Combining more than a decade of probe-design experience with an improved probe-manufacturing process, the new KAPA HyperExome probe pools enable efficient, uniform hybridization-based capture for Whole Exome Sequencing (WES). Achieve sensitive, reliable detection of genomic alterations, including single-nucleotide variations (SNVs), indels, copy-number variations (CNVs), gene fusions, inversions, and other rearrangements within exonic regions.
- Reduce sequencing costs and save time through superior capture uniformity that lowers the amount of sequencing required to detect variants
- Reliably enrich challenging, previously inaccessible exonic regions
- Ensure accurate sample identification with 387 sample-tracking SNPs
- Streamline targeted sequencing with our HyperCap Workflow v3, driven by KAPA HyperPrep or KAPA HyperPlus Library Prep Kits