全基因组关联研究
单核苷酸多态性
遗传关联
机器学习
计算生物学
人口
人工智能
计算机科学
SNP公司
上位性
生物
遗传学
基因型
医学
基因
环境卫生
作者
David O. Enoma,Janet Bishung,Theresa Nkechi Abiodun,Olubanke Olujoke Ogunlana,Victor Chukwudi Osamor
标识
DOI:10.1016/j.jksus.2022.101847
摘要
Genome-wide Association Studies (GWAS) are conducted to identify single nucleotide polymorphisms (variants) associated with a phenotype within a specific population. These variants associated with diseases have a complex molecular aetiology with which they cause the disease phenotype. The genotyping data generated from subjects of study is of high dimensionality, which is a challenge. The problem is that the dataset has a large number of features and a relatively smaller sample size. However, statistical testing is the standard approach being applied to identify these variants that influence the phenotype of interest. The wide applications and abilities of Machine Learning (ML) algorithms promise to understand the effects of these variants better. The aim of this work is to discuss the applications and future trends of ML algorithms in GWAS towards understanding the effects of population genetic variant. It was discovered that algorithms such as classification, regression, ensemble, and neural networks have been applied to GWAS for which this work has further discussed comprehensively including their application areas. The ML algorithms have been applied to the identification of significant single nucleotide polymorphisms (SNP), disease risk assessment & prediction, detection of epistatic non-linear interaction, and integrated with other omics sets. This comprehensive review has highlighted these areas of application and sheds light on the promise of innovating machine learning algorithms into the computational and statistical pipeline of genome-wide association studies. This will be beneficial for better understanding how variants are affected by disease biology and how the same variants can influence risk by developing a particular phenotype for favourable natural selection.
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