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Fused multi-modal similarity network as prior in guiding brain imaging genetic association
INTRODUCTION: Brain imaging genetics aims to explore the genetic architecture underlying brain structure and functions. Recent studies showed that the incorporation of prior knowledge, such as subject diagnosis information and brain regional correlation, can help identify significantly stronger imag...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10196480/ https://www.ncbi.nlm.nih.gov/pubmed/37215688 http://dx.doi.org/10.3389/fdata.2023.1151893 |
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author | He, Bing Xie, Linhui Varathan, Pradeep Nho, Kwangsik Risacher, Shannon L. Saykin, Andrew J. Yan, Jingwen |
author_facet | He, Bing Xie, Linhui Varathan, Pradeep Nho, Kwangsik Risacher, Shannon L. Saykin, Andrew J. Yan, Jingwen |
author_sort | He, Bing |
collection | PubMed |
description | INTRODUCTION: Brain imaging genetics aims to explore the genetic architecture underlying brain structure and functions. Recent studies showed that the incorporation of prior knowledge, such as subject diagnosis information and brain regional correlation, can help identify significantly stronger imaging genetic associations. However, sometimes such information may be incomplete or even unavailable. METHODS: In this study, we explore a new data-driven prior knowledge that captures the subject-level similarity by fusing multi-modal similarity networks. It was incorporated into the sparse canonical correlation analysis (SCCA) model, which is aimed to identify a small set of brain imaging and genetic markers that explain the similarity matrix supported by both modalities. It was applied to amyloid and tau imaging data of the ADNI cohort, respectively. RESULTS: Fused similarity matrix across imaging and genetic data was found to improve the association performance better or similarly well as diagnosis information, and therefore would be a potential substitute prior when the diagnosis information is not available (i.e., studies focused on healthy controls). DISCUSSION: Our result confirmed the value of all types of prior knowledge in improving association identification. In addition, the fused network representing the subject relationship supported by multi-modal data showed consistently the best or equally best performance compared to the diagnosis network and the co-expression network. |
format | Online Article Text |
id | pubmed-10196480 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101964802023-05-20 Fused multi-modal similarity network as prior in guiding brain imaging genetic association He, Bing Xie, Linhui Varathan, Pradeep Nho, Kwangsik Risacher, Shannon L. Saykin, Andrew J. Yan, Jingwen Front Big Data Big Data INTRODUCTION: Brain imaging genetics aims to explore the genetic architecture underlying brain structure and functions. Recent studies showed that the incorporation of prior knowledge, such as subject diagnosis information and brain regional correlation, can help identify significantly stronger imaging genetic associations. However, sometimes such information may be incomplete or even unavailable. METHODS: In this study, we explore a new data-driven prior knowledge that captures the subject-level similarity by fusing multi-modal similarity networks. It was incorporated into the sparse canonical correlation analysis (SCCA) model, which is aimed to identify a small set of brain imaging and genetic markers that explain the similarity matrix supported by both modalities. It was applied to amyloid and tau imaging data of the ADNI cohort, respectively. RESULTS: Fused similarity matrix across imaging and genetic data was found to improve the association performance better or similarly well as diagnosis information, and therefore would be a potential substitute prior when the diagnosis information is not available (i.e., studies focused on healthy controls). DISCUSSION: Our result confirmed the value of all types of prior knowledge in improving association identification. In addition, the fused network representing the subject relationship supported by multi-modal data showed consistently the best or equally best performance compared to the diagnosis network and the co-expression network. Frontiers Media S.A. 2023-05-05 /pmc/articles/PMC10196480/ /pubmed/37215688 http://dx.doi.org/10.3389/fdata.2023.1151893 Text en Copyright © 2023 He, Xie, Varathan, Nho, Risacher, Saykin, Yan and the Alzheimer's Disease Neuroimaging Initiative. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Big Data He, Bing Xie, Linhui Varathan, Pradeep Nho, Kwangsik Risacher, Shannon L. Saykin, Andrew J. Yan, Jingwen Fused multi-modal similarity network as prior in guiding brain imaging genetic association |
title | Fused multi-modal similarity network as prior in guiding brain imaging genetic association |
title_full | Fused multi-modal similarity network as prior in guiding brain imaging genetic association |
title_fullStr | Fused multi-modal similarity network as prior in guiding brain imaging genetic association |
title_full_unstemmed | Fused multi-modal similarity network as prior in guiding brain imaging genetic association |
title_short | Fused multi-modal similarity network as prior in guiding brain imaging genetic association |
title_sort | fused multi-modal similarity network as prior in guiding brain imaging genetic association |
topic | Big Data |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10196480/ https://www.ncbi.nlm.nih.gov/pubmed/37215688 http://dx.doi.org/10.3389/fdata.2023.1151893 |
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