Case organization, worklists and variant interpretation are all accessed through an intuitive interface that's easy-to-use for clinical genomicists and molecular pathologists.
Clinicians perform variant characterization, prioritization and interpretation through the interactive environment using toggle like features.
Ability to easily add phenotype, medical data and mine external sources to characterize variants based on disease association.
Establish workflows for variant confirmation with the ability to keep track of variants at any filtering stage.
All novel variants, annotation and interpretations are stored in the variant knowledgebase and can be accessed via the application.
Report findings with auto generated templates or customizable reports with the ability to securely send to external systems with electronic sign off.