Medical Scientist Training Program, Vanderbilt University, Nashville, TN, USA.
Vanderbilt Genetics Institute, Vanderbilt University Medical Center, Nashville, TN, USA.
BMC Bioinformatics. 2024 Oct 8;25(1):325. doi: 10.1186/s12859-024-05936-x.
We present the NeuroimaGene resource as an R package designed to assist researchers in identifying genes and neurologic features relevant to psychiatric and neurological health. While recent studies have identified hundreds of genes as potential components of pathophysiology in neurologic and psychiatric disease, interpreting the physiological consequences of this variation is challenging. The integration of neuroimaging data with molecular findings is a step toward addressing this challenge. In addition to sharing associations with both molecular variation and clinical phenotypes, neuroimaging features are intrinsically informative of cognitive processes. NeuroimaGene provides a tool to understand how disease-associated genes relate to the intermediate structure of the brain.
We created NeuroimaGene, a user-friendly, open access R package now available for public use. Its primary function is to identify neuroimaging derived brain features that are impacted by genetically regulated expression of user-provided genes or gene sets. This resource can be used to (1) characterize individual genes or gene sets as relevant to the structure and function of the brain, (2) identify the region(s) of the brain or body in which expression of target gene(s) is neurologically relevant, (3) impute the brain features most impacted by user-defined gene sets such as those produced by cohort level gene association studies, and (4) generate publication level, modifiable visual plots of significant findings. We demonstrate the utility of the resource by identifying neurologic correlates of stroke-associated genes derived from pre-existing analyses.
Integrating neurologic data as an intermediate phenotype in the pathway from genes to brain-based diagnostic phenotypes increases the interpretability of molecular studies and enriches our understanding of disease pathophysiology. The NeuroimaGene R package is designed to assist in this process and is publicly available for use.
我们提出了 NeuroimaGene 资源,它是一个 R 包,旨在帮助研究人员识别与精神和神经健康相关的基因和神经特征。虽然最近的研究已经确定了数百个基因作为神经和精神疾病病理生理学的潜在组成部分,但解释这种变异的生理后果具有挑战性。将神经影像学数据与分子发现相结合是解决这一挑战的一步。除了与分子变异和临床表型共享关联外,神经影像学特征还可以提供关于认知过程的内在信息。NeuroimaGene 提供了一种工具,可以了解疾病相关基因与大脑中间结构的关系。
我们创建了 NeuroimaGene,这是一个用户友好的、开放获取的 R 包,现在可供公众使用。它的主要功能是识别受基因调控表达的用户提供的基因或基因集影响的神经影像学衍生的大脑特征。该资源可用于:(1)描述与大脑结构和功能相关的个体基因或基因集;(2)识别目标基因表达在其中具有神经相关性的大脑区域或身体区域;(3)推断受用户定义的基因集(例如,由队列水平基因关联研究产生的基因集)影响最大的大脑特征;(4)生成具有出版物水平的、可修改的显著发现的可视化图形。我们通过识别来自先前分析的与中风相关基因的神经相关性,展示了该资源的实用性。
将神经数据作为从基因到基于大脑的诊断表型的途径中的中间表型进行整合,可以提高分子研究的可解释性,并丰富我们对疾病病理生理学的理解。NeuroimaGene R 包旨在协助这一过程,并且可供公众使用。