NGS Variant Analysis

Identify human genome variations of functional significance through variant analysis by mapping next generation sequencing data to known elements such as disease mutations and regulatory sites.

Interested in whole genome or exome sequencing data?  Discover how to identify relevant variations in research and learn how to upload a complete genome’s worth of variations and, within minutes, identify the relevant subset that have been described as characterized mutations or that are novel but fall within a candidate disease gene with Genome TraxTM database.

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