Metascape
Metascape performs gene-list annotation, functional enrichment, and interactome/network analysis for OMICs datasets by integrating over 40 independent knowledgebases to support pathway inference and protein complex identification.
Key Features:
- Functional Enrichment Analysis: Identifies statistically enriched biological pathways and processes associated with input gene lists.
- Interactome Analysis: Analyzes protein-protein interactions and network context to reveal modules and complexes.
- Gene Annotation: Aggregates annotations from over 40 independent knowledgebases to provide comprehensive gene-level information.
- Membership Search: Searches gene membership across pathways, protein complexes, and curated biological entities.
- Comparative Analysis: Compares multiple independent and orthogonal datasets to highlight shared and distinct biological signals.
Scientific Applications:
- OMICs Data Interpretation: Interprets OMICs-derived gene lists to derive biological insights.
- Pathway and Process Discovery: Discovers enriched pathways and biological processes underlying experimental gene sets.
- Protein Interaction and Complex Identification: Identifies protein-protein interaction modules and candidate protein complexes from gene sets.
- Cross-study Comparative Analysis: Integrates and contrasts results across independent experiments to validate and prioritize findings.
Methodology:
Integrates diverse biological databases and over 40 independent knowledgebases into a unified analytical pipeline for annotation, enrichment, interactome analysis, membership search, and comparative analysis.
Topics
Details
- License:
- Unlicense
- Maturity:
- Mature
- Cost:
- Free of charge
- Tool Type:
- web application
- Operating Systems:
- Linux, Windows, Mac
- Added:
- 7/4/2019
- Last Updated:
- 6/16/2020
Operations
Publications
Zhou Y, Zhou B, Pache L, Chang M, Khodabakhshi AH, Tanaseichuk O, Benner C, Chanda SK. Metascape provides a biologist-oriented resource for the analysis of systems-level datasets. Nature Communications. 2019;10(1). doi:10.1038/s41467-019-09234-6. PMID:30944313. PMCID:PMC6447622.