We frequently host webinars on key topics in genomics medicine or demonstrations of our work. Take a look below at our upcoming webinars or explore the videos from our previous sessions.
Maximizing Diagnostic Yield with an Optimized Variant Interpretation Platform
Register for Webinar This webinar will discuss the use of next-generation sequencing and an optimized variant interpretation workflow to increase diagnostic yield in complex…
Real-World Examples of Efficiency Gains in the Analysis & Interpretation of Genomic Data
In this webinar, Genomenon’s Founder & Chief Science Officer , Dr. Mark Kiel welcomed Dr. Eva Serra, who demonstrated Congenica, a way to overcome…
Achieving a Definitive Diagnosis for Epilepsy Patients
Dr Charles Steward, speaks on best practices for diagnosing epilepsy; the existing technologies and techniques, and the pathways to diagnosis. Dr Steward provides case…
Discovering the Missing Link between my Rare Disease and an Olympic Athlete
Jill Viles, an Iowa mother with no clinical training, shares her story of how she self-diagnosed her rare condition, a muscle-wasting disease caused by…
Rare Inherited Disease: 30 Min from data to report
Andrea Haworth, Head of Clinical Services and Laura Reed, Pre-Registered Clinical Scientist at Congenica share their experiences and challenges of Whole Genome Analysis and the insights gained from using Sapientia with the Genomics England 100K project.
Practical Applications of Genome Interpretation for Rare Disease Diagnosis and Research
Dr Matt Hurles, Dominic McMullan FRCPath, and Dr Hywel Williams speak about their experiences in genome interpretation for rare disease diagnosis and discovery. Each presentation covers discoveries made during each of their projects, and the lessons learnt and applied.