Abstract
Plant scientists are rapidly integrating single-cell RNA sequencing (scRNA-seq) into their workflows. Maximizing the potential of scRNA-seq requires a proper understanding of the spatiotemporal context of cells. However, positional information is inherently lost during scRNA-seq, limiting its potential to characterize complex biological systems. In this review we highlight how current single-cell analysis pipelines cannot completely recover spatial information, which confounds biological interpretation. Various strategies exist to identify the location of RNA, from classical RNA in situ hybridization to spatial transcriptomics. Herein we discuss the possibility of utilizing this spatial information to supervise single-cell analyses. An integrative approach will maximize the potential of each technology, and lead to insights which go beyond the capability of each individual technology.
Original language | English |
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Pages (from-to) | 1018-1028 |
Journal | Trends in Plant Science |
Volume | 29 |
Issue number | 9 |
Early online date | 2 Apr 2024 |
DOIs | |
Publication status | Published - 2024 |
Keywords
- cellular ontogeny
- dimension reduction
- RNA-seq
- single-cell
- spatial transcriptomics