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Stoica, A.-F.

Publications and source records attributed to Stoica, A.-F..

3 recordsLinked to original sources

CSOA: A Novel Single-Cell Gene Set Enrichment Analysis Method with Comprehensive Benchmarking

Single-cell gene set enrichment analysis is widely used to evaluate the activity of gene sets in individual cells, as measured by single-cell sequencing technologies. However, existing methods often generate ambiguous scores that cannot reliably distinguish cells enriched for a biological signal from background cells. To address this limitation, we developed Cell Set Overlap Analysis (CSOA), a novel method for gene set enrichment analysis that leverages gene pair relationships by quantifying pairwise overlaps between high-expression cell sets constructed for each signature gene. We benchmarked CSOA against sixteen established methods representing five methodological classes: direct scoring, rank-based scoring, model-based scoring, matrix decomposition, and overrepresentation analysis. Our evaluation framework introduces novel metrics tailored for the gene set scoring problem, such as score coverage and silhouette rank alignment. They are used alongside traditional metrics for binary classification, such as the Matthews correlation coefficient and area under the receiver operating characteristic (AUROC). CSOA showed superior accurate annotation of cell types and specific biological processes compared with competing approaches. This advantage was particularly pronounced in the class boundary determination benchmark, where it ranked the first in all evaluated datasets. CSOA also outperformed most of the compared methods in computational efficiency. Notably, CSOAs combination of outstanding performance in the score coverage metric and solid overall performance positions it as a uniquely well-suited method for distinguishing cells enriched for specific biological signals.

bioinformatics↗

An Integrated Single-Cell Atlas Reveals Hepatic Stellate Cell Heterogeneity and Spatiotemporal Dynamics after Liver Injury

BackgroundHepatic stellate cells (HSCs) orchestrate fibrosis-free repair after acute liver injury (ALI) and sustain fibrogenesis in chronic liver injury (CLI). However, the heterogeneity and spatiotemporal dynamics of HSCs across these different injury models remain elusive. This study sought to construct a cross-etiological HSC atlas to delineate HSC states and transitions during liver injury. MethodsWe integrated 86,072 single-cell transcriptomes from 84 mouse samples across four etiologies and validated findings using multi-omics data from 277 mouse and 798 human samples. Cellular dynamics were characterized through clustering, trajectory inference, spatial analysis, and multicellular coordination network analysis. Experimental validation included liver injury models and gain-of-functional assays in primary mouse HSCs and LX-2 cells. ResultsWe established a cross-etiological, spatiotemporally resolved HSC atlas comprising 11 subpopulations. Trajectory analysis delineated a continuous quiescence-activation-attenuation (QAA) trajectory, recapitulating the in vivo full spectrum of state transitions and being supported by sequential pathway activation validated in vitro. In ALI, HSCs spatiotemporally completed the QAA trajectory around injury zones, whereas collagen-producing S100a6 HSCs pathologically accumulated in mouse and human CLI due to trajectory dysregulation. Notably, the atlas identified a previously unrecognized apoptosis-prone Mrc2 HSC subtype strongly co-localized with p53 in both mice and humans. Overexpression of transcription factors confirmed that Hbp1, Tbx20, Atoh8, and Plagl1 enriched in Mrc2+ HSCs promoted HSC apoptosis. Finally, we revealed the microenvironment of distinct cellular modules which coordinated HSC progression along the QAA trajectory. A 531-gene signature derived from the inflammatory-fibrotic cellular module significantly correlated with fibrosis stage and hepatocellular carcinoma risk in human cohorts. ConclusionsWe established a comprehensive HSC atlas and delineates HSC heterogeneity and spatiotemporal dynamic across etiologies. Dysregulation of the QAA trajectory underlies fibrotic progression, providing a resource for identifying antifibrotic targets.

cell biology↗

scRetinaDB: A Comprehensive Database of Single-Cell and Spatial Omics from Cross-Species Retinas

The retina is essential for encoding visual signals, and its dysregulation can lead to retinal diseases. Recent advances in single-cell and spatial sequencing technologies have yielded extensive omics data from retinal tissues across species and biological conditions. However, existing retinal omics data are dispersed across various repositories without uniform processing, which limits integrative analysis. To address this we developed scRetinaDB (https://casapp.dnayun.com/scretina/), a comprehensive resource that aggregates single-cell RNA sequencing (scRNA-seq), single-cell assay for transposase-accessible chromatin using sequencing (scATAC-seq), and spatial RNA sequencing (spRNA-seq) data from retinas across species and diverse biological conditions. The database comprises over 2.79 million retinal cells collected from 453 scRNA-seq datasets spanning 34 studies, 17 species and 27 biological conditions. For each species, these scRNA-seq datasets were integrated to construct a retinal cell atlas. In addition, scRetinaDB also contains 107 scATAC-seq and 18 spRNA-seq datasets from human and mouse retinas. The scRetinaDB website provides four major modules separately for browsing species-specific omics data, searching cross-species omics profiles, performing analyses of cell type annotation and cell similarity analysis, and downloading preprocessed multi-omics datasets. Overall, scRetinaDB is a valuable resource for retinal single-cell and spatial omics, advancing cross-species studies particularly in vision research.

bioinformatics↗