Cancer genomic data contain views from different sources that provide complementary information about genetic activity. This provides a new way for cancer research. Feature selection and multi-view clustering are hot topics in bioinformatics, and they can make full use of complementary information to improve the effect. In this paper, a novel integrated model called Multi-view Non-negative Matrix Factorization (MvNMF) is proposed for the selection of common differential genes (co-differential genes) and multi-view clustering. In order to encode the geometric information in the multi-view genomic data, graph regularized MvNMF (GMvNMF) is further proposed by applying the graph regularization constraint in the objective function. GMvNMF can not only obtain the potential shared feature structure and shared cluster group structure, but also capture the manifold structure of multi-view data. The validity of the proposed GMvNMF method was tested in four multi-view genomic data. Experimental results showed that the GMvNMF method has better performance than other representative methods.

There is much evidence that long non-coding RNA (lncRNA) is associated with many diseases. However, it is time-consuming and expensive to identify meaningful lncRNA-disease associations (LDAs) through medical or biological experiments. Therefore, investigating how to identify more meaningful LDAs is necessary, and at the same time it is conducive to the prevention, diagnosis and treatment of complex diseases. Considering the limitations of some current prediction models, a novel model based on bipartite local model with nearest profile-based association inferring, BLM-NPAI, is developed for predicting LDAs. This model predicts novel LDAs from the lncRNA side and the disease side, respectively. More importantly, for some lncRNAs and diseases without any association, the model can also be predicted by their nearest neighbors. Leave-one-out cross validation (LOOCV) and 5-fold cross validation are implemented for BLM-NPAI to evaluate the performance of this model. Our model is superior to current advanced methods in most cases. In addition, to verify the validity and reliability of BLM-NPAI, three disease cases and three lncRNA cases are analyzed to further evaluate BLM-NPAI. Finally, these predicted novel LDAs are confirmed by using the LncRNADisease database.

Detecting genomes with similar expression patterns using clustering techniques plays an important role in gene expression data analysis. Non-negative matrix factorization (NMF) is an effective method for clustering the analysis of gene expression data. However, the NMF-based method is performed within the Euclidean space, and it is usually inappropriate for revealing the intrinsic geometric structure of data space. In order to overcome this shortcoming, Cai et al. proposed a novel algorithm, called graph regularized non-negative matrices factorization (GNMF). Motivated by the topological structure of the GNMF-based method, we propose improved graph regularized non-negative matrix factorization (GNMF) to facilitate the display of geometric structure of data space. Robust manifold non-negative matrix factorization (RM-GNMF) is designed for cancer gene clustering, leading to an enhancement of the GNMF-based algorithm in terms of robustness. We combine the $l_{2,1}$ -norm NMF with spectral clustering to conduct the wide-ranging experiments on the three known datasets. Clustering results indicate that the proposed method outperforms the previous methods, which displays the latest application of the RM-GNMF-based method in cancer gene clustering.

In recent years, with the increasing application of highthroughput sequencing technology, researchers have obtained and accumulated a large amount of multi-omics data, making it possible to diagnose cancer at the gene expression level. The proliferation of various omics data can provide a large amount of biological information, which brings new opportunities and great challenges as well to cancer classification and diagnosis. Machine learning algorithms for early diagnosis of lung cancer have emerged that distinguish cancers of the early and late stages by using genomic features. Omics data are generally characterized with low sample size, high dimensionality and high noise. Therefore, simple direct application of common classification methods cannot achieve better performance and must be improved in a targeted manner. This paper puts forward a combined convolutional neural network and convolutional auto-encoders approach to construct a deep migratory learning classification model for early lung cancer diagnosis. First, the convolutional auto-encoders algorithm is used to reduce the dimensionality of the dataset in order to make it better meet the requirements of migration learning. Second, a neural network model is constructed with the original dataset and the existing labeled dataset, and the model migration rules are set as well. Finally, a small number of labeled target datasets are used in the training to complete the construction of the classification model. The proposed convolutional neural network method based on model migration and five other popular machine learning models are used to classify and predict the three lung cancer gene datasets and the integrated dataset. The experimental results show that such four evaluation metrics as accuracy, precision, recall, and f1-score with our proposed method have obtained better prediction performance, and the average area under curve result also shows our proposed method is optimal.

Night vision imaging is a technology that converts objects not visible to the human eye into visible images for night scenes and other low-light environments. However, conventional night vision imaging can directly produce only grayscale images. Here, we report a novel, to the best of our knowledge, color night vision imaging method based on a ghost imaging framework and optimized coincidence measurement based on wavelet transformation. An interesting phenomenon is that color night vision image can be directly produced by this new method. To our knowledge, this is the first direct color night vision imaging method without any conventional pseudocolor image fusion techniques. The experimental results show that this method can restore color very well for some objects. Moreover, the color of the night vision image is more natural and friendly to the human eye than that of conventional color night vision images. Due to the advantages of wavelet transforms, this method has high reconstruction ability for distorted signals.