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Gene expression analysis of Unstimulated follicular B cells and follicular B cells stimulated with IFNa, CpG and CpG plus IFNa.

GSE244442 Mus musculus (mouse) RNA-seq (gene expression) 12 samples Submitted 2024/04/22 Platform GPL24247
At a glance

RNA-seq (gene expression) · mouse · 12 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
12 samples: 3 × Unstimulated FO B cells (Unstimulated), vs 3 × FO B cells stimulated with IFNa (IFNa), vs 3 × FO B cells stimulated with CpG (CpG), vs 3 × FO B cells stimulated with CpG plus IFNa (CpG + IFNa),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
Type I interferon promotes the fate of Toll-like receptor 9-stimulated follicular B cells to plasma cell differentiationPNAS nexus · 2024
Summary (written by the submitters)
We report the grobal gene expression in follicular (FO) B cells stimulated with CpG, IFNa, and CpG plus IFNa for 12 hours prior to the onset of PC differentiation. We found that stimulation with CpG plus IFNa upregulates metabolic processes compared to stimulation with CpG alone. This study highlight the pivotal role of IFNa in determining the fate of PC differentiation of TLR9-activated FO B cells.
Published in
Type I interferon promotes the fate of Toll-like receptor 9-stimulated follicular B cells to plasma cell differentiation
Higuchi R, Tanaka K, Saito Y et al. · PNAS nexus 2024 · PMID 38659975 · doi:10.1093/pnasnexus/pgae152
This dataset
Open GSE244442 in finder → Find more mouse RNA-seq datasets →
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.

Series matrix ↓
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 GSE244442_RAW.tar (it can run to tens of gigabytes).

All supplementary files ↗ Whole study · RAW.tar ↓
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.

Raw reads on ENA ↗

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 PRJNA1023174 and SRA study SRP464151. Searching any of these in the dataset finder brings you back here.

NCBI GEO page ↗ Paper (PMID 38659975) ↗
Study design
3 × Unstimulated FO B cells (Unstimulated), vs 3 × FO B cells stimulated with IFNa (IFNa), vs 3 × FO B cells stimulated with CpG (CpG), vs 3 × FO B cells stimulated with CpG plus IFNa (CpG + IFNa),

Supports a between-group comparison across 12 samples.

How we read this: 4 replicated groups read from 12 sample titles; they account for 12 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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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.