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Browsing by Subject "Canonical correlation analysis"
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Item Identification of discriminative imaging proteomics associations in Alzheimer's Disease via a novel sparse correlation model(World Scientific, 2016-12) Yan, Jingwen; Risacher, Shannon L.; Nho, Kwangsik; Saykin, Andrew J.; Shen, Li; Department of Biohealth Informatics, School of Informatics and ComputingBrain imaging and protein expression, from both cerebrospinal fluid and blood plasma, have been found to provide complementary information in predicting the clinical outcomes of Alzheimer's disease (AD). But the underlying associations that contribute to such a complementary relationship have not been previously studied yet. In this work, we will perform an imaging proteomics association analysis to explore how they are related with each other. While traditional association models, such as Sparse Canonical Correlation Analysis (SCCA), can not guarantee the selection of only disease-relevant biomarkers and associations, we propose a novel discriminative SCCA (denoted as DSCCA) model with new penalty terms to account for the disease status information. Given brain imaging, proteomic and diagnostic data, the proposed model can perform a joint association and multi-class discrimination analysis, such that we can not only identify disease-relevant multimodal biomarkers, but also reveal strong associations between them. Based on a real imaging proteomic data set, the empirical results show that DSCCA and traditional SCCA have comparable association performances. But in a further classification analysis, canonical variables of imaging and proteomic data obtained in DSCCA demonstrate much more discrimination power toward multiple pairs of diagnosis groups than those obtained in SCCA.Item Structured sparse CCA for brain imaging genetics via graph OSCAR(Biomed Central, 2016) Du, Lei; Huang, Heng; Yan, Jingwen; Kim, Sungeun; Risacher, Shannon; Inlow, Mark; Moore, Jason; Saykin, Andrew J.; Shen, Li; Department of Radiology and Imaging Sciences, IU School of MedicineRecently, structured sparse canonical correlation analysis (SCCA) has received increased attention in brain imaging genetics studies. It can identify bi-multivariate imaging genetic associations as well as select relevant features with desired structure information. These SCCA methods either use the fused lasso regularizer to induce the smoothness between ordered features, or use the signed pairwise difference which is dependent on the estimated sign of sample correlation. Besides, several other structured SCCA models use the group lasso or graph fused lasso to encourage group structure, but they require the structure/group information provided in advance which sometimes is not available.