<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/GSE304nnn/GSE304967/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Other</omics_type><species>synthetic construct</species><gds_type>Other</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE304967</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>HNRNPH controls alternative splicing cooperatively on a transcriptome-wide scale [RTstop profiling]</name><description>High-throughput experimental validation of G-quadruplex formation for RNAs with HNRNPH binding sites is not available. Hence, we performed an in vitro Reverse Transcriptase Stop-Profiling (RT-Stop profiling) in high-throughput to map G-quadruplex structure formation of 2000 individual RNAs that have been identified to be bound by HNRNPH.</description><dates><publication>2026/04/14</publication></dates><accession>GSE304967</accession><cross_references><GSM>GSM9160408</GSM><GSM>GSM9160407</GSM><GSM>GSM9160409</GSM><GSM>GSM9160411</GSM><GSM>GSM9160410</GSM><GSM>GSM9160413</GSM><GSM>GSM9160412</GSM><GSM>GSM9160415</GSM><GSM>GSM9160414</GSM><GSM>GSM9160406</GSM><GSM>GSM9160416</GSM><GSM>GSM9160405</GSM><GPL>19424</GPL><GSE>304967</GSE><taxon>synthetic construct</taxon><PMID>[41867855]</PMID></cross_references></HashMap>