<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/GSE335nnn/GSE335431/</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=GSE335431</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>H4R3me2a ChIP-seq in HCT116 cells</name><description>ChIP-seq was performed to profile H4R3me2a occupancy in HCT116 colorectal cancer cells with matched input DNA control. Libraries were sequenced as paired-end 150 bp reads on an Illumina NovaSeq 6000. Reads were aligned to GRCh38 with Bowtie2, peaks were called with MACS2 (q &lt; 0.05), and metagene profiles were generated with deepTools.</description><dates><publication>2026/06/20</publication></dates><accession>GSE335431</accession><cross_references><GSM>GSM9813557</GSM><GSM>GSM9813556</GSM><GPL>24676</GPL><GSE>335431</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>