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Unravel the Threads of Cancer’s Complexity

Explore pathways. Discover biomarkers. Change lives.

Tapestri Designer software allows you to complete a custom DNA design within minutes. Primer design algorithms and multiplex PCR biochemistry have been optimized with AI technology for the Tapestri Platform so that you can be confident in robust results. Custom DNA panels can also be paired with olio-conjugated antibodies to enable simultaneous detection of genotype and phenotype from the same cell for true single-cell multi-omics insights.

START YOUR DESIGN

Tapestri Designer for custom DNA panels:
Get the biomarkers at the sources of disease

Best single-cell custom panel performance
Order with confidence using optimized design parameters with high coverage and uniformity for the Tapestri workflow
Expansive application set
Support for human and mouse genomes to design oncology panels for SNV and CNV analysis or genome editing panels covering on- and off-target edits
Simple workflow
Quickly enter the target coordinates or database IDs to create a curated panel in minutes, then visualize the targeted coverage

The Tapestri Designer Workflow

Design a custom DNA panel in 3 easy steps.

With the easy-to-use and intuitive Tapestri Designer software, your custom design can be completed within minutes. Primer design algorithms and multiplex PCR biochemistry have been optimized for the Tapestri Platform, so you can be confident of high design coverage and high panel uniformity. Custom DNA panels can also be paired with oligo-conjugated antibodies to enable simultaneous detection of genotype and phenotype from the same cell for true single-cell multi-omics insights.

Account SETUP
Enter credentials to access Tapestri Designer, Tapestri Pipeline, and Tapestri Insights.
UPLOAD/ENTER TARGETS
Upload your csv files or enter gene, ID, or coordinate targets.
SUBMIT DESIGN
Submit your targets, and results are available within minutes.

Have novel applications or challenging panel design requirements?

Our team of experts is ready to support requests for DNA fusions, unique target sequences (CRISPR translocation events, viral integration, etc.), regions with high GC content, or large panels.

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Questions?

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