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Single-cell parallel analysis of DNA damage and transcriptome reveals selective genome vulnerability

GSE268567 Mus musculus (mouse) Single-cell RNA-seq 30 samples Submitted 2025/01/03 Platform GPL24247Platform GPL24676
At a glance

Single-cell RNA-seq · mouse · 30 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
30 samples: 28 distinct titles, 2 of them repeatedGroups 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 parallel analysis of DNA damage and transcriptome reveals selective genome vulnerabilityNature methods · 2025
Summary (written by the submitters)
We used a new technology, named Paired-Damage-seq, to perform simultaneous profiling of DNA damage and mRNA on HeLa cells and mouse cortex at single-cell level.
Published in
Single-cell parallel analysis of DNA damage and transcriptome reveals selective genome vulnerability
Bai D, Cao Z, Attada N et al. · Nature methods 2025 · PMID 40128288 · doi:10.1038/s41592-025-02632-3
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 GSE268567_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 PRJNA1117815 and SRA study SRP510448. Searching any of these in the dataset finder brings you back here.

Study design
28 distinct titles, 2 of them repeated
Hela_Paired_Damage_DNA ×2 Hela_Paired_Damage_RNA ×2

How we read this: Read from 30 sample titles: 28 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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