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Alternative splicing plays a key role in the regulation of the central dogma. Four major types of alternative splicing have been classified as intron retention, exon skipping, alternative 5 splice sites or alternative donor sites, and alternative 3 splice sites or alternative acceptor sites. A few algorithms have been developed to detect splice junctions from RNA-Seq reads. However, there are few tools targeting at the major alternative splicing types at the exon/intron level. This type of analysis may reveal subtle, yet important events of alternative splicing, and thus help gain deeper understanding of the mechanism of alternative splicing. This paper describes a user-friendly R package, extracting, annotating and analyzing alternative splicing types for sequence alignment files from RNA-Seq. SplicingTypesAnno can: (1) provide annotation for major alternative splicing at exon/intron level. By comparing the annotation from GTF/GFF file, it identifies the novel alternative splicing sites; (2) offer a convenient two-level analysis: genome-scale annotation for users with high performance computing environment, and gene-scale annotation for users with personal computers; (3) generate a user-friendly web report and additional BED files for IGV visualization. SplicingTypesAnno is a user-friendly R package for extracting, annotating and analyzing alternative splicing types at exon/intron level for sequence alignment files from RNA-Seq. It is publically available at https://sourceforge.net/projects/splicingtypes/files/ or http://genome.sdau.edu.cn/research/software/SplicingTypesAnno.html . [ABSTRACT FROM AUTHOR]

Abstract: This paper presents a new visualization software called pairheatmap, which is able to generate and compare two heatmaps so as to compare expression patterns of gene groups. It adds a conditioning variable such as time to the heatmap, and provides separate clustering for row groups in the first heatmap in order to visualize pattern changes between two heatmaps. pairheatmap is developed in R statistical environment. It provides: (1) the flexible framework for comparing two heatmaps; and (2) high-quality figures based on R package grid. The general architecture can be efficiently incorporated into bioinformatics pipeline. The package and user documentation are free to download at http://cran.r-project.org/web/packages/pairheatmap/index.html. [Copyright &y& Elsevier]

Abstract: Population pharmacokinetic (PopPK) modeling has become increasing important in drug development because it handles unbalanced design, sparse data and the study of individual variation. However, the increased complexity of the model makes it more of a challenge to diagnose the fit. Graphics can play an important and unique role in PopPK model diagnostics. The software described in this paper, PKgraph, provides a graphical user interface for PopPK model diagnosis. It also provides an integrated and comprehensive platform for the analysis of pharmacokinetic data including exploratory data analysis, goodness of model fit, model validation and model comparison. Results from a variety of modeling fitting software, including NONMEM, Monolix, SAS and R, can be used. PKgraph is programmed in R, and uses the R packages lattice, ggplot2 for static graphics, and rggobi for interactive graphics. [Copyright &y& Elsevier]

• The proposed model is adaptively adjusted. • The average accuracy of the proposed model exceeds 85% on several datasets. • The model ensures better accuracy for each subject. • The proposed data augmentation method is applicable to many types of data. • The proposed model captures both intra- and inter-channel features of EEG. Background and objective: The development of deep learning has led to significant improvements in the decoding accuracy of Motor Imagery (MI) EEG signal classification. However, current models are inadequate in ensuring high levels of classification accuracy for an individual. Since MI EEG data is primarily used in medical rehabilitation and intelligent control, it is crucial to ensure that each individual's EEG signal is recognized with precision. Methods: We propose a multi-branch graph adaptive network (MBGA-Net), which matches each individual EEG signal with a suitable time-frequency domain processing method based on spatio-temporal domain features. We then feed the signal into the relevant model branch using an adaptive technique. Through an enhanced attention mechanism and deep convolutional method with residual connectivity, each model branch more effectively harvests the features of the related format data. Results: We validate the proposed model using the BCI Competition IV dataset 2a and dataset 2b. On dataset 2a, the average accuracy and kappa values are 87.49 % and 0.83, respectively. The standard deviation of individual kappa values is only 0.08. For dataset 2b, the average classification accuracies obtained by feeding the data into the three branches of MBGA-Net are 85.71 % , 85.83 % , and 86.99 % , respectively. Conclusions: The experimental results demonstrate that MBGA-Net could effectively perform the classification task of motor imagery EEG signals, and it exhibits strong generalization performance. The proposed adaptive matching technique enhances the classification accuracy of each individual, which is beneficial for the practical application of EEG classification. [ABSTRACT FROM AUTHOR]