Solutions to enable CGP using tissue or liquid biopsy samples
The TruSight Oncology product family includes in vitro diagnostic (IVD) and clinical research solutions for solid tumor genomic analysis. Maximize insights by consolidating multiple iterative tests into one assay to assess DNA and RNA* biomarkers across more than 500 genes. Keep samples local and save time with testing in your own lab.
Integrated, sample to report IVD workflow enabling labs to interrogate both DNA and RNA content from FFPE tissue samples in ~5 days. Generate a comprehensive genomic profile (CGP) of a patient's tumor and improve chances of identifying a targeted therapy based on the latest clinical guidelines.
Multiple assay configurations enable labs to perform in-house CGP using solid tumor tissue or circulating tumor DNA (ctDNA) in blood plasma for research. Similar content and workflow design across an innovative portfolio of products enable labs to consolidate platforms for more streamlined in-house operations.
*RNA variants are not included with TruSight Oncology 500 ctDNA v2 assays.
†For In Vitro Diagnostic Use. Not available in all regions and countries.
As an industry leader in NGS with 25+ years of innovation, you can rely on Illumina as your preferred provider of CGP solutions. As a single supplier with expertise across the entire workflow—from library preparation to sequencing through bioinformatics—Illumina can help you efficiently enable CGP in your lab. The Illumina portfolio provides a variety of options tailored to meet the needs of your institution.
Contact an Illumina representative to learn more about the TruSight Oncology product line and find the right solutions for your needs.