Velsera clinical genomics knowledgebase

Clinical next-generation sequencing (NGS) testing is a growing area as new approvals are introduced for targeted therapies and commercial availability increases. The challenges faced for this is ensuring quality interpretation and variant classification. To address this challenge, Velsera has developed the Clinical Genomics Workspace, a platform for streamlining complex genomics workflows.

The Velsera Knowledgebase includes expertly curated content, real-world medical data, and public data sources, as well as ready-to-use interpretations synthesized from aggregated Knowledgebase information that can be used to rapidly and accurately classify and interpret variants to produce an actionable report.

Find out more about the Velsera Knowledgebase workflow and how it was used for somatic cancer biomarker reporting.