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NSPA: characterizing the disease association of multiple genetic interactions at single-subject resolution

MOTIVATION: The interaction between genetic variables is one of the major barriers to characterizing the genetic architecture of complex traits. To consider epistasis, network science approaches are increasingly being used in research to elucidate the genetic architecture of complex diseases. Networ...

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Detalles Bibliográficos
Autores principales: Sha, Zhendong, Chen, Yuanzhu, Hu, Ting
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9927570/
https://www.ncbi.nlm.nih.gov/pubmed/36818729
http://dx.doi.org/10.1093/bioadv/vbad010
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author Sha, Zhendong
Chen, Yuanzhu
Hu, Ting
author_facet Sha, Zhendong
Chen, Yuanzhu
Hu, Ting
author_sort Sha, Zhendong
collection PubMed
description MOTIVATION: The interaction between genetic variables is one of the major barriers to characterizing the genetic architecture of complex traits. To consider epistasis, network science approaches are increasingly being used in research to elucidate the genetic architecture of complex diseases. Network science approaches associate genetic variables’ disease susceptibility to their topological importance in the network. However, this network only represents genetic interactions and does not describe how these interactions attribute to disease association at the subject-scale. We propose the Network-based Subject Portrait Approach (NSPA) and an accompanying feature transformation method to determine the collective risk impact of multiple genetic interactions for each subject. RESULTS: The feature transformation method converts genetic variants of subjects into new values that capture how genetic variables interact with others to attribute to a subject’s disease association. We apply this approach to synthetic and genetic datasets and learn that (1) the disease association can be captured using multiple disjoint sets of genetic interactions and (2) the feature transformation method based on NSPA improves predictive performance comparing with using the original genetic variables. Our findings confirm the role of genetic interaction in complex disease and provide a novel approach for gene–disease association studies to identify genetic architecture in the context of epistasis. AVAILABILITY AND IMPLEMENTATION: The codes of NSPA are now available in: https://github.com/MIB-Lab/Network-based-Subject-Portrait-Approach CONTACT: ting.hu@queensu.ca SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics Advances online.
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spelling pubmed-99275702023-02-16 NSPA: characterizing the disease association of multiple genetic interactions at single-subject resolution Sha, Zhendong Chen, Yuanzhu Hu, Ting Bioinform Adv Original Paper MOTIVATION: The interaction between genetic variables is one of the major barriers to characterizing the genetic architecture of complex traits. To consider epistasis, network science approaches are increasingly being used in research to elucidate the genetic architecture of complex diseases. Network science approaches associate genetic variables’ disease susceptibility to their topological importance in the network. However, this network only represents genetic interactions and does not describe how these interactions attribute to disease association at the subject-scale. We propose the Network-based Subject Portrait Approach (NSPA) and an accompanying feature transformation method to determine the collective risk impact of multiple genetic interactions for each subject. RESULTS: The feature transformation method converts genetic variants of subjects into new values that capture how genetic variables interact with others to attribute to a subject’s disease association. We apply this approach to synthetic and genetic datasets and learn that (1) the disease association can be captured using multiple disjoint sets of genetic interactions and (2) the feature transformation method based on NSPA improves predictive performance comparing with using the original genetic variables. Our findings confirm the role of genetic interaction in complex disease and provide a novel approach for gene–disease association studies to identify genetic architecture in the context of epistasis. AVAILABILITY AND IMPLEMENTATION: The codes of NSPA are now available in: https://github.com/MIB-Lab/Network-based-Subject-Portrait-Approach CONTACT: ting.hu@queensu.ca SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics Advances online. Oxford University Press 2023-02-07 /pmc/articles/PMC9927570/ /pubmed/36818729 http://dx.doi.org/10.1093/bioadv/vbad010 Text en © The Author(s) 2023. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Paper
Sha, Zhendong
Chen, Yuanzhu
Hu, Ting
NSPA: characterizing the disease association of multiple genetic interactions at single-subject resolution
title NSPA: characterizing the disease association of multiple genetic interactions at single-subject resolution
title_full NSPA: characterizing the disease association of multiple genetic interactions at single-subject resolution
title_fullStr NSPA: characterizing the disease association of multiple genetic interactions at single-subject resolution
title_full_unstemmed NSPA: characterizing the disease association of multiple genetic interactions at single-subject resolution
title_short NSPA: characterizing the disease association of multiple genetic interactions at single-subject resolution
title_sort nspa: characterizing the disease association of multiple genetic interactions at single-subject resolution
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9927570/
https://www.ncbi.nlm.nih.gov/pubmed/36818729
http://dx.doi.org/10.1093/bioadv/vbad010
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