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Tags: genes, plot, R, KEGG, GO, pathway
Download the file WT_vs_K3R_sig_GO_top5.txt
Step-by-Step Guide for KEGG and GO Analysis from Differentially Expressed Genes:
Identify differentially expressed genes: Using the significance threshold (p-value <= 0.05, log2foldchange <= -0.58 and log2foldchange >= 0.58 or log2foldchange <= -2 and => +2), filter the significantly differentially expressed genes from your dataset.
Perform KEGG and GO enrichment analysis: Use a reliable tool like DAVID (https://david.ncifcrf.gov/) to perform KEGG pathway analysis and GO term enrichment based on the significantly differentially expressed genes. Export the enrichment results in text format.
Rank the enrichment results: Rank the KEGG pathway and GO term results using -log10(FDR) or -log10(p-adjusted) to better display the differences in values, especially when the values are too small to differentiate.
Visualize the enrichment results using R-scripts: Use the provided R-scripts to generate bubble plots for the KEGG pathway and GO term enrichment results.
Here's a detailed breakdown of the steps for visualization using R-scripts:
Install required R packages: Install the necessary R packages, such as ggplot2, for generating the bubble plots.
Load enrichment results: Import the text format output from DAVID or other web enrichment portals into your R environment.
Generate bubble plots: Use the attached R-scripts to create bubble plots for the KEGG pathway and GO term enrichment results.
Interpret and report the results: Analyze the bubble plots to identify the most significant KEGG pathways and GO terms associated with your differentially expressed genes. Include these findings in your research reports or publications.
library(ggplot2)
library(dplyr)
library(magrittr)
library(tidyr)
library(forcats)
mydat <- read.csv("WT_vs_K3R_sig_GO_top5.txt", sep="\t", header=TRUE)
mydat$GeneRatio <- sapply(mydat$GeneRatio_frac, function(x) eval(parse(text=x)))
#mydat$FoldEnrichment <- as.numeric(mydat$FoldEnrichment)
mydat$Category <- factor(mydat$Category, levels=c("CC","BP","MF"))
mydat$Comparison <- factor(mydat$Comparison, levels=c("WT dox vs K3R dox","WT dox+chase vs K3R dox+chase"))
#mydat$Description <- factor(mydat$Description)
#mydat <- mydat %>% mutate(Description = fct_reorder(Description, row_number()))
description_order <- rev(c("transmembrane transporter complex","transporter complex","ion channel complex","melanosome membrane","chitosome", "pigment granule membrane","specific granule","tertiary granule", "sensory perception of sound","sensory perception of mechanical stimulus","cellular potassium ion transport","potassium ion transmembrane transport","potassium ion transport", "leukocyte proliferation","regulation of leukocyte proliferation","peptidyl-tyrosine phosphorylation","peptidyl-tyrosine modification","tissue remodeling", "ion channel activity","substrate-specific channel activity","channel activity","passive transmembrane transporter activity","metal ion transmembrane transporter activity", "cytokine binding","heparin binding","calmodulin binding","glycosaminoglycan binding","3',5'-cyclic-GMP phosphodiesterase activity"))
mydat$Description <- factor(mydat$Description, levels = description_order)
png("bubble_plot.png", 1000, 800)
ggplot(mydat, aes(y = Description, x = Comparison)) +
geom_point(aes(color = Category, size = Count, alpha = abs(log10(p.adjust)))) +
scale_color_manual(values = c("CC" = "red", "BP" = "blue", "MF"="green")) +
scale_size_continuous(range = c(4, 10)) +
labs(x = "", y = "", color="Category", size="Count", alpha="-log10(p.adjust)") +
theme(axis.text.x = element_text(angle = 20, vjust = 0.5)) +
theme(axis.text = element_text(size = 20)) +
theme(legend.text = element_text(size = 20)) +
theme(legend.title = element_text(size = 20)) +
guides(color = guide_legend(override.aes = list(size = 10)), alpha = guide_legend(override.aes = list(size = 10)))
dev.off()
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