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

"The Accel-NGS 2S Plus Kit generates good ChIP-seq data, even with less than 50 pg ChIP DNA." - Chang Lu, PhD, Virginia Tech

Accel-NGS® XL Library Kit for Pacific Biosciences®

The Swift Biosciences Accel-NGS XL Library Kit designed for the Pacific Biosciences platform is the fastest sequencing solution for genome assembly and haplotype sequencing on PacBio platforms. Long-read sequencing technology provides better coverage to sequence difficult genomic regions including low complexity, repetitive elements, or large structural variation. more »

Similar Products

Swift Biosciences Launches Novel Long-Insert Library Kit to Improve Data Quality on Pacific Biosciences® Sequencing Platforms

Posted February 14, 2017

Results from Mount Sinai, Washington University, and Cold Spring Harbor Laboratories to be presented at AGBT 2017 General Meeting (ANN ARBOR, Mich. – February 14, 2017) Swift Biosciences today announced the commercial release of its Accel-NGS® XL Library Prep Kit, the fastest sequencing solution for whole genome sequencing on Pacific… more »

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Tue - Sat Mar 21-25 2017

ACMG 2017 Annual Meeting

Phoenix, AZ | Booth #1015