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Shai Dickman

Publications and source records attributed to Shai Dickman.

2 recordsLinked to original sources

Spectral Feedback for Test-Time Alignment of Protein Diffusion Models

Reward maximization alignment methods for discrete diffusion models have primarily focused on steering the reverse process, either by influencing token logits or by selecting favorable sequences at intermediate steps. These approaches largely treat inference as a unidirectional process, lacking mechanisms for revisiting undesirable token selections. We introduce Spectral Feedback, an algorithm that selects edit-positions in a feedback loop, allowing the model to iteratively correct its own generations. This approach leverages the mask structure of discrete diffusion models by re-masking and re-sampling tokens, analogous to image editing methods that reintroduce noisy latents and re-run the reverse process. While prior alignment methods focus on what token labels to assign to maximize a target reward, we instead treat which tokens to revisit as the central alignment problem. Selecting edit-positions is challenging because edit effects are interdependent: the impact of modifying one token depends on which others are edited simultaneously. We define an edit-set as a set of token positions to re-mask and re-sample. Motivated by prior work on sparse interactions in biological systems, we find empirically that edit-set value functions for protein inverse folding admit sparse Fourier representations. This structure enables Spectral Feedback to efficiently learn and optimize the value functions for edit-position selection. Spectral Feedback is model-agnostic and can be applied to pretrained, test-time aligned, and fine-tuned diffusion models. For all of these models, the algorithm improves alignment performance without modifying the underlying generative process. Applied to inverse folding with a protein stability reward oracle, it achieves a 32.3% increase in stable proteins for a pretrained model, 24.8% for Best-of-10, and 5.8% for a state-of-the-art RL fine-tuned diffusion model.

cs.AI↗

Panoramic Voltage-Sensitive Optical Mapping of Contracting Hearts using Cooperative Multi-View Motion Tracking with 12 to 24 Cameras

Voltage-sensitive fluorescence imaging is widely used to image action potential waves in the heart. However, while the electrical waves trigger mechanical contraction, imaging needs to be performed with pharmacologically contraction-inhibited hearts, limiting studies of the coupling between cardiac electrophysiology and tissue mechanics. Here, we introduce a high-resolution multi-camera optical mapping system with which we image action potential waves at high resolutions across the entire ventricular surface of the beating and strongly deforming heart. We imaged intact isolated rabbit hearts inside a soccer-ball shaped imaging chamber facilitating even illumination and panoramic imaging. Using 12 high-speed cameras, ratiometric voltage-sensitive imaging, and three-dimensional (3D) multi-view motion tracking, we reconstructed the entire 3D deforming ventricular surface and performed corresponding voltage-sensitive measurements during sinus rhythm, paced rhythm, and ventricular fibrillation. Our imaging setup defines a new state-of-the-art in the field and can be used to study the heart's electromechanical physiology during health and disease at unprecedented resolutions. For instance, we measured electrical activation times and observed mechanical strain waves following electrical activation fronts during pacing, observed electromechanical vortices during ventricular fibrillation, and measured action potential duration and contractile changes in response to pharmacological blockage of potassium ion channels.

physics.med-ph↗