Elucidating dynamic cell lineages and gene networks in time-course single cell differentiation

被引:0
|
作者
Zhang, Mengrui [3 ]
Chen, Yongkai [1 ]
Yu, Dingyi [2 ]
Zhong, Wenxuan [1 ]
Zhang, Jingyi [2 ]
Ma, Ping [1 ]
机构
[1] Univ Georgia, Dept Stat, Athens, GA 30602 USA
[2] Tsinghua Univ, Ctr Stat Sci, Dept Ind Engn, Beijing, Peoples R China
[3] Surrozen Inc, South San Francisco, CA USA
来源
ARTIFICIAL INTELLIGENCE IN THE LIFE SCIENCES | 2023年 / 3卷
基金
美国国家科学基金会; 国家重点研发计划;
关键词
scRNA-seq; Optimal Transport; Smoothing Spline; Dynamic Gene Networks; INFERENCE; STATES;
D O I
10.1016/j.ailsci.2023.100068
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Single cell RNA sequencing (scRNA-seq) technologies provide researchers with an unprecedented opportunity to exploit cell heterogeneity. For example, the sequenced cells belong to various cell lineages, which may have different cell fates in stem and progenitor cells. Those cells may differentiate into various mature cell types in a cell differentiation process. To trace the behavior of cell differentiation, researchers reconstruct cell lineages and predict cell fates by ordering cells chronologically into a trajectory with a pseudo-time. However, in scRNAseq experiments, there are no cell-to-cell correspondences along with the time to reconstruct the cell lineages, which creates a significant challenge for cell lineage tracing and cell fate prediction. Therefore, methods that can accurately reconstruct the dynamic cell lineages and predict cell fates are highly desirable. In this article, we develop an innovative machine-learning framework called Cell Smoothing Transformation (CellST) to elucidate the dynamic cell fate paths and construct gene networks in cell differentiation processes. Unlike the existing methods that construct one single bulk cell trajectory, CellST builds cell trajectories and tracks behaviors for each individual cell. Additionally, CellST can predict cell fates even for less frequent cell types. Based on the individual cell fate trajectories, CellST can further construct dynamic gene networks to model gene-gene relationships along the cell differentiation process and discover critical genes that potentially regulate cells into various mature cell types.
引用
收藏
页数:10
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