SureSelect Cancer Custom Panels
RUO
Rapidly design your NGS panels for tumor genomic profiling to fit your specific requirements, including incorporation of new and emerging biomarkers. Leverage the curated content of the SureSelect Cancer CGP and Tumor-Specific catalog DNA panels to add or subtract gene content in the SureDesign web portal.
Powered by the SureSelect XT HS2 library preparation and target enrichment workflows featuring 90-min hybridization, NGS libraries can be generated from low input DNA in less than a day. Perform robust and confident detection of somatic variants (SNVs, indels, CNVs, DNA translocations), TMB, MSI, and HRD.
Powered by the SureSelect XT HS2 library preparation and target enrichment workflows featuring 90-min hybridization, NGS libraries can be generated from low input DNA in less than a day. Perform robust and confident detection of somatic variants (SNVs, indels, CNVs, DNA translocations), TMB, MSI, and HRD.
For Research Use Only. Not for use in diagnostic procedures.
Product Details
Features
- Guided, easy-to-use design process using SureDesign software
- Flexibility to design a range of custom panel sizes (1 Kb to 24 Mb)
- Start with globally curated gene content from SureSelect Cancer catalog DNA panels (SureSelect Cancer CGP panel, SureSelect Cancer Tumor-Specific panels) predefined in SureDesign software
- Easily include content for TMB and MSI assessment
- Automations options with scalability and as little as 15 minutes hands-on time
- Combine with SureSelect Cancer CGP RNA assay (80 genes) for gene fusion detection
- Enzymatic fragmentation option eliminates the need for physical shearing equipment
- 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, with rapid turnaround time to results
- Compatible data analysis options with customer in-house informatics and third-party analysis software
