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Main Authors: Eshkiki, Hassan, Costa, Sarah, Mohammadpour, Mostafa, Tanhaei, Farinaz, George, Christopher H., Caraffini, Fabio
Format: Preprint
Published: 2026
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Online Access:https://arxiv.org/abs/2601.10392
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author Eshkiki, Hassan
Costa, Sarah
Mohammadpour, Mostafa
Tanhaei, Farinaz
George, Christopher H.
Caraffini, Fabio
author_facet Eshkiki, Hassan
Costa, Sarah
Mohammadpour, Mostafa
Tanhaei, Farinaz
George, Christopher H.
Caraffini, Fabio
contents Fluorescence microscopy is widely employed for the analysis of living biological samples; however, the utility of the resulting recordings is frequently constrained by noise, temporal variability, and inconsistent visualisation of signals that oscillate over time. We present a unique computational framework that integrates information from multiple time-resolved frames into a single high-quality image, while preserving the underlying biological content of the original video. We evaluate the proposed method through an extensive number of configurations (n = 111) and on a challenging dataset comprising dynamic, heterogeneous, and morphologically complex 2D monolayers of cardiac cells. Results show that our framework, which consists of a combination of explainable techniques from different computer vision application fields, is capable of generating composite images that preserve and enhance the quality and information of individual microscopy frames, yielding 44% average increase in cell count compared to previous methods. The proposed pipeline is applicable to other imaging domains that require the fusion of multi-temporal image stacks into high-quality 2D images, thereby facilitating annotation and downstream segmentation.
format Preprint
id arxiv_https___arxiv_org_abs_2601_10392
institution arXiv
publishDate 2026
record_format arxiv
spellingShingle Multi-Temporal Frames Projection for Dynamic Processes Fusion in Fluorescence Microscopy
Eshkiki, Hassan
Costa, Sarah
Mohammadpour, Mostafa
Tanhaei, Farinaz
George, Christopher H.
Caraffini, Fabio
Computer Vision and Pattern Recognition
Fluorescence microscopy is widely employed for the analysis of living biological samples; however, the utility of the resulting recordings is frequently constrained by noise, temporal variability, and inconsistent visualisation of signals that oscillate over time. We present a unique computational framework that integrates information from multiple time-resolved frames into a single high-quality image, while preserving the underlying biological content of the original video. We evaluate the proposed method through an extensive number of configurations (n = 111) and on a challenging dataset comprising dynamic, heterogeneous, and morphologically complex 2D monolayers of cardiac cells. Results show that our framework, which consists of a combination of explainable techniques from different computer vision application fields, is capable of generating composite images that preserve and enhance the quality and information of individual microscopy frames, yielding 44% average increase in cell count compared to previous methods. The proposed pipeline is applicable to other imaging domains that require the fusion of multi-temporal image stacks into high-quality 2D images, thereby facilitating annotation and downstream segmentation.
title Multi-Temporal Frames Projection for Dynamic Processes Fusion in Fluorescence Microscopy
topic Computer Vision and Pattern Recognition
url https://arxiv.org/abs/2601.10392