Multi-biomaker NGS assay for solid tumors that evaluates >500 genes for SNVs, Indels, CNVs, LOH, Gene Fusions and also includes TMB and MSI. (FFPE samples)
Comprehensive Cancer Panel PLUS + HRD
This panel covers 46 genes of the HRR pathway and the Pan-Cancer Comprehensive Assay Plus provides clinically relevant information related to TMB, MSI, hotspot SNVs and Indels, CNVs and gene fusions, through the analysis of more than 500 genes.
Multi-biomaker NGS assay that covers 161 of the most clinically relevant cancer genes in solid tumors (FFPE samples)
Evaluate 52 genes of great relevance on multiple cancer types. Compatible with as little as 10 ng of genetic material extracted from FFPE tissue samples.
Evaluation of 46 genes of the homologous recombination repair pathway on solid tumors, detection of variants on genes of the HRR pathway that may cause HRD and Genomic Instability Metrics (GIM), gives information about genomic scarring/instability.
Includes 19 relevant genes for colorectal cancer assessment including MMR (mismatch repair pathway) genes: MLH1, MSH2, MSH6 and PMS2
Somatic and germline patogenic variants for BRCA1 and BRCA2 genes (FFPE + blood)
Analysis of 21 cancer genes including homologus repair pathway and MMR in FFPE biopsies
(Germline testing also available)
Evaluates 12 genes with proven clinical utility in genetic material, extracted from paraffin-embedded tumor tissue (FFPE) samples
Analysis of more than 200 genes relevant in Hereditary Cancer Syndromes (germline mutations).
Clarity Test is designed to screen 39 genes associated with hereditary cancer syndromes.