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Comprehensive Evaluation of Differential Methylation Analysis Methods for Bisulfite Sequencing Data

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  • Yongjun Piao

    (School of Medicine, Nankai University, Tianjin 300071, China
    Tianjin Key Laboratory of Human Development and Reproductive Regulation, Tianjin Central Hospital of Gynecology Obstetrics, Tianjin 300199, China
    These authors are contributed equally to this work.)

  • Wanxue Xu

    (Center for Reproductive Medicine, Department of Obstetrics and Gynecology, Peking University Third Hospital, Beijing 100191, China
    These authors are contributed equally to this work.)

  • Kwang Ho Park

    (Department of Computer Science, College of Electrical and Computer Engineering, Chungbuk National University, Cheongju 28644, Korea)

  • Keun Ho Ryu

    (Faculty of Information Technology, Ton Duc Thang University, Ho Chi Minh City 700000, Vietnam)

  • Rong Xiang

    (School of Medicine, Nankai University, Tianjin 300071, China)

Abstract

Background: With advances in next-generation sequencing technologies, the bisulfite conversion of genomic DNA followed by sequencing has become the predominant technique for quantifying genome-wide DNA methylation at single-base resolution. A large number of computational approaches are available in literature for identifying differentially methylated regions in bisulfite sequencing data, and more are being developed continuously. Results: Here, we focused on a comprehensive evaluation of commonly used differential methylation analysis methods and describe the potential strengths and limitations of each method. We found that there are large differences among methods, and no single method consistently ranked first in all benchmarking. Moreover, smoothing seemed not to improve the performance greatly, and a small number of replicates created more difficulties in the computational analysis of BS-seq data than low sequencing depth. Conclusions: Data analysis and interpretation should be performed with great care, especially when the number of replicates or sequencing depth is limited.

Suggested Citation

  • Yongjun Piao & Wanxue Xu & Kwang Ho Park & Keun Ho Ryu & Rong Xiang, 2021. "Comprehensive Evaluation of Differential Methylation Analysis Methods for Bisulfite Sequencing Data," IJERPH, MDPI, vol. 18(15), pages 1-15, July.
  • Handle: RePEc:gam:jijerp:v:18:y:2021:i:15:p:7975-:d:603205
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    References listed on IDEAS

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    1. Ryan Lister & Mattia Pelizzola & Robert H. Dowen & R. David Hawkins & Gary Hon & Julian Tonti-Filippini & Joseph R. Nery & Leonard Lee & Zhen Ye & Que-Minh Ngo & Lee Edsall & Jessica Antosiewicz-Bourg, 2009. "Human DNA methylomes at base resolution show widespread epigenomic differences," Nature, Nature, vol. 462(7271), pages 315-322, November.
    2. Francesco Neri & Stefania Rapelli & Anna Krepelova & Danny Incarnato & Caterina Parlato & Giulia Basile & Mara Maldotti & Francesca Anselmi & Salvatore Oliviero, 2017. "Intragenic DNA methylation prevents spurious transcription initiation," Nature, Nature, vol. 543(7643), pages 72-77, March.
    3. Harrison W. Gabel & Benyam Kinde & Hume Stroud & Caitlin S. Gilbert & David A. Harmin & Nathaniel R. Kastan & Martin Hemberg & Daniel H. Ebert & Michael E. Greenberg, 2015. "Disruption of DNA-methylation-dependent long gene repression in Rett syndrome," Nature, Nature, vol. 522(7554), pages 89-93, June.
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