| iobr_deg | R Documentation |
Performs differential expression analysis on gene expression data using either DESeq2 or limma. Includes pre-processing steps like filtering low count data, and calculates fold changes and adjusted p-values. Optionally generates volcano plots and heatmaps.
iobr_deg(
eset,
annotation = NULL,
id_anno = NULL,
pdata,
group_id = "group",
pdata_id = "ID",
array = FALSE,
method = c("DESeq2", "limma"),
contrast = c("High", "Low"),
path = NULL,
padj_cutoff = 0.01,
logfc_cutoff = 0.5,
volcano_plot = FALSE,
col_volcano = 1,
heatmap = TRUE,
col_heatmap = 1,
parallel = FALSE
)
eset |
A matrix of gene expression data where rows represent genes and columns represent samples. |
annotation |
Optional data frame for mapping gene IDs to gene names. Default is 'NULL'. |
id_anno |
Character string specifying the identifier column in annotation. Default is 'NULL'. |
pdata |
A data frame containing sample information and grouping labels. |
group_id |
Character string specifying the column name in 'pdata' containing grouping labels. Default is '"group"'. |
pdata_id |
Character string specifying the column name in 'pdata' for sample IDs. Default is '"ID"'. |
array |
Logical indicating whether to perform quantile normalization. Default is 'FALSE'. |
method |
Character string specifying the method: '"DESeq2"' or '"limma"'. Default is '"DESeq2"'. |
contrast |
Character vector of length 2 specifying contrast groups. Default is 'c("High", "Low")'. |
path |
Character string for output directory. Default is 'NULL'. |
padj_cutoff |
Numeric cutoff for adjusted p-values. Default is '0.01'. |
logfc_cutoff |
Numeric log2 fold change cutoff. Default is '0.5'. |
volcano_plot |
Logical indicating whether to generate a volcano plot. Default is 'FALSE'. |
col_volcano |
Integer specifying color index for volcano plot. Default is '1'. |
heatmap |
Logical indicating whether to generate a heatmap. Default is 'TRUE'. |
col_heatmap |
Integer specifying color index for heatmap. Default is '1'. |
parallel |
Logical indicating whether to run in parallel. Default is 'FALSE'. |
Data frame containing differentially expressed genes with statistics including log2 fold changes and adjusted p-values.
Dongqiang Zeng
# Simulate data
set.seed(123)
sim_eset <- matrix(abs(rnorm(100 * 20)), 100, 20)
rownames(sim_eset) <- paste0("Gene", 1:100)
colnames(sim_eset) <- paste0("Sample", 1:20)
sim_pdata <- data.frame(
ID = paste0("Sample", 1:20),
group = rep(c("High", "Low"), each = 10)
)
# Run DEG analysis
deg <- iobr_deg(
eset = sim_eset, pdata = sim_pdata,
group_id = "group", pdata_id = "ID",
method = "limma", contrast = c("High", "Low"),
heatmap = FALSE
)
if (!is.null(deg)) head(deg)
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