Leveraging spatial transcriptomics data to recover cell locations in single-cell RNA-seq with CeLEry.
Qihuang ZhangShunzhou JiangAmelia SchroederJian HuKejie LiBaohong ZhangDavid DaiEdward B LeeRui XiaoMingyao LiPublished in: Nature communications (2023)
Single-cell RNA sequencing (scRNA-seq) has revolutionized our understanding of cellular heterogeneity in health and disease. However, the lack of physical relationships among dissociated cells has limited its applications. To address this issue, we present CeLEry (Cell Location recovEry), a supervised deep learning algorithm that leverages gene expression and spatial location relationships learned from spatial transcriptomics to recover the spatial origins of cells in scRNA-seq. CeLEry has an optional data augmentation procedure via a variational autoencoder, which improves the method's robustness and allows it to overcome noise in scRNA-seq data. We show that CeLEry can infer the spatial origins of cells in scRNA-seq at multiple levels, including 2D location and spatial domain of a cell, while also providing uncertainty estimates for the recovered locations. Our comprehensive benchmarking evaluations on multiple datasets generated from brain and cancer tissues using Visium, MERSCOPE, MERFISH, and Xenium demonstrate that CeLEry can reliably recover the spatial location information for cells using scRNA-seq data.
Keyphrases
- single cell
- rna seq
- induced apoptosis
- high throughput
- gene expression
- cell cycle arrest
- deep learning
- electronic health record
- healthcare
- public health
- oxidative stress
- mental health
- physical activity
- stem cells
- endoplasmic reticulum stress
- cell death
- dna methylation
- bone marrow
- air pollution
- cell therapy
- multiple sclerosis
- cell proliferation
- squamous cell carcinoma
- soft tissue
- papillary thyroid
- artificial intelligence