Integration of single cell multiomics data by deep transfer hypergraph neural network.

IF 2.5 3区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Yulong Kan, Zhongxiao Zhang, Yingjie Wang, Yunjing Qi, Haoxin Chang, Weihao Wang, Zheng Zhang, Quanhong Liu, Xiaoran Shi
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Abstract

Multi-omics characterization of individual cells offers remarkable potential for analyzing the dynamics and relationships of gene regulatory states across millions of cells. How to integrate multimodal data is an open problem, existing integration methods struggle with accuracy and modality-specific biological variation retention. In this paper, we present scHyper (scalable, interpretable machine learning for single cell integration), a low-code and data-efficient deep transfer model designed for integrating paired and unpaired single-cell multimodal data. We benchmark scHyper against datasets from different multimodal data. ScHyper learns a low-dimensional representation and aligns the covariance matrices of the measured modalities, achieving high accuracy even with large scale atlas-level datasets with low memory and computational time across different cell lines, shedding light on regulatory relationships between different types of omics. Altogether, we show that scHyper is a versatile and robust tool for cell-type label transfer and integration from multimodal single-cell datasets.

Abstract Image

Abstract Image

Abstract Image

基于深度传递超图神经网络的单细胞多组学数据集成。
单个细胞的多组学表征为分析数百万细胞中基因调控状态的动态和关系提供了显着的潜力。如何集成多模态数据是一个开放的问题,现有的集成方法在准确性和模态特异性生物变异保留方面存在问题。在本文中,我们提出了scHyper(可扩展,可解释的单细胞集成机器学习),这是一种低代码和数据高效的深度传输模型,旨在集成成对和非成对的单细胞多模态数据。我们对来自不同多模态数据集的scHyper进行基准测试。ScHyper学习低维表示并对齐测量模式的协方差矩阵,即使使用跨不同细胞系的低内存和计算时间的大规模图谱级数据集也能实现高精度,从而揭示不同类型组学之间的调节关系。总之,我们表明scHyper是一个多功能和强大的工具,用于多模态单细胞数据集的细胞类型标签转移和集成。
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来源期刊
Briefings in Functional Genomics
Briefings in Functional Genomics BIOTECHNOLOGY & APPLIED MICROBIOLOGY-GENETICS & HEREDITY
CiteScore
6.30
自引率
2.50%
发文量
37
审稿时长
6-12 weeks
期刊介绍: Briefings in Functional Genomics publishes high quality peer reviewed articles that focus on the use, development or exploitation of genomic approaches, and their application to all areas of biological research. As well as exploring thematic areas where these techniques and protocols are being used, articles review the impact that these approaches have had, or are likely to have, on their field. Subjects covered by the Journal include but are not restricted to: the identification and functional characterisation of coding and non-coding features in genomes, microarray technologies, gene expression profiling, next generation sequencing, pharmacogenomics, phenomics, SNP technologies, transgenic systems, mutation screens and genotyping. Articles range in scope and depth from the introductory level to specific details of protocols and analyses, encompassing bacterial, fungal, plant, animal and human data. The editorial board welcome the submission of review articles for publication. Essential criteria for the publication of papers is that they do not contain primary data, and that they are high quality, clearly written review articles which provide a balanced, highly informative and up to date perspective to researchers in the field of functional genomics.
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