Modal-nexus auto-encoder for multi-modality cellular data integration and imputation

Heterogeneous feature spaces and technical noise hinder the cellular data integration and imputation. The high cost of obtaining matched data across modalities further restricts analysis. Thus, there’s a critical need for deep learning approaches to effectively integrate and impute unpaired multi-mo...

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Veröffentlicht in:Nature communications 2024-10, Vol.15 (1), p.9021-15, Article 9021
Hauptverfasser: Tang, Zhenchao, Chen, Guanxing, Chen, Shouzhi, Yao, Jianhua, You, Linlin, Chen, Calvin Yu-Chian
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Sprache:eng
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Zusammenfassung:Heterogeneous feature spaces and technical noise hinder the cellular data integration and imputation. The high cost of obtaining matched data across modalities further restricts analysis. Thus, there’s a critical need for deep learning approaches to effectively integrate and impute unpaired multi-modality single-cell data, enabling deeper insights into cellular behaviors. To address these issues, we introduce the Mo dal- N exus A uto- E ncoder (Monae). Leveraging regulatory relationships between modalities and employing contrastive learning within modality-specific auto-encoders, Monae enhances cell representations in the unified space. The integration capability of Monae furnishes it with modality-complementary cellular representations, enabling the generation of precise intra-modal and cross-modal imputation counts for extensive and complex downstream tasks. In addition, we develop Monae-E (Monae-Extension), a variant of Monae that can converge rapidly and support biological discoveries. Evaluations on various datasets have validated Monae and Monae-E’s accuracy and robustness in multi-modality cellular data integration and imputation. Heterogeneous feature spaces and technical noise hinder the cellular data integration and further analysis. Here, authors report a Modal-Nexus Auto-Encoder (Monae) to effectively integrate unpaired multi-modality cellular data and generate imputation counts for downstream analysis.
ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-024-53355-6