bioRxiv Science⌕ Search

Biology subjects

Hossain, M. Z.

Publications and source records attributed to Hossain, M. Z..

3 recordsLinked to original sources

Machine Learning to Predict Gut Microbiomes of Agricultural Pests

ContextWhile current efforts to control agricultural insect pests largely focus on the widespread use of insecticides, predicting microbiome composition can provide important data for creating more efficient and long-lasting pest control methods by analysing the pests food-digesting capacity and resistance to bacteria or viruses. AimsInstead of using computationally expensive techniques, we aim to investigate the dynamics of these microbiome compositions using metagenomic samples taken from fruit flies. MethodsIn this paper, we propose the three machine learning-based biological models. Firstly, we propose the intrafamilial successor prediction, which predicts the relative abundance of each bacterial family using the past four generations. Next, we propose our interfamilial quantitative prediction, where the model predicts the amount of a given bacterial family in each sample using the amount of all other bacteria present in the sample. Lastly. we propose our interfamilial qualitative prediction, which predicts the relative abundance of each bacterial family within a sample using binary information of all bacterial families. Key ResultsAll three models were tested against Least Angle Regression, Random Forest, Elastic-Net, and Lasso. The third approach exhibits promising results by applying a Random Forest with the lowest mean Coefficient of Variance of 1.25. ConclusionThe overall results of this study highlight how complex these dynamic systems are and demonstrate that more computationally efficient methods can characterise them quickly.

bioinformatics↗

Bilayer tension-induced clustering of the UPR sensor IRE1

The endoplasmic reticulum acts as a protein quality control center where a range of chaperones and foldases facilitates protein folding. IRE1 is a sensory trans-membrane protein that transduces signals of proteotoxic stress by forming clusters and activating a cellular program called the unfolded protein response (UPR). Recently, membrane thickness variation due to membrane compositional changes have been shown to drive IRE1 cluster formation, activating the UPR even in the absence of proteotoxic stress. Here, we demonstrate a direct relationship between bilayer tension and UPR activation based on IRE1 dimer stability. The stability of the IRE1 dimer in a (50%DOPC-50%POPC) membrane at different applied bilayer tensions was analyzed via molecular dynamics simulations. The potential of mean force for IRE1 dimerization predicts a higher concentration of IRE1 dimers for both tensed and compressed ER membranes. This study shows that IRE1 may be a mechanosensitive membrane protein and establishes a direct biophysical relationship between bilayer tension and UPR activation. HighlightsO_LIMechanical perturbation of the ER membrane favor oligomerization. C_LIO_LIBoth tension and compression promote IRE1 dimer formation. C_LIO_LIIRE1 is mechanosensitive, potentially the UPR to changes in ER membrane tension and compression. C_LI

biophysics↗

Spatial Transcriptomics Analysis of Gene Expression Prediction using Exemplar Guided Graph Neural Network

Spatial transcriptomics (ST) is essential for understanding diseases and developing novel treatments. It measures the gene expression of each fine-grained area (i.e., different windows) in the tissue slide with low throughput. This paper proposes an exemplar guided graph network dubbed EGGN to accurately and efficiently predict gene expression from each window of a tissue slide image. We apply exemplar learning to dynamically boost gene expression prediction from nearest/similar exemplars of a given tissue slide image window. Our framework has three main components connected in a sequence: i) an extractor to structure a feature space for exemplar retrievals; ii) a graph construction strategy to connect windows and exemplars as a graph; iii) a graph convolutional network backbone to process window and exemplar features, and a graph exemplar bridging block to adaptively revise the window features using its exemplars. Finally, we complete the gene expression prediction task with a simple attention-based prediction block. Experiments on standard benchmark datasets indicate the superiority of our approach when compared with past state-of-the-art methods. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=108 SRC="FIGDIR/small/534914v1_ufig1.gif" ALT="Figure 1"> View larger version (29K): org.highwire.dtl.DTLVardef@6507f5org.highwire.dtl.DTLVardef@ed7ea5org.highwire.dtl.DTLVardef@159fd5org.highwire.dtl.DTLVardef@1b09270_HPS_FORMAT_FIGEXP M_FIG C_FIG In this paper, we aim to predict gene expression of each window in a tissue slide image. Given a tissue slide image, we encode the windows to feature space, retrieve its exemplars from the reference dataset, construct a graph, and then dynamically predict gene expression of each window with our exemplar guided graph network. HighlightsO_LIWe propose an exemplar guided graph network to accurately predict gene expression from a slide image window. C_LIO_LIWe design a graph construction strategy to connect windows and exemplars for performing exemplar learning of gene expression prediction. C_LIO_LIWe propose a graph exemplar bridging block to revise the window feature by using its nearest exemplars. C_LIO_LIExperiments on two standard benchmark datasets demonstrate our superiority when compared with state-of-the-art approaches. C_LI

bioinformatics↗