DAVID Bioinformatics 6.7
The Database for Annotation, Visualization and Integrated Discovery
DAVID Bioinformatics Resources 6.8
Laboratory of Human Retrovirology and Immunoinformatics (LHRI)

*** Welcome to DAVID 6.8 ***
*** If you are looking for DAVID 6.7, please visit our development site. ***
Untitled Document
Shortcut to DAVID Tools
   Functional Annotation
Gene-annotation enrichment analysis, functional annotation clustering , BioCarta & KEGG pathway mapping, gene-disease association, homologue match, ID translation, literature match and more
   Gene Functional Classification
Provide a rapid means to reduce large lists of genes into functionally related groups of genes to help unravel the biological content captured by high throughput technologies.  More
   Gene ID Conversion  
Convert list of gene ID/accessions to others of your choice with the most comprehensive gene ID mapping repository. The ambiguous accessions in the list can also be determined semi-automatically. More
   Gene Name Batch Viewer
Display gene names for a given gene list; Search functionally related genes within your list or not in your list; Deep links to enriched detailed information. 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, Leidos Biomedical Research, Inc., Frederick National Laboratory for Cancer Research
   DAVID Publications
Publications for DAVID
 
    
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Recommending: A paper published in Nature Protocols describes step-by-step procedure to use DAVID!

Welcome to DAVID 6.8

2003 - 2020

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

 
a  What's Important in DAVID? a  Statistics of DAVID

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
2-D View of Gene-Annotation
Screen Shot 1
Gene Functional Classification
Screen Shot 2
Functional Annotation
Screen Shot 3



 Please cite Nature Protocols 2009; 4(1):44 & Nucleic Acids Res. 2009;37(1):1 within any publication that makes use of any methods inspired by DAVID.
                          

        

                 
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