Evidence map›Paper›PMID 41309785›Full record

ArticleScientific reports2025

Enhancing classification of rare white blood cells in FPM with a physics-inspired GAN.

Houda Hassini, Bernadette Dorizzi, Vincent Leymarie, Jacques Klossa, Yaneck Gottesman

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited 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

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Houda HassiniSamovar, Télécom SudParis, Institut Polytechnique de Paris, 91120, Palaiseau, France.
Bernadette DorizziSamovar, Télécom SudParis, Institut Polytechnique de Paris, 91120, Palaiseau, France.
Vincent LeymarieLaboratoire d'Hématologie, HUPSSD, Hôpital Avicenne, AP-HP, 93009, Bobigny, France.
Jacques KlossaTRIBVN, 92200, Neuilly, France.
Yaneck GottesmanSamovar, Télécom SudParis, Institut Polytechnique de Paris, 91120, Palaiseau, France. yaneck.gottesman@telecom-sudparis.eu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this work, we propose a novel GAN-based architecture, termed Physics-Inspired GAN (PI-GAN), to generate synthetic bimodal data comprising both intensity and phase images as produced through Fourier Ptychographic Microscopy (FPM). By explicitly incorporating the forward model of image formation into the GAN architecture, our approach ensures that the physical relationship between the intensity and phase modalities is preserved throughout the training and generation processes, therefore solving the mode collapse problem encountered in classical GANs. Our approach is evaluated for the classification of the five major types of white blood cells (WBCs) in peripheral blood smears, a domain where severe class imbalance is a major challenge. In particular, basophils represent less than 1% of circulating WBCs, making it difficult to train robust classifiers without synthetic augmentation. To overcome the scarcity of basophil data, we proposed a two-step fine-tuning strategy: first training the PI-GAN to generate neutrophils (a more abundant but morphologically similar class), and then adapting the model to produce basophils. Our results show that the addition of synthetic basophil images allows a great improvement (5% in precision) in the ability to correctly classify basophils. Our approach offers great potential for future hybrid models that combine physics-based priors with the flexibility of deep generative networks.

Indexed as

Image Processing, Computer-AssistedLeukocytesMicroscopyAlgorithmsBasophilsFourier AnalysisHumans

Identifiers

PMID41309785
PMCPMC12660895

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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.