A user interface for exploring and evaluating results from the ClarityNLP clinical phenotype application.
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Updated
Dec 9, 2022 - JavaScript
A user interface for exploring and evaluating results from the ClarityNLP clinical phenotype application.
The phenogrid widget
The Genomic Variations Explorer (GenVarX) is a toolset that consists of promoter region component and CNV component for users to perform queries, visualize data, and conduct annotations using genotypic and phenotypic differences.
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