Deep neural networks, particularly Transformers, have been widely adopted for predicting the functional properties of proteins. In this work, we focus on exploring whether Protein Transformers can capture biological intelligence among protein sequences. To achieve our goal, we first introduce a protein function dataset, namely Protein-FN, providing over 9000 protein data with meaningful labels. Second, we devise a new Transformer architecture, namely Sequence Protein Transformers (SPT), for computationally efficient protein function predictions. Third, we develop a novel Explainable Artificial Intelligence (XAI) technique called Sequence Score, which can efficiently interpret the decision-making processes of protein models, thereby overcoming the difficulty of deciphering biological intelligence bided in Protein Transformers. Remarkably, even our smallest SPT-Tiny model, which contains only 5.4M parameters, demonstrates impressive predictive accuracy, achieving 94.3% on the Antibiotic Resistance (AR) dataset and 99.6% on the Protein-FN dataset, all accomplished by training from scratch. Besides, our Sequence Score technique helps reveal that our SPT models can discover several meaningful patterns underlying the sequence structures of protein data, with these patterns aligning closely with the domain knowledge in the biology community. We have officially released our Protein-FN dataset on Hugging Face Datasets https://huggingface.co/datasets/Protein-FN/Protein-FN. Our code is available at https://github.com/fudong03/BioIntelligence.
While several feature embedding models have been developed in the literature, comparisons of these embeddings have largely focused on their numerical performance in classification-related downstream applications. However, an interpretable comparison of different embeddings requires identifying and analyzing mismatches between sample groups clustered within the embedding spaces. In this work, we propose the \emph{Spectral Pairwise Embedding Comparison (SPEC)} framework to compare embeddings and identify their differences in clustering a reference dataset. Our approach examines the kernel matrices derived from two embeddings and leverages the eigendecomposition of the difference kernel matrix to detect sample clusters that are captured differently by the two embeddings. We present a scalable implementation of this kernel-based approach, with computational complexity that grows linearly with the sample size. Furthermore, we introduce an optimization problem using this framework to align two embeddings, ensuring that clusters identified in one embedding are also captured in the other model. We provide numerical results demonstrating the SPEC's application to compare and align embeddings on large-scale datasets such as ImageNet and MS-COCO. The code is available at [https://github.com/mjalali/embedding-comparison](github.com/mjalali/embedding-comparison).
Inverse folding models have proven to be highly effective zero-shot predictors of protein stability. Despite this success, the link between the amino acid preferences of an inverse folding model and the free-energy considerations underlying thermodynamic stability remains incompletely understood. A better understanding would be of interest not only from a theoretical perspective, but also potentially provide the basis for stronger zero-shot stability prediction. In this paper, we take steps to clarify the free-energy foundations of inverse folding models. Our derivation reveals the standard practice of likelihood ratios as a simplistic approximation and suggests several paths towards better estimates of the relative stability. We empirically assess these approaches and demonstrate that considerable gains in zero-shot performance can be achieved with fairly simple means.
As a core mechanism of epigenetic regulation in eukaryotes, protein post-translational modifications (PTMs) require precise prediction to decipher dynamic life activity networks. To address the limitations of existing deep learning models in cross-modal feature fusion, domain generalization, and architectural optimization, this study proposes UniPTMs: the first unified framework for multi-type PTM prediction. The framework innovatively establishes a "Master-Slave" dual-path collaborative architecture: The master path dynamically integrates high-dimensional representations of protein sequences, structures, and evolutionary information through a Bidirectional Gated Cross-Attention (BGCA) module, while the slave path optimizes feature discrepancies and recalibration between structural and traditional features using a Low-Dimensional Fusion Network (LDFN). Complemented by a Multi-scale Adaptive convolutional Pyramid (MACP) for capturing local feature patterns and a Bidirectional Hierarchical Gated Fusion Network (BHGFN) enabling multi-level feature integration across paths, the framework employs a Hierarchical Dynamic Weighting Fusion (HDWF) mechanism to intelligently aggregate multimodal features. Enhanced by a novel Hierarchical Contrastive loss function for feature consistency optimization, UniPTMs demonstrates significant performance improvements (3.2%-11.4% MCC and 4.2%-14.3% AP increases) over state-of-the-art models across five modification types and transcends the Single-Type Prediction Paradigm. To strike a balance between model complexity and performance, we have also developed a lightweight variant named UniPTMs-mini.
