Artificial intelligence-based air quality index (AQI) forecasting is a hot research topic in the fields of sustainable and smart industrial environment design. There are mainly two obstacles that hinder the existing machine learning (ML) and deep learning (DL) technologies providing accurate forecasting results to protect the environment, which include the intercorrelation between different AQI components and the highly volatile AQI pattern changes. In this article, a novel DL framework combining multiple nested long short term memory networks (MTMC-NLSTM) is proposed for accurate AQI forecasting enlightened with the federated learning. The performance of the proposed MTMC-NLSTM model is compared with conventional ML models, DL methods, as well as hybrid DL models. The experimental results show that the performance of the proposed method is superior to those of all compared models.

Efficient and accurate recognition of protein–DNA interactions is vital for understanding the molecular mechanisms of related biological processes and further guiding drug discovery. Although the current experimental protocols are the most precise way to determine protein–DNA binding sites, they tend to be labor-intensive and time-consuming. There is an immediate need to design efficient computational approaches for predicting DNA-binding sites. Here, we proposed ULDNA, a new deep-learning model, to deduce DNA-binding sites from protein sequences. This model leverages an LSTM-attention architecture, embedded with three unsupervised language models that are pre-trained on large-scale sequences from multiple database sources. To prove its effectiveness, ULDNA was tested on 229 protein chains with experimental annotation of DNA-binding sites. Results from computational experiments revealed that ULDNA significantly improves the accuracy of DNA-binding site prediction in comparison with 17 state-of-the-art methods. In-depth data analyses showed that the major strength of ULDNA stems from employing three transformer language models. Specifically, these language models capture complementary feature embeddings with evolution diversity, in which the complex DNA-binding patterns are buried. Meanwhile, the specially crafted LSTM-attention network effectively decodes evolution diversity-based embeddings as DNA-binding results at the residue level. Our findings demonstrated a new pipeline for predicting DNA-binding sites on a large scale with high accuracy from protein sequence alone.

A deep transfer learning framework adapting mixed subdomains is proposed for cross-species plant disease diagnosis. Most existing deep transfer learning studies focus on knowledge transfer between highly correlated domains. These methods may fail dealing with domains that are poorly correlated. In this study, mixed domain images were generated from source and target image groups for improving the correlation between the mixed domain (training dataset) and target domain (testing dataset). A subdomain alignment mechanism is employed to transfer knowledge from the mixed domain to the target domain. The proposed framework captures the fine-grained information more effectively. Extensive experiments were conducted and prove that the proposed method produces a more effective result compared with existing deep transfer learning technologies for poorly related subdomains.

Anomalies in time series, also called “discord,” are the abnormal subsequences. The occurrence of anomalies in time series may indicate that some faults or disease will occur soon. Therefore, development of novel computational approaches for anomaly detection (discord search) in time series is of great significance for state monitoring and early warning of real-time system. Previous studies show that many algorithms were successfully developed and were used for anomaly classification, e.g., health monitoring, traffic detection, and intrusion detection. However, the anomaly detection of time series was not well studied. In this paper, we proposed a long short-term memory- (LSTM-) based anomaly detection method (LSTMAD) for discord search from univariate time series data. LSTMAD learns the structural features from normal (nonanomalous) training data and then performs anomaly detection via a statistical strategy based on the prediction error for observed data. In our experimental evaluation using public ECG datasets and real-world datasets, LSTMAD detects anomalies more accurately than other existing approaches in comparison.

Most life activities in organisms are regulated through protein complexes, which are mainly controlled via Protein–Protein Interactions (PPIs). Discovering new interactions between proteins and revealing their biological functions are of great significance for understanding the molecular mechanisms of biological processes and identifying the potential targets in drug discovery. Current experimental methods only capture stable protein interactions, which lead to limited coverage. In addition, expensive cost and time consuming are also the obvious shortcomings. In recent years, various computational methods have been successfully developed for predicting PPIs based only on protein homology, primary sequences of protein or gene ontology information. Computational efficiency and data complexity are still the main bottlenecks for the algorithm generalization. In this study, we proposed a novel computational framework, HNSPPI, to predict PPIs. As a hybrid supervised learning model, HNSPPI comprehensively characterizes the intrinsic relationship between two proteins by integrating amino acid sequence information and connection properties of PPI network. The experimental results show that HNSPPI works very well on six benchmark datasets. Moreover, the comparison analysis proved that our model significantly outperforms other five existing algorithms. Finally, we used the HNSPPI model to explore the SARS-CoV-2-Human interaction system and found several potential regulations. In summary, HNSPPI is a promising model for predicting new protein interactions from known PPI data.