<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/GSE275nnn/GSE275651/</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=GSE275651</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Dispensable role of RPB1 CTD in co-transcriptional splicing in mouse ESC (Fraction chrRNA-seq)</name><description>To define the function of CTD on co-transcriptional splicing, we used auxin-inducible CTD degron system in mouse embryonic stem cells (mESCs) with auxin treatment for 3 hours to sufficiently deplete Rpb9. To measure co-transcriptional splicing, we fractionated mESCs cells (spiked in with Drosophila S2 cells for data normalization) into cytosolic (Cyt), nucleoplasm (NP), and chromatin/particle (Chr) fractions. We purified total RNA from Chr compartment, depleted ribosomal RNAs, and constructed two independent libraries for RNA-seq, which showed excellent reproducibility.</description><dates><publication>2026/05/04</publication></dates><accession>GSE275651</accession><cross_references><GSM>GSM8481950</GSM><GSM>GSM8481949</GSM><GSM>GSM8481947</GSM><GSM>GSM8481948</GSM><GPL>24247</GPL><GSE>275651</GSE><taxon>Mus musculus</taxon><PMID>[25772140]</PMID></cross_references></HashMap>