一种基于哈希的框架,用于增强高维单细胞轮廓的聚类描绘。

IF 3.7 Q2 GENETICS & HEREDITY Phenomics (Cham, Switzerland) Pub Date : 2022-05-19 eCollection Date: 2022-10-01 DOI:10.1007/s43657-022-00056-z
Xiao Liu, Ting Zhang, Ziyang Tan, Antony R Warden, Shanhe Li, Edwin Cheung, Xianting Ding
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引用次数: 2

摘要

尽管已经开发了许多方法来通过聚类高维(HD)单细胞组学数据来探索细胞的功能,但所有细胞中蛋白质或基因的生物标志物的不明显差异表达干扰了细胞聚类的描绘和下游分析。在这里,我们引入了一个基于哈希的框架来改进细胞簇的描绘,该框架基于这样的假设,即一个没有显著差异的变量可以分解为更多样的潜在变量来区分细胞。通过将原始数据投影到稀疏HD空间中,fly和densefly哈希预处理保留了数据的局部结构,并改进了现有聚类方法(如PhenoGraph)的聚类描绘。此外,对质谱数据集的分析表明,我们基于哈希的框架成功地揭示了细胞簇中新的隐藏异质性。所提出的框架通过引入更多的潜在变量来促进细胞生物标志物的利用,并丰富生物学发现。补充信息:在线版本包含补充材料,可访问10.1007/s43657-022-00056-z。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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A Hashing-Based Framework for Enhancing Cluster Delineation of High-Dimensional Single-Cell Profiles.

Although many methods have been developed to explore the function of cells by clustering high-dimensional (HD) single-cell omics data, the inconspicuously differential expressions of biomarkers of proteins or genes across all cells disturb the cell cluster delineation and downstream analysis. Here, we introduce a hashing-based framework to improve the delineation of cell clusters, which is based on the hypothesis that one variable with no significant differences can be decomposed into more diversely latent variables to distinguish cells. By projecting the original data into a sparse HD space, fly and densefly hashing preprocessing retain the local structure of data, and improve the cluster delineation of existing clustering methods, such as PhenoGraph. Moreover, the analyses on mass cytometry dataset show that our hashing-based framework manages to unveil new hidden heterogeneities in cell clusters. The proposed framework promotes the utilization of cell biomarkers and enriches the biological findings by introducing more latent variables.

Supplementary information: The online version contains supplementary material available at 10.1007/s43657-022-00056-z.

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