<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/GSE333nnn/GSE333803/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></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=GSE333803</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Distinct media requirements for dopaminergic neuron reprogramming from human glia and fibroblasts</name><description>Bulk RNA sequencing was performed on human glial progenitor cells (hGPCs) derived from the hESC line RC17 and reprogrammed toward a dopaminergic neuron fate using Ascl1, Lmx1a, Nurr1 and shREST (ALNRi). Cells were cultured under two media conditions; standard NDiff medium or a B27/Neurobasal-based medium without small molecules (new media) and harvested at day 10 and day 21 post-transduction (three technical replicates per condition). The dataset was generated to identify transcriptional differences underlying the improved dopaminergic reprogramming efficiency observed with the new media. Gene-level counts were quantified using Salmon (alignment-based mode, GRCh38/hg38) and merged across samples using tximport.</description><dates><publication>2026/08/21</publication></dates><accession>GSE333803</accession><cross_references><GSM>GSM9773572</GSM><GSM>GSM9773571</GSM><GSM>GSM9773574</GSM><GSM>GSM9773573</GSM><GSM>GSM9773570</GSM><GSM>GSM9773581</GSM><GSM>GSM9773580</GSM><GSM>GSM9773579</GSM><GSM>GSM9773576</GSM><GSM>GSM9773575</GSM><GSM>GSM9773578</GSM><GSM>GSM9773577</GSM><GPL>24676</GPL><GSE>333803</GSE><taxon>Homo sapiens</taxon><PMID>[42608437]</PMID></cross_references></HashMap>