
PanHemeOnc panel
Fast and streamlined NGS profiling for both lymphoid and myeloid disorders

Actionable mutation panel
Detect low frequency variants in key oncogenes of the Epidermal Growth Factor Receptor

Carrier screening panel
Accurately analyze carrier status of 448 inherited childhood disorders using a single workflow

Familial Hypercholesterolemia Panel
Comprehensive coverage of clinically relevant variants of Familial Hypercholesterolemia.