Join our interactive webinars to connect with CENTOGENE’s international team of experts and discuss topics ranging from clinical diagnostic practices to cutting-edge research. Together, we can revolutionize patient care.
Get in touch with the CentoTalk support team
By registering, you will receive a recording of the webinar even if you could not attend the event. If you encounter any problems, please contact us.
Our CentoTalks are live and on-demand webinars that feature key developments in clinical diagnostics as well as insights into the latest research findings in the field of rare diseases. Learn from our renowned speakers, and let us support you in delivering transformative solutions to rare disease patients.
CentoArray – Opening the Door to Early and Accurate Diagnosis
Join us on May 25 as we open our digital doors to provide you with an exclusive look into our Extensive Genome-Wide Cytogenetic Analysis – NEW CentoArray.
Biomarkers for Lysosomal Storage Disorders
Interested in the latest innovations in metabolic disease diagnostics and assessing the effects of therapy? Do you want to learn more about biochemical genetic testing at CENTOGENE? Join this webinar […]
Complete Oncogenetic Workflow
Looking for a one-stop-solution for your laboratory? Join this webinar to learn more about our CentoCloud® for diagnostic NGS panels, clinical bioinformatics & medical interpretation in the […]
- Hereditary Cancer
Illumina and CENTOGENE: Using NIPT to Screen for the Most Common Fetal Chromosomal Abnormalities
Everybody is talking about it: Non-invasive prenatal testing (NIPT) to screen for the most common fetal chromosomal abnormalities. With CentoNIPT® CENTOGENE now offers non-invasive prenatal testing […]
- Reproductive Genetics
A Journey to the Future – Whole Genome Sequencing for the Diagnosis of Heterogeneous Genetic Disorders
Last year CENTOGENE announced its new sequencing facility for rare hereditary disorders, which uses Illumina’s HiSeq X® sequencer. Some months after our journey started, our CSO Prof. Peter Bauer […]
Solving the Diagnostic Riddle – Diagnosing Heterogeneous Genetic Disorders with Whole Exome Sequencing
Most of the disease-causing mutations that science has been able to identify so far are located within the exons. Whereas most genetic tests focus on a single gene or on a set number of predetermined […]
A Race Against the Clock – Diagnosing Genetic Conditions in Newborns and Children
Up to one third of all babies and children admitted to the intensive care unit (ICU) have a genetic disease. For many of them early identification can make a difference for their immediate and later […]
- Metabolic Disorders
Oncogenetics in the Clinical Practice
In this webinar you will learn the last insights in oncogenetics testing and how CENTOGENE gene panels can support you to assess the risk of a patient to develop an inherited cancer.
- BRCA 1/2
- Hereditary Cancer
Genetic Testing of Mitochondrial Diseases
Mitochondrial diseases are genetic conditions that occur when mitochondria are failing to produce enough energy for the cell.