4.8 Article

The Human Disease Ontology 2022 update

Journal

NUCLEIC ACIDS RESEARCH
Volume 50, Issue D1, Pages D1255-D1261

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/nar/gkab1063

Keywords

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Funding

  1. National Institutes of Health-National Human Genome Research Institute (NHGRI) [U41 HG008735-01A1]
  2. NIH/NHGRI [U41 HG008735-01A1]

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The Human Disease Ontology database has significantly expanded its disease content and userbase since 2018, providing a key reference framework for biomedical data integration across numerous research projects worldwide. The updated website offers enhanced search capabilities, documentation, and educational resources to users.
The Human Disease Ontology (DO) (www.disease-ontology.org) database, has significantly expanded the disease content and enhanced our userbase and website since the DO's 2018 Nucleic Acids Research DATABASE issue paper. Conservatively, based on available resource statistics, terms from the DO have been annotated to over 1.5 million biomedical data elements and citations, a 10x increase in the past 5 years. The DO, funded as a NHGRI Genomic Resource, plays a key role in disease knowledge organization, representation, and standardization, serving as a reference framework for multiscale biomedical data integration and analysis across thousands of clinical, biomedical and computational research projects and genomic resources around the world. This update reports on the addition of 1,793 new disease terms, a 14% increase of textual definitions and the integration of 22 137 new SubClassOf axioms defining disease to disease connections representing the DO's complex disease classification. The DO's updated website provides multifaceted etiology searching, enhanced documentation and educational resources.

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