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PNAS Plus: Robust single-cell Hi-C clustering by convolution- and random-walk–based imputation

机译:PNAS Plus:通过基于卷积和随机游走的插补进行可靠的单细胞Hi-C聚类

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摘要

Three-dimensional genome structure plays a pivotal role in gene regulation and cellular function. Single-cell analysis of genome architecture has been achieved using imaging and chromatin conformation capture methods such as Hi-C. To study variation in chromosome structure between different cell types, computational approaches are needed that can utilize sparse and heterogeneous single-cell Hi-C data. However, few methods exist that are able to accurately and efficiently cluster such data into constituent cell types. Here, we describe scHiCluster, a single-cell clustering algorithm for Hi-C contact matrices that is based on imputations using linear convolution and random walk. Using both simulated and real single-cell Hi-C data as benchmarks, scHiCluster significantly improves clustering accuracy when applied to low coverage datasets compared with existing methods. After imputation by scHiCluster, topologically associating domain (TAD)-like structures (TLSs) can be identified within single cells, and their consensus boundaries were enriched at the TAD boundaries observed in bulk cell Hi-C samples. In summary, scHiCluster facilitates visualization and comparison of single-cell 3D genomes.
机译:三维基因组结构在基因调控和细胞功能中起着关键作用。使用成像和染色质构象捕获方法(例如Hi-C)已经实现了基因组架构的单细胞分析。为了研究不同细胞类型之间染色体结构的变异,需要可以利用稀疏和异构单细胞Hi-C数据的计算方法。但是,几乎没有方法能够将这些数据准确有效地聚类为组成细胞类型。在这里,我们描述scHiCluster,这是一种用于Hi-C接触矩阵的单细胞聚类算法,该算法基于使用线性卷积和随机游走的插补。与现有方法相比,使用模拟和实际单细胞Hi-C数据作为基准,scHiCluster应用于低覆盖率数据集时,可显着提高聚类准确性。通过scHiCluster进行插补后,可以在单个细胞中鉴定出拓扑关联域(TAD)样结构(TLS),并且它们的共有边界在大细胞Hi-C样品中观察到的TAD边界处富集。总之,scHiCluster有助于单细胞3D基因组的可视化和比较。

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