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Experience the new SureSeq Myeloid MRD Panel, for ultra-low variant detection enabling stronger characterization of your sample's AML status

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Includes FDA-cleared Class II IVD FISH Probe Kits for AML and MDS, along with over 150 ASR FISH probes. Custom FISH probes and ancillary products also available.

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Featuring the new constitutional NGS platform for cytogenetic research, alongside a broad range of arrays for rare disease and cancer research.

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Choose from preloaded NGS panels for hematological and solid tumor cancer research or we can help you create your own.

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Ultra-low variant detection down to 0.05% VAF

SureSeq Myeloid MRD NGS Panel

The highly targeted SureSeq Myeloid MRD Panel enables the detection of 13 key AML MRD-associated biomarkers to provide a more comprehensive picture of the current AML status of your samples. Key targets include very large, ultra-low frequency FLT3-ITDs (even up to 300 bp) that are traditionally challenging to detect. The streamlined, guideline-driven panel content expands on OGT customer’s MRD detection capabilities to deliver a better understanding of the current AML status, and ensures genomic insights are not missed.

Graph showing example coverage profile of target regions in the SureSeq Myeloid MRD Panel, including NPM1 exon 11.

For deeper insights into CLL progression

SureSeq CLL + CNV V3 NGS Panel

Improving upon existing SureSeq technology, this latest SureSeq NGS panel unlocks more efficient and expansive genetic profiling for CLL samples. The figure (right) illustrates the panel's uniformity and high depth of coverage, allowing the confident detection of [A] a SF3B1 exon 15 hotspot variant Lys700Glu with 4.8% allele frequency and [B] a TP53 exon 4 frameshift deletion (TP53 c.124del) with frequency 38.9%.

NGS software data showing detection of a SF3B1 exon 15 hotspot variant Lys700Glu and a TP53 exon 4 frameshift deletion.

New high-quality ASR solid tumor FISH probes

CDKN2A / 3 alpha satellite / 7 alpha satellite / 17 alpha satellite

The CDKN2A Probe covers CDKN2A (P16) gene and flanking regions, and is labeled in gold. The Centromere 17 Probe covers the chromosome 17 centromere (D17Z1) region and is labeled in aqua. The Centromere 3 Probe covers the chromosome 3 centromere (D3Z1) region and is labeled in red. The Centromere 7 Probe covers the chromosome 7 centromere (D7Z1) region and is labeled in green.

Fluorescence in situ hybridization (FISH) microscope images of CDKN2A, 17 centromere, 3 centromere and 7 centromere probes.

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What binds us, makes us.

We believe that collaboration is key to improving patient lives. By sharing our knowledge and expertise, we ensure that we move forward with our customers, bound by a collective commitment to unlocking the future of genetic clinical care. See our story.

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Latest OGT news

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OGT delivers superior MRD detection capabilities with new SureSeq Myeloid MRD Panel Image

OGT delivers superior MRD detection capabilities with new SureSeq Myeloid MRD Panel

22 Jan 2025

Ultra-low variant detection (including very large FLT3-ITDs) enables a stronger characterization of a sample’s current AML status.

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OGT unveils the enhanced SureSeq CLL + CNV V3 Panel for deeper insights into CLL progression Image

OGT unveils the enhanced SureSeq CLL + CNV V3 Panel for deeper insights into CLL progression

02 Dec 2024

Improving upon existing SureSeq™ technology, this latest SureSeq NGS panel unlocks more efficient and expansive genetic profiling for CLL samples

Read
OGT launches new SureSeq Myeloid Fusion Panel to help drive advances in myeloid cancer research   Image

OGT launches new SureSeq Myeloid Fusion Panel to help drive advances in myeloid cancer research

30 Apr 2024

Enables users to replace multiple techniques with a single streamlined NGS process for faster results.

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