Full-length RNA sequencing

Splice variants are important.

Transcript isoformsShort-read sequencingLong-read sequencing

Nearly all human genes produce multiple transcript isoforms. Short reads can't tell you which.

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offerings
Single-cell analysis

Untargeted long-read sequencing

Full-length transcript capture with isoform-level quantification. Available as a service for bulk tissue or single-cell samples.

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Bundled software
Analyze from the same assay.
Integrated tools for read processing, V(D)J resolution, and interactive exploration.
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specifications

5' Long-Read Sequencing

Untargeted polyA transcript capture. Available for bulk tissue or single-cell samples.

Input

  • Bulk tissue or single-cell suspension
  • Cryopreserved, viability post-thaw >70%

Optional

  • V(D)J enrichment for TCR/BCR clonotypes
  • Cell selection
  • Custom tissue dissociation protocol development (available upon request)

Outputs

  • RNA expression
  • Whole-exome variant calls
  • V(D)J clonotypes (single-cell)
  • Cell type classification (single-cell)
  • Access to HoX software analysis suite

Coming soon: surface protein profiling via ADT, isoform-resolved expression tables and analysis tools.

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