Diagnostic Methods

Optimized for a wide range of questions from medical diagnostics

Our Service Portfolio

Exome Diagnostics

Finding the genetic cause of rare diseases

Keyvisual Seltene Erkrankungen

Panel Diagnostics

Parallel analysis of all genes considered for differential diagnosis of a disease

Keyvisual Array CGH

Array CGH

For a genome-wide deletion and duplication analysis

Single Gene and Segregation Analysis

Single gene analysis, deletion/duplication, or fragment length analysis

What is Genetic Diagnostics?

Molecular genetics is an interdisciplinary field combining both natural sciences and medicine, and requires expertise in biochemistry, biology and bioinformatics. Recent developments in our understanding of the human genome have made it possible to detect disease – causing changes to DNA, which facilitates accurate medical diagnosis.

Using molecular genetic diagnostics, we support the referring physician in making a diagnosis, and in many cases, we can also make recommendations for treatments and therapies. We can also provide accurate information on disease progression and prognosis. Family members may also receive a risk assessment based on heredity.

Our Accreditations

Binding standards guarantee the quality of our work: Our laboratory services are accredited according to CAP/CLIA and DIN EN ISO 15189. You can find further accreditations and certifications here.

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You Are also Welcome to Take a Look at the Following Areas

General Information

Receive general information on our genetic diagnostics


View our publications and inform yourself about the latest results

Contact Us

Do you have a question, or are you interested in our service?

Diagnostic Support

We will assist you in selecting the diagnostic strategy – for each patient.

Diagnostic support team of CeGaT