scholarly journals Efficient framework for predicting MiRNA-disease associations based on improved hybrid collaborative filtering

2021 ◽  
Vol 21 (S1) ◽  
Author(s):  
Ru Nie ◽  
Zhengwei Li ◽  
Zhu-hong You ◽  
Wenzheng Bao ◽  
Jiashu Li
Keyword(s):  
Collaborative Filtering ◽  
Disease Association ◽  
Human Diseases ◽  
Gaussian Kernel ◽  
Predictive Score ◽  
Disease Associations ◽  
Similar Disease ◽  
Hybrid Collaborative Filtering ◽  
Case Validation ◽  
The Impact

Abstract Background Accumulating studies indicates that microRNAs (miRNAs) play vital roles in the process of development and progression of many human complex diseases. However, traditional biochemical experimental methods for identifying disease-related miRNAs cost large amount of time, manpower, material and financial resources. Methods In this study, we developed a framework named hybrid collaborative filtering for miRNA-disease association prediction (HCFMDA) by integrating heterogeneous data, e.g., miRNA functional similarity, disease semantic similarity, known miRNA-disease association networks, and Gaussian kernel similarity of miRNAs and diseases. To capture the intrinsic interaction patterns embedded in the sparse association matrix, we prioritized the predictive score by fusing three types of information: similar disease associations, similar miRNA associations, and similar disease-miRNA associations. Meanwhile, singular value decomposition was adopted to reduce the impact of noise and accelerate predictive speed. Results We then validated HCFMDA with leave-one-out cross-validation (LOOCV) and two types of case studies. In the LOOCV, we achieved 0.8379 of AUC (area under the curve). To evaluate the performance of HCFMDA on real diseases, we further implemented the first type of case validation over three important human diseases: Colon Neoplasms, Esophageal Neoplasms and Prostate Neoplasms. As a result, 44, 46 and 44 out of the top 50 predicted disease-related miRNAs were confirmed by experimental evidence. Moreover, the second type of case validation on Breast Neoplasms indicates that HCFMDA could also be applied to predict potential miRNAs towards those diseases without any known associated miRNA. Conclusions The satisfactory prediction performance demonstrates that our model could serve as a reliable tool to guide the following research for identifying candidate miRNAs associated with human diseases.

scholarly journals A Novel Network-Based Computational Model for Prediction of Potential LncRNA–Disease Association

2019 ◽  
Vol 20 (7) ◽  
pp. 1549 ◽  
Author(s):  
Yang Liu ◽  
Xiang Feng ◽  
Haochen Zhao ◽  
Zhanwei Xuan ◽  
Lei Wang
Keyword(s):  
Computational Models ◽  
Disease Association ◽  
Label Propagation ◽  
Human Diseases ◽  
Weighted Matrix ◽  
Disease Associations ◽  
Resource Allocation Strategy ◽  
Simulation Results ◽  
Leave One Out ◽  
Treatment Prognosis

Accumulating studies have shown that long non-coding RNAs (lncRNAs) are involved in many biological processes and play important roles in a variety of complex human diseases. Developing effective computational models to identify potential relationships between lncRNAs and diseases can not only help us understand disease mechanisms at the lncRNA molecular level, but also promote the diagnosis, treatment, prognosis, and prevention of human diseases. For this paper, a network-based model called NBLDA was proposed to discover potential lncRNA–disease associations, in which two novel lncRNA–disease weighted networks were constructed. They were first based on known lncRNA–disease associations and topological similarity of the lncRNA–disease association network, and then an lncRNA–lncRNA weighted matrix and a disease–disease weighted matrix were obtained based on a resource allocation strategy of unequal allocation and unbiased consistence. Finally, a label propagation algorithm was applied to predict associated lncRNAs for the investigated diseases. Moreover, in order to estimate the prediction performance of NBLDA, the framework of leave-one-out cross validation (LOOCV) was implemented on NBLDA, and simulation results showed that NBLDA can achieve reliable areas under the ROC curve (AUCs) of 0.8846, 0.8273, and 0.8075 in three known lncRNA–disease association datasets downloaded from the lncRNADisease database, respectively. Furthermore, in case studies of lung cancer, leukemia, and colorectal cancer, simulation results demonstrated that NBLDA can be a powerful tool for identifying potential lncRNA–disease associations as well.

