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Structural perturbation of chromatin domains with multiple developmental regulators can severely impact gene regulation and development

GSE271760 Mus musculus (mouse) ChIP-seq / ATAC-seq (genome binding and open chromatin) 88 samples Submitted 2024/08/06 Platform GPL24247
At a glance

ChIP-seq / ATAC-seq (genome binding and open chromatin) · mouse · 88 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
88 samples: 21 conditions, mostly in triplicateGroups 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
Structural perturbation of chromatin domains with multiple developmental regulators can severely impact gene regulation and developmentbioRxiv : the preprint server for biology · 2024
SuperSeries — this record groups several sub-series.
Summary (written by the submitters)
This SuperSeries is composed of the SubSeries listed below.
Published in
Structural perturbation of chromatin domains with multiple developmental regulators can severely impact gene regulation and development
Chakraborty S, Wenzlitschke N, Anderson MJ et al. · bioRxiv : the preprint server for biology 2024 · PMID 39372737 · doi:10.1101/2024.08.03.606480
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 GSE271760_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 PRJNA1133039 and SRA study SRP517346. Searching any of these in the dataset finder brings you back here.

Study design
21 conditions, mostly in triplicate
es_wt ×7 C1-C4flxflx;CRE ×7 xen_wt ×5 C1-C4flxflx ×5 es_c5-c6d ×4 E4.5_C7-C10_WT_SC ×4 E4.5_C7-C10_HOM_SC ×4 E4.5_C5-C6_HOM_SC ×4 +27 more

Supports a between-group comparison across 74 samples.

How we read this: 21 replicated groups read from 88 sample titles; they account for 74 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

+ 48 more — browse all 88 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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