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1.
IEEE J Biomed Health Inform ; 26(6): 2405-2416, 2022 06.
Article in English | MEDLINE | ID: mdl-33764880

ABSTRACT

N6-methyladenosine (m6A) has been shown to play crucial roles in RNA metabolism, physiology, and pathological processes. However, the specific regulatory mechanisms of most methylation sites remain uncharted due to the complexity of life processes. Biological experimental methods are costly to solve this problem, and computational methods are relatively lacking. The discovery of local co-methylation patterns (LCPs) of m6A epi-transcriptome data can benefit to solve the above problems. Based on this, we propose a novel biclustering algorithm based on the beta distribution (BDBB), which realizes the mining of LCPs of m6A epi-transcriptome data. BDBB employs the Gibbs sampling method to complete parameter estimation. In the process of modeling, LCPs are recognized as sharp beta distributions compared to the background distribution. Simulation study showed BDBB can extract all the three actual LCPs implanted in the background data and the overlap conditions between them with considerable accuracy (almost close to 100%). On MeRIP-Seq data of 69,446 methylation sites under 32 experimental conditions from 10 human cell lines, BDBB unveiled two LCPs, and Gene Ontology (GO) enrichment analysis showed that they were enriched in histone modification and embryo development, etc. important biological processes respectively. The GOE_Score scoring indicated that the biclustering results of BDBB in the m6A epi-transcriptome data are more biologically meaningful than the results of other biclustering algorithms.


Subject(s)
Algorithms , Gene Expression Profiling , Cluster Analysis , Computer Simulation , Gene Expression Profiling/methods , Humans , Methylation , Transcriptome/genetics
2.
Front Neuroinform ; 15: 781551, 2021.
Article in English | MEDLINE | ID: mdl-35002667

ABSTRACT

Early diagnosis of pathological brains leads to early interventions in brain diseases, which may help control the illness conditions, prolong the life of patients, and even cure them. Therefore, the classification of brain diseases is a challenging but helpful task. However, it is hard to collect brain images, and the superabundance of images is also a great challenge for computing resources. This study proposes a new approach named TReC: Transferred Residual Networks (ResNet)-Convolutional Block Attention Module (CBAM), a specific model for small-scale samples, to detect brain diseases based on MRI. At first, the ResNet model, which is pre-trained on the ImageNet dataset, serves as initialization. Subsequently, a simple attention mechanism named CBAM is introduced and added into every ResNet residual block. At the same time, the fully connected (FC) layers of the ResNet are replaced with new FC layers, which meet the goal of classification. Finally, all the parameters of our model, such as the ResNet, the CBAM, and new FC layers, are retrained. The effectiveness of the proposed model is evaluated on brain magnetic resonance (MR) datasets for multi-class and two-class tasks. Compared with other state-of-the-art models, our model reaches the best performance for two-class and multi-class tasks on brain diseases.

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