TRPC4/TRPC5 are critical for neuronal modulation by transcranial focused ultrasound in retrosplenial cortex in male mice.
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- [1] § Methods › RNA-seq based on fluorescence-activated cell sorting (FACS) ↔ Bulk RNA-seq analysis workflow.R, lines 1–71 · score 0.56 · DEGseq, fold change, adj, log2, RNA
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The authors' code
R · 304 lines · 12 KB · CC-BY-4.0 · 1 match
- Sys.setenv(LANGUAGE = "en")
- options(stringsAsFactors = FALSE)
- #####Differential analysis
- BiocManager::install(c("DEGseq","qvalue"))
- library(qvalue)
- library(DEGseq)
- library(data.table)
- geneExpFile <-data.frame(fread("gene_count_matrix.csv",header=T))
- geneExpFile$name<-make.unique(geneExpFile$name)
- row.names(geneExpFile) <-geneExpFile$name
- geneExpFile1<-geneExpFile[3:14]
- geneExpFile1<-geneExpFile1+1
- write.csv(geneExpFile1,file="gene+count+matrix.csv")
- treatment_positive_df <-readGeneExp(file = "gene+count+matrix.csv",geneCol = 1,valCol = c(2,4,6),sep = ",")
- control_positive_df <-readGeneExp(file = "gene+count+matrix.csv",geneCol = 1,valCol = c(8,10,12),sep = ",")
- treatment_df <-readGeneExp(file = "gene+count+matrix.csv",geneCol = 1,valCol = c(3,5,7),sep = ",")
- control_df <-readGeneExp(file = "gene+count+matrix.csv",geneCol = 1,valCol = c(9,11,13),sep = ",")
- treatment_positive_depth <-c(48359508,52611832,50916518)
- control_positive_depth <-c(41714122,48820574,49144424)
- treatment_depth<-c(49698164,42923092,63185328)
- control_depth <-c(50013002,47967490,47360832)
- #options(digits = 22)
- #Comparison within the control group
- DEGexp(geneExpMatrix2 = control_positive_df, geneCol1 = 1, expCol1 = 2:4, depth1 = control_positive_depth, groupLabel1 = "Tre",
- geneExpMatrix1 = control_df, geneCol2 = 1, expCol2 = 2:4, depth2 = control_depth, groupLabel2 = "Con",
- method = "LRT", normalMethod = "median", outputDir = "tmp")
- #Comparison within the tFus group
- DEGexp(geneExpMatrix2 = treatment_positive_df, geneCol1 = 1, expCol1 = 2:4, depth1 = treatment_positive_depth, groupLabel1 = "Tre",
- geneExpMatrix1 = treatment_df, geneCol2 = 1, expCol2 = 2:4, depth2 = treatment_depth, groupLabel2 = "Con",
- method = "LRT", normalMethod = "median", outputDir = "tmp")
- #Comparison between the control and the tFus group
- DEGexp(geneExpMatrix2 = treatment_positive_df, geneCol1 = 1, expCol1 = 2:4, depth1 = treatment_positive_depth, groupLabel1 = "Tre",
- geneExpMatrix1 = control_positive_df, geneCol2 = 1, expCol2 = 2:4, depth2 = control_positive_depth, groupLabel2 = "Con",
- method = "LRT", normalMethod = "median", outputDir = "tmp")
- #Rename each output txt file and saved as csv format
- ########vocalno painting
- library(ggplot2)
- contr_compare<-data.frame(fread("control+G vs -G adj.csv",header=T))
- Tfus_compare<-data.frame(fread("tfus+G vs -G adj.csv",header=T))
- Tfus_contr_compare<-data.frame(fread("tfus+G vs control +G adj.csv",header=T))
- M<-contr_compare
- M<-Tfus_compare
