Copy Number Analysis on the Tapestri Platform Now Available.
Get SNVs and CNVs from one single-cell platform
The only single-cell targeted DNA solution that provides both copy number variants (CNVs) and single nucleotide variants (SNVs) from the same cell. Characterize genomic heterogeneity using a single platform, with comprehensive single-cell DNA analysis to co-detect both SNVs and CNVs.
Call genotypes and copy number variants on up to 10,000 cells
Resolve gene-level to chromosome-level events including amplifications, deletions, and loss of heterozygosity (LOH)
Complete simple 1.5 day workflow from cells or nuclei to libraries
Compatible with Tapestri Catalog and Custom Panels