CentoWebinar
At CENTOGENE, we established a free webinars series (live and on demand) on key developments in clinical diagnostics as well as giving insights into the latest research findings in the field of rare disease. Benefit from our renowned speakers and let us support you with daily routine implementation.
Upcoming webinars
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Genetics in Parkinson’s Disease – Lessons from a Global Cohort
Join our next webinar discussing Parkinson’s Disease, one of the most common neurodegenerative disorders manifested by a broad spectrum of motor and non-motor features. Prof. Peter Bauer, MD, will be introducing the genetics of this progressive nervous system disorder and outlining genetic…
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Why it’s time to consider WGS as first-line genetic testing
Last year CENTOGENE announced its new sequencing facility for rare hereditary disorders, which uses Illumina’s HiSeq X® sequencer. Now, some months after our journey started, our CSO Prof. Peter Bauer will explain CENTOGENE’s experience using this groundbreaking next generation sequencing (NGS)…
Recorded webinars - CentoWebinars on demand
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Gaucher Disease – Update on diagnosing and therapy monitoring
Knowing Gaucher Disease (GD), the most common lysosomal storage disorder, is crucial when being faced with unspecific abnormalities in many organs like brain, liver, spleen and bones. Right at Gaucher Disease Awareness Month, we will host the next webinar “Gaucher Disease: beyond the paradigms based…
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Enfermedad de Gaucher – Enfoque en el diagnóstico y seguimiento de la terapia
Conocer la enfermedad de Gaucher (EG), el trastorno de almacenamiento lisosomal más común, es crucial cuando su paciente presenta anormalidades inespecíficas en diversos órganos como cerebro, hígado, bazo y sistema óseo. Justo el día de la concienciación de la Enfermedad de Gaucher, organizaremos el…
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Enfermedad de Hunter: Cuando sospecharla, como diagnosticarla y el estudio clínico de CENTOGENE: Bio-Hunter
¿Estas interesado en aprender más sobre la enfermedad de Hunter- un desorden de depósito lisosomal causante de una serie de alteraciones en órganos como el corazón, sistema nervioso central y óseo?
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‘PICoP global‘ – an international collaboration assessing neoepitopes for patient-specific vaccination in Colon and Pankreas Cancer
This webinar will cover the opportunities and challenges with clinical Whole Genome Sequencing (cWGS), value of curated digital data, re-classification and re-analysis and the utility of cWGS
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Genome First. Last. Fast: the One Step Approach to Genetic Testing
This webinar will cover the opportunities and challenges with clinical Whole Genome Sequencing (cWGS), value of curated digital data, re-classification and re-analysis and the utility of cWGS
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The critical role of clinical information in producing a diagnostic report
This webinar reviews how Human Phenotype Ontology (HPO) terms allows the genetic and medical community to provide patients’ clinical information in a high quality format and their importance in increasing diagnostic yield.
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Fibrosis Quística: presente y futuro
¿Estas interesado en aprender más sobre el diagnóstico de fibrosis quística, una enfermedad genética común, con altas tasas de morbilidad y mortalidad? Puedes ver nuestro Webinar acerca de fibrosis quística y los métodos disponibles para el diagnóstico confiable. Además, durante esta sesión…
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Is Pancreatitis a Genetic Disease?
Pancreatitis is a common cause of life-threatening abdominal symptoms and pain. If diagnosed, especially in the young, the question as to the etiology arises. Join our guest speaker, Prof. Matthias Löhr, and co-host Prof. Peter Bauer, as they examine how genetic markers can indicate different…
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Variant Reclassification: When, Why, How
Discover how CENTOGENE’s variant reclassification enables us to provide you with the latest and highest quality data for the most up-to-date diagnosis.
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Niemann-Pick Type C Disease Often Overlooked: Fast & Efficient Screening Programs
Discover how CENTOGENE’s fast and efficient screening program for NP-C can enable diagnosis, prediction and therapy monitoring for your patients.