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ARAşTıRMA · BILGISAYARLı GöRü arXiv:2609.03080 2 Eyl 2026 · v3

Exemplar: Few-Shot Biomedical Segmentation That Fits in Seconds

Michal Průšek, Adam Novozámský, Filip Šroubek

YAYIN:2 Eyl 2026 ALAN:cs.CV OKUMA:2

Özet

Segmenting a new microscopy dataset usually means training a deep network on its annotations, and training again for every added image. Exemplar solves a segmentation readout in closed form and updates it exactly with each new mask in seconds, as accurately as networks trained for minutes. The updated readout is identical to a fit from all masks at once. Its linear readout combines frozen DINOv3 features, read at a magnification chosen from the masks, with classical filter responses at native resolution. Its regularisation and its pixel weighting are chosen exactly by leaving out one annotated image at a time, so none is set aside for validation. On ten biomedical datasets from cells to vessels and filaments, Exemplar is more accurate than every few-shot method that only applies a pretrained model, and on average than nnU-Net trained on the same masks. A fine-tuned Cellpose-SAM, the strongest baseline, is as accurate on average, but each of its fits takes a median of 25 minutes against 8.5 seconds, and each new mask means fine-tuning it again.

Özetle: Segmenting a new microscopy dataset usually means training a deep network on its annotations, and training again for every added image.

Özet

Segmenting a new microscopy dataset usually means training a deep network on its annotations, and training again for every added image. Exemplar solves a segmentation readout in closed form and updates it exactly with each new mask in seconds, as accurately as networks trained for minutes. The updated readout is identical to a fit from all masks at once. Its linear readout combines frozen DINOv3 features, read at a magnification chosen from the masks, with classical filter responses at native resolution. Its regularisation and its pixel weighting are chosen exactly by leaving out one annotated image at a time, so none is set aside for validation. On ten biomedical datasets from cells to vessels and filaments, Exemplar is more accurate than every few-shot method that only applies a pretrained model, and on average than nnU-Net trained on the same masks. A fine-tuned Cellpose-SAM, the strongest baseline, is as accurate on average, but each of its fits takes a median of 25 minutes against 8.5 seconds, and each new mask means fine-tuning it again.

Orijinal Özet (İngilizce)

Segmenting a new microscopy dataset usually means training a deep network on its annotations, and training again for every added image. Exemplar solves a segmentation readout in closed form and updates it exactly with each new mask in seconds, as accurately as networks trained for minutes. The updated readout is identical to a fit from all masks at once. Its linear readout combines frozen DINOv3 features, read at a magnification chosen from the masks, with classical filter responses at native resolution. Its regularisation and its pixel weighting are chosen exactly by leaving out one annotated image at a time, so none is set aside for validation. On ten biomedical datasets from cells to vessels and filaments, Exemplar is more accurate than every few-shot method that only applies a pretrained model, and on average than nnU-Net trained on the same masks. A fine-tuned Cellpose-SAM, the strongest baseline, is as accurate on average, but each of its fits takes a median of 25 minutes against 8.5 seconds, and each new mask means fine-tuning it again.

Kaynak: arXiv:2609.03080 · PDF

BibTeX

@article{prek2026exemplar,
  title   = {Exemplar: Few-Shot Biomedical Segmentation That Fits in Seconds},
  author  = {Michal Průšek and Adam Novozámský and Filip Šroubek},
  journal = {arXiv preprint arXiv:2609.03080},
  year    = {2026},
  url     = {https://arxiv.org/abs/2609.03080}
}

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