Development and Characterization of Reference Materials for Genetic Testing: Focus on Public Partnerships
Lisa V Kalman1, Vivekananda Datta2, Mickey Williams2
1Centers for Disease Control and Prevention, Atlanta, GA, USA.
Abstract:
Characterized reference materials (RMs) are needed for clinical laboratory test development and validation, quality control procedures, and proficiency testing to assure their quality. In this article, we review the development and characterization of RMs for clinical molecular genetic tests. We describe various types of RMs and how to access and utilize them, especially focusing on the Genetic Testing Reference Materials Coordination Program (Get-RM) and the Genome in a Bottle (GIAB) Consortium. This review also reinforces the need for collaborative efforts in the clinical genetic testing community to develop additional RMs.


