Join us at our next event!
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Join us in Anaheim! | June 26 - 30
Add us to your ADLM agenda, and stop by booth 4429 for a personalized demo.
Join us in Houston! | August 1 - 5
Add us to your CGC agenda, and stop by the SeqOne booth for a personalized demo.
Join us in San Diego! | September 14 - 26
Add us to your AGBT agenda, and join our stop by the SeqOne booth for a personalized demo.
Join us in Montreal! | October 20 - 24
Add us to your ASHG agenda, and stop by booth 521 for a personalized demo.
Join us in Seattle! | November 10 - 14
Add us to your AMP agenda, and stop by booth 1903 for a personalized demo.
Miss our ACMG Exhibit Theater? Get the slides on-demand
From Complexity to Clarity: Streamlining CNV and SV Interpretation in Clinical Genomics
Here's what you'll walk away with:
✔️ Effortless Integration: SeqOne fits right into your existing analytical workflow — no rip-and-replace required.
✔️ Accelerated Interpretation: DiagAI, our explainable AI-driven algorithm, dramatically speeds up variant interpretation while keeping your team in the driver's seat.
✔️ Intuitive Visualization: The Large Variant Viewer (LVV) makes even the most complex genomic variants easy to see and interpret, rounding out your end-to-end workflow.
