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