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Adipogenic Transcriptional Regulation Mediated by PARP7 Through NAD+ Sensing Mechanism

GSE282161 Mus musculus (mouse) ChIP-seq / ATAC-seq (genome binding and open chromatin) 65 samples Submitted 2025/12/24 Platform GPL30172
At a glance

ChIP-seq / ATAC-seq (genome binding and open chromatin) · mouse · 65 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
65 samples: 18 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
NAD (+) Sensing by PARP7 Regulates the C/EBPβ-Dependent Transcription Program in Adipose Tissue In VivobioRxiv : the preprint server for biology · 2025
SuperSeries — this record groups several sub-series.
Summary (written by the submitters)
This SuperSeries is composed of the SubSeries listed below.
Published in
NAD (+) Sensing by PARP7 Regulates the C/EBPβ-Dependent Transcription Program in Adipose Tissue In Vivo
Stokes MS, Kim YJ, Kim Y et al. · bioRxiv : the preprint server for biology 2025 · PMID 40291749 · doi:10.1101/2025.04.07.647692
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 GSE282161_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 PRJNA1187495 and SRA study SRP545669. Searching any of these in the dataset finder brings you back here.

Study design
18 conditions, mostly in duplicate
Control siRNA 0 day ×4 Parp7 siRNA1 0 day ×4 Parp7 siRNA2 0 day ×4 Control siRNA 2 day ×4 Parp7 siRNA1 2 day ×4 Parp7 siRNA2 2 day ×4 Vehicle Treatment ×3 MG132 Treatment ×3 +24 more

Supports a between-group comparison across 51 samples.

How we read this: 18 replicated groups read from 65 sample titles; they account for 51 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

+ 25 more — browse all 65 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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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.