Variant prioritization remains one of the most time-consuming and critical bottlenecks in modern genomic analysis, especially as labs transition to whole-genome and long-read data.

In this webinar, experts from Uppsala University Hospital and SeqOne will demonstrate how bringing multi-technology workflows onto a single, explainable AI platform can dramatically streamline in-house variant interpretation without sacrificing clinical control.

What you'll walk away with:

  • ‍Accelerate interpretation: Practical strategies to dramatically cut variant review time without losing clinical sensitivity.‍
  • Unify complex workflows: How a leading lab integrated short-read, long-read, and array data onto a single platform.‍
  • Scale advanced variants: Proven approaches for interpreting structural variants and long-read data at scale.‍
  • Master explainable AI: Clear criteria to evaluate AI model transparency and retain full clinical control.

🗓️ Date: 29 September 2026

🖥️ Format: Live webinar

⏳ 1 hour

🕐 Time: 7 AM PT  |  10 AM ET  |  4 PM CET

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👉 Register now

Scheduling conflict? You can still participate! All registrants will receive a link to view an on-demand recording of the event.

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