Swift Products

Swift products enable the most efficient and reproducible output from routine and challenging samples, for next-generation sequencing of DNA.

NEW! SWIFT AMPLICON 16S+ITS PANEL

Comprehensive Microbial Identification

The Swift Amplicon 16S+ITS Panel enables highly efficient, sensitive and specific microbial identification by targeting the 16S rRNA (V1-V9) and ITS genes in a single primer pool, along with a simple two-hour workflow.

NEW! SWIFT NORMALASE™ KITS

Revolutionary Library Normalization Technology for NGS Laboratories

The Swift Normalase Kit offers a novel enzymatic library normalization technology that is augmented by the power to consolidate library normalization and pooling for loading on Illumina® sequencing platforms. The Normalase workflow eliminates the need for library quantification and concentration adjustment prior to library pooling, resulting in optimal cluster density and library balance. The Swift normalization method can easily be integrated into standard protocols to improve turnaround time loading and accuracy for NGS laboratories.

SWIFT 2S TURBO DNA LIBRARY KITS

The Easy-to-Use Library Prep Kits for Sequencing Production Labs

The NEW Swift 2S Turbo DNA Library Kits are a fast, efficient and cost-effective library prep solution.  Leveraging a robust enzymatic fragmentation prep and flexible indexing, you can prepare high-quality whole genome and exome libraries using a broad range of input amounts and sample types.

The Accel-NGS 2S family of products employ a combination of unique fragment repair mechanisms and an exceptionally efficient adapter technology to generate the most diverse libraries for Illumina® platforms. The synergy in this process allows for processing DNA inputs as low as 10 pg while minimizing base composition bias in final libraries. All of the Accel-NGS 2S Kits permit for single-tube processing of just a few samples with a simple protocol while easily being automated for high-throughput labs.

ACCEL-AMPLICON™ NGS PANELS

Prepare Targeted Libraries in 2 Hours

Accel-Amplicon NGS Panels utilize multiple amplicons in a single tube, using a rapid, 2-hour workflow to prepare ready-to-sequence libraries. Primer pairs in Accel-Amplicon NGS Panels are compatible with short DNA fragments and are designed for generating libraries from input DNA as low as 10 ng. This unique design enables applications utilizing limiting or damaged samples such as FFPE and cfDNA, and provides powerful solutions for detecting variants and screening clinically-relevant mutations with limit of detection down to 1%.

ACCEL-AMPLICON™ PLUS CANCER PANELS

One Enabling Workflow. Infinite Possibilities.

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 your scientific needs..

ACCEL-NGS® 1S DNA LIBRARY KITS

NGS DNA Library Construction from Samples with Limiting Amounts of Degraded DNA

The Accel-NGS 1S DNA Library Kits enable users to make libraries from the impossible. Libraries can be made from damaged and degraded samples by using Swift’s Adaptase™ technology. Unlike other library methods, the Adaptase technology can generate library molecules from single-stranded DNA fragments, which allow researchers to recover more of their input DNA from difficult samples compared to other commercially-available products.

The Accel-NGS Methyl-Seq DNA Library prep utilizes Adaptase technology for capturing single-stranded DNA molecules in an unbiased manner. As bisulfite treatment of samples damages DNA, Swift Biosciences’ single-strand compatible Adaptase technology maximizes recovery of DNA from bisulfite-converted samples.

ACCEL-NGS® XL LIBRARY KIT FOR PACIFIC BIOSCIENCES®

Reliable Long-Read Sequencing Solutions for Genome Assembly and Genomic Phasing

The Swift Biosciences Accel-NGS XL Library Kit designed for the Pacific Biosciences (PacBio®) 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. Until now, the standard protocol has had a long workflow that reduces your productivity.