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Shreya Saxena

Shreya Saxena contributes to research discovery and scholarly infrastructure.

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Published work

2 published item(s)

preprint2026arXiv

FLUX: Geometry-Aware Longitudinal Flow Matching with Mixture of Experts

Many biological systems evolve through continuous local dynamics while switching between latent regimes defined by learning, stimulus context, internal state, or developmental stage. These processes are often observed only as unpaired longitudinal snapshots: the same cells, neurons, or animals are not tracked as matched trajectories, even though population states are sampled across successive stages. This creates two coupled challenges. First, trajectories must respect curved low-dimensional manifolds embedded in high-dimensional biological measurements. Second, the model must identify when the transport mechanism itself changes. We introduce FLUX (FLow matching for Unpaired longitudinal data with miXture-of-experts), a geometry-aware longitudinal flow-matching framework for joint transport modeling and unsupervised regime discovery. FLUX learns a data-dependent metric from pooled labeled and unlabeled observations, uses that metric to construct geometry-aware conditional paths between adjacent marginals, and decomposes the resulting velocity field into sparse expert vector fields selected by a Straight-Through Gumbel-Softmax router. Across manifold controls, a regime-switching Lorenz system, widefield cortical calcium imaging during associative learning, and embryoid body single-cell differentiation, FLUX reconstructs longitudinal transport while recovering interpretable regime structure. Ablations show that mixture-of-experts routing alone is insufficient: FLUX without geometric learning can fit local transport but fails or weakens regime discovery when regimes are encoded in local dynamics. These results suggest that geometry-aware velocity decomposition provides a general strategy for discovering latent biological state transitions from unpaired longitudinal snapshots.

preprint2020arXiv

Nonlinear Evolution via Spatially-Dependent Linear Dynamics for Electrophysiology and Calcium Data

Latent variable models have been widely applied for the analysis of time series resulting from experimental neuroscience techniques. In these datasets, observations are relatively smooth and possibly nonlinear. We present Variational Inference for Nonlinear Dynamics (VIND), a variational inference framework that is able to uncover nonlinear, smooth latent dynamics from sequential data. The framework is a direct extension of PfLDS; including a structured approximate posterior describing spatially-dependent linear dynamics, as well as an algorithm that relies on the fixed-point iteration method to achieve convergence. We apply VIND to electrophysiology, single-cell voltage and widefield imaging datasets with state-of-the-art results in reconstruction error. In single-cell voltage data, VIND finds a 5D latent space, with variables akin to those of Hodgkin-Huxley-like models. VIND's learned dynamics are further quantified by predicting future neural activity. VIND excels in this task, in some cases substantially outperforming current methods.