Multi-distance based spectral embedding fusion for clustering single-cell methylation data

Qi Tian, Jianxiao Zou, Jianxiong Tang, Shicai Fan
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引用次数: 1

Abstract

Advances in high throughput sequencing have enabled DNA methylation profiling at single-cell resolution. The generation of single-cell methylation sequencing (scM-Seq) data provides unprecedented opportunities for a comprehensive dissection of epigenetic heterogeneity. An important step of exploring epigenetic heterogeneity is clustering cells according to their single-cell methylation profiles. However, the inherent sparsity and stochastic measurement characteristic of the data make it challenging. To this end, we introduce SINCEF, using spectral embedding fusion to reconstruct cell-to-cell pairwise distance for clustering single-cell methylation data. SIN CEF first calculates multiple basic distance matrices to capture cell-to-cell methylation dissimilarity relationships according to the global methylation status. Then it adopts spectral embedding to transform these basic distance matrices into the latent representations, pooling information from the basic distance measures. Finally, it reconstructs a novel distance matrix and implements hierarchical clustering to yield cell partitions. Assessments on several public scM-Seq datasets demonstrated that SINCEF could generate a more appropriate distance matrix to measure the methylation distance between cells, which considerably improved the clustering performance. As an additional benefit, the reconstructed novel distance matrix could help to visually assess the heterogeneity across cell populations through presenting the block structures in the hierarchical clustering heat maps. SINCEF is freely available on GitHub at https://github.com/TQBio/SINCEF.
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基于多距离谱嵌入融合的单细胞甲基化数据聚类
在高通量测序的进步使DNA甲基化分析在单细胞分辨率。单细胞甲基化测序(scM-Seq)数据的产生为表观遗传异质性的全面解剖提供了前所未有的机会。研究表观遗传异质性的一个重要步骤是根据单细胞甲基化谱对细胞进行聚类。然而,数据固有的稀疏性和随机测量特性使其具有挑战性。为此,我们引入了SINCEF,利用光谱嵌入融合重建细胞间的成对距离,用于聚类单细胞甲基化数据。SIN CEF首先计算多个基本距离矩阵,根据全局甲基化状态捕获细胞间甲基化不相似关系。然后采用谱嵌入的方法将这些基本距离矩阵转化为潜在表示,池化基本距离度量的信息。最后,重构新的距离矩阵,实现分层聚类,得到细胞分区。对几个公开的scM-Seq数据集的评估表明,SINCEF可以生成更合适的距离矩阵来测量细胞之间的甲基化距离,从而大大提高了聚类性能。作为一个额外的好处,重建的新型距离矩阵可以通过在分层聚类热图中呈现块结构来帮助直观地评估细胞群体的异质性。SINCEF可以在GitHub上免费获得,网址为https://github.com/TQBio/SINCEF。
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