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.
