Abstract
AbstractTime-series spatial transcriptome data with single-cell resolution provide an opportunity to study cell differentiation, growth and migration in physical space over time. Due to the destructive nature of sequencing, simultaneous reconstruction of cell differentiation, growth and migration trajectories remains challenging, especially migration in physical space, as the coordinates obtained at different temporal snapshots are not in the same coordinate system. To realize this potential, we developed stVCR, which is an optimal transport algorithm with dynamical form, unbalanced setting and invariance to rigid body transformations. stVCR extends the previous algorithm, which only reconstructs differentiation trajectories and population growth, to end-to-end simultaneously reconstruct cell differentiation, growth, migration in physical space and align spatial coordinates of multiple snapshots. In addition, stVCR allows the study of the interaction between gene expression and spatial migration and the effect of gene expression and spatial migration on growth. We verified the effectiveness of stVCR on simulated data and axolotl brain regeneration data.
Publisher
Cold Spring Harbor Laboratory
Cited by
1 articles.
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