Accel-NGS 2S Hyb DNA Library Kit for Illumina - 24 reactions Add to Cart
Select an indexing kit matching your hybridization capture technology:
||NimbleGen SeqCap EZ
||IDT xGen Lockdown Probes
NGS Prep for Hybridization Capture
Whole Exome Sequencing and specific gene panel targeted sequencing -
minimize duplicates, maximize sequencing data
• Compatible with all major capture technologies
• Validated for as low as 1 ng human DNA
• Sequential repair steps for damaged samples
• Compatiblity with low input cfDNA and FFPE samples
• Exceptional library prep efficiency and library complexity for deep sequencing
• Proprietary adapter attachment chemistry minimizes bias and supports low input
• Excellent evenness of coverage, balanced coverage of AT-/GC-rich regions
• Readily automatable
A variety of indexing kits allow for compatiblity with all major hybridization capture technologies:
- Agilent SureSelectXT and SureSelectXT2
- NimbleGen™ SeqCap™ EZ
- IDT® xGen® Lockdown® Probes
Go to the product line overview to choose the indexing kit for your application. For complete functionality of the kit an Indexing Kit is always required.
The Accel-NGS 2S Hyb kit is the right choice for users working with samples of limiting quantity or quality who are looking to take advantage of the sequencing cost savings associated with hybridization capture. The kit utilizes Illumina-compatible adapter sequences and has been validated on the MiSeq® and HiSeq® platforms.
Accel-NGS 2S Hyb Workflow:
Each step is color-coded to make the protocol easy to follow.
Clean-up beads are not provided with the kit, we recommend the SPRIselect™ Reagent Kit from Beckman Coulter.
- Girotti MR et al. (2016) Application of sequencing, liquid biopsies, and patient-derived xenografts for personalized medicine in melanoma. Cancer Discov. 6(3):286-299.
- Williamson SC et al. (2016) Vasculogenic mimicry in small cell lung cancer. Nature Communications 7:13322. doi:10.1038/ncomms13322.