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Integration of multiple genomic imaging data for the study of schizophrenia using joint nonnegative matrix factorization

机译:使用联合非负矩阵分解法整合多个基因组成像数据以研究精神分裂症

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Schizophrenia (SZ) is a complex disease caused by a lot genetic variants, epigenetic and brain region abnormalities. In this study, we adopted a joint nonnegative matrix factorization method to integrate three datasets including single nucleotide polymorphism (SNP), brain activity measured by functional magnetic resonance imaging (fMRI) and DNA Methylation to identify multi-dimensional modules associated with SZ. They are then used to study the coordination between regulatory mechanisms at multiple levels. This method projects multiple types of data onto a common feature space, in which heterogeneous variables with large coefficients on the same projected bases form a multi-dimensional module. The genomic factors in such modules have significant correlations and likely functional associations with brain activities. We applied this method to the real data analysis and identified multi-dimensional modules including SNP, fMRI and DNA methylation sites. These selected biomarkers were finally used to identify genes and voxels, which were confirmed to be significantly associated with SZ.
机译:精神分裂症(SZ)是由许多遗传变异,表观遗传和大脑区域异常引起的复杂疾病。在这项研究中,我们采用联合非负矩阵分解方法来整合三个数据集,包括单核苷酸多态性(SNP),通过功能磁共振成像(fMRI)和DNA甲基化测量的大脑活动,以识别与SZ相关的多维模块。然后将它们用于研究多个级别的监管机制之间的协调。该方法将多种类型的数据投影到一个公共特征空间中,在该特征空间中,在相同投影基上具有大系数的异类变量形成一个多维模块。此类模块中的基因组因素与脑部活动具有显着的相关性,并且可能与功能相关。我们将此方法应用于实际数据分析,并确定了包括SNP,fMRI和DNA甲基化位点在内的多维模块。这些选择的生物标记物最终被用于鉴定基因和体素,这些基因和体素被证实与SZ显着相关。

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