scholarly journals NEMPD: A network embedding-based miRNA-protein-disease network method for the miRNA-disease association prediction

2020 ◽  
Author(s):  
Bo-Ya Ji ◽  
Zhu-Hong You ◽  
Zhan-Heng Chen ◽  
Leon Wong ◽  
Hai-Cheng Yi
Keyword(s):  
Structural Information ◽  
Disease Association ◽  
Human Diseases ◽  
Single Type ◽  
Mirna Sequence ◽  
Sequence Information ◽  
Network Embedding ◽  
Disease Network ◽  
Graph Representations ◽  
Disease Associations

Abstract Background As an important non-coding RNA newly discovered in recent years, MicroRNA (miRNA) plays an important role in a series of life processes and is closely associated with a variety of human diseases. Hence, the identification of potential miRNA-disease associations can make great contributions to the research and treatment of human diseases. However, to our knowledge, many of the existing state-of-the-art computational methods only utilize the single type of known association information between miRNAs and diseases to predict their potential associations, without focusing on their interactions or associations with other types of molecules. Results In this paper, a network embedding-based the tripartite miRNA-protein-disease network (NEMPD) method was proposed for the prediction of miRNA-disease associations. Firstly, a tripartite miRNA-protein-disease network is created by integrating known miRNA-protein and protein-disease associations. Then, we utilize the network representation method-Learning Graph Representations with Global Structural Information (GraRep) to obtain the behavior information (associations with proteins in the network) of miRNAs and diseases. Secondly, the behavior information of miRNAs and diseases is combined with the attribute information of them (disease semantic similarity and miRNA sequence information) to represent miRNA-disease pairs. Thirdly, the prediction model was established based on these known miRNA-disease pairs and the Random Forest algorithm. In the results, under five-fold cross validation, the average prediction accuracy, sensitivity, and AUC of NEMPD is 85.41%, 80.96%, and 91.58%. Furthermore, the performance of NEMPD was also validated by the case studies. Among the top 50 predicted disease-related miRNAs, 48 (breast neoplasms), 47 (colon neoplasms), 47 (lung neoplasms) were confirmed by two other databases. Conclusions NEMPD has a good performance in predicting the potential associations between miRNAs and diseases and has great potency in the field of miRNA-disease association prediction in the future.

scholarly journals ILPMDA: Predicting miRNA–Disease Association Based on Improved Label Propagation

2021 ◽  
Vol 12 ◽  
Author(s):  
Yu-Tian Wang ◽  
Lei Li ◽  
Cun-Mei Ji ◽  
Chun-Hou Zheng ◽  
Jian-Cheng Ni
Keyword(s):  
Disease Association ◽  
Label Propagation ◽  
Human Diseases ◽  
Biological Information ◽  
Disease Similarity ◽  
Kernel Fusion ◽  
Disease Associations ◽  
Non Coding Rnas ◽  
Similarity Networks ◽  
Association Data

MicroRNAs (miRNAs) are small non-coding RNAs that have been demonstrated to be related to numerous complex human diseases. Considerable studies have suggested that miRNAs affect many complicated bioprocesses. Hence, the investigation of disease-related miRNAs by utilizing computational methods is warranted. In this study, we presented an improved label propagation for miRNA–disease association prediction (ILPMDA) method to observe disease-related miRNAs. First, we utilized similarity kernel fusion to integrate different types of biological information for generating miRNA and disease similarity networks. Second, we applied the weighted k-nearest known neighbor algorithm to update verified miRNA–disease association data. Third, we utilized improved label propagation in disease and miRNA similarity networks to make association prediction. Furthermore, we obtained final prediction scores by adopting an average ensemble method to integrate the two kinds of prediction results. To evaluate the prediction performance of ILPMDA, two types of cross-validation methods and case studies on three significant human diseases were implemented to determine the accuracy and effectiveness of ILPMDA. All results demonstrated that ILPMDA had the ability to discover potential miRNA–disease associations.

