Gene expression profile at the single-cell level of skin and PBMC samples collected from patients with severe cutaneous adverse drug reactions (SCADR).
Single-cell RNA-seq · human · 14 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
- 14 samples: 14 samples, each with a distinct title — no replicated groupsGroups 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.
Read the full summary ↓
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.
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.
Supplementary files
The count tables and other files the authors uploaded. Take only the samples you need, or the whole study as GSE235512_RAW.tar (it can run to tens of gigabytes).
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 PRJNA986170 and SRA study SRP445245. Searching any of these in the dataset finder brings you back here.
Any grouping that defines a comparison lives in the sample characteristics, which GEO records separately from the titles.
How we read this: Read from 14 sample titles: 14 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.
- GSM7504437 S1_TEN
- GSM7504438 S2_SJS
- GSM7504439 S3_AGEP
- GSM7504440 S4_MPR
- GSM7504441 S5_Healthy_Control_1
- GSM7504442 S6_Healthy_Control_2
- GSM7504443 S7_Healthy_Control_3
- GSM7504444 S8_TEN
- GSM7504445 S9_SJS
- GSM7504446 S10_AGEP
- GSM7504447 S11_MPR
- GSM7504448 S12_Healthy_Control_1
- GSM7504449 S13_Healthy_Control_2
- GSM7504450 S14_Healthy_Control_3
- GSE227835 Single-cell RNA-seq data of human PBMC from Myasthenia Gravis patients 40 samples shares pbmc, single-cell
- GSE279945 OP3: single-cell multimodal dataset in PBMCs for perturbation prediction benchmarking 102 samples shares pbmc, single-cell
- GSE334588 Single-cell transcriptomic atlas of adult dermatomyositis, cutaneous lupus erythematosus and healthy skin 48 samples shares single-cell, cutaneous
- GSE316832 Comprehensive single-cell transcriptomic profiling of the scalp from patients with moderate-to-severe alopecia areata 30 samples shares single-cell, severe
- GSE272005 Genomic and single-cell landscape of transformed cutaneous T-cell lymphoma 32 samples shares single-cell, cutaneous
- GSE205672 Transcriptomes of human PBMCs and monocytes in sepsis patients 460 samples shares pbmc
- GSE267718 Single cell RNA sequencing (scRNAseq) of urine-derived cells, peripheral blood mononuclear (PBMC), and tumor cells from bladder cancer patients. 33 samples shares pbmc
- GSE267023 scRNA-seq analysis of PBMCs from ischemic stroke patients 16 samples shares pbmc
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.