Webinar 

Stay ahead of relapse: Pioneer HLA loss research with precision

Watch and learn how Devyser HLA Loss is designed to support researchers and laboratories studying post-transplant relapse pathways.

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Webinar 

Devyser RHD: High performance without complexity 

Watch to learn how Devyser RHD sets a new standard for fetal RHD screening. Discover how Devyser RHD’s unique single-exon assay simplifies analysis and reduces inconclusive results.

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Webinar 

Devyser Thalassemia v2: The all-in-one NGS solution for alpha & beta thalassemia 

Watch to learn how Devyser Thalassemia v2 can help your laboratory simplify genetic testing by integrating alpha and beta thalassemia detection—including SNV and CNV analysis, and beta modifiers—into a single, efficient assay. 

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Webinar 

The new guidelines on Y-chromosomal microdeletion testing

Join us for an exclusive webinar, where renowned expert Prof. Csilla Krausz will delve into the 2023 AZF testing guidelines, how they impact AZF testing, and their clinical relevance.   

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Webinar 

Implementación del panel Devyser BRCA para la detección de SNVs y CNVs por NGS 

Les invitamos a nuestro próximo webinar sobre BRCA, con Juan Torres Gregorio, especialista en Biología Molecular en CARPERMOR. Descubra cómo se implementaron las pruebas para diagnóstico de BRCA en un laboratorio acreditado por CAP en México.    

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Webinar 

Familial Hypercholesterolemia: The importance of genetic testing

In this webinar Dr. Mafalda Bourbon talks about the role of genetic testing in familial hypercholesterolemia (FH) and preventing early cardiovascular events.  

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Webinar 

Establishing a modern standard to provide personalized RhD prophylaxis

Professor Agneta Wikman presents how testing can help provide personalized prophylaxis for expectant mothers.

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Webinar 

Familial  hypercholesterolemia: How an early genetic pediatric screening can guide treatment

Prof. Albert Wiegman (MD, PhD), paediatric cardiologist at Amsterdam UMC, talks about how early paediatric screening and genetic testing can guide detection and treatment of familial hypercholesterolemia (FH).

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Webinar 

One size fits all: Addressing hemoglobinopathy using NGS

Dr. Robert Akkers, presents the shifting distribution of hemoglobinopathy, and the need for expanded thalassemia genetic testing.

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Webinar 

The utility of broader CFTR genotyping in cystic fibrosis populations

Prof. Milan Macek discusses how changing demographics are driving a need for extended CFTR analysis and the value of sequencing in establishing global equitable CF diagnostics.

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Webinar 

Overcome the challenges of PMS2 variant calling with Devyser LynchFAP – our new NGS solution

Learn why PMS2 is the most challenging gene when it comes to variant calling in relation to hereditary colorectal cancer syndromes.  Discover how Devyser LynchFAP can help you overcome this challenge.

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Webinar 

Spotlight on Familial Hypercholesterolemia (FH) – Uncovering the importance of genetic testing

Watch an insightful, educational session where Magdalena Daccord, Chief Executive of FH Europe, the European patient network, puts a spotlight on Familial hypercholesterolemia (FH) and the importance of genetic testing.

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Webinar 

NGS for thalassemia genetic testing – insights from a customer implementation journey

Watch our webinar featuring Dr. Thessalia Papasavva at the Cyprus Institute of Neurology and Genetics is performing genetic testing for thalassemia in Cyprus, both for diagnostics and as part of the national screening programs.

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Webinar

Post-transplant monitoring: The future of chimerism testing

Join our webinar featuring Dr. Helena Devos, MD, Clinical Biologist and Dr. Freidel Nollet, PhD, Molecular Biologist at AZ Sint-Jan in Bruges, Belgium. Where we will talk about the implementation of an NGS solution for chimerism testing and the clinical perspectives.

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