<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Vaidya H</submitter><funding>NCI NIH HHS</funding><funding>NIH</funding><pagination>27</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9933260</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>24(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Epigenetic marks are encoded by DNA methylation and accumulate errors as organisms age. This drift correlates with lifespan, but the biology of how this occurs is still unexplained. We analyze DNA methylation with age in mouse intestinal stem cells and compare them to nonstem cells.&lt;h4>Results&lt;/h4>Age-related changes in DNA methylation are identical in stem and nonstem cells, affect most prominently CpG islands and correlate weakly with gene expression. Age-related DNA methylation entropy, measured by the Jensen-Shannon Distribution, affects up to 25% of the detectable CpG sites and is a better measure of aging than individual CpG methylation. We analyze this entropy as a function of age in seven other tissues (heart, kidney, skeletal muscle, lung, liver, spleen, and blo</pubmed_abstract><journal>Genome biology</journal><pubmed_title>DNA methylation entropy as a measure of stem cell replication and aging.</pubmed_title><pmcid>PMC9933260</pmcid><funding_grant_id>P50 CA254897</funding_grant_id><funding_grant_id>CA254897</funding_grant_id><funding_grant_id>CA100632</funding_grant_id><funding_grant_id>CA214005</funding_grant_id><pubmed_authors>Vaidya H</pubmed_authors><pubmed_authors>Keith K</pubmed_authors><pubmed_authors>Maegawa S</pubmed_authors><pubmed_authors>Calendo G</pubmed_authors><pubmed_authors>Jelinek J</pubmed_authors><pubmed_authors>Jeong HS</pubmed_authors><pubmed_authors>Issa JJ</pubmed_authors><pubmed_authors>Madzo J</pubmed_authors></additional><is_claimable>false</is_claimable><name>DNA methylation entropy as a measure of stem cell replication and aging.</name><description>&lt;h4>Background&lt;/h4>Epigenetic marks are encoded by DNA methylation and accumulate errors as organisms age. This drift correlates with lifespan, but the biology of how this occurs is still unexplained. We analyze DNA methylation with age in mouse intestinal stem cells and compare them to nonstem cells.&lt;h4>Results&lt;/h4>Age-related changes in DNA methylation are identical in stem and nonstem cells, affect most prominently CpG islands and correlate weakly with gene expression. Age-related DNA methylation entropy, measured by the Jensen-Shannon Distribution, affects up to 25% of the detectable CpG sites and is a better measure of aging than individual CpG methylation. We analyze this entropy as a function of age in seven other tissues (heart, kidney, skeletal muscle, lung, liver, spleen, and blo</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Feb</publication><modification>2026-04-12T20:07:48.461Z</modification><creation>2025-05-29T20:01:09.078Z</creation></dates><accession>S-EPMC9933260</accession><cross_references><pubmed>36797759</pubmed><doi>10.1186/s13059-023-02866-4</doi></cross_references></HashMap>