Over the last decade, the field of molecular diagnostics has undergone tremendous transformation, catalyzed by the clinical implementation of next-generation sequencing (NGS).
Today, commercial molecular diagnostic labs are competing to offer an ever-expanding menu of NGS tests. But there’s an inherent problem: as NGS panels grow, test interpretation becomes more complex and time-consuming.
Overcoming this bottleneck requires sophisticated curation methods and processes to find, prioritize, transform, and constantly update relevent publications at scale.
This white paper provides an overview of Qiagen's variant interpretation software and services, which take advantage of different curation methods to accurately transform the literature into biological and clinical insights.
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