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.
Disease Prevention Panel
Understand genetic risk factors and plan health care.
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 Us
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
Sample
Shipping
