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Enrichment Map: A Network-Based Method for Gene-Set Enrichment Visualization and Interpretation
Open accessAbstract
BACKGROUND: Gene-set enrichment analysis is a useful technique to help functionally characterize large gene lists, such as the results of gene expression experiments. This technique finds functionally coherent gene-sets, such as pathways, that are statistically over-represented in a given gene list. Ideally, the number of resulting sets is smaller than the number of genes in the list, thus simplifying interpretation. However, the increasing number and redundancy of gene-sets used by many current enrichment analysis software works against this ideal. PRINCIPAL FINDINGS: To overcome gene-set redundancy and help in the interpretation of large gene lists, we developed "Enrichment Map", a network-based visualization method for gene-set enrichment results. Gene-sets are organized in a network, where each set is a node and edges represent gene overlap between sets. Automated network layout groups related gene-sets into network clusters, enabling the user to quickly identify the major enriched functional themes and more easily interpret the enrichment results. CONCLUSIONS: Enrichment Map is a significant advance in the interpretation of enrichment analysis. Any research project that generates a list of genes can take advantage of this visualization framework. Enrichment Map is implemented as a freely available and user friendly plug-in for the Cytoscape network visualization software (http://baderlab.org/Software/EnrichmentMap/).
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“Furthermore, gene set enrichment analysis (GSEA) revealed that the hypoxia pathway is impaired in miR-140G/G, but not in miR-140−/− chondrocytes”
From Gain-of-function mutation of microRNA-140 in human skeletal dysplasia (2019) · cites this paper as [26]
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Metadata
- Authors
- Merico, D., Isserlin, R., Stueker, O., Emili, A., & Bader, G. D.
- Affiliations
- University of Toronto (CA)
- Corresponding author
- Merico, Daniele
- Bader, Gary D.
- Venue
- PLoS ONE
- Publisher
- Public Library of Science (PLoS)
- Published
- 2010-11-15
- Volume
- 5
- Issue
- 11
- Pages
- e13984
- ISSN
- 1932-6203 (ISSN-L)
- PMC
- PMC2981572
- OpenAlex
- W2097948046
- Cited by
- 2,235
- References
- 58
- Citations by year
- 2026: 89 · 2025: 145 · 2024: 176 · 2023: 216 · 2022: 238 · 2021: 233 · 2020: 237 · 2019: 164 · 2018: 158 · 2017: 145 · 2016: 127 · 2015: 101 · 2014: 79 · 2013: 69 · 2012: 43
- FWCI
- 16.30
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- PLoS ONE (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Figshare (submittedVersion, cc-by)
- Funders
- Heart and Stroke Foundation of Canada
- Genome Canada
- Ontario Genomics
- Ontario Genomics Institute
- Hospital for Sick Children
- National Institutes of Health
- National Human Genome Research Institute (P41 P41HG04118, P41HG04118, P41HG004118)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bioinformatics and Genomic Networks
- Health Sciences › Medicine › Health Informatics › Biomedical Text Mining and Ontologies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
- Keywords
- gene set enrichment analysis, network visualization, gene set overlap, network clustering, pathway over-representation, gene expression data interpretation, Cytoscape plugin
- MeSH terms
- Algorithms, Breast Neoplasms, Colonic Neoplasms, Estrogens, Female, Humans, Software, Reproducibility of Results, Gene Expression Regulation, Neoplastic, Cluster Analysis, Computational Biology, Internet, Gene Expression Profiling, Gene Regulatory Networks
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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