Tissue-specific network-based genome wide study of amygdala imaging phenotypes to identify functional interaction modules
dc.contributor.author | Yao, Xiaohui | |
dc.contributor.author | Yan, Jingwen | |
dc.contributor.author | Liu, Kefei | |
dc.contributor.author | Kim, Sungeun | |
dc.contributor.author | Nho, Kwangsik | |
dc.contributor.author | Risacher, Shannon L. | |
dc.contributor.author | Greene, Casey S. | |
dc.contributor.author | Moore, Jason H. | |
dc.contributor.author | Saykin, Andrew J. | |
dc.contributor.author | Shen, Li | |
dc.contributor.author | Alzheimer’s Disease Neuroimaging Initiative | |
dc.contributor.department | BioHealth Informatics, School of Informatics and Computing | en_US |
dc.date.accessioned | 2019-08-15T14:19:10Z | |
dc.date.available | 2019-08-15T14:19:10Z | |
dc.date.issued | 2017-10-15 | |
dc.description.abstract | Motivation: Network-based genome-wide association studies (GWAS) aim to identify functional modules from biological networks that are enriched by top GWAS findings. Although gene functions are relevant to tissue context, most existing methods analyze tissue-free networks without reflecting phenotypic specificity. Results: We propose a novel module identification framework for imaging genetic studies using the tissue-specific functional interaction network. Our method includes three steps: (i) re-prioritize imaging GWAS findings by applying machine learning methods to incorporate network topological information and enhance the connectivity among top genes; (ii) detect densely connected modules based on interactions among top re-prioritized genes; and (iii) identify phenotype-relevant modules enriched by top GWAS findings. We demonstrate our method on the GWAS of [18F]FDG-PET measures in the amygdala region using the imaging genetic data from the Alzheimer's Disease Neuroimaging Initiative, and map the GWAS results onto the amygdala-specific functional interaction network. The proposed network-based GWAS method can effectively detect densely connected modules enriched by top GWAS findings. Tissue-specific functional network can provide precise context to help explore the collective effects of genes with biologically meaningful interactions specific to the studied phenotype. | en_US |
dc.eprint.version | Final published version | en_US |
dc.identifier.citation | Yao, X., Yan, J., Liu, K., Kim, S., Nho, K., Risacher, S. L., … Alzheimer’s Disease Neuroimaging Initiative (2017). Tissue-specific network-based genome wide study of amygdala imaging phenotypes to identify functional interaction modules. Bioinformatics (Oxford, England), 33(20), 3250–3257. doi:10.1093/bioinformatics/btx344 | en_US |
dc.identifier.uri | https://hdl.handle.net/1805/20370 | |
dc.language.iso | en_US | en_US |
dc.publisher | Oxford University Press | en_US |
dc.relation.isversionof | 10.1093/bioinformatics/btx344 | en_US |
dc.relation.journal | Bioinformatics | en_US |
dc.rights | Publisher Policy | en_US |
dc.source | PMC | en_US |
dc.subject | Aged, 80 and over | en_US |
dc.subject | Alzheimer Disease | en_US |
dc.subject | Amygdala | en_US |
dc.subject | Computational Biology | en_US |
dc.subject | Genetic Predisposition to Disease | en_US |
dc.subject | Genome-Wide Association Study | en_US |
dc.subject | Machine Learning | en_US |
dc.subject | Middle Aged | en_US |
dc.subject | Male | en_US |
dc.subject | Phenotype | en_US |
dc.subject | Polymorphism, Genetic | en_US |
dc.subject | Positron Emission Tomography | en_US |
dc.subject | Software | en_US |
dc.title | Tissue-specific network-based genome wide study of amygdala imaging phenotypes to identify functional interaction modules | en_US |
dc.type | Article | en_US |
ul.alternative.fulltext | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6410887/ | en_US |