Evidence map›Paper›PMID 39099678›Full record

ArticleJournal of biomedical optics2024

DermoGAN: multi-task cycle generative adversarial networks for unsupervised automatic cell identification on

Imane Lboukili, Georgios Stamatas, Xavier Descombes

Abstract read
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Article in Journal of biomedical optics, 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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0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Imane LboukiliJohnson & Johnson Santé Beauté France, Paris, France.ORCID 0000-0003-4964-8142
Georgios StamatasJohnson & Johnson Santé Beauté France, Paris, France.ORCID 0000-0003-4544-7597
Xavier DescombesUCA, INRIA, I3S/CNRS, Sophia Antipolis, France.ORCID 0000-0002-7611-6021

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Significance: Accurate identification of epidermal cells on reflectance confocal microscopy (RCM) images is important in the study of epidermal architecture and topology of both healthy and diseased skin. However, analysis of these images is currently done manually and therefore time-consuming and subject to human error and inter-expert interpretation. It is also hindered by low image quality due to noise and heterogeneity. Aim: We aimed to design an automated pipeline for the analysis of the epidermal structure from RCM images. Approach: Two attempts have been made at automatically localizing epidermal cells, called keratinocytes, on RCM images: the first is based on a rotationally symmetric error function mask, and the second on cell morphological features. Here, we propose a dual-task network to automatically identify keratinocytes on RCM images. Each task consists of a cycle generative adversarial network. The first task aims to translate real RCM images into binary images, thus learning the noise and texture model of RCM images, whereas the second task maps Gabor-filtered RCM images into binary images, learning the epidermal structure visible on RCM images. The combination of the two tasks allows one task to constrict the solution space of the other, thus improving overall results. We refine our cell identification by applying the pre-trained StarDist algorithm to detect star-convex shapes, thus closing any incomplete membranes and separating neighboring cells. Results: The results are evaluated both on simulated data and manually annotated real RCM data. Accuracy is measured using recall and precision metrics, which is summarized as the Conclusions: We demonstrate that the proposed fully unsupervised method successfully identifies keratinocytes on RCM images of the epidermis, with an accuracy on par with experts' cell identification, is not constrained by limited available annotated data, and can be extended to images acquired using various imaging techniques without retraining.

Indexed as

EpidermisKeratinocytesMicroscopy, ConfocalAlgorithmsEpidermal CellsHumansImage Processing, Computer-AssistedNeural Networks, ComputerUnsupervised Machine Learningcycle generative adversarial networkidentificationkeratinocytesmulti-taskreflectance confocal microscopysegmentation

Identifiers

PMID39099678
PMCPMC11294601

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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.