<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Haoqing Hu</submitter><organism>Homo sapiens</organism><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-16152</full_dataset_link><description>Engineered SOX17 (eSOX17) factors were used to replace Yamanaka factor SOX2 in induced expanded potential stem cell (EPSC) reprogramming. eSOX17 achieved more efficient reprogramming under both feeder and feeder-free conditions. We have compared the iEPSC cell lines generated during the reprogramming with the embryo-derived EPSC control and found a similar gene expression pattern.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Library Construction - Library was prepared by AZENTA using Poly-A selection</sample_protocol><sample_protocol>Sample Collection - Total RNA was extracted using Trizol (Invitrogen, #15596018) and more than 2 μg total RNA of each sample was submitted to AZENTA (Suzhou, China) for 150 bp paired-end RNA-seq</sample_protocol><sample_protocol>Nucleic Acid Extraction - Total RNA was extracted using Trizol (Invitrogen, #15596018)</sample_protocol><sample_protocol>Sequencing - Sequencing was performed on the Illumina Novaseq platform, in a 2x150bp paired-end (PE) configuration, with ~6.0 Gb PF data per sample</sample_protocol><figure_sub>Organization</figure_sub><figure_sub>MINSEQE Score</figure_sub><figure_sub>Assays and Data</figure_sub><figure_sub>Processed Data</figure_sub><figure_sub>MAGE-TAB Files</figure_sub><data_protocol>Data Transformation - Raw RNA-seq reads in fastq format were aligned to the hg38 transcriptome using RSEM and bowtie 2.0. Alignment results at the gene levels for multiple samples were merged and annotated using glbase3. Read counts per gene were calculated using RSEM and normalized to GC content using EDAseq. GC-normalized read counts ≥ 20 in at least two samples were kept. PCA was performed in R (stats::prcomp) on log2-transformed (rounded counts + 1), centered data; results were visualized with ggplot2/ggrepel.</data_protocol><omics_type>Metabolomics</omics_type><omics_type>Unknown</omics_type><omics_type>Transcriptomics</omics_type><omics_type>Genomics</omics_type><omics_type>Proteomics</omics_type><instrument_platform>Not applicable</instrument_platform><instrument_platform>Illumina NovaSeq 6000</instrument_platform><study_type>RNA-seq of coding RNA</study_type><species>Homo sapiens</species><pubmed_authors>Haoqing Hu</pubmed_authors></additional><is_claimable>false</is_claimable><name>Enhancing reprogramming towards human expanded pluripotency</name><description>Engineered SOX17 (eSOX17) factors were used to replace Yamanaka factor SOX2 in induced expanded potential stem cell (EPSC) reprogramming. eSOX17 achieved more efficient reprogramming under both feeder and feeder-free conditions. We have compared the iEPSC cell lines generated during the reprogramming with the embryo-derived EPSC control and found a similar gene expression pattern.</description><dates><release>2026-03-12T00:00:00Z</release><modification>2026-03-17T14:46:17.095Z</modification><creation>2025-11-17T11:42:22.084Z</creation></dates><accession>E-MTAB-16152</accession><cross_references><ENA>ERP185158</ENA><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003816</EFO><EFO>EFO_0003738</EFO><EFO>EFO_0004184</EFO></cross_references></HashMap>