype$phenotype_description!="",]
UniPort.rs.OGlcNAc.Clinc <- UniPort.rs.OGlcNAc[UniPort.rs.OGlcNAc$refsnp_id%in%unique(SNP.Phenotype$refsnp_id),]
UniPort.rs.OGlcNAc.Clinc <- merge(UniPort.rs.OGlcNAc.Clinc, SNP.Phenotype, by="refsnp_id")
```

## 02-07. Visualization of the gene regulatory network {.tabset .tabset-fade}

### Code {.tabset .tabset-fade}

Filter out the TFs that doesn't have pathogenic SNP on O-GlcNAc sites.
```{r 02-07.a}
temp <- nodes[nodes$group=="TF",]
temp <- temp[temp$title%in%unique(UniPort.rs.OGlcNAc.Clinc$UniPort_ID),]
nodes <- rbind(
  nodes[nodes$group!="TF",],
  temp
)
edges <- edges[edges$from%in%nodes$id & edges$to%in%nodes$id,]
nodes<-nodes[nodes$id%in%unique(c(edges$from,edges$to)),]
```
<br>

Add url link to nodes.
```{r 02-07.b}
for(i in nodes$title[nodes$group=="TF"]){
  OGlcNAc.site <- OGlcNAc_Anno[OGlcNAc_Anno$Query==i,]$Position_in_Protein %>%
    unique() %>% paste(., collapse = ";")
  temp <- UniPort.rs.OGlcNAc.Clinc[UniPort.rs.OGlcNAc.Clinc$UniPort_ID==i, ]
  temp <- temp[!duplicated(temp$refsnp_id), ]
  SNP.list <- c()
  for (k in temp$refsnp_id) {
    SNP.list <- c(
      SNP.list,
      paste0(
        "<br><a href='https://www.ensembl.org/Homo_sapiens/Variation/Phenotype?db=core;r=",
        paste0(temp$chr_name[temp$refsnp_id==k],":",temp$chrom_start[temp$refsnp_id==k],"-",temp$chrom_end[temp$refsnp_id==k]),
        ";v=", k, ";vdb=variation' target='_blank'>SNP: ",
        k, "; on AA site: ", temp$translation_start[temp$refsnp_id==k],
        " of ", temp$ensembl_transcript_stable_id[temp$refsnp_id==k], "</a>"
      )
    )
  }
  nodes$title[nodes$title==i] <- HTML(
    paste0(
      '<a href="https://www.uniprot.org/uniprotkb/',i,'/entry" target="_blank">', i, '</a><br>',
      '<a href="https://oglcnac.org/atlas/detail/', i, '" target="_blank">O-GlcNAc Site: ', OGlcNAc.site, '</a><br>',
      'O-GlcNAc site with pathogenic SNP:'
    ), HTML(SNP.list)
  )
}
for(i in nodes$title[nodes$group!="TF"]){
  nodes$title[nodes$title==i] <- HTML(
    paste0(
      '<a href="https://www.uniprot.org/uniprotkb/',i,'/entry" target="_blank">', i, '</a>'
    )
  )
}
TFs.Mesh.keep <- TFs.Mesh$literature.mining[TFs.Mesh$literature.mining$GeneSymbol%in%nodes$label[nodes$group=="TF"],]
MitoCySk.Mesh.keep <- MitoCySk.Mesh$literature.mining[MitoCySk.Mesh$literature.mining$GeneSymbol%in%nodes$label[nodes$group!="TF"],]
Mesh.keep <- rbind(
  TFs.Mesh.keep, MitoCySk.Mesh.keep
)
R.max <- max(Mesh.keep$R)
R.min <- min(Mesh.keep$R)
for(i in nodes$label){
  nodes$value[nodes$label==i]<-1+(((Mesh.keep$R[Mesh.keep$GeneSymbol==i]-R.min)/R.max)*100)
}
TF_ls <- TFLink$Name.TF %>% unique()
for(i in nodes$label[nodes$group!="TF"]){
  if(i %in% TF_ls){
    nodes$shape[nodes$label==i] <- "dot"
  }
}
```
<br>

Add url link to edge.
```{r 02-07.c}
edges <- cbind(
  edges, title = 1, width = 1, color="lightblue", highlight = "red"
)
for(i in 1:nrow(edges)){
  from <- edges[i,]$from
  to <- edges[i,]$to
  from <- nodes$label[nodes$id==from]
  to <- nodes$label[nodes$id==to]
  temp <- TFLink_related_filter[TFLink_related_filter$Name.TF==from & TFLink_related_filter$Name.Target==to,]
  PubMed.ls <- temp$PubmedID %>%
    str_split(.,";") %>% unlist() %>%
    paste0(
      "<a href='https://pubmed.ncbi.nlm.nih.gov/", ., "/' target='_blank'>",
      ., "</a><br>"
    )
  edges$title[i] <- paste0(
    "Has Small-scale Evidence: ", temp$`Small-scale.evidence`, "<br>", HTML(PubMed.ls)
  ) %>% HTML()
  edges$width[i] <- length(PubMed.ls)
  if(temp$`Small-scale.evidence`=="Yes"){
    edges$color[i] <- "#9999FF"
  }
}
e.Max <- max(edges$width)
e.Min <- min(edges$width)
edges$width <- round(log(edges$width - e.Min + 1, base = 2) + 1)
```
<br>

Add legends
```{r 02-07.d}
# nodes data.frame for legend
lnodes <- data.frame(
  label = c(
    "TFs related to cytoskeleton\nwithout O-GlcNAc site records\nand is not DEGs in GSE138783",
    "TFs related to cytoskeleton\nwith O-GlcNAc site records\nand is DEGs in GSE138783",
    "TFs with O-GlcNAc site records\nand is not DEGs in GSE138783",
    "TFs with O-GlcNAc site records\nand is DEGs in GSE138783",
    "Targets related to cytoskeleton", "Targets related to mitochondria",
    "Targets related to\nboth of cytoskeleton and mitochondria",
    "Size of node indicates the amount\nof articles related to osteoblast",
    "Width of edge indicates\nthe amount of articles"
  ),
  shape = c(
    "dot", "star", "square", "star", "triangle", "triangle", "diamond", "text", "text"
  ),
  color = c(
    "red", "red", "blue", "blue", "red", "orange", "black", "#FFFFFF", "#FFFFFF"
  ),
  title = "Legends",
  id = 1:9
)
# edges data.frame for legend
ledges <- data.frame(
  color = c("#9999FF", "lightblue"),
  label = c("Has small-scale\nevidence", "No small-scale\nevidence"),
  arrows =c("to", "to"), width = 10
)
```
<br>

Make interactive network
```{r 02-07.e}
network <- visNetwork(nodes, edges, height = "800px", width = "100%") %>%
  visNodes(physics = TRUE) %>%
  visPhysics(stabilization = TRUE, solver = "repulsion", maxVelocity = 1) %>%
  visEdges(
    smooth = TRUE, shadow = FALSE,
    arrows =list(to = list(enabled = TRUE, scaleFactor = 0.5))
  ) %>%
  visOptions(
    nodesIdSelection = TRUE, selectedBy = "group", manipulation = FALSE,
    highlightNearest = list(enabled = TRUE, degree = 9999, algorithm = "hierarchical")
  ) %>%
  visLegend(addEdges = ledges, addNodes = lnodes, useGroups = FALSE)
network %>% visSave(file = "network.html")
```

### Result {.tabset .tabset-fade}

```{r 02-07.f}
print(network)
```


# 03. Supplementary

```{r 03.Supplementary}
save.image("./CheckPoint.RData")
sessionInfo()
```