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dc.contributor.authorHeyn, Holger-
dc.contributor.authorHernando-Herraez, Irene-
dc.contributor.authorMarqués-Bonet, Tomàs-
dc.contributor.authorEsteller, Manel-
dc.date.accessioned2015-03-12T12:53:55Z-
dc.date.available2015-03-12T12:53:55Z-
dc.date.issued2013-
dc.identifierdoi: 10.1101/gr.154187.112-
dc.identifierissn: 1088-9051-
dc.identifiere-issn: 1549-5469-
dc.identifier.citationGenome Research 23: 1363-1372 (2013)-
dc.identifier.urihttp://hdl.handle.net/10261/112296-
dc.descriptionHeyn, Holger el al.-- This article, published in Genome Research, is available under a Creative Commons License (Attribution-NonCommercial 3.0 Unported).-
dc.description.abstractDNA methylation patterns are important for establishing cell, tissue, and organism phenotypes, but little is known about their contribution to natural human variation. To determine their contribution to variability, we have generated genomescale DNA methylation profiles of three human populations (Caucasian-American, African-American, and Han Chinese-American) and examined the differentially methylated CpG sites. The distinctly methylated genes identified suggest an influence of DNA methylation on phenotype differences, such as susceptibility to certain diseases and pathogens, and response to drugs and environmental agents. DNA methylation differences can be partially traced back to genetic variation, suggesting that differentially methylated CpG sites serve as evolutionarily established mediators between the genetic code and phenotypic variability. Notably, one-third of the DNA methylation differences were not associated with any genetic variation, suggesting that variation in population-specific sites takes place at the genetic and epigenetic levels, highlighting the contribution of epigenetic modification to natural human variation. © 2013, Published by Cold Spring Harbor Laboratory Press.-
dc.description.sponsorshipThe research leading to these results received funding from the European Research Council (ERC) grant EPINORC under agreement number 268626, ERC Starting Grant (260372), NIH grants CA138461 and GM61388 (Pharmacogenomics Research Network), the MICINN Projects SAF2011-22803 and BFU2011-28549, the Cellex Foundation, the European Community's Seventh Framework Programme (FP7/2007-2013) from grant HEALTH-F5-2011-282510 (BLUEPRINT), and the Health and Science Departments of the Generalitat de Catalunya. I.H.H. is a fellow of the Generalitat de Catalunya (FI 2011).-
dc.publisherCold Spring Harbor Laboratory Press-
dc.relationinfo:eu-repo/grantAgreement/EC/FP7/268626-
dc.relationinfo:eu-repo/grantAgreement/EC/FP7/282510-
dc.relation.isversionofPublisher's version-
dc.rightsopenAccess-
dc.titleDNA methylation contributes to natural human variation-
dc.typeartículo-
dc.identifier.doi10.1101/gr.154187.112-
dc.relation.publisherversionhttp://dx.doi.org/10.1101/gr.154187.112-
dc.date.updated2015-03-12T12:53:55Z-
dc.description.versionPeer Reviewed-
dc.language.rfc3066eng-
dc.rights.licensehttp://creativecommons.org/licenses/by-nc/3.0/-
dc.contributor.funderEuropean Commission-
dc.contributor.funderMinisterio de Ciencia e Innovación (España)-
dc.contributor.funderFundació Privada Cellex-
dc.contributor.funderGeneralitat de Catalunya-
dc.relation.csic-
dc.identifier.funderhttp://dx.doi.org/10.13039/501100000780es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100004837es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100002809es_ES
dc.identifier.pmid23908385-
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.openairetypeartículo-
item.grantfulltextopen-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextWith Fulltext-
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