Full-length RNA sequencing
Long-read sequencing with isoform-level resolution, for bulk tissue or single cells.
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Nearly all human genes produce multiple transcript isoforms. Short reads can't tell you which.
Untargeted long-read sequencing
Full-length transcript capture with isoform-level quantification. Available as a service for bulk tissue or single-cell samples.
Analyze from the same assay
Explore cell populations and expression patterns with integrated tools for read processing, V(D)J resolution, and interactive exploration.
Visualize RNA alignments
Navigate full-length transcript alignments with smooth, responsive visualization.
Immune repertoire resolution
Explore immune clonotypes and their recombinations, linked back to source alignments and assembly.
Everything connects
Link transcripts back to alignments and assembly. Navigate from expression to reads in a single click.
30kb+ reads, smooth navigation
Handle long reads with responsive, fluid navigation across the full length of each alignment.
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.
Making biology computable.
Bringing science out of the lab and into the world.