- M<-Tfus_contr_compare
- logFC_cutoff <-2
- Pvalue_cutoff<-0.001
- #Let each comparison data equals to M and repeat the following codes
- M$change[M$log2.Fold_change.>=logFC_cutoff & M$q.value.Benjamini.et.al..1995.<Pvalue_cutoff] <-"Down"
- M$change[(M$log2.Fold_change.<logFC_cutoff &
- M$log2.Fold_change.>-logFC_cutoff)
- | M$q.value.Benjamini.et.al..1995.>Pvalue_cutoff] <-"No"
- M$change[M$log2.Fold_change.<=-logFC_cutoff & M$q.value.Benjamini.et.al..1995.<Pvalue_cutoff] <-"Up"
- table(M$change)
- M$change <-as.factor(M$change)
- p<-ggplot(M,aes(x=log2.Fold_change.,y=-log10(q.value.Benjamini.et.al..1995.),color=change))+
- geom_point(alpha=0.4,size=1)+
- scale_color_manual(values = c("Down"='#006699',"No"='#bebebe',"Up"='#ffad21'))+
- geom_vline(xintercept = c(-logFC_cutoff,logFC_cutoff),linetype="dashed",color="black",linewidth=1)+
- geom_hline(yintercept=-log10(Pvalue_cutoff),linetype="dashed",color="black",linewidth=1)+
- labs(x="log2(Fold Change)",y="-log10(P Value)")+
- theme_bw()+
- theme(legend.position = "right")
- p1<-p+scale_y_continuous(limits = c(0,20))
- ggsave('vocalno.pdf',plot = p1,width = 8,height = 6)
- contr_compare<-merge(M,geneExpFile1[,7:12],by.x = 1,by.y = 0)
- Tfus_compare<-merge(M,geneExpFile1[,1:6],by.x = 1,by.y = 0)
- Tfus_contr_compare<-merge(M,geneExpFile1[,c(1,3,5,7,9,11)],by.x = 1,by.y = 0)
- write.csv(contr_compare,file="contr_compare.csv")
- write.csv(Tfus_compare,file="Tfus_compare.csv")
- write.csv(Tfus_contr_compare,file="Tfus_contr_compare.csv")
- ############Venn painting
- install.packages("vctrs")
- install.packages("devtools")
- devtools::install_github("yanlinlin82/ggvenn")
- library(grid)
- library(vctrs)
- library(ggvenn)
- conUp<-data.frame(fread("conUp.csv",header=T))
- tfusUp<-data.frame(fread("tfusUp.csv",header=T))
- tvcUp<-data.frame(fread("tvcUp.csv",header=T))
- x <-list('Control'=conUp$GeneNames,
- 'Tfus vs Control'=tvcUp$GeneNames,
- 'Tfus'=tfusUp$GeneNames)
- Up<-ggvenn(x,
- show_percentage = F,
- stroke_color = "white",
- fill_color = c("#b2e7cb","#b2d4ec","#ffb2b2"),
- set_name_color = c("#4a9b83","#1d6295","#ff0000"))
- ggsave('venn_Up.pdf',plot = Up,width = 8,height = 6)
- conDown<-data.frame(fread("conDown.csv",header=T))
- tfusDown<-data.frame(fread("tfusDown.csv",header=T))
- tvcDown<-data.frame(fread("tvcDown.csv",header=T))
- x <-list('Control'=conDown$GeneNames,
- 'Tfus vs Control'=tvcDown$GeneNames,
- 'Tfus'=tfusDown$GeneNames)
- Down<-ggvenn(x,
- show_percentage = F,
- stroke_color = "white",
- fill_color = c("#b2e7cb","#b2d4ec","#ffb2b2"),
- set_name_color = c("#4a9b83","#1d6295","#ff0000"))
- ggsave('venn_Down.pdf',plot = Down,width = 8,height = 6)
- #########intersection filtering
- df1<-tvcUp$GeneNames
- df2<-conUp$GeneNames
- df3<-tfusUp$GeneNames
- tvcup_re<-setdiff(df1,df2)
- tfusup_re<-setdiff(df3,df2)
- tvc_plus_tfus<-intersect(tvcup_re,tfusup_re)
- write.csv(tvc_plus_tfus, 'tvc_plus_tfus.csv')
- #############GO analysis
- BiocManager::install("org.Mm.eg.db")
- library(org.Mm.eg.db)
