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Single-cell dynamic RNA and glycosylation sequencing reveal the process of iPSC differentiation into HSCs in vitro

GSE263152 Homo sapiens (human) Single-cell RNA-seq 18 samples Submitted 2025/01/01 Platform GPL24676
At a glance

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.
Organism
Homo sapiens (human)
Samples
18 samples: 18 samples, each with a distinct title — no replicated groupsGroups are read from the sample names, not from the paper. Check the list below.
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 dynamic RNA and glycosylation sequencing reveals the mechanism underlying the differentiation of pluripotent stem cells into hematopoietic stem cellsHuman cell · 2025
Summary (written by the submitters)
Understanding the differentiation process of human induced pluripotent stem cells (iPSCs) into hematopoietic stem/progenitor cells (HSPCs) is essential for advancing regenerative medicine and gaining insights into embryonic hematopoiesis. However, the connection between transcriptomic dynamics and glycation levels during this process remains unclear.
Read the full summary ↓
In this study, we conducted a systematic analysis of the dynamic transcriptome and glycation changes of HSPCs derived from iPSCs during in vitro differentiation. Comprehensive analysis showed that there is a significant correlation between staged hematopoietic differentiation of iPSC-derived HSPCs and the degree of glycation, particularly during the endothelial differentiation stage. Additionally, there are similarities between in vivo embryonic hematopoiesis and in vitro differentiation models, which reinforces the utility of these models for studying human hematopoiesis. This study provides important insights into the link between the transcriptome and glycation of HSPCs derived from iPSCs.
Published in
Single-cell dynamic RNA and glycosylation sequencing reveals the mechanism underlying the differentiation of pluripotent stem cells into hematopoietic stem cells
Feng W, Zeng S, Liu D et al. · Human cell 2025 · PMID 40425941 · doi:10.1007/s13577-025-01234-7
This dataset
Download · which file do I need?

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.

1 · Just have a look

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.

2 · Re-analyse it

Supplementary files

The count tables and other files the authors uploaded. Take only the samples you need, or the whole study as GSE263152_RAW.tar (it can run to tens of gigabytes).

3 · Start from the raw reads

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 PRJNA1095986 and SRA study SRP499593. Searching any of these in the dataset finder brings you back here.

Study design
18 samples, each with a distinct title — no replicated groups

Any grouping that defines a comparison lives in the sample characteristics, which GEO records separately from the titles.

How we read this: Read from 18 sample titles: 18 distinct titles with little repetition. These groups are guessed from the sample names, not taken from the paper, so check them against the sample list below before relying on them.

Samples in this study
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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.