Table 1 A comparative table of mathematical framework for modeling spatiotemporal scRNA-seq data

From: Deciphering cell-fate trajectories using spatiotemporal single-cell transcriptomic data

Mathematical framework

Core goal

Advantages

Limitations

Static OT

Map cells across time points.

Provide baseline matching of cell states between two discrete snapshots.

Deliver a static map; no continuous trajectories or temporal dynamics.

Dynamical OT

Infer velocity along trajectories.

Yield continuous, kinetic-consistent trajectories and a velocity field in gene space.

Assume mass conservation—ignores proliferation, death, and stochasticity.

GWOT

Align cell-state across conditions.

Match datasets without shared features by preserving intra-condition geometry.

The dynamical form remains unclear; do not generate continuous trajectory

Dynamical Unbalanced OT

Infer velocity and proliferation.

Add a source-sink term to capture net growth/death while keeping continuous paths.

Treat dynamics as deterministic; stochastic fluctuations remain unmodeled.

Mean-field Schrödinger bridge

Infer velocity, stochasticity, and interaction.

Introduce both Brownian noise and cell-cell interaction forces within one framework.

Require prior knowledge of cell-cell interaction.

Regularized unbalanced OT

Infer velocity, proliferation, and stochasticity.

Combine diffusion, creation/destruction, and continuous paths in a single objective.

Neglect cell-cell communication such that cellular interaction effects are absent.

Unbalanced mean-field Schrödinger bridge

Infer velocity, proliferation, stochasticity, and interaction.

Unified model that simultaneously handles noise, net growth, and interaction forces.

Require prior knowledge of cell-cell interaction.

Hamilton–Jacobi–Bellman equation

Simplify the difficulty of numerical solution.

Reduce vector-field optimization to learning one scalar field; faster, more stable.

Requires computing second-order spatial derivatives, making numerical solution costly.

Rigid body transformation invariant OT

Map cells and infers velocity in unpaired spatiotemporal data

Simultaneously infer the rigid spatial transformation and optimal transport mapping for joint alignment of spatial coordinates and gene expression.

Limited to rigid transformations; do not correct nonrigid tissue deformation or local morphogenesis.