We present a comprehensive investigation into plant bioelectric responses to human presence and emotional states, building on five years of systematic research. Using custom-built plant sensors and machine learning classification, we demonstrate that plants generate distinct bioelectric signals correlating with human proximity, emotional states, and physiological conditions. A deep learning model based on ResNet50 architecture achieved 97% accuracy in classifying human emotional states through plant voltage spectrograms, while control models with shuffled labels achieved only 30% accuracy. This study synthesizes findings from multiple experiments spanning 2020-2025, including individual recognition (66% accuracy), eurythmic gesture detection, stress prediction, and responses to human voice and movement. We propose that these phenomena represent evolved anti-herbivory early warning systems, where plants detect approaching animals through bioelectric field changes before physical contact. Our results challenge conventional understanding of plant sensory capabilities and suggest practical applications in agriculture, healthcare, and human-plant interaction research.
Deep neural networks trained to predict neural activity from visual input and behaviour have shown great potential to serve as digital twins of the visual cortex. Per-neuron embeddings derived from these models could potentially be used to map the functional landscape or identify cell types. However, state-of-the-art predictive models of mouse V1 do not generate functional embeddings that exhibit clear clustering patterns which would correspond to cell types. This raises the question whether the lack of clustered structure is due to limitations of current models or a true feature of the functional organization of mouse V1. In this work, we introduce DECEMber -- Deep Embedding Clustering via Expectation Maximization-based refinement -- an explicit inductive bias into predictive models that enhances clustering by adding an auxiliary $t$-distribution-inspired loss function that enforces structured organization among per-neuron embeddings. We jointly optimize both neuronal feature embeddings and clustering parameters, updating cluster centers and scale matrices using the EM-algorithm. We demonstrate that these modifications improve cluster consistency while preserving high predictive performance and surpassing standard clustering methods in terms of stability. Moreover, DECEMber generalizes well across species (mice, primates) and visual areas (retina, V1, V4). The code is available at https://github.com/Nisone2000/sensorium/tree/neuroips_version.
The detection of ligand binding sites for proteins is a fundamental step in Structure-Based Drug Design. Despite notable advances in recent years, existing methods, datasets, and evaluation metrics are confronted with several key challenges: (1) current datasets and methods are centered on individual protein-ligand complexes and neglect that diverse binding sites may exist across multiple complexes of the same protein, introducing significant statistical bias; (2) ligand binding site detection is typically modeled as a discontinuous workflow, employing binary segmentation and subsequent clustering algorithms; (3) traditional evaluation metrics do not adequately reflect the actual performance of different binding site prediction methods. To address these issues, we first introduce UniSite-DS, the first UniProt (Unique Protein)-centric ligand binding site dataset, which contains 4.81 times more multi-site data and 2.08 times more overall data compared to the previously most widely used datasets. We then propose UniSite, the first end-to-end ligand binding site detection framework supervised by set prediction loss with bijective matching. In addition, we introduce Average Precision based on Intersection over Union (IoU) as a more accurate evaluation metric for ligand binding site prediction. Extensive experiments on UniSite-DS and several representative benchmark datasets demonstrate that IoU-based Average Precision provides a more accurate reflection of prediction quality, and that UniSite outperforms current state-of-the-art methods in ligand binding site detection. The dataset and codes will be made publicly available at https://github.com/quanlin-wu/unisite.
Recently, extensive deep learning architectures and pretraining strategies have been explored to support downstream protein applications. Additionally, domain-specific models incorporating biological knowledge have been developed to enhance performance in specialized tasks. In this work, we introduce $\textbf{Protap}$, a comprehensive benchmark that systematically compares backbone architectures, pretraining strategies, and domain-specific models across diverse and realistic downstream protein applications. Specifically, Protap covers five applications: three general tasks and two novel specialized tasks, i.e., enzyme-catalyzed protein cleavage site prediction and targeted protein degradation, which are industrially relevant yet missing from existing benchmarks. For each application, Protap compares various domain-specific models and general architectures under multiple pretraining settings. Our empirical studies imply that: (i) Though large-scale pretraining encoders achieve great results, they often underperform supervised encoders trained on small downstream training sets. (ii) Incorporating structural information during downstream fine-tuning can match or even outperform protein language models pretrained on large-scale sequence corpora. (iii) Domain-specific biological priors can enhance performance on specialized downstream tasks. Code and datasets are publicly available at https://github.com/Trust-App-AI-Lab/protap.
