Description: Neurocarta is a knowledgebase that consolidates information on genes and phenotypes across multiple resources and allows tracking and exploring of the associations. The system enables automatic and manual curation of evidence supporting each association, as well as user-enabled entry of their own annotations. Phenotypes are recorded using controlled vocabularies such as the Disease Ontology to facilitate computational inference and linking to external data sources. The gene-to-phenotype associations are filtered by stringent criteria to focus on the annotations most likely to be relevant. Neurocartas in-depth annotation of neurodevelopmental disorders makes it a unique resource for neuroscientists working on brain development.

Institution: University of British Columbia

Contacts: Dr. Paul Pavlidis

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Ontologies Used