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.
Exome Diagnostics
Parallel analysis of all coding regions of the genome.
Prevention
We identify genetic risk factors – for you and your family
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
Dedicated Support
We’re available to support you in choosing the diagnostic strategy for individual patients and to discuss the results of the analysis.
