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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"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
The Accel-NGS 2S Hyb DNA Library Kit, designed for Illumina® platforms, produces 45% fewer duplicates at 1 ng to save you money on sequencing costs. A variety of indexing kits allow for compatibility with multiple hybridization capture technologies. This kit is the right choice for researchers working with applications pertaining to low input… more »
Company completes Series D funding and adds two new directors to board. Swift Biosciences, a leading provider of innovative library prep solutions for genomic sequencing, today announced the completion of a Series D funding raise of $12.2 million. The company also announced the addition of two new directors to its board, positioning the company for accelerated growth. The Series D round was led by Arboretum Ventures more »