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Connectome-scale group-wise consistent resting-state network analysis in autism spectrum disorder
Understanding the organizational architecture of human brain function and its alteration patterns in diseased brains such as Autism Spectrum Disorder (ASD) patients are of great interests. In-vivo functional magnetic resonance imaging (fMRI) offers a unique window to investigate the mechanism of bra...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4916065/ https://www.ncbi.nlm.nih.gov/pubmed/27358766 http://dx.doi.org/10.1016/j.nicl.2016.06.004 |
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author | Zhao, Yu Chen, Hanbo Li, Yujie Lv, Jinglei Jiang, Xi Ge, Fangfei Zhang, Tuo Zhang, Shu Ge, Bao Lyu, Cheng Zhao, Shijie Han, Junwei Guo, Lei Liu, Tianming |
author_facet | Zhao, Yu Chen, Hanbo Li, Yujie Lv, Jinglei Jiang, Xi Ge, Fangfei Zhang, Tuo Zhang, Shu Ge, Bao Lyu, Cheng Zhao, Shijie Han, Junwei Guo, Lei Liu, Tianming |
author_sort | Zhao, Yu |
collection | PubMed |
description | Understanding the organizational architecture of human brain function and its alteration patterns in diseased brains such as Autism Spectrum Disorder (ASD) patients are of great interests. In-vivo functional magnetic resonance imaging (fMRI) offers a unique window to investigate the mechanism of brain function and to identify functional network components of the human brain. Previously, we have shown that multiple concurrent functional networks can be derived from fMRI signals using whole-brain sparse representation. Yet it is still an open question to derive group-wise consistent networks featured in ASD patients and controls. Here we proposed an effective volumetric network descriptor, named connectivity map, to compactly describe spatial patterns of brain network maps and implemented a fast framework in Apache Spark environment that can effectively identify group-wise consistent networks in big fMRI dataset. Our experiment results identified 144 group-wisely common intrinsic connectivity networks (ICNs) shared between ASD patients and healthy control subjects, where some ICNs are substantially different between the two groups. Moreover, further analysis on the functional connectivity and spatial overlap between these 144 common ICNs reveals connectomics signatures characterizing ASD patients and controls. In particular, the computing time of our Spark-enabled functional connectomics framework is significantly reduced from 240 hours (C ++ code, single core) to 20 hours, exhibiting a great potential to handle fMRI big data in the future. |
format | Online Article Text |
id | pubmed-4916065 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-49160652016-06-29 Connectome-scale group-wise consistent resting-state network analysis in autism spectrum disorder Zhao, Yu Chen, Hanbo Li, Yujie Lv, Jinglei Jiang, Xi Ge, Fangfei Zhang, Tuo Zhang, Shu Ge, Bao Lyu, Cheng Zhao, Shijie Han, Junwei Guo, Lei Liu, Tianming Neuroimage Clin Regular Article Understanding the organizational architecture of human brain function and its alteration patterns in diseased brains such as Autism Spectrum Disorder (ASD) patients are of great interests. In-vivo functional magnetic resonance imaging (fMRI) offers a unique window to investigate the mechanism of brain function and to identify functional network components of the human brain. Previously, we have shown that multiple concurrent functional networks can be derived from fMRI signals using whole-brain sparse representation. Yet it is still an open question to derive group-wise consistent networks featured in ASD patients and controls. Here we proposed an effective volumetric network descriptor, named connectivity map, to compactly describe spatial patterns of brain network maps and implemented a fast framework in Apache Spark environment that can effectively identify group-wise consistent networks in big fMRI dataset. Our experiment results identified 144 group-wisely common intrinsic connectivity networks (ICNs) shared between ASD patients and healthy control subjects, where some ICNs are substantially different between the two groups. Moreover, further analysis on the functional connectivity and spatial overlap between these 144 common ICNs reveals connectomics signatures characterizing ASD patients and controls. In particular, the computing time of our Spark-enabled functional connectomics framework is significantly reduced from 240 hours (C ++ code, single core) to 20 hours, exhibiting a great potential to handle fMRI big data in the future. Elsevier 2016-06-07 /pmc/articles/PMC4916065/ /pubmed/27358766 http://dx.doi.org/10.1016/j.nicl.2016.06.004 Text en © 2016 Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Regular Article Zhao, Yu Chen, Hanbo Li, Yujie Lv, Jinglei Jiang, Xi Ge, Fangfei Zhang, Tuo Zhang, Shu Ge, Bao Lyu, Cheng Zhao, Shijie Han, Junwei Guo, Lei Liu, Tianming Connectome-scale group-wise consistent resting-state network analysis in autism spectrum disorder |
title | Connectome-scale group-wise consistent resting-state network analysis in autism spectrum disorder |
title_full | Connectome-scale group-wise consistent resting-state network analysis in autism spectrum disorder |
title_fullStr | Connectome-scale group-wise consistent resting-state network analysis in autism spectrum disorder |
title_full_unstemmed | Connectome-scale group-wise consistent resting-state network analysis in autism spectrum disorder |
title_short | Connectome-scale group-wise consistent resting-state network analysis in autism spectrum disorder |
title_sort | connectome-scale group-wise consistent resting-state network analysis in autism spectrum disorder |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4916065/ https://www.ncbi.nlm.nih.gov/pubmed/27358766 http://dx.doi.org/10.1016/j.nicl.2016.06.004 |
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