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Subclonal evolution revealed by single-cell profiles of expressed mutations identifies adaptation mechanisms to immunotherapy in melanoma.

GSE215963 Mus musculus (mouse) Single-cell RNA-seq 1497 samples Submitted 2024/10/27 Platform GPL21103Platform GPL21493Platform GPL24247
At a glance

Single-cell RNA-seq · mouse · 1497 samples

What it is
Single-cell RNA-seqGene activity measured in thousands of individual cells, so cell types can be told apart.
Organism
Mus musculus (mouse)
Samples
1497 samples: 34 conditions, mostly with about 12 replicates eachGroups 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
Stochastic modeling of single-cell gene expression adaptation reveals non-genomic contribution to evolution of tumor subclonesCell systems · 2025
SuperSeries — this record groups several sub-series.
Summary (written by the submitters)
This SuperSeries is composed of the SubSeries listed below.
Published in
Stochastic modeling of single-cell gene expression adaptation reveals non-genomic contribution to evolution of tumor subclones
Hirsch MG, Pal S, Rashidi Mehrabadi F et al. · Cell systems 2025 · PMID 39701099 · doi:10.1016/j.cels.2024.11.013
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 GSE215963_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 PRJNA891346 and SRA study SRP403101. Searching any of these in the dataset finder brings you back here.

Study design
34 conditions, mostly with about 12 replicates each
103_P05_A ×12 103_P05_B ×12 103_P05_C ×12 103_P05_D ×12 103_P05_E ×12 103_P05_F ×12 103_P05_G ×12 103_P05_H ×12 +26 more

Supports a between-group comparison across 400 samples.

How we read this: 34 replicated groups read from the first 400 of 1497 sample titles; they account for 400 of them. 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

+ 1457 more — browse all 1497 samples with per-sample file links →

Datasets on a similar topic

Search all mouse RNA-seq datasets in GEO →

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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.