Covering NGS, array and FISH probe technologies and cancer, constitutional and rare disease applications.
"Pre-designed Arrays" videos:
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Use of NGS panels and microarrays for CNV detection
Hear Douglas Hurd describe some of our recent advances in next generation sequencing (NGS) panel design to allow detection of both copy number variation (CNV) and single nucleotide variation (SNV) from a single assay.
Customisable, single exon resolution CNV analysis complements NGS for additional insights into genetic disorders
Hear Dr Tracey Lewis from the R&D Molecular Genomics Group, ARUP Laboratories Salt Lake City, USA discuss the importance of single exon CNV changes in a variety of genetic conditions.
Identifying a broader range of genetic syndromes using exon-focussed array designs
This workshop outlines the development of the new CytoSure Constitutional v3 arrays and how Emory University School of Medicine complements its NGS workflows using the CytoSure™ Medical Research Exome array.
ASHG Workshop 2014
Held at the American Society of Human Genetics (ASHG), this workshop featured presentations from Professor Madhuri Hegde, Professor of Human Genetics, Emory University and Dr Mike Evans, CEO at OGT.