Cargando…
Comparative analysis of 12 different kits for bisulfite conversion of circulating cell-free DNA
Blood circulating cell-free DNA (cfDNA) is becoming popular in the search of promising predictive and prognostic biomarkers. Among these biomarkers, cfDNA methylation markers have especially gained considerable attention. A significant challenge in the utilization of cfDNA methylation markers is the...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5687322/ https://www.ncbi.nlm.nih.gov/pubmed/28557629 http://dx.doi.org/10.1080/15592294.2017.1334024 |
_version_ | 1783278935374561280 |
---|---|
author | Worm Ørntoft, Mai-Britt Jensen, Sarah Østrup Hansen, Thomas Birkballe Bramsen, Jesper Bertram Andersen, Claus Lindbjerg |
author_facet | Worm Ørntoft, Mai-Britt Jensen, Sarah Østrup Hansen, Thomas Birkballe Bramsen, Jesper Bertram Andersen, Claus Lindbjerg |
author_sort | Worm Ørntoft, Mai-Britt |
collection | PubMed |
description | Blood circulating cell-free DNA (cfDNA) is becoming popular in the search of promising predictive and prognostic biomarkers. Among these biomarkers, cfDNA methylation markers have especially gained considerable attention. A significant challenge in the utilization of cfDNA methylation markers is the limited amount of cfDNA available for analyses; reportedly, bisulfite conversion (BSC) reduce cfDNA amounts even further. Nevertheless, few efforts have focused on ensuring high cfDNA conversion efficiency and recovery after BSC. To compare cfDNA recovery of different BSC methods, we compared 12 different commercially available BSC kits. We tested whether DNA recovery was affected by the molecular weight and/or quantity of input DNA. We also tested BSC efficiency for each kit. We found that recovery varied for DNA fragments of different lengths: certain kits recovered short fragments better than others, and only 3 kits recovered DNA fragments of <100 bp well. In contrast, DNA input amount did not seem to affect DNA recovery: for quantities spanning between 820 and ∼25,000 genome equivalents per BSC, a linear relation was found between input and recovery amount. Overall, mean recovery ranged between 9 and 32%, with BSC efficiency of 97–99.9%. When plasma cfDNA was used as input for BSC, recovery varied from 22% for the poorest and 66% for the best performing kits, while conversion efficiency ranged from 96 to 100% among different kits. In conclusion, clear performance differences exist between commercially available BSC kits, both in terms of DNA recovery and conversion efficiency. The choice of BSC kit can substantially impact the amount of converted cfDNA available for downstream analysis, which is critical in a cfDNA methylation marker setting. |
format | Online Article Text |
id | pubmed-5687322 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-56873222017-11-21 Comparative analysis of 12 different kits for bisulfite conversion of circulating cell-free DNA Worm Ørntoft, Mai-Britt Jensen, Sarah Østrup Hansen, Thomas Birkballe Bramsen, Jesper Bertram Andersen, Claus Lindbjerg Epigenetics Research Papers Blood circulating cell-free DNA (cfDNA) is becoming popular in the search of promising predictive and prognostic biomarkers. Among these biomarkers, cfDNA methylation markers have especially gained considerable attention. A significant challenge in the utilization of cfDNA methylation markers is the limited amount of cfDNA available for analyses; reportedly, bisulfite conversion (BSC) reduce cfDNA amounts even further. Nevertheless, few efforts have focused on ensuring high cfDNA conversion efficiency and recovery after BSC. To compare cfDNA recovery of different BSC methods, we compared 12 different commercially available BSC kits. We tested whether DNA recovery was affected by the molecular weight and/or quantity of input DNA. We also tested BSC efficiency for each kit. We found that recovery varied for DNA fragments of different lengths: certain kits recovered short fragments better than others, and only 3 kits recovered DNA fragments of <100 bp well. In contrast, DNA input amount did not seem to affect DNA recovery: for quantities spanning between 820 and ∼25,000 genome equivalents per BSC, a linear relation was found between input and recovery amount. Overall, mean recovery ranged between 9 and 32%, with BSC efficiency of 97–99.9%. When plasma cfDNA was used as input for BSC, recovery varied from 22% for the poorest and 66% for the best performing kits, while conversion efficiency ranged from 96 to 100% among different kits. In conclusion, clear performance differences exist between commercially available BSC kits, both in terms of DNA recovery and conversion efficiency. The choice of BSC kit can substantially impact the amount of converted cfDNA available for downstream analysis, which is critical in a cfDNA methylation marker setting. Taylor & Francis 2017-05-30 /pmc/articles/PMC5687322/ /pubmed/28557629 http://dx.doi.org/10.1080/15592294.2017.1334024 Text en Published with license by Taylor & Francis Group, LLC © Mai-Britt Worm Ørntoft, Sarah Østrup Jensen, Thomas Birkballe Hansen, Jesper Bertram Bramsen, and Claus Lindbjerg Andersen. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way. |
spellingShingle | Research Papers Worm Ørntoft, Mai-Britt Jensen, Sarah Østrup Hansen, Thomas Birkballe Bramsen, Jesper Bertram Andersen, Claus Lindbjerg Comparative analysis of 12 different kits for bisulfite conversion of circulating cell-free DNA |
title | Comparative analysis of 12 different kits for bisulfite conversion of circulating cell-free DNA |
title_full | Comparative analysis of 12 different kits for bisulfite conversion of circulating cell-free DNA |
title_fullStr | Comparative analysis of 12 different kits for bisulfite conversion of circulating cell-free DNA |
title_full_unstemmed | Comparative analysis of 12 different kits for bisulfite conversion of circulating cell-free DNA |
title_short | Comparative analysis of 12 different kits for bisulfite conversion of circulating cell-free DNA |
title_sort | comparative analysis of 12 different kits for bisulfite conversion of circulating cell-free dna |
topic | Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5687322/ https://www.ncbi.nlm.nih.gov/pubmed/28557629 http://dx.doi.org/10.1080/15592294.2017.1334024 |
work_keys_str_mv | AT wormørntoftmaibritt comparativeanalysisof12differentkitsforbisulfiteconversionofcirculatingcellfreedna AT jensensarahøstrup comparativeanalysisof12differentkitsforbisulfiteconversionofcirculatingcellfreedna AT hansenthomasbirkballe comparativeanalysisof12differentkitsforbisulfiteconversionofcirculatingcellfreedna AT bramsenjesperbertram comparativeanalysisof12differentkitsforbisulfiteconversionofcirculatingcellfreedna AT andersenclauslindbjerg comparativeanalysisof12differentkitsforbisulfiteconversionofcirculatingcellfreedna |