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name: bio-pathway-gsea description: Gene Set Enrichment Analysis using clusterProfiler gseGO and gseKEGG. Use when analyzing ranked gene lists to find coordinated expression changes in gene sets without arbitrary significance cutoffs. Detects subtle but coordinated expression changes. tool_type: r primary_tool: clusterProfiler

Gene Set Enrichment Analysis (GSEA)

Core Concept

GSEA uses all genes ranked by a statistic (log2FC, signed p-value) rather than a subset of significant genes. It finds gene sets where members are enriched at the top or bottom of the ranked list.

Prepare Ranked Gene List

library(clusterProfiler)
library(org.Hs.eg.db)

de_results <- read.csv('de_results.csv')

# Create named vector: values = statistic, names = gene IDs
gene_list <- de_results$log2FoldChange
names(gene_list) <- de_results$gene_id

# Sort in decreasing order (REQUIRED)
gene_list <- sort(gene_list, decreasing = TRUE)

Convert Gene IDs for GSEA

# Convert symbols to Entrez IDs
gene_ids <- bitr(names(gene_list), fromType = 'SYMBOL', toType = 'ENTREZID', OrgDb = org.Hs.eg.db)

# Create ranked list with Entrez IDs
gene_list_entrez <- gene_list[names(gene_list) %in% gene_ids$SYMBOL]
names(gene_list_entrez) <- gene_ids$ENTREZID[match(names(gene_list_entrez), gene_ids$SYMBOL)]
gene_list_entrez <- sort(gene_list_entrez, decreasing = TRUE)

Alternative Ranking Statistics

# Signed p-value (recommended for detecting both up and down)
gene_list <- -log10(de_results$pvalue) * sign(de_results$log2FoldChange)
names(gene_list) <- de_results$gene_id
gene_list <- sort(gene_list, decreasing = TRUE)

# Wald statistic (from DESeq2)
gene_list <- de_results$stat
names(gene_list) <- de_results$gene_id
gene_list <- sort(gene_list, decreasing = TRUE)

GSEA with GO

gse_go <- gseGO(
    geneList = gene_list_entrez,
    OrgDb = org.Hs.eg.db,
    ont = 'BP',                     # BP, MF, CC, or ALL
    minGSSize = 10,
    maxGSSize = 500,
    pvalueCutoff = 0.05,
    verbose = FALSE,
    pAdjustMethod = 'BH'
)

# Make readable
gse_go <- setReadable(gse_go, OrgDb = org.Hs.eg.db, keyType = 'ENTREZID')

GSEA with KEGG

gse_kegg <- gseKEGG(
    geneList = gene_list_entrez,
    organism = 'hsa',
    minGSSize = 10,
    maxGSSize = 500,
    pvalueCutoff = 0.05,
    verbose = FALSE
)

# Make readable
gse_kegg <- setReadable(gse_kegg, OrgDb = org.Hs.eg.db, keyType = 'ENTREZID')

GSEA with Custom Gene Sets

# Read GMT file (Gene Matrix Transposed)
gene_sets <- read.gmt('msigdb_hallmarks.gmt')

gse_custom <- GSEA(
    geneList = gene_list_entrez,
    TERM2GENE = gene_sets,
    minGSSize = 10,
    maxGSSize = 500,
    pvalueCutoff = 0.05
)

MSigDB Gene Sets

# Use msigdbr package for MSigDB gene sets
library(msigdbr)

# Hallmark gene sets
hallmarks <- msigdbr(species = 'Homo sapiens', category = 'H')
hallmarks_t2g <- hallmarks[, c('gs_name', 'entrez_gene')]

gse_hallmark <- GSEA(
    geneList = gene_list_entrez,
    TERM2GENE = hallmarks_t2g,
    pvalueCutoff = 0.05
)

# Other categories: C1 (positional), C2 (curated), C3 (motif), C5 (GO), C6 (oncogenic), C7 (immunologic)

Understanding Results

# View results
head(gse_go)
results <- as.data.frame(gse_go)

# Key columns:
# - NES: Normalized Enrichment Score (positive = upregulated, negative = downregulated)
# - pvalue: Nominal p-value
# - p.adjust: FDR-adjusted p-value
# - core_enrichment: Leading edge genes

Interpreting NES (Normalized Enrichment Score)

NES	Interpretation
Positive (> 0)	Gene set enriched in upregulated genes
Negative (< 0)	Gene set enriched in downregulated genes
	NES

Key Parameters

Parameter	Default	Description
geneList	required	Named, sorted numeric vector
OrgDb	required	Organism database (for gseGO)
organism	hsa	KEGG organism code (for gseKEGG)
ont	BP	Ontology: BP, MF, CC, ALL
minGSSize	10	Min genes in gene set
maxGSSize	500	Max genes in gene set
pvalueCutoff	0.05	P-value threshold
pAdjustMethod	BH	Adjustment method
nPerm	10000	Permutations (if permutation test used)
eps	1e-10	Boundary for p-value calculation

Export Results

results_df <- as.data.frame(gse_go)
write.csv(results_df, 'gsea_go_results.csv', row.names = FALSE)

# Get leading edge genes for a term
leading_edge <- strsplit(results_df$core_enrichment[1], '/')[[1]]

Notes

• Must be sorted - gene list must be sorted in decreasing order
• Named vector - names are gene IDs, values are statistics
• No arbitrary cutoffs - uses all genes, not just significant ones
• NES sign matters - positive = upregulated enrichment
• Leading edge - core_enrichment contains driving genes

Related Skills

• go-enrichment - Over-representation analysis for GO
• kegg-pathways - Over-representation analysis for KEGG
• enrichment-visualization - GSEA plots, ridge plots