SGANRDA: semi-supervised generative adversarial networks for predicting circRNA–disease associations

Author(s):  
Lei Wang ◽  
Xin Yan ◽  
Zhu-Hong You ◽  
Xi Zhou ◽  
Hao-Yuan Li ◽  
...  

Abstract Emerging research shows that circular RNA (circRNA) plays a crucial role in the diagnosis, occurrence and prognosis of complex human diseases. Compared with traditional biological experiments, the computational method of fusing multi-source biological data to identify the association between circRNA and disease can effectively reduce cost and save time. Considering the limitations of existing computational models, we propose a semi-supervised generative adversarial network (GAN) model SGANRDA for predicting circRNA–disease association. This model first fused the natural language features of the circRNA sequence and the features of disease semantics, circRNA and disease Gaussian interaction profile kernel, and then used all circRNA–disease pairs to pre-train the GAN network, and fine-tune the network parameters through labeled samples. Finally, the extreme learning machine classifier is employed to obtain the prediction result. Compared with the previous supervision model, SGANRDA innovatively introduced circRNA sequences and utilized all the information of circRNA–disease pairs during the pre-training process. This step can increase the information content of the feature to some extent and reduce the impact of too few known associations on the model performance. SGANRDA obtained AUC scores of 0.9411 and 0.9223 in leave-one-out cross-validation and 5-fold cross-validation, respectively. Prediction results on the benchmark dataset show that SGANRDA outperforms other existing models. In addition, 25 of the top 30 circRNA–disease pairs with the highest scores of SGANRDA in case studies were verified by recent literature. These experimental results demonstrate that SGANRDA is a useful model to predict the circRNA–disease association and can provide reliable candidates for biological experiments.

Author(s):  
Xing Chen ◽  
Tian-Hao Li ◽  
Yan Zhao ◽  
Chun-Chun Wang ◽  
Chi-Chi Zhu

Abstract MicroRNA (miRNA) plays an important role in the occurrence, development, diagnosis and treatment of diseases. More and more researchers begin to pay attention to the relationship between miRNA and disease. Compared with traditional biological experiments, computational method of integrating heterogeneous biological data to predict potential associations can effectively save time and cost. Considering the limitations of the previous computational models, we developed the model of deep-belief network for miRNA-disease association prediction (DBNMDA). We constructed feature vectors to pre-train restricted Boltzmann machines for all miRNA-disease pairs and applied positive samples and the same number of selected negative samples to fine-tune DBN to obtain the final predicted scores. Compared with the previous supervised models that only use pairs with known label for training, DBNMDA innovatively utilizes the information of all miRNA-disease pairs during the pre-training process. This step could reduce the impact of too few known associations on prediction accuracy to some extent. DBNMDA achieves the AUC of 0.9104 based on global leave-one-out cross validation (LOOCV), the AUC of 0.8232 based on local LOOCV and the average AUC of 0.9048 ± 0.0026 based on 5-fold cross validation. These AUCs are better than other previous models. In addition, three different types of case studies for three diseases were implemented to demonstrate the accuracy of DBNMDA. As a result, 84% (breast neoplasms), 100% (lung neoplasms) and 88% (esophageal neoplasms) of the top 50 predicted miRNAs were verified by recent literature. Therefore, we could conclude that DBNMDA is an effective method to predict potential miRNA-disease associations.


2020 ◽  
Vol 10 (24) ◽  
pp. 9133
Author(s):  
Lloyd A. Courtenay ◽  
Diego González-Aguilera

The fossil record is notorious for being incomplete and distorted, frequently conditioning the type of knowledge that can be extracted from it. In many cases, this often leads to issues when performing complex statistical analyses, such as classification tasks, predictive modelling, and variance analyses, such as those used in Geometric Morphometrics. Here different Generative Adversarial Network architectures are experimented with, testing the effects of sample size and domain dimensionality on model performance. For model evaluation, robust statistical methods were used. Each of the algorithms were observed to produce realistic data. Generative Adversarial Networks using different loss functions produced multidimensional synthetic data significantly equivalent to the original training data. Conditional Generative Adversarial Networks were not as successful. The methods proposed are likely to reduce the impact of sample size and bias on a number of statistical learning applications. While Generative Adversarial Networks are not the solution to all sample-size related issues, combined with other pre-processing steps these limitations may be overcome. This presents a valuable means of augmenting geometric morphometric datasets for greater predictive visualization.


Author(s):  
Lloyd A. Courtenay ◽  
Diego González-Aguilera

The fossil record is notorious for being incomplete and distorted, frequently conditioning the type of knowledge that can be extracted from it. In many cases, this often leads to issues when performing complex statistical analyses, such as classification tasks, predictive modelling, and variance analyses, such as those used in Geometric Morphometrics. Here different Generative Adversarial Network architectures are experimented with, testing the effects of sample size and domain dimensionality on model performance. For model evaluation, robust statistical methods were used. Each of the algorithms were observed to produce realistic data. Generative Adversarial Networks using different loss functions produced multidimensional synthetic data significantly equivalent to the original training data. Conditional Generative Adversarial Networks were not as successful. The methods proposed are likely to reduce the impact of sample size and bias on a number of statistical learning applications. While Generative Adversarial Networks are not the solution to all sample-size related issues, combined with other pre-processing steps these limitations may be overcome. This presents a valuable means of augmenting geometric morphometric datasets for greater predictive visualization.


