Webinars
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.
Upcoming webinars
Prenatal exome analysis – finding the molecular cause of fetal anomalies, faster
July 14, 2020; 10am (ET) – Suzanne Drury, PhD shares how refined workflows lead to rapid causal variant identification and streamlined reporting in a…
Past webinars
Increasing case throughput: How to gain immediate insight into clinically relevant evidence
In this webinar we look at a key part of the clinical interpretation workflow and reveal how a combination of new tools is helping…
The Genetics of COVID-19
In this webinar, Nick Lench, PhD, reviews the current state of knowledge regarding the genetics of COVID-19 and the potential application of pharmacogenetics to…
Influencing prenatal clinical management using exome sequencing
St George’s University Hospital implemented prenatal exome sequencing in cases of fetal structural abnormality in ongoing pregnancies as part of a service improvement project…
Clinically relevant CNV detection via WGS and ExomeCG WES – towards a single assay approach
As part of the ESHG 2020 Virtual Annual Meeting, Dominic McMullan speaks on how Birmingham Women’s and Children’s NHS Foundation Trust have been detecting…
Phenotype-based prioritisation of variants with Exomiser
In this talk, Damian describes a phenotype-based approach to rare disease variant prioritisation and how Exomiser is used in Genomic England’s 100,000 Genomes Project…
Faster Analysis of Neurodevelopmental Disorders with Congenica Neuro
Around 300 million people worldwide are thought to have epilepsy or a neurodevelopmental disorder. 1,2 Many of these disorders are now known to have…