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CentoTalks

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.

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What Can Science Do for You?

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.

CentoTalks – Upcoming Webinars

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.

Webinar
May 25, 2022
  • CMA
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CentoTalks – Webinars on Demand

Niemann-Pick tipo C: Dos genes – muchos cuadros clínicos – un biomarcador unificador

Mira nuestro webinar sobre Niemann-Pick tipo C, un raro trastorno genético progresivo caracterizado por la incapacidad del cuerpo para transportar el colesterol y otras sustancias grasas (lípidos) […]

Webinar
Mar 03, 2020
  • Biomarker
  • Hematology
  • Hepatology
  • WGS
  • WES
  • Ophthalmology
  • Neurology
  • Metabolic Disorders
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Niemann-Pick Type C: Two Genes - Many Clinical Pictures - One Unifying Biomarker

Watch our webinar “Niemann-Pick type C: Two Genes – Many Clinical Pictures – One Unifying Biomarker” hosted by Prof. Peter Bauer. Throughout the webinar, he will provide an overview of this rare […]

Webinar
Mar 02, 2020
  • Biomarker
  • Hepatology
  • Metabolic Disorders
  • WES
  • WGS
  • Hematology
  • Ophthalmology
  • Neurology
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CentoLCV – El nuevo estándar para detectar desequilibrios cromosómicos

Mira el webinar sobre CentoLCV™, nuestro nuevo análisis integral de variación de número de copias (CNV), y aprender por qué es el nuevo estándar para establecer diagnósticos moleculares más precisos […]

Webinar
Jan 29, 2020
  • Neurology
  • WGS
  • NGS
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CentoLCV – The New Standard for Detecting Chromosomal Imbalances

Watch Dr. Peter Bauer, MD, Chief Genomic Officer at CENTOGENE, as he discusses CentoLCV, our comprehensive Large Copy number Variation (CNV) analysis, and why it is the new standard for establishing […]

Webinar
Jan 26, 2020
  • Neurology
  • WGS
  • NGS
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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, […]

Webinar
Dec 04, 2019
  • Neurology
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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 […]

Webinar
Nov 21, 2019
  • WGS
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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 […]

Webinar
Oct 06, 2019
  • WES
  • WGS
  • NGS
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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, […]

Webinar
Sep 16, 2019
  • WES
  • WGS
  • NGS
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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?

Webinar
Jul 10, 2019
  • Nephrology
  • Biomarker
  • Endocrinology
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