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bioconductor-clusterprofiler

This package supports functional characteristics of both coding and non-coding genomics data for thousands of species with up-to-date gene annotation. It provides a univeral interface for gene functional annotation from a variety of sources

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bioconductor-clusterprofiler

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Use bioconductor-clusterprofiler to plan and run an ORA or GSEA analysis of [gene list or ranked genes] for [species and annotation source] in an R environment, returning enrichment plots and interpretation.

Required inputs

  • [gene list or ranked genes]
  • [species and annotation source]

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SKILL.md

name: bioconductor-clusterprofilerdescription: This package supports functional characteristics of both coding and non-coding genomics data for thousands of species with up-to-date gene annotation. It provides a univeral interface for gene functional annotation from a variety of sourceswhen_to_use: "Use when: Performing Over-Representation Analysis or Gene Set Enrichment Analysis.; Comparing biological themes among gene clusters.; Visualizing functional profiles of genomic coordinates (supported by ChIPseeker), genes, and gene clusters.; Querying Gene Ontology annotations online via AnnotationHub or KEGG Pathway and Module data.. Not for: For purely interactive web-based enrichment without an R environment (use web portals like DAVID directly).; When analyzing species not supported by online databases (unless providing customized user annotations)."user-invocable: false

clusterProfiler

Dependencies & Environment

Package-intrinsic requirements from the Bioconductor landing page — reproduce in any R environment.

  • Version: 4.20.0 · Bioconductor: 3.23 · R: ≥ 4.6
  • Imports: aisdk, AnnotationDbi, dplyr, enrichit, enrichplot, ggplot2, GO.db, GOSemSim, gson, httr, igraph, jsonlite, magrittr, plyr, qvalue, rlang, tidyr, yulab.utils
  • Install: BiocManager::install("clusterProfiler")

When to Use

  • Performing Over-Representation Analysis or Gene Set Enrichment Analysis.
  • Comparing biological themes among gene clusters.
  • Visualizing functional profiles of genomic coordinates (supported by ChIPseeker), genes, and gene clusters.
  • Querying Gene Ontology annotations online via AnnotationHub or KEGG Pathway and Module data.

When NOT to Use

  • For purely interactive web-based enrichment without an R environment (use web portals like DAVID directly).
  • When analyzing species not supported by online databases (unless providing customized user annotations).

Data Requirements

  • Genomic coordinates, gene lists, or gene clusters.
  • Annotations from supported ontologies/pathways (e.g., Disease Ontology, DisGeNET, Gene Ontology, KEGG, Reactome, Molecular Signatures Database) or customized user ontologies.

Key Parameters

  • No specific parameters are detailed in the provided vignette text.

Best Practices

  • Utilize the package's built-in visualization functions such as barplot, cnetplot, dotplot, emapplot, gseaplot, goplot, and upsetplot to interpret enrichment results.
  • When querying Gene Ontology, use AnnotationHub to support many species with online annotation queries.
  • Provide a reproducible example when posting bugs to the GitHub issue tracker.

Common Pitfalls

  • Failing to find answers to common problems because the user did not visit the clusterProfiler homepage documentation first.
  • Posting questions to the Bioconductor support site without tagging the post with clusterProfiler, leading to delayed responses.
  • Attempting to analyze unsupported species without supplying a customized ontology or user annotation.

Alternatives

  • DOSE: Specifically focused on Disease Ontology and Network of Cancer Gene enrichment.
  • ReactomePA: Specifically tailored for Reactome Pathway analysis.
  • goseq: Alternative for GO enrichment that explicitly corrects for RNA-seq transcript length bias.

Citations

  • G Yu, LG Wang, Y Han, QY He. clusterProfiler: an R package for comparing biological themes among gene clusters. OMICS: A Journal of Integrative Biology 2012, 16(5):284-287. doi: 10.1089/omi.2011.0118.

References


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