Cancer research products
Find kits and reagents that enable researchers to identify genomic changes in cancer, from somatic variants to gene fusions, epigenetic alterations, and more.
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Illumina Complete Long Read Prep, Human | Highly Comprehensive Long-Read WGS
Highly accurate, high-performance full workflow solution for comprehensive human WGS with long-read data from NovaSeq platforms.
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TruSight Oncology 500 ctDNA v2 | Enable CGP from ctDNA in blood plasma
Enable CGP with a pan-cancer panel capable of detecting key IO gene signatures (TMB, MSI) plus all main variant classes from ctDNA in blood plasma.
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NGS-based cancer sequencing methods provide more information in less time compared to single-gene and array-based approaches.
Access a broad range of fixed and custom next-generation sequencing panels targeting known cancer-related gene variants.
Our sequencing and microarray technologies support a broad range of cancer genomics research applications, from DNA to RNA analysis, epigenetics, and more.