Because a change in our blueprint is where cancer begins.
The Tapestri Platform is the only single-cell targeted DNA solution that provides both single nucleotide variants (SNVs) and copy number variants (CNVs) from the same cell. Characterize genomic heterogeneity using a single platform, with comprehensive single-cell DNA analysis to co-detect all the changes in our blueprint that matter.
When determining the clonal heterogeneity across a cancer sample, it’s important to comprehensively measure both DNA mutations and copy number variants in every cell to give us higher resolution to explore tumor evolution and heterogeneity.
Gain unprecedented insight into the diversity of genomic changes with simultaneous SNV and CNV analysis from the same cell.
Obtain quality for your research with best-in-class single-cell DNA accessibility using the Tapestri two-step workflow
Use a single workflow for co-detection of gene-level to chromosome-level CNVs, LOH, and SNVs at the single-cell level
Start from cells or nuclei with maximum sample flexibility for CNV analysis
Discover how single-cell SNV and CNV analysis helps better resolve the heterogeneity in renal cell carcinoma (RCC) samples.