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Analysis of individual patient pathway coordination in a cross-species single-cell kidney atlas

GSE291551 Homo sapiens; Mus musculus Expression profiling by high throughput sequencing 11 samples Submitted 2025/06/23 Platform GPL21103Platform GPL24676
Summary
The use of single-cell RNA sequencing in clinical and translational research is limited by cross-species differences and the challenge of identifying cell-type-specific, targetable molecular changes in individual patients. Here, we created an Integrated Single-cell Kidney Atlas including over one million cells from 140 samples, defining more than 70 conserved cell states in human and rodent models. We developed CellSpectra, a computational tool that quantifies changes in gene expression coordination across cellular functions, which we applied to kidney and lung cancer data. This tool powers our Patient-Level Single-Cell Functional Profiling Report, which highlights cell-type-specific changes in pathway gene expression coordination in individuals. Our cross-species atlas facilitates the selection of a rodent model that closely reflects the cellular and pathway-level signatures observed in a patient sample, advancing the application of single-cell methodologies in clinical precision medicine. Finally, by using experimental models, we demonstrate how our informatics approach can be applied for the potential selection of suitable therapeutics.
Published in
Analysis of individual patient pathway coordination in a cross-species single-cell kidney atlas
Klötzer KA, Abedini A, Li S et al. · Nature genetics 2025 · PMID 40775269 · doi:10.1038/s41588-025-02285-0
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Direct links to NCBI, no account and no request form: the whole study as GSE291551_RAW.tar, processed values as the series matrix, the supplementary file directory, and per-sample supplementary files for any of the 11 samples. Raw sequencing reads are also available from ENA.

Also filed as BioProject PRJNA1234133 and SRA study SRP569200. Searching any of these in the dataset finder brings you back here.

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