seqWell

seqWell

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Contact information, map and directions, contact form, opening hours, services, ratings, photos, videos and announcements from seqWell, Biotechnology company, 66 Cherry Hill Drive, Beverly, MA.

Our plexWell™ platform is a transformative library prep technology that allows for simple, scalable multiplexing of 100s to 1000s of samples without time- and cost-consuming normalization.

06/11/2026

Loaded TnX transposase from seqWell.

Looking for a high-performance, fully QC'd transposase loaded with Illumina-compatible universal adapters? Look no further - Tagify TnX Universal Adapters!

- Rapid tagmentation-based library prep
- Fully QC’d for batch-to-batch consistency
- TnX for uniform sequence coverage

https://hubs.ly/Q04l230s0

06/09/2026

🌱🧬 Join us for an upcoming webinar exploring how population-scale, low-pass whole genome sequencing is accelerating crop improvement.

In this webinar, we will discuss:
- High-throughput NGS library prep for agrigenomics
- Pangenome-enabled genomic discovery
- Low-pass WGS for trait mapping and genomic selection
- Case study using AgriPrep™ to identify peanut disease resistance

Register now to learn how scalable sequencing workflows are helping advance agrigenomics.

https://hubs.ly/Q04kKGmL0

06/02/2026

seqWell is excited to present new data at ASM Microbe evaluating one-step library prep for microbial WGS.

Our poster benchmarks our latest advancement, ExpressPlex™ Plus, against Tn5-based and fragmentation, highlighting:
- Workflow simplicity
- Consistent coverage
- And scalability for high-throughput sequencing

If you’re attending ASM Microbe, stop by on Sunday, June 7th and connect with the seqWell team at Poster: AEM-SUN-729

05/28/2026

BLOG Part 2: Scaling sequencing projects shouldn’t mean scaling complexity. Solution - the ExpressPlex™ Workflow!

In the latest blog from our ongoing library prep workflow series, we explore how the ExpressPlex™ workflow impacts throughput, reproducibility, and operational efficiency in large-scale NGS applications.

Explore the blog: https://hubs.ly/Q04jc5Py0

Missed the first blog in our library prep series? Catch up here: https://hubs.ly/Q04jc8_D0

05/26/2026

We're always excited to engage with the scientific community, and ASM Microbe is one of the biggest highlights of the year.

We'll be attending the conference and highlighting a new one-step NGS library prep kit for scalable microbial WGS.

We hope to see you there!

05/20/2026

🧬 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

05/14/2026

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.

05/07/2026

🐄🌱Agrigenomic Scientists - Check out seqWell's benchmarking study for AgriPrep™ Library Prep Kit vs. traditional library prep workflows for low pass WGS.

The RESULTS?
🧬 Higher mean coverage, lower duplication rates, & larger estimated library sizes
🎯 ≥ Performance for imputation accuracy & variant detection sensitivity
🔄 >60% faster workflow across plant, animal & human samples

Explore how you can scale low pass WGS without the bottlenecks. https://hubs.ly/Q04fQLWl0

05/05/2026

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.

04/29/2026

Don't want to load your own transposase? We've got you covered.

With Tagify™ Custom, you get a commercial source of fully QC'd transposase loaded with your adapter of choice for maximum flexibility. Get assays like GUIDE-seq2, ATAC-seq, CHANGE-seq, SHARE-seq, and more up and running faster.

https://hubs.ly/Q04dTJJg0

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66 Cherry Hill Drive
Beverly, MA
01915