Accel-NGS® 2S Hyb DNA LIBRARY KITS

Next-Generation Sequencing Prep for Hybridization Capture

Swift Accel NGS 2S Hyb

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. A variety of indexing kits allow for compatibility with multiple hybridization capture technologies: Agilent SureSelect, NimbleGen SeqCap EZ, and IDT® xGen®Lockdown® Probes. 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.

Features:

  • Sequential repair steps
  • Superior library preparation efficiency
  • Exceptional library complexity
  • Balanced coverage of AT-/GC-rich regions
  • No adapter titration or heat steps involved

Benefits:

  • 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
  • Readily automatable

Frequently Asked Questions →

PLACE ORDER

First, select a product and quantity:

Next, an Indexing Kit is required for complete functionality. Please select from the following:

Accel-NGS 2S Single Indexed Adapters 96-PLEX

Accel-NGS 2S Single Indexed Adapters with MIDs

Accel-NGS 2S Dual Indexed Adapters 768-PLEX

Accel-NGS® Unique Dual Indexing Kit

For Agilent SureSelect Target Enrichment, choose:

For NimbleGen SeqCap EZ Target Enrichment, choose:

For IDT xGen Lockdown Probes, choose:

The below solutions are included with your Library Kit. If you require extra, please add now:

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For Customers Outside the United States: Please request a quote or select from our list of distributors.

DATA SHEET
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SCIENTIFIC POSTER (AACR 2018)
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WORKFLOW
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PERFORMANCE DATA
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PROTOCOLS, TOOLS & TECHNICAL NOTES
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BUNDLE WITH SWIFT HYBRIDIZATION CAPTURE KITS & NORMALASE

Swift Hybridization Capture Kits
Swift Normalese Normalization Kits

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