As large language models (LLMs) continue to revolutionize AI research, there is a growing interest in building large-scale brain foundation models to advance neuroscience. While most existing brain foundation models are pre-trained on time-series signals or region-of-interest (ROI) features, we propose a novel graph-based pre-training paradigm for constructing a brain graph foundation model. In this paper, we introduce the Brain Graph Foundation Model, termed BrainGFM, a unified framework that leverages graph contrastive learning and graph masked autoencoders for large-scale fMRI-based pre-training. BrainGFM is pre-trained on a diverse mixture of brain atlases with varying parcellations, significantly expanding the pre-training corpus and enhancing the model's ability to generalize across heterogeneous fMRI-derived brain representations. To support efficient and versatile downstream transfer, we integrate both graph prompts and language prompts into the model design, enabling BrainGFM to flexibly adapt to a wide range of atlases, neurological and psychiatric disorders, and task settings. Furthermore, we employ meta-learning to optimize the graph prompts, facilitating strong generalization to previously unseen disorders under both few-shot and zero-shot learning conditions via language-guided prompting. BrainGFM is pre-trained on 27 neuroimaging datasets spanning 25 common neurological and psychiatric disorders, encompassing 2 types of brain atlases (functional and anatomical) across 8 widely-used parcellations, and covering over 25,000 subjects, 60,000 fMRI scans, and a total of 400,000 graph samples aggregated across all atlases and parcellations. The code is available at: https://github.com/weixinxu666/BrainGFM
Inspired by the success of unsupervised pre-training paradigms, researchers have applied these approaches to DNA pre-training. However, we argue that these approaches alone yield suboptimal results because pure DNA sequences lack sufficient information, since their functions are regulated by genomic profiles like chromatin accessibility. Here, we demonstrate that supervised training for genomic profile prediction serves as a more effective alternative to pure sequence pre-training. Furthermore, considering the multi-species and multi-profile nature of genomic profile prediction, we introduce our $\textbf{S}$pecies-$\textbf{P}$rofile $\textbf{A}$daptive $\textbf{C}$ollaborative $\textbf{E}$xperts (SPACE) that leverages Mixture of Experts (MoE) to better capture the relationships between DNA sequences across different species and genomic profiles, thereby learning more effective DNA representations. Through extensive experiments across various tasks, our model achieves state-of-the-art performance, establishing that DNA models trained with supervised genomic profiles serve as powerful DNA representation learners. The code is available at https://github.com/ZhuJiwei111/SPACE.
Understanding behavior requires datasets that capture humans while carrying out complex tasks. The kitchen is an excellent environment for assessing human motor and cognitive function, as many complex actions are naturally exhibited in kitchens from chopping to cleaning. Here, we introduce the EPFL-Smart-Kitchen-30 dataset, collected in a noninvasive motion capture platform inside a kitchen environment. Nine static RGB-D cameras, inertial measurement units (IMUs) and one head-mounted HoloLens~2 headset were used to capture 3D hand, body, and eye movements. The EPFL-Smart-Kitchen-30 dataset is a multi-view action dataset with synchronized exocentric, egocentric, depth, IMUs, eye gaze, body and hand kinematics spanning 29.7 hours of 16 subjects cooking four different recipes. Action sequences were densely annotated with 33.78 action segments per minute. Leveraging this multi-modal dataset, we propose four benchmarks to advance behavior understanding and modeling through 1) a vision-language benchmark, 2) a semantic text-to-motion generation benchmark, 3) a multi-modal action recognition benchmark, 4) a pose-based action segmentation benchmark. We expect the EPFL-Smart-Kitchen-30 dataset to pave the way for better methods as well as insights to understand the nature of ecologically-valid human behavior. Code and data are available at https://github.com/amathislab/EPFL-Smart-Kitchen
Episodic memory enables humans to recall past experiences by associating semantic elements such as objects, locations, and time into coherent event representations. While large pretrained models have shown remarkable progress in modeling semantic memory, the mechanisms for forming associative structures that support episodic memory remain underexplored. Inspired by hippocampal CA3 dynamics and its role in associative memory, we propose the Latent Structured Hopfield Network (LSHN), a biologically inspired framework that integrates continuous Hopfield attractor dynamics into an autoencoder architecture. LSHN mimics the cortical-hippocampal pathway: a semantic encoder extracts compact latent representations, a latent Hopfield network performs associative refinement through attractor convergence, and a decoder reconstructs perceptual input. Unlike traditional Hopfield networks, our model is trained end-to-end with gradient descent, achieving scalable and robust memory retrieval. Experiments on MNIST, CIFAR-10, and a simulated episodic memory task demonstrate superior performance in recalling corrupted inputs under occlusion and noise, outperforming existing associative memory models. Our work provides a computational perspective on how semantic elements can be dynamically bound into episodic memory traces through biologically grounded attractor mechanisms. Code: https://github.com/fudan-birlab/LSHN.
