Comprehensive Target Enrichment Panel for Genome-Wide Copy Number, LOH and Targeted Mutations - in ONE assay
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.
No need to invest in multiple technologies or perform deep WGS.
Discover CNVs, LOH, SNVs, Indels, and aneuploidies in one NGS assay.
Accelerate sample to answer with one simple workflow and data analysis automation using SureCall Data Analysis Software.