Simplifying your everyday genetic testing
Detect all mutations in BRCA1 and BRCA2
Measure chimerism accurately down to 0.05% minority fraction
Perform complete thalassemia testing in a single tube
Perform non-invasive prenatal RHD screening
NGS-based chimerism monitoring combines the benefits of STR and qPCR without the drawbacks.
Next generation sequencing of multiple genes for oncology testing can be challenging and time-consuming. A rapid, user-friendly protocol resolves the bottlenecks.
Both the demand and complexity of thalassemia testing are increasing. NGS enables variant detection of alpha and beta thalassemias on the first try, in one simple procedure.
”The workflow is easier, the analysis is easier and more efficient”
© Devyser 2021