Customisable, single exon resolution CNV analysis complements NGS for additional insights into genetic disorders

Thursday 7 April 2016
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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. She illustrates the benefits of using customizable exon-focused aCGH microarrays, with exon level resolution, as a complementary technology to next generation sequencing to better understand the full mutation spectrum in inherited disease.