Improve quality, reduce error with Sunquest Mitogen™ Genetics
Assessing the clinical significance of novel variants is a sizable task –time-consuming, rife with data, and requires management and ranking of evidence amassed from multiple sources. Sunquest Mitogen™ Genetics helps you take control of this process by bringing order and consistency to the variant assessment process. With our capabilities, you can:
Access a robust information resource library, including ClinVar, PubMed, ExAC and gnomAD.
Process evidence against pre-loaded ACMG guidelines, using features such as visual cues and drag-and-drop functionality to guide your efforts in building evidence.
Benefit from a dynamic scoring algorithm that provides real-time calculation of a final compiled interpretation score with regard to pathogenicity.