- install.packages("Rcpp")
- library(Rcpp)
- library(clusterProfiler)
- gene1<-tvc_plus_tfus
- gene_ENTREZID <- unlist(na.omit(mapIds(x = org.Mm.eg.db,
- keys = gene1,
- keytype = "SYMBOL",
- column = "ENTREZID",
- multiVals = "first")))
- go_enrich_results_ALL <- enrichGO(gene = gene_ENTREZID,
- OrgDb = "org.Mm.eg.db",
- ont = "ALL" ,
- pvalueCutoff = 0.05,
- qvalueCutoff = 0.05,
- readable = TRUE)
- write.csv(go_enrich_results_ALL@result, 'GO_gene_ALL_enrichresults.csv')
- #####KEGG analysis
- kegg_enrich_results <- enrichKEGG(gene = gene_ENTREZID,
- organism = "mmu",
- keyType = "kegg",
- pAdjustMethod = "BH",
- pvalueCutoff = 0.05,
- qvalueCutoff = 0.05)
- kk_read <- DOSE::setReadable(kegg_enrich_results,
- OrgDb="org.Mm.eg.db",
- keyType='ENTREZID')#ENTREZID to gene Symbol
- write.csv(kk_read@result,'KEGG_gene_enrichresults.csv')
- ########GO terms painting
- library(enrichplot)
- library(ggplot2)
- bp <-data.frame(fread("GO_gene_ALL_enrichresults_tfusplustvcBP.csv",header = T))
- mf <-data.frame(fread("GO_gene_ALL_enrichresults_tfusplustvcMF.csv",header = T))
- cc <-data.frame(fread("GO_gene_ALL_enrichresults_tfusplustvcCC.csv",header = T))
- d<-bp
- d<-mf
- d<-cc
- #Let each GO ontology equals to d and repeat the following codes
- d<-d[order(-d$Count),]
- d <-d[1:13,]
- d$Description <- factor(d$Description,levels=d$Description)
- mytheme <- theme(axis.title=element_text(face="bold", size=14,colour = 'black'),
- axis.text.y =element_text(face="bold", size=14,colour = 'black'),
- axis.text.x=element_text(size=8),
- axis.line = element_line(linewidth=0.5, colour = 'black'),
- panel.background = element_rect(color='black'),
- legend.key = element_blank()
- )
- p <- ggplot(d,aes(x=Count,y=Description,colour=-1*log10(p.adjust),size=Count))+
- geom_point()+
- scale_size(range=c(2, 8))+
- scale_colour_gradient(low = "blue",high = "red")+
- theme_bw()+
- ylab("GO_BP Pathway Terms")+
- xlab("Gene numbers")+
- labs(color=expression(-log[10](PValue)))+mytheme
- ggsave('GO_BP.pdf',plot = p,width = 10,height = 6)
- #########KEGG terms painting
- kegg_up <-data.frame(fread("KEGG_gene_enrichresults_tfusplustvc.csv",header = T))
- kegg_down <-data.frame(fread("KEGG_gene_enrichresults_tfusdowntvc.csv",header = T))
- d<-kegg_up
- d<-d[order(-d$Count),]
- d <-d[1:10,]
- d$Description <- factor(d$Description,levels=d$Description)
- kegg_up<-d
- d<-kegg_down
- d<-d[order(-d$Count),]
- d <-d[1:10,]
- d$Description <- factor(d$Description,levels=d$Description)
- kegg_down<-d
- kegg<-rbind(kegg_up,kegg_down)
- kegg$number <- factor(rev(1:nrow(kegg)))
- kegg$type<-factor(c(rep("Up", 10),rep("Down", 10)),levels=c("Up", "Down"))
- p <- ggplot(data=kegg, aes(x=number, y=Count, fill=type)) +
- geom_bar(stat="identity", width=0.8) + coord_flip() +
- scale_fill_manual(values = c('#FD8D62',"#8DA1CB")) + theme_test() +
- scale_x_discrete(labels=kegg$Description) +
- xlab("KEGG term") +
- theme(axis.text=element_text(face = "bold", color="gray50")) +
- labs(title = "The Most Enriched KEGG Terms")
