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Abstract
We describe a suite of predictive models, coined FASTmC, for nonreference, 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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1 Department of Genetics, University of Georgia, Athens, Georgia 30602
2 Institute of Bioinformatics, University of Georgia, Athens, Georgia 30602
3 Department of Plant Biology, University of Georgia, Athens, Georgia 30602
4 Department of Genetics, University of Georgia, Athens, Georgia 30602; Department of Genetics, University of Georgia, Athens, Georgia 30602





