Foundation models are increasingly applied to computational pathology, yet their behavior under cross-cancer and cross-species transfer remains unspecified. This study investigated how fine-tuning CPath-CLIP affects cancer detection under same-cancer, cross-cancer, and cross-species conditions using whole-slide image patches from canine and human histopathology. Performance was measured using area under the receiver operating characteristic curve (AUC). Few-shot fine-tuning improved same-cancer (64.9% to 72.6% AUC) and cross-cancer performance (56.84% to 66.31% AUC). Cross-species evaluation revealed that while tissue matching enables meaningful transfer, performance remains below state-of-the-art benchmarks (H-optimus-0: 84.97% AUC), indicating that standard vision-language alignment is suboptimal for cross-species generalization. Embedding space analysis revealed extremely high cosine similarity (greater than 0.99) between tumor and normal prototypes. Grad-CAM shows prototype-based models remain domain-locked, while language-guided models attend to conserved tumor morphology. To address this, we introduce Semantic Anchoring, which uses language to provide a stable coordinate syst
Cross-species antimicrobial resistance (AMR) prediction is fundamentally an out-of-distribution (OOD) generalization problem: models trained on one set of bacterial taxa must transfer to phylogenetically distinct genomes that may rely on different resistance mechanisms. Across species, resistance arises from a heterogeneous mixture of localized, horizontally transferred gene cassettes and diffuse species-specific genomic backgrounds, making successful transfer inherently mechanism-dependent. Using a strict species holdout protocol, we first establish an interpretable k-mer baseline with Kover and show that strong within-species performance collapses under true cross-species evaluation. This motivates representation-level approaches that preserve transferable biological signals rather than amplify phylogenetic shortcuts. We investigate genomic foundation model embeddings derived from Evo-1-8k-base and introduce diagnostics for layer selection based on activation scale, isotropy, effective rank, and cross-seed stability under native bfloat16 inference. These analyses identify a stability boundary in deeper layers and reveal that embeddings extracted near this boundary provide more ro
Veterinary pharmacovigilance systems are essential for monitoring adverse drug events (ADEs), yet existing approaches often fail to capture region-specific toxicity patterns shaped by local biological and regulatory contexts. In Japan, these challenges are amplified by species-specific metabolic differences and reporting practices defined by the Ministry of Agriculture, Forestry, and Fisheries (MAFF). Most prior work relies on prediction-oriented models, limiting mechanistic interpretability. This study proposes a regulatory-integrated unsupervised framework for pattern discovery using the National Veterinary Assay Laboratory (NVAL) database. ADEs are encoded into organ system-aligned representations and adjusted for species-specific reporting biases, enabling cross-species comparison. Similarity-based clustering and dimensionality reduction are applied to identify latent toxicity structures. Analysis of 4,120 high-confidence ADE reports (9,080 drug-ADE combinations) identified three significant species clusters (p < 0.01), including hepatic-dominant patterns in companion animals (0.42 $\pm$ 0.06), renal toxicity in ruminants (0.39 $\pm$ 0.07), and dermatological sensitivity in
We present density response estimators for Monte Carlo simulations that are based on a reweighting procedure, where the samples of an unperturbed system are used to estimate the properties of a system perturbed by an external harmonic potential. This allows the linear and nonlinear static density response to be estimated purely from simulations of the unperturbed system. The method is demonstrated for the uniform electron gas under warm dense matter and strongly coupled conditions using ab initio path integral Monte Carlo simulations. The performance of the method with respect to the number of particles and the number of imaginary time slices is investigated. The scheme is generalised to consider multiple external perturbations, acting on different species and with different wavenumbers, giving one access to additional cross-species density response functions and the complete quadratic response function resolved for both wave number arguments through mode coupling. The flexibility of the methodology opens the possibility to investigate numerous new density response properties to further advance our understanding of interacting quantum many-body systems across a broad range of appli
The investigation of plant transcriptional regulation constitutes a fundamental basis for crop breeding, where cis-regulatory elements (CREs), as the key factor determining gene expression, have become the focus of crop genetic improvement research. Deep learning techniques, leveraging their exceptional capacity for high-dimensional feature extraction and nonlinear regulatory relationship modeling, have been extensively employed in this field. However, current methodologies present notable limitations: single CNN-based architectures struggle to capture long-range regulatory interactions, while existing CNN-Transformer hybrid models demonstrate proneness to overfitting and inadequate generalization in cross-species prediction contexts. To address these challenges, this study proposes DeepPlantCRE, a deep-learning framework for plant gene expression prediction and CRE Extraction. The model employs a Transformer-CNN hybrid architecture that achieves enhanced Accuracy, AUC-ROC, and F1-score metrics over existing baselines (DeepCRE and PhytoExpr), with improved generalization performance and overfitting inhibiting. Cross-species validation experiments conducted on gene expression datase
Decoding the orchestration of neural activity in electroencephalography (EEG) signals is a central challenge in bridging neuroscience with artificial intelligence. Foundation models have made strides in generalized EEG decoding, yet many existing frameworks primarily relying on separate temporal and spectral masking of raw signals during self-supervised pretraining. Such strategies often tend to bias learning toward high-frequency oscillations, as low-frequency rhythmic patterns can be easily inferred from the unmasked signal. We introduce a foundation model that utilizes a novel Gaussian-smoothed masking scheme applied to short-time Fourier transform (STFT) maps. By jointly applying time, frequency, and time-frequency Gaussian masks, we make the reconstruction task much more challenging, forcing the model to learn intricate neural patterns across both high- and low-frequency domains. To effectively recover signals under this aggressive masking strategy, we design SpecHi-Net, a U-shaped hierarchical architecture with multiple encoding and decoding stages. To accelerate large-scale pretraining, we partition the data into three subsets, each used to train an independent expert model.
