The semantic segmentation of a brain tumor is of paramount importance for its treatment and prevention. Recently, researches have proposed various neural network-based architectures to improve the performance of segmentation of brain tumor sub-regions. Brain tumor segmentation, being a challenging area of research, requires improvement in its performance. This paper proposes a 2D image segmentation method, BU-Net, to contribute to brain tumor segmentation research. Residual extended skip (RES) and wide context (WC) are used along with the customized loss function in the baseline U-Net architecture. The modifications contribute by finding more diverse features, by increasing the valid receptive field. The contextual information is extracted with the aggregating features to get better segmentation performance. The proposed BU-Net was evaluated on the high-grade glioma (HGG) datasets of the BraTS2017 Challenge—the test datasets of the BraTS 2017 and 2018 Challenge datasets. Three major labels to segmented were tumor core (TC), whole tumor (WT), and enhancing core (EC). To compare the performance quantitatively, the dice score was utilized. The proposed BU-Net outperformed the existing state-of-the-art techniques. The high performing BU-Net can have a great contribution to researchers from the field of bioinformatics and medicine.

Efficient segmentation of Magnetic Resonance (MR) brain tumor images is of the utmost value for the diagnosis of tumor region. In recent years, advancement in the field of neural networks has been used to refine the segmentation performance of brain tumor sub-regions. The brain tumor segmentation has proven to be a complicated task even for neural networks, due to the small-scale tumor regions. These small-scale tumor regions are unable to be identified, the reason being their tiny size and the huge difference between area occupancy by different tumor classes. In previous state-of-the-art neural network models, the biggest problem was that the location information along with spatial details gets lost in deeper layers. To address these problems, we have proposed an encoder–decoder based model named BrainSeg-Net. The Feature Enhancer (FE) block is incorporated into the BrainSeg-Net architecture which extracts the middle-level features from low-level features from the shallow layers and shares them with the dense layers. This feature aggregation helps to achieve better performance of tumor identification. To address the problem associated with imbalance class, we have used a custom-designed loss function. For evaluation of BrainSeg-Net architecture, three benchmark datasets are utilized: BraTS2017, BraTS 2018, and BraTS 2019. Segmentation of Enhancing Core (EC), Whole Tumor (WT), and Tumor Core (TC) is carried out. The proposed architecture have exhibited good improvement when compared with existing baseline and state-of-the-art techniques. The MR brain tumor segmentation by BrainSeg-Net uses enhanced location and spatial features, which performs better than the existing plethora of brain MR image segmentation approaches.

DNA N6-methyladenine (6mA) has been demonstrated to have an essential function in epigenetic modification in eukaryotic species in recent research. 6mA has been linked to various biological processes. It’s critical to create a new algorithm that can rapidly and reliably detect 6mA sites in genomes to investigate their biological roles. The identification of 6mA marks in the genome is the first and most important step in understanding the underlying molecular processes, as well as their regulatory functions. In this article, we proposed a novel computational tool called i6mA-Caps which CapsuleNet based a framework for identifying the DNA N6-methyladenine sites. The proposed framework uses a single encoding scheme for numerical representation of the DNA sequence. The numerical data is then used by the set of convolution layers to extract low-level features. These features are then used by the capsule network to extract intermediate-level and later high-level features to classify the 6mA sites. The proposed network is evaluated on three datasets belonging to three genomes which are Rosaceae, Rice and Arabidopsis thaliana. Proposed method has attained an accuracy of 96.71%, 94% and 86.83% for independent Rosaceae dataset, Rice dataset and A.thaliana dataset respectively. The proposed framework has exhibited improved results when compared with the existing top-of-the-line methods. A user-friendly web-server is made available for the biological experts which can be accessed at: http://nsclbio.jbnu.ac.kr/tools/i6mA-Caps/. Supplementary data are available at Bioinformatics online.