arXiv subjects

Kaden Stillwagon

Publications and source records attributed to Kaden Stillwagon.

2 recordsLinked to original sources

arXiv2026

Maximum Matching Accuracy: An Instance Segmentation Evaluation Metric Utilizing Globally Optimal Matching

Reliable evaluation of instance segmentation models requires metrics that accurately and consistently reflect segmentation quality. However, the metrics most widely used in biological imaging carry fundamental mathematical weaknesses: hard Intersection-over-Union (IoU) thresholds that produce discontinuous, low sensitivity scoring; per-object normalization that distorts scores under object size variation; and greedy or one-to-many matching procedures that yield non-optimal, order-dependent correspondences. Together, these properties produce unintuitive and unreliable model rankings under common failure modes such as split cells, merged cells, and cell boundary imprecision. We propose Maximum Matching Accuracy (MMA), a threshold-free continuous metric that finds a globally optimal one-to-one matching between predicted and ground truth objects and aggregates total overlap using per-pixel normalization. We evaluate MMA against AP@50, PQ, SEG, and AJI across three experiments: synthetic failure cases, progressive corruption tests, and a model ranking comparison. MMA produces scores that are more stable, more sensitive, and more interpretable than existing alternatives, providing a principled foundation for fair instance segmentation benchmarking in biological cell imaging.

cs.CV↗

arXiv2026

Self-supervised Pretraining of Cell Segmentation Models

Instance segmentation enables the analysis of spatial and temporal properties of cells in microscopy images by identifying the pixels belonging to each cell. However, progress is constrained by the scarcity of high-quality labeled microscopy datasets. Many recent approaches address this challenge by initializing models with segmentation-pretrained weights from large-scale natural-image models such as Segment Anything Model (SAM). However, representations learned from natural images often encode objectness and texture priors that are poorly aligned with microscopy data, leading to degraded performance under domain shift. We propose DINOCell, a self-supervised framework for cell instance segmentation that leverages representations from DINOv2 and adapts them to microscopy through continued self-supervised training on unlabeled cell images prior to supervised fine-tuning. On the LIVECell benchmark, DINOCell achieves a SEG score of 0.784, improving by 10.42% over leading SAM-based models, and demonstrates strong zero-shot performance on three out-of-distribution microscopy datasets. These results highlight the benefits of domain-adapted self-supervised pretraining for robust cell segmentation.

cs.CV↗