These enrichment-based next-generation sequencing (NGS) reagents enable simultaneous analysis of DNA and RNA, and can cover a wide range of cancer variant types. This methodology provides laboratories with a deep view into the genetics of cancer.
Analysis of TruSight Oncology 500 data with PierianDx Clinical Genomics Workspace Software
Brochure | PDF < 1 MB
TruSight Oncology 500 Demo Program Flyer
Brochure | PDF < 1 MB
Analysis of TMB and MSI Status with TruSight Oncology 500
Application note | HTML
Optimizing RNA input to detect gene fusions with TruSight Oncology 500 High-Throughput
Technical note | PDF < 1 MB
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