Sunquest Mitogen™ Genetics
Genomic Analysis & Reporting Solution for Clinical Laboratories that Perform Next-Generation Sequencing (NGS)
Sunquest Mitogen™ Genetics helps laboratories start and grow next-generation sequencing (NGS) services by implementing scalable processes that allow labs to quickly produce concise, clinically actionable genetic reports in minutes, from next-generation sequencing data. Sunquest Mitogen Genetics simplifies the laboratory’s task of variant annotation and interpretation. When used in combination with Sunquest Mitogen LIMS in the wet lab, the two products together provide customers a comprehensive NGS workflow solution.
Automate Filtration & Annotation
Quickly process data to identify variants of interest
Leverage Meaningful Content
Access content from trusted sources
Produce Clinically Actionable Reports
Apply in-app support to identify clinically significant variants
Expedite Reporting
Generate ~80% of each report automatically
Minimize IT Overhead
Deploy quickly with a small, cloud-based footprint
Engage in Peer Networking
Share de-identified variant and condition data with other labs
Sunquest Mitogen Genetics together with Sunquest Mitogen LIMS provides customers a comprehensive NGS support solution from the wet lab to the dry lab.
Genomic Analysis Software for Precision Medicine
Quickly find meaningful genetic variants and deliver concise, clinically actionable genetic reports in less time.
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- Automate annotation and filtration to identify variants of interest
- Scale your lab to achieve higher test volume and faster report turnaround time
- Standardize variant interpretation and reporting
- Use a powerful variant assessment tool to help classify variants using built-in ACMG guidelines
- Deliver concise, patient-specific, clinically-actionable, EHR-ready reports that are ~80% automated
- Create, search, share, and repurpose variant filters, report templates, sections and content for interpretation consistency across your team
- Create enhanced, customized individual reports through a real-time visual editor
- Integrate your lab’s variant knowledgebase and benefit from knowledgebase management with advanced search
- Use meaningful content from trusted sources, including ClinVar, dbSNP, COSMIC and the Monarch Initiative’s ontology
- Explore integration with Sunquest Mitogen LIMS, which is continually evolving
- Share de-identified variant and condition data with other labs