Detection and Classification of a brain tumor is an important step to better understanding its mechanism. Magnetic Reasoning Imaging (MRI) is an experimental medical imaging technique that helps the radiologist find the tumor region. However, it is a time taking process and requires expertise to test the MRI images, manually. Nowadays, the advancement of Computer-assisted Diagnosis (CAD), machine learning, and deep learning in specific allow the radiologist to more reliably identify brain tumors. The traditional machine learning methods used to tackle this problem require a handcrafted feature for classification purposes. Whereas deep learning methods can be designed in a way to not require any handcrafted feature extraction while achieving accurate classification results. This paper proposes two deep learning models to identify both binary (normal and abnormal) and multiclass (meningioma, glioma, and pituitary) brain tumors. We use two publicly available datasets that include 3064 and 152 MRI images, respectively. To build our models, we first apply a 23-layers convolution neural network (CNN) to the first dataset since there is a large number of MRI images for the training purpose. However, when dealing with limited volumes of data, which is the case in the second dataset, our proposed “23-layers CNN” architecture faces overfitting problem. To address this issue, we use transfer learning and combine VGG16 architecture along with the reflection of our proposed “23 layers CNN” architecture. Finally, we compare our proposed models with those reported in the literature. Our experimental results indicate that our models achieve up to 97.8% and 100% classification accuracy for our employed datasets, respectively, exceeding all other state-of-the-art models. Our proposed models, employed datasets, and all the source codes are publicly available at: (https://github.com/saikat15010/Brain-Tumor-Detection).

Motivation: Extracting useful feature set which contains significant discriminatory information is a critical step in effectively presenting sequence data to predict structural, functional, interaction and expression of proteins, DNAs and RNAs. Also, being able to filter features with significant information and avoid sparsity in the extracted features require the employment of efficient feature selection techniques. Here we present PyFeat as a practical and easy to use toolkit implemented in Python for extracting various features from proteins, DNAs and RNAs. To build PyFeat we mainly focused on extracting features that capture information about the interaction of neighboring residues to be able to provide more local information. We then employ AdaBoost technique to select features with maximum discriminatory information. In this way, we can significantly reduce the number of extracted features and enable PyFeat to represent the combination of effective features from large neighboring residues. As a result, PyFeat is able to extract features from 13 different techniques and represent context free combination of effective features. The source code for PyFeat standalone toolkit and employed benchmarks with a comprehensive user manual explaining its system and workflow in a step by step manner are publicly available. Results: https://github.com/mrzResearchArena/PyFeat/blob/master/RESULTS.md. Availability and implementation: Toolkit, source code and manual to use PyFeat: https://github.com/mrzResearchArena/PyFeat/ Supplementary information: Supplementary data are available at Bioinformatics online.

Bacteriophage proteins are viruses that can significantly impact on the functioning of bacteria and can be used in phage based therapy. The functioning of Bacteriophage in the host bacteria depends on its location in those host cells. It is very important to know the subcellular location of the phage proteins in a host cell in order to understand their working mechanism. In this paper, we propose iPHLoc-ES, a prediction method for subcellular localization of bacteriophage proteins. We aim to solve two problems: discriminating between host located and non-host located phage proteins and discriminating between the locations of host located protein in a host cell (membrane or cytoplasm). To do this, we extract sets of evolutionary and structural features of phage protein and employ Support Vector Machine (SVM) as our classifier. We also use recursive feature elimination (RFE) to reduce the number of features for effective prediction. On standard dataset using standard evaluation criteria, our method significantly outperforms the state-of-the-art predictor. iPHLoc-ES is readily available to use as a standalone tool from: https://github.com/swakkhar/iPHLoc-ES/ and as a web application from: http://brl.uiu.ac.bd/iPHLoc-ES/.

Bioinformatics and computational biology have significantly contributed to the generation of vast and important knowledge that can lead to great improvements and advancements in biology and its related fields. Over the past three decades, a wide range of tools and methods have been developed and proposed to enhance performance, diagnosis, and throughput while maintaining feasibility and convenience for users. Here, we propose a new user-friendly comprehensive tool called VIRMOTIF to analyze DNA sequences. VIRMOTIF brings different tools together as one package so that users can perform their analysis as a whole and in one place. VIRMOTIF is able to complete different tasks, including computing the number or probability of motifs appearing in DNA sequences, visualizing data using the matplotlib and heatmap libraries, and clustering data using four different methods, namely K-means, PCA, Mean Shift, and ClusterMap. VIRMOTIF is the only tool with the ability to analyze genomic motifs based on their frequency and representation (D-ratio) in a virus genome.