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Characterization of TLR signaling in Ticam2-/- macrophages

GSE321707 Mus musculus (mouse) RNA-seq (gene expression) 30 samples Submitted 2026/08/07 Platform GPL24247
At a glance

RNA-seq (gene expression) · mouse · 30 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
30 samples: 10 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.
Summary (written by the submitters)
Early Toll-like receptor (TLR) signaling termination in TRAM (Ticam2) KO macrophages selectively impairs activation of secondary response genes (SRG) and interferon-stimulated genes (ISGs), whereas primary response gene (PRG) induction remains largely intact. We performed bulk RNA-Seq on LTA- or LPS-stimulated primary WT and Ticam2-/- BMDMs after 2 h and 6 h of PAMP-treatment to analyze this phenomenom.
This dataset
Open GSE321707 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 GSE321707_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 PRJNA1429322 and SRA study SRP679818. Searching any of these in the dataset finder brings you back here.

NCBI GEO page ↗
Study design
10 conditions, mostly in triplicate
primary TRAM (Ticam2) KO macrophages, LPS-tre… ×3 primary TRAM (Ticam2) KO macrophages, LTA-tre… ×3 primary TRAM (Ticam2) KO macrophages, ×3 primary TRAM (Ticam2) KO macrophages, LPS-tre… ×3 primary TRAM (Ticam2) KO macrophages, LTA-tre… ×3 primary WT macrophages, LPS-treated, 6 hrs, ×3 primary WT macrophages, LTA-treated, 6 hrs, ×3 primary WT macrophages, ×3 +2 more

Supports a case/control comparison: 12 samples read as cases, 3 as controls.

How we read this: 10 replicated groups read from 30 sample titles; they account for 30 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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