<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/GSE176nnn/GSE176248/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Methylation profiling</omics_type><species>Homo sapiens</species><gds_type>Methylation profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE176248</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Pivotal Role of the NuRD Complex in Remodeling Chromatin Environment and Maintaining Genome Architecture at CTCF Sites [BS-seq]</name><description>The currently available data of CTCF binding in mammalian cells are exclusively obtained with ChIP-seq. In order to fully retain the dynamic information of CTCF binding, we have developed a new method called GpC-Methylation Assisted Tracing (G-MAT) of a nuclear protein, which leverages DNA cytosine methylation to record the footprints of a protein within a given period of time.</description><dates><publication>2026/05/04</publication></dates><accession>GSE176248</accession><cross_references><GSM>GSM5681639</GSM><GSM>GSM5681638</GSM><GSM>GSM5360664</GSM><GSM>GSM5681640</GSM><GSM>GSM5360663</GSM><GSM>GSM5360666</GSM><GSM>GSM5360665</GSM><GSM>GSM5360668</GSM><GSM>GSM5360667</GSM><GSM>GSM5681646</GSM><GSM>GSM5681635</GSM><GSM>GSM5681634</GSM><GSM>GSM5681645</GSM><GSM>GSM5681648</GSM><GSM>GSM5681637</GSM><GSM>GSM5681636</GSM><GSM>GSM5681647</GSM><GSM>GSM5681642</GSM><GSM>GSM5681641</GSM><GSM>GSM5681644</GSM><GSM>GSM5681643</GSM><GPL>20301</GPL><GPL>23227</GPL><SRA>SRP322970</SRA><GSE>176248</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>