Sunquest Mitogen™ Genetics
Genetic Variant 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-gen sequencing data. Sunquest Mitogen simplifies the laboratory’s task of variant annotation and interpretation.
Produce Clinically Actionable Reports
Identify significant variants, diseases, clinical trials and therapeutics
Automate Filtration & Annotation
Manage variants for inherited diseases, cancer, pharmacogenetics
Expedite Reporting
Generate 80% of each report automatically
Tap Into Content Sources
Access global knowledge databases and curated content
Minimize IT Overhead
Deploy quickly with a small, cloud-based footprint
Enable Interoperability And Data Sharing
Connect with clinical LIS/LIMS, physician EMRs, and peer lab networks
Growing your genetic testing business requires scalable processes. Genetic analysis software, curated variant knowledge sources, and the option of real-time collaboration with peer labs allows you to quickly identify and report on clinically actionable information from a sea of variant data from next generation sequencing (NGS) instruments.
Genetic Analysis Software For Precision Medicine
Quickly find meaningful genetic variants and deliver concise, clinically actionable genetic reports in less time.
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- Scale your genetic testing lab to achieve higher volume and faster turnaround time
- Use standardized processes for consistent variant interpretation and reporting
- Repurpose curated data from trusted sources
- Utilize powerful variant assessment tool to assay and classify variants with built-in ACMG guidelines
- Automatically generate about 80% of each customizable report
- Create, search, share, and repurpose variant filters, report templates, sections and content
- Edit reports using a visual editor, including charts, graphs and images
- Easily create compound variants, manage test panels with more than 5,000 genes, and add genes in bulk
- Generate concise, patient-specific, clinically actionable, enhanced reports
- Integrate and develop your lab’s own variant knowledgebase
- Use curated content from trusted sources such as ClinVar, dbSNP and COSMIC
- Use Monarch Initiative’s ontology, connecting genes, diseases and phenotypes
- Use the cancer mutation knowledgebase from the Dana Farber Cancer Institute
- Tie somatic mutations to cancers, therapeutics and clinical trials
- Dedicated implementation team focuses on your workflows and tests
- 24 x 7, 365 support
- Connect with LIMS to import test results
- PDF, HL7, and FHIR compatible for integration with EMR and other healthcare systems
- Share de-identified data with other labs
- Leverage a feature-rich API to integrate with all your other systems
- Built-in integration with N-of-One