Our diagnostic services

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.

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.

How does it work?

Test selection

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

Genetic counceling

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.