Bridging the Gap

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The SureSelect Human All Exon V6 is a high performing design that targets updated content, including challenging regions, from the databases relevant to both the clinical and translational researchers. Optimized bait selection and boosting enables highly uniform coverage of the exome and each individual targeted exon. This improvement helps address the current observation of the inverse correlation between depth of coverage and breadth of coverage providing balanced coverage, maximizing variant information output for per exome sequenced.

Most comprehensive content, an exome solution for every application
  • Up-to-date core content from relevant databases, targets more genes/ exons including hard-to-capture regions
  • Easily add UTRs for translational research, COSMIC for cancer research or custom content for specific applications

Deep and complete target coverage for definitive answers
  • Highly optimized design for superior coverage and uniformity
  • Increased breadth of coverage of targeted regions

Complete and flexible solutions from sample to data
  • Compatible with SureSelect workflows for faster time to results
  • Solutions from design, library prep, sample QC, automation and data analysis

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For Research Use Only. Not for Use in Diagnostic Procedures
NGS Constitutional Disease Research Resource Center

This NGS Resource Center
contains a tremendous amount
of useful material to help you
get the most out of your NGS
solution when it comes to
Clinical research on
Constitutional Diseases!
NGS Brochure

Enabling your Success with Agilent
Next Generation Sequencing
Complete Solutions
Technical Information

Download the SureSelect Human
All Exon V6 datasheet and learn
more about the technology

Store Type: Genomics