4.7 Article Proceedings Paper

stPlus: a reference-based method for the accurate enhancement of spatial transcriptomics

期刊

BIOINFORMATICS
卷 37, 期 -, 页码 I299-I307

出版社

OXFORD UNIV PRESS
DOI: 10.1093/bioinformatics/btab298

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资金

  1. National Key Research and Development Program of China [2018YFC0910404]
  2. National Natural Science Foundation of China [61873141, 61721003, 61573207]

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This study introduces a reference-based method called stPlus, which leverages scRNA-seq data to enhance spatial transcriptomics research. stPlus outperforms baseline methods in terms of gene and cell-level Spearman correlation coefficients, and its performance can be systematically evaluated through a clustering-based approach.
Motivation: Single-cell RNA sequencing (scRNA-seq) techniques have revolutionized the investigation of transcriptomic landscape in individual cells. Recent advancements in spatial transcriptomic technologies further enable gene expression profiling and spatial organization mapping of cells simultaneously. Among the technologies, imaging-based methods can offer higher spatial resolutions, while they are limited by either the small number of genes imaged or the low gene detection sensitivity. Although several methods have been proposed for enhancing spatially resolved transcriptomics, inadequate accuracy of gene expression prediction and insufficient ability of cell-population identification still impede the applications of these methods. Results: We propose stPlus, a reference-based method that leverages information in scRNA-seq data to enhance spatial transcriptomics. Based on an auto-encoder with a carefully tailored loss function, stPlus performs joint embedding and predicts spatial gene expression via a weighted k-nearest-neighbor. stPlus outperforms baseline methods with higher gene-wise and cell-wise Spearman correlation coefficients. We also introduce a clustering-based approach to assess the enhancement performance systematically. Using the data enhanced by stPlus, cell populations can be better identified than using the measured data. The predicted expression of genes unique to scRNA-seq data can also well characterize spatial cell heterogeneity. Besides, stPlus is robust and scalable to datasets of diverse gene detection sensitivity levels, sample sizes and number of spatially measured genes. We anticipate stPlus will facilitate the analysis of spatial transcriptomics.

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