seqWell innovation began in 2014 by harnessing the power of tagmentation – the simultaneous fragmenting and tagging (ligating NGS adapter sequences) of DNA – to replace traditional library preparation methods that use complex and lengthy protocols and to increase the power of multiplexing. Our latest innovations include TnX, an engineered next-generation transposase and high-performance alternative to Tn5, and seqWell directional tagmentation.
seqWell uses a variety of NGS library preparation workflows — from one-step tagmentation & amplification, to single and dual tagmentation, as well as directional tagmentation — to address a variety of needs.
TnX, seqWell’s next generation transposase and alternative to Tn5, was developed using fit-for-purpose engineering that targeted improvements in 3 key enzyme attributes: activity, insertion bias and robustness. These improved attributes translate into enhanced sequencing performance by improving NGS data quality and uniformity.
Read start site insertion bias was measured by examining the frequency of bases in the first 9 bases of each read. Positions with higher per-base nucleotide bias are represented by heights for hyperactive Tn5 and TnX, and illustrate the reduced bias of TnX.
TnX loaded with universal adapters, i5/i7 adapters, UMIs or customer-specified oligos – used for sensitive targeted gene editing QC analysis assays, as well as other custom assays.
Ready-to-use, one-step library preparation kit for plasmid, amplicon and small genome sequencing
90-minute library prep using TnX-based directional tagmentation for production of high complexity libraries.
Combine the workflow simplicity of tagmentation, the reduced insertion bias of TnX, & the performance benefits of ligation and you’ve got seqWell’s directional tagmentation used in our ready-to-use MosaiX kit. This 90-minute workflow requires less than 35 minutes of hands-on time and produces complex libraries required for population genomics.
Our library prep and multiplexing kits are available to support all your short and long-read sequencing applications. Contact us to find out which is right for you!