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WES Case Study
Identifying a Clinically Relevant Mitochondrial Variant

Download Our Free Whole Exome Sequencing (WES) Case Study Today!

It takes approx. seven years to diagnose a patient with a rare disease. With NEW CentoXome®, this doesn’t have to be the case.

Through utilizing NEW CentoXome, our enhanced Whole Exome Sequencing (WES), we were able to provide a twenty-year-old female and her family with answers.

Take a look at our Case Study to see how we were able shorten this young rare disease patient's diagnostic odyssey.

By clicking “Download now” I agree that CENTOGENE will get in touch via email on latest news regarding our clinical diagnostics and scientific developments on rare diseases, including but not limited to upcoming events and commercial offers. I can withdraw my consent at any time for the future by clicking the “Unsubscribe” button in the emails or by contacting CENTOGENE directly.

How NEW CentoXome Can Help You

CENTOGENE Diagnostics Whole Exome Sequencing Icon DNA Search

Access enhanced coverage across the entire exome, full mitochondrial genome, and nearly 100% coverage of all known clinically relevant genes and variants throughout the genome

CENTOGENE Diagnostics Whole Exome Sequencing Icon Report

Increase diagnostic yield by up to 20% compared to conventional WES


CENTOGENE Icon Network

Leverage deeper insights to guide the best patient care possible, thanks of the CENTOGENE Biodatabank