Genetic Diagnostics – our Portfolio

Single Gene Testing

Analysis of variation of single genes by conventional Sanger sequencing, deletion or duplication analysis, or fragment length analysis.

Diagnostic Panels

Simultaneous, fast, and effective analysis of all known genes associated with a certain disease.

Focused Panels

Cost-effective and fast genetic analyses for well characterized clinical features.

Tumor Diagnostics

Molecular genetic characterization of tumor tissue to aid in the selection of the best therapeutic intervention.

Exome Diagnostics

Parallel analysis of all coding regions of the genome.

Array-CGH

Analysis of large deletions and duplications across the whole genome.

Non-invasive prenatal test (NIPT)

A non-invasive prenatal test by Cenata GmbH, which can reliably detect the risk of the chromosomal disorders trisomy 21, trisomy 18, and trisomy 13.

Contact CeGaT Diagnostic Support

We’re available to support you in choosing the diagnostic strategy for individual patients and to discuss the results of the analysis.

How does the ordering process work?

Test selection

If you need help finding an appropriate test please contact our Diagnostic Support team.

Genetic counseling

Patient receives genetic counseling and signs the order form with consent form.

Sample

Blood samples (3-5 ml purple top EDTA tube) or genomic DNA (5 μg) can be sent directly to us. More information is available under notes for sample requirements.

Shipping

Dispatch of sample together with the order form.