NEXTflex® NSeq Kits offers robust genome coverage to identify variants in over 350 genes.
For Research Use Only. Not for use in diagnostic proceedures.
Our NEXTflex® NSeq kits Offer robust genome coverage to identify variants in over 350 genes. Targeted regions are designed for comprehensive research of early onset disorders. Library prep is also Illumina® and Element BioSciences compatible.
Shipping Conditions |
Dual Temperature
|
---|
Brochure that outlines our newborn sequencing research workflow.
One pager that details the flexibility of our newborn sequencing research workflow.
We are here to answer your questions.