Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/30490
Title: Evaluating DNA recovery efficiency following bisulphite modification from plasma samples submitted for cell-free DNA methylation analysis.
Austin Authors: Cox, Daniel R A ;Wong, Boris Ka Leong;Lee, Eunice ;Testro, Adam G ;Muralidharan, Vijayaragavan ;Dobrovic, Alexander ;Goh, Su Kah 
Affiliation: Victorian Liver Transplant Unit
Surgery (University of Melbourne)
Translational Genomics and Epigenomics Laboratory, Department of Surgery (Austin Precinct), The University of Melbourne, Heidelberg, Australia..
Hepatopancreatobiliary Surgery
Issue Date: 28-Jun-2022
Date: 2022
Publication information: Epigenetics 2022; 17(13)
Abstract: The detection of methylated templates in cell-free DNA (cfDNA) is increasingly recognized as a valuable, non-invasive tool for diagnosis, monitoring and prognostication in a range of medical contexts. The importance of controlling pre-analytical conditions in laboratory workflows prior to cfDNA quantification is well-established. Significant variations in the recovery of DNA following processes such as cfDNA extraction and sodium bisulphite modification may confound downstream analysis, particularly when accurate quantification of templates is required. Given the wealth of potential applications for this emerging molecular technology, attention has turned to the requirement to recognize and minimize pre-analytical variables prior to cfDNA methylation analysis. We recently described the development of an approach using an exogenous DNA construct to evaluate the recovery efficiency of cfDNA following the extraction and bisulphite modification steps (CEREBIS). Here, we report our experience in the practical application of this technique in 107 consecutive patient plasma samples submitted for quantitative cfDNA methylation analysis. The mean recovery of cfDNA (as estimated using cerebis), following extraction and bisulphite modification, was 37% ± 7%. Nine (8.4%) of the 107 samples were found to be outside of control limits, where the recovery of cerebis indicated significant differences in the efficiency of the pre-analytical processing of these samples. Recognition of these out-of-control samples precluded subsequent molecular analysis. Implementation of data-driven quality control measures, such as the one described, has the potential to improve the quality of liquid biopsy methylation analysis, interpretation and reporting.
URI: https://ahro.austin.org.au/austinjspui/handle/1/30490
DOI: 10.1080/15592294.2022.2091821
ORCID: 0000-0002-5092-4370
0000-0002-6684-2521
0000-0002-1522-3499
0000-0001-6776-3115
0000-0001-8247-8937
0000-0003-3414-112X
Journal: Epigenetics
PubMed URL: 35763697
PubMed URL: https://pubmed.ncbi.nlm.nih.gov/35763697/
Type: Journal Article
Subjects: DNA controls
DNA methylation
cell-free DNA
digital PCR
pre-analytical
quality control
Appears in Collections:Journal articles

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