Based on primer extension technology, KAPA HyperPETE technology provides a single workday workflow for target enrichment. The integrated end-to-end offering makes for more efficient and effective processes, enabling you to shift your focus to what matters most. Providing both catalog or custom panels with an integrated analysis solution (NAVIFY® Mutation Caller), KAPA HyperPETE Workflow is especially suited for small panel oncology research applications.
High uniformity for better sequencing efficiency with less optimization
Single day workflow by shorter incubations and reduced hands-on-time
Custom design expertise enables access to difficult genomic regions
Suitable for small panel oncology research applications, KAPA HyperPETE catalog panels have been optimized for somatic oncology research workflows and provide precise variant calling for SNV, CNV, indels, fusions and MSI. The KAPA HyperPETE Workflow offers integrated secondary analysis provided by NAVIFY® Mutation Caller.
Learn moreKAPA HyperPETE Choice and KAPA HyperPETE Explore Panels enable custom panel design up to 250Kb for DNA inputs and 50Kb for RNA inputs. Based on Roche’s renowned design and content expertise, our workflow is specifically optimized for small design sizes and validated to detect all major mutation classes. The KAPA HyperPETE Workflow offers integrated secondary analysis provided by NAVIFY® Mutation Caller.
Learn moreStreamlining every step of the process from pipetting to purchasing, Roche Sample Prep Solutions encompass all the steps required to convert a sample to a sequencing-ready library. From sample collection to library quantification, we offer integrated workflow solutions for different sample types and sequencing applications that are proven, simple and complete.
KAPA HyperPETE Workflow | KAPA HyperCap Workflow | Amplicon-based workflow | |
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Performance |
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Technology | Primer Extension Target Enrichment | Hybridization-based capture | PCR amplification |
Turnaround time | Single day | 1.5 days | Single shift |
Panel size | Up to 250 Kb | Up to Whole Exome and beyond | Up to a few megabases |
Applications |
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Secondary analysis support |
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Various vendor offerings
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