OncoFull


OncoFull panel includes NGS (next generation sequencing) molecular diagnostic test and three FISH analysis as well as molecular interpretations plus selection of targeted therapies. OncoFull panel is designed to cover the widest spectrum of mutations from oncogenes to tumour suppressor genes. This includes around 1000 COSMIC mutations from 56 genes in the first in Poland full somatic cancer panel.

OncoFull gene list:ABL1, CSF1R, FBXW7, GNAS, KIT, NPM1, STK11, AKT1, CTNNB1, FGFR1, HNF1A, KRAS, NRAS, SMAD4, ALK, DDR2, FGFR2, HRAS, MAP2K1, PDGFRA, SMARCB1, APC, DNMT3A, FGFR3, IDH1, MET, PIK3CA, SMO, ATM, EGFR, FLT3, IDH2, MLH1, PTEN, SRC, BRAF, ERBB2, FOXL2, JAK2, MPL, PTPN11, TP53, CDH1, ERBB4, GNA11, JAK3, MSH6, RB1, TSC1, CDKN2A, EZH2, GNAQ, KDR, NOTCH1, RET, VHL

Type of cancer covered by OncoFull panel:

Colorectal cancer Breast cancer Gastric cancer Gardner Syndrome Adenoma
Adenomatous polyposis coli NSCLC Neuroblastoma Melanoma Lung cancer
Ovarian cancer Endometrial cancer Prostate cancer Hepatocellular cancer Granulosa cell tumors of the ovary
Biliary tract cancer Uveal melanoma CML, GIST Brain cancer
Renal cell cancer Mismatch repair cancer syndrome hereditary nonpolyposis type-5, Epidermal Nevus familial thyroid cance
hypereosinophilic syndrome Soft tissue sarcoma Hamartomas, Malignant melanomas SCC Head and Neck
Thyroid cancer, Meningioma, Pancreatic cancer Polyposis juvenile intestinal Advanced colon cancer
Testicular tumor Li-Fraumeni syndrome, osteocarcinoma nasopharyngeal carcinoma squamos cell lung carcinoma
myelodysplastic syndromes acute myeloid leukemia acute lymphoblastic leukemia basal cell carcinoma medulloblastoma