Tracking by weakly-supervised learning and graph optimization for whole-embryo C. elegans lineages
Peter Hirsch, Caroline Malin-Mayor, Anthony Santella, Stephan, Preibisch, Dagmar Kainmueller, Jan Funke

TL;DR
This paper introduces a weakly-supervised learning and graph optimization approach for accurate whole-embryo C. elegans lineage tracking in noisy microscopy data, addressing challenges like frequent cell divisions and polar bodies.
Contribution
It develops a novel method combining learned cell division and polar body detectors with automated ILP weight tuning, outperforming previous methods on multiple datasets.
Findings
Outperforms previous leader on Fluo-N3DH-CE dataset
Improves detection of cell division events
Increases length and correctness of track segments
Abstract
Tracking all nuclei of an embryo in noisy and dense fluorescence microscopy data is a challenging task. We build upon a recent method for nuclei tracking that combines weakly-supervised learning from a small set of nuclei center point annotations with an integer linear program (ILP) for optimal cell lineage extraction. Our work specifically addresses the following challenging properties of C. elegans embryo recordings: (1) Many cell divisions as compared to benchmark recordings of other organisms, and (2) the presence of polar bodies that are easily mistaken as cell nuclei. To cope with (1), we devise and incorporate a learnt cell division detector. To cope with (2), we employ a learnt polar body detector. We further propose automated ILP weights tuning via a structured SVM, alleviating the need for tedious manual set-up of a respective grid search. Our method outperforms the previous…
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Taxonomy
TopicsGenetics, Aging, and Longevity in Model Organisms · Gut microbiota and health · Single-cell and spatial transcriptomics
MethodsSupport Vector Machine
