Simple, digital detection of single nucleotide variants (SNVs) and small InDels from as little as 5 ng of DNA from FFPE in a single tube. Designed for compatibility with other 3D B...
Vantage 3D™ SNV Solid Tumor Panel
Designed to identify the most meaningful variants across a variety of solid tumor types, this panel includes somatic variants (SNVs, DNVs, and small InDels) associated with lung adenocarcinoma, thyroid carcinoma, pancreatic adenocarcinoma, colorectal adenocarcinoma, and melanoma. The genes and mutations covered are relevant to new and existing clinical trials, drug pipelines, tumor subtypes, drug resistance, and response.
- 104 driver mutations from 25 key solid tumor genes
- Only 5 ng DNA input requirement from FFPE, fresh/frozen, and cells
- Sensitivity and Specificity above 95% on solid tumor samples with >5% allele frequency*
- Concordance with gold standard mutational analysis techniques
- Simultaneous multi-analyte profiling with Vantage 3D RNA and Protein Assays
*Validated on internal reference materials. Data may vary with the various quality of FFPE samples.
Curated Content
