<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/GSE326623/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Danio rerio</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=GSE326623</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>inDropsPilot_29hpf-ef1a-mCherry</name><description>We profiled gene expression during zebrafish development. This inDrops single-cell RNA-seq dataset comprises 12,603 cells collected from 29 hpf Danio rerio embryos. Here, nuclear-tagged mCherry2 is driven by a ~2.2 kb upstream regulatory region of eef1a1l1, enabling ubiquitous nuclear labeling (Tg(eef1a1l1:h2b-mCherry2) /+). Single-cell analysis shows that reporter expression covaries with endogenous eef1a1l1 transcripts, serving as a proxy for eef1a1l1 expression.</description><dates><publication>2026/04/01</publication></dates><accession>GSE326623</accession><cross_references><GSM>GSM9635845</GSM><GSM>GSM9635847</GSM><GSM>GSM9635846</GSM><GSM>GSM9635849</GSM><GSM>GSM9635848</GSM><GSM>GSM9635850</GSM><GSM>GSM9635852</GSM><GSM>GSM9635851</GSM><GPL>30614</GPL><GSE>326623</GSE><taxon>Danio rerio</taxon></cross_references></HashMap>