Bulk Liver in MAFLD/MASH
Single-cell RNA-seq · human · 18 samples
- What it is
- Single-cell RNA-seqGene activity measured in thousands of individual cells, so cell types can be told apart. Read from the summary: GEO's own type field only says 'expression profiling by sequencing', so confirm it in the paper.
- Organism
- Homo sapiens (human)
- Samples
- 18 samples
- Data you can get
- A processed table (series matrix) and supplementary files from NCBI; the raw sequencing reads from ENA. Which of these hold counts depends on the study, so check the file list.
- Paper
- Single-cell landscape of peripheral immune cells in MASLD/MASHHepatology communications · 2025
Read the full summary ↓
Direct links to NCBI and ENA, no account and no request form. Pick by what you want to do: take the small processed table to look, the supplementary files to re-analyse, or the original raw data to start over.
Processed table
The series matrix: one table of values per sample as the submitters processed it. The smallest download, and it opens in Excel or R. Start here to see what the data look like.
Supplementary files
The count tables and other files the authors uploaded. Take only the samples you need, or the whole study as GSE267031_RAW.tar (it can run to tens of gigabytes).
Raw sequencing reads
The original FASTQ files, straight from the sequencer, held at ENA. Large, and you align them yourself, so only choose this if you need to re-process the study from scratch.
What the files usually look like: Single-cell studies usually ship their counts as 10x files (matrix.mtx, barcodes.tsv, features.tsv), an .h5 file, or an .rds / .h5ad object that Seurat or Scanpy can open. Look for those among the supplementary files.
Also filed as BioProject PRJNA1109378 and SRA study SRP506569. Searching any of these in the dataset finder brings you back here.
The grouping that defines any comparison lives in the sample characteristics, which GEO records separately from the titles.
How we read this: Sample titles run Liver_patient_10 … Liver_patient_36 and carry no group information.
- GSM8258728 Liver_patient_10
- GSM8258729 Liver_patient_18
- GSM8258730 Liver_patient_7
- GSM8258731 Liver_patient_4
- GSM8258732 Liver_patient_14
- GSM8258733 Liver_patient_9
- GSM8258734 Liver_patient_8
- GSM8258735 Liver_patient_6
- GSM8258736 Liver_patient_12
- GSM8258737 Liver_patient_17
- GSM8258738 Liver_patient_11
- GSM8258739 Liver_patient_13
- GSM8258740 Liver_patient_16
- GSM8258741 Liver_patient_21
- GSM8258742 Liver_patient_20
- GSM8258743 Liver_patient_15
- GSM8258744 Liver_patient_19
- GSM8258745 Liver_patient_36
- GSE309979 GeoMx GeoMx-DSP Toxic Lipid-induced Epigenetic Activation of ICAM1 in Liver Sinusoidal Endothelium Regulates Myeloid-Driven Fibro-inflammatory Response in MASH 217 samples shares mash, liver
- GSE255312 Spatial transcriptomics landscape for liver from patients with metabolic dysfunction-associated steatohepatitis (MASH) 72 samples shares mash, liver
- GSE287540 Transcriptomic and proteomic characterization of cell and protein biomarkers of checkpoint inhibitor-induced liver injury [bulk RNA-seq] 128 samples shares liver, bulk
- GSE217649 Bulk RNA sequencing for gene expression profileing of primary liver sinusoidal endothelial cells and iPSC-derived hepatic endoderm, septum mesenchymal cells, endothelial cells, and liver bud organoids 26 samples shares liver, bulk
- GSE268518 Duodenal-derived organoids from MASH patients exhibit altered digestive homeostasis. 39 samples shares mash
- GSE205154 Bulk RNA-Seq gene expression data for 289 primary and metastatic pancreatic ductal adenocarcinoma (PDAC) tumor samples from FFPE blocks. 289 samples shares bulk
- GSE297742 Bulk RNA-seq of primary tumor biopsy samples from prostate adenocarcinoma patients 234 samples shares bulk
- GSE263733 Single-cell transcriptome analysis reveals subtype-specific clonal evolution and microenvironmental changes in liver metastasis of pancreatic adenocarcinoma and their clinical implications 218 samples shares liver
Metadata from NCBI GEO, cached and refreshed periodically — the NCBI page above is authoritative. Downloads link straight to NCBI/ENA; nothing is proxied through BioTransfer.