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In vivo systematic detection of the outcomes of CRISPR/Cas9 mediated DNA repair in skeletal muscle stem cells

GSE327708 Mus musculus (mouse) ChIP-seq / ATAC-seq (genome binding and open chromatin) 365 samples Submitted 2026/04/23 Platform GPL34328Platform GPL24247Platform GPL18480Platform GPL24973
At a glance

ChIP-seq / ATAC-seq (genome binding and open chromatin) · mouse · 365 samples

What it is
ChIP-seq / ATAC-seq (genome binding and open chromatin)Where proteins bind the genome, or which regions are open and active.
Organism
Mus musculus (mouse)
Samples
365 samples: 117 conditions, mostly in duplicateGroups 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
In vivo systematic detection of the outcomes of CRISPR-Cas9-mediated DNA repair in skeletal muscle stem cellsMolecular therapy : the journal of the American Society of Gene Therapy · 2026
SuperSeries — this record groups several sub-series.
Summary (written by the submitters)
This SuperSeries is composed of the SubSeries listed below.
Published in
In vivo systematic detection of the outcomes of CRISPR-Cas9-mediated DNA repair in skeletal muscle stem cells
He L, Fu Y, Wang Z et al. · Molecular therapy : the journal of the American Society of Gene Therapy 2026 · PMID 42015511 · doi:10.1016/j.ymthe.2026.04.032
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 GSE327708_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: Look for peak files (.bed, .narrowPeak) and signal tracks (.bigWig) among the supplementary files; the raw reads are on ENA.

Also filed as BioProject PRJNA1451905. Searching any of these in the dataset finder brings you back here.

Study design
117 conditions, mostly in duplicate
control for D ×51 control for S ×19 Lig4-KO ×9 Ctrl-for-Lig4 ×9 Ctrl-for-Ku80 ×8 Ku80-KO ×8 Ctrl-for-Nbn ×6 Nbn-KO ×6 +128 more

Supports a between-group comparison across 346 samples.

How we read this: 117 replicated groups read from 365 sample titles; they account for 346 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

+ 325 more — browse all 365 samples with per-sample file links →

Datasets on a similar topic

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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.