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Announcing new Tapestri Platform updates including lowered input threshold and expanded heme-onc menu. Learn More
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technical note

Copy number variants (CNV) and single nucleotide variants (SNV) simultaneously detected in single cells

Cancer begins in a single cell within the DNA. These genetic mutations are often caused by single nucleotide variants (SNVs) and gene copy number variants (CNVs), including loss of heterozygosity (LOH). Differences in SNVs and CNVs contribute to cancer heterogeneity, making some clonal populations more virulent and drug-resistant than others. Accurately defining clonal populations and reconstructing clonal phylogenies can only be achieved through single-cell analysis and is critical for informed clinical research. Learn how to obtain both CNVs and SNVs from the Tapestri Platform using Tapestri Single-cell DNA Panels.



technical note
MGI Sequencing Platforms Produce High-Quality Performance Metrics from Tapestri Single-cell Experiments (Language: Mandarin)
technical note
Deep understanding of cell and gene therapy genome editing protocols enabled with single-cell sequencing (Language: Mandarin)
technical note
In-depth quantification of cell and gene therapy DNA integrations enabled with single-cell sequencing (Language: Mandarin)
technical note
MGI Sequencing Platforms Produce High-Quality Performance Metrics from Tapestri Single-cell Experiments
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