Ruilin Su, Binyang Huang, Junyan Tan, Zhencai Shen, Ping Zhong, Jianfeng Liu
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引用次数: 0
Abstract
Genomic prediction is a crucial technique for phenotype estimation, with the genomic best linear unbiased prediction (GBLUP) being the most widely adopted method. Yet, GBLUP falls short in capturing the intricate nonlinear relationships between genomic data and phenotypes. Given its ability to more effectively capture nonlinear genetic effects, machine learning (ML) has become increasingly appealing in genomic prediction. However, almost GBLUP and ML methods utilize all single nucleotide polymorphisms (SNPs) data for prediction, ignoring the fact that only a subset of SNPs are effective. This not only consumes computation time but also has poor prediction accuracy. So, this paper proposed a mutual information stacking method (MISM). Firstly, mutual information was introduced to select the SNPs with effect and remove the redundant SNPs. Then, we constructed a stacking model that can capture both linear and nonlinear relationships between SNPs and phenotypes to improve the prediction accuracy. To assess the effectiveness of MISM, we compared its performance on pig growth traits with GBLUP and other ML methods. The statistical analysis results indicated that MISM outperformed other ML models and GBLUP.
期刊介绍:
Briefings in Bioinformatics is an international journal serving as a platform for researchers and educators in the life sciences. It also appeals to mathematicians, statisticians, and computer scientists applying their expertise to biological challenges. The journal focuses on reviews tailored for users of databases and analytical tools in contemporary genetics, molecular and systems biology. It stands out by offering practical assistance and guidance to non-specialists in computerized methodologies. Covering a wide range from introductory concepts to specific protocols and analyses, the papers address bacterial, plant, fungal, animal, and human data.
The journal's detailed subject areas include genetic studies of phenotypes and genotypes, mapping, DNA sequencing, expression profiling, gene expression studies, microarrays, alignment methods, protein profiles and HMMs, lipids, metabolic and signaling pathways, structure determination and function prediction, phylogenetic studies, and education and training.