<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE285nnn/GSE285671/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Genomics</omics_type><species>Homo sapiens</species><gds_type>Genome binding/occupancy profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE285671</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>H3K4me3 ChIP-seq Identifies EMT-TFs in TGF-β-Induced A549 cells</name><description>H3K4me3 marks active gene regions and broad H3K4me3 occupancy is associated with genes critical for cell identity and function. To identify novel EMT-inducing transcription factors (EMT-TFs), we analyzed changes in broad H3K4me3 occupancy during TGF-β-induced epithelial-to-mesenchymal transition (EMT) in A549 lung adenocarcinoma cells using H3K4me3 ChIP-seq.</description><dates><publication>2026/07/31</publication></dates><accession>GSE285671</accession><cross_references><GSM>GSM8706617</GSM><GSM>GSM8706615</GSM><GSM>GSM8706616</GSM><GSM>GSM8706614</GSM><GPL>16791</GPL><GSE>285671</GSE><taxon>Homo sapiens</taxon><PMID>[42230580]</PMID></cross_references></HashMap>