Transforming NGS Library Prep Applications

Get the most efficient and reproducible output from low sample input. Our products are designed for sequencing analysis of DNA in whole genome, whole exome, epigenetics, or amplicon applications. Swift technologies help to accelerate workflow, improve uniformity, reduce library bias, and diminish coverage gaps.

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Peer-reviewed publications showcasing Swift's product portfolio.


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What Swift Clients Say

"This indicates that A-LA [Accel-NGS 1S Plus] would be the library preparation method of choice when targeting both ssDNA and dsDNA viruses in surveys of natural communities." - Roux et al. (2016), PeerJ 4:e2777

Accel-Amplicon™ Plus Cancer Panels

Accel-Amplicon Plus Panels combine the easiest, fastest workflow with flexible content to accelerate your variant discovery and screening. Simply leverage our pre-designed, validated core content and add your own targets. With our fast results and robust on-target performance and coverage uniformity, you’ll have the most informative panel with the best data quality for… more »

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Swift Biosciences Launches Swift 2S Turbo Library Kit, Accelerating Whole Genome, Exome and Large Gene Studies with One Universal Approach

Posted July 18, 2018

(ANN ARBOR, Mich. – July 18, 2018) Swift Biosciences, a leading provider of innovative library prep solutions for next-generation sequencing (NGS), today announced early access to its Swift 2S Turbo Library Kit. These new kits offer a fast, robust enzymatic fragmentation prep and flexible adapter options to produce high-quality libraries for production-scale sequencing. With an automation more »

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