Principles and challenges of modeling temporal and spatial omics data

被引:31
作者
Velten, Britta [1 ,2 ,3 ,4 ]
Stegle, Oliver [1 ,2 ,5 ]
机构
[1] German Canc Res Ctr, Div Computat Genom & Syst Genet, Heidelberg, Germany
[2] Wellcome Sanger Inst, Cellular Genet Programme, Cambridge, England
[3] Heidelberg Univ, Ctr Organismal Studies, Heidelberg, Germany
[4] Heidelberg Univ, Interdisciplinary Ctr Sci Comp IWR, Heidelberg, Germany
[5] European Mol Biol Lab, Genome Biol Unit, Heidelberg, Germany
关键词
GENE REGULATORY NETWORKS; COMMON COORDINATE FRAMEWORK; LONGITUDINAL MULTI-OMICS; CELL RNA-SEQ; SINGLE-CELL; BREAST-CANCER; EXPRESSION; TIME; DYNAMICS; INFERENCE;
D O I
10.1038/s41592-023-01992-y
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Studies with temporal or spatial resolution are crucial to understand the molecular dynamics and spatial dependencies underlying a biological process or system. With advances in high-throughput omic technologies, time- and space-resolved molecular measurements at scale are increasingly accessible, providing new opportunities to study the role of timing or structure in a wide range of biological questions. At the same time, analyses of the data being generated in the context of spatiotemporal studies entail new challenges that need to be considered, including the need to account for temporal and spatial dependencies and compare them across different scales, biological samples or conditions. In this Review, we provide an overview of common principles and challenges in the analysis of temporal and spatial omics data. We discuss statistical concepts to model temporal and spatial dependencies and highlight opportunities for adapting existing analysis methods to data with temporal and spatial dimensions.
引用
收藏
页码:1462 / 1474
页数:13
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