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单细胞数据中的正交多模态整合与聚类

Orthogonal multimodality integration and clustering in single-cell data.

作者信息

Liu Yufang, Chen Yongkai, Lu Haoran, Zhong Wenxuan, Yuan Guo-Cheng, Ma Ping

机构信息

Department of Statistics, University of Georgia, Athens, GA, 30602, USA.

Department of Genetics and Genomics, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.

出版信息

BMC Bioinformatics. 2024 Apr 25;25(1):164. doi: 10.1186/s12859-024-05773-y.

DOI:10.1186/s12859-024-05773-y
PMID:38664601
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11045458/
Abstract

Multimodal integration combines information from different sources or modalities to gain a more comprehensive understanding of a phenomenon. The challenges in multi-omics data analysis lie in the complexity, high dimensionality, and heterogeneity of the data, which demands sophisticated computational tools and visualization methods for proper interpretation and visualization of multi-omics data. In this paper, we propose a novel method, termed Orthogonal Multimodality Integration and Clustering (OMIC), for analyzing CITE-seq. Our approach enables researchers to integrate multiple sources of information while accounting for the dependence among them. We demonstrate the effectiveness of our approach using CITE-seq data sets for cell clustering. Our results show that our approach outperforms existing methods in terms of accuracy, computational efficiency, and interpretability. We conclude that our proposed OMIC method provides a powerful tool for multimodal data analysis that greatly improves the feasibility and reliability of integrated data.

摘要

多模态整合结合来自不同来源或模态的信息,以更全面地理解一种现象。多组学数据分析中的挑战在于数据的复杂性、高维度和异质性,这需要复杂的计算工具和可视化方法来对多组学数据进行恰当的解释和可视化。在本文中,我们提出了一种用于分析CITE-seq的新方法,称为正交多模态整合与聚类(OMIC)。我们的方法使研究人员能够整合多种信息来源,同时考虑它们之间的依赖性。我们使用CITE-seq数据集进行细胞聚类来证明我们方法的有效性。我们的结果表明,我们的方法在准确性、计算效率和可解释性方面优于现有方法。我们得出结论,我们提出的OMIC方法为多模态数据分析提供了一个强大的工具,极大地提高了整合数据的可行性和可靠性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b118/11046773/65af0cb641e4/12859_2024_5773_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b118/11046773/67f31ca31c1a/12859_2024_5773_Fig1_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b118/11046773/31b597c11bff/12859_2024_5773_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b118/11046773/86454d8b8439/12859_2024_5773_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b118/11046773/915675b7d74f/12859_2024_5773_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b118/11046773/f954e895ba22/12859_2024_5773_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b118/11046773/1a4e69ff28e5/12859_2024_5773_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b118/11046773/65af0cb641e4/12859_2024_5773_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b118/11046773/67f31ca31c1a/12859_2024_5773_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b118/11046773/e8026d7990b2/12859_2024_5773_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b118/11046773/5d8b9a972ade/12859_2024_5773_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b118/11046773/31b597c11bff/12859_2024_5773_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b118/11046773/86454d8b8439/12859_2024_5773_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b118/11046773/915675b7d74f/12859_2024_5773_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b118/11046773/f954e895ba22/12859_2024_5773_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b118/11046773/1a4e69ff28e5/12859_2024_5773_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b118/11046773/65af0cb641e4/12859_2024_5773_Fig9_HTML.jpg

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本文引用的文献

1
High-plex protein and whole transcriptome co-mapping at cellular resolution with spatial CITE-seq.高多重蛋白和全转录组共定位与空间 CITE-seq 在细胞分辨率下。
Nat Biotechnol. 2023 Oct;41(10):1405-1409. doi: 10.1038/s41587-023-01676-0. Epub 2023 Feb 23.
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A single-cell and spatially resolved atlas of human breast cancers.人类乳腺癌的单细胞和空间分辨图谱。
Nat Genet. 2021 Sep;53(9):1334-1347. doi: 10.1038/s41588-021-00911-1. Epub 2021 Sep 6.
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Multi-omics integration in the age of million single-cell data.多组学整合在百万单细胞数据时代。
Nat Rev Nephrol. 2021 Nov;17(11):710-724. doi: 10.1038/s41581-021-00463-x. Epub 2021 Aug 20.
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Integrated analysis of multimodal single-cell data.多模态单细胞数据的综合分析。
Cell. 2021 Jun 24;184(13):3573-3587.e29. doi: 10.1016/j.cell.2021.04.048. Epub 2021 May 31.
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Single-cell profiling of myeloid cells in glioblastoma across species and disease stage reveals macrophage competition and specialization.跨物种和疾病阶段对胶质母细胞瘤中髓样细胞进行单细胞分析揭示了巨噬细胞的竞争和特化。
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Joint probabilistic modeling of single-cell multi-omic data with totalVI.单细胞多组学数据的总变分联合概率建模。
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Multiplex digital spatial profiling of proteins and RNA in fixed tissue.固定组织中蛋白质和 RNA 的多重数字空间分析。
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MOFA+: a statistical framework for comprehensive integration of multi-modal single-cell data.MOFA+:一种全面整合多模态单细胞数据的统计框架。
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BREM-SC: a bayesian random effects mixture model for joint clustering single cell multi-omics data.BREM-SC:一种用于联合聚类单细胞多组学数据的贝叶斯随机效应混合模型。
Nucleic Acids Res. 2020 Jun 19;48(11):5814-5824. doi: 10.1093/nar/gkaa314.
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CiteFuse enables multi-modal analysis of CITE-seq data.CiteFuse 支持 CITE-seq 数据的多模式分析。
Bioinformatics. 2020 Aug 15;36(14):4137-4143. doi: 10.1093/bioinformatics/btaa282.