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Multi-omics analysis of thermogenic lipolysis in brown adipocytes

GSE291567 Mus musculus (mouse) RNA-seq (gene expression) 18 samples Submitted 2025/07/30 Platform GPL24247
At a glance

RNA-seq (gene expression) · mouse · 18 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
18 samples: 6 × BMC, 0 h, vs 6 × BMC, 4 h, vs 6 × BMC, 24 h,Groups 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
Multi-omics analysis of thermogenic lipolysis in brown adipocytesiScience · 2025
Summary (written by the submitters)
The integration of omics technologies into molecular biological research has transformed it into a field where a system can be investigated as a whole by combining information from multiple biochemical layers. This extension of traditional molecular biology, where various data sources are considered independently, offers novel insights into complex molecular interactions.
Read the full summary ↓
Here, we present a multi-omics analysis of murine brown adipocytes undergoing thermogenic lipolysis, which is part of the non-shivering response to cold. Through combining information from multiple types of biomolecules, we describe what is important for each biochemical layer, and the coordinated molecular responses across different layers at the system level, at different time points. Furthermore, a classification of data integration approaches for multi-omics data analysis is presented, and their applications in our study are compared, providing insights into the focus and effectiveness of these methods.
Published in
Multi-omics analysis of thermogenic lipolysis in brown adipocytes
Anagho-Mattanovich M, Anagho-Mattanovich HA, Argemi-Muntadas L et al. · iScience 2025 · PMID 40949097 · doi:10.1016/j.isci.2025.113382
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 GSE291567_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 PRJNA1234155 and SRA study SRP569248. Searching any of these in the dataset finder brings you back here.

Study design
6 × BMC, 0 h, vs 6 × BMC, 4 h, vs 6 × BMC, 24 h,

Supports a between-group comparison across 18 samples.

How we read this: 3 replicated groups read from 18 sample titles; they account for 18 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
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