- ggsave('kegg_all.pdf',plot = p,width = 10,height = 8)
- ################preparation file for cytoscape and Upset of GO terms
- library(UpSetR)
- go_results<- data.frame(fread("pathway_select.csv",header = T))
- colnames(go_results)[colnames(go_results)=="Type"]<-"Ontology"
- nodes_list <- list()
- edges_list <- list()
- for (i in 1:nrow(go_results)) {
- pathway <- go_results[i, ]
- genes <- unlist(strsplit(pathway$geneID, "/"))
- pathway_node <- data.frame(
- ID = pathway$ID,
- name = pathway$Description,
- Type = "Pathway",
- Ontology = pathway$Ontology,
- stringsAsFactors = FALSE
- )
- nodes_list[[i]] <- pathway_node
- gene_nodes <- data.frame(
- ID = genes,
- name = genes,
- Type = "Gene",
- Ontology = NA,
- stringsAsFactors = FALSE
- )
- nodes_list[[i]] <- rbind(nodes_list[[i]], gene_nodes)
- pathway_edges <- data.frame(
- fromNode_ID = rep(pathway$ID, length(genes)),
- fromNode_name = rep(pathway$Description, length(genes)),
- toNode_ID = genes,
- toNode_name = genes,
- Relations_Type = rep("Path-gene", length(genes)),
- Ontology = rep(pathway$Ontology, length(genes)),
- stringsAsFactors = FALSE
- )
- edges_list[[i]] <- pathway_edges
- }
- nodes <- do.call(rbind, nodes_list)
- edges <- do.call(rbind, edges_list)
- gene_freq<-table(edges$toNode_name)
- gene_freq_df <- as.data.frame(gene_freq)
- colnames(gene_freq_df) <- c("Gene", "Frequency")
- gene_freq_df <- gene_freq_df[order(-gene_freq_df$Frequency), ]
- select<-gene_freq_df[gene_freq_df$Frequency>=5,]
- p<-ggplot(select, aes(x = Gene, y = Frequency)) +
- geom_bar(stat = "identity") +
- theme(axis.text.x = element_text(angle = 90, hjust = 1)) +
- labs(title = "Gene Frequency in GO Pathways", x = "Gene", y = "Frequency")
- ggsave('gene_frequency_GO.pdf',plot =p,width = 10,height=6 )
- write.table(nodes, "nodes.txt", sep = "\t", row.names = FALSE)
- write.table(edges, "edges.txt", sep = "\t", row.names = FALSE)
- x <-list('GO:0042391'=edges_list[[1]]$toNode_ID,
- 'GO:1990351'=edges_list[[2]]$toNode_ID,
- 'GO:1902495'=edges_list[[3]]$toNode_ID,
- 'GO:0022804'=edges_list[[4]]$toNode_ID,
- 'GO:0046873'=edges_list[[5]]$toNode_ID,
- 'GO:0005216'=edges_list[[6]]$toNode_ID)
- p<-upset(fromList(x),
- nsets = 6,
- order.by = "freq",
- mainbar.y.label = "Intersection size",
- sets.x.label = "Set size",
- sets.bar.color = c("#b2e7cb","#ff0000","#ff0000","#b2d4ec","#b2d4ec","#ff0000"
- ),
- matrix.color = "black",
- main.bar.color = "black",
- text.scale = c(1.5, 1.5, 1.5, 1.5, 1.5, 1),
- shade.color = "gray88")
- #####heatmap painting
- library(ggplot2)
- library(reshape2)
- select <- data.frame(fread("filtered_expr.csv",header = T))
- row.names(select)<-select$GeneNames
- select<-select[,11:16]
- select<-log2(select+0.01)
- scaled_matrix <- scale(t(select))
- row.names(scaled_matrix)<-c('tFUS-1','tFUS-2','tFUS-3','Ctrl-1','Ctrl-2','Ctrl-3')
- melted_matrix <- melt(scaled_matrix)
- p<-ggplot(melted_matrix, aes(x = Var2, y = Var1, fill = value)) +
- geom_tile() +
