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Single-cell RNA and TCR sequencing from skin, blood and cerebral spinal fluid (CSF) samples from Degos disease patients

GSE279392 Homo sapiens (human) Single-cell RNA-seq 116 samples Submitted 2026/06/11 Platform GPL34284Platform GPL21290Platform GPL24676Platform GPL30173
At a glance

Single-cell RNA-seq · human · 116 samples

What it is
Single-cell RNA-seqGene activity measured in thousands of individual cells, so cell types can be told apart.
Organism
Homo sapiens (human)
Samples
116 samples: 103 distinct titles, 12 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.
SuperSeries — this record groups several sub-series.
Summary (written by the submitters)
This SuperSeries is composed of the SubSeries listed below.
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 GSE279392_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: Single-cell studies usually ship their counts as 10x files (matrix.mtx, barcodes.tsv, features.tsv), an .h5 file, or an .rds / .h5ad object that Seurat or Scanpy can open. Look for those among the supplementary files.

Also filed as BioProject PRJNA1172604 and SRA study SRP536700. Searching any of these in the dataset finder brings you back here.

Study design
103 distinct titles, 12 of them repeated
Degos_3_PBMC_PostRuxo_Wk ×3 Degos_1_Skin_Inflam ×2 Degos_2_Skin_Inflam_Lesion ×2 Degos_3_Skin_Inflam_PostRuxo_Wk_0 ×2 Degos_1_Skin_Scar ×2 Degos_3_Skin_Scar ×2 Degos_14_Skin_Scar_Lesion_1 ×2 Degos_3_PBMC_PostRuxo_Wk_4 ×2 +4 more

How we read this: Read from 116 sample titles: 103 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

+ 76 more — browse all 116 samples with per-sample file links →

Datasets on a similar topic

Search all human RNA-seq datasets in GEO →

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