To speed up the reporting workflow, we uniquely embed the N-of-One variant database or your own curated knowledgebase natively on the platform. This integration enables lighting-up clinically actionable variants through filtering for rapid selection.
Our unique integration with N-of-One brings together one of the most
comprehensive genomic databases right inside IntelliSpace Genomics. This is in addition to all of the available public data sources the platform brings for comprehensive annotation, filtering and reliable prioritization.
To focus on information and/or actionable variants from the large number detected by NGS, we provide flexible and visual filtering options. To make the filters easily accessible, we have classified them in QC, frequency, functional impact scores and database presence categories. Our visual filtering interface displays distribution of variants by read depth and allele frequency so that you can optimize your filters at a glance.
