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The performance of existing traditional Chinese medicine (TCM) recommendation models is generally poor because of their weak generalization ability, overfitting, and inability to use known biological networks. Therefore, building a TCM recommendation model based on artificial intelligence has currently become an important bioinformatics task. This study aimed to design a multitask meta-learning model with good biological interpretation for TCM formula recommendation (MBI-TCMR) for deep learning regularization. This method was based on the known biological network structure to sparse the deep learning network, solve the overfitting problem of the model, and enhance the biological interpretability of the model. Furthermore, a multi-learning framework based on meta-learning was also proposed. The framework allowed the MBI-TCMR model to mine knowledge of TCM formulas and quickly adapt to different types of TCM formula recommendation tasks. Finally, we used a gradient-based deep learning feature backtracking method to calculate the feature weight for each neuron. This weight could provide valuable explanatory information for researchers to study how the model made its medicine recommendations. We designed three independent experiments. The experimental results showed that the hit ratio (HR), AUC, and recall and precision value of the MBI-TCMR model outperformed the existing TCM formula recommendation models. The MBI-TCMR model’s HR of top 1–10 reached 0.15–0.9 (Gynecologic Disease Dataset). HR was 10 for the MBI-TCMR model, which was an improvement of 11.1% compared with the best baseline model. The bio-enrichment analysis showed that the model exhibited good bio-interpretation. In summary, this study proposed a novel TCM formula recommendation model, which expanded the application of the artificial intelligence model and achieved good results.

Trading cryptocurrencies (digital currencies) are currently performed by applying methods similar to what is applied to the stock market or commodities; however, these algorithms are not necessarily well-suited for predicting cryptocurrency prices. Unlike stock exchanges, which shut down for several hours or days at a time, digital currency prediction and trading seem to be of a more consistent and predictable nature. In this work, we benefit from sentiment analysis of tweets using both an existing sentiment analysis package and a manually tailored “objective analysis,” to calculate one impact value for each analysis every 15min. We then select the most appropriate training method by applying evolutionary techniques and discover the best subset of the generated features to include, as well as other parameters. One of the unique contributions of this work is the analysis of both English and Japanese tweets with a tailored “objective analysis” tool. This resulted in implementation of predictors which yielded 28% to 122% profit in a four-week simulation, much more than simply holding a digital currency for the same period of time.

The study and treatment of cancer is traditionally specialized to the cancer’s site of origin. However, certain phenotypes are shared across cancer types and have important implications for clinical care. To date, automating the identification of these characteristics from routine clinical data - irrespective of the type of cancer - is impaired by tissue-specific variability and limited labeled data. Whole-genome doubling is one such phenotype; whole-genome doubling events occur in nearly every type of cancer and have significant prognostic implications. Using digitized histopathology slide images of primary tumor biopsies, we train a deep neural network end-to-end to accurately generalize few-shot classification of whole-genome doubling across 17 cancer types. By taking a meta-learning approach, cancer types are treated as separate but jointly-learned tasks. This approach outperforms a traditional neural network classifier and quickly generalizes to both held-out cancer types and batch effects. These results demonstrate the unrealized potential for meta-learning to not only account for between-cancer type variability but also remedy technical variability, enabling real-time identification of cancer phenotypes that are too often costly and inefficient to obtain.