SeqOne DiagAI | Rare and hereditary diseases

Unleash the power of genomic insights with SeqOne DiagAI

Discover a groundbreaking approach to rare and hereditary diseases through SeqOne DiagAI.

Accelerate your understanding of genomic data with ultra-fast interpretation, offering a shortlist of ~11 variant candidates, and a remarkable 96% probability of identifying the causal variant.

Dive into the future:

  • Fast and efficient variant prioritization with SeqOne’s AI models.
  • Automatic phenotype integration for enhanced prioritization performance.

Embark on a journey with SeqOne DiagAI – where cutting-edge technology meets the intricacies of genomic interpretation.

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