- scale_fill_gradient2(low = "#008B8B", high = "red", mid = "white", midpoint = 0) +
- theme_minimal() +
- theme(axis.text.x =element_text(angle = 60, vjust = 0.5, hjust = 0.3))
- ggsave('heat_map_select.pdf',plot = p,width = 12,height = 3)
Bulk RNA-seq analysis workflow.R, under CC-BY-4.0 · at the source
Overview
- Department of Psychiatry, The Fourth Affiliated Hospital, School of Medicine, Zhejiang University,Yiwu, China
- Center for Membrane Receptors and Brain Medicine, the Fourth Affiliated Hospital of School of Medicine, and International School of Medicine, International Institutes of Medicine, Zhejiang University,Yiwu, China
- NHC and CAMS Key Laboratory of Medical Neurobiology, MOE Frontier Science Center for Brain, Research and Brain-Machine Integration, School of Brain Science and Brain Medicine, Zhejiang University,Hangzhou, China
- School of Biomedical Engineering, Guangdong Medical University,Dongguan, China
- Core Facilities of the School of Medicine, Zhejiang University,Hangzhou, China
- Department of Biophysics, Institute of Neuroscience, Zhejiang University School of Medicine,Hangzhou, Zhejiang China
- Chinese Institute for Brain Research,Beijing, China
- Shenzhen Key Laboratory of Ultrasound Imaging and Therapy, Paul C. Lauterbur Research Center for Biomedical Imaging, State Key Laboratory of Biomedical Imaging Science and System, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences,Shenzhen, China
Abstract
The abstract is not reproduced here: the paper's license (CC BY-NC-ND) does not allow it. Read it in the paper, at the publisher or on Europe PMC.
Repositories
Its files are read in the Code ↔ Paper reader above, with 1 match between paragraphs and lines of code.
awnsjjj/TRPC4-TRPC5-are-critical-for-neuronal-modulation-by-tFUS-in-retrosplenial-cortex-in-male-mice
75e43d721d002c15561d5cf15136cf3906eef43c, 17 May 2026Availability: 1 check, the latest on 27 September 2026: the link answers
- 27 September 2026: the link answers
3 files
- code/
Bulk RNA-seq analysis workflow.R , R, 311 lines - LICENSE, License, 21 lines
- README.md, Text, 108 lines
Zenodo 15128201
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1 file
- Bulk RNA-seq analysis workflow.R, R, 304 lines, 1 match
codeocean:1809197
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Code availability statement
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- it points to the authors' code: codeocean:1809197, awnsjjj/
TRPC4-TRPC5-are-critical , Zenodo 15128201-for-neuronal-modulation -by-tFUS-in-retrosplenia l-cortex-in-male-mice
Read it in the paper: doi.org/10.1038/s41467-026-74779-2.
Tracing map
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What the map holds:
- 3 repositories of the authors' code, each at its verified commit, with its license and how the link was found in the paper;
- 2 scripts, each with its path and the digest of its content;
- 1 match between paragraphs of the paper and lines of the code (method lexical-v1);
- neither the text of the paper nor the code itself.
