by Nabil Hafez | Sep 7, 2017 | Blog
Genetic testing has the power to improve patient care, but putting that power to work for everyday use requires tools that make it easier to connect the work of the laboratory with decisions made in the clinic.
When MedComp Sciences prepared to update its lab to meet this demand, they worked with Sunquest to develop a workflow system that would modernize its laboratory system and ensure that genetic interpretations were made with the most accurate and up-to-date variant knowledge.
MedComp Sciences had three specific objectives:
- Developing a 21st-century laboratory information management system (LIMS) purpose-built for molecular diagnostics
- Facilitating report generation that clearly indicates the clinical significance of variants and, where appropriate, the implications for treatment
- Improving the accuracy of genetic interpretations to complement and extend clinical data for better healthcare decisions
MedComp Sciences chose the Sunquest Mitogen™ platform. Because Sunquest’s engineering team has both laboratory expertise and strong history in data management, the development and implementation process was responsive and efficient. Sunquest “knows what has and hasn’t worked in the past,” said MedComp Sciences Lead Geneticist Jason Walker, PhD. “The finished product is something we are truly proud of at MedComp Sciences. It is an investment we have made in laboratory quality and in our future.”
Reporting and variant interpretation tools from Sunquest Mitogen complemented the modernized LIMS system, to create an automated workflow system integrated from sample acquisition and processing through interpretation and report creation. Automation is the key to allowing MedComp Sciences to keep expanding their service. The ability to scale both tests and reporting makes it possible to add new tests and more volume quickly and at a lower cost. MedComp Sciences also joined Sunquest’s VariantWire initiative. VariantWire® empowers laboratories in the United States and Canada to share structured genetic data in real time. Through collaborative exchange of variant knowledge, labs can make variant calls with greater accuracy and more confidence. The end result is better, more accurate diagnoses for individual patients.
About the author
Sr. Director Product Management and Marketing, Sunquest Mitogen
After cutting his teeth on the Human Genome Project, Nabil was hooked on genetics. Sixteen years later, his passion remains focused on enabling technologies to bring precision medicine to mainstream medicine.