<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Lao Z</submitter><funding>National Medical Research Council (NMRC)</funding><funding>NCI NIH HHS</funding><funding>National Medical Research Council</funding><pagination>2170-2180</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11096012</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>30(10)</volume><pubmed_abstract>&lt;h4>Purpose&lt;/h4>DNA methylation alterations are widespread in acute myelogenous leukemia (AML) and myelodysplastic syndrome (MDS), some of which appear to have evolved independently of somatic mutations in epigenetic regulators. Although the presence of somatic mutations in peripheral blood can predict the risk of development of AML and MDS, its accuracy remains unsatisfactory.&lt;h4>Experimental design&lt;/h4>We performed global DNA methylation profiling in a case control study nested within the Singapore Chinese Health Study to evaluate whether DNA methylation alterations were associated with AML/MDS development. Targeted deep sequencing and methylated DNA immunoprecipitation sequencing (MeDIP-seq) were performed on peripheral blood collected a median of 9.9 years before diagnosis of AML or MD</pubmed_abstract><journal>Clinical cancer research : an official journal of the American Association for Cancer Research</journal><pubmed_title>A Pre-Leukemic DNA Methylation Signature in Healthy Individuals at Higher Risk for Developing Myeloid Malignancy.</pubmed_title><pmcid>PMC11096012</pmcid><funding_grant_id>R01 CA144034</funding_grant_id><funding_grant_id>UM1 CA182876</funding_grant_id><funding_grant_id>MOH-OFIRG21nov-0007</funding_grant_id><funding_grant_id>NMRC/Fellowship/0036/2016</funding_grant_id><funding_grant_id>NMRC/TA/0051/2016</funding_grant_id><pubmed_authors>Yang H</pubmed_authors><pubmed_authors>Yuan JM</pubmed_authors><pubmed_authors>Chng WJ</pubmed_authors><pubmed_authors>Ng AY</pubmed_authors><pubmed_authors>Lao Z</pubmed_authors><pubmed_authors>Grigoropoulos N</pubmed_authors><pubmed_authors>Koeffler HP</pubmed_authors><pubmed_authors>Jia L</pubmed_authors><pubmed_authors>Ying L</pubmed_authors><pubmed_authors>Goh YT</pubmed_authors><pubmed_authors>Koh WP</pubmed_authors><pubmed_authors>Wang R</pubmed_authors><pubmed_authors>Sun QY</pubmed_authors><pubmed_authors>Yan B</pubmed_authors><pubmed_authors>Capinpin SM</pubmed_authors><pubmed_authors>Ding LW</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Pre-Leukemic DNA Methylation Signature in Healthy Individuals at Higher Risk for Developing Myeloid Malignancy.</name><description>&lt;h4>Purpose&lt;/h4>DNA methylation alterations are widespread in acute myelogenous leukemia (AML) and myelodysplastic syndrome (MDS), some of which appear to have evolved independently of somatic mutations in epigenetic regulators. Although the presence of somatic mutations in peripheral blood can predict the risk of development of AML and MDS, its accuracy remains unsatisfactory.&lt;h4>Experimental design&lt;/h4>We performed global DNA methylation profiling in a case control study nested within the Singapore Chinese Health Study to evaluate whether DNA methylation alterations were associated with AML/MDS development. Targeted deep sequencing and methylated DNA immunoprecipitation sequencing (MeDIP-seq) were performed on peripheral blood collected a median of 9.9 years before diagnosis of AML or MD</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 May</publication><modification>2026-06-03T05:17:11.64Z</modification><creation>2025-04-04T14:50:57.483Z</creation></dates><accession>S-EPMC11096012</accession><cross_references><pubmed>38437679</pubmed><doi>10.1158/1078-0432.CCR-22-3804</doi><doi>10.1158/1078-0432.ccr-22-3804</doi></cross_references></HashMap>