Single-cell electrophysiological recordings provide a powerful window into neuronal functional diversity and offer an interpretable route for linking intrinsic physiology to transcriptomic identity. Here, we replicate and extend the electrophysiology-to-transcriptomics framework introduced by Gouwens et al. (2020) using publicly available Allen Institute Patch-seq datasets from both mouse and human cortex. We focus on GABAergic inhibitory interneurons to target a subclass structure (Lamp5, Pvalb, Sst, Vip) that is comparable and conserved across species. After quality control, we analyzed 3,699 mouse visual cortex neurons and 506 human neocortical neurons from neurosurgical resections. Using standardized electrophysiological features and sparse PCA, we reproduced the major class-level separations reported in the original mouse study. For supervised prediction, a class-balanced random forest provided a strong feature-engineered baseline in mouse data and a reduced but still informative baseline in human data. We then developed an attention-based BiLSTM that operates directly on the structured IPFX feature-family representation, avoiding sPCA and providing feature-family-level interp
Speech brain-computer interfaces (BCIs) aim to restore communication for people with paralysis by translating neural activity into text. Most systems use cascaded frameworks that decode phonemes before assembling sentences with an n-gram language model (LM), preventing joint optimization of all stages simultaneously. Here, we introduce an end-to-end BraIn-to-Text (BIT) framework that translates neural activity into coherent sentences using a single differentiable neural network. Central to our approach is a cross-task, cross-species pretrained neural encoder, whose representations transfer to both attempted and imagined speech. In a cascaded setting with an n-gram LM, the pretrained encoder establishes a new state-of-the-art (SOTA) on the Brain-to-Text '24 and '25 benchmarks. Integrated end-to-end with audio large language models (LLMs) and trained with contrastive learning for cross-modal alignment, BIT reduces the word error rate (WER) of the prior end-to-end method from 24.69% to 10.22%. Notably, we find that small-scale audio LLMs markedly improve end-to-end decoding. Beyond record-setting performance, BIT aligns attempted and imagined speech embeddings to enable cross-task gen
Accurate plant counting provides valuable information for agriculture such as crop yield prediction, plant density assessment, and phenotype quantification. Vision-based approaches are currently the mainstream solution. Prior art typically uses a detection or a regression model to count a specific plant. However, plants have biodiversity, and new cultivars are increasingly bred each year. It is almost impossible to exhaust and build all species-dependent counting models. Inspired by class-agnostic counting (CAC) in computer vision, we argue that it is time to rethink the problem formulation of plant counting, from what plants to count to how to count plants. In contrast to most daily objects with spatial and temporal invariance, plants are dynamic, changing with time and space. Their non-rigid structure often leads to worse performance than counting rigid instances like heads and cars such that current CAC and open-world detection models are suboptimal to count plants. In this work, we inherit the vein of the TasselNet plant counting model and introduce a new extension, TasselNetV4, shifting from species-specific counting to cross-species counting. TasselNetV4 marries the local cou
Recent video editing advancements rely on accurate pose sequences to animate subjects. However, these efforts are not suitable for cross-species animation due to pose misalignment between species (for example, the poses of a cat differs greatly from that of a pig due to differences in body structure). In this paper, we present AnimateZoo, a zero-shot diffusion-based video generator to address this challenging cross-species animation issue, aiming to accurately produce animal animations while preserving the background. The key technique used in our AnimateZoo is subject alignment, which includes two steps. First, we improve appearance feature extraction by integrating a Laplacian detail booster and a prompt-tuning identity extractor. These components are specifically designed to capture essential appearance information, including identity and fine details. Second, we align shape features and address conflicts from differing subjects by introducing a scale-information remover. This ensures accurate cross-species animation. Moreover, we introduce two high-quality animal video datasets featuring a wide variety of species. Trained on these extensive datasets, our model is capable of gen
Pose estimation serves as a cornerstone of computer vision for understanding animal posture, behavior, and welfare. Yet, agricultural applications remain constrained by the scarcity of large, annotated datasets for livestock, especially dairy cattle. This study evaluates the potential and limitations of cross-species transfer learning by adapting ZebraPose - a vision transformer-based model trained on synthetic zebra imagery - for 27-keypoint detection in dairy cows under real barn conditions. Using three configurations - a custom on-farm dataset (375 images, Sussex, New Brunswick, Canada), a subset of the APT-36K benchmark dataset, and their combination, we systematically assessed model accuracy and generalization across environments. While the combined model achieved promising performance (AP = 0.86, AR = 0.87, PCK 0.5 = 0.869) on in-distribution data, substantial generalization failures occurred when applied to unseen barns and cow populations. These findings expose the synthetic-to-real domain gap as a major obstacle to agricultural AI deployment and emphasize that morphological similarity between species is insufficient for cross-domain transfer. The study provides practical i
