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.
Discover moreFeaturing the new constitutional NGS platform for cytogenetic research, alongside a broad range of arrays for rare disease and cancer research.
Discover moreChoose from preloaded NGS panels for hematological and solid tumor cancer research or we can help you create your own.
Discover moreThe 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.
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%.
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.
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.
Ultra-low variant detection (including very large FLT3-ITDs) enables a stronger characterization of a sample’s current AML status.
ReadImproving upon existing SureSeq™ technology, this latest SureSeq NGS panel unlocks more efficient and expansive genetic profiling for CLL samples
ReadEnables users to replace multiple techniques with a single streamlined NGS process for faster results.
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