RNA sequencing of naïve, activated and HIV-1 infected CD4+ T cells
RNA-seq (gene expression) · human · 9 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
- 9 samples: 9 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 GSE328010_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 PRJNA1453501 and SRA study SRP691796. Searching any of these in the dataset finder brings you back here.
Supports a case/control comparison: 3 samples read as cases, 3 as controls.
How we read this: Read from 9 sample titles: 9 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.
- GSM9670305 Naive CD4+ T cells, donor D, biological replicate 1
- GSM9670306 Naive CD4+ T cells, donor E, biological replicate 2
- GSM9670307 Naive CD4+ T cells, donor F, biological replicate 3
- GSM9670308 Activated CD4+ T cells, donor D, biological replicate 1
- GSM9670309 Activated CD4+ T cells, donor E, biological replicate 2
- GSM9670310 Activated CD4+ T cells, donor F, biological replicate 3
- GSM9670311 Activated HIV-1 infected CD4+ T cells, donor D, biological replicate 1
- GSM9670312 Activated HIV-1 infected CD4+ T cells, donor E, biological replicate 2
- GSM9670313 Activated HIV-1 infected CD4+ T cells, donor F, biological replicate 3
- GSE247196 Productively HIV-1 infected and bystander primary human CD4+ T-cells 18 samples shares hiv-1, cd4, infected
- GSE319139 The HIV-1 Vpr R77Q mutant alters host apoptotic gene regulation in CD4+ T cells 33 samples shares hiv-1, cd4
- GSE280563 HIV-1 m6A methylome investigation by m6A-SAC-seq [CD4+ T cells] 12 samples shares hiv-1, cd4
- GSE329693 Microbiome-Derived Metabolites Shape CD4⁺ T-Cell Differentiation and Immune Aging in Chronic HIV-1 Infection [RNA-Seq] 36 samples shares hiv-1, cd4
- GSE299125 Paracrine Signals from HIV-1 Infected Immune Cells Reprogram Cervical Cancer Pathways 35 samples shares hiv-1, infected
- GSE342431 Transcriptomic effects of combined AZD4573 and SMAP-2 treatment in resting and anti-CD3/CD28-activated primary human CD4+ T cells 12 samples shares cd4, activated
- GSE299348 Single-cell epigenetic, transcriptional, protein, and TCR states of HIV-1-infected cells in gut 117 samples shares hiv-1, infected
- GSE313059 Single cell multiomic analysis of the impact of Delta-9-tetrahydrocannabinol on HIV infected CD4 T cells 16 samples shares cd4, infected
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.