OneSeq:
Technology tailored to your specific needs

OneSeq harnesses the power of the SureSelect target enrichment platform to detect Copy Number Variations (CNVs) and Loss Of Heterozygosity (LOH) genome-wide, as well as SNVs and Indels in targeted regions in one streamlined assay.

• Reduce Cost: No need to invest in multiple technologies or perform deep WGS.
• Maximize Efficiency: Discover CNVs, LOH, SNVs, Indels, and aneuploidies in one NGS assay.
• Save Time: Accelerate sample to answer with one simple workflow and data analysis automation using SureCall Data Analysis Software.

Comprehensive Target Enrichment Panel for Genome-Wide Copy Number, LOH and Targeted Mutations - in ONE assay