Webinars

We frequently host webinars on key topics in precision medicine or work with partners and customers to demonstrate the benefits of our world-leading Clinical Decision Support Platform.  They are all available on this page for you to either sign up for, or watch at a time convenient to you. 

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The Real Costs of Rare Disease – 16 November 2022

November 1, 2022
16 November 2022   15:00 - 1600 GMT / 10:00 - 11:00 CDT / 16:00 - 17:00 CET  The cost of rare disease is high, much higher than many other diseases,…
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Genomics in Medicine: Working with National Genome Programmes

August 18, 2022
Professor Philip Beales, MD FRCP FMedSci, CMO at Congenica was involved in the 1000,000 Genomes Project from the beginning. Here he talks about the project in detail, the challenges, how…
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Latest developments in next-generation genomic data analysis

August 17, 2022
Enabling Genomic Medicine (EGM) 2021: Best practice in genomic analysis   During Congenica's Enabling Genomic Medicine 2021 virtual event, Alistair Johnson, Chief Product Officer at Congenica presented: Latest developments in…
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Prenatal diagnosis using Whole Exome Sequencing (WES)

August 17, 2022
Enabling Genomic Medicine (EGM) 2021: Best practice in genomic analysis During Congenica's Enabling Genomic Medicine 2021 virtual event, Dr. Luis Izquierdo, Chief Medical Officer, Doctor of Medicine and Surgery and…
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Improving Rare Disease Diagnosis in the 100,000 Genomes Project (UK 100K)

August 17, 2022
During this webinar, you will hear from Dr Meriel McEntagart, a consultant clinical geneticist at St George’s Hospital in London, who was directly involved in the 100,000 project. Dr McEntagart…
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From bench to bedside: Best practices in diagnosing and treating pediatric patients with epilepsy

August 17, 2022
Enabling Genomic Medicine (EGM) 2021: Best practice in genomic analysis During Congenica's Enabling Genomic Medicine 2021 virtual event, Parul Jayakar, MD, MS, FACMG, Director Division of Genetics and Metabolism, Nicklaus…
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Chris Wigley, CEO Genomics England: To Infinity and Beyond – working together to bring genomic medicine to EVERYONE

August 17, 2022
Enabling Genomic Medicine (EGM) 2021: Best practice in genomic analysis During Congenica's Enabling Genomic Medicine 2021 virtual event, Chris Wigley, CEO at Genomics England, provided a presentation entitled:    To…
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Richard Durbin, PhD, Informatics Director, Congenica and Professor of Genetics, University of Cambridge: Long-read sequencing and new reference genomes

August 17, 2022
Enabling Genomic Medicine (EGM) 2021: Best practice in genomic analysis During Congenica's Enabling Genomic Medicine 2021 virtual event, Richard Durbin, PhD, Informatics Director, Congenica and Professor of Genetics, University of…
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Priorisation des variants entièrement interprétable basée sur l’Intelligence Artificielle Fournit des résultats rapides et exploitables pour les patients

July 28, 2022
Yacine Dahman,  Machine Learning Software Developer chez Congenica, présente : Le classement des variants entièrement interprétable basée sur l’Intelligence Artificielle pouvant fournir des résultats rapides et exploitables pour les patients …
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Why choose a professional solution?

November 24, 2021
Congenica customer Anna Miller, technical specialist at NOAH Clinical Laboratory, and Victoria Hewitt, HCPC Lead, Clinical Interpretation Services at Congenica, discuss the essential attributes needed in a professional solution to…
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Polygenic Risk Scores & the Future of Precision Medicine: Challenges and Opportunities

August 19, 2021
Discover the role of Polygenic Risk Score (PRS) in advanced genomic risk assessment and precision healthcare in the UK. In this webinar, experts will explore the current clinical application of…
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Automating standardized analysis of cases

August 19, 2021
In this on-demand webinar, Helen Savage, Lead Clinical Scientist, Product Innovation at Congenica highlights the case for automating standardized analysis of cases, demonstrating how automated variant classification workflows maintain quality…
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Practical Applications of Genome Interpretation for Rare Disease Diagnosis and Research

April 21, 2021
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…
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Rare Inherited Disease: 30 Min from data to report

April 21, 2021
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…
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Discovering the Missing Link between my Rare Disease and an Olympic Athlete

April 21, 2021
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…
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Achieving a Definitive Diagnosis for Epilepsy Patients

April 21, 2021
Dr Charles Steward, speaks on best practices for diagnosing epilepsy; the existing technologies and techniques, and the pathways to diagnosis. Dr Steward provides case…
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Real-World Examples of Efficiency Gains in the Analysis & Interpretation of Genomic Data

April 21, 2021
In this webinar, Genomenon’s Founder & Chief Science Officer , Dr. Mark Kiel welcomed Dr. Eva Serra, who demonstrated Congenica, a way to overcome…
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Maximizing Diagnostic Yield with an Optimized Variant Interpretation Platform

April 21, 2021
Using specific case examples as illustrations, Dr. Katherine Benson of the Royal College of Surgeons Ireland discusses how her team has implemented an all-in-one solution for…
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