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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.

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.


Technology tailored to your specific needs

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For Research Use Only. Not for Use in Diagnostic Procedures