<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/GSE336nnn/GSE336192/</Other></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Homo sapiens</species><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE336192</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Paired CRISPR screens to map gene regulation in cis and trans (RNA-seq)</name><description>In this study, we develop a scalable approach that pairs discovery of cis- and trans-acting elements to systematically decipher the gene regulatory network. We explore the regulation of the immune checkpoint PD-L1 under both basal and IFNγ-stimulated contexts. PD-L1 expression on tumor cells serves as a clinically-actionable diagnostic for immune checkpoint blockade therapy across multiple cancer types.</description><dates><publication>2026/06/24</publication></dates><accession>GSE336192</accession><cross_references><GSM>GSM9829759</GSM><GSM>GSM9829757</GSM><GSM>GSM9829758</GSM><GSM>GSM9829764</GSM><GSM>GSM9829762</GSM><GSM>GSM9829763</GSM><GSM>GSM9829760</GSM><GSM>GSM9829761</GSM><GPL>34281</GPL><GSE>336192</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>