An Investigation of Complex Interactions Between Genetically Determined Protein Expression and the Metabolic Phenotype of Human Islet Cells Using Deep Learning

The relationship between gene modules and several genome-scale metrics was examined, including heterozygosity that caused type 2 diabetes due to insulin deuteration, differential expression, genotyping association, methylation, and copy number changes. This work investigates the complex relationships between protein expression, genetic polymorphisms, and metabolic properties of human islet cells using expression quantitative trait loci (eQTL) detection. We looked at the genomic, transcriptomic, and proteomic information from islet cells in persons with type 2 diabetes. From the information from different levels, we noticed novel eQTLs that regulate crucial metabolic and signaling pathways in islet cells. Our study highlights the importance of a systems-level approach in understanding the complicated biological processes by highlighting the complexity of the link between genetic variants, protein expression, and metabolic abnormalities using the PIMA Indian dataset. Our findings provide novel insights into the molecular mechanisms behind islet cell failure in type 2 diabetes, potential targets for emerging treatment strategies, and the genomic implications of variations in gene expression, mutations, and other factors. To accomplish this purpose, we proposed a novel BLB model and obtained 99.89%.