Speaker
Description
Spatial transcriptomics studies are becoming increasingly large and commonplace, necessitating the simultaneous analysis of a large number of spatially resolved variables. Correspondingly, a diverse range of methodologies have been proposed to compare the spatial expression structure of genes. Here we apply persistent homology, a method from topological data analysis, to produce a continuous quantification of spatial structure in a given gene’s expression, and show how this metric can be used for downstream tasks such as spatially variable gene identification. We explore the unique advantages of topology for this task, deriving biologically meaningful insights into kidney disease and myocardial infarction using public spatial transcriptomics data. We also show how the non-parametric nature of homology enables our methodology to extend naturally to other spatial omics modalities, demonstrating this on a spatial metabolomics sample. Our work showcases the advantages of using a continuous quantification of spatial structure over p-value based approaches to spatially variable gene identification, the potential for developing unified methods for the analysis of different spatial omics modalities, and the utility of persistent homology in big data applications.
