Oxford, UK – 16 July 2015. OGT, The Molecular Genetics Company, has made its European Human Genetics (ESHG) Conference workshop freely available to view online. The presentation, entitled ‘The Next Generation of Microarrays: Identifying a Broader Range of Genetic Syndromes Using Exon–Focussed Array Designs’, took place at the ESHG conference in Glasgow, UK on 8th June 2015. OGT also launched its CytoSure® Constitutional v3 Arrays at the event.
Having become one of the premier events in the field of human genetics, ESHG is a forum for all workers in human and medical genetics to review the latest advances and develop research collaborations. OGT’s workshop was one of the best attended workshops of the conference, with over 150 delegates turning up to learn how OGT has coupled its microarray design expertise with the latest developmental disorder content to create CytoSure Constitutional v3 arrays. Launched at the ESHG conference, these are the only arrays available with enhanced content from the Deciphering Developmental Disorders (DDD) study1,2 and ClinGen (formerly ISCA/ICCG) — enabling high-resolution CNV detection across ~500 genes of interest.
Senior Computational Biologist at OGT, Duarte Molha, discussed OGT’s advanced microarray design strategies to deliver the latest generation of exon-focused arrays for the accurate detection of small DNA deletions and duplications. In addition, Professor Madhuri Hegde PhD, FACMG, Professor of Human Genetics at Emory University School of Medicine presented how Emory University complements its next generation sequencing workflows with OGT’s CytoSure Medical Research Exome array to provide gold-standard CNV detection at the exon level.
OGT, a Sysmex Group company, is a leading global provider of clinical and diagnostic genomic solutions that are created for scientists by scientists - including CytoCell®, CytoSure® and SureSeq™ ranges of FISH, microarray and NGS products. The company is dedicated to creating products that enable researchers and clinical decision makers to reach the right care decisions for each patient, every time. OGT strives to unlock the future of genetic clinical care with a commitment to working in partnership with its customers - not only by sharing its expertise of 25 years at the forefront of genetic endeavour, but also by working closely with scientists to understand their unique challenges, and to customise its approach to meet their exact needs. Dedicated to improving clinical care, OGT believes that through partnership—together—we’ll achieve more.
For more information on the Company, please visit our website at ogt.com
CytoSure®, SureSeq™ and myProbes®: For Research Use Only, not for use in diagnostic procedures. CytoCell: Some products may not be available in your region.
About Sysmex Corporation
Sysmex Corporation is a world leader in clinical laboratory systemization and solutions, including laboratory diagnostics, laboratory automation and clinical information systems. Serving customers for more than 50 years, Sysmex focuses on technological leadership in diagnostic science and information tools that make a difference in the health of people worldwide. The company is also exploring emerging opportunities in the life science field. Its R&D efforts focus on the development of high-value-added testing and diagnostic technologies that are innovative, original and optimize individual health. Sysmex also seeks to leverage its state-of-the-art technologies for cell, gene and protein analysis. The company, headquartered in Kobe, Japan, has subsidiaries in North America, Latin America, Europe, the Middle East, Africa, China and Asia Pacific and employs more than 9,000 employees worldwide. Sysmex Corporation is listed in the top tier of the Tokyo Stock Exchange.
For more information about Sysmex Corporation and its affiliate companies, please visit www.sysmex.co.jp/en/.
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Paper published in npj Genomic Medicine demonstrates identification of more reportable CNVs with CytoSure v3 vs traditional array design.Read