Find the key
signatures of cancer.

You seek more than patterns. You seek the sources of disease. That is why our Tapestri Platform analyzes genotype and phenotype simultaneously from the same single cells, letting you reveal clonal heterogeneity and target comprehensive biomarkers that help stratify patients more precisely, signal resistance as it begins, and predict relapse.

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Why Single Cell for DNA and Protein?

Cancer is a complex disease with a mix of cells with varied states, and understanding of the disease state at the cellular level is required for better therapies. A single-cell multi-omics approach is the only way to achieve full resolution, revealing the complex interplay between genotype and phenotype. Perform true multi-omics with simultaneous detection of SNVs, CNVs, and protein at the single-cell level.

Correlate immunophenotype with genotype from the same cell.

Distinguish subclones from minimal residual disease with multiple analytes in the cell using SNVs, CNVs, and protein expression.

Eliminate inferences while saving on research budgets and analysis times.

Explore insights of single-cell multi-omics in myeloid malignancies.

Ross Levine, M.D., Memorial Sloan Kettering Cancer Center

View Panels

Target the diversity that matters with content in a custom panel, or start with one of our pre-designed panels.

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Explore Hematology

See how single-cell DNA sequencing transforms the study of hematological malignancies.

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The Tapestri Workflow

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.

Target Selection

Choose a pre-designed or custom DNA panel