Focus your CLL analysis with help from OGT

SureSeq™: For Research Use Only. Not for Use in Diagnostic Procedures.

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Transition your CLL CNV analysis into the molecular era

Are you running multiple assays to obtain a comprehensive genetic profile of your CLL specimen?

OGT’s hybridization experts are here to help you streamline your CLL research into one NGS assay.

SureSeq™ CLL + CNV NGS panel investigates a wide variety of chromosomal abnormalities associated with CLL, ranging from SNVs & indels up to large copy number variations (CNVs), including trisomies.

Got a minute? Watch the video

SureSeq™: For Research Use Only. Not for Use in Diagnostic Procedures.

Privacy Policy © Oxford Gene Technology IP Limited – 2022. All rights reserved.