Epileptic seizure forecasting is a clinically important yet challenging problem in epilepsy research. Existing approaches predominantly rely on neural signals such as electroencephalography (EEG), which require specialized equipment and limit long-term deployment in real-world settings. In contrast, video data provide a non-invasive and accessible alternative, yet existing video-based studies mainly focus on post-onset seizure detection, leaving seizure forecasting largely unexplored. In this work, we formulate a novel task of video-based epileptic seizure forecasting, where short pre-ictal video segments (3-10 seconds) are used to predict whether a seizure will occur within the subsequent 5 seconds. To address the scarcity of annotated human epilepsy videos, we propose a cross-species transfer learning framework that leverages large-scale rodent video data for auxiliary pretraining. This enables the model to capture seizure-related behavioral dynamics that generalize across species. Experimental results demonstrate that our approach achieves over 70% prediction accuracy under a strictly video-only setting and outperforms existing baselines. These findings highlight the potential o
Epilepsy significantly impacts global health, affecting about 65 million people worldwide, along with various animal species. The diagnostic processes of epilepsy are often hindered by the transient and unpredictable nature of seizures. Here we propose a multi-space alignment approach based on cross-species and cross-modality electroencephalogram (EEG) data to enhance the detection capabilities and understanding of epileptic seizures. By employing deep learning techniques, including domain adaptation and knowledge distillation, our framework aligns cross-species and cross-modality EEG signals to enhance the detection capability beyond traditional within-species and with-modality models. Experiments on multiple surface and intracranial EEG datasets of humans and canines demonstrated substantial improvements in the detection accuracy, achieving over 90% AUC scores for cross-species and cross-modality seizure detection with extremely limited labeled data from the target species/modality. To our knowledge, this is the first study that demonstrates the effectiveness of integrating heterogeneous data from different species and modalities to improve EEG-based seizure detection performance
Accurate delineation of the boundaries between the renal cortex and medulla is crucial for subsequent functional structural analysis and disease diagnosis. Training high-quality deep-learning models for layer segmentation relies on the availability of large amounts of annotated data. However, due to the patient's privacy of medical data and scarce clinical cases, constructing pathological datasets from clinical sources is relatively difficult and expensive. Moreover, using external natural image datasets introduces noise during the domain generalization process. Cross-species homologous data, such as mouse kidney data, which exhibits high structural and feature similarity to human kidneys, has the potential to enhance model performance on human datasets. In this study, we incorporated the collected private Periodic Acid-Schiff (PAS) stained mouse kidney dataset into the human kidney dataset for joint training. The results showed that after introducing cross-species homologous data, the semantic segmentation models based on CNN and Transformer architectures achieved an average increase of 1.77% and 1.24% in mIoU, and 1.76% and 0.89% in Dice score for the human renal cortex and medul
Understanding how genes influence phenotype across species is a fundamental challenge in genetic engineering, which will facilitate advances in various fields such as crop breeding, conservation biology, and personalized medicine. However, current phenotype prediction models are limited to individual species and expensive phenotype labeling process, making the genotype-to-phenotype prediction a highly domain-dependent and data-scarce problem. To this end, we suggest taking images as morphological proxies, facilitating cross-species generalization through large-scale multimodal pretraining. We propose the first genotype-to-phenotype diffusion model (G2PDiffusion) that generates morphological images from DNA considering two critical evolutionary signals, i.e., multiple sequence alignments (MSA) and environmental contexts. The model contains three novel components: 1) a MSA retrieval engine that identifies conserved and co-evolutionary patterns; 2) an environment-aware MSA conditional encoder that effectively models complex genotype-environment interactions; and 3) an adaptive phenomic alignment module to improve genotype-phenotype consistency. Extensive experiments show that integrat
Research organisms provide invaluable insights into human biology and diseases, serving as essential tools for functional experiments, disease modeling, and drug testing. However, evolutionary divergence between humans and research organisms hinders effective knowledge transfer across species. Here, we review state-of-the-art methods for computationally transferring knowledge across species, primarily focusing on methods that utilize transcriptome data and/or molecular networks. Our review addresses four key areas: (1) transferring disease and gene annotation knowledge across species, (2) identifying functionally equivalent molecular components, (3) inferring equivalent perturbed genes or gene sets, and (4) identifying equivalent cell types. We conclude with an outlook on future directions and several key challenges that remain in cross-species knowledge transfer, including introducing the concept of "agnology" to describe functional equivalence of biological entities, regardless of their evolutionary origins. This concept is becoming pervasive in integrative data-driven models where evolutionary origins of functions can remain unresolved.
