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Reliable detection of copy number changes and loss of heterozygosity on a single array for haematological malignancies and solid cancers.
The CytoSure Cancer +SNP array delivers: ■ Flexible choice of reference sample ■ Confident de... Read more...
OGT can help you get straight to the variant of interest with whole exome or custom targeted sequencing services.
Genefficiency™ targeted sequencing services are designed to be different, leading you all the way from project conceptio... Read more...
A high-quality RNA sequencing service designed to deliver cost-effective and rapid access to meaningful transcriptomics results.
The Genefficiency™ RNA-Seq Service from OGT provides a new level of assay customisation to ensure each ex... Read more...
Reliable detection of copy number changes for research into a range of genetic disorders.
CytoSure Molecular Arrays are designed to accurately identify small intragenic copy number variations (CNVs) in genes associated with a variety ... Read more...