The RNA BaseCode Kit

Get superior long-read data using widely available short-read sequencers—no need for specialized equipment. Our technology works with low RNA input and delivers unmatched base accuracy.

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Laboratory kits labeled RNABaseCode cDNA Kit and Sequencing Library Kit, three small sample vials, and a pink rack with multiple wells on a white surface.

  • Precision in Isoform Detection

    Resolves transcript variants missed by conventional methods, critical for studying splicing-related diseases.

  • Seamless Integration

    Works with established short-read platforms, avoiding costly infrastructure upgrades.

  • Scalability

    Processes millions of reads efficiently, ideal for large-scale studies.

FAQs

  • We recommend having at least 5ng of total RNA in 2ul as input for each reaction.

  • If possible, we recommend starting with RNA with RIN 7 or higher. Starting with lower RIN RNA may reduce performance.

  • We recommend sequencing your RNA BaseCode samples to a depth of 50M reads / sample using PE150 sequencing chemistry.