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Comprehensive transcriptomic analysis of immune-related genes in diabetic foot ulcers: New insights into mechanisms and therapeutic targets

GSE199939 Homo sapiens Expression profiling by high throughput sequencing 21 samples Submitted 2024/05/30 Platform GPL24676
Summary
We performed RNA-seq on tissue biopsies derived from patients with DFU and compared it to healthy controls who had similar foot surgery to identify the significant immune related differentially expressed genes between normal and DFU samples. Our results identified that there was a total of 8800 DEGs detected by RNA-seq data analysis, among which 2351 were upregulated and 6449 downregulated genes in DFU. 526 differential IRGs were obtained from intersection of DEGs and IRGs. These results suggest that a deregulated immune cells contribute to pathogenesis of DFUs.The purpose of this study was to identify the key biomarkers of the abnormally expressed genes and immune infiltration in the diabetic wound and to provide diagnostic and therapeutic targets for DFU.
Published in
Comprehensive transcriptomic analysis of immune-related genes in diabetic foot ulcers: New insights into mechanisms and therapeutic targets
Jiang N, Xu C, Xu Y et al. · International immunopharmacology 2024 · PMID 39079197 · doi:10.1016/j.intimp.2024.112638
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Direct links to NCBI, no account and no request form: the whole study as GSE199939_RAW.tar, processed values as the series matrix, the supplementary file directory, and per-sample supplementary files for any of the 21 samples. Raw sequencing reads are also available from ENA.

Also filed as BioProject PRJNA822286 and SRA study SRP367217. Searching any of these in the dataset finder brings you back here.

Study design
21 conditions, each sampled once — no replicated groups

Read from 21 sample titles: 21 distinct titles with little repetition. Check it against the sample list below before relying on it.

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