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Differential roles of copper-binding transcription factors and the subfamilies of the SWI/SNF complex in the transcriptional regulation of the skeletal muscle lineage

GSE253379 Mus musculus (mouse) RNA-seq (gene expression) 36 samples Submitted 2024/10/26 Platform GPL30172
At a glance

RNA-seq (gene expression) · mouse · 36 samples

What it is
RNA-seq (gene expression)Gene activity measured by sequencing. The summary does not mention single-cell work, so this is most likely bulk: one average per sample, the usual starting point for comparing groups.
Organism
Mus musculus (mouse)
Samples
36 samples: 12 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
The PBAF chromatin remodeling complex contributes to metal homeostasis through MTF1 regulationMetallomics : integrated biometal science · 2026
SuperSeries — this record groups several sub-series.
Summary (written by the submitters)
This SuperSeries is composed of the SubSeries listed below.
Published in
The PBAF chromatin remodeling complex contributes to metal homeostasis through MTF1 regulation
Carulli N, Johnston EE, Klein DC et al. · Metallomics : integrated biometal science 2026 · PMID 42246576 · doi:10.1093/mtomcs/mfag019
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 GSE253379_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: For RNA-seq the counts are usually a table among the supplementary files (look for 'counts', 'expression', 'FPKM' or 'TPM' in the file name). The series matrix of a sequencing study is sometimes nearly empty.

Also filed as BioProject PRJNA1065431 and SRA study SRP484009. Searching any of these in the dataset finder brings you back here.

Study design
12 conditions, mostly in duplicate
BAF180_Cu_RNA-seq ×2 BAF180_notreat_RNA-seq ×2 BAF180_Zn_RNA-seq ×2 BAF250_Cu_RNA-seq ×2 BAF250_notreat_RNA-seq ×2 BAF250_Zn_RNA-seq ×2 BRD9_Cu_RNA-seq ×2 BRD9_notreat_RNA-seq ×2 +16 more

Supports a between-group comparison across 24 samples.

How we read this: 12 replicated groups read from 36 sample titles; they account for 24 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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