Scalable genetic analysis for your clinical next generation sequencing (NGS) laboratory
Sunquest Mitogen™ provides scalable genetic analysis for clinical laboratories performing next generation sequencing (NGS)-based testing. This is the dry lab component of DNA sequencing used by pathologists, data scientists and lab directors to perform variant annotation, interpretation and clinical reporting. The secure, cloud-based application scales from single gene tests to panels, exomes, and whole genomes.
Cancer genetic testing
From inherited cancer panels (e.g., BRCA, Lynch Syndrome) to solid tumor profiling, our clinical genetic analysis and reporting software provides the insights oncologists need to properly diagnose and treat their patients.
Inherited disease testing
At all stages of life - from pre-conception carrier screening to prenatal, newborn, and adult testing, our variant analysis software can quickly identify the significance of variants in genetic disorders, so you can best advise patients and their families on how to treat and prevent disease.
By having access to information on variations in gene response to the latest medications, clinicians can avoid adverse reactions to improve patient safety and drug treatment efficacy, even before treatments begins, to ensure your patients have the best outcomes.
At Sunquest we understand the value of your time, as the available genetic knowledge exponentially expands and your lab testing volume grows, you need a solution that can be highly automated to quickly produce clinical genetic reports. Sunquest Mitogen's templates, automated filters, and user-configured logic allow you to quickly and easily generate full-featured and editable reports that are timely and clinically actionable.
Clinicians receive electronic test results through HL7 and PDF output that integrates seamlessly with EMR systems, the variant interpretive process doesn’t end once a report is delivered; clinicians receive updates linked to the patient record that alert them when new information is learned about their patients’ variants.
Sunquest Mitogen's genetic analysis software helps you to identify meaningful variants in a sea of data, enabling you to annotate and filter your dataset using genomic, biological, population, and phenotypic variant databases. Quickly analyze your patient samples and produce consistent, actionable, and rich clinical reports.
Integrated into Sunquest Mitogen are third-party professionally curated content from:
The Monarch Initiative is an integrative data and analytic platform connecting phenotypes to genotypes across species. For example, a mutation may give rise to similar diseases in multiple species, including humans. Monarch Initiative brings this data together to help identify a patient’s clinical features.
Our genetic analysis software helps power data sharing through the VariantWire network where de-identified, clinically validated variant and gene data can be shared in real time with participating member labs for high quality variant interpretation.
Each laboratory can choose to participate and can grow its own genetic knowledgebase for standardized interpretations and exchange knowledge across a network of peer institutions.
ISO 9001 (Quality Management) & ISO 13485 (Quality Management System for Medical Devices) are internationally recognized and independently verified certifications that document Sunquest has implemented quality management systems to ensure products and services consistently meet customer needs and applicable regulatory requirements.