Welcome to the latest edition of DNA Dispatch, the quarterly newsletter from OGT, your hybridization experts.
We are excited to be attending the AMP 2024 Annual Meeting and Expo in Vancouver, Canada!
Visit us at booth #820 where our experts will be around to chat about our full range of CytoCell® FISH probes, CytoSure® arrays and SureSeq™ NGS panels which give you the clearest insights into hematological malignancies.
At OGT, we know it can sometimes be difficult to find the exact FISH probe you need for your workflow. Our myProbes® service delivers high quality, fully quality-assured custom FISH probes for virtually any sequence in the entire human genome.
And we are constantly updating our offering of CytoCell myProbes with an expansive range of targets and fluorophores. Check out some of our latest additions to the myProbes catalog...
OGT delivers innovative hematological malignancy NGS solutions, enabling labs to streamline their workflows and unlock clinically relevant insights.
See how leading labs leverage OGT’s NGS panels for targeted genomic profiling across the world at their posters during AMP 2024.
Watch Alex Hobbs', Account Manager (UK South) at OGT, presentation from ACGS 2024 that highlights how your lab can achieve more accurate sample classification with the SureSeq Myeloid Fusion Panel.
In his presentation he provides an overview of how you can simultaneously interrogate multiple baited target fusions to enhance your sample classification and reliably detect MECOM overexpression to support the identification of GATA2::MECOM translocations
Get to know the SureSeq Myeloid Fusion NGS Panel today...
When FISHing, high background fluorescence is more than just a nuisance – it’s a significant issue that obscures critical data, complicates interpretation and may result in erroneous conclusions.
In this blog, we cover key areas including sample preparation and hybridization conditions.
Learn how to combat high background fluorescence in your FISH assays with our inside tips today...
Our CytoSure arrays are used in a variety of clinical research applications*, ranging from validation of novel genome mapping methods to investigating intragenic deletions and duplications.
CytoSure arrays are available in a variety of different formats for different targets and can be customized to meet your research needs.
Don’t forget…Our FAS team can be contacted online with free support advice
*Providing links to these publications is intended for educational purposes only and does not replace independent professional judgment. Statements of fact and opinions expressed are those of the publications’ authors and, unless expressly stated to the contrary, are not the opinion or position of the Oxford Gene Technology Group (OGT). OGT does not endorse or approve, and assumes no responsibility for, the content, accuracy or completeness of the information presented in these publications.
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