Biology

New Software Preserves Delicate Cell Branch Structures for Better Analysis

How the science connects

Fluorescence micro…Image analysis

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MorphoBranch is a new computational tool designed to analyze the branching structures of neurons and microglia from fluorescence microscopy images while preserving fine cellular details that are often lost or misrepresented in existing methods. The system combines a deterministic image-processing pipeline with a large language model interface that translates natural language requests into analytical actions, achieving superior accuracy in measuring skeleton structure and branch length compared to existing methods across three test datasets. Testing showed 94% success rate in executing user requests while maintaining reproducible and human-reviewable analysis workflows.


Accurate measurement of neuronal and microglial branching patterns is critical for understanding brain development, neural connectivity, and neurological diseases, but current methods struggle with fragile cellular processes. This tool could improve the reliability and accessibility of brain cell morphology studies by reducing measurement errors and allowing researchers to interact with complex analysis pipelines using plain language.


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Fluorescence microscopy Concept coming soon Image analysis Concept coming soon

⚠️ Preprint – Noch nicht peer-reviewed

Dieser Artikel wurde noch nicht von unabhängigen Experten begutachtet. Die Ergebnisse sind vorläufig und sollten mit Vorsicht interpretiert werden.

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Abstract: Background and Objectives: Fluorescence-labeled cellular arbors provide readouts of neuronal and microglial morphology, but fine and weakly labeled processes are prone to fragmentation and false connections that bias skeleton-based measurements. We present MorphoBranch, a fine-structure-preserving, human-reviewable workbench for morphometry of branched cellular structures. Methods: MorphoBranch combines a deterministic Morphometry Engine with an LLM-assisted Refinement Engine. The Mor- phometry Engine implements an image-to-graph workflow integrating multiscale structural evidence extraction, hysteresis segmen- tation, evidence-constrained skeleton refinement, and graph-based morphometry. The Refinement Engine maps natural-language requests to registered actions for parameter adjustment, preview execution, metric reporting, and unsupported-request handling, while image processing and quantitative computation remain deterministic and reviewable. Results: MorphoBranch was evaluated on two public neuronal axon datasets, AxonMIP and AxonStack, and the in-house Cell- Morph dataset of microglial fluorescence images. It achieved the highest Skeleton F1 and clDice and the lowest length-estimation error among the evaluated methods on all three datasets, while also achieving the highest Dice and IoU on AxonMIP and Axon- Stack. Across 150 natural-language tasks, the Refinement Engine achieved a 94.0% end-to-end success rate. Conclusions: These results demonstrate that MorphoBranch provides a reproducible, human-reviewable workflow for mor- phometric analysis of branched cellular structures. It supports fine-structure-preserving quantification across neuronal axon and microglial fluorescence images while maintaining inspectable and reproducible analysis workflows.

Source: MorphoBranch: A Fine-Structure-Preserving Workbench for Morphometric Analysis of Branched Cellular Structures