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Improve quality, reduce error and expedite reporting with Sunquest Mitogen™ Genetics

Analyzing and reporting on next-generation sequencing, including assessing the clinical significance of novel variants, is a sizable task –time-consuming, rife with data, and requires managing and ranking evidence amassed from multiple sources. Sunquest Mitogen™ Genetics helps you take control of this process with order, consistency and automation. With our capabilities, you can in one place:

Access a robust information resource library,
including ClinVar, PubMed, ExAC and gnomAD.

Process evidence against pre-loaded
ACMG guidelines

Benefit from a dynamic scoring algorithm that
provides real-time calculation of a final compiled
interpretation score with regard to pathogenicity.

Produce clinically-actionable reports
in minutes instead of hours, with
automation and customization

Download the Product Brief Today!

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