Incorporating network diffusion and peak location information for better single-cell ATAC-seq data analysis

Author:

Yu Jiating1234,Leng Jiacheng2345ORCID,Hou Zhichao234,Sun Duanchen6ORCID,Wu Ling-Yun234ORCID

Affiliation:

1. School of Mathematics and Statistics, Nanjing University of Information Science & Technology , Nanjing 210044, China

2. IAM , MADIS, NCMIS, Academy of Mathematics and Systems Science, , Beijing 100190, China

3. Chinese Academy of Sciences , MADIS, NCMIS, Academy of Mathematics and Systems Science, , Beijing 100190, China

4. School of Mathematical Sciences, University of Chinese Academy of Sciences , Beijing 100049, China

5. Zhejiang Lab , Hangzhou 311121, China

6. School of Mathematics, Shandong University , Jinan 250100, China

Abstract

Abstract Single-cell assay for transposase-accessible chromatin using sequencing (scATAC-seq) data provided new insights into the understanding of epigenetic heterogeneity and transcriptional regulation. With the increasing abundance of dataset resources, there is an urgent need to extract more useful information through high-quality data analysis methods specifically designed for scATAC-seq. However, analyzing scATAC-seq data poses challenges due to its near binarization, high sparsity and ultra-high dimensionality properties. Here, we proposed a novel network diffusion–based computational method to comprehensively analyze scATAC-seq data, named Single-Cell ATAC-seq Analysis via Network Refinement with Peaks Location Information (SCARP). SCARP formulates the Network Refinement diffusion method under the graph theory framework to aggregate information from different network orders, effectively compensating for missing signals in the scATAC-seq data. By incorporating distance information between adjacent peaks on the genome, SCARP also contributes to depicting the co-accessibility of peaks. These two innovations empower SCARP to obtain lower-dimensional representations for both cells and peaks more effectively. We have demonstrated through sufficient experiments that SCARP facilitated superior analyses of scATAC-seq data. Specifically, SCARP exhibited outstanding cell clustering performance, enabling better elucidation of cell heterogeneity and the discovery of new biologically significant cell subpopulations. Additionally, SCARP was also instrumental in portraying co-accessibility relationships of accessible regions and providing new insight into transcriptional regulation. Consequently, SCARP identified genes that were involved in key Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways related to diseases and predicted reliable cis-regulatory interactions. To sum up, our studies suggested that SCARP is a promising tool to comprehensively analyze the scATAC-seq data.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Publisher

Oxford University Press (OUP)

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