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Detection of germline and somatic mutations in BRCA1, BRCA2, PALB2 genes.
NGS DNA panels for the detection of SNV, InDel and CNV somatic variants using AMP technology
NGS RNA panels for the detection of gene fusions, alternative splicing, SNV and InDel variants using AMP technology
Detection of somatic SNV and InDel mutations in 42 genes using NGS.
Detection of somatic SNV and InDel mutations in 42 genes and 137 gene fusions by NGS.
NGS solution for detection of variants of 28 HRR genes and determination of genomic integrity to determine HRD status.
NGS panels for the detection of SNVs, InDels and CNVs in 4-28 HRR genes.
NGS RNA panels for the detection of SNVs, InDels and gene fusions even with unknown binding partners.
NGS panel for detection of SNVs, InDels and CNVs in 477 genes. It also allows determination of MSI and TMB.
Kits for determining the risk of developing cervical cancer using the bisulfite reaction and rtPCR.
Kits for detection of EGFR, KRAS, NRAS, BRAF gene mutations by PNAClamp technology
A kit for the detection of the 6 most frequent mutations of the POLE gene based on the analysis of DNA isolated from FFPE samples using qPCR.