Clinical Bioinformatician Body of Knowledge—Clinical Laboratory Regulation and Data Security Core

• Published in: The Journal of molecular diagnostics : JMD Vol. 27; no. 7; pp. 583 - 601
• Main Authors: Schmidt, Ryan J., Furtado, Larissa V., Fussell, Amber M., Jordan, Danielle, Lebo, Matthew, Syed, Aijazuddin, Temple-Smolkin, Robyn L., Venner, Eric, Worthey, Elizabeth, Carter, Alexis B.
• Format: Journal Article
• Language: English
• Published: Elsevier Inc 01.07.2025
• ISSN: 1525-1578
• DOI: 10.1016/j.jmoldx.2025.04.003

Clinical bioinformaticians have come to play an essential role in clinical molecular diagnostic laboratories. However, the core knowledge needed for the clinical practice and training of this emerging group of professionals has not been previously established. Clinical laboratories are subject to a complex set of legal and accreditation requirements from numerous governmental and nongovernmental bodies that cover the generation, processing, storage, and distribution of patient data in the form of test results and intermediate data files. Clinical bioinformaticians are intimately involved in the development and maintenance of systems that perform these activities. This third article in the Association for Molecular Pathology's Clinical Bioinformatician Body of Knowledge Core series presents a body of knowledge for the clinical bioinformatician describing relevant laboratory regulations and data security in the domains of hardware, software, networks, and interoperability. Although this article does not substitute for legal counsel, it provides a resource for clinical bioinformaticians to identify and familiarize themselves with regulations affecting their professional functions within the laboratory.