Laboratory products
Automated Sample Preparation for Next-Generation Sequencing
Mar 20 2012
Beckman Coulter Life Sciences has launched SPRIworks HT, a high-throughput solution for fragment library preparation on Illumina next-generation sequencers. The system allows researchers to process libraries with greater speed and sample reproducibility and decreases processing costs. SPRIworks HT utilises built-in SPRI (Solid Phase Reversible Immobilization)-based per-well size selection. User interaction is seamless and requires as little as 15 minutes of hands-on time.
Up to 96 samples can be prepared in as little as three hours without size selection, or six hours with size selection. The simplicity of SPRIworks HT enables users to seamlessly perform automated sample preparation protocols upon their first interaction with the system. SPRIworks HT offers a reagent kit for library preparation that includes sizing solution and PCR reagents. Protocols are automated via a suite of methods built on the Beckman Coulter Biomek FXP Liquid Handling Workstation. Per-well size selection provides users with the flexibility to process samples for multiple applications in a single run. For added efficiency, methods are also included for downstream processes such as PCR setup, PCR cleanup, qPCR setup, quantitation, normalisation and sample pooling. The overall system increases reproducibility, decreases processing costs and eliminates most manual preparation steps in next
generation sequencing sample prep.
"SPRIworks HT is the only high-throughput system that automates not only library construction, but size selection and enzymatic cleanups as well," said Julie Moore, director of strategic marketing at Beckman Coulter. "We are excited to deliver a product that will enable genomic laboratories to eliminate bottlenecks, increase throughput and maximise returns on instrument investments."
The SPRIworks HT system complements existing SPRIworks platforms, SPRI paramagnetic bead-based chemistry and Biomek liquid handling platforms, which are used to support genomic researchers in their work to solve biological problems through sequencing.
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