OGT launches first Fusion MRD NGS Panel for acute myeloid leukaemia

New RNA-based NGS panel helps to detect, analyze and track high-impact AML-associated fusion events across multiple timepoints

27 Oct 2026
OGT launches first Fusion MRD NGS Panel for acute myeloid leukaemia

OGT has launched the SureSeq™ myPanel Myeloid Fusion MRD Panel, the first-to-market dedicated fusion MRD next-generation sequencing (NGS) panel for acute myeloid leukaemia (AML).

Genomic AML workflows traditionally cover only part of the genomic landscape, with important fusion events being potentially undetected. This new myPanel, a custom SureSeq NGS panel, developed in collaboration with Roswell Park Comprehensive Cancer Center using the myPanel custom service, enables the detection of AML-associated fusion events and identifies MECOM expression levels at MRD-level sensitivity, generating broader fusion insights for AML sample cohorts in a single assay.

In an initial study of clinical research samples, carried out at Roswell Park Comprehensive Cancer Center, the SureSeq myPanel Fusion MRD NGS workflow was shown to detect key disease-associated fusion events, including BCR::ABL1 and PML::RARA in serial dilutions as low as 1% tumor cells.

“The addition of RNA fusion detection represents an important opportunity to broaden the reach of molecular MRD assessment to the approximately 20–25% of AML cases associated with fusion-driven disease," said Dr Sean Glenn, Director of the Advanced Molecular Diagnostics Laboratory, Roswell Park Comprehensive Cancer Center.

“By providing molecular markers of residual leukaemia that can be monitored over time, fusion transcripts can support residual disease assessment, including in samples that lack an informative DNA mutation.”

As part of the end-to-end SureSeq NGS workflow, OGT’s complimentary NGS analysis software, Interpret, allows laboratories to analyze, track and visualize variants, including fusion events, across multiple timepoints within a single software environment. Available through cloud and local installation options, and with options for integration of third party tools including QIAGEN Clinical Insight (QCI®) Interpret, clinical researchers can easily follow AML disease dynamics and generate key genomic insights from their NGS data.

The launch reflects OGT’s commitment to creating genomic solutions for scientists, by scientists. The SureSeq myPanel Myeloid Fusion MRD Panel can be used as a standalone assay for fusion event detection or used alongside the SureSeq Myeloid MRD Plus NGS Panel for broader MRD characterization.

Together, these panels support MRD-level detection of SNVs, indels, ITDs and fusion events in AML samples, enabling researchers to expand the range of detectable variants without relying on multiple single-analyte assays.

Adrian Smith, CEO at OGT, said, “We’re proud to launch the first dedicated Fusion MRD NGS panel for AML that empowers laboratories with a focused tool to detect, analyze and track fusion events at MRD-level sensitivity. Used independently or alongside our SureSeq Myeloid MRD Plus NGS Panel, this panel has the potential to capture a wide range of disease-associated fusion events at MRD-levels of sensitivity that may otherwise be missed, and thus provides a broader genomic profile of AML samples for deeper insights.”

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Next-Generation SequencingNext-generation sequencing (NGS), also known as whole-genome sequencing, high-throughput sequencing and massive parallel sequencing, produces and analyses thousands to millions of nucleotide sequences at once. Sequencing systems operate via varying technologies depending on the manufacturer, including sequencing by synthesis, ligation, pyrosequencing, ion semiconductor and single-molecule real-time sequencing. For NGS, library preparation is paramount to successful sequencing. In this section, explore a range of library preparation kits, from targeted, amplicon-based or hybridization-based kits including epigenomic, transcriptomic and genomic workflows to fragmentation kits. Find the best next-generation sequencing products in our peer-reviewed product directory: compare products, check customer reviews and receive pricing direct from manufacturers.Acute Myeloid LeukemiaGenomicsGenomics is the study of genomes, focusing on the sequencing, analysis, and interpretation of genetic material. It is key in understanding genetic diseases, evolutionary biology, and personalized medicine. Techniques like next-generation sequencing (NGS) are commonly used in genomics research. Browse our peer-reviewed product directory to find the best genomics tools, compare products, check reviews, and get pricing directly from manufacturers.Cancer ResearchCancer research aims to understand the mechanisms of cancer development and progression to improve prevention, diagnosis, and treatment. From molecular biology to clinical trials, research spans a wide range of disciplines, including immunotherapy, targeted therapies, and drug discovery. Explore the best cancer research products in our peer-reviewed product directory; compare products, check reviews, and get pricing directly from manufacturers.Cancer DiagnosticsThere are a wide variety of diagnostic tests for cancer available, and this range continues to expand as our knowledge of cancer improves. Current diagnostic methods include biopsy, imaging and blood tests for known biomarkers. New methods in research development include liquid biopsies and cancer breathalyzers.

Frequently asked questions

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What is OGT’s SureSeq myPanel Myeloid Fusion MRD Panel?

It is the first-to-market dedicated fusion measurable residual disease (MRD) next-generation sequencing panel for acute myeloid leukaemia (AML). Developed with Roswell Park Comprehensive Cancer Center, it detects AML-associated fusion events and identifies MECOM expression levels at MRD-level sensitivity in a single assay.

Which AML fusion events can the SureSeq Fusion MRD NGS workflow detect?

In an initial study of clinical research samples at Roswell Park Comprehensive Cancer Center, the workflow detected key disease-associated fusion events, including BCR::ABL1 and PML::RARA, in serial dilutions containing as little as 1% tumor cells.

How does OGT’s Interpret software support AML MRD analysis?

OGT’s complimentary Interpret NGS analysis software enables laboratories to analyze, track and visualize variants, including fusion events, across multiple timepoints. It offers cloud and local installation options and can integrate third-party tools such as QIAGEN Clinical Insight (QCI) Interpret, helping researchers follow AML disease dynamics and generate genomic insights.