Greetings there,
I'm excited to share the latest edition of The seqWell Scope!
In this issue we’re taking a deeper dive into purePlex, the latest product in our expanding portfolio of multiplexed NGS library solutions. Our new products team at seqWell created the purePlex™ DNA Library Prep Kit to help address the large and growing number of NGS applications that depend on the sensitivity provided by unique dual indexing (UDI). purePlex builds on seqWell’s core technology for multiplexing and library normalization to provide a new indexing format that expands the number of applications that can be addressed with our unique transposase-based library chemistry.
In the blogs and video links below you’ll have a chance to learn and explore more about how and why UDI indexing matters, and how purePlex was built to use UDIs to solve some of the common needs and workflow challenges associated with implementing UDIs in the lab.
We also take a deeper look at one of the growing areas in NGS: low-pass whole genome sequencing, where multiplexed library prep has an important role to play in allowing sequencing to become a cost-effective method of routine genotyping applications.
October kicks off an exciting stretch for the whole team here at seqWell. We’ll be attending and presenting at a variety of upcoming conferences such as the
Tri-Omics Summit (Boston), NERLSCD (Rochester), MWACD (Rochester), Single Cell Genomics (Utrecht), ASHG (Los Angeles) and more. I hope we have a chance to meet in-person at one of these events!
Enjoy the start of autumn!
Best regards,
