Superior Data from a Wide Range of RNA Inputs
The Swift RNA Library Kit offers a fast, robust NGS transcriptomics workflow with optimal transcript coverage and NGS data quality from a broad range of input quantities for Illumina® sequencing platforms. Leveraging patented Adaptase® technology, this kit enables stranded RNA library construction directly from 1st strand cDNA without the requirement for 2nd strand cDNA synthesis and degradation, or template-switching methods.
Accelerate Your RNA-Seq Discovery
The Swift Rapid RNA Library Kit offers the fastest, lowest cost NGS transcriptomics workflow for Illumina® sequencing platforms. Leveraging patented Adaptase® technology, this kit enables stranded RNA library construction directly from 1st strand cDNA without the requirement for 2nd strand cDNA synthesis and degradation, or template-switching methods.
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.
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.
Now compatible with indexing by PCR and indexing by ligation for both DNA and RNA library prep workflows
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.
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%.
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..
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 gold standard for single-base resolution of methylomes
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.
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.