NCBI Webinar: Using NCBI Resources and Variant Interpretation Tools for the Clinical Community on June 15, 2016

NCBI Webinar: Using NCBI Resources and Variant Interpretation Tools for the Clinical Community on June 15, 2016. NLM Tech Bull. 2016 May-Jun;(410):b8.

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 show a phenotype-driven whole-genome sequence analysis using tools from Golden Helix, Omicia and SimulConsult will follow the overview.

Date and time: Wednesday, June 15, 2016 1:00 pm EDT

To register: Go to https://attendee.gotowebinar.com/register/6974809559951440644

After registering, you will receive a confirmation email with information about attending the Webinar. After the live presentation, the Webinar will be uploaded to the NCBI YouTube channel. Any related materials will be accessible on the Webinars and Courses homepage where you can also learn about future Webinars on this page.