4.6 Article

DEEPsc: A Deep Learning-Based Map Connecting Single-Cell Transcriptomics and Spatial Imaging Data

期刊

FRONTIERS IN GENETICS
卷 12, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fgene.2021.636743

关键词

spatial gene expression atlas; scRNA-seq data; spatial information imputation; deep learning; metric learning; comprehensive evaluation metric

资金

  1. NIH [U01AR073159, P30AR075047]
  2. NSF [DMS1763272, MCB2028424]
  3. Simons Foundation [594598]

向作者/读者索取更多资源

Single-cell RNA sequencing (scRNA-seq) data provides valuable information on cell fate decisions, but lacks spatial arrangement. A deep learning-based method called DEEPsc is developed to impute spatial information onto scRNA-seq data using a reference atlas, showing improved balance between precision and robustness compared to existing methods. DEEPsc serves as a data-adaptive tool for analyzing cell fate decisions by connecting scRNA-seq datasets with spatial imaging datasets.
Single-cell RNA sequencing (scRNA-seq) data provides unprecedented information on cell fate decisions; however, the spatial arrangement of cells is often lost. Several recent computational methods have been developed to impute spatial information onto a scRNA-seq dataset through analyzing known spatial expression patterns of a small subset of genes known as a reference atlas. However, there is a lack of comprehensive analysis of the accuracy, precision, and robustness of the mappings, along with the generalizability of these methods, which are often designed for specific systems. We present a system-adaptive deep learning-based method (DEEPsc) to impute spatial information onto a scRNA-seq dataset from a given spatial reference atlas. By introducing a comprehensive set of metrics that evaluate the spatial mapping methods, we compare DEEPsc with four existing methods on four biological systems. We find that while DEEPsc has comparable accuracy to other methods, an improved balance between precision and robustness is achieved. DEEPsc provides a data-adaptive tool to connect scRNA-seq datasets and spatial imaging datasets to analyze cell fate decisions. Our implementation with a uniform API can serve as a portal with access to all the methods investigated in this work for spatial exploration of cell fate decisions in scRNA-seq data. All methods evaluated in this work are implemented as an open-source software with a uniform interface.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据