Single-nucleotide polymorphism (SNP)-SNP interactions are crucial for understanding the association between disease-related multifactorials for disease analysis. Existing statistical methods for determining such interactions are limited by the considerable computation required for evaluating all potential associations between disease-related multifactorials. Identifying SNP-SNP interactions is thus a major challenge in genetic association studies. This paper proposes a catfish Taguchi-based binary differential evolution (CT-BDE) algorithm for identifying SNP-SNP interactions. In the search space, the catfish effect prevents the premature convergence of the population, and the Taguchi method improves the search ability of the BDE algorithm. Hence, the proposed algorithm enables obtaining a favorable solution regarding the identification of high-order SNP-SNP interactions. Additionally, the proposed algorithm applies an effective fitness function derived from a multifactor dimensionality reduction (MDR) operation to evaluate the solutions from BDE-based algorithms. Simulated and real data sets were used to evaluate the ability of several BDE-based algorithms in identifying specific SNP-SNP interactions. We compared the fitness function derived from the MDR operation with that derived according to the difference between cases and controls, by using the different BDE-based algorithms. The results showed that the proposed CT-BDE algorithm applying the fitness function derived from the MDR operation exhibited a superior ability in identifying SNP-SNP interactions compared with the other BDE-based algorithms.
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http://dx.doi.org/10.1109/TNB.2018.2844342 | DOI Listing |
Mol Genet Genomics
December 2024
Department of Plant Sciences, North Dakota State University, Fargo, 58108, USA.
Detecting genome-wide SNP-SNP interactions (epistasis) efficiently is essential to harnessing the vast data now available from modern biobanks. With millions of SNPs and genetic information from hundreds of thousands of individuals, researchers are positioned to uncover new insights into complex disease pathways. However, this data scale brings significant computational and statistical challenges.
View Article and Find Full Text PDFJ Integr Neurosci
December 2024
Laboratory of Genomic Research, Research Institute for Genetic and Molecular Epidemiology, Kursk State Medical University, 305041 Kursk, Russia.
Background: Heat shock proteins (HSPs) play a critical role in the molecular mechanisms of ischemic stroke (IS). A possible role for HSP40 family proteins in atherosclerosis progression has already been revealed; however, to date, molecular genetic studies on the involvement of genes encoding proteins of the HSP40 family in IS have not yet been carried out.
Aim: We sought to determine whether nine single nucleotide polymorphisms (SNPs) in genes encoding HSP40 family proteins (, , , , and ) are associated with the risk and clinical features of IS.
Respir Med
December 2024
Department of Pulmonary and Critical Care Medicine, Hainan General Hospital, Hainan Affiliated Hospital of Hainan Medical University, Haikou 570311, Hainan, China. Electronic address:
Background: Chronic obstructive pulmonary disease (COPD) is characterized by persistent respiratory symptoms and airflow limitation. Interleukin-13 (IL13), associated with T-helper type 2 cells, plays a crucial role in COPD pathophysiology. This study aimed to investigate the relationship of single nucleotide polymorphisms (SNPs) in IL13 to COPD risk.
View Article and Find Full Text PDFJ Orthop Surg Res
December 2024
Department of Endocrinology, Hebei Medical University Third Hospital, Shijiazhuang, Hebei, China.
Background: The influence of the glucagon-like peptide-1 receptor (GLP-1R) on bone metabolism is well-established. However, it has been observed that single nucleotide polymorphisms (SNPs) in the GLP-1R gene can partially affect its function. Therefore, this study aims to investigate the association between SNPs in the GLP-1R gene and postmenopausal osteoporosis (PMOP) within the Chinese Han population.
View Article and Find Full Text PDFInt J Chron Obstruct Pulmon Dis
December 2024
Department of Respiratory and Critical Care Medicine, Hainan Affiliated Hospital of Hainan Medical University, Hainan General Hospital, Haikou City, Hainan Province, People's Republic of China.
Background: Mutations in ADGRG6 are associated with a variety of cancers and multiple types of diseases. However, the impact of genetic variations in ADGRG6 on chronic obstructive pulmonary disease (COPD) susceptibility has not yet been evaluated.
Methods: Considering the high prevalence of COPD among the elderly population in China, this study specifically targets the elderly Han population in Southern China as the study subject.
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