Geneticist Assistant NGS Interpretative Workbench provides Variant Interpretation, Population Frequency, Functional Prediction, Conservation Scores and Disease Associations on each found variant from multiple sources in a single view. Once a variant call has been made, it is stored in the database and then displayed for any samples that contain the variant, significantly reducing time and effort on future analysis.
Sample’s Variants: Example configuration of variant table. Columns can be customized to show the fields needed. Variant pathogenicity is set by the user and shown in other samples.