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Synovial Dysregulation in Ankle Osteoarthritis: Molecular Insights and Pathogenetic Pathways [RNA-Seq 1]

GSE293276 Homo sapiens (human) RNA-seq (gene expression) 34 samples Submitted 2025/07/03 Platform GPL24676
At a glance

RNA-seq (gene expression) · human · 34 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
Homo sapiens (human)
Samples
34 samples: 26 × Synovium, End-stage Ankle Osteoarthritis, Sample vs 8 × Synovium, Ankle, Control, SampleGroups 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
Synovial Dysregulation in Ankle Osteoarthritis: Molecular Insights and Pathogenetic PathwaysJournal of orthopaedic research : official publication of the Orthopaedic Research Society · 2025
Summary (written by the submitters)
Osteoarthritis (OA) of the ankle is a debilitating condition that impacts almost 20% of adults in the United States. Little is known about the tissue, cellular and molecular basis of the disease, nor is the contribution of the synovium to the disease process understood. Here, we aimed to examine the gene expression profile of the synovium in ankle OA to uncover unique biological pathways altered in this condition.
Published in
Synovial Dysregulation in Ankle Osteoarthritis: Molecular Insights and Pathogenetic Pathways
Matthias J, Buckley S, David M et al. · Journal of orthopaedic research : official publication of the Orthopaedic Research Society 2025 · PMID 40605342 · doi:10.1002/jor.70016
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 GSE293276_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 PRJNA1243472 and SRA study SRP574041. Searching any of these in the dataset finder brings you back here.

Study design
26 × Synovium, End-stage Ankle Osteoarthritis, Sample vs 8 × Synovium, Ankle, Control, Sample

Supports a between-group comparison across 34 samples.

How we read this: 2 replicated groups read from 34 sample titles; they account for 34 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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