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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What Swift Clients Say

"We are hopeful that Swift's library prep will allow us to ask more questions and get a more comprehensive view of the epigenetic changes associated with oncogenesis." - Prakash Rao, Dana Farber Cancer Institute

Accel-NGS® 2S Plus DNA Library Kit

The Accel-NGS 2S Plus DNA Library Kit, designed for Illumina platforms, utilizes a proprietary adapter attachment chemistry which minimizes bias and supports inputs as low as 10 pg. The Accel-NGS 2S Plus kit offers exceptional performance for a broad range of applications pertaining to whole genome sequencing of limiting more »

Similar Products

Swift Biosciences and Fluxion Biosciences Announce Jointly Developed NGS Workflow for Somatic Mutation Detection from Liquid Biopsy Samples

Posted October 27, 2016

South San Francisco, CA and Ann Arbor, MI, October 27, 2016 – In advance of the 2016 American Molecular Pathology (AMP) meeting, Swift Biosciences, Inc. and Fluxion Biosciences, Inc. announced a key advancement in cancer sequencing—improving the sensitivity to detect mutations at very low frequencies using low input samples. This… more »

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