Evidence map›Paper›PMID 39591424›Full record

ArticlePloS one2024

Deep learning-enhanced automated mitochondrial segmentation in FIB-SEM images using an entropy-weighted ensemble approach.

Yubraj Gupta, Rainer Heintzmann, Carlos Costa, Rui Jesus, Eduardo Pinho

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Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Yubraj GuptaDepartamento de Electrónica, Telecomunicações e Informática (DETI), University of Aveiro, Aveiro, Portugal.ORCID 0000-0002-8404-5411
Rainer HeintzmannLeibniz-Institute of Photonic Technology (Leibniz-IPHT), Jena, Germany.
Carlos CostaDepartamento de Electrónica, Telecomunicações e Informática (DETI), University of Aveiro, Aveiro, Portugal.
Rui JesusBMD Software, Aveiro, Portugal.
Eduardo PinhoBMD Software, Aveiro, Portugal.ORCID 0000-0002-4397-8792

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mitochondria are intracellular organelles that act as powerhouses by breaking down nutrition molecules to produce adenosine triphosphate (ATP) as cellular fuel. They have their own genetic material called mitochondrial DNA. Alterations in mitochondrial DNA can result in primary mitochondrial diseases, including neurodegenerative disorders. Early detection of these abnormalities is crucial in slowing disease progression. With recent advances in data acquisition techniques such as focused ion beam scanning electron microscopy, it has become feasible to capture large intracellular organelle volumes at data rates reaching 4Tb/minute, each containing numerous cells. However, manually segmenting large data volumes (gigapixels) can be time-consuming for pathologists. Therefore, there is an urgent need for automated tools that can efficiently segment mitochondria with minimal user intervention. Our article proposes an ensemble of two automatic segmentation pipelines to predict regions of interest specific to mitochondria. This architecture combines the predicted outputs from both pipelines using an ensemble learning-based entropy-weighted fusion technique. The methodology minimizes the impact of individual predictions and enhances the overall segmentation results. The performance of the segmentation task is evaluated using various metrics, ensuring the reliability of our results. We used four publicly available datasets to evaluate our proposed method's effectiveness. Our proposed fusion method has achieved a high score in terms of the mean Jaccard index and dice coefficient for all four datasets. For instance, in the UroCell dataset, our proposed fusion method achieved scores of 0.9644 for the mean Jaccard index and 0.9749 for the Dice coefficient. The mean error rate and pixel accuracy were 0.0062 and 0.9938, respectively. Later, we compared it with state-of-the-art methods like 2D and 3D CNN algorithms. Our ensemble approach shows promising segmentation efficiency with minimal intervention and can potentially aid in the early detection and mitigation of mitochondrial diseases.

Indexed as

Deep LearningEntropyMitochondriaAlgorithmsHumansImage Processing, Computer-AssistedMicroscopy, Electron, ScanningVolume Electron Microscopy

Identifiers

PMID39591424
PMCPMC11593762

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.