About This Resource:

As clinical NGS testing volumes grow in light of expanded medical knowledge and new targeted therapy approvals, commercial availability of large comprehensive gene panels, and favorable coverage decisions, the challenge of quality clinical interpretation and variant classification will also grow. To address this challenge, Velsera has developed the Clinical Genomics Workspace, a platform for streamlining complex genomics workflows.

The Velsera Clinical Genomics Knowledgebase is a key component of the Clinical Genomics Workspace. Built using an ideal combination of technology and human expertise, the Knowledgebase enables users to rapidly and accurately classify and interpret variants to produce an actionable report.

This technical note describes the Velsera Knowledgebase in the context of somatic cancer biomarker reporting.