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Biology subjects

Altay, G.

Publications and source records attributed to Altay, G..

5 recordsLinked to original sources

Gene Regulatory Cross Networks: Inferring Gene Level Cell-to-Cell Communications of Immune Cells

BackgroundGene level cell-to-cell communications are crucial part of biology as they may be potential targets of drugs and vaccines against a disease condition of interest. Yet, there are only few studies that propose algorithms on this particularly important research field.\n\nResultsIn this study, we first overview the current literature and define two general terms for the types of approaches in general for gene level cell-to-cell communications: Gene Regulatory Cross Networks (GRCN) and Gene Co-Expression Cross Networks (GCCN). We then propose two algorithms for each type, named as GRCNone and GCCNone. We applied them to reveal communications among 8 different immune cell types and evaluate their performances mainly via membrane protein database. Also, we show the biological relevance of the predicted cross-networks with pathway enrichment analysis. We then provide an approach that prioritize the targets by ranking them before experimental validations.\n\nConclusionsWe establish two main approaches and propose algorithms for genome-wide scale gene level cell-to-cell communications between any two different cell-types. This study aims accelerating this relatively new avenue of research in cross-networks and points out the gap of it with the well-established single cell type gene networks. The proposed algorithms have the potential to reveal gene level interactions between normal and disease cell types. For instance, they might reveal the interaction of genes between tumor and normal cells, which are the potential drug-targets and thus can help finding new cures that might prevent the prevailing of tumor cells.

bioinformatics

Tensorflow Based Deep Learning Model and Snakemake Workflow for Peptide-Protein Binding Predictions

In this study, we first present a Tensorflow based Deep Learning (DL) model that provides high performances in predicting the binding of peptides to major histocompatibility complex (MHC) class I protein. Second, we provide the necessary Python codes to run the model and also easily input large train and test peptide binding benchmark dataset. Third, we provide Snakemake based workflow that allows to run all the model and performance analysis over all the different test alleles at once in parallel over computer and clusters. We also provide comparison analysis of the performances of various models. Finally, in order to help attaining to the best possible DL model by a community effort, this work is intended to be a ready to modify base model and workflow for the global Deep Learning community with no domain knowledge in MHC-peptide binding problem and thus provides all the necessary reference code templates and benchmarking data sets for further developments on the presented model architecture. All the reproducible Python codes, Snakemake workflow and benchmark data sets and a tutorial are available online at https://github.com/altayg/Deep-Learning-MHCI.

bioinformatics

Directed Conservative Causal Core Gene Networks

MotivationInferring large scale directional networks with higher accuracy has important applications such as gene regulatory network or finance.\n\nResultsWe modified a well-established conservative causal core network inference algorithm, C3NET, to be able to infer very large scale networks with direction information. This advanced version is called Ac3net. We demonstrate that Ac3net outperforms C3NET and many other popular algorithms when considering the directional interaction information of gene/protein networks. We provide and R package and present performance results that are reproducible via the Supplementary file.\n\nAvailabilityAc3net is available on CRAN and at github.com/altayg/Ac3net\n\nContactaltay@lji.org\n\nSupplementary informationSupplementary file is available online.

bioinformatics

Genome-Wide Differential Gene Network Analysis R Software And Its Application In LnCap Prostate Cancer

We present an R software package that performs at genome-wide level differential network analysis and infers only disease-specific molecular interactions between two different cell conditions. This helps revealing the disease mechanism and predicting most influential genes as potential drug targets or biomarkers of the disease condition of interest. As an exemplary analysis, we performed an application of the software over LNCaP datasets and, out of approximately 25000 genes, predicted CXCR7 and CXCR4 together as drug targets of LNCaP prostate cancer dataset. We further successfully validated them with our initial wet-lab experiments. The introduced software can be applied to all the diseases, especially cancer, with gene expression data of two different conditions (e.g. tumor vs normal) and thus has the potential of a global benefit. As a distinct remark, our software provide the causal disease mechanism with multiple potential drug-targets rather than a single independent target prediction. AvailabilityThe introduced R software package for the analysis is available in CRAN at https://cran.r-project.org/web/packages/dc3net and also at https://github.com/altayg/dc3net

bioinformatics

DepEst: an R package of important dependency estimators for gene network inference algorithms

Gene network inference algorithms (GNI) are popular in bioinformatics area. In almost all GNI algorithms, the main process is to estimate the dependency (association) scores among the genes of the dataset.\n\nWe present a bioinformatics tool, DepEst (Dependency Estimators), which is a powerful and flexible R package that includes 11 important dependency score estimators that can be used in almost all GNI Algorithms. DepEst is the first bioinformatics package that includes such a large number of estimators that runs both in parallel and serial.\n\nDepEst is currently available at https://github.com/altayg/Depest. Package access link, instructions, various workflows and example data sets are provided in the supplementary file.

bioinformatics