‘Leveling’ the playing field for analyses of single-base resolution DNA methylomes

Over the past few years the cost of DNA sequencing has plummeted while the numbers and lengths of sequencing reads have increased. This sequencing revolution has led to widespread adoption of methods to investigate genome-wide patterns of DNA methylation, collectively referred to as whole-genome bisulfite sequencing (WGBS). Single-base resolution DNA methylomes are now routinely being decoded by combining high-throughput sequencing with sodium bisulfite conversion, the gold-standard method for the detection of cytosine DNA methylation [1,2]. With increasing acquisition and analysis of DNA methylomes there is a growing need to reach a consensus on the definition(s) of the amount of methylation at a specific cytosine or region. ‘Methylation level’ is often poorly defined, and can vary significantly depending on the experimenter and the queries being addressed. Therefore, we propose a set of guidelines to be considered when analyzing ‘methylation levels’ from WGBS data.