Its JSON (tracing-map.json) is deposited on Zenodo with its DOI once the map is validated.
Data
Datasets cited
- figshare:30284812, at figshare; found in DataCite
Data availability statement
The paper has a data availability statement. Its license (CC BY-NC-ND) does not allow reproducing it here; in short, from what the harvester recognized in it:
- no repository, dataset or request procedure was recognized in it
Read it in the paper: doi.org/10.1038/s41467-026-74779-2.
Versions
The history of this record: each version stored by the harvester or made by a correction of its authors or of the maintainers of its code, and what changed in its facts. The texts of the paper (its abstract, its availability statements) are not part of it; versions that changed only those are not listed.
Version 1, 27 September 2026: the first record
Recorded: type, language, journal, volume, issue, pages, dates, 13 authors, 3 keywords, 8 MeSH terms, 1 funder, 69 references.
Cite
This paper
Wu, C., You, J., Sheng, T., Li, G.-F., Zhang, C., Liu, L., Xu, L.-Z., Xiong, W., Yang, F., Yang, W., Qiu, W.-B., Zheng, H.-R., & Li, X.-Y. (2026). TRPC4/
BibTeX
@article{wu2026trpc4,
author = {Wu, Cheng and You, Jie and Sheng, Tao and Li, Guo-Feng and Zhang, Can and Liu, Li and Xu, Li-Zhen and Xiong, Wei and Yang, Fan and Yang, Wei and Qiu, Wei-Bao and Zheng, Hai-Rong and Li, Xiang-Yao},
title = {{TRPC4/
journal = {Nature communications},
year = {2026},
month = jun,
volume = {17},
number = {1},
pages = {8129},
publisher = {Nature Publishing Group},
issn = {2041-1723},
doi = {10.1038/
url = {https://
pmid = {42373633},
pmcid = {PMC13458073}
}
RIS
TY - JOUR
AU - Wu, Cheng
AU - You, Jie
AU - Sheng, Tao
AU - Li, Guo-Feng
AU - Zhang, Can
AU - Liu, Li
AU - Xu, Li-Zhen
AU - Xiong, Wei
AU - Yang, Fan
AU - Yang, Wei
AU - Qiu, Wei-Bao
AU - Zheng, Hai-Rong
AU - Li, Xiang-Yao
TI - TRPC4/
T2 - Nature communications
J2 - Nat Commun
PY - 2026
DA - 2026/
VL - 17
IS - 1
SP - 8129
SN - 2041-1723
PB - Nature Publishing Group
DO - 10.1038/
UR - https://
LA - en
ER -
CSL-JSON
{
"id": "10.1038/
"type": "article-journal",
"title": "TRPC4/
"container-title": "Nature communications",
"author": [
{
"family": "Wu",
"given": "Cheng"
},
{
"family": "You",
"given": "Jie"
},
{
"family": "Sheng",
"given": "Tao"
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{
"family": "Li",
"given": "Guo-Feng"
},
{
"family": "Zhang",
"given": "Can"
},
{
"family": "Liu",
"given": "Li"
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{
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{
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"family": "Yang",
"given": "Fan"
},
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"given": "Wei"
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{
"family": "Qiu",
"given": "Wei-Bao"
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"given": "Hai-Rong"
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{
"family": "Li",
"given": "Xiang-Yao"
}
],
"container-title-short":
"volume": "17",
"issue": "1",
"page": "8129",
"DOI": "10.1038/
"PMID": "42373633",
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"ISSN": "2041-1723",
"publisher": "Nature Publishing Group",
"URL": "https://
"language": "en",
"issued": {
"date-parts": [
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}
}
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- cGAS-mediated type I IFN signaling contributes to disease progression in drug-refractory epilepsy.Journal: Nature neuroscienceIn common: clusterProfiler, reshape2, data.table, 1 other tool, mouse, cellular / molecular
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