Method

metilene: fast and sensitive calling of differentially methylated regions from bisulfite sequencing data

    • 1Transcriptome Bioinformatics Group, LIFE - Leipzig Research Center for Civilization Diseases, University of Leipzig, 04107 Leipzig, Germany;
    • 2Interdisciplinary Center for Bioinformatics and Bioinformatics Group, Faculty of Computer Science, University of Leipzig, 04107 Leipzig, Germany;
    • 3RNomics Group, Fraunhofer Institute for Cell Therapy and Immunology - IZI, 04103 Leipzig, Germany;
    • 4Santa Fe Institute, Santa Fe, New Mexico 87501, USA;
    • 5Department of Theoretical Chemistry, University of Vienna, 1090 Vienna, Austria;
    • 6Max Planck Institute for Mathematics in Sciences, 04103 Leipzig, Germany
    • 7 These authors contributed equally to this work.
Published December 2, 2015. Vol 26 Issue 2, pp. 256-262. https://doi.org/10.1101/gr.196394.115
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Abstract

The detection of differentially methylated regions (DMRs) is a necessary prerequisite for characterizing different epigenetic states. We present a novel program, metilene, to identify DMRs within whole-genome and targeted data with unrivaled specificity and sensitivity. A binary segmentation algorithm combined with a two-dimensional statistical test allows the detection of DMRs in large methylation experiments with multiple groups of samples in minutes rather than days using off-the-shelf hardware. metilene outperforms other state-of-the-art tools for low coverage data and can estimate missing data. Hence, metilene is a versatile tool to study the effect of epigenetic modifications in differentiation/development, tumorigenesis, and systems biology on a global, genome-wide level. Whether in the framework of international consortia with dozens of samples per group, or even without biological replicates, it produces highly significant and reliable results.

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