VarSeq 2.3.0 facilitates the evaluation of a multitude of somatic genomic variations with a more refined user interface to streamline variant evaluation. Our recent webcasts have shown the full range of these newly developed upgrades:

Now, we are showing it all in action from the user’s perspective. This webcast provides a comprehensive demonstration of performing somatic variation analysis and reporting. We review how to use workflow automation to expedite the NGS project creation process and report rendering. We also demonstrate the streamlined capture of knowledge during variant evaluation by leveraging our clinical expert-curated interpretations with the Golden Helix Cancer Knowledge Base (CancerKB).

We hope you watch below to see VarSeq 2.3.0 from a user’s perspective, covering:

Watch on demand

Please enjoy this webcast recording. Should you have any questions about the content covered, please reach out to our team here.