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Titlebook: Software Engineering 1; Abstraction and Mode Dines Bj?rner Textbook 2006 Springer-Verlag Berlin Heidelberg 2006 design.formal method.lambda

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發(fā)表于 2025-3-25 05:46:40 | 只看該作者
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發(fā)表于 2025-3-25 16:06:11 | 只看該作者
d engineering requires a thorough study about what is happening in the real world that will motivate a mathematician or engineer to mathematicize?the incident. The deeper one can observe and analyze ?the incident, the better will be for mathematical?modeling. The topic here is to visualize scientifi
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發(fā)表于 2025-3-25 20:56:12 | 只看該作者
ctures, which integrate function and matter from lower to upper levels, and b) from a practical point of view by proposing future tracks for cancer therapeutics, as cancer is primarily a failure of multicellularity in animals and humans. This approach resorts to the emergent field of knowledge known
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發(fā)表于 2025-3-26 01:38:01 | 只看該作者
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發(fā)表于 2025-3-26 05:13:42 | 只看該作者
n comparison to conventional serum markers in previous studies. Moreover, 2 proteins, F12 and CFD, were not previously associated with GC and were not utilized for serum-based testing of other malignancies. Proposed approach has a high potential to be used for serum marker identification in other ty
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發(fā)表于 2025-3-26 09:18:17 | 只看該作者
s and non-linear effects of random subsets of these variables. Models were compared using the concordance index and integrated Brier score. We applied the methods to the METABRIC breast cancer data set, including 1,960 patients, 6 clinical covariates and the expression of 863 genes.. In the simulati
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發(fā)表于 2025-3-26 13:12:52 | 只看該作者
d Dataverse to develop deep-learning algorithms that aid in skin self-examination. ResNet-50, DenseNet-121, and VGG-16 models were used to distinguish low-risk lesions (melanocytic nevi, dermatofibroma, and benign keratosis-like lesions) from high-risk lesions (melanoma, basal cell carcinoma, actini
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發(fā)表于 2025-3-26 19:24:42 | 只看該作者
0201 for these software tools. Two studies were performed, one using the data that the neural networks were trained on and the other using a sample of the human proteome. A significant bias within NetMHC-4.0 towards predicting highly hydrophobic peptides as strong binders was observed in both studie
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