Minimize Duplicates, Maximize Sequencing Data
The Accel-NGS 2S Hyb DNA Library Kit, designed for Illumina® platforms, produces 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: Swift Hybridization Capture Kits, IDT® xGen®Lockdown® Probes, Twist Human Core Exome Kit and Agilent SureSelect. This kit is the right choice for researchers working with applications pertaining to low input FFPE DNA or whole genome sequencing of liquid biopsy and cfDNA samples.
Sequential repair steps
Superior library preparation efficiency
Exceptional library complexity
Balanced coverage of AT-/GC-rich regions
No adapter titration or heat steps involved
Compatibility with limiting FFPE and cfDNA samples
More unique molecules available for capture
Meaningful data from low input samples
Suitable for a diverse set of panels
Accel-NGS 2S DNA Library Kits produce high quality libraries
with an all-inclusive, easy-to-use format. The kits contain all
reagents necessary to build high complexity libraries from a
wide range of input quantities and a variety of sample types,
including microbial samples, FFPE, and cell- free DNA (cfDNA).
They can be used for PCR-free whole genome sequencing and
ChIP-Seq, as well as targeted sequencing by hybridization
capture. The Accel-NGS 2S Kits have been optimized for use
with sample indices (barcodes) for multiplex sequencing, as
well as with molecular identifiers (MIDs), which are used to filter
duplicates during data analysis.