Identification of Human Cell Cycle Phase Markers Based on Single-Cell RNA-Seq Data by Using Machine Learning Methods.

The cell cycle is composed of a series of ordered, highly regulated processes through which a cell grows and duplicates its genome and eventually divides into two daughter cells. According to the complex changes in cell structure and biosynthesis, the cell cycle is divided into four phases: gap 1 (G...

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Publicado en:BioMed Research International Vol. 2022; pp. 1 - 20
Autores principales: Huang, FeiMing, Chen, Lei, Guo, Wei, Huang, Tao, Cai, Yu-dong
Formato: equations & formulas pictorial research tables/charts Journal Article
Publicado: Wiley-Blackwell 8/13/2022
Acceso en línea:Ver este registro en EBSCOhost
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      dt: 8/13/2022
      vid: 2022
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      pub: Wiley-Blackwell
      place: Malden, Massachusetts
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        10.1155/2022/2516653
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        atl: Identification of Human Cell Cycle Phase Markers Based on Single-Cell RNA-Seq Data by Using Machine Learning Methods.
      aug:
        au:
          Huang, FeiMing
          Chen, Lei
          Guo, Wei
          Huang, Tao
          Cai, Yu-dong
        affil: School of Life Sciences, Shanghai University, Shanghai 200444, China
      sug:
        subj:
          Cell Cycle
          Biological Markers
          Cytological Techniques Methods
          Machine Learning Methods
          Human
          Cell Physiology
          Mutation
      ab: The cell cycle is composed of a series of ordered, highly regulated processes through which a cell grows and duplicates its genome and eventually divides into two daughter cells. According to the complex changes in cell structure and biosynthesis, the cell cycle is divided into four phases: gap 1 (G1), DNA synthesis (S), gap 2 (G2), and mitosis (M). Determining which cell cycle phases a cell is in is critical to the research of cancer development and pharmacy for targeting cell cycle. However, current detection methods have the following problems: (1) they are complicated and time consuming to perform, and (2) they cannot detect the cell cycle on a large scale. Rapid developments in single-cell technology have made dissecting cells on a large scale possible with unprecedented resolution. In the present research, we construct efficient classifiers and identify essential gene biomarkers based on single-cell RNA sequencing data through Boruta and three feature ranking algorithms (e.g., mRMR, MCFS, and SHAP by LightGBM) by utilizing four advanced classification algorithms. Meanwhile, we mine a series of classification rules that can distinguish different cell cycle phases. Collectively, we have provided a novel method for determining the cell cycle and identified new potential cell cycle-related genes, thereby contributing to the understanding of the processes that regulate the cell cycle.
      pubtype: Academic Journal
      doctype:
        equations & formulas
        pictorial
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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