Basic Genomics
Unlocking the full potential of RNA research for a healthier Future.
Basic Genomics specializes in advanced RNA sequencing technologies that enable precise detection and quantification of RNA molecules. With our BaseCode platform, we empower researchers and clinicians to uncover critical insights into gene regulation, disease mechanisms, and therapeutic targets.
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Basic Genomics has developed a unique high-throughput isoform-aware RNA-sequencing method that enables precise detection and quantification of RNA molecules.
Our cutting-edge BaseCode technology platform offers a synthetic long-read sequencing solution that combines the efficiency of short-read sequencing with the ability to produce high-quality data.
This powerful platform empowers researchers to investigate RNA isoforms and understand the critical role that splicing plays in human health and disease.
Long read data you can trust
Introducing our cutting-edge synthetic long read RNA sequencing technology, designed to provide unparalleled isoform resolution.
“By delivering high-resolution data, our RNA sequencing facilitates deeper insights into cellular functions, disease mechanisms, and potential therapeutic targets”
RNA BaseCode Kit
By bridging the gap between short-read practicality and long-read detail, BaseCode positions itself as a transformative tool for researchers and investors aiming to decode transcriptomic complexity.
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Nobels Väg, 16171 65 Solna, Sweden