MultiGAI: Global Attention-Based Integration of Single-Cell Multi-Omics with Batch Effects Correction

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Multi-GAI is a variational autoencoder framework that uses global attention to integrate single-cell multi-omics data while correcting for batch effects, effectively preserving biological signals.

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The paper introduces Multi-GAI, a variational autoencoder with a global attention mechanism for integrating single-cell multi-omics data (e.g., scRNA-seq with scATAC-seq or scRNA-seq with ADT) while correcting technical batch effects. Using specially designed components intended to limit batch-information propagation during encoding, the method aims to generate high-quality latent cell representations that preserve biological signals despite differences in modality distributions and noise. The authors report good performance not only for multi-omics batch correction but also for transcriptomic batch correction and integration involving spatial transcriptomic data. The paper does not state a specific limitation in the provided text. The paper does not explicitly discuss endometriosis or adenomyosis; it was included in the corpus via a keyword match in the upstream search index.

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Abstract

Single-cell multi-omics technologies allow the simultaneous measurement of multiple molecular modalities within the same cell, such as gene expression and chromatin accessibility (scRNA-seq + scATAC-seq) or gene expression and cell surface protein abundance (scRNA-seq + ADT), providing a multidimensional perspective on cellular states and regulatory mechanisms. However, these modalities often differ substantially in their distributions and noise levels and are affected by technical biases during experimental batches and sample processing, which can obscure true biological signals. To address these challenges, we present Multi-GAI, a variational autoencoder (VAE) framework with a global attention mechanism. MultiGAI integrates global information from the dataset during encoding and employs specially designed components to limit the propagation of batch information. This design allows effective batch effects correction while preserving key biological signals, generating high-quality latent representations of cells. Notably, in addition to performing well on single-cell multi-omics data, MultiGAI also demonstrates good performance in batch effects correction for single-cell transcriptomic data and in the integration of spatial transcriptomic data. Overall, MultiGAI provides a novel strategy for batch effects correction while retaining biological information, offering new insights for future single-cell multi-omics data integration.
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Abstract Single-cell multi-omics technologies allow the simultaneous measurement of multiple molecular modalities within the same cell, such as gene expression and chromatin accessibility (scRNA-seq + scATAC-seq) or gene expression and cell surface protein abundance (scRNA-seq + ADT), providing a multidimensional perspective on cellular states and regulatory mechanisms. However, these modalities often differ substantially in their distributions and noise levels and are affected by technical biases during experimental batches and sample processing, which can obscure true biological signals. To address these challenges, we present Multi-GAI, a variational autoencoder (VAE) framework with a global attention mechanism. MultiGAI integrates global information from the dataset during encoding and employs specially designed components to limit the propagation of batch information. This design allows effective batch effects correction while preserving key biological signals, generating high-quality latent representations of cells. Notably, in addition to performing well on single-cell multi-omics data, MultiGAI also demonstrates good performance in batch effects correction for single-cell transcriptomic data and in the integration of spatial transcriptomic data. Overall, MultiGAI provides a novel strategy for batch effects correction while retaining biological information, offering new insights for future single-cell multi-omics data integration. Competing Interest Statement The authors have declared no competing interest. Footnotes Added batch correction methods for single-cell transcriptomics and integration methods for spatial transcriptomics.

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last seen: 2026-05-20T01:45:00.602351+00:00