seqWell

🧬 NGS scientists take note! 🧬 Your library prep workflow matters!

When library prep workflows become too complex, labs face slower timelines, lower throughput, and operational bottlenecks that limit scientific progress.

Our latest blog explores why simplicity and scalability are essential for modern high-throughput NGS workflows, and how features like tagmentation, early pooling, and high-level multiplexing can unlock:

✔️ Faster turnaround times
✔️ More reproducible data
✔️ Greater operational efficiency
✔️ Lower total cost of operation

Read the full blog to learn more: https://hubs.ly/Q04hh4dZ0

Join us at the SLAS Europe Conference May 19-21.

Sabina Gude will be presenting our latest work on a fully automated, highly miniaturized, one-step TnX-based NGS library preparation workflow designed for ultra-high-throughput sequencing.

If you’ll be on-site, stop by to learn how we’re enabling scalable, automation-friendly library prep workflows and to connect with our team.

Microarrays have long been the standard, but low-pass WGS is emerging as a cost-effective alternative that captures genome-wide variation.

Instead of being limited to predefined SNP panels, lpWGS enables:
🔍 Discovery of novel variants
📈 Genome-wide detection of copy number variants
💡 Greater long-term value from your data

Our latest poster shows how easy it is to make the switch, using AgriPrep™ to deliver scalable lpWGS with >98% concordance to array data.

We're happy to welcome the latest member of the seqWell team - Brett Fritz - as the VP of Sales.

Really excited to have him on board—already looking forward to the ideas, energy, and perspective he’ll bring.

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