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ChIP-seq analysis of control and DOT1L HET cortical nuclei.

GSE292609 Mus musculus (mouse) ChIP-seq / ATAC-seq (genome binding and open chromatin) 18 samples Submitted 2025/11/13 Platform GPL32159
At a glance

ChIP-seq / ATAC-seq (genome binding and open chromatin) · mouse · 18 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
18 samples: 8 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
Loss of DOT1L disrupts neuronal transcription and leads to a neurodevelopmental disorderBrain : a journal of neurology · 2026
Summary (written by the submitters)
We aimed to understand the changes in H3K79me2 deposition upon monoallelic DOT1L loss in cortical nuclei from 10 week old mice.
Published in
Loss of DOT1L disrupts neuronal transcription and leads to a neurodevelopmental disorder
Maroni MJ, Barton M, Lynch K et al. · Brain : a journal of neurology 2026 · PMID 40494548 · doi:10.1093/brain/awaf212
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 GSE292609_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 PRJNA1240293 and SRA study SRP572229. Searching any of these in the dataset finder brings you back here.

Study design
8 conditions, mostly in duplicate
Control_Female_H3K79me2 ×2 HET_Female_H3K79me2 ×2 HET_Male_H3K79me2 ×2 Control_Female_input ×2 HET_Female_input ×2 Control_Male_input ×2 HET_Male_input ×2 IgG_control ×2 +2 more

Supports a between-group comparison across 16 samples.

How we read this: 8 replicated groups read from 18 sample titles; they account for 16 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
Datasets on a similar topic

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