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All-in-one AI-powered platform for precise, scalable, and comprehensive genomic analysis
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ASHG Industry Session: Lucid Genomics x Pawel T. Stankiewicz (Baylor College of Medicine)
Many disease-causing variants remain undetected. Lucid Genomics uses machine learning with short- and long-read data to improve detection and interpretation of structural and non-coding variants. Pawel Stankiewicz, MD, PhD (Baylor College of Medicine) will present key cases and a live demo of Lucid’s platform.
⏱︎ October 17, 12:00 PM - 1:00 PM
⚲ Room 151A, Level 1
Pawel Stankiewicz, M.D., Ph.D.
Professor of Molecular and Human Genetics at Baylor College of Medicine and expert in structural variants and non-coding regulatory element.
