The Database for Annotation, Visualization and Integrated Discovery
DAVID Bioinformatics Resources 6.8
Laboratory of Human Retrovirology and Immunoinformatics (LHRI)
Overview

The Database for Annotation, Visualization and Integrated Discovery (DAVID ) v6.8 comprises a full Knowledgebase update to the sixth version of our original web-accessible programs. DAVID now provides a comprehensive set of functional annotation tools for investigators to understand biological meaning behind large list of genes. For any given gene list, DAVID tools are able to:

    Identify enriched biological themes, particularly GO terms
     Discover enriched functional-related gene groups
     Cluster redundant annotation terms
     Visualize genes on BioCarta & KEGG pathway maps
     Display related many-genes-to-many-terms on 2-D view.
     Search for other functionally related genes not in the list
     List interacting proteins
     Explore gene names in batch
     Link gene-disease associations
     Highlight protein functional domains and motifs
     Redirect to related literatures
     Convert gene identifiers from one type to another.
     And more

Hot Links

  •  Call for papers 
    Submit papers for a Special Issue:"DNA or RNA-Mediated Innate Immune Response" of the International Journal of Molecular Sciences
  • DAVID Forum
    Forum for DAVID users to ask questions, suggest new functions and help other users by answering their questions.
  • FAQ
    Frequently Asked Questions
  • LHRI Publications
    Publications of the Laboratory of Human Retrovirology and Immunoinformatics, Frederick National Laboratory for Cancer Research
  • DAVID Publications
    Publications about DAVID
What's New

DAVID Statistics

DAVID Bioinformatic Resources Citations

  • > 47,000 Citations (Updated 8/20/2020)
  • Average Daily Usage: ~2,700 gene lists/sublists from ~900 unique researchers.
  • Average Annual Usage: ~1,000,000 gene lists/sublists from >100 countries