De novo analysis of bulk RNA-seq data at spatially resolved single-cell resolution.
|
IF: 17.694
|
Cited by: 10
|

Abstract

Uncovering the tissue molecular architecture at single-cell resolution could help better understand organisms' biological and pathological processes. However, bulk RNA-seq can only measure gene expression in cell mixtures, without revealing the transcriptional heterogeneity and spatial patterns of single cells. Herein, we introduce Bulk2Space ( https://github.com/ZJUFanLab/bulk2space ), a deep learning framework-based spatial deconvolution algorithm that can simultaneously disclose the spatial and cellular heterogeneity of bulk RNA-seq data using existing single-cell and spatial transcriptomics references. The use of bulk transcriptomics to validate Bulk2Space unveils, in particular, the spatial variance of immune cells in different tumor regions, the molecular and spatial heterogeneity of tissues during inflammation-induced tumorigenesis, and spatial patterns of novel genes in different cell types. Moreover, Bulk2Space is utilized to perform spatial deconvolution analysis on bulk transcriptome data from two different mouse brain regions derived from our in-house developed sequencing approach termed Spatial-seq. We have not only reconstructed the hierarchical structure of the mouse isocortex but also further annotated cell types that were not identified by original methods in the mouse hypothalamus.

Keywords

Spatial Transcriptomics

MeSH terms

Mice
Animals
RNA-Seq
Transcriptome
Algorithms
Exome Sequencing
Neoplasms
Single-Cell Analysis
Sequence Analysis, RNA
Gene Expression Profiling

Authors

Liao, Jie
Qian, Jingyang
Fang, Yin
Chen, Zhuo
Zhuang, Xiang
Zhang, Ningyu
Shao, Xin
Hu, Yining
Yang, Penghui
Cheng, Junyun
Hu, Yang
Yu, Lingqi
Yang, Haihong
Zhang, Jinlu
Lu, Xiaoyan
Shao, Li
Wu, Dan
Gao, Yue
Chen, Huajun
Fan, Xiaohui