Genome-wide CNV Panel

Assessing the integrity of the genome is vital for ensuring the safety of gene-edited and stem-cell therapies by avoiding potential oncogenic risks. Genome integrity is also crucial for studying cancer clonal heterogeneity, as it uncovers genomic variations in subclones behind tumor evolution and therapy resistance. This panel uniformly covers copy number variations (CNV) in nearly the entire human genome to assess genome integrity, including sub-chromosomal deletions and duplications, and whole chromosomal aneuploidy.

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Tapestri Single-cell DNA Genome-wide CNV Panel Panel

Assess the genomic integrity of primary cells and stem cells to evaluate cell and gene therapy safety or to interrogate cancer clonal heterogeneity by targeting genome-wide CNVs with 500 amplicons for single-cell DNA sequencing. This panel has been verified in a wet lab to meet performance specifications.

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Genome-wide CNV Panel

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