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Multi-source feature learning for joint analysis of incomplete multiple heterogeneous neuroimaging data

机译:联合分析不完整的多个异质神经影像数据的多源特征学习

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Analysis of incomplete data is a big challenge when integrating large-scale brain imaging datasets from different imaging modalities. In the Alzheimer's Disease Neuroimaging Initiative (ADNI), for example, over half of the subjects lack cerebrospinal fluid (CSF) measurements; an independent half of the subjects do not have fluorodeoxyglucose positron emission tomography (FDG-PET) scans; many lack proteomics measurements. Traditionally, subjects with missing measures are discarded, resulting in a severe loss of available information. In this paper, we address this problem by proposing an incomplete Multi-Source Feature (iMSF) learning method where all the samples (with at least one available data source) can be used. To illustrate the proposed approach, we classify patients from the ADNI study into groups with Alzheimer's disease (AD), mild cognitive impairment (MCI) and normal controls, based on the multi-modality data. At baseline, ADNI's 780 participants (172. AD, 397 MCI, 211 NC), have at least one of four data types: magnetic resonance imaging (MRI), FDG-PET, CSF and proteomics. These data are used to test our algorithm. Depending on the problem being solved, we divide our samples according to the availability of data sources, and we learn shared sets of features with state-of-the-art sparse learning methods. To build a practical and robust system, we construct a classifier ensemble by combining our method with four other methods for missing value estimation. Comprehensive experiments with various parameters show that our proposed iMSF method and the ensemble model yield stable and promising results.
机译:当整合来自不同成像方式的大规模脑成像数据集时,不完整数据的分析是一个巨大的挑战。例如,在阿尔茨海默氏病神经影像学倡议(ADNI)中,超过一半的受试者缺乏脑脊液(CSF)测量;独立的一半受试者没有进行氟脱氧葡萄糖正电子发射断层扫描(FDG-PET)扫描;许多人缺乏蛋白质组学测量。传统上,缺少措施的对象将被丢弃,从而导致大量可用信息丢失。在本文中,我们通过提出一种不完整的多源特征(iMSF)学习方法来解决此问题,该方法可以使用所有样本(至少有一个可用的数据源)。为了说明所提出的方法,我们根据多模态数据将来自ADNI研究的患者分为阿尔茨海默氏病(AD),轻度认知障碍(MCI)和正常对照的组。在基线时,ADNI的780名参与者(172. AD,397 MCI,211 NC)至少具有以下四种数据类型之一:磁共振成像(MRI),FDG-PET,CSF和蛋白质组学。这些数据用于测试我们的算法。根据要解决的问题,我们根据数据源的可用性对样本进行划分,并使用最新的稀疏学习方法学习功能的共享集。为了构建一个实用且健壮的系统,我们通过将我们的方法与其他四种用于估计缺失值的方法相结合来构建分类器集合。综合各种参数的实验表明,我们提出的iMSF方法和集成模型产生了稳定而有希望的结果。

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