NEXTalk - From sample to insights: Revolutionizing Rare DiseaseGenomics with AI
Key Takeaway: • How AI automates and scales genomic workflows • Faster, more accurate rare disease identification • Boosting clinical confidence in decision-making • End-to-end workflow: from sample to actionable insight • Real-world examples from leading laboratories • Scaling rare disease diagnosis efficiently Speaker: Vanisha Mistry, PhD Vice President of Customer Success Fabric Genomics
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