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Accessing clinical content for improved variant assessment and reporting – Oct. 13

Date: 2022/10/13 Duration: 01:00:00 Presented by: Ruth Burton and Tim Bonnert

In this 60-minute webinar, you will learn how to access the most comprehensive collection of germline and somatic variant information and see how access to Human Gene Mutation Database (HGMD) Professional, Human Somatic Mutation Database (HSMD), Catalogue of Somatic Mutations in Cancer (COSMIC), and QIAGEN Clinical Insight Knowledge Base (QCI KB) can improve the quality and decrease the time needed for variant classification and interpretation.

Click here to register.