Hybrid quantum-classical machine learning offers a path to leverage noisy intermediate-scale quantum (NISQ) devices for drug discovery, but optimal model architectures remain unclear. We systematically optimize the quantum-classical bridge architecture for generative adversarial networks (GANs) in molecular discovery using multi-objective Bayesian optimization. Our optimized model (BO-QGAN) significantly improves performance, achieving a 2.27-fold higher Drug Candidate Score (DCS) than prior quantum-hybrid benchmarks and 2.21-fold higher than the classical baseline, using over 60% fewer parameters. Key findings favor layering multiple (3-4) shallow (4-8 qubit) quantum circuits sequentially, while classical architecture shows less sensitivity above a minimum capacity. This work provides the first empirically grounded architectural guidelines for hybrid models, enabling more effective integration of current quantum computers into pharmaceutical research pipelines.
Single-cell RNA sequencing (scRNA-seq) has revolutionized our understanding of cellular processes by enabling gene expression analysis at the individual cell level. Clustering allows for the identification of cell types and the further discovery of intrinsic patterns in single-cell data. However, the high dimensionality and sparsity of scRNA-seq data continue to challenge existing clustering models. In this paper, we introduce JojoSCL, a novel self-supervised contrastive learning framework for scRNA-seq clustering. By incorporating a shrinkage estimator based on hierarchical Bayesian estimation, which adjusts gene expression estimates towards more reliable cluster centroids to reduce intra-cluster dispersion, and optimized using Stein's Unbiased Risk Estimate (SURE), JojoSCL refines both instance-level and cluster-level contrastive learning. Experiments on ten scRNA-seq datasets substantiate that JojoSCL consistently outperforms prevalent clustering methods, with further validation of its practicality through robustness analysis and ablation studies. JojoSCL's code is available at: https://github.com/ziwenwang28/JojoSCL.
Accurately predicting gene mutations, mutation subtypes and their exons in lung cancer is critical for personalized treatment planning and prognostic assessment. Faced with regional disparities in medical resources and the high cost of genomic assays, using artificial intelligence to infer these mutations and exon variants from routine histopathology images could greatly facilitate precision therapy. Although some prior studies have shown that deep learning can accelerate the prediction of key gene mutations from lung cancer pathology slides, their performance remains suboptimal and has so far been limited mainly to early screening tasks. To address these limitations, we have assembled PathGene, which comprises histopathology images paired with next-generation sequencing reports from 1,576 patients at the Second Xiangya Hospital, Central South University, and 448 TCGA-LUAD patients. This multi-center dataset links whole-slide images to driver gene mutation status, mutation subtypes, exon, and tumor mutational burden (TMB) status, with the goal of leveraging pathology images to predict mutations, subtypes, exon locations, and TMB for early genetic screening and to advance precision oncology. Unlike existing datasets, we provide molecular-level information related to histopathology images in PathGene to facilitate the development of biomarker prediction models. We benchmarked 11 multiple-instance learning methods on PathGene for mutation, subtype, exon, and TMB prediction tasks. These experimental methods provide valuable alternatives for early genetic screening of lung cancer patients and assisting clinicians to quickly develop personalized precision targeted treatment plans for patients. Code and data are available at https://github.com/panliangrui/NIPS2025/.
