June 15th webinar: Using NCBI Resources and Variant Interpretation Tools for the Clinical Community

In two weeks, NCBI will present a webinar that will show you how to use three clinical variant interpretation tools geared to clinicians through an overview of NCBI variation and medical genetics databases. A demonstration using a clinical case to demonstrate a phenotype-driven whole-genome sequence analysis using tools from Golden Helix, Omicia and SimulConsult will follow the overview.
Source: NCBI Announcements - Category: Databases & Libraries Source Type: news