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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

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Contact us atTel: (66) 02 080 5663 Fax: (66) 02 116 7676
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Visit usPathumwan, Bangkok 10330, Thailand