Enhance the assessment of copy number variation (CNV) signatures in human pluripotent stem cells (hPSCs), including embryonic stem cells (ESCs) and induced pluripotent stem cells (iPSCs), with our virtual panel with 46 amplicons. Designed to be used in combination with the Tapestri Single-cell Genome-Wide CNV (gwCNV) Panel, this dual-panel approach covers 76.2% of recurrent CNVs in hPSCs, including Chr20q11.21 (Assou et al. 2020, Avery et al., 2013, Halliwell et al., 2020). This powerful tool elevates CNV analysis for improved quality control and characterization of stem cells in regenerative medicine and cell-based therapies.
REQUEST A QUOTEAssess the genome integrity in hPSCs to characterize stem cells in regenerative medicine and cell-based therapies by targeting 76.2% of recurrent CNVs in hPSCs with 46 amplicons for single-cell DNA sequencing. This panel has been verified in a wet lab to meet performance specifications.
Use Tapestri Designer to add or remove content from existing catalog panels and make this panel your own with content that is relevant to your research. Or start from scratch and upload your human (hg19) or mouse (mm10) targets using gene names, genomic coordinates, or SNV IDs. Target anywhere in the whole human or mouse genome and advance your research with targeted single-cell DNA sequencing.
DESIGN PANEL