SCPLPA: An miRNA-disease association prediction model based on spatial consistency projection and label propagation algorithm.

Identifying the association between miRNA and diseases is helpful for disease prevention, diagnosis and treatment. It is of great significance to use computational methods to predict potential human miRNA disease associations. Considering the shortcomings of existing computational methods, such as low prediction accuracy and weak generalization, we propose a new method called SCPLPA to predict miRNA-disease associations. First, a heterogeneous disease similarity network was constructed using the disease semantic similarity network and the disease Gaussian interaction spectrum kernel similarity network, while a heterogeneous miRNA similarity network was constructed using the miRNA functional similarity network and the miRNA Gaussian interaction spectrum kernel similarity network. Then, the estimated miRNA-disease association scores were evaluated by integrating the outcomes obtained by implementing label propagation algorithms in the heterogeneous disease similarity network and the heterogeneous miRNA similarity network. Finally, the spatial consistency projection algorithm of the network was used to extract miRNA disease association features to predict unverified associations between miRNA and diseases. SCPLPA was compared with four classical methods (MDHGI, NSEMDA, RFMDA and SNMFMDA), and the results of multiple evaluation metrics showed that SCPLPA exhibited the most outstanding predictive performance. Case studies have shown that SCPLPA can effectively identify miRNAs associated with colon neoplasms and kidney neoplasms. In summary, our proposed SCPLPA algorithm is easy to implement and can effectively predict miRNA disease associations, making it a reliable auxiliary tool for biomedical research.

KATZNCP: a miRNA-disease association prediction model integrating KATZ algorithm and network consistency projection.

BACKGROUND: Clinical studies have shown that miRNAs are closely related to human health. The study of potential associations between miRNAs and diseases will contribute to a profound understanding of the mechanism of disease development, as well as human disease prevention and treatment. MiRNA-disease associations predicted by computational methods are the best complement to biological experiments. RESULTS: In this research, a federated computational model KATZNCP was proposed on the basis of the KATZ algorithm and network consistency projection to infer the potential miRNA-disease associations. In KATZNCP, a heterogeneous network was initially constructed by integrating the known miRNA-disease association, integrated miRNA similarities, and integrated disease similarities; then, the KATZ algorithm was implemented in the heterogeneous network to obtain the estimated miRNA-disease prediction scores. Finally, the precise scores were obtained by the network consistency projection method as the final prediction results. KATZNCP achieved the reliable predictive performance in leave-one-out cross-validation (LOOCV) with an AUC value of 0.9325, which was better than the state-of-the-art comparable algorithms. Furthermore, case studies of lung neoplasms and esophageal neoplasms demonstrated the excellent predictive performance of KATZNCP. CONCLUSION: A new computational model KATZNCP was proposed for predicting potential miRNA-drug associations based on KATZ and network consistency projections, which can effectively predict the potential miRNA-disease interactions. Therefore, KATZNCP can be used to provide guidance for future experiments.

Inferring Latent Disease-lncRNA Associations by Label-Propagation Algorithm and Random Projection on a Heterogeneous Network.

Long noncoding RNA (lncRNA), a type of more than 200 nucleotides non-coding RNA, is related to various complex diseases. To precisely identify the potential lncRNA-disease association is important to understand the disease pathogenesis, to develop new drugs, and to design individualized diagnosis and treatment methods for different human diseases. Compared with the complexity and high cost of biological experiments, computational methods can quickly and effectively predict potential lncRNA-disease associations. Thus, it is a promising avenue to develop computational methods for lncRNA-disease prediction. However, owing to the low prediction accuracy ofstate of the art methods, it is vastly challenging to accurately and effectively identify lncRNA-disease at present. This article proposed an integrated method called LPARP, which is based on label-propagation algorithm and random projection to address the issue. Specifically, the label-propagation algorithm is initially used to obtain the estimated scores of lncRNA-disease associations, and then random projections are used to accurately predict disease-related lncRNAs.The empirical experiments showed that LAPRP achieved good prediction on three golddatasets, which is superior to existing state-of-the-art prediction methods. It can also be used to predict isolated diseases and new lncRNAs. Case studies of bladder cancer, esophageal squamous-cell carcinoma, and colorectal cancer further prove the reliability of the method. The proposed LPARP algorithm can predict the potential lncRNA-disease interactions stably and effectively with fewer data. LPARP can be used as an effective and reliable tool for biomedical research.

A novel miRNA-disease association prediction model using dual random walk with restart and space projection federated method.

