<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/GSE341nnn/GSE341158/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Other</omics_type><species>Mus musculus</species><gds_type>Other</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE341158</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>GFP ChIL-seq mapping of H3mm15-EGFP chromatin incorporation in transgenic mouse testis</name><description>H3mm15 is a testis-specific histone H3 variant whose genomic distribution has remained undefined. We applied chromatin integration labeling followed by sequencing (ChIL-seq) with an anti-GFP antibody to map H3mm15-EGFP incorporation in testes of transgenic mice expressing the fusion protein under the CAG enhancer/promoter. H3mm15-EGFP signal accumulated preferentially around transcription start sites, and incorporated genes were biased toward the transcriptionally active fraction of the genome. Non-transgenic littermates, which lack the EGFP fusion protein, were processed in parallel as controls.</description><dates><publication>2026/08/31</publication></dates><accession>GSE341158</accession><cross_references><GSM>GSM9901115</GSM><GSM>GSM9901114</GSM><GSM>GSM9901113</GSM><GSM>GSM9901116</GSM><GPL>30172</GPL><GSE>341158</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>