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DAVID: Database for Annotation, Visualization, and Integrated Discovery
Open accessAbstract
BACKGROUND: Functional annotation of differentially expressed genes is a necessary and critical step in the analysis of microarray data. The distributed nature of biological knowledge frequently requires researchers to navigate through numerous web-accessible databases gathering information one gene at a time. A more judicious approach is to provide query-based access to an integrated database that disseminates biologically rich information across large datasets and displays graphic summaries of functional information. RESULTS: Database for Annotation, Visualization, and Integrated Discovery (DAVID; http://www.david.niaid.nih.gov) addresses this need via four web-based analysis modules: 1) Annotation Tool - rapidly appends descriptive data from several public databases to lists of genes; 2) GoCharts - assigns genes to Gene Ontology functional categories based on user selected classifications and term specificity level; 3) KeggCharts - assigns genes to KEGG metabolic processes and enables users to view genes in the context of biochemical pathway maps; and 4) DomainCharts - groups genes according to PFAM conserved protein domains. CONCLUSIONS: Analysis results and graphical displays remain dynamically linked to primary data and external data repositories, thereby furnishing in-depth as well as broad-based data coverage. The functionality provided by DAVID accelerates the analysis of genome-scale datasets by facilitating the transition from data collection to biological meaning.
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“DAVID yielded consistent results with 59 pathways enriched in probands and 19 in siblings (p=0.01, permutation analysis)”
From Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism (2011) · cites this paper as Dennis et al., 2003
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Metadata
- Authors
- Dennis, G., Sherman, B. T., Hosack, D. A., Yang, J., Gao, W., Lane, H. C., & Lempicki, R. A.
- Affiliations
- National Cancer Institute (US)
- National Institutes of Health (US)
- Corresponding author
- Dennis, Glynn
- Venue
- Genome Biology
- Published
- 2003-04-03
- Volume
- 4
- Issue
- 5
- Pages
- P3-P3
- ISSN
- 1465-6906 (ISSN-L)
- 1474-760X
- PMC
- PMC193660
- OpenAlex
- W2122683221
- Cited by
- 9,327
- References
- 16
- Citations by year
- 2026: 164 · 2025: 352 · 2024: 394 · 2023: 412 · 2022: 486 · 2021: 528 · 2020: 459 · 2019: 429 · 2018: 392 · 2017: 413 · 2016: 377 · 2015: 456 · 2014: 437 · 2013: 484 · 2012: 527
- FWCI
- 38.46
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Genome biology (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion, other-oa)
- PubMed Central (publishedVersion, other-oa)
- PubMed (publishedVersion)
- Funders
- U.S. Public Health Service (N01-C056000)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bioinformatics and Genomic Networks
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
- Health Sciences › Medicine › Health Informatics › Biomedical Text Mining and Ontologies
- Keywords
- David, functional annotation, differentially expressed genes, microarray data analysis, Gene Ontology, KEGG pathways, online databases, gene function classification
- MeSH terms
- Humans, Leukocytes, Mononuclear, Macrophages, HIV-1, Computational Biology, Internet, Oligonucleotide Array Sequence Analysis, Gene Expression Profiling, Databases, Nucleic Acid
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.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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