NCMCMDA: miRNA–disease association prediction through neighborhood constraint matrix completion

2020 ◽  
Author(s):  
Xing Chen ◽  
Lian-Gang Sun ◽  
Yan Zhao
Keyword(s):  
Computational Models ◽  
Cross Validation ◽  
Matrix Completion ◽  
Critical Role ◽  
Disease Association ◽  
Human Diseases ◽  
Superior Performance ◽  
Main Task ◽  
Constraint Matrix ◽  
Disease Associations

Abstract Emerging evidence shows that microRNAs (miRNAs) play a critical role in diverse fundamental and important biological processes associated with human diseases. Inferring potential disease related miRNAs and employing them as the biomarkers or drug targets could contribute to the prevention, diagnosis and treatment of complex human diseases. In view of that traditional biological experiments cost much time and resources, computational models would serve as complementary means to uncover potential miRNA–disease associations. In this study, we proposed a new computational model named Neighborhood Constraint Matrix Completion for MiRNA–Disease Association prediction (NCMCMDA) to predict potential miRNA–disease associations. The main task of NCMCMDA was to recover the missing miRNA–disease associations based on the known miRNA–disease associations and integrated disease (miRNA) similarity. In this model, we innovatively integrated neighborhood constraint with matrix completion, which provided a novel idea of utilizing similarity information to assist the prediction. After the recovery task was transformed into an optimization problem, we solved it with a fast iterative shrinkage-thresholding algorithm. As a result, the AUCs of NCMCMDA in global and local leave-one-out cross validation were 0.9086 and 0.8453, respectively. In 5-fold cross validation, NCMCMDA achieved an average AUC of 0.8942 and standard deviation of 0.0015, which demonstrated NCMCMDA’s superior performance than many previous computational methods. Furthermore, NCMCMDA was applied to three different types of case studies to further evaluate its prediction reliability and accuracy. As a result, 84% (colon neoplasms), 98% (esophageal neoplasms) and 98% (breast neoplasms) of the top 50 predicted miRNAs were verified by recent literature.

scholarly journals NEMPD: A Network Embedding-Based miRNA-Protein-Disease Network Method for the miRNA-Disease Association Prediction

2020 ◽  
Author(s):  
Bo-Ya Ji ◽  
Zhu-Hong You ◽  
Zhan-Heng Chen ◽  
Leon Wong ◽  
Hai-Cheng Yi
Keyword(s):  
Structural Information ◽  
Disease Association ◽  
Human Diseases ◽  
Single Type ◽  
Mirna Sequence ◽  
Sequence Information ◽  
Network Embedding ◽  
Disease Network ◽  
Graph Representations ◽  
Disease Associations

Abstract Background: As an important non-coding RNA newly discovered in recent years, MicroRNA (miRNA) plays an important role in a series of life processes and is closely associated with a variety of human diseases. Hence, the identification of potential miRNA-disease associations can make great contributions to the research and treatment of human diseases. However, to our knowledge, many of the existing state-of-the-art computational methods only utilize the single type of known association information between miRNAs and diseases to predict their potential associations, without focusing on their interactions or associations with other types of molecules.Results: In this paper, a network embedding-based the tripartite miRNA-protein-disease network (NEMPD) method was proposed for the prediction of miRNA-disease associations. Firstly, a tripartite miRNA-protein-disease network is created by integrating known miRNA-protein and protein-disease associations. Then, we utilize the network representation method-Learning Graph Representations with Global Structural Information (GraRep) to obtain the behavior information (associations with proteins in the network) of miRNAs and diseases. Secondly, the behavior information of miRNAs and diseases is combined with the attribute information of them (disease semantic similarity and miRNA sequence information) to represent miRNA-disease pairs. Thirdly, the prediction model was established based on these known miRNA-disease pairs and the Random Forest algorithm. In the results, under five-fold cross validation, the prediction accuracy, sensitivity, and AUC of NEMPD is 85.41%, 80.96%, and 91.58%. Furthermore, the performance of NEMPD was also validated by the case studies. Among the top 50 predicted disease-related miRNAs, 48 (breast neoplasms), 47 (colon neoplasms), 47 (lung neoplasms) were confirmed by two other databases.Conclusions: NEMPD has a good performance in predicting the potential associations between miRNAs and diseases and has great potency in the field of miRNA-disease association prediction in the future.

