转录组全根因推断

Eric V Strobl, Eric R Gamazon
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引用次数: 0

摘要

根部致病基因对应于发病过程中受遗传或非遗传因素干扰的第一个基因表达水平。针对病根因果基因,有可能在发病初期消除病理现象,从而完全缓解疾病。目前还没有一种算法能够仅从观察数据中发现根源性因果基因。因此,我们提出了转录组全根因推断(TWRCI)算法,该算法结合基因变异和未扰动的大容量 RNA 测序数据来识别根因基因及其因果图。TWRCI 采用新颖的竞争回归程序,将顺式和反式遗传变异注释为其直接导致的基因表达水平。该算法同时还能恢复表达水平的因果排序,从而精确定位底层因果图并估算根因果效应。TWRCI 通过直接定位根源因果基因,同时考虑远端关系、连锁不平衡、患者异质性和广泛的多义性,在各种指标上优于其他方法。我们通过揭示两种复杂疾病的根源因果机制来演示该算法,并利用独立的全基因组汇总统计进行了复制确认。
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Transcriptome-Wide Root Causal Inference
Root causal genes correspond to the first gene expression levels perturbed during pathogenesis by genetic or non-genetic factors. Targeting root causal genes has the potential to alleviate disease entirely by eliminating pathology near its onset. No existing algorithm discovers root causal genes from observational data alone. We therefore propose the Transcriptome-Wide Root Causal Inference (TWRCI) algorithm that identifies root causal genes and their causal graph using a combination of genetic variant and unperturbed bulk RNA sequencing data. TWRCI uses a novel competitive regression procedure to annotate cis and trans-genetic variants to the gene expression levels they directly cause. The algorithm simultaneously recovers a causal ordering of the expression levels to pinpoint the underlying causal graph and estimate root causal effects. TWRCI outperforms alternative approaches across a diverse group of metrics by directly targeting root causal genes while accounting for distal relations, linkage disequilibrium, patient heterogeneity and widespread pleiotropy. We demonstrate the algorithm by uncovering the root causal mechanisms of two complex diseases, which we confirm by replication using independent genome-wide summary statistics.
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