← BioTransfer GEO Dataset Finder
GEO series

Bulk RNA-seq data of orbital fibroblasts and peripheral blood mononuclear cells (PBMCs) from thyroid eye disease patients

GSE280114 Homo sapiens (human) RNA-seq (gene expression) 59 samples Submitted 2025/12/09 Platform GPL30209Platform GPL29480
At a glance

RNA-seq (gene expression) · human · 59 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
59 samples: 45 distinct titles, 7 of them repeatedGroups 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
Integrative transcriptomic profiling and machine learning reveal hypoxia-associated molecular signatures for precision diagnosis in thyroid eye diseaseHuman genomics · 2025
Summary (written by the submitters)
Smoking affects the severity of TED manifestations as well as patients’ responses to medication. However, the underlying pathogenic mechanisms of smoking remain largely unclear in TED.To address these issues, we conducted bulk RNA-seq to distinguish orbital fibroblats under different time of treatment of cigarette smoking extract (CSE) from control. Besides, bulk RNA-seq was performed to unravel transcriptional differences between TED patients with or without smoking habits.
Published in
Integrative transcriptomic profiling and machine learning reveal hypoxia-associated molecular signatures for precision diagnosis in thyroid eye disease
Qian W, Zhu T, Liu J et al. · Human genomics 2025 · PMID 41287009 · doi:10.1186/s40246-025-00860-4
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 GSE280114_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 PRJNA1176489 and SRA study SRP540350. Searching any of these in the dataset finder brings you back here.

Study design
45 distinct titles, 7 of them repeated
fibroblast, control, ×3 fibroblast, CSE treatment, 6h, ×3 fibroblast, CSE treatment, 8h, ×3 fibroblast, CSE treatment, 12h, ×3 fibroblast, CSE treatment, 24h, ×3 fibroblast, CSE treatment, 48h, ×3 fibroblast, CSE treatment, 72h, ×3

Supports a case/control comparison: 38 samples read as cases, 3 as controls.

How we read this: Read from 59 sample titles: 45 distinct titles with little repetition. 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

+ 19 more — browse all 59 samples with per-sample file links →

Datasets on a similar topic

Search all human RNA-seq datasets in GEO →

Share this dataset

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.