The Solid Tumor Multi-gene Combined Detection Kit is designed to identify actionable genomic alterations in multiple types of cancer, including single nucleotide variants (SNV), insertions and deletions (InDel), copy number variants (CNV), tumor mutational burden (TMB), microsatellite instability (MSI), and fusions, across cancer-related genes. Tissue samples are supported. It provides clinicians with comprehensive and accurate NGS based testing solutions for identifying clinically actionable mutations and discovering novel variants with important functions in cancer.
Solid Tumor
Next-Generation Sequencing (NGS)