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.
NGS library prep for hybridization capture
Optimal sequencing of your cfDNA, FFPE and ChIP DNA
Optimal sequencing of your cfDNA, FFPE and ChIP DNA
The Accel-NGS 2S MID Indexing Kits have been designed, optimized, and validated for use withAccel-NGS 2S DNA Library Kits on Illumina platforms, and aid in low frequency variant detection, as well as accurate de-duplication of single read sequencing and sequencing from samples with non-random fragmentation. Get the most out of your NGS sequencing data with this powerful tool. Improve detection of low frequency alleles Identify unique library molecules Retain more sequencing data Designed for exome sequencing Compatible with circulating, cell-free DNA Supported DNA Sequencing Applications: Whole exome sequencing (WES) Deep targeted sequencing Cell-free DNA sequencing Single-end sequencing, such as ChIP-Seq
PCR-free NGS prep with highest library diversity, lowest inputs
PCR-free NGS prep with highest library diversity, lowest inputs
NGS library prep for hybridization capture
