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Welcome to the latest edition of DNA Dispatch, the quarterly newsletter from OGT, your hybridization experts.

Innovative research using OGT’s solutions is taking place all over the world

We’re showcasing a selection of publications* featuring OGT products that have caught our interest over the last month:

Cytogenomic characterization of pediatric T-cell acute lymphoblastic leukemia reveals TCR rearrangements as predictive factors for exceptional prognosis

The use of CGH arrays for identifying copy number variations in children with Autism Spectrum Disorder

ZNF217 gene copy number as a marker of response to standard therapy drugs according to ERα status in Breast Cancer

Combined tumor-based BRCA1/2 and TP53 mutation testing in Ovarian cancer

Innovative research using OGT’s solutions is taking place all over the world Image

Struggling to find the exact FISH probes you need?  Image

Struggling to find the exact FISH probes you need? 

At OGT, we are constantly updating our offering of CytoCell myProbes® with an expansive range of targets and fluorophores.

OGT at ACGS 2024

Re-defining the landscape for Myeloid Malignancies with new NGS panels from OGT

Watch Alex Hobbs, Account Manager at OGT, discuss the key features of our SureSeq™ Myeloid Fusion Panel and the benefits it can bring to your lab!

Re-defining the landscape for Myeloid Malignancies with new NGS panels from OGT Image

CytoSure helps further understand the genetic basis of Autism Spectrum Disorder Image

CytoSure helps further understand the genetic basis of Autism Spectrum Disorder

In this recent paper, researchers at the Polish Mother’s Memorial Hospital-Research Institute examined the role of copy number variations (CNVs) in Autism Spectrum Disorder (ASD) using CytoSure® arrays.

Involving 180 children aged 2-17, DNA analysis identified nine pathogenic and six likely pathogenic imbalances underscoring the importance of aCGH in understanding the genetic basis of Autism Spectrum Disorder.

OGT blog

Read our blog posts providing clarity on your most pressing NGS questions

NGS: Six top tips to improve your sequencing library. When it comes to next-generation sequencing (NGS), how do you ensure that what you put in is good enough to get the quality of results that you need

Summoning insights: NGS variant calling best practices. Differentiating between ‘true variants’ and ‘noise’ in sequencing data can present a challenge in clinical research, so what are the best practices for an accurate variant calling strategy?

What lies ahead: The future of Next Generation Sequencing. Next Generation Sequencing (NGS) is a transformative tool revolutionizing clinical and research fields alike so where might the future of NGS take us

Read our blog posts providing clarity on your most pressing NGS questions Image

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.