Comprehensive Cancer Variant Analysis in VarSeq: From Targeted Panels to Long Read Genomes 

About this webinar

Wednesday, February 18th, 2026 // 12:00 PM EST

Presented By: Darby Kammeraad, Director of Field Application Services, and Julia Love, Associate Director of Product Quality

In this webcast, we’ll dive into why labs are turning to long-read sequencing for better fusion detection and how methylation can add meaningful diagnostic yield. With expert-curated knowledgebases like Golden Helix CancerKB for clinical actionability and Genomenon for literature-backed evidence, interpretation becomes faster, more consistent, and far less manual- no guideline hunting required.

In this webcast, we will walk through real-world examples, including:
  • A PacBio-powered somatic workflow generating clinically actionable results for an acute myeloid leukemia case.
  • A TSO500 comprehensive panel applied to non–small cell lung cancer
  • Join us for a discussion on how WGS long-read can boost clinical yield and how our VSWarehouse platform integrates somatic workflows so labs can leverage the full potential of these technologies.


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