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@ARTICLE{Rehn:1050784,
author = {Rehn, Fabian and Pils, Marlene and Bujnicki, Tuyen and
Bannach, Oliver and Willbold, Dieter},
title = {{A}rtifact detection in fluorescence microscopy using
convolutional autoencoder},
journal = {Scientific reports},
volume = {15},
number = {1},
issn = {2045-2322},
address = {[London]},
publisher = {Springer Nature},
reportid = {FZJ-2026-00508},
pages = {32482},
year = {2025},
abstract = {To ensure analytical accuracy in fluorescence microscopy
image analysis, robust artifact detection is essential. For
large datasets or time-sensitive analyses, automation is
advisable, as it not only reduces time and costs but also
eliminates human bias and enhances reproducibility. Although
artificial intelligence is commonly employed for artifact
detection, it is typically limited to recognizing artifact
types that have been previously learned, often necessitating
large training datasets. This study proposes an approach for
an automated detection of previously unseen artifacts
without the need for a training set of artifact-laden
images. Multiple datasets were assembled using images
generated by our surface-based intensity distribution
analysis (sFIDA) technology during different experiments. A
convolutional autoencoder was trained on a dataset of
artifact-free images to reproduce preprocessed images
accurately. Artifact-laden images are subsequently detected
by computing the difference between the input and output of
the model, with increased discrepancies indicating the
presence of artifacts. The proposed model is capable of
classifying artifacts across different datasets with an
average accuracy of $95.5\%.$ Additionally, the model was
able to detect unseen artifacts of various types, including
differences in cause, structure, size and intensity. The
findings demonstrate that convolutional autoencoders provide
a lightweight, but effective method for detecting
artifact-laden images. While the method was tested only on
sFIDA images, its design, which does not rely on an artifact
specific training set, suggests potential for use across
various microscopy techniques.},
cin = {IBI-7},
ddc = {600},
cid = {I:(DE-Juel1)IBI-7-20200312},
pnm = {5241 - Molecular Information Processing in Cellular Systems
(POF4-524)},
pid = {G:(DE-HGF)POF4-5241},
typ = {PUB:(DE-HGF)16},
doi = {10.1038/s41598-025-18943-6},
url = {https://juser.fz-juelich.de/record/1050784},
}