<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/GSE348nnn/GSE348087/</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=GSE348087</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Detecting Fusion Transcripts in Huh7 cells with Long-Read RNA-seq</name><description>This study is a comparison of sequencing technologies and library preparations protocols performed on RNA extracted from Huh-7 cells, a human hepatocellular carcinoma (HCC) cell line, for which a few characteristic fusion transcripts have previously been reported. The sequencing platforms and library types include Oxford Nanopore Technologies (ONT) MinION direct-cDNA, ONT MinION direct-RNA and ONT MinION PCR-cDNA, PacBio Revio Kinnex sequencing. Additionally, this study includes matched short-read sequencing data from the Illumina NovaSeq platform.</description><dates><publication>2026/09/26</publication></dates><accession>GSE348087</accession><cross_references><GSM>GSM10066200</GSM><GSM>GSM10066201</GSM><GSM>GSM10066198</GSM><GSM>GSM10066199</GSM><GSM>GSM10066202</GSM><GSM>GSM10066193</GSM><GSM>GSM10066196</GSM><GSM>GSM10066197</GSM><GSM>GSM10066194</GSM><GSM>GSM10066195</GSM><GPL>34284</GPL><GPL>34382</GPL><GPL>24106</GPL><GSE>348087</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>