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Interpretive JIVE: Connections with CCA and an application to brain connectivity

Joint and Individual Variation Explained (JIVE) is a model that decomposes multiple datasets obtained on the same subjects into shared structure, structure unique to each dataset, and noise. JIVE is an important tool for multimodal data integration in neuroimaging. The two most common algorithms are...

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Autores principales: Murden, Raphiel J., Zhang, Zhengwu, Guo, Ying, Risk, Benjamin B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9614436/
https://www.ncbi.nlm.nih.gov/pubmed/36312020
http://dx.doi.org/10.3389/fnins.2022.969510
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author Murden, Raphiel J.
Zhang, Zhengwu
Guo, Ying
Risk, Benjamin B.
author_facet Murden, Raphiel J.
Zhang, Zhengwu
Guo, Ying
Risk, Benjamin B.
author_sort Murden, Raphiel J.
collection PubMed
description Joint and Individual Variation Explained (JIVE) is a model that decomposes multiple datasets obtained on the same subjects into shared structure, structure unique to each dataset, and noise. JIVE is an important tool for multimodal data integration in neuroimaging. The two most common algorithms are R.JIVE, an iterative approach, and AJIVE, which uses principal angle analysis. The joint structure in JIVE is defined by shared subspaces, but interpreting these subspaces can be challenging. In this paper, we reinterpret AJIVE as a canonical correlation analysis of principal component scores. This reformulation, which we call CJIVE, (1) provides an intuitive view of AJIVE; (2) uses a permutation test for the number of joint components; (3) can be used to predict subject scores for out-of-sample observations; and (4) is computationally fast. We conduct simulation studies that show CJIVE and AJIVE are accurate when the total signal ranks are correctly specified but, generally inaccurate when the total ranks are too large. CJIVE and AJIVE can still extract joint signal even when the joint signal variance is relatively small. JIVE methods are applied to integrate functional connectivity (resting-state fMRI) and structural connectivity (diffusion MRI) from the Human Connectome Project. Surprisingly, the edges with largest loadings in the joint component in functional connectivity do not coincide with the same edges in the structural connectivity, indicating more complex patterns than assumed in spatial priors. Using these loadings, we accurately predict joint subject scores in new participants. We also find joint scores are associated with fluid intelligence, highlighting the potential for JIVE to reveal important shared structure.
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spelling pubmed-96144362022-10-29 Interpretive JIVE: Connections with CCA and an application to brain connectivity Murden, Raphiel J. Zhang, Zhengwu Guo, Ying Risk, Benjamin B. Front Neurosci Neuroscience Joint and Individual Variation Explained (JIVE) is a model that decomposes multiple datasets obtained on the same subjects into shared structure, structure unique to each dataset, and noise. JIVE is an important tool for multimodal data integration in neuroimaging. The two most common algorithms are R.JIVE, an iterative approach, and AJIVE, which uses principal angle analysis. The joint structure in JIVE is defined by shared subspaces, but interpreting these subspaces can be challenging. In this paper, we reinterpret AJIVE as a canonical correlation analysis of principal component scores. This reformulation, which we call CJIVE, (1) provides an intuitive view of AJIVE; (2) uses a permutation test for the number of joint components; (3) can be used to predict subject scores for out-of-sample observations; and (4) is computationally fast. We conduct simulation studies that show CJIVE and AJIVE are accurate when the total signal ranks are correctly specified but, generally inaccurate when the total ranks are too large. CJIVE and AJIVE can still extract joint signal even when the joint signal variance is relatively small. JIVE methods are applied to integrate functional connectivity (resting-state fMRI) and structural connectivity (diffusion MRI) from the Human Connectome Project. Surprisingly, the edges with largest loadings in the joint component in functional connectivity do not coincide with the same edges in the structural connectivity, indicating more complex patterns than assumed in spatial priors. Using these loadings, we accurately predict joint subject scores in new participants. We also find joint scores are associated with fluid intelligence, highlighting the potential for JIVE to reveal important shared structure. Frontiers Media S.A. 2022-10-14 /pmc/articles/PMC9614436/ /pubmed/36312020 http://dx.doi.org/10.3389/fnins.2022.969510 Text en Copyright © 2022 Murden, Zhang, Guo and Risk. 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 Neuroscience
Murden, Raphiel J.
Zhang, Zhengwu
Guo, Ying
Risk, Benjamin B.
Interpretive JIVE: Connections with CCA and an application to brain connectivity
title Interpretive JIVE: Connections with CCA and an application to brain connectivity
title_full Interpretive JIVE: Connections with CCA and an application to brain connectivity
title_fullStr Interpretive JIVE: Connections with CCA and an application to brain connectivity
title_full_unstemmed Interpretive JIVE: Connections with CCA and an application to brain connectivity
title_short Interpretive JIVE: Connections with CCA and an application to brain connectivity
title_sort interpretive jive: connections with cca and an application to brain connectivity
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9614436/
https://www.ncbi.nlm.nih.gov/pubmed/36312020
http://dx.doi.org/10.3389/fnins.2022.969510
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