Integration of unpaired single cell omics data by deep transfer graph convolutional network

The rapid advance of large-scale atlas-level single cell RNA sequences and single-cell chromatin accessibility data provide extraordinary avenues to broad and deep insight into complex biological mechanism. Leveraging the datasets and transfering labels from scRNA-seq to scATAC-seq will empower the exploration of single-cell omics data. However, the current label transfer methods have limited performance, largely due to the lower capable of preserving fine-grained cell populations and intrinsic or extrinsic heterogeneity between datasets. Here, we present a robust deep transfer model based graph convolutional network, scTGCN, which achieves versatile performance in preserving biological variation, while achieving integration hundreds of thousands cells in minutes with low memory consumption. We show that scTGCN is powerful to the integration of mouse atlas data and multimodal data generated from APSA-seq and CITE-seq. Thus, scTGCN shows high label transfer accuracy and effectively knowledge transfer across different modalities.

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Publication Details

Journal
PLoS Computational Biology
Published
2025-01-16
DOI
https://doi.org/10.1371/journal.pcbi.1012625
Citations
2
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
1.61

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article

Integration of unpaired single cell omics data by deep transfer graph convolutional network

Shuilin Jin, Zhongxiao Zhang, Yulong Kan, Weihao Wang et al.
2 citations
PLoS Computational Biology
Single-cell and spatial transcriptomics
1.61
article

Integration of unpaired single cell omics data by deep transfer graph convolutional network

Shuilin Jin, Zhongxiao Zhang, Yulong Kan, Weihao Wang, Xikeng Liang, Yunjing Qi
article en
2 citations

Abstract

The rapid advance of large-scale atlas-level single cell RNA sequences and single-cell chromatin accessibility data provide extraordinary avenues to broad and deep insight into complex biological mechanism. Leveraging the datasets and transfering labels from scRNA-seq to scATAC-seq will empower the exploration of single-cell omics data. However, the current label transfer methods have limited performance, largely due to the lower capable of preserving fine-grained cell populations and intrinsic or extrinsic heterogeneity between datasets. Here, we present a robust deep transfer model based graph convolutional network, scTGCN, which achieves versatile performance in preserving biological variation, while achieving integration hundreds of thousands cells in minutes with low memory consumption. We show that scTGCN is powerful to the integration of mouse atlas data and multimodal data generated from APSA-seq and CITE-seq. Thus, scTGCN shows high label transfer accuracy and effectively knowledge transfer across different modalities.

PLoS Computational BiologyVol. 21(1)
Harbin Institute of Technology (CN)
National Natural Science Foundation of China, Harbin Institute of Technology
Openalex Percentile: Top 20%
Single-cell and spatial transcriptomics
1.61
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