This white paper, first published in Genomic Medicine, demonstrates that OGT’s CytoSure Constitutional v3 array, with an enhanced targeted exon-level resolution design, offered a significant increase in reporting rate (4.49%) for developmental disorder (DD) research, compared to traditional arrays.
Read and download the White paperCytoSure arrays offer robust copy-number detection with high resolution – detecting CNVs of a few hundred base pairs at the single-exon level. However, a number of different factors need to be taken into account when designing microarrays to make sure that they offer robust performance across the targeted regions. Learn more about the process that we undertake to make sure our arrays perform the best they possibly can.
Read and download the App noteThis application note illustrates the use of the InnoScan 710 scanner and Mapix with a range of OGT CytoSure cytogenetic array formats.
Read and download the App noteThis whitepaper from Dominic McMullan, West Midlands Regional Genetics Laboratory, Birmingham, UK, demonstrates that the CytoSure Constitutional v3 microarray can detect variants not detectable by other microarray platforms.
Read and download the White paperIn this white paper, Kris Van Den Bogaert describes how the most current microarray technology is set to increase the detection of disease-relevant variants following a validation and implementation programme at the Department of Human Genetics, University Hospitals Leuven, Belgium.
Read and download the White paperIn this white paper, genetic scientists Dr Tracey Lewis and Dr Emily Farrow discuss how customisable, exon focused array designs complement next generation sequencing (NGS) for clinical genetic research.
Read and download the White paperThis application note provides a technical evaluation of CytoSure Genomic DNA Labelling Kits compared with another leading DNA labelling kit.
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