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Systematic benchmarking of tools for CpG methylation detection from Nanopore sequencing

View ORCID ProfileZaka Wing-Sze Yuen, View ORCID ProfileAkanksha Srivastava, View ORCID ProfileDennis McNevin, View ORCID ProfileCameron Jack, View ORCID ProfileEduardo Eyras
doi: https://doi.org/10.1101/2020.10.14.340315
Zaka Wing-Sze Yuen
1EMBL Australia Partner Laboratory Network at the Australian National University, Acton ACT 2601, Canberra, Australia
2The John Curtin School of Medical Research, Australian National University, Acton ACT 2601, Canberra, Australia
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Akanksha Srivastava
1EMBL Australia Partner Laboratory Network at the Australian National University, Acton ACT 2601, Canberra, Australia
2The John Curtin School of Medical Research, Australian National University, Acton ACT 2601, Canberra, Australia
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Dennis McNevin
3Centre for Forensic Science, School of Mathematical & Physical Sciences, Faculty of Science, University of Technology Sydney, Australia
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Cameron Jack
2The John Curtin School of Medical Research, Australian National University, Acton ACT 2601, Canberra, Australia
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  • For correspondence: cameron.jack@anu.edu.au eduardo.eyras@anu.edu.au
Eduardo Eyras
1EMBL Australia Partner Laboratory Network at the Australian National University, Acton ACT 2601, Canberra, Australia
2The John Curtin School of Medical Research, Australian National University, Acton ACT 2601, Canberra, Australia
4Catalan Institution for Research and Advanced Studies (ICREA), E08010 Barcelona, Spain
5Hospital del Mar Medical Research Institute (IMIM), E08003 Barcelona, Spain
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  • For correspondence: cameron.jack@anu.edu.au eduardo.eyras@anu.edu.au
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Abstract

DNA methylation plays a fundamental role in the control of gene expression and genome integrity. Although there are multiple tools that enable its detection from Nanopore sequencing, their accuracy remains largely unknown. Here, we present a systematic benchmarking of tools for the detection of CpG methylation from Nanopore sequencing using individual reads, control mixtures of methylated and unmethylated reads, and bisulfite sequencing. We found that tools showed a tradeoff between false positives and false negatives, and presented a high dispersion with respect to the expected methylation frequency values. We described various strategies to improve the accuracy of these tools and proposed a new method, METEORE (https://github.com/comprna/METEORE), based on the combination of the predictions from two or more tools that has improved accuracy over individual tools. Snakemake pipelines are provided for reproducibility and to enable the systematic application of our analyses to other datasets.

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

  • Fixed title on biorxiv

  • https://github.com/comprna/METEORE

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY 4.0 International license.
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Posted October 15, 2020.
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Systematic benchmarking of tools for CpG methylation detection from Nanopore sequencing
Zaka Wing-Sze Yuen, Akanksha Srivastava, Dennis McNevin, Cameron Jack, Eduardo Eyras
bioRxiv 2020.10.14.340315; doi: https://doi.org/10.1101/2020.10.14.340315
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Systematic benchmarking of tools for CpG methylation detection from Nanopore sequencing
Zaka Wing-Sze Yuen, Akanksha Srivastava, Dennis McNevin, Cameron Jack, Eduardo Eyras
bioRxiv 2020.10.14.340315; doi: https://doi.org/10.1101/2020.10.14.340315

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