INDIBATOR: Diverse and Fact-Grounded Individuality for Multi-Agent Debate in Molecular Discovery

Multi-agent systems have emerged as a powerful paradigm for automating scientific discovery. To differentiate agent behavior in the multi-agent system, current frameworks typically assign generic role-based personas such as ''reviewer'' or ''writer'' or rely on coarse grained keyword-based personas. While functional, this approach oversimplifies how human scientists operate, whose contributions are shaped by their unique research trajectories. In response, we propose INDIBATOR, a framework for molecular discovery that grounds agents in individualized scientist profiles constructed from two modalities: publication history for literature-derived knowledge and molecular history for structural priors. These agents engage in multi-turn debate through proposal, critique, and voting phases. Our evaluation demonstrates that these fine-grained individuality-grounded agents consistently outperform systems relying on coarse-grained personas, achieving competitive or state-of-the-art performance. These results validate that capturing the ``scientific DNA'' of individual agents is essential for high-quality discovery.

Learning Collective Variables from Time-lagged Generation

Rare events such as state transitions are difficult to observe directly with molecular dynamics simulations due to long timescales. Enhanced sampling techniques overcome this by introducing biases along carefully chosen low-dimensional features, known as collective variables (CVs), which capture the slow degrees of freedom. Machine learning approaches (MLCVs) have automated CV discovery, but existing methods typically focus on discriminating meta-stable states without fully encoding the detailed dynamics essential for accurate sampling. We propose TLC, a framework that learns CVs directly from time-lagged conditions of a generative model. Instead of modeling the static Boltzmann distribution, TLC models a time-lagged conditional distribution yielding CVs to capture the slow dynamic behavior. We validate TLC on the Alanine Dipeptide system using two CV-based enhanced sampling tasks: (i) steered molecular dynamics (SMD) and (ii) on-the-fly probability enhanced sampling (OPES), demonstrating equal or superior performance compared to existing MLCV methods in both transition path sampling and state discrimination.

Collective Variable Free Transition Path Sampling with Generative Flow Network

Understanding transition paths between meta-stable states in molecular systems is fundamental for material design and drug discovery. However, sampling these paths via molecular dynamics simulations is computationally prohibitive due to the high-energy barriers between the meta-stable states. Recent machine learning approaches are often restricted to simple systems or rely on collective variables (CVs) extracted from expensive domain knowledge. In this work, we propose to leverage generative flow networks (GFlowNets) to sample transition paths without relying on CVs. We reformulate the problem as amortized energy-based sampling over molecular trajectories and train a bias potential by minimizing the squared log-ratio between the target distribution and the generator, derived from the flow matching objective of GFlowNets. Our evaluation on three proteins (Alanine Dipeptide, Polyproline, and Chignolin) demonstrates that our approach, called TPS-GFN, generates more realistic and diverse transition paths than the previous CV-free machine learning approach.

Non-backtracking Graph Neural Networks

The celebrated message-passing updates for graph neural networks allow the representation of large-scale graphs with local and computationally tractable updates. However, the local updates suffer from backtracking, i.e., a message flows through the same edge twice and revisits the previously visited node. Since the number of message flows increases exponentially with the number of updates, the redundancy in local updates prevents the graph neural network from accurately recognizing a particular message flow for downstream tasks. In this work, we propose to resolve such a redundancy via the non-backtracking graph neural network (NBA-GNN) that updates a message without incorporating the message from the previously visited node. We further investigate how NBA-GNN alleviates the over-squashing of GNNs, and establish a connection between NBA-GNN and the impressive performance of non-backtracking updates for stochastic block model recovery. We empirically verify the effectiveness of our NBA-GNN on long-range graph benchmark and transductive node classification problems.

NTIRE 2022 Challenge on High Dynamic Range Imaging: Methods and Results

This paper reviews the challenge on constrained high dynamic range (HDR) imaging that was part of the New Trends in Image Restoration and Enhancement (NTIRE) workshop, held in conjunction with CVPR 2022. This manuscript focuses on the competition set-up, datasets, the proposed methods and their results. The challenge aims at estimating an HDR image from multiple respective low dynamic range (LDR) observations, which might suffer from under- or over-exposed regions and different sources of noise. The challenge is composed of two tracks with an emphasis on fidelity and complexity constraints: In Track 1, participants are asked to optimize objective fidelity scores while imposing a low-complexity constraint (i.e. solutions can not exceed a given number of operations). In Track 2, participants are asked to minimize the complexity of their solutions while imposing a constraint on fidelity scores (i.e. solutions are required to obtain a higher fidelity score than the prescribed baseline). Both tracks use the same data and metrics: Fidelity is measured by means of PSNR with respect to a ground-truth HDR image (computed both directly and with a canonical tonemapping operation), while complexity metrics include the number of Multiply-Accumulate (MAC) operations and runtime (in seconds).