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An atlas of evidence-based phenotypic associations across the mouse phenome
To date, reliable relationships between mammalian phenotypes, based on diagnostic test measurements, have not been reported on a large scale. The purpose of this study was to present a large mouse phenotype-phenotype relationships dataset as a reference resource, alongside detailed evaluation of the...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7054260/ https://www.ncbi.nlm.nih.gov/pubmed/32127602 http://dx.doi.org/10.1038/s41598-020-60891-w |
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author | Tanaka, Nobuhiko Masuya, Hiroshi |
author_facet | Tanaka, Nobuhiko Masuya, Hiroshi |
author_sort | Tanaka, Nobuhiko |
collection | PubMed |
description | To date, reliable relationships between mammalian phenotypes, based on diagnostic test measurements, have not been reported on a large scale. The purpose of this study was to present a large mouse phenotype-phenotype relationships dataset as a reference resource, alongside detailed evaluation of the resource. We used bias-minimized comprehensive mouse phenotype data and applied association rule mining to a dataset consisting of only binary (normal and abnormal phenotypes) data to determine relationships among phenotypes. We present 3,686 evidence-based significant associations, comprising 345 phenotypes covering 60 biological systems (functions), and evaluate their characteristics in detail. To evaluate the relationships, we defined a set of phenotype-phenotype association pairs (PPAPs) as a module of phenotypic expression for each of the 345 phenotypes. By analyzing each PPAP, we identified phenotype sub-networks consisting of the largest numbers of phenotypes and distinct biological systems. Furthermore, using hierarchical clustering based on phenotype similarities among the 345 PPAPs, we identified seven community types within a putative phenome-wide association network. Moreover, to promote leverage of these data, we developed and published web-application tools. These mouse phenome-wide phenotype-phenotype association data reveal general principles of relationships among mammalