ABSTRACT
We describe a suite of predictive models, coined FASTmC, for non-reference, cost-effective exploration and comparative analysis of context-specific DNA methylation levels. Accurate estimations of true DNA methylation levels can be obtained from as few as several thousand short-reads generated from whole genome bisulfite sequencing. These models make high-resolution time course or developmental, and large diversity studies practical regardless of species, genome size and availability of a reference genome.
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