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In previous sections, we have described the drawbacks of the Snake model.
Finally, the GVF snake model is adopted for tongue body segmentation.
But the classical snake model presents one limitation that topological changes which occur during the curve evolution are difficult.
As we mentioned briefly in Section 1, Daugman, in [5], proposed a method for iris segmentation using Snake model [21].
Geodesic active contours [43, 44] can be used to address the limited capture range problem of the conventional snake model.
In [4 6], several PolSAR image object segmentation methods based on the classical snake model [5] were proposed.
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Apart from problems that arise due to the definition of this snake models, there are other items which are not manages with snakes.
Alarm chirps used as playback stimuli were elicited by the presentation of leopard and snake models.
In particular, whilst snake models occasionally prompted subjects to jump into trees at <2 m, leopard models always resulted in subjects climbing higher (>2 m) into a tree.
We used a generalised linear mixed model (GLMM) with binomial error structure and logit link function to test whether snake models were more likely than leopard models to elicit bipedal behaviour, with bipedal behaviour scored as absent or present.
As an example, Powell [ 39] used captive birds of prey attacking moving weasel models to explore the adaptive function of tail coloration; a similar system could be used to explore the issues considered here, perhaps using snake models.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com