Matrix Factorization Techniques for Recommender Systems

System Identification I

Rolling element bearing fault diagnosis using convolutional neural network and vibration image

Time-series forecasting is an important research and application area. Much effort has been devoted over the past several decades to develop and improve the time-series forecasting models. This paper introduces a new time-series forecasting model based on the flexible neural tree (FNT). The FNT model is generated initially as a flexible multi-layer feed-forward neural network and evolved using an evolutionary procedure. Very often it is a difficult task to select the proper input variables or time-lags for constructing a time-series model. Our research demonstrates that the FNT model is capable of handing the task automatically. The performance and effectiveness of the proposed method are evaluated using time series prediction problems and compared with those of related methods.

Time-series forecasting using flexible neural tree model

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Annual Review of Information Science and Technology

It is well known that DNA sequence contains a certain amount of transcription factors (TF) binding sites, and only part of them are identified through biological experiments. However, these experiments are expensive and time-consuming. To overcome these problems, some computational methods, based on k-mer features or convolutional neural networks, have been proposed to identify TF binding sites from DNA sequences. Although these methods have good performance, the context information that relates to TF binding sites is still lacking. Research indicates that standard recurrent neural networks (RNN) and its variants have better performance in time-series data compared with other models. In this study, we propose a model, named KEGRU, to identify TF binding sites by combining Bidirectional Gated Recurrent Unit (GRU) network with k-mer embedding. Firstly, DNA sequences are divided into k-mer sequences with a specified length and stride window. And then, we treat each k-mer as a word and pre-trained word representation model though word2vec algorithm. Thirdly, we construct a deep bidirectional GRU model for feature learning and classification. Experimental results have shown that our method has better performance compared with some state-of-the-art methods. Additional experiments about embedding strategy show that k-mer embedding will be helpful to enhance model performance. The robustness of KEGRU is proved by experiments with different k-mer length, stride window and embedding vector dimension.

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Recurrent Neural Network for Predicting Transcription Factor Binding Sites

Accumulating biological and clinical reports have indicated that imbalance of microbial community is closely associated with occurrence and development of various complex human diseases. Identifying potential microbe-disease associations, which could provide better understanding of disease pathology and further boost disease diagnostic and prognostic, has attracted more and more attention. However, hardly any computational models have been developed for large scale microbe-disease association prediction. In this article, based on the assumption that microbes with similar functions tend to share similar association or non-association patterns with similar diseases and vice versa, we proposed the model of Network Consistency Projection for Human Microbe-Disease Association prediction (NCPHMDA) by integrating known microbe-disease associations and Gaussian interaction profile kernel similarity for microbes and diseases. NCPHMDA yielded outstanding AUCs of 0.9039, 0.7953 and average AUC of 0.8918 in global leave-one-out cross validation, local leave-one-out cross validation and 5-fold cross validation, respectively. Furthermore, colon cancer, asthma and type 2 diabetes were taken as independent case studies, where 9, 9 and 8 out of the top 10 predicted microbes were successfully confirmed by recent published clinical literature. NCPHMDA is a non-parametric universal network-based method which can simultaneously predict associated microbes for investigated diseases but does not require negative samples. It is anticipated that NCPHMDA would become an effective biological resource for clinical experimental guidance.

/pdf/novel-human-microbe-disease-association-prediction-using-n1dmfsmrk9.pdf

Novel human microbe-disease association prediction using network consistency projection.

Although convolutional neural networks (CNN) have outperformed conventional methods in predicting the sequence specificities of protein-DNA binding in recent years, they do not take full advantage of the intrinsic weakly-supervised information of DNA sequences that a bound sequence may contain multiple TFBS(s). Here, we propose a weakly-supervised convolutional neural network architecture (WSCNN), combining multiple-instance learning (MIL) with CNN, to further boost the performance of predicting protein-DNA binding. WSCNN first divides each DNA sequence into multiple overlapping subsequences (instances) with a sliding window, and then separately models each instance using CNN, and finally fuses the predicted scores of all instances in the same bag using four fusion methods, including Max , Average , Linear Regression , and Top-Bottom Instances . The experimental results on in vivo and in vitro datasets illustrate the performance of the proposed approach. Moreover, models built on in vitro data using WSCNN can predict in vivo protein-DNA binding with good accuracy. In addition, we give a quantitative analysis of the importance of the reverse-complement mode in predicting in vivo protein-DNA binding, and explain why not directly use advanced pooling layers to combine MIL with CNN, through a series of experiments.

Weakly-Supervised Convolutional Neural Network Architecture for Predicting Protein-DNA Binding

Post translational modification plays a significiant role in the biological processing. The potential post translational modification is composed of the center sites and the adjacent amino acid residues which are fundamental protein sequence residues. It can be helpful to perform their biological functions and contribute to understanding the molecular mechanisms that are the foundations of protein design and drug design. The existing algorithms of predicting modified sites often have some shortcomings, such as lower stability and accuracy. In this paper, a combination of physical, chemical, statistical, and biological properties of a protein have been ulitized as the features, and a novel framework is proposed to predict a protein's post translational modification sites. The multi-layer neural network and support vector machine are invoked to predict the potential modified sites with the selected features that include the compositions of amino acid residues, the E-H description of protein segments, and several properties from the AAIndex database. Being aware of the possible redundant information, the feature selection is proposed in the propocessing step in this research. The experimental results show that the proposed method has the ability to improve the accuracy in this classification issue.

/pdf/mutli-features-prediction-of-protein-translational-1a6ikekq8a.pdf

Wenzheng Bao

Papers

Recurrent Neural Network for Predicting Transcription Factor Binding Sites

Novel human microbe-disease association prediction using network consistency projection.

Weakly-Supervised Convolutional Neural Network Architecture for Predicting Protein-DNA Binding

Mutli-Features Prediction of Protein Translational Modification Sites

A novel deep model with multi-loss and efficient training for person re-identification