<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kim M</submitter><funding>NSF</funding><funding>NIBIB NIH HHS</funding><funding>NIA NIH HHS</funding><funding>NIA</funding><funding>NIMH NIH HHS</funding><funding>National Research Foundation of Korea</funding><funding>National Institutes of Health</funding><funding>NIBIB</funding><funding>NLM</funding><funding>McDonnell Center for Systems Neuroscience</funding><funding>NIH Blueprint for Neuroscience Research</funding><funding>NLM NIH HHS</funding><funding>NIH HHS</funding><funding>National Science Foundation</funding><pagination>102297</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8792314</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>76</volume><pubmed_abstract>The advances in technologies for acquiring brain imaging and high-throughput genetic data allow the researcher to access a large amount of multi-modal data. Although the sparse canonical correlation analysis is a powerful bi-multivariate association analysis technique for feature selection, we are still facing major challenges in integrating multi-modal imaging genetic data and yielding biologically meaningful interpretation of imaging genetic findings. In this study, we propose a novel multi-task learning based structured sparse canonical correlation analysis (MTS2CCA) to deliver interpretable results and improve integration in imaging genetics studies. We perform comparative studies with state-of-the-art competing methods on both simulation and real imaging genetic data. On the simulatio</pubmed_abstract><journal>Medical image analysis</journal><pubmed_title>Multi-task learning based structured sparse canonical correlation analysis for brain imaging genetics.</pubmed_title><pmcid>PMC8792314</pmcid><funding_grant_id>S10 OD023495</funding_grant_id><funding_grant_id>RF1 AG063481</funding_grant_id><funding_grant_id>IIS 1837964</funding_grant_id><funding_grant_id>U01 AG068057</funding_grant_id><funding_grant_id>R01 LM013463</funding_grant_id><funding_grant_id>U54 MH091657</funding_grant_id><funding_grant_id>R01 EB022574</funding_grant_id><funding_grant_id>R01 AG058854</funding_grant_id><funding_grant_id>NRF-2020R1A6A3A03038525</funding_grant_id><pubmed_authors>Saykin AJ</pubmed_authors><pubmed_authors>Shen L</pubmed_authors><pubmed_authors>Moore JH</pubmed_authors><pubmed_authors>Liu K</pubmed_authors><pubmed_authors>Yan J</pubmed_authors><pubmed_authors>Min EJ</pubmed_authors><pubmed_authors>Long Q</pubmed_authors><pubmed_authors>Kim M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Multi-task learning based structured sparse canonical correlation analysis for brain imaging genetics.</name><description>The advances in technologies for acquiring brain imaging and high-throughput genetic data allow the researcher to access a large amount of multi-modal data. Although the sparse canonical correlation analysis is a powerful bi-multivariate association analysis technique for feature selection, we are still facing major challenges in integrating multi-modal imaging genetic data and yielding biologically meaningful interpretation of imaging genetic findings. In this study, we propose a novel multi-task learning based structured sparse canonical correlation analysis (MTS2CCA) to deliver interpretable results and improve integration in imaging genetics studies. We perform comparative studies with state-of-the-art competing methods on both simulation and real imaging genetic data. On the simulatio</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Feb</publication><modification>2026-04-08T10:46:05.525Z</modification><creation>2025-04-21T15:51:45.081Z</creation></dates><accession>S-EPMC8792314</accession><cross_references><pubmed>34871929</pubmed><doi>10.1016/j.media.2021.102297</doi></cross_references></HashMap>