A targeted NGS solution for streamlined tumor profiling and precision oncology

Presented by

Adeline Pek, MSc, MPharm, Medical Affairs Oncology, Liu Xi, MSc, Principal Scientist, Jo-Anne Penkler, MSc, Sr. Scientist

About this talk

In this webinar, we highlight 3 of these tools: - KAPA HyperPETE, a novel NGS target enrichment technology that combines the performance of hybrid-capture target enrichment with the speed and simplicity of amplicon workflows. KAPA HyperPETE is optimized to detect all major somatic variants—including SNVs, short indels, CNVs, MSI status, and known and novel fusion transcripts—in cfDNA, FFPET, and RNA samples. - NAVIFY Mutation Caller*, a cloud-based standalone secondary analysis software for NGS that analyzes raw sequencing data from KAPA HyperPETE to identify variants - NAVIFY Mutation Profiler, a tertiary analysis and reporting solution for NGS that works in conjunction with NAVIFY Mutation Caller to help labs accurately and efficiently interpret the biological significance of mutations Research Use Only. Not for use in diagnostics procedures. *Product in development. Not for sale in the United States. In the US, NAVIFY Mutation Profiler, and NAVIFY Mutation Caller are for Research Use Only. Not for use in diagnostics procedures. Presented by: MC-US-10274
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Next-generation sequencing (NGS) is driving advances in translational and clinical research. From expanding our understanding of cancer, reproductive and developmental biology to unravelling complex microbial populations, NGS is touching all facets of human disease and well­being. Sample prep for NGS holds the key to unlocking the potential of every sample. Explore our integrated Roche Sample Preparation Solutions, encompassing all the steps required to convert a sample to a sequencing-ready library. From sample collection to library quantification, we offer sample prep solutions for different sample types and sequencing applications that are proven, simple, and complete.