Pattern illustration of DNA helix with a yellow background and ATCG bases graphic for the SureSeq NGS product range.

Discover SureSeq's innovative NGS solutions

Developed by scientists, for scientists, experience the superior hybridisation-based approach of OGT's SureSeq™ portfolio for haematology, solid tumour and constitutional cytogenetics, with pre-designed and custom NGS solutions optimised for the enhanced detection of low-frequency SNVs and indels, as well as complex structural aberrations such as ITDs, PTDs, CNVs, LOH and translocations.

Discover the efficiency of streamlined next generation sequencing (NGS) workflows and unlock clinically relevant insights

  • Unlock more comprehensive genomic profiling of your samples our highly sensitive bait designs effortlessly achieve high coverage uniformity minimising the risk of missing low-frequency variants
  • Reduce assay times and speed up your lab’s sample-to-result process with our streamlined workflow for faster sample insights
  • Experience our quality-driven customisation service to tailor our panels to your specific targets of interest, so you can ensure maximal efficiency for your data generation
Next generation sequencing (NGS) laboratory scientist studying a FlowCell.

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ready-to-order pre-designed NGS panels

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expert-curated, pre-optimised genes for cancer

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day streamlined hybridisation-based NGS workflow

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years' experience developing NGS products

What our customers say about SureSeq...

Have a question or want to know more about our SureSeq NGS products?

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