At OGT we understand that making the change from microarrays to NGS is a daunting prospect, particularly when it comes to data analysis.
That’s why we’ve developed the Interpret NGS analysis software for use in conjunction with the CytoSure® Constitutional NGS panel for constitutional cytogenetics research. To facilitate the easy transition for copy number variant (CNV) and loss of heterozygosity (LOH) analysis as well as streamlining single nucleotide variant (SNV) and insertion/deletion (indel) calling, we’ve provided familiar visualisation and interpretation tools alongside an intuitive web interface.
This application note outlines some of the key features we’ve incorporated to help make the change from arrays to NGS as painless as possible.
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