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Single-agent vs. Multi-agents for Automated Video Analysis of On-Screen Collaborative Learning Behaviors

arXiv:2604.03631v1 Announce Type: new Abstract: On-screen learning behavior provides valuable insights into how students seek, use, and create information during learning. Analyzing on-screen behavioral engagement is essential for capturing students' cognitive and collaborative processes. The recent development of Vision Language Models (VLMs) offers new opportunities to automate the labor-intensive manual coding often required for multimodal video data analysis. In this study, we compared the performance of both leading closed-source VLMs (Claude-3.7-Sonnet, GPT-4.1) and open-source VLM (Qwen2.5-VL-72B) in single- and multi-agent settings for automated coding of screen recordings in collaborative learning contexts based on the ICAP framework. In particular, we proposed and compared two multi-agent frameworks: 1) a three-agent workflow multi-agent system (MAS) that segments screen videos by scene and detects on-screen behaviors using cursor-informed VLM prompting with evidence-based verification; 2) an autonomous-decision MAS inspired by ReAct that iteratively interleaves reasoning, tool-like operations (segmentation/ classification/ validation), and observation-driven self-correction to produce interpretable on-screen behavior labels. Experimental results demonstrated that the two proposed MAS frameworks achieved viable performance, outperforming the single VLMs in scene and action detection tasks. It is worth noting that the workflow-based agent achieved best on scene detection, and the autonomous-decision MAS achieved best on action detection. This study demonstrates the effectiveness of VLM-based Multi-agent System for video analysis and contributes a scalable framework for multimodal data analytics.

Integrated multi-omics analysis reveals that MARCKS reprograms the immunosuppressive microenvironment to drive hepatocellular carcinoma progression

NPJ Precis Oncol. 2026 Mar 11. doi: 10.1038/s41698-026-01372-7. Online ahead of print.

ABSTRACT

Hepatocellular carcinoma (HCC) is one of the most lethal malignancies worldwide, and its progression is closely linked to the establishment of an immunosuppressive tumor microenvironment. Myristoylated alanine-rich C kinase substrate (MARCKS) has been implicated in tumor biology; however, its role in regulating immune interactions in HCC remains poorly defined. Here, we performed an integrated multi-omics analysis combining bulk transcriptomics, single-cell RNA sequencing, and spatial transcriptomics to systematically investigate the expression pattern and functional relevance of MARCKS in HCC. We found that MARCKS was significantly upregulated in HCC tissues and that high MARCKS expression was associated with aggressive clinicopathological features and unfavorable prognosis. Single-cell and spatial analyses revealed that MARCKS expression was enriched in myeloid cell populations within the tumor microenvironment. Functional annotation and mIF(Multiple immunofluorescence) validation demonstrated that MARCKS expression was associated with enhanced JAK/STAT3 signaling and M2-like macrophage polarization. Consistently, MARCKS silencing in HCC cell lines reduced STAT3 phosphorylation, suppressed malignant phenotypes in vitro, inhibited tumor growth in vivo, and diminished the capacity of tumor-derived conditioned media to promote macrophage M2 polarization. Together, these findings identify MARCKS as a key regulator of the immunosuppressive tumor microenvironment in HCC and highlight its potential as a therapeutic target for overcoming immune evasion.

PMID:41813922 | DOI:10.1038/s41698-026-01372-7

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