Swift Accel-NGS® 2S Hyb DNA Library Kit (96 reactions)
NGS library prep for hybridization capture
Accel-NGS® 2S Hyb DNA Library Kit
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Minimize duplicates, maximize sequencing data. 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.
Benefits include:
- Validated as low as 1 ng human DNA
- Sequential repair steps for damaged samples
- Compatiblity with low input cfDNA and FFPE samples
- Increased library complexity. Balanced coverage of AT-/GC-rich regions
The right choice for users with samples of limiting quantity or quality who are looking to take advantage of the sequencing cost savings associated with hybridization capture.
Accel-NGS® 2S DNA Library Kits
The application notes provides an overview of Accel-NGS® 2S DNA Library Kits. Accel-NGS 2S DNA Library Kits produce high quality libraries with an all-inclusive, easy-to-use format. Applications of the Library Kits, including use in sequencing liquid biopsy samples and Pico-Scale ChIP-Seq are also covered.
Understanding NGS Intricacy and Single-Cell Sequencing
The application note describes the sequence coverage performance and preservation of molecular complexity of next generation sequencing (NGS) libraries, generated from human and microbial genomic DNA using Accel-NGS® 2S DNA Library Kits for whole-genome sequencing (WGS) on the Illumina® platform. Comparisons to the leading commercially available methods are also presented.
Accurate De-Duplication of Sequencing Data with New Molecular IDs from Swift Biosciences
Kate Cunningham, PhD, Applications Scientist at Swift Biosciences, introduces the new range of molecular IDs for Accel-NGS® 2S library kits. Hear how the molecular IDs label each individual library molecules, to enable low frequency variant detection, as well as accurate de-duplication of single read sequencing and sequencing from samples with non-random fragmentation. The technology is ideal for applications including whole exome sequencing (WES), deep targeted sequencing, cell-free DNA sequencing and ChIP-Seq.
Advances in Sequencing Technology Facilitate Gene Expression Analyses at the Epigenomic Level
Three leading scientists discuss their research and the benefits of ChIP-Sequencing
Effective Library Preparation for NGS Analysis of Liquid Biopsies at Cancer Research UK Manchester Institute
Using circulating cell-free DNA to analyze pancreatic cancer
