GEO series
Multiomics Analyses Unveil Immune Landscape in Pediatric and Adult Sepsis [CITE-seq]
GSE279451
Homo sapiens
Expression profiling by high throughput sequencing; Other
40 samples
2025/09/28
GPL24676
Summary
Sepsis is defined as a life-threatening organ dysfunction caused by a dysregulated host response to infection. The immune response varies significantly based on the anatomical source of infection. This study uses cellular indexing of transcriptomes and epitopes by sequencing (CITE-seq) to profile surface protein expression and transcriptomics at the single-cell level in PBMC samples from 40 adults: 3 healthy controls, 5 ICU controls, and 32 sepsis patients. The sepsis patients are categorized by infections originating from different anatomical sites. The findings aim to support sepsis stratification and guide the development of targeted therapies based on infection sources.
Download
NCBI GEO page ↗
{# Names what the click gives you. "Open in finder" meant nothing to a
visitor who arrived from a search engine and has never seen the tool. #}
Find more
human RNA-seq datasets →
Similar datasets
- GSE296419 The critical role of the host endogenous immune compartment after intracerebroventricular CAR T cell therapy in recurrent GBM 143 samples
- GSE335494 B-cell depletion improves therapeutic index of combination checkpoint blockade in patients with advanced melanoma 44 samples
- GSE332623 Immunological Differences in Atopic Dermatitis Across Age Groups: Insights from Single-Cell Multi-Omics 54 samples
- GSE320042 High-resolution and noninvasive profiling of the tumor microenvironment with spatial ecotypes 38 samples
- GSE325670 Promoter mutagenesis and a massively parallel reporter screen of the MAPT locus identifies cis-regulatory elements and genetic variation effects 140 samples
- GSE317520 Mitochondrial DNA Mutations Drive Tumor Heterogeneity in Papillary Thyroid Carcinoma 92 samples
- GSE319236 Spatially resolved maternal and fetal cell contributions to severe Preeclampsia 152 samples
- GSE301785 The molecular basis for fate determination of nuclear polyadenylated RNA 131 samples
Share this dataset
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.