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Genetic Analysis of the Cardiac Methylome at Single Nucleotide Resolution in a Model of Human Cardiovascular Disease

Publication at First Faculty of Medicine |
2014

Abstract

Epigenetic marks such as cytosine methylation are important determinants of cellular and whole-body phenotypes. However, the extent of, and reasons for inter-individual differences in cytosine methylation, and their association with phenotypic variation are poorly characterised.

Here we present the first genome-wide study of cytosine methylation at single-nucleotide resolution in an animal model of human disease.