ENAapplication/xmlftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR123/060/ERR12357260/ERR12357260_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR123/075/ERR12357275/ERR12357275.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR123/077/ERR12357277/ERR12357277.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR123/062/ERR12357262/ERR12357262_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR123/060/ERR12357260/ERR12357260_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR123/074/ERR12357274/ERR12357274.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR123/061/ERR12357261/ERR12357261_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR123/058/ERR12357258/ERR12357258_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR123/076/ERR12357276/ERR12357276.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR123/061/ERR12357261/ERR12357261_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR123/057/ERR12357257/ERR12357257_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR123/059/ERR12357259/ERR12357259_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR123/057/ERR12357257/ERR12357257_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR123/062/ERR12357262/ERR12357262_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR123/078/ERR12357278/ERR12357278.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR123/073/ERR12357273/ERR12357273.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR123/059/ERR12357259/ERR12357259_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR123/058/ERR12357258/ERR12357258_1.fastq.gzprimaryOK200GenomicsMAINZInstitute of Molecular Genetic, University of Mainzhttps://www.ebi.ac.uk/ena/browser/view/PRJEB70417Transcriptome analyses of public datasets from human tissues and cells revealed that the alternative isoform V-3 represented the predominant variant of the globin cytoglobin (CYGB) in hepatoblastoma (HB) cell lines and in the majority of analysed normal and HB liver tissues. RNA-seq analyses on CYGB+/+ and gene-edited CYGB‐/‐ HepG2 cell lines were performed to investigate possible transcriptomic effects of the CYGB knockout and gain knowledge on the potential function of CYGB V-3 in HB cells. The submitted libraries consist of reads trimmed for quality and adapter sequences and filtered for quality. Each library, which was sequenced as paired reads, is composed of a forward reads file, a reverse reads file, and a single end reads file consisting of the reads whose respective pair was discarded in the processing step.xref:PubMed:38016326ENAfalseMolecular analysis of the human cytoglobin mRNA isoformsTranscriptome of CYGB+/+ and gene-edited CYGB‐/‐ HepG2 HB cells2023-12-122023-12-12PRJEB7041738016326