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

agilent oneseq chart


Contact us atTel: 65-6777 1886Fax: 65-6777 3090
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Visit us 237 Pandan Loop, #06-03 Westech Building, Singapore 128424