The New Exome V8

Ignite Something that Lasts

How will your exome studies impact future generations?

Your exome research can ignite inspiration.

We have been with you on your exome journey since the beginning. With the new SureSelect Human All Exon V8 panel, we are continuing to support your journey and help you impact the future. Explore the advantages of the latest edition.

Your exome research can impact the future.

The SureSelect Human All Exon V8 is part of a seamless exome sequencing solution that enables labs to focus on their inspired research. Recent advancements include:

Probe printings that target both DNA strands to minimize base-specific biases
Intelligent probe selection and placement to deliver improved performance and efficiency
Probes that target the protein coding regions from CCDS, RefSeq, and GENCODE to ensure you have the most up-to-date content
Deeper and more uniform coverage across targeted regions, delivering confident variant calls
Option to include UTRs, clinical, and customized content for enhanced utility
Natively automated to provide high throughput and rapid workflow solutions for any genomics lab
Seamlessly integrated with the Agilent Alissa Interpret Informatics platform for efficient and optimized variant analysis and reporting

The SureSelect Human All Exon V8 datasheet highlights key performance metrics.

Performance that inspires.

Spanning a 35.1 Mb target region of the human genome, the SureSelect Human All Exon V8 delivers comprehensive and updated coverage of the protein-coding regions from RefSeq, CCDS, and GENCODE. Explore the datasheet for mapping metrics, including uniformity and on-target rate, plus learn how the new probe design reduces GC dropout.

Instant access

Customer Testimonials

"Our initial evaluation of SureSelect Human All Exon V8 indicates that its uniformity of coverage is better than exomes from other vendors. With this significant improvement, we believe that we will be more confident with our CNV analysis on the Exome data." – Medical genetics laboratory at a university hospital in France.

“The first run showed that SureSelect Human All Exon V8 libraries prepared using the Magnis Dx NGS Prep System provide highly uniform coverage, and the quality of the reads meets our expectations. We are convinced that this solution will enable us to achieve automation of exome library preparation in our laboratory and in the near future, we will test also for DNA custom panels.” – Rare disease genetics laboratory at a university hospital in France.

For Research Use Only. Not for use in diagnostic procedures.

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