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Follow on Google News | Free NGS report demo — Bypass the data bottleneck with Genefficiency servicesRapidly identify meaningful results with OGT’s Genefficiency™ NGS Report
By: Oxford Gene Technology The demo allows researchers to explore the easy-to-use features of the software with publicly-available sequence data from Tariq et al (2011)1, which identified a novel candidate gene (SHROOM3) for heterotaxy, a severe form of congenital heart disease. It provides researchers with a unique opportunity to experience the interactive report format, discovering what’s possible with OGT’s Genefficiency NGS Services. The report offers rapid filtering options, built-in quality control metrics and the ability to retrospectively analyse the data with additional or new selection criteria. On completion of all OGT Genefficiency NGS exome and targeted panel projects, customers receive their results pre-loaded into the Genefficiency NGS Variant Analysis Report, so that they can quickly and easily identify relevant data. OGT’s services cover the complete NGS pipeline, from project conception through to the delivery of high-quality, meaningful results via the software, bypassing the bottleneck of complex data analysis. The Genefficiency NGS Variant Analysis Report is an intuitive solution to NGS data analysis and reporting. Thousands of variations can be filtered within minutes to just a handful requiring further validation — with no requirement for additional bioinformatics resources. Bespoke analysis is easily integrated into the reporting software, allowing variants to be filtered based on biological function or other tailored criteria, for the easy identification of the most significant regions of genetic variation relevant to each individual study. Furthermore, the readily accessible in-depth quality metrics provide maximum confidence that the results are of the highest quality. To download the demo, register here (http://www.ogt.com/ For more information on OGT’s Genefficiency services contact OGT (mailto:contact@ References: Tariq M, et al (2011). SHROOM3 is a novel candidate for heterotaxy identified by whole exome sequencing. Genome Biol. Sep 21;12(9):R91. doi: 10.1186/gb-2011- For further information, please contact: Oxford Gene Technology, Begbroke Science Park, Begbroke Hill, Woodstock Road, Begbroke, Oxfordshire, OX5 1PF, U.K. T: +44 (0) 1865 856826 ; F: +44 (0) 1865 848684 ; E: contact@ogt.com W: www.ogt.com ; Twitter: @OxfordGeneTech (https://twitter.com/#!/ End
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