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Biology subjects

Adilina, S.

Publications and source records attributed to Adilina, S..

3 recordsLinked to original sources

ACP-MHCNN: An Accurate Multi-Headed Deep-Convolutional Neural Network to Predict Anticancer peptides

Although advancing the therapeutic alternatives for treating deadly cancers has gained much attention globally, still the primary methods such as chemotherapy have significant downsides and low specificity. Most recently, Anticancer peptides (ACPs) have emerged as a potential alternative to therapeutic alternatives with much fewer negative side-effects. However, the identification of ACPs through wet-lab experiments is expensive and time-consuming. Hence, computational methods have emerged as viable alternatives. During the past few years, several computational ACP identification techniques using hand-engineered features have been proposed to solve this problem. In this study, we propose a new multi headed deep convolutional neural network model called ACP-MHCNN, for extracting and combining discriminative features from different information sources in an interactive way. Our model extracts sequence, physicochemical, and evolutionary based features for ACP identification through simultaneous interaction with different numerical peptide representations while restraining parameter overhead. It is evident through rigorous experiments using cross-validation and independent-dataset that ACP-MHCNN outperforms other models for anticancer peptide identification by a substantial margin. ACP-MHCNN outperforms state-of-the-art model by 6.3%, 8.6%, 3.7%, 4.0%, and 0.20 in terms of accuracy, sensitivity, specificity, precision, and MCC respectively. ACP-MHCNN and its relevant codes and datasets are publicly available at: https://github.com/mrzResearchArena/Anticancer-Peptides-CNN.

bioinformatics↗

SubFeat: Feature Subspacing Ensemble Classifier for Function Prediction of DNA, RNA and Protein Sequences

The information of a cell is primarily contained in Deoxyribonucleic Acid (DNA). There is a flow of information of DNA to protein sequences via Ribonucleic acids (RNA) through transcription and translation. These entities are vital for the genetic process. Recent developments in epigenetic also show the importance of the genetic material and knowledge of their attributes and functions. However, the growth in known attributes or functionalities of these entities are still in slow progression due to the time consuming and expensive in vitro experimental methods. In this paper, we have proposed an ensemble classification algorithm called SubFeat to predict the functionalities of biological entities from different types of datasets. Our model uses a feature subspace based novel ensemble method. It divides the feature space into sub-spaces which are then passed to learn individual classifier models and the ensemble is built on this base classifiers that uses a weighted majority voting mechanism. SubFeat tested on four datasets comprising two DNA, one RNA and one protein dataset and it outperformed all the existing single classifiers and as well as the ensemble classifiers. SubFeat is made availalbe as a Python-based tool. We have made the package SubFeat available online along with a user manual. It is freely accessible from here: https://github.com/fazlulhaquejony/SubFeat.

bioinformatics↗

DeepDBP: Deep Neural Networks for Identification of DNA-binding Proteins

DNA-Binding proteins (DBP) are associated with many cellular level functions which includes but not limited to bodys defense mechanism and oxygen transportation. They bind DNAs and interact with them. In the past DBPs were identified using experimental lab based methods. However, in the recent years researchers are using supervised learning to identify DBPs solely from protein sequences. In this paper, we apply deep learning methods to identify DBPs. We have proposed two different deep learning based methods for identifying DBPs: DeepDBP-ANN and DeepDBP-CNN. DeepDBP-ANN uses a generated set of features trained on traditional neural network and DeepDBP-CNN uses a pre-learned embedding and Convolutional Neural Network. Both of our proposed methods were able to produce state-of-the-art results when tested on standard benchmark datasets.DeepDBP-ANN had a train accuracy of 99.02% and test accuracy of 82.80%.And DeepDBP-CNN though had train accuracy of 94.32%, it excelled at identifying test instances with 84.31% accuracy. All methods are available codes and methods are available for use at: https://github.com/antorkhan/DNABinding.

bioinformatics↗