Checklist for Optimization and Validation of Real-Time PCR Assays

被引:141
作者
Raymaekers, Marijke [1 ]
Smets, Rita [1 ]
Maes, Brigitte [1 ]
Cartuyvels, Reinoud [1 ]
机构
[1] Virga Jesse Hosp, Clin Lab, B-3500 Hasselt, Belgium
关键词
real-time PCR; checklist; molecular diagnostics; optimization; validation; HARMONIZING CURRENT METHODOLOGY; BCR-ABL TRANSCRIPTS; NUCLEIC-ACID; BASIC REQUIREMENTS; MOLECULAR BEACONS; DNA AMPLIFICATION; QUANTITATIVE PCR; TECHNICAL REPORT; PROBES; QUANTIFICATION;
D O I
10.1002/jcla.20307
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Real-time polymerase chain reaction (PCR) is a frequently used technique in molecular diagnostics. To date, practical guidelines for the complete process of optimization and validation of commercial and in-house developed molecular diagnostic methods are scare. Therefore, we propose a practical guiding principle for the optimization and validation of real-time PCR assays. Based on literature, existing guidelines, and personal experience, we created a checklist that can be used in different steps of the development and validation process of commercial and in-house developed real-time PCR assays. Furthermore, determination of target values and reproducibility of internal quality controls are included, which allows a statistical follow-up of the performance of the assay. Recently, we used this checklist for the development of various qualitative and quantitative assays for microbiological and hematological applications, for which accreditation according to ISO 15189:2007 was obtained. In our experience, the use of the proposed guidelines leads to a more efficient and standardized optimization and validation. Ultimately, this results in reliable and robust molecular diagnostics. The proposed checklist is independent of environment, equipment, and specific applications and can be used in other laboratories. A worldwide consensus on this kind of checklist should be aimed at. J. Clin. Lab. Anal. 23:145-151, 2009. (C) 2009 Wiley-Liss, Inc.
引用
收藏
页码:145 / 151
页数:7
相关论文
共 85 条
[1]   BASIC LOCAL ALIGNMENT SEARCH TOOL [J].
ALTSCHUL, SF ;
GISH, W ;
MILLER, W ;
MYERS, EW ;
LIPMAN, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) :403-410
[2]  
Amos J, 2006, TECHNICAL STANDARDS
[3]  
[Anonymous], 2001, Rapid Cycle Real-Time PCR [Internet], DOI [DOI 10.1007/978-3-642-59524-0_3, 10.1007/978-3-642-59524-0_3]
[4]   Basic principles of real-time quantitative PCR [J].
Arya, M ;
Shergill, IS ;
Williamson, M ;
Gommersall, L ;
Arya, N ;
Patel, HRH .
EXPERT REVIEW OF MOLECULAR DIAGNOSTICS, 2005, 5 (02) :209-219
[5]  
Aslanzadeh J, 2004, ANN CLIN LAB SCI, V34, P389
[6]   AMPLIFICATION OF NUCLEIC-ACIDS BY POLYMERASE CHAIN-REACTION (PCR) AND OTHER METHODS AND THEIR APPLICATIONS [J].
BEJ, AK ;
MAHBUBANI, MH ;
ATLAS, RM .
CRITICAL REVIEWS IN BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1991, 26 (3-4) :301-334
[7]   A GENERAL METHOD FOR ISOLATION OF RNA COMPLEMENTARY TO DNA [J].
BOLTON, ET ;
MCCARTHY, BJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1962, 48 (08) :1390-&
[8]   Locked nucleic acid (LNA): fine-tuning the recognition of DNA and RNA [J].
Braasch, DA ;
Corey, DR .
CHEMISTRY & BIOLOGY, 2001, 8 (01) :1-7
[9]   Rationale for the recommendations for harmonizing current methodology for detecting BCR-ABL transcripts in patients with chronic myeloid leukaemia [J].
Branford, S. ;
Cross, N. C. P. ;
Hochhaus, A. ;
Radich, J. ;
Saglio, G. ;
Kaeda, J. ;
Goldman, J. ;
Hughes, T. .
LEUKEMIA, 2006, 20 (11) :1925-1930
[10]   PREDICTING DNA DUPLEX STABILITY FROM THE BASE SEQUENCE [J].
BRESLAUER, KJ ;
FRANK, R ;
BLOCKER, H ;
MARKY, LA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (11) :3746-3750