EQUAL-qual: A European Program for External Quality Assessment of Genomic DNA Extraction and PCR Amplification

Author:

Orlando Claudio1,Verderio Paolo2,Maatman Ronald3,Danneberg Jan3,Ramsden Simon4,Neumaier Michael5,Taruscio Domenica6,Falbo Vincenzo6,Jansen Robert7,Casini-Raggi Claudia1,Malentacchi Francesca1,Marubini Ettore8,Pizzamiglio Sara2,Vernelen Kris9,Libeer Jean-Claude9,Palicka Vladimir10,Pazzagli Mario1

Affiliation:

1. Department of Clinical Physiopathology, University of Florence, Florence, Italy

2. Operative Unit of Medical Statistics and Biometry, Instituto Nazionale per lo Studio e la Cura dei Tumori, Milan, Italy

3. Department of Clinical Chemistry, ZiekenhuisGroep Twente, Zilvermeeuw, Almelo, The Netherlands

4. National Genetics Reference Laboratory, Saint Mary’s Hospital, Manchester, United Kingdom

5. Institute for Clinical Chemistry, University Hospital Mannheim of the University of Heidelberg, Mannheim, Germany

6. National Center Rare Diseases, Department of Cell Biology and Neuroscience, Istituto Superiore di Sanità, Rome, Italy

7. Department of Clinical Chemistry, St. Anna Hospital, Geldrop, The Netherlands

8. Istituto di Statistica Medica e Biometria, Universitàdegli Studi di Milano, Milan, Italy

9. Department of Clinical Biology, Institute of Public Health, Brussels, Belgium

10. Institute for Clinical Chemistry and Diagnostics, School of Medicine, University Hospital Sokolska, Hradec Kralove, Czech Republic

Abstract

Abstract Background: Despite the rapid transition into routine clinical practice of molecular techniques based on PCR, external quality assessment (EQA) is still not widely available. The European Union and European Communities Confederation of Clinical Chemistry have supported the EQUAL project as a series of 3 different EQA programs for the assessment of molecular methods independently from analytes. We present the results from the EQUAL-qual program designed to evaluate the analytical aspects of DNA analysis by means of a conventional qualitative PCR experiment. Methods: The EQUAL-qual program provided DNA, blood samples, and primer sets to participant laboratories to assess DNA extraction and PCR amplification. We have developed statistical procedures to identify laboratories performing poorly in DNA extraction (quality and quantity), PCR efficiency, and data interpretation after electrophoresis. Results: An application to participate was obtained from 213 laboratories (from 25 countries), and 175 (82%) of laboratories submitted results for assessment. Questionable results in terms of quality and/or quantity of DNA derived from blood extractions were returned by 27% of laboratories (46 of 166). PCR efficiency showed high variability, with 3% of laboratories (5 of 163) showing a consistently low rate of amplification and 10% (18 of 175) not reporting the expected number of bands of the amplified targets. Conclusions: The results showed considerable variability in all phases of the experiment. The approach confirms the validity of EQA as a method for evaluating analytical aspects of PCR-based tests.

Funder

European Union Sixth Framework

Publisher

Oxford University Press (OUP)

Subject

Biochemistry (medical),Clinical Biochemistry

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