Cancer All-In-One Solid Tumor Assay
Single NGS assay for Single Nucleotide Variants, indels, Copy Number Variations, and translocations relevant to multiple solid tumor types.
- All-in-one profiling of SNVs, indels, CNVs, and translocations relevant to multiple solid tumors from a single DNA sample of 50 ng or less
- Compatible with FFPE and low-quality DNA samples
- Streamlined workflow to achieve target-enriched NGS libraries from DNA within a day
- Robust detection of somatic CNVs, including gene amplifications and deletions down to 15% tumor cells
- High-sensitivity translocation detection by targeting translocation driver genes regardless of partner genes
- Complementary data analysis supported by Agilent SureCall software