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OGT’s response during COVID-19 outbreak
During these unprecedented times, OGT remains committed and ready to support you...
Thinking of switching your constitutional ID and DD analysis from aCGH to NGS?
The CytoSureTM Constitutional NGS solution delivers robust CNV analysis down to single-exon level and loss of heterozygosity (LOH) as well as SNV and indel detection, all in a single assay. Find out more
OGT’s transformative CytoSure NGS panel for constitutional disorders has been profiled in GenomeWeb – read more about this exciting new solution
Streamline your CLL analysis and alleviate the burden of running multiple assays
In addition to SNVs and indels, the SureSeq™ CLL + CNV Panel also accurately detects small and large CNVs, trisomy 12 and LOH, to obtain a more complete understanding of the genetic makeup of your CLL research samples in a single NGS assay.
Cytocell® FISH Probes for AML and MDS Poster
This poster provides a quick guide to abnormal results expected from our line of FDA-cleared FISH probes for AML and MDS.
NGS software with array users in mind
We understand that making the change from aCGH to NGS is a daunting prospect, particularly when it comes to data analysis.
That’s why we’ve developed Interpret NGS analysis software for use in conjunction with the CytoSure Constitutional NGS panel for constitutional cytogenetics research.
Considering switching your CLL CNV and LOH analysis to an NGS panel?
Presented at AMP 2019, this poster demonstrates the capability of the SureSeq CLL + CNV panel to overcome the challenges of detecting CNVs in CLL samples.
New Video now available: CytoSure Interpret™ Software – Case Status
Learn how to track the progress of a case in the Case Status field. The video details the various stages, transitioning between them and how the function can be used to search for samples in database management.
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