Covering NGS, array and FISH probe technologies and cancer, constitutional and rare disease applications.
"Rare Disease Research" videos:
Introduction to Interpret™ NGS analysis software
Learn about Interpret, OGT’s powerful and easy-to-use next generation sequencing analysis solution, designed to work seamlessly with SureSeq™ and CytoSure™ NGS panels.
Make our expertise work for you
See how you can discover more when you take advantage of our aCGH design expertise.
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.