<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/GSE304955/</Other></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></file_versions><scores/><additional><omics_type>Other</omics_type><species>Homo sapiens</species><gds_type>Other</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE304955</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Chimeric AGO2-miR-eCLIP analysis of LIMD1 deficient (CRISPR-Cas9 edited) human SAEC cells</name><description>To assess AGO2:miRNA:target interactions under LIMD1 deficiency, we performed chimeric AGO2-miR-eCLIP on CRISPR-edited hSAECs. This technique ligates miRNAs to their AGO2-bound targets, capturing endogenous AGO2:miRNA:target complexes. After successful IP with anti-AGO2 antibody, post-processing mapped reads were identified as AGO2-miRNA, AGO2-mRNA, or chimeric peaks.</description><dates><publication>2026/06/23</publication></dates><accession>GSE304955</accession><cross_references><GSM>GSM9160220</GSM><GSM>GSM9160222</GSM><GSM>GSM9160211</GSM><GSM>GSM9160210</GSM><GSM>GSM9160221</GSM><GSM>GSM9160209</GSM><GSM>GSM9160224</GSM><GSM>GSM9160213</GSM><GSM>GSM9160212</GSM><GSM>GSM9160223</GSM><GSM>GSM9160204</GSM><GSM>GSM9160215</GSM><GSM>GSM9160226</GSM><GSM>GSM9160225</GSM><GSM>GSM9160214</GSM><GSM>GSM9160217</GSM><GSM>GSM9160206</GSM><GSM>GSM9160227</GSM><GSM>GSM9160205</GSM><GSM>GSM9160216</GSM><GSM>GSM9160219</GSM><GSM>GSM9160208</GSM><GSM>GSM9160207</GSM><GSM>GSM9160218</GSM><GPL>30173</GPL><GSE>304955</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>