BioMARS: A Multi-Agent Robotic System for Autonomous Biological Experiments

Large language models (LLMs) and vision-language models (VLMs) have the potential to transform biological research by enabling autonomous experimentation. Yet, their application remains constrained by rigid protocol design, limited adaptability to dynamic lab conditions, inadequate error handling, and high operational complexity. Here we introduce BioMARS (Biological Multi-Agent Robotic System), an intelligent platform that integrates LLMs, VLMs, and modular robotics to autonomously design, plan, and execute biological experiments. BioMARS uses a hierarchical architecture: the Biologist Agent synthesizes protocols via retrieval-augmented generation; the Technician Agent translates them into executable robotic pseudo-code; and the Inspector Agent ensures procedural integrity through multimodal perception and anomaly detection. The system autonomously conducts cell passaging and culture tasks, matching or exceeding manual performance in viability, consistency, and morphological integrity. It also supports context-aware optimization, outperforming conventional strategies in differentiating retinal pigment epithelial cells. A web interface enables real-time human-AI collaboration, while a modular backend allows scalable integration with laboratory hardware. These results highlight the feasibility of generalizable, AI-driven laboratory automation and the transformative role of language-based reasoning in biological research.

Intermediate Domain-guided Adaptation for Unsupervised Chorioallantoic Membrane Vessel Segmentation

The chorioallantoic membrane (CAM) model is widely employed in angiogenesis research, and distribution of growing blood vessels is the key evaluation indicator. As a result, vessel segmentation is crucial for quantitative assessment based on topology and morphology. However, manual segmentation is extremely time-consuming, labor-intensive, and prone to inconsistency due to its subjective nature. Moreover, research on CAM vessel segmentation algorithms remains limited, and the lack of public datasets contributes to poor prediction performance. To address these challenges, we propose an innovative Intermediate Domain-guided Adaptation (IDA) method, which utilizes the similarity between CAM images and retinal images, along with existing public retinal datasets, to perform unsupervised training on CAM images. Specifically, we introduce a Multi-Resolution Asymmetric Translation (MRAT) strategy to generate intermediate images to promote image-level interaction. Then, an Intermediate Domain-guided Contrastive Learning (IDCL) module is developed to disentangle cross-domain feature representations. This method overcomes the limitations of existing unsupervised domain adaptation (UDA) approaches, which primarily concentrate on directly source-target alignment while neglecting intermediate domain information. Notably, we create the first CAM dataset to validate the proposed algorithm. Extensive experiments on this dataset show that our method outperforms compared approaches. Moreover, it achieves superior performance in UDA tasks across retinal datasets, highlighting its strong generalization capability. The CAM dataset and source codes are available at https://github.com/Light-47/IDA.

Label-free Prediction of Vascular Connectivity in Perfused Microvascular Networks in vitro

Continuous monitoring and in-situ assessment of microvascular connectivity have significant implications for culturing vascularized organoids and optimizing the therapeutic strategies. However, commonly used methods for vascular connectivity assessment heavily rely on fluorescent labels that may either raise biocompatibility concerns or interrupt the normal cell growth process. To address this issue, a Vessel Connectivity Network (VC-Net) was developed for label-free assessment of vascular connectivity. To validate the VC-Net, microvascular networks (MVNs) were cultured in vitro and their microscopic images were acquired at different culturing conditions as a training dataset. The VC-Net employs a Vessel Queue Contrastive Learning (VQCL) method and a class imbalance algorithm to address the issues of limited sample size, indistinctive class features and imbalanced class distribution in the dataset. The VC-Net successfully evaluated the vascular connectivity with no significant deviation from that by fluorescence imaging. In addition, the proposed VC-Net successfully differentiated the connectivity characteristics between normal and tumor-related MVNs. In comparison with those cultured in the regular microenvironment, the averaged connectivity of MVNs cultured in the tumor-related microenvironment decreased by 30.8%, whereas the non-connected area increased by 37.3%. This study provides a new avenue for label-free and continuous assessment of organoid or tumor vascularization in vitro.

Efficient Multiple Object Tracking Using Mutually Repulsive Active Membranes

Studies of social and group behavior in interacting organisms require high-throughput analysis of the motion of a large number of individual subjects. Computer vision techniques offer solutions to specific tracking problems, and allow automated and efficient tracking with minimal human intervention. In this work, we adopt the open active contour model to track the trajectories of moving objects at high density. We add repulsive interactions between open contours to the original model, treat the trajectories as an extrusion in the temporal dimension, and show applications to two tracking problems. The walking behavior of Drosophila is studied at different population density and gender composition. We demonstrate that individual male flies have distinct walking signatures, and that the social interaction between flies in a mixed gender arena is gender specific. We also apply our model to studies of trajectories of gliding Myxococcus xanthus bacteria at high density. We examine the individual gliding behavioral statistics in terms of the gliding speed distribution. Using these two examples at very distinctive spatial scales, we illustrate the use of our algorithm on tracking both short rigid bodies (Drosophila) and long flexible objects (Myxococcus xanthus). Our repulsive active membrane model reaches error rates better than $5\times 10^{-6}$ per fly per second for Drosophila tracking and comparable results for Myxococcus xanthus.