RNA-seq of activated murine CD8+ T-cells cultured in high (0.625 mg/mL holotransferrin) or low iron (0.001 mg/mL holotransferrin) conditions with or without 40 mM aspartate
RNA-seq (gene expression) · mouse · 12 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
- 12 samples: 12 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.
- Paper
- Iron deficiency causes aspartate-sensitive dysfunction in CD8(+) T cellsNature communications · 2025
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 GSE251963_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: 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 PRJNA1056036 and SRA study SRP479751. 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 12 sample titles: 12 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.
- GSM7990633 CD8+ T-cells, mouse 1, 0.625 mg/mL holotransferrin
- GSM7990634 CD8+ T-cells, mouse 1, 0.625 mg/mL holotransferrin + 40 mM aspartate
- GSM7990635 CD8+ T-cells, mouse 1, 0.001 mg/mL holotransferrin
- GSM7990636 CD8+ T-cells, mouse 1, 0.001 mg/mL holotransferrin + 40 mM aspartate
- GSM7990637 CD8+ T-cells, mouse 2, 0.625 mg/mL holotransferrin
- GSM7990638 CD8+ T-cells, mouse 2, 0.625 mg/mL holotransferrin + 40 mM aspartate
- GSM7990639 CD8+ T-cells, mouse 2, 0.001 mg/mL holotransferrin
- GSM7990640 CD8+ T-cells, mouse 2, 0.001 mg/mL holotransferrin + 40 mM aspartate
- GSM7990641 CD8+ T-cells, mouse 3, 0.625 mg/mL holotransferrin
- GSM7990642 CD8+ T-cells, mouse 3, 0.625 mg/mL holotransferrin + 40 mM aspartate
- GSM7990643 CD8+ T-cells, mouse 3, 0.001 mg/mL holotransferrin
- GSM7990644 CD8+ T-cells, mouse 3, 0.001 mg/mL holotransferrin + 40 mM aspartate
- GSE334845 Discovery of Tcf7 regulators with clonally-resolved CRISPR screens identifies Trim28 as a mediator of CD8 T cell differentiation in tumors [RNA-Seq] 86 samples shares cd8, rna-seq
- GSE306744 Pre-division TCF1 downregulation determines long-term effector and memory CD8 T cell fates [RNA-Seq] 31 samples shares cd8, rna-seq
- GSE290839 PD-1 regulates tumor-infiltrating CD8+ T cells in both a cell-intrinsic and cell-extrinsic fashion [scRNA-seq] 20 samples shares cd8, rna-seq
- GSE269347 Daunorubicin-induced T cell remodeling facilitates a high antitumor response to PD-1 blockade therapy by promoting the expansion and effector function of CD8+ prolifeating T cells [scRNA-Seq] 16 samples shares cd8, rna-seq
- GSE253492 Transcriptional Regulation by NFATc1 and NFATc2 in chronically activated CD8+ T cells 16 samples shares cd8, activated
- GSE215759 Mettl3-dependent m6A modification is essential for effector differentiation and memory formation of CD8+ T cells [RNA-seq] 15 samples shares cd8, rna-seq
- GSE320177 All -trans retinoic acid suppresses CD8+ T cell terminal exhaustion which enhances anti–PD-1 efficacy against glioblastoma [RNA-Seq] 12 samples shares cd8, rna-seq
- GSE290455 RNAseq of activated CD8+ T cells with and without Glutamine Synthetase 10 samples shares cd8, activated
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.