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NEBNext Direct for target enrichment


NEBNext Direct® employs a unique technology that enables highly specific target enrichment of genomic regions of interest. The result of a partnership between New England Biolabs® (NEB®) and Directed Genomics™, this innovative approach to target enrichment balances the speed and precision of multiplexed PCR-based approaches with the content scalability typical of hybridization-based methods. This flexibility allows a single workflow for assays ranging from single gene tests to comprehensive panels including several hundred genes. Regardless of sample type or assay content, NEBNext Direct allows you to enrich your targets with precision. Read what other people are saying.

 

Advantages

  • Generate a higher percentage of your sequencing reads aligning to your targets
  • Obtain uniform sequencing of ALL targets, regardless of GC content
  • Save time with a streamlined workflow that couples enrichment and library preparation
  • Generate high quality libraries with limited input amounts and degraded DNA samples, including FFPE and ctDNA
  • Distinguish molecular duplicates, reducing false positive variants and improving sensitivity
  • On-bead sample preparation is ideal for automated workflows

 

Request More info or a free sample

 

NEBNext Direct Workflow


View our tutorial for help visualizing NEBNext Directs's unique and enabling workflow:
 

 

 

 

What People are Saying

 
"NEBNext Direct enrichment technology is by far the fastest and most automation friendly protocol available today. I can have samples on the sequencer in 6 hours starting from genomic DNA. The technology produces very high on target percentages (>90%) for even very small panels, and in combination with molecular barcoding produces low duplication rates. From an optimization perspective, NEBNext Direct enrichment allows me to assign individual captured fragments to a probe unambiguously, thus giving the opportunity for optimizing the coverage distribution of any target."

– Eric C. Olivares,   Founder, SEQanswers.com
 
"Using the NEBNext Direct kit, we were able to detect all known single nucleotide variants and indels in DNA extracted from fresh frozen or FFPE tissue derived from glioma biopsies. We could also clearly see amplification in genes like EGFR or PDGFR. The workflow is really easy and fast and can be rapidly implemented in a lab."
– Yannick Marie,   Sequencing Core Facility Manager,   Brain and Spine Institute (ICM)
 
"The kit and its technology are easy to use and easy to automate, allowing us to get up and running quickly. The protocol itself is fast and efficient to obtain deep coverage of targets, giving homogeneous results for FFPE and frozen tumors, therefore opening doors for customized panels."
– Francis Rousseau, Ph.D.   Director of Genomics for IntegraGen SA


 

Request: more information or a free sample
 

Please select the below option that best describes your laboratory (select only one)

  • Basic Research Laboratory
  • Translational Research Laboratory
  • Contract Research Organization
  • Clinical Diagnostics Laboratory
  • Other


Sample: Which NEBNext Direct panel would you like to sample? Each sample contains 8 reactions. (choose 1)

  • NEBNext Direct Cancer HotSpot Panel (E7000S)
  • NEBNext Direct BRCA1/BRCA2 Panel (E6627S)


What is the primary source of genomic DNA for which you expect you will be testing with the Cancer HotSpot Panel? (select all that apply)*

    • FFPE tissue
    • Whole blood
    • Fresh/frozen Tissue
    • Plasma (cell-free DNA)
    • Cell line
      Other


    Information: please send me information about the following products

    • NEBNext Direct Cancer HotSpot Panel (E7000S)
    • NEBNext Direct BRCA1/BRCA2 Panel (E6627S)
    • Customized Panels
       
    Mr *
    Ms *
    Mrs *



    *Mandatory fields

    This offer is valid in the BeNeLux countries only 
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