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AbstractSpatial transcriptomic studies are becoming increasingly common and large, posing important statistical and computational challenges for many analytic tasks. Here, we present SPARK-X, a non-parametric method for rapid and effective detection of spatially expressed genes in large spatial transcriptomic studies. SPARK-X not only produces effective type I error control and high power but also brings orders of magnitude computational savings. We apply SPARK-X to analyze three large datasets, one of which is only analyzable by SPARK-X. In these data, SPARK-X identifies many spatially expressed genes including those that are spatially expressed within the same cell type, revealing new biological insights.
QH301-705.5, Method, Datasets as Topic, Non-parametric modeling, QH426-470, Spatial transcriptomics, Mice, Covariance test, Models, Spatial Interaction, HDST, Cerebellum, Genetics, Animals, Humans, Computer Simulation, RNA, Messenger, Biology (General), Slide-seq, Ovarian Neoplasms, SE analysis, Olfactory Bulb, Gene Expression Regulation, Female, Single-Cell Analysis, Transcriptome, Algorithms
QH301-705.5, Method, Datasets as Topic, Non-parametric modeling, QH426-470, Spatial transcriptomics, Mice, Covariance test, Models, Spatial Interaction, HDST, Cerebellum, Genetics, Animals, Humans, Computer Simulation, RNA, Messenger, Biology (General), Slide-seq, Ovarian Neoplasms, SE analysis, Olfactory Bulb, Gene Expression Regulation, Female, Single-Cell Analysis, Transcriptome, Algorithms
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