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首页> 外文期刊>NeuroImage >Multi-site genetic analysis of diffusion images and voxelwise heritability analysis: A pilot project of the ENIGMA-DTI working group
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Multi-site genetic analysis of diffusion images and voxelwise heritability analysis: A pilot project of the ENIGMA-DTI working group

机译:扩散图像的多站点遗传分析和体素遗传分析:ENIGMA-DTI工作组的试点项目

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摘要

The ENIGMA (Enhancing NeuroImaging Genetics through Meta-Analysis) Consortium was set up to analyze brain measures and genotypes from multiple sites across the world to improve the power to detect genetic variants that influence the brain. Diffusion tensor imaging (DTI) yields quantitative measures sensitive to brain development and degeneration, and some common genetic variants may be associated with white matter integrity or connectivity. DTI measures, such as the fractional anisotropy (FA) of water diffusion, may be useful for identifying genetic variants that influence brain microstructure. However, genome-wide association studies (GWAS) require large populations to obtain sufficient power to detect and replicate significant effects, motivating a multi-site consortium effort. As part of an ENIGMA-DTI working group, we analyzed high-resolution FA images from multiple imaging sites across North America, Australia, and Europe, to address the challenge of harmonizing imaging data collected at multiple sites. Four hundred images of healthy adults aged 18-85 from four sites were used to create a template and corresponding skeletonized FA image as a common reference space. Using twin and pedigree samples of different ethnicities, we used our common template to evaluate the heritability of tract-derived FA measures. We show that our template is reliable for integrating multiple datasets by combining results through meta-analysis and unifying the data through exploratory mega-analyses. Our results may help prioritize regions of the FA map that are consistently influenced by additive genetic factors for future genetic discovery studies. Protocols and templates are publicly available at (http://enigma.loni.ucla.edu/ongoing/dti-working-group/).
机译:建立了ENIGMA(通过元分析来增强神经成像遗传学)联盟,以分析来自全球多个地点的大脑指标和基因型,以提高检测影响大脑的遗传变异的能力。扩散张量成像(DTI)产生对大脑发育和变性敏感的定量测量,并且一些常见的遗传变异可能与白质完整性或连通性有关。 DTI度量(例如水扩散的分数各向异性(FA))可能对识别影响大脑微结构的遗传变异有用。但是,全基因组关联研究(GWAS)需要大量的人口来获得足够的能力来检测和复制重大影响,从而推动多站点联合体的努力。作为ENIGMA-DTI工作组的一部分,我们分析了北美,澳大利亚和欧洲多个成像站点的高分辨率FA图像,以应对统一在多个站点收集的成像数据的挑战。使用来自四个地点的18岁至85岁健康成年人的400张图像来创建模板和相应的骨架化FA图像,作为共同的参考空间。通过使用不同种族的双胞胎和家谱样本,我们使用了通用模板来评估基于泳道的FA测量的遗传性。我们证明了我们的模板通过通过荟萃分析合并结果并通过探索性的大型分析统一数据来可靠地集成多个数据集。我们的研究结果可能有助于确定FA图的区域,这些区域始终受到附加遗传因素的影响,以便将来进行遗传发现研究。协议和模板可在(http://enigma.loni.ucla.edu/ongoing/dti-working-group/)上公开获得。

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