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Rens Janssens

dblp:211/7112 · DBLP profile ↗
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1ranked-venue papers
1as first author
1since 2021 · last 2021
0000-0001-5717-0340ORCID · reported

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 1 · 1 first-author · 1 since 2021

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%

Topics — the 2 heaviest of 2, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › biological imaging
cellular imaging
0.512021
Fully unsupervised deep mode of action learning for phenotyping high-content cellular images · Bioinform. 2021
Bioinformatics and computational biology
high-content screening
0.512021
Fully unsupervised deep mode of action learning for phenotyping high-content cellular images · Bioinform. 2021

Methods — techniques the papers use, named apart from their topics

deep learning · 0.5clustering · 0.5batch effect correction · 0.5
YearPublicationVenuePosition
2021 Fully unsupervised deep mode of action learning for phenotyping high-content cellular images
abstract
MOTIVATION: The identification and discovery of phenotypes from high content screening images is a challenging task. Earlier works use image analysis pipelines to extract biological features, supervised training methods or generate features with neural networks pretrained on non-cellular images. We introduce a novel unsupervised deep learning algorithm to cluster cellular images with similar Mode-of-Action (MOA) together using only the images' pixel intensity values as input. It corrects for batch effect during training. Importantly, our method does not require the extraction of cell candidates and works from the entire images directly. RESULTS: The method achieves competitive results on the labeled subset of the BBBC021 dataset with an accuracy of 97.09% for correctly classifying the MOA by nearest neighbors matching. Importantly, we can train our approach on unannotated datasets. Therefore, our method can discover novel MOAs and annotate unlabeled compounds. The ability to train end-to-end on the full resolution images makes our method easy to apply and allows it to further distinguish treatments by their effect on proliferation. AVAILABILITY AND IMPLEMENTATION: Our code is available at https://github.com/Novartis/UMM-Discovery. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Rens Janssens, Audrey Kauffmann, Antoine de Weck, Eric Y. Durand
Bioinform.1