Study Objectives: Fetal sleep is a vital yet underexplored aspect of prenatal neurodevelopment. Its cyclic organization reflects the maturation of central neural circuits, and disturbances in these patterns may offer some of the earliest detectable signs of neurological compromise. This is the first review to integrate more than seven decades of research into a unified, cross-species synthesis of fetal sleep. We examine: (i) Physiology and Ontogeny-comparing human fetuses with animal models; and (ii) Methodological Evolution-transitioning from invasive neurophysiology to non-invasive monitoring and deep learning frameworks. Methods: A structured narrative synthesis was guided by a systematic literature search across four databases (PubMed, Scopus, IEEE Xplore, and Google Scholar). From 2,925 identified records, 171 studies involving fetal sleep-related physiology, sleep-state classification, or signal-based monitoring were included in this review. Results: Across the 171 studies, fetal sleep states become clearly observable as the brain matures. In fetal sheep and baboons, organized cycling between active and quiet sleep emerges at approximately 80%-90% gestation. In humans, this d
Deep learning techniques are dominating automated animal activity recognition (AAR) tasks with wearable sensors due to their high performance on large-scale labelled data. However, current deep learning-based AAR models are trained solely on datasets of individual animal species, constraining their applicability in practice and performing poorly when training data are limited. In this study, we propose a one-for-many framework, dubbed Cross-species Knowledge Sharing and Preserving (CKSP), based on sensor data of diverse animal species. Given the coexistence of generic and species-specific behavioural patterns among different species, we design a Shared-Preserved Convolution (SPConv) module. This module assigns an individual low-rank convolutional layer to each species for extracting species-specific features and employs a shared full-rank convolutional layer to learn generic features, enabling the CKSP framework to learn inter-species complementarity and alleviating data limitations via increasing data diversity. Considering the training conflict arising from discrepancies in data distributions among species, we devise a Species-specific Batch Normalization (SBN) module, that invol
Gene regulatory networks (GRNs) are essential for understanding cell fate decisions and disease mechanisms, yet cross-species GRN inference from single-cell RNA-seq data remains challenging due to noise, sparsity, and cross-species distribution shifts. We propose GP-DHT (GenePair DualHeadTransformer), a cross-species single-cell GRN inference framework that models genes and cells in a heterogeneous graph with multi-level expression relations and learns structured regulatory representations via multi-relational graph attention. A dual-head Transformer further captures local gene pair regulatory dependencies and global cross-cell interaction patterns. To improve robustness under sparse and cross-species settings, GP-DHT introduces gene pair level supervised contrastive learning. Experiments on seven BEELINE benchmark datasets show consistent gains over representative baselines, improving AUROC and AUPRC by approximately 5 to 7 percent on most datasets. GP-DHT also recovers known regulatory modules and helps distinguish conserved from species-specific regulations.
Species interactions through cross-feeding via leakage and uptake of chemicals are important in microbial communities, and play an essential role in the coexistence of diverse species. Here, we study a simple dynamical model of a microbial community in which species interact by competing for the uptake of common metabolites that are leaked by other species. The model includes coupled dynamics of species populations and chemical concentrations in the medium, allowing for a variety of uptake and leakage networks among species. Depending on the structure of these networks, the system exhibits different attractors, including fixed points, limit cycles, low-dimensional chaos, and high-dimensional chaos. In the fixed-point and limit-cycle cases, the number of coexisting species is bounded by the number of exchangeable chemicals, consistent with the well-known competitive exclusion principle. In contrast, in the low-dimensional chaotic regime, the number of coexisting species exhibits noticeable but limited excess over this limit. Remarkably, in the high-dimensional chaotic regime, a much larger number of species beyond this limit coexist persistently over time. In this case, the rank-abu