Analysis of variation of single genes by conventional Sanger sequencing, deletion or duplication analysis, or fragment length analysis.
Simultaneous, fast, and effective analysis of all known genes associated with a certain disease.
Molecular genetic characterization of tumor tissue to aid in the selection of the best therapeutic intervention.
Parallel analysis of all coding regions of the genome.
Analysis of large deletions and duplications across the whole genome.
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.
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