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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.

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Automate Filtration & Annotation

Quickly process data to identify variants of interest

Leverage Meaningful Content
Leverage Meaningful Content

Access content from trusted sources

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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

Growing your genetic testing business requires scalable processes

Sunquest Mitogen Genetics together with Sunquest Mitogen LIMS provides customers a comprehensive NGS support solution from the wet lab to the dry lab.

Growing your genetic testing business requires scalable processes

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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Mitogen Genetics Product Brief
Manage Complexity at Scale
  • 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
Increase Report Throughput
  • 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
Improve Report Quality
  • 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
Maximize Interoperability
  • Explore integration with Sunquest Mitogen LIMS, which is continually evolving
  • Share de-identified variant and condition data with other labs