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DOGMA-seq of opioid addiction treatment in HIV-1 infected individuals

GSE234521 Homo sapiens (human) RNA-seq (gene expression) 27 samples Submitted 2024/07/01 Platform GPL24676
At a glance

RNA-seq (gene expression) · human · 27 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
27 samples: 6 conditions, mostly with about 6 replicates eachGroups 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
Medications for opioid use disorder shape immune responses during chronic HIV infectionCell reports. Medicine · 2025
Summary (written by the submitters)
Opioid use and HIV-1 infection a impact immune function independently, but their impact on the immune system together is unknown. To understand the impact of opioids on immune function in HIV-1 infected individuals we used DOGMA-seq to examine the transcriptome, chromatin accessibility, and surface protein expression in HIV-1-infected individuals undergoing opioid addiction treatment.
Published in
Medications for opioid use disorder shape immune responses during chronic HIV infection
Collora JA, Steinhauser SF, Davenport TC et al. · Cell reports. Medicine 2025 · PMID 40460829 · doi:10.1016/j.xcrm.2025.102159
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 GSE234521_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 PRJNA981575 and SRA study SRP441904. Searching any of these in the dataset finder brings you back here.

Study design
6 conditions, mostly with about 6 replicates each
CD4, scRNA-seq group ×6 CD4, scATAC-seq group ×6 CD4, CITE-seq group ×6 PBMC, scRNA-seq group ×3 PBMC, scATAC-seq group ×3 PBMC, CITE-seq group ×3

Supports a between-group comparison across 27 samples.

How we read this: 6 replicated groups read from 27 sample titles; they account for 27 of them. 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
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