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KAPA HyperExome

RocheAvailable: United States

Efficient, and uniform hybridization-based capture for Whole Exome Sequencing 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).

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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

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