PVT inhibition mitigates neuropathology and cognitive deficits in chronic cerebral hypoperfusion.
The 1 match
- [1] § STAR★Methods › Method details › Weighted gene co-expression network analysis ↔ WGCNA_Analysis.R, lines 1–61 · score 0.55 · soft thresholding, TOM, cutting, WGCNA, power, network
Paper
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The authors' code
R · 94 lines · 3.1 KB · no license · 1 match
- library(WGCNA)
- library(openxlsx)
- library(readxl)
- library(dplyr)
- options(stringsAsFactors = FALSE)
- enableWGCNAThreads()
- df <- read_excel("result.xlsx")
- femData_clean <- na.omit(df)
- datExpr0 <- as.data.frame(t(femData_clean[, -c(1)]))
- names(datExpr0) <- femData_clean[[1]]
- rownames(datExpr0) <- colnames(femData_clean[, -c(1)])
- gsg <- goodSamplesGenes(datExpr0, verbose = 3)
- if (!gsg$allOK) {
- datExpr0 <- datExpr0[gsg$goodSamples, gsg$goodGenes]
- }
- sample_names <- rownames(datExpr0)
- group_vector <- ifelse(grepl("^group_1", sample_names), "group1",
- ifelse(grepl("^group_2", sample_names), "group2", "Unknown"))
- traitData <- data.frame(
- sample = sample_names,
- Group = group_vector,
- ADG = rnorm(length(sample_names), 1.1, 0.3)
- )
- traitData$Group_numeric <- ifelse(traitData$Group == "group2", 1, 0)
- Samples <- rownames(datExpr0)
- traitRows <- match(Samples, traitData$sample)
- datTraits <- traitData[traitRows, c("ADG", "Group_numeric")]
- rownames(datTraits) <- traitData[traitRows, 1]
- powers <- c(c(1:10), seq(from = 12, to = 30, by = 2))
- sft <- pickSoftThreshold(datExpr0, powerVector = powers, verbose = 5, networkType = "signed")
- sft_index <- which(abs(sft$fitIndices[, 3]) > 0.8)
- if (length(sft_index) > 0) {
- chosen_power <- sft$fitIndices[min(sft_index), 1]
- } else {
- chosen_power <- sft$fitIndices[which.max(abs(sft$fitIndices[, 3])), 1]
- }
- net <- blockwiseModules(datExpr0, power = chosen_power,
- TOMType = "signed",
- networkType = "signed",
- minModuleSize = 15,
- reassignThreshold = 0,
- mergeCutHeight = 0.25,
- numericLabels = TRUE,
- pamRespectsDendro = FALSE,
- saveTOMs = TRUE,
- saveTOMFileBase = "BTOM",
- verbose = 3)
- moduleLabels <- net$colors
- moduleColors <- labels2colors(net$colors)
- MEs <- net$MEs
- nGenes <- ncol(datExpr0)
- nSamples <- nrow(datExpr0)
- MEs0 <- moduleEigengenes(datExpr0, moduleColors)$eigengenes
- MEs <- orderMEs(MEs0)
- moduleTraitCor <- cor(MEs, datTraits, use = "p")
- moduleTraitPvalue <- corPvalueStudent(moduleTraitCor, nSamples)
- trait_of_interest <- "Group_numeric"
- trait_data <- as.data.frame(datTraits[, trait_of_interest])
- names(trait_data) <- trait_of_interest
- GS <- as.data.frame(cor(datExpr0, trait_data, use = "p"))
- colnames(GS) <- paste("GS", trait_of_interest, sep=".")
- modNames <- substring(names(MEs), 3)
- MM <- as.data.frame(cor(datExpr0, MEs, use = "p"))
- colnames(MM) <- paste("MM", modNames, sep=".")
- gene_module_mm_gs <- data.frame(
- BrainRegion = colnames(datExpr0),
- Module = moduleColors
- )
- for(mod in unique(moduleColors)) {
- if(mod == "grey") next
- module_genes <- (moduleColors == mod)
- gene_module_mm_gs[module_genes, "MM"] <- MM[module_genes, paste0("MM.", mod)]
- }
- gene_module_mm_gs$GS <- GS[, paste0("GS.", trait_of_interest)]
- write.csv(gene_module_mm_gs, "All_BrainRegions_MM_GS.csv", row.names = FALSE)
WGCNA_Analysis.R at commit f0cca60, no license · at the source
Overview
- Beijing Institute of Brain Disorders, Laboratory of Brain Disorders, Ministry of Science and Technology, Collaborative Innovation Center for Brain Disorders, Capital Medical University, Beijing, China
- Institute of Basic Theory for Traditional Chinese Medicine, China Academy of Chinese Medical Sciences, Beijing, 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.
Repository
Its files are read in the Code ↔ Paper reader above, with 1 match between paragraphs and lines of code.
SunLab-code/WGCNA-CCH-iScience
f0cca6060cfcc56e64f163fcc688808985dbcc5b, 1 July 2026Availability: 1 check, the latest on 27 September 2026: the link answers
- 27 September 2026: the link answers
2 files
- WGCNA_Analysis.R, R, 94 lines, 1 match
- README.md, Text, 1 line
The paper's code and data availability statement is in the Data section.
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Data
Datasets cited
- zenodo:21107938, at Zenodo; found in “Data and code availability”
Code and data availability statement
The paper has a code and data availability statement. Its license (CC BY-NC-ND) does not allow reproducing it here; in short, from what the harvester recognized in it:
- it points to a dataset: Zenodo 21107938
- it points to the authors' code: SunLab-code/
WGCNA-CCH-iScience - it says that the data are available on request
- it says that the code is available on request
Read it in the paper: doi.org/10.1016/j.isci.2026.117108.
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Version 3, 28 September 2026
- Authors: added Le Sun (0000-0001-9399-6772); removed Le Sun
Version 1, 27 September 2026: the first record
Recorded: type, language, journal, volume, issue, pages, dates, 7 authors, 5 keywords, 1 funder, 62 references, 6 RRIDs.
Cite
This paper
Guan, Y., Ma, J., Li, R., Xu, J., Xu, T., Li, G., & Sun, L. (2026). PVT inhibition mitigates neuropathology and cognitive deficits in chronic cerebral hypoperfusion. iScience, 29(8), 117108. https://
BibTeX
@article{guan2026pvt,
author = {Guan, Yuying and Ma, Jinghao and Li, Rui and Xu, Jialu and Xu, Taoyue and Li, Gaifen and Sun, Le},
title = {{PVT inhibition mitigates neuropathology and cognitive deficits in chronic cerebral hypoperfusion}},
journal = {iScience},
year = {2026},
month = aug,
volume = {29},
number = {8},
pages = {117108},
publisher = {Elsevier},
issn = {2589-0042},
doi = {10.1016/
url = {https://
pmid = {42602569},
pmcid = {PMC13474078}
}
RIS
TY - JOUR
AU - Guan, Yuying
AU - Ma, Jinghao
AU - Li, Rui
AU - Xu, Jialu
AU - Xu, Taoyue
AU - Li, Gaifen
AU - Sun, Le
TI - PVT inhibition mitigates neuropathology and cognitive deficits in chronic cerebral hypoperfusion
T2 - iScience
J2 - iScience
PY - 2026
DA - 2026/
VL - 29
IS - 8
SP - 117108
SN - 2589-0042
PB - Elsevier
DO - 10.1016/
UR - https://
LA - en
ER -
CSL-JSON
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