Beyond Continuity: Simulation-free Reconstruction of Discrete Branching Dynamics from Single-cell Snapshots

arXiv cs.AI / 5/4/2026

💬 OpinionModels & Research

Key Points

  • The paper addresses how to infer cellular trajectories from destructive single-cell snapshots, where stochasticity and non-conservative mass effects (e.g., proliferation and apoptosis) complicate inference.
  • It criticizes existing unbalanced optimal transport approaches that treat cell mass as a continuous fluid, noting they can miss the inherently discrete, jump-like behavior of birth-death events at single-cell resolution.
  • The authors introduce Unbalanced Schrödinger Bridge (USB), a simulation-free framework that learns underlying stochastic dynamics while explicitly modeling discrete birth-death jumps at the single-cell level.
  • USB is presented as having a theoretical connection to the Branching Schrödinger Bridge (BSB) problem, with a microscopic interpretation in which each cell undergoes both Brownian motion and discrete birth-death jumps.
  • Experiments on simulated and real omics datasets show USB improves or matches deterministic baselines for trajectory reconstruction and uniquely supports realistic discrete birth-death simulations at single-cell resolution.

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 Schr\"odinger 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 Schr\"odinger 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.