SureSelect Cancer Tumor-Specific Assays
SureSelect Cancer Tumor-Specific assays offer genomic profiling for solid tumors from lung, colon, pancreas, kidney, or bladder tissue, to detect single nucleotide variants (SNVs), copy number variants (CNVs), insertions/deletions (indels), and translocations (TLs). These small cancer panels enable affordable tumor genomic profiling.
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Powered by SureSelect XT HS2 library preparation and target enrichment reagents, the assays feature fast hybridization, low sample input, enzymatic fragmentation, and a one-day workflow to generate NGS sequencing-ready libraries. Automation options reduce hands-on time to maximize lab efficiency.
For Research Use Only. Not for use in diagnostic procedures.
- Small cancer panels of approximately 50 genes each for lung, colon, pancreas, bladder, and kidney, based on subsets of gene content from the SureSelect Cancer CGP assay
- Compatibility with low throughput sequencers (Illumina MiSeq and MiniSeq) for lower cost tumor genomic profiling
- Globally curated, clinically relevant biomarker content
- Walkaway convenience using the benchtop Agilent Magnis NGS Prep system with only 15-min hands on time
- For gene fusion detection, modular workflow allows the option to combine a SureSelect Cancer Tumor-Specific DNA assay with the SureSelect Cancer CGP RNA assay (80 genes) together in the same sequencing run
- Start with input as low as 10 ng DNA (recommended 50 ng) to enable profiling of more samples
- Fast hybridization (90 minutes) for library preparation in a single day
- Flexible data analysis options, including Agilent Alissa, customer in-house, and third-party software
