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.