mobile-back.jpg

Basic Genomics

Long-read data you can trust.

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.

↓

By bridging the gap between short-read practicality and long-read detail, RNA BaseCode positions itself as a transformative tool for researchers to decode transcriptomic complexity.

RNA BaseCode

Explore RNA BaseCode Products
Laboratory materials for RNA sequencing, including two boxes labeled 'RNABaseCode cDNA Kit' and 'RNABaseCode Sequencing Library Kit,' three small vials with blue, purple, and light blue caps, and a pink plastic rack with multiple wells.

The RNA BaseCode chemistry and software leverage our proprietary reverse-transcription error signatures to unambiguously identify short reads originating from the same RNA molecule and assemble them into high-quality synthetic long reads.

Learn more about RNA BaseCode Technology
Open box of RNA BaseCode's sequencing library kit with 24 tubes, pens, and scientific papers on a table.
Infographic showing six features of a sequencing platform: 1) Relative and absolute RNA counting, 2) Quantitative and qualitative RNA isoform detection, 3) Unprecedented sequencing accuracy for improved signal-to-noise, 4) Uses widely available short-read sequencing platforms, 5) Low sample input requirements, 6) Fusion-transcript and multi-mapping transcript detection.
Quote about the high sensitivity of lowly expressed genes, attributed to a postdoctoral researcher at St. Anna Children's Cancer Research Institute in Vienna, Austria.

“By delivering high-resolution data, our RNA sequencing facilitates deeper insights into cellular functions, disease mechanisms, and potential therapeutic targets”

Get In Touch!

Nobels Väg, 16
171 65 Solna, Sweden