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1.
Complex Intell Systems ; : 1-12, 2023 Mar 29.
Artigo em Inglês | MEDLINE | ID: mdl-37361966

RESUMO

In recent years, federated learning has been believed to play a considerable role in cross-silo scenarios (e.g., medical institutions) due to its privacy-preserving properties. However, the non-IID problem in federated learning between medical institutions is common, which degrades the performance of traditional federated learning algorithms. To overcome the performance degradation problem, a novelty distribution information sharing federated learning approach (FedDIS) to medical image classification is proposed that reduce non-IIDness across clients by generating data locally at each client with shared medical image data distribution from others while protecting patient privacy. First, a variational autoencoder (VAE) is federally trained, of which the encoder is uesd to map the local original medical images into a hidden space, and the distribution information of the mapped data in the hidden space is estimated and then shared among the clients. Second, the clients augment a new set of image data based on the received distribution information with the decoder of VAE. Finally, the clients use the local dataset along with the augmented dataset to train the final classification model in a federated learning manner. Experiments on the diagnosis task of Alzheimer's disease MRI dataset and the MNIST data classification task show that the proposed method can significantly improve the performance of federated learning under non-IID cases.

2.
Org Lett ; 21(22): 9223-9227, 2019 11 15.
Artigo em Inglês | MEDLINE | ID: mdl-31687829

RESUMO

An efficient silver-assisted oxidative coupling of simple ethers with tert-butyl isocyanide was realized in the presence of DDQ. The direct synthesis of high density functional ß-carbonyl α-iminonitriles was achieved in a single step with high yields through the synergetic cascade isocyanide insertion into C(sp3)-H bond, where the isocyanide was used as crucial "CN" and "C═N" sources and the tert-butoxyl group acted as the carbonyl source. Diverse reactivity of ß-carbonyl α-iminonitriles has been demonstrated.

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