2025-12-17T16:26:58Z
2025-12-17T16:26:58Z
2025-10-21
2025-12-17T16:26:58Z
DNA methylation is a widely studied epigenetic mark and a powerful biomarker of cell type, age, environmental exposures, and disease. Whole-genome sequencing following selective conversion of unmethylated cytosines into thymines via bisulfite treatment or enzymatic methods remains the reference method for DNA methylation profiling genome-wide. While numerous software tools facilitate processing of DNA methylation sequencing reads, a comprehensive benchmarking study has been lacking. In this study, we systematically compared complete computational workflows for processing DNA methylation sequencing data using a dedicated benchmarking dataset generated with five whole-genome profiling protocols. As an evaluation reference, we employed accurate locus-specific measurements from our previous benchmark of targeted DNA methylation assays. Based on this experimental gold-standard assessment and multiple performance metrics, we identified workflows that consistently demonstrated superior performance and revealed major workflow development trends. To ensure the long-term utility of our benchmark, we implemented an interactive workflow execution and data presentation platform, adaptable to user-defined criteria and readily expandable to future software.
Article
Published version
English
Biologia computacional; Seqüència de nucleòtids; Epigènesi; Computational biology; Nucleotide sequence; Epigenesis
Oxford University Press
Reproducció del document publicat a: https://doi.org/10.1093/nar/gkaf970
Nucleic Acids Research, 2025, vol. 53, num.19
https://doi.org/10.1093/nar/gkaf970
cc-by (c) Lin, Y.Y. et al., 2025
https://creativecommons.org/licenses/by/4.0/