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Using Gaussian-Process Regression for Meta-Analytic Neuroimaging Inference Based on Sparse Observations

机译:基于稀疏观测值的高斯过程回归进行元分析神经成像推断

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The purpose of neuroimaging meta-analysis is to localize the brain regions that are activated consistently in response to a certain intervention. As a commonly used technique, current coordinate-based meta-analyses (CBMA) of neuroimaging studies utilize relatively sparse information from published studies, typically only using (x,y,z) coordinates of the activation peaks. Such CBMA methods have several limitations. First, there is no way to jointly incorporate deactivation information when available, which has been shown to result in an inaccurate statistic image when assessing a difference contrast. Second, the scale of a kernel reflecting spatial uncertainty must be set without taking the effect size (e.g., Z-stat) into account. To address these problems, we employ Gaussian-process regression (GPR), explicitly estimating the unobserved statistic image given the sparse peak activation “coordinate” and “standardized effect-size estimate” data. In particular, our model allows estimation of effect size at each voxel, something existing CBMA methods cannot produce. Our results show that GPR outperforms existing CBMA techniques and is capable of more accurately reproducing the (usually unavailable) full-image analysis results.
机译:神经影像荟萃分析的目的是定位响应某些干预而一致激活的大脑区域。作为一种常用的技术,神经影像研究的当前基于坐标的荟萃分析(CBMA)利用来自已发表研究的相对稀疏的信息,通常仅使用激活峰的(x,y,z)坐标。这样的CBMA方法具有几个局限性。首先,没有办法在可用时共同合并停用信息,这已显示出在评估差异对比时会导致不准确的统计图像。其次,必须设置反映空间不确定性的核的尺度,而不必考虑效应大小(例如Z-stat)。为了解决这些问题,我们使用高斯过程回归(GPR),在稀疏峰激活“坐标”和“标准化效应量估计”数据的情况下,显式估计未观察到的统计图像。特别是,我们的模型允许估算每个体素的效果大小,而现有CBMA方法无法产生这种效果。我们的结果表明,GPR优于现有的CBMA技术,并且能够更准确地再现(通常不可用)全图像分析结果。

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