The Tapestri Platform is the only single-cell multi-omics 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 SNV and CNV analysis to co-detect all the changes in our blueprint.
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 microfluidic workflow.
Use a single workflow for co-detection of gene-level to chromosome-level CNVs, LOH, and SNVs in single cells.
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.
Integrate seamlessly into your existing NGS workflow with sample prep and analysis solutions using the Tapestri single-cell sequencing platform
With our single-cell sequencing platform, use the Tapestri Instrument, reagents, and consumables up-front of your NGS system and then Tapestri Pipeline and Tapestri Insights software for data analysis and visualization.