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Tranposable Element Control by TRIM28 Safeguards PGC Sex Determination Program

GSE266178 Mus musculus (mouse) ChIP-seq / ATAC-seq (genome binding and open chromatin) 81 samples Submitted 2025/04/29 Platform GPL24247Platform GPL34290
At a glance

ChIP-seq / ATAC-seq (genome binding and open chromatin) · mouse · 81 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
81 samples: 24 conditions, mostly with about 4 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
Sex-specific expression and function of TRIM28 during mouse primordial germ differentiationiScience · 2025
SuperSeries — this record groups several sub-series.
Summary (written by the submitters)
This SuperSeries is composed of the SubSeries listed below.
Published in
Sex-specific expression and function of TRIM28 during mouse primordial germ differentiation
DiRusso JA, Zhan L, Tao Y et al. · iScience 2025 · PMID 41019377 · doi:10.1016/j.isci.2025.113474
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 GSE266178_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 PRJNA1106062 and SRA study SRP504772. Searching any of these in the dataset finder brings you back here.

Study design
24 conditions, mostly with about 4 replicates each
E10.5_PGC_Male_TRIM28KO_ATAC ×5 E10.5_PGC_Male_Control_ATAC ×4 E10.5_PGC_Female_Control_ATAC ×4 E10.5_PGC_Female_TRIM28KO_ATAC ×4 E14.5_PGC_Male_Control_ATAC ×4 E14.5_PGC_Female_Control_ATAC ×4 E11.5_PGC_Control_Male ×4 E11.5_PGC_TRIM28KO_Male ×4 +16 more

Supports a between-group comparison across 81 samples.

How we read this: 24 replicated groups read from 81 sample titles; they account for 81 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

+ 41 more — browse all 81 samples with per-sample file links →

Datasets on a similar topic

Search all mouse ChIP / ATAC / CUT&Tag datasets in GEO →

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