本文へ移動
cccskills
無料GitHub で公開

bio-pathway-go-enrichment

Gene Ontology over-representation analysis using clusterProfiler enrichGO. Use when identifying biological functions enriched in a gene list from differential expression or other analyses. Supports all three ontologies (BP, MF, CC), multiple ID types, and customizable statistical thresholds.

インストール方法を見る

含まれるファイル(4)

  • SKILL.md6.4 KB
  • examples/go_all_ontologies.R1.1 KB
  • examples/go_enrichment_basic.R832 B
  • usage-guide.md2.6 KB

SKILL.md(原文)

インストールする前に、エージェントに与えられる指示の中身を確認できます。

Version Compatibility

Reference examples tested with: R stats (base), clusterProfiler 4.10+

Before using code patterns, verify installed versions match. If versions differ:

  • R: packageVersion('<pkg>') then ?function_name to verify parameters

If code throws ImportError, AttributeError, or TypeError, introspect the installed package and adapt the example to match the actual API rather than retrying.

GO Over-Representation Analysis

Core Pattern

Goal: Identify enriched Gene Ontology terms in a gene list from differential expression or similar analyses.

Approach: Test for over-representation of GO terms using the hypergeometric test via clusterProfiler enrichGO.

"Run GO enrichment on my gene list" → Test whether biological process, molecular function, or cellular component terms are over-represented among significant genes.

library(clusterProfiler)
library(org.Hs.eg.db)  # Human - change for other organisms

ego <- enrichGO(
    gene = gene_list,           # Character vector of gene IDs
    OrgDb = org.Hs.eg.db,       # Organism annotation database
    keyType = 'ENTREZID',       # ID type: ENSEMBL, SYMBOL, ENTREZID, etc.
    ont = 'BP',                 # BP, MF, CC, or ALL
    pAdjustMethod = 'BH',       # p-value adjustment method
    pvalueCutoff = 0.05,
    qvalueCutoff = 0.2
)

Prepare Gene List from DE Results

Goal: Extract significant gene IDs from differential expression results and convert to the format required by enrichGO.

Approach: Filter DE results by adjusted p-value and fold change, then convert gene symbols to Entrez IDs using bitr.

library(dplyr)

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

sig_genes <- de_results %>%
    filter(padj < 0.05, abs(log2FoldChange) > 1) %>%
    pull(gene_id)

# If using gene symbols, convert to Entrez IDs
gene_ids <- bitr(sig_genes, fromType = 'SYMBOL', toType = 'ENTREZID', OrgDb = org.Hs.eg.db)
gene_list <- gene_ids$ENTREZID

ID Conversion with bitr

Goal: Convert between gene identifier types (Ensembl, Symbol, Entrez) for compatibility with enrichment tools.

Approach: Use clusterProfiler bitr to map between ID types using organism annotation databases.

# Check available key types
keytypes(org.Hs.eg.db)

# Convert between ID types
converted <- bitr(genes, fromType = 'ENSEMBL', toType = 'ENTREZID', OrgDb = org.Hs.eg.db)

# Multiple output types
converted <- bitr(genes, fromType = 'SYMBOL', toType = c('ENTREZID', 'ENSEMBL'), OrgDb = org.Hs.eg.db)

With Background Universe

Goal: Improve enrichment specificity by restricting the background to genes actually tested in the experiment.

Approach: Pass all expressed genes (not just significant ones) as the universe parameter to enrichGO.

# Use all expressed genes as background (recommended)
all_genes <- de_results$gene_id
universe_ids <- bitr(all_genes, fromType = 'SYMBOL', toType = 'ENTREZID', OrgDb = org.Hs.eg.db)

ego <- enrichGO(
    gene = gene_list,
    universe = universe_ids$ENTREZID,  # Background gene set
    OrgDb = org.Hs.eg.db,
    keyType = 'ENTREZID',
    ont = 'BP',
    pAdjustMethod = 'BH',
    pvalueCutoff = 0.05
)

All Three Ontologies

# Run all ontologies at once
ego_all <- enrichGO(
    gene = gene_list,
    OrgDb = org.Hs.eg.db,
    keyType = 'ENTREZID',
    ont = 'ALL',  # BP, MF, and CC combined
    pAdjustMethod = 'BH',
    pvalueCutoff = 0.05
)

# Results include ONTOLOGY column
head(as.data.frame(ego_all))

Make Results Readable

# Convert Entrez IDs to gene symbols in results
ego_readable <- setReadable(ego, OrgDb = org.Hs.eg.db, keyType = 'ENTREZID')

# Or use readable = TRUE directly (only works with ENTREZID input)
ego <- enrichGO(
    gene = gene_list,
    OrgDb = org.Hs.eg.db,
    keyType = 'ENTREZID',
    ont = 'BP',
    readable = TRUE  # Converts to symbols
)

Extract and Export Results

# View top results
head(ego)

# Convert to data frame
results_df <- as.data.frame(ego)

# Key columns: ID, Description, GeneRatio, BgRatio, pvalue, p.adjust, qvalue, geneID, Count

# Export to CSV
write.csv(results_df, 'go_enrichment_results.csv', row.names = FALSE)

# Filter for specific criteria
sig_terms <- results_df[results_df$p.adjust < 0.01 & results_df$Count >= 5, ]

Simplify Redundant Terms

Goal: Remove highly similar GO terms to reduce redundancy in enrichment results.

