孟德尔随机化
全基因组关联研究
生物
因果关系(物理学)
电池类型
表达数量性状基因座
细胞
计算生物学
遗传关联
遗传学
基因
疾病
遗传变异
单核苷酸多态性
医学
基因型
病理
物理
量子力学
作者
Ruo-Han Hao,Tian-Pei Zhang,Feng Jiang,Jun-Hui Liu,Shan‐Shan Dong,Meng Li,Yan Guo,Tie‐Lin Yang
标识
DOI:10.1038/s41467-024-49263-4
摘要
Abstract The human brain has been implicated in the pathogenesis of several complex diseases. Taking advantage of single-cell techniques, genome-wide association studies (GWAS) have taken it a step further and revealed brain cell-type-specific functions for disease loci. However, genetic causal associations inferred by Mendelian randomization (MR) studies usually include all instrumental variables from GWAS, which hampers the understanding of cell-specific causality. Here, we developed an analytical framework, Cell-Stratified MR (csMR), to investigate cell-stratified causality through colocalizing GWAS signals with single-cell eQTL from different brain cells. By applying to obesity-related traits, our results demonstrate the cell-type-specific effects of GWAS variants on gene expression, and indicate the benefits of csMR to identify cell-type-specific causal effect that is often hidden from bulk analyses. We also found csMR valuable to reveal distinct causal pathways between different obesity indicators. These findings suggest the value of our approach to prioritize target cells for extending genetic causation studies.
科研通智能强力驱动
Strongly Powered by AbleSci AI