EHAI: Enhanced Human Microbe-Disease Association Identification

2020 ◽  
Vol 21 (11) ◽  
pp. 1078-1084
Author(s):  
Ruizhi Fan ◽  
Chenhua Dong ◽  
Hu Song ◽  
Yixin Xu ◽  
Linsen Shi ◽  
...  
Keyword(s):  
Microbial Community ◽  
Human Health ◽  
Complex Diseases ◽  
Disease Association ◽  
Computational Results ◽  
Computational Approaches ◽  
Disease Diagnostics ◽  
Disease Associations ◽  
Association Discovery ◽  
Biological Tool

: Recently, an increasing number of biological and clinical reports have demonstrated that imbalance of microbial community has the ability to play important roles among several complex diseases concerning human health. Having a good knowledge of discovering potential of microbe-disease relationships, which provides the ability to having a better understanding of some issues, including disease pathology, further boosts disease diagnostics and prognostics, has been taken into account. Nevertheless, a few computational approaches can meet the need of huge scale of microbe-disease association discovery. In this work, we proposed the EHAI model, which is Enhanced Human microbe- disease Association Identification. EHAI employed the microbe-disease associations, and then Gaussian interaction profile kernel similarity has been utilized to enhance the basic microbe-disease association. Actually, some known microbe-disease associations and a large amount of associations are still unavailable among the datasets. The ‘super-microbe’ and ‘super-disease’ were employed to enhance the model. Computational results demonstrated that such super-classes have the ability to be helpful to the performance of EHAI. Therefore, it is anticipated that EHAI can be treated as an important biological tool in this field.

scholarly journals Current insights into the implications of m6A RNA methylation and autophagy interaction in human diseases

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Xuechai Chen ◽  
Jianan Wang ◽  
Muhammad Tahir ◽  
Fangfang Zhang ◽  
Yuanyuan Ran ◽  
...  
Keyword(s):  
Intervertebral Disc Degeneration ◽  
Rna Binding ◽  
Rna Binding Proteins ◽  
Degradation Process ◽  
Human Diseases ◽  
Rna Modification ◽  
Rna Methylation ◽  
M6a Rna Methylation ◽  
The Impact

AbstractAutophagy is a conserved degradation process crucial to maintaining the primary function of cellular and organismal metabolism. Impaired autophagy could develop numerous diseases, including cancer, cardiomyopathy, neurodegenerative disorders, and aging. N6-methyladenosine (m6A) is the most common RNA modification in eukaryotic cells, and the fate of m6A modified transcripts is controlled by m6A RNA binding proteins. m6A modification influences mRNA alternative splicing, stability, translation, and subcellular localization. Intriguingly, recent studies show that m6A RNA methylation could alter the expression of essential autophagy-related (ATG) genes and influence the autophagy function. Thus, both m6A modification and autophagy could play a crucial role in the onset and progression of various human diseases. In this review, we summarize the latest studies describing the impact of m6A modification in autophagy regulation and discuss the role of m6A modification-autophagy axis in different human diseases, including obesity, heart disease, azoospermatism or oligospermatism, intervertebral disc degeneration, and cancer. The comprehensive understanding of the m6A modification and autophagy interplay may help in interpreting their impact on human diseases and may aid in devising future therapeutic strategies.

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