Approach: Cluster GO terms by semantic similarity and retain representative terms using the simplify function.

# Remove redundant GO terms (keeps representative terms)
ego_simplified <- simplify(ego, cutoff = 0.7, by = 'p.adjust', select_fun = min)

Different Organisms

# Mouse
library(org.Mm.eg.db)
ego_mouse <- enrichGO(gene = genes, OrgDb = org.Mm.eg.db, ont = 'BP')

# Zebrafish
library(org.Dr.eg.db)
ego_zfish <- enrichGO(gene = genes, OrgDb = org.Dr.eg.db, ont = 'BP')

# Yeast
library(org.Sc.sgd.db)
ego_yeast <- enrichGO(gene = genes, OrgDb = org.Sc.sgd.db, ont = 'BP', keyType = 'ORF')

Group GO Terms by Ancestor

Goal: Classify genes by broad GO slim categories for a high-level functional overview.

Approach: Use groupGO to assign genes to GO terms at a specific hierarchy level.

# Classify genes by GO slim categories
ggo <- groupGO(
    gene = gene_list,
    OrgDb = org.Hs.eg.db,
    ont = 'BP',
    level = 3,  # GO hierarchy level
    readable = TRUE
)

Key Parameters

ParameterDefaultDescription
generequiredVector of gene IDs
OrgDbrequiredOrganism database
keyTypeENTREZIDInput ID type
ontBPBP, MF, CC, or ALL
pvalueCutoff0.05P-value threshold
qvalueCutoff0.2Q-value (FDR) threshold
pAdjustMethodBHBH, bonferroni, etc.
universeNULLBackground genes
minGSSize10Min genes per term
maxGSSize500Max genes per term
readableFALSEConvert to symbols

Related Skills

  • kegg-pathways - KEGG pathway enrichment
  • gsea - Gene Set Enrichment Analysis for GO
  • enrichment-visualization - Visualize enrichment results
  • differential-expression - Generate input gene lists

レビュー

まだレビューはありません。使ってみた感想をお寄せください。

同じリポジトリのスキル

概要と使いどころ

adaptyv

無料

Cloud laboratory platform for automated protein testing and validation. Use when designing proteins and needing experimental validation including binding assays, expression testing, thermostability measurements, enzyme activity assays, or protein sequence optimization. Also use for submitting experiments via API, tracking experiment status, downloading results, optimizing protein sequences for better expression using computational tools (NetSolP, SoluProt, SolubleMPNN, ESM), or managing protein design workflows with wet-lab validation.

日本語の概要は準備中です。原文の説明を表示しています。

FreedomIntelligence/OpenClaw-Medical-Skills3,0622026年7月21日 更新

Time-blind friendly planning, executive function support, and daily structure for ADHD brains. Specializes in realistic time estimation, dopamine-aware task design, and building systems that actually work for neurodivergent minds.

日本語の概要は準備中です。原文の説明を表示しています。

FreedomIntelligence/OpenClaw-Medical-Skills3,0622026年7月21日 更新

aeon

無料

This skill should be used for time series machine learning tasks including classification, regression, clustering, forecasting, anomaly detection, segmentation, and similarity search. Use when working with temporal data, sequential patterns, or time-indexed observations requiring specialized algorithms beyond standard ML approaches. Particularly suited for univariate and multivariate time series analysis with scikit-learn compatible APIs.

日本語の概要は準備中です。原文の説明を表示しています。

FreedomIntelligence/OpenClaw-Medical-Skills3,0622026年7月21日 更新

Browse the web for any task — research topics, read articles, interact with web apps, fill forms, take screenshots, extract data, and test web pages. Use whenever a browser would be useful, not just when the user explicitly asks.

日本語の概要は準備中です。原文の説明を表示しています。

FreedomIntelligence/OpenClaw-Medical-Skills3,0622026年7月21日 更新

AI驱动的综合健康分析系统,整合多维度健康数据、识别异常模式、预测健康风险、提供个性化建议。支持智能问答和AI健康报告生成。

日本語の概要は準備中です。原文の説明を表示しています。

FreedomIntelligence/OpenClaw-Medical-Skills3,0622026年7月21日 更新

alphafold

無料

Validate protein designs using AlphaFold2 structure prediction. Use this skill when: (1) Validating designed sequences fold correctly, (2) Predicting binder-target complex structures, (3) Calculating confidence metrics (pLDDT, pTM, ipTM), (4) Self-consistency validation of designs, (5) Multi-chain complex prediction with AlphaFold-Multimer. For faster single-chain prediction, use esm. For QC thresholds, use protein-qc.

日本語の概要は準備中です。原文の説明を表示しています。

FreedomIntelligence/OpenClaw-Medical-Skills3,0622026年7月21日 更新

FreedomIntelligence のスキルをすべて見る

このスキルの問題を報告する