A large number of studies have shown that the variation and disorder of miRNAs are important causes of diseases. The recognition of disease-related miRNAs has become an important topic in the field of biological research. However, the identification of disease-related miRNAs by biological experiments is expensive and time consuming. Thus, computational prediction models that predict disease-related miRNAs must be developed. A novel network projection-based dual random walk with restart (NPRWR) was used to predict potential disease-related miRNAs. The NPRWR model aims to estimate and accurately predict miRNA-disease associations by using dual random walk with restart and network projection technology, respectively. The leave-one-out cross validation (LOOCV) was adopted to evaluate the prediction performance of NPRWR. The results show that the area under the receiver operating characteristic curve(AUC) of NPRWR was 0.9029, which is superior to that of other advanced miRNA-disease associated prediction methods. In addition, lung and kidney neoplasms were selected to present a case study. Among the first 50 miRNAs predicted, 50 and 49 miRNAs have been proven by in databases or relevant literature. Moreover, NPRWR can be used to predict isolated diseases and new miRNAs. LOOCV and the case study achieved good prediction results. Thus, NPRWR will become an effective and accurate disease-miRNA association prediction model.

A Transfer Learning-Based Approach for Lysine Propionylation Prediction.

Lysine propionylation is a newly discovered posttranslational modification (PTM) and plays a key role in the cellular process. Although proteomics techniques was capable of detecting propionylation, large-scale detection was still challenging. To bridge this gap, we presented a transfer learning-based method for computationally predicting propionylation sites. The recurrent neural network-based deep learning model was trained firstly by the malonylation and then fine-tuned by the propionylation. The trained model served as feature extractor where protein sequences as input were translated into numerical vectors. The support vector machine was used as the final classifier. The proposed method reached a matthews correlation coefficient (MCC) of 0.6615 on the 10-fold crossvalidation and 0.3174 on the independent test, outperforming state-of-the-art methods. The enrichment analysis indicated that the propionylation was associated with these GO terms (GO:0016620, GO:0051287, GO:0003735, GO:0006096, and GO:0005737) and with metabolism. We developed a user-friendly online tool for predicting propoinylation sites which is available at http://47.113.117.61/.

A novel information diffusion method based on network consistency for identifying disease related microRNAs.

The abnormal expression of miRNAs is directly related to the development of human diseases. Predicting the potential candidate miRNAs associated with diseases can contribute to the detection, diagnosis, treatment and prevention of human complex diseases. The effective inference of the calculation method of the relationship between miRNAs and diseases is an effective supplement to biological experiments. It is of great help in the prevention, treatment and prognosis of complex diseases. This paper proposes a novel information diffusion method based on network consistency (IDNC) for identifying disease related microRNAs. The model first synthesizes the miRNA family information and the miRNA function similarity to reconstruct the miRNA network, and reconstruct the disease network by using the known disease and miRNA-related information and the semantic score between diseases. Then the global similarity of the two networks is obtained by using the Laplacian score of graphs. The global similarity score is a measure of the similarity between diseases and miRNAs. The disease-miRNA relation network was reconstructed by integrating the global similarity relation. The network consistency diffusion seed is then obtained by combining the global similarity network with the reconstructed disease-miRNA association network. Thereafter, the stable diffusion spectrum is generated as the prediction score by using the restarted random walk algorithm. The AUC value obtained by performing the LOOCV in the gold benchmark dataset is 0.8814. The AUC value obtained by performing the LOOCV in the predictive dataset is 0.9512. Compared with other frontier methods, our method has higher accuracy, which is further illustrated by case studies of breast neoplasms and colon neoplasms to prove that IDNC is valuable.

A Novel Gene Selection Method Based on Sparse Representation and Max-Relevance and Min-Redundancy.

AIM AND OBJECTIVE: Gene selection method as an important data preprocessing work has been followed. The criteria Maximum relevance and minimum redundancy (MRMR) has been commonly used for gene selection, which has a satisfactory performance in evaluating the correlation between two genes. However, for viewing genes in isolation, it ignores the influence of other genes. METHODS: In this study, we propose a new method based on sparse representation and MRMR algorithm (SRCMRM), using the sparse representation coefficient to represent the relevance of genes and correlation between genes and categories. The SRCMRMR algorithm contains two steps. Firstly, the genes irrelevant to the classification target are removed by using sparse representation coefficient. Secondly, sparse representation coefficient is used to calculate the correlation between genes and the most representative gene with the highest evaluation. RESULTS: To validate the performance of the SRCMRM, our method is compared with various algorithms. The proposed method achieves better classification accuracy for all datasets. CONCLUSION: The effectiveness and stability of our method have been proven through various experiments, which means that our method has practical significance.