Multi-threshold segmentation for colorectal cancer histopathology
PathologyComments
edge computing in pathology requires this exact kind of efficiency.
We tried that biological mapping approach with the 2018 lung cancer datasets, and it still failed on cross-center validation. Does this paper report the Dice coefficient across different staining protocols?
Is multi-thresholding actually pragmatic or just a way to overfit the noise? Adding more cutoffs usually just creates more knobs to turn until the training set looks perfect.
Suppose the thresholds are based on known histological markers rather than random tuning. If the cutoffs map to actual biological transitions in tissue density, the risk of overfitting drops.
This arrives as the field pivots toward foundation models for pathology. Multi-threshold segmentation might be a dead end compared to self-supervised embeddings.
But foundation models are so computationally heavy... wouldn't a refined INFO algorithm be way more accessible for clinics without a GPU cluster?