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.

Documentation