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.