Beyond Continuity: Simulation-free Reconstruction of Discrete Branching Dynamics from Single-cell Snapshots
Junda Ying, Yuxuan Wang, Bowen Yang, Peijie Zhou, Lei Zhang
TLDR
Unbalanced Schrödinger Bridge (USB) reconstructs discrete branching cell dynamics from snapshots, integrating stochastic and birth-death events.
Key contributions
- Introduces Unbalanced Schrödinger Bridge (USB) for learning discrete, jump-like birth-death dynamics.
- Provides a tractable solution to the Branching Schrödinger Bridge (BSB) problem with microscopic interpretation.
- Implements an efficient, simulation-free training objective for high-dimensional omics data.
- Achieves superior or comparable trajectory reconstruction and enables realistic discrete birth-death simulations.
Why it matters
Existing methods struggle with discrete birth-death events in single-cell trajectory inference. This paper introduces USB, a novel framework that accurately models these jump-like dynamics. This advancement provides a more precise understanding of cell lineage and fate decisions, crucial for fields like developmental biology and disease research.
Original Abstract
Inferring cellular trajectories from destructive snapshots is complicated by the challenges of stochasticity and non-conservative mass dynamics such as cell proliferation and apoptosis. Existing unbalanced Optimal Transport (OT) methods treat mass as a continuous fluid, performing inference at the population level. However, this macroscopic view often fails to capture the discrete, jump-like nature of birth-death events at single-cell resolution, which is essential for understanding lineage branching and fate decisions. We present Unbalanced Schrödinger Bridge (USB), a simulation-free framework for learning underlying dynamics that effectively integrates both stochastic and unbalanced effects which also models the discrete, jump-like birth-death dynamics at single-cell resolution. Theoretically, USB provides a tractable solution to the Branching Schrödinger Bridge (BSB) problem, offering a rigorous microscopic interpretation where individual cells undergo both Brownian motion and discrete birth-death jumps. Technically, the method implements an efficient solver by introducing a simulation-free training objective that effectively scales to high-dimensional omics data. Empirically, we demonstrate on both simulated and real-world datasets that USB not only achieves trajectory reconstruction performance better than or comparable to deterministic baselines but also uniquely enables realistic discrete simulation of birth-death dynamics at single-cell resolution.
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