全基因组关联研究
表达数量性状基因座
计算生物学
可解释性
生物
背景(考古学)
基因组学
遗传关联
基因
基因调控网络
基因组
遗传学
基因表达
计算机科学
机器学习
单核苷酸多态性
基因型
古生物学
作者
Marc Subirana-Granés,Jill A. Hoffman,Haoyu Zhang,Christina Akirtava,Sutanu Nandi,Kevin Fotso,Milton Pividori
出处
期刊:Annual review of biomedical data science
[Annual Reviews]
日期:2025-02-20
标识
DOI:10.1146/annurev-biodatasci-103123-095355
摘要
Understanding the genetic basis of complex traits is a longstanding challenge in the field of genomics. Genome-wide association studies (GWAS) have identified thousands of variant-trait associations, but most of these variants are located in non-coding regions, making the link to biological function elusive. While traditional approaches, such as transcriptome-wide association studies (TWAS), have advanced our understanding by linking genetic variants to gene expression, they often overlook gene-gene interactions. Here, we review current approaches to integrate different molecular data, leveraging machine learning methods to identify gene modules based on co-expression and functional relationships. These integrative approaches, like PhenoPLIER, combine TWAS and drug-induced transcriptional profiles to effectively capture biologically meaningful gene networks. This integration provides a context-specific understanding of disease processes while highlighting both core and peripheral genes. These insights pave the way for novel therapeutic targets and enhance the interpretability of genetic studies in personalized medicine.
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