MarkovHC: Markov hierarchical clustering for the topological structure of high-dimensional single-cell omics data with transition pathway and critical point detection

Author:

Wang Zhenyi1ORCID,Zhong Yanjie23,Ye Zhaofeng4,Zeng Lang5,Chen Yang1,Shi Minglei4,Yuan Zhiyuan1,Zhou Qiming6,Qian Minping2,Zhang Michael Q147

Affiliation:

1. MOE Key Laboratory of Bioinformatics; Bioinformatics Division and Center for Synthetic & Systems Biology, BNRist; Department of Automation, Tsinghua University, Beijing 100084, China

2. School of Mathematical Sciences, Peking University, Beijing 100871, China

3. Department of Mathematics and Statistics, Washington University in St. Louis, St. Louis, MO 63130, USA

4. MOE Key Laboratory of Bioinformatics; Bioinformatics Division and Center for Synthetic & Systems Biology, BNRist; School of Medicine, Tsinghua University, Beijing 100084, China

5. Department of Biostatistics, University of Michigan, Ann Arbor, MI 48109, USA

6. MOE Key Laboratory of Bioinformatics; Bioinformatics Division and Center for Synthetic & Systems Biology, BNRist; School of Life Sciences, Tsinghua University, Beijing 100084, China

7. Department of Biological Sciences, Center for Systems Biology, The University of Texas, Richardson, TX 75080-3021, USA

Abstract

Abstract Clustering cells and depicting the lineage relationship among cell subpopulations are fundamental tasks in single-cell omics studies. However, existing analytical methods face challenges in stratifying cells, tracking cellular trajectories, and identifying critical points of cell transitions. To overcome these, we proposed a novel Markov hierarchical clustering algorithm (MarkovHC), a topological clustering method that leverages the metastability of exponentially perturbed Markov chains for systematically reconstructing the cellular landscape. Briefly, MarkovHC starts with local connectivity and density derived from the input and outputs a hierarchical structure for the data. We firstly benchmarked MarkovHC on five simulated datasets and ten public single-cell datasets with known labels. Then, we used MarkovHC to investigate the multi-level architectures and transition processes during human embryo preimplantation development and gastric cancer procession. MarkovHC found heterogeneous cell states and sub-cell types in lineage-specific progenitor cells and revealed the most possible transition paths and critical points in the cellular processes. These results demonstrated MarkovHC’s effectiveness in facilitating the stratification of cells, identification of cell populations, and characterization of cellular trajectories and critical points.

Funder

Natural Science Foundation of China

National Key Research and Development Program

Publisher

Oxford University Press (OUP)

Subject

Genetics

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