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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.

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