Download case study: Accelerating rare variant analysis and interpretation

Atil Bisgin, MD, PhD, and his colleagues at Çukurova University Hospital in Adana, Turkey, manage one of the largest databases for rare hereditary diseases in the world. With over 50,000 samples spanning the Eurasian continent from patients afflicted with rare genetic disease, this state-of-the-art database will assist researchers and clinicians in identifying causative mutations.

To keep up with caseload demand and ensure patients and their doctors receive test results in days — not weeks — Dr. Bisgin knew AGENTEM would have to automate portions of their variant interpretation process, so he turned to QIAGEN Clinical Insights (QCI) Interpret for help.

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Download this case study to learn how QCI Interpret is helping AGENTEM accelerate rare variant analysis and interpretation and shorten the diagnostic odyssey.

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