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Variational group-PCA for intrinsic dimensionality determination in fMRI data

机译:fMRI数据中固有维数的变分组PCA

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Functional Magnetic Resonance Imaging (fMRI) is widely used to gain a better understanding of the human brain's functional organization. As fMRI data are high dimensional it is challenging to analyse using conventional methods thus low-rank approximations such as principal component analysis (PCA), and independent component analysis (ICA) is often applied as a preprocessing step before any additional analysis. Low-rank methods generally require that the rank or latent dimensionality is known beforehand. When this is not the case a range of plausible dimensionalities have to be tested and compared. Furthermore, in an fMRI-context it is not fully understood how information from multiple subjects should best be incorporated when applying dimensionality reduction. We propose a Bayesian group principal component analysis (Group-BPCA) model with an automatic relevance determination (ARD) prior to determine the number of active components supported by the data. All subjects share the same spatial maps (components), but the uncertainties on these maps as well as the noise is subject specific. We find an approximate solution using the mature variational Bayesian framework and develop a fast and scalable implementation using a graphical processing unit (GPU). We test the model on fMRI data from 29 healthy subjects performing a block-design fingertapping experiment. The model identified 10 active components. Neither variational Bayesian PCA on temporally concatenated data nor Group-BPCA, where uncertainties on the spatial maps are shared, leads to pruning components, but provide better generalization in two of three scenarios. We show that the right level of subject variability is highly dependent on the chosen validation scheme.
机译:功能磁共振成像(fMRI)被广泛用于更好地了解人脑的功能组织。由于fMRI数据是高维的,因此使用常规方法进行分析具有挑战性,因此在进行任何其他分析之前,通常将低阶近似法(例如主成分分析(PCA)和独立成分分析(ICA))用作预处理步骤。低等级方法通常要求等级或潜在维数事先已知。如果不是这种情况,则必须测试和比较一系列合理的尺寸。此外,在功能磁共振成像的背景下,当应用降维时,如何最好地结合来自多个受试者的信息尚不完全清楚。我们提出一种具有自动相关性确定(ARD)的贝叶斯组主成分分析(Group-BPCA)模型,然后再确定该数据支持的活动成分的数量。所有对象共享相同的空间图(组件),但是这些图上的不确定性以及噪声是特定于对象的。我们使用成熟的变分贝叶斯框架找到了一种近似解决方案,并使用图形处理单元(GPU)开发了一种快速且可扩展的实现。我们对来自29位健康受试者的fMRI数据进行了模型设计的敲击实验,测试了该模型。该模型确定了10个活动组件。时间连接数据上的变分贝叶斯PCA或Group-BPCA(共享空间图上的不确定性)都不会导致修剪分量,但在三种情况中的两种情况下都无法提供更好的概括性。我们显示正确的主题可变性水平高度依赖于所选的验证方案。

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