The RNA BaseCode Products and Services

Slide titled 'Solving long-standing Biological questions' with text about RNA BaseCode pilot study, a quote, and logos of NIH and Hide & Seek Foundation.
A scientist wearing green gloves is pipetting from a RNA BaseCode reagent tube.

The RNA BaseCode Kit

Introducing the new RNA BaseCode Kit for high-accuracy synthetic long-read RNA sequencing.

By exploiting an advanced barcoding strategy, RNA BaseCode reconstructs complete RNA transcripts from short-read data with exceptional accuracy at scale. The result is a powerful, easy-to-use solution for researchers seeking deeper insight into isoforms, splicing, and transcript complexity, all from standard short-read sequencing platforms.

Two people working together on a computer in an office setting, with one person pointing at the monitor displaying code and graphs relating to RNA BaseCode data.

RNA BaseCode Kit features:

  • 24 reactions per kit.

  • Go from total RNA to sequencing-ready libraries in 2 days.

  • 5 ng total RNA input.

  • No dedicated liquid handling equipment or instruments required.

  • Works with existing short-read sequencing instruments.

  • Uses our freely available RNA BaseCode data processing software to produce synthetic long-reads.

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.

RNA BaseCode Service

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Try RNA BaseCode, no pipetting, no sequencing, just data.

Our RNA BaseCode Service gives you fast and easy access to high-quality synthetic long-read RNA sequencing data generated with our proprietary chemistry and analysis pipeline. Simply send us your RNA and we’ll deliver fully processed, isoform-resolved synthetic long-read data straight to your inbox. It’s the easiest way to explore the power of RNA BaseCode before bringing the technology into your own lab.

An infographic illustrating the process of RNA sequencing in biology and genomics. It shows a pipette, a storage box, a scientist with a test tube, a sequencer machine, computer screens displaying DNA sequences, a test tube with pink liquid, and a BAM file document. The text explains isolating RNA, preparing sequencing libraries, discovering new biology and disease mechanisms, and delivering a BAM file after 3-6 weeks.

Key Features and Benefits of RNA BaseCode

Diagram with six icons and text describing RNA analysis technologies. Top row: relative and absolute RNA counting, quantitative and qualitative RNA isoform detection. Middle row: unmatched sequencing accuracy (>Q90), uses widely available short-read platforms. Bottom row: low sample input requirements, fusion-transcript and multi-mapping transcript detection.

  • Precision in Isoform Detection

    Resolves transcript variants missed by conventional methods. Don’t miss out on critical Biology or Biomarkers!

  • Seamless Integration

    RNA BaseCode brings the scale, quality, availability and ease-of-use of short-read sequencing platforms to RNA isoform discovery.

  • Quantitative and Qualitative

    With RNA BaseCode there is no need to run separate assays to obtain long-read data and quantitative short-read data. Get all your data from a single assay!

  • Low input requirement

    RNA BaseCode requires only 5 ng of total RNA per sample.

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.