{"title":"QuadST identifies cell-cell interaction-changed genes in spatially resolved transcriptomics data","authors":"Xiaoyu Song, Yuqing Shang, Michelle Ehrlich, Panos Roussos, Guo-Cheng Yuan, Pei Wang","doi":"10.1101/gr.279859.124","DOIUrl":null,"url":null,"abstract":"Recent advances in spatially resolved transcriptomics (SRT) have provided valuable avenues for identifying cell-cell interactions and their critical roles in diseases. We introduce QuadST, a novel statistical method for the robust and powerful identification of cell-cell interactions and their impacted genes in single-cell SRT. QuadST models interactions at different cell-cell distance quantile levels and innovatively contrasts signals to identify interaction-changed genes, which exhibit stronger signals at shorter distances. Unlike other methods, QuadST does not require the specification of interacting cell pairs. It is also robust against unmeasured confounding factors and measurement errors of the data. Simulation studies demonstrate that QuadST effectively controls the type I error, even in misspecified settings, and significantly improves power over existing methods. Applications of QuadST to real datasets have successfully revealed biologically significant interaction-changed genes across various cell types.","PeriodicalId":12678,"journal":{"name":"Genome research","volume":"19 1","pages":""},"PeriodicalIF":5.5000,"publicationDate":"2025-06-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Genome research","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1101/gr.279859.124","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Recent advances in spatially resolved transcriptomics (SRT) have provided valuable avenues for identifying cell-cell interactions and their critical roles in diseases. We introduce QuadST, a novel statistical method for the robust and powerful identification of cell-cell interactions and their impacted genes in single-cell SRT. QuadST models interactions at different cell-cell distance quantile levels and innovatively contrasts signals to identify interaction-changed genes, which exhibit stronger signals at shorter distances. Unlike other methods, QuadST does not require the specification of interacting cell pairs. It is also robust against unmeasured confounding factors and measurement errors of the data. Simulation studies demonstrate that QuadST effectively controls the type I error, even in misspecified settings, and significantly improves power over existing methods. Applications of QuadST to real datasets have successfully revealed biologically significant interaction-changed genes across various cell types.
期刊介绍:
Launched in 1995, Genome Research is an international, continuously published, peer-reviewed journal that focuses on research that provides novel insights into the genome biology of all organisms, including advances in genomic medicine.
Among the topics considered by the journal are genome structure and function, comparative genomics, molecular evolution, genome-scale quantitative and population genetics, proteomics, epigenomics, and systems biology. The journal also features exciting gene discoveries and reports of cutting-edge computational biology and high-throughput methodologies.
New data in these areas are published as research papers, or methods and resource reports that provide novel information on technologies or tools that will be of interest to a broad readership. Complete data sets are presented electronically on the journal''s web site where appropriate. The journal also provides Reviews, Perspectives, and Insight/Outlook articles, which present commentary on the latest advances published both here and elsewhere, placing such progress in its broader biological context.