Sensors ◽  
2021 ◽  
Vol 21 (15) ◽  
pp. 4953
Author(s):  
Sara Al-Emadi ◽  
Abdulla Al-Ali ◽  
Abdulaziz Al-Ali

Drones are becoming increasingly popular not only for recreational purposes but in day-to-day applications in engineering, medicine, logistics, security and others. In addition to their useful applications, an alarming concern in regard to the physical infrastructure security, safety and privacy has arisen due to the potential of their use in malicious activities. To address this problem, we propose a novel solution that automates the drone detection and identification processes using a drone’s acoustic features with different deep learning algorithms. However, the lack of acoustic drone datasets hinders the ability to implement an effective solution. In this paper, we aim to fill this gap by introducing a hybrid drone acoustic dataset composed of recorded drone audio clips and artificially generated drone audio samples using a state-of-the-art deep learning technique known as the Generative Adversarial Network. Furthermore, we examine the effectiveness of using drone audio with different deep learning algorithms, namely, the Convolutional Neural Network, the Recurrent Neural Network and the Convolutional Recurrent Neural Network in drone detection and identification. Moreover, we investigate the impact of our proposed hybrid dataset in drone detection. Our findings prove the advantage of using deep learning techniques for drone detection and identification while confirming our hypothesis on the benefits of using the Generative Adversarial Networks to generate real-like drone audio clips with an aim of enhancing the detection of new and unfamiliar drones.


2021 ◽  
Vol 14 ◽  
Author(s):  
Eric Nathan Carver ◽  
Zhenzhen Dai ◽  
Evan Liang ◽  
James Snyder ◽  
Ning Wen

Every year thousands of patients are diagnosed with a glioma, a type of malignant brain tumor. MRI plays an essential role in the diagnosis and treatment assessment of these patients. Neural networks show great potential to aid physicians in the medical image analysis. This study investigated the creation of synthetic brain T1-weighted (T1), post-contrast T1-weighted (T1CE), T2-weighted (T2), and T2 Fluid Attenuated Inversion Recovery (Flair) MR images. These synthetic MR (synMR) images were assessed quantitatively with four metrics. The synMR images were also assessed qualitatively by an authoring physician with notions that synMR possessed realism in its portrayal of structural boundaries but struggled to accurately depict tumor heterogeneity. Additionally, this study investigated the synMR images created by generative adversarial network (GAN) to overcome the lack of annotated medical image data in training U-Nets to segment enhancing tumor, whole tumor, and tumor core regions on gliomas. Multiple two-dimensional (2D) U-Nets were trained with original BraTS data and differing subsets of the synMR images. Dice similarity coefficient (DSC) was used as the loss function during training as well a quantitative metric. Additionally, Hausdorff Distance 95% CI (HD) was used to judge the quality of the contours created by these U-Nets. The model performance was improved in both DSC and HD when incorporating synMR in the training set. In summary, this study showed the ability to generate high quality Flair, T2, T1, and T1CE synMR images using GAN. Using synMR images showed encouraging results to improve the U-Net segmentation performance and shows potential to address the scarcity of annotated medical images.


2021 ◽  
Vol 21 (S1) ◽  
Author(s):  
Yu-Tian Wang ◽  
Qing-Wen Wu ◽  
Zhen Gao ◽  
Jian-Cheng Ni ◽  
Chun-Hou Zheng

Abstract Background MicroRNAs (miRNAs) have been confirmed to have close relationship with various human complex diseases. The identification of disease-related miRNAs provides great insights into the underlying pathogenesis of diseases. However, it is still a big challenge to identify which miRNAs are related to diseases. As experimental methods are in general expensive and time‐consuming, it is important to develop efficient computational models to discover potential miRNA-disease associations. Methods This study presents a novel prediction method called HFHLMDA, which is based on high-dimensionality features and hypergraph learning, to reveal the association between diseases and miRNAs. Firstly, the miRNA functional similarity and the disease semantic similarity are integrated to form an informative high-dimensionality feature vector. Then, a hypergraph is constructed by the K-Nearest-Neighbor (KNN) method, in which each miRNA-disease pair and its k most relevant neighbors are linked as one hyperedge to represent the complex relationships among miRNA-disease pairs. Finally, the hypergraph learning model is designed to learn the projection matrix which is used to calculate uncertain miRNA-disease association score. Result Compared with four state-of-the-art computational models, HFHLMDA achieved best results of 92.09% and 91.87% in leave-one-out cross validation and fivefold cross validation, respectively. Moreover, in case studies on Esophageal neoplasms, Hepatocellular Carcinoma, Breast Neoplasms, 90%, 98%, and 96% of the top 50 predictions have been manually confirmed by previous experimental studies. Conclusion MiRNAs have complex connections with many human diseases. In this study, we proposed a novel computational model to predict the underlying miRNA-disease associations. All results show that the proposed method is effective for miRNA–disease association predication.