In cognition, response times and choices in decision-making tasks are commonly modeled using Drift Diffusion Models (DDMs), which describe the accumulation of evidence for a decision as a stochastic process, specifically a Brownian motion, with the drift rate reflecting the strength of the evidence. In the same vein, the Poisson counter model describes the accumulation of evidence as discrete events whose counts over time are modeled as Poisson processes, and has a spiking neurons interpretation as these processes are used to model neuronal activities. However, these models lack a learning mechanism and are limited to tasks where participants have prior knowledge of the categories. To bridge the gap between cognitive and biological models, we propose a biologically plausible Spiking Neural Network (SNN) model for decision-making that incorporates a learning mechanism and whose neurons activities are modeled by a multivariate Hawkes process. First, we show a coupling result between the DDM and the Poisson counter model, establishing that these two models provide similar categorizations and reaction times and that the DDM can be approximated by spiking Poisson neurons. To go further, we show that a particular DDM with correlated noise can be derived from a Hawkes network of spiking neurons governed by a local learning rule. In addition, we designed an online categorization task to evaluate the model predictions. This work provides a significant step toward integrating biologically relevant neural mechanisms into cognitive models, fostering a deeper understanding of the relationship between neural activity and behavior.
We present a continuous-time portfolio selection framework that reflects goal-based investment principles and mental accounting behavior. In this framework, an investor with multiple investment goals constructs separate portfolios, each corresponding to a specific goal, with penalties imposed on fund transfers between these goals, referred to as mental costs. By applying the stochastic Perron's method, we demonstrate that the value function is the unique constrained viscosity solution of a Hamilton-Jacobi-Bellman equation system. Numerical analysis reveals several key features: the free boundaries exhibit complex shapes with bulges and notches; the optimal strategy for one portfolio depends on the wealth level of another; investors must diversify both among stocks and across portfolios; and they may postpone reallocating surplus from an important goal to a less important one until the former's deadline approaches.
We introduce an open-source Python framework for generating synthetic ECG image datasets to advance critical deep learning-based tasks in ECG analysis, including ECG digitization, lead region and lead name detection, and pixel-level waveform segmentation. Using the PTB-XL signal dataset, our proposed framework produces four open-access datasets: (1) ECG images in various lead configurations paired with time-series signals for ECG digitization, (2) ECG images annotated with YOLO-format bounding boxes for detection of lead region and lead name, (3)-(4) cropped single-lead images with segmentation masks compatible with U-Net-based models in normal and overlapping versions. In the overlapping case, waveforms from neighboring leads are superimposed onto the target lead image, while the segmentation masks remain clean. The open-source Python framework and datasets are publicly available at https://github.com/rezakarbasi/ecg-image-and-signal-dataset and https://doi.org/10.5281/zenodo.15484519, respectively.
We present a generic Branch-and-Bound procedure designed to solve L0-penalized optimization problems. Existing approaches primarily focus on quadratic losses and construct relaxations using "Big-M" constraints and/or L2-norm penalties. In contrast, our method accommodates a broader class of loss functions and allows greater flexibility in relaxation design through a general penalty term, encompassing existing techniques as special cases. We establish theoretical results ensuring that all key quantities required for the Branch-and-Bound implementation admit closed-form expressions under the general blanket assumptions considered in our work. Leveraging this framework, we introduce El0ps, an open-source Python solver with a plug-and-play workflow that enables user-defined losses and penalties in L0-penalized problems. Through extensive numerical experiments, we demonstrate that El0ps achieves state-of-the-art performance on classical instances and extends computational feasibility to previously intractable ones.
Combinatorial Optimization problems are widespread in domains such as logistics, manufacturing, and drug discovery, yet their NP-hard nature makes them computationally challenging. Recent Neural Combinatorial Optimization methods leverage deep learning to learn solution strategies, trained via Supervised or Reinforcement Learning (RL). While promising, these approaches often rely on task-specific augmentations, perform poorly on out-of-distribution instances, and lack robust inference mechanisms. Moreover, existing latent space models either require labeled data or rely on pre-trained policies. In this work, we propose LGS-Net, a novel latent space model that conditions on problem instances, and introduce an efficient inference method, Latent Guided Sampling (LGS), based on Markov Chain Monte Carlo and Stochastic Approximation. We show that the iterations of our method form a time-inhomogeneous Markov Chain and provide rigorous theoretical convergence guarantees. Empirical results on benchmark routing tasks show that our method achieves state-of-the-art performance among RL-based approaches.