- Indicated for the detection of variants that are targets for cancer therapeutic or prognosis.
- Covers hotspots, full exons or the entire gene within 26 of the most relevant cancer genes involved in solid tumors.
- Offers at least 94% sensitivity and 100% specificity and positive predictive values for SNVs and indels with ≥3% and 5% variant allele frequency, respectively.
- Can be performed on DNA extracted from formalin-fixed, paraffin-embedded (FFPE).
Genes tested in the assay
AKT1
ALK
APC
BRAF
CDH1
CTNNB1
EGFR
ERBB2
FBXW7
FGFR2
FOXL2
GNAQ
GNAS
KIT
KRAS
MAP2K1
MET
MSH6
NRAS
PDGFRA
PIK3CA
PTEN
SMAD4
SRC
STK11
TP53