<HashMap><database>biostudies-arrayexpress</database><scores/><additional><omics_type>Unknown</omics_type><omics_type>Transcriptomics</omics_type><omics_type>Genomics</omics_type><omics_type>Proteomics</omics_type><submitter>xiao yang</submitter><instrument_platform>NextSeq 500</instrument_platform><study_type>RNA-seq of coding RNA</study_type><organism>Homo sapiens</organism><species>Homo sapiens</species><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-17157</full_dataset_link><description>This study contains bulk RNA sequencing datasets generated from THP1-derived macrophages and primary monocyte-derived macrophages under M0 and M1 polarization conditions. Wild-type and TET2-deficient cells were analyzed to characterize transcriptional programs associated with TET2 loss-of-function and phagocytosis-related pathways.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Sample Collection - THP1-derived macrophages and primary monocyte-derived macrophages were cultured under M0 and M1 polarization conditions. Cells were harvested at the indicated experimental endpoints and collected for RNA extraction.</sample_protocol><sample_protocol>Library Construction - RNA sequencing libraries were prepared from purified total RNA according to the manufacturer's instructions. Libraries were quality controlled and quantified before sequencing.</sample_protocol><sample_protocol>Sequencing - Paired-end RNA sequencing was performed on an Illumina platform with a read length of 150 bp. Sequencing generated paired FASTQ files for downstream transcriptomic analysis.Paired-end RNA sequencing was performed on an Illumina platform with a read length of 150 bp. Sequencing generated paired FASTQ files for downstream transcriptomic analysis.</sample_protocol><sample_protocol>Nucleic Acid Extraction - Total RNA was extracted from THP1-derived macrophages and primary monocyte-derived macrophages using a standard RNA isolation procedure. RNA quality and quantity were assessed prior to library preparation.</sample_protocol><figure_sub>Organization</figure_sub><figure_sub>MINSEQE Score</figure_sub><figure_sub>Assays and Data</figure_sub><figure_sub>MAGE-TAB Files</figure_sub><pubmed_authors>xiao yang</pubmed_authors></additional><is_claimable>false</is_claimable><name>Supporting datasets for: Mutation-resolved single-cell transcriptomics reveals enhanced β-amyloid clearance in TET2-mutant human monocytes</name><description>This study contains bulk RNA sequencing datasets generated from THP1-derived macrophages and primary monocyte-derived macrophages under M0 and M1 polarization conditions. Wild-type and TET2-deficient cells were analyzed to characterize transcriptional programs associated with TET2 loss-of-function and phagocytosis-related pathways.</description><dates><release>2026-06-16T00:00:00Z</release><modification>2026-06-16T20:16:29.519Z</modification><creation>2026-06-12T14:50:44.461Z</creation></dates><accession>E-MTAB-17157</accession><cross_references><ENA>ERP194992</ENA><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003738</EFO><EFO>EFO_0004184</EFO></cross_references></HashMap>