What is carrier screening research?
In today’s multiethnic society, some genetic disorders previously thought to be confined to specific ethnic groups are increasingly being found in broader populations. Next-generation sequencing (NGS) enables rapid carrier screening research across the broadest range of disorders, crossing ancestries and geographic regions, with a scalable, cost-effective solution.
Having genetic information by carrier screening research helps intended parents to understand their risk and probability of passing on an inherited genetic disorder to their children.
Discover our workflow
Prepare your sample
NA quantification
Pipettes and tips
Vortex mixers
NA extraction and purification
Resources
Analyse your sample
Microarray
NGS
qPCR and dPCR
Capillary electrophoresis
Resources
Expand your capabilities for reproductive health genetic testing
For Research Use Only. Not for use in diagnostic procedures.
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