Author(s):  
A. Courtial ◽  
G. Touya ◽  
X. Zhang

Abstract. This article presents how a generative adversarial network (GAN) can be employed to produce a generalised map that combines several cartographic themes in the dense context of urban areas. We use as input detailed buildings, roads, and rivers from topographic datasets produced by the French national mapping agency (IGN), and we expect as output of the GAN a legible map of these elements at a target scale of 1:50,000. This level of detail requires to reduce the amount of information while preserving patterns; covering dense inner cities block by a unique polygon is also necessary because these blocks cannot be represented with enlarged individual buildings. The target map has a style similar to the topographic map produced by IGN. This experiment succeeded in producing image tiles that look like legible maps. It also highlights the impact of data and representation choices on the quality of predicted images, and the challenge of learning geographic relationships.


2020 ◽  
Vol 20 (6) ◽  
pp. 452-460
Author(s):  
Lin Tang ◽  
Yu Liang ◽  
Xin Jin ◽  
Lin Liu ◽  
Wei Zhou

Background: Accumulating experimental studies demonstrated that long non-coding RNAs (LncRNAs) play crucial roles in the occurrence and development progress of various complex human diseases. Nonetheless, only a small portion of LncRNA–disease associations have been experimentally verified at present. Automatically predicting LncRNA–disease associations based on computational models can save the huge cost of wet-lab experiments. Methods and Result: To develop effective computational models to integrate various heterogeneous biological data for the identification of potential disease-LncRNA, we propose a hierarchical extension based on the Boolean matrix for LncRNA-disease association prediction model (HEBLDA). HEBLDA discovers the intrinsic hierarchical correlation based on the property of the Boolean matrix from various relational sources. Then, HEBLDA integrates these hierarchical associated matrices by fusion weights. Finally, HEBLDA uses the hierarchical associated matrix to reconstruct the LncRNA– disease association matrix by hierarchical extending. HEBLDA is able to work for potential diseases or LncRNA without known association data. In 5-fold cross-validation experiments, HEBLDA obtained an area under the receiver operating characteristic curve (AUC) of 0.8913, improving previous classical methods. Besides, case studies show that HEBLDA can accurately predict candidate disease for several LncRNAs. Conclusion: Based on its ability to discover the more-richer correlated structure of various data sources, we can anticipate that HEBLDA is a potential method that can obtain more comprehensive association prediction in a broad field.


Author(s):  
Xing Chen ◽  
Lian-Gang Sun ◽  
Yan Zhao

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.


2021 ◽  
Author(s):  
Dang Huang ◽  
JiYong An ◽  
Lei Zhang ◽  
BaiLong Liu

Abstract Background: A large number of evidences from biological experiments have confirmed that miRNAs play an important role in the progression and development of various human complex diseases. However, the traditional experiment methods are expensive and time-consuming. Therefore, it is a challenging task that how to develop more accurate and efficient methods for predicting potential associations between miRNA and disease. Results: In the study, we developed a computational model that combined Heterogeneous Graph Convolutional Network with Enhanced Layer for miRNA-Disease Association prediction (HGCNELMDA). The major improvement of our method lies in through restarting the random walk optimized the original features of nodes and adding a Reinforcement layer to the hidden layer of graph convolutional network retained similar information between nodes in the feature space. In addition, the proposed approach recalculated the influence of neighborhood nodes on target nodes by introducing the attention mechanism. The reliable performance of the HGCNELMDA was certified by the AUC of 93.47% in global leave-one-out cross-validation (LOOCV), and the average AUCs of 93.01% in fivefold cross-validation. Meanwhile, we compared the HGCNELMDA with the state‑of‑the‑art methods. Comparative results indicated that o the HGCNELMDA is very promising and may provide a cost‑effective alternative for miRNA-Disease Association prediction. Moreover, we applied HGCNELMDA to 3 different case studies to predict potential miRNAs related to lung cancer, prostate cancer, and pancreatic cancer. Results showed that 48, 50, and 50 of the top 50 predicted miRNAs were supported by experimental association evidence. Therefore, the HGCNELMDA is a reliable method for predicting disease-related miRNAs. Conclusions: The results of the HGCNELMDA method in the LOOCV (leave-one-out cross validation, LOOCV) and 5-cross validations were 93.47% and 93.01%, respectively. Compared with other typical methods, the performance of HGGCNMA is higher. Three cases of lung cancer, prostate cancer, and pancreatic cancer were studied. Among the predicted top 50 candidate miRNAs, 48, 50, and 50 were verified in the biological database HDMMV2.0.Therefore; this further confirms the feasibility and effectiveness of our method. To facilitate extensive studies for future disease-related miRNAs research, we developed a freely available web server called HGCNELMDA is available at http://132.232.17.50:8080/HGCNELMDA.jsp.


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