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Lab Med Online.  2022 Oct;12(4):227-234. 10.47429/lmo.2022.12.4.227.

Recommendations for the Verification of Quantitative Molecular Hemato-Oncology Tests

Affiliations
  • 1Department of Laboratory Medicine, Yonsei University College of Medicine, Seoul, Korea
  • 2Department of Laboratory Medicine, Keimyung University School of Medicine, Daegu, Korea
  • 3Department of Laboratory Medicine, Hallym University College of Medicine, Chuncheon, Korea
  • 4Department of Laboratory Medicine, Hanyang University College of Medicine, Seoul, Korea

Abstract

Quantitative molecular genetic tests are increasingly used for the detection and quantification of target molecules or genetic alterations. When introducing a new assay into clinical laboratories, it is necessary to verify the manufacturers’ claimed performance characteristics within individual laboratories. Appropriate assay verification procedures are essential to ensure the quality of test results in clinical laboratories. This study aimed to provide recommendations for the verification of quantitative molecular genetic testing focused on the hemato-oncology field in clinical genetic laboratories. Based on a literature review, we provide recommendations for the performance verification of quantitative molecular hemato-oncology tests. The performance characteristic elements that comprise the verification procedures are presented and exemplified. These recommendations can assist individual clinical laboratories in verifying quantitative molecular diagnostic assays.

Keyword

Verification; Quantitative PCR; Digital PCR; Real-time PCR; Molecular diagnostic techniques
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