In this paper, a new method is designed to effectively determine the parameters of proton exchange membrane fuel cells (PEMFCs), i.e., ξ 1 , ξ 2 , ξ 3 , ξ 4 , R C , λ , and b . The fuel cells (FCs) involve multiple variable quantities with complex non-linear behaviours, demanding accurate modelling to ensure optimal operation. An accurate model of these FCs is essential to evaluate their performance accurately. Furthermore, the design of the FCs significantly impacts simulation studies, which are crucial for various technological applications. This study proposed an improved parameter estimation procedure for PEMFCs by using the GOOSE algorithm, which was inspired by the adaptive behaviours found in geese during their relaxing and foraging times. The orthogonal learning mechanism improves the performance of the original GOOSE algorithm. This FC model uses the root mean squared error as the objective function for optimizing the unknown parameters. In order to validate the proposed algorithm, a number of experiments using various datasets were conducted and compared the outcomes with different state-of-the-art algorithms. The outcomes indicate that the proposed GOOSE algorithm not only produced promising results but also exhibited superior performance in comparison to other similar algorithms. This approach demonstrates the ability of the GOOSE algorithm to simulate complex systems and enhances the robustness and adaptability of the simulation tool by integrating essential behaviours into the computational framework. The proposed strategy facilitates the development of more accurate and effective advancements in the utilization of FCs.
Primary angle closure glaucoma (PACG) is a major cause of blindness worldwide. We conducted a genome-wide association study (GWAS) followed by replication in a combined total of 10,503 PACG cases and 29,567 controls drawn from 24 countries across Asia, Australia, Europe, North America, and South America. We observed significant evidence of disease association at five new genetic loci upon meta-analysis of all patient collections. These loci are at EPDR1 rs3816415 (odds ratio (OR) = 1.24, P = 5.94 × 10(-15)), CHAT rs1258267 (OR = 1.22, P = 2.85 × 10(-16)), GLIS3 rs736893 (OR = 1.18, P = 1.43 × 10(-14)), FERMT2 rs7494379 (OR = 1.14, P = 3.43 × 10(-11)), and DPM2-FAM102A rs3739821 (OR = 1.15, P = 8.32 × 10(-12)). We also confirmed significant association at three previously described loci (P < 5 × 10(-8) for each sentinel SNP at PLEKHA7, COL11A1, and PCMTD1-ST18), providing new insights into the biology of PACG.