<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/GSE326nnn/GSE326774/</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=GSE326774</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>SNHG29 knockdown by CRISPRi and shRNA in M07e acute myeloid leukemia cells</name><description>The long non-coding RNA SNHG29 has been identified as a candidate essential gene in acute myeloid leukemia (AML) through a genome-wide CRISPRi depletion screen. To characterize the transcriptomic consequences of SNHG29 loss, we performed RNA-seq in M07e AML cells following SNHG29 knockdown using two independent methods: CRISPRi (two sgRNAs targeting the SNHG29 promoter, with Luciferase-targeting sgRNA as control) and shRNA (two shRNAs targeting SNHG29, with scrambled shRNA as control). Three biological replicates were generated per condition. Differential expression analysis was performed using DESeq2.</description><dates><publication>2026/06/30</publication></dates><accession>GSE326774</accession><cross_references><GSM>GSM9639029</GSM><GSM>GSM9639028</GSM><GSM>GSM9639027</GSM><GSM>GSM9639026</GSM><GSM>GSM9639037</GSM><GSM>GSM9639032</GSM><GSM>GSM9639031</GSM><GSM>GSM9639030</GSM><GSM>GSM9639036</GSM><GSM>GSM9639025</GSM><GSM>GSM9639024</GSM><GSM>GSM9639035</GSM><GSM>GSM9639023</GSM><GSM>GSM9639034</GSM><GSM>GSM9639033</GSM><GPL>24676</GPL><GSE>326774</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>