<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/GSE318nnn/GSE318410/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Mus musculus</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=GSE318410</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>The effects of RBM27 on heart function</name><description>The goal of this study is to investigate how RBM27 regulates heart function. Total RNA was extracted using Tripure Isolation Reagent (Roche, Mannheim, Germany) from hearts of Rbm27flox/flox and Rbm27-CKO mice at 12 weeks old. Three independent biological replicates for each group were used for RNA-seq. RNA-seq was performed by deep sequencing using an Illumina Novaseq 6000 platform. Paired-end clean reads were aligned to the mouse reference genome(GRCm38/mm10) with Hisat2 v2.0.5, and the aligned reads were used to quantify mRNA expression by using featureCounts v1.5.0-p3.</description><dates><publication>2026/08/18</publication></dates><accession>GSE318410</accession><cross_references><GSM>GSM9494024</GSM><GSM>GSM9494023</GSM><GSM>GSM9494022</GSM><GSM>GSM9494027</GSM><GSM>GSM9494026</GSM><GSM>GSM9494025</GSM><GPL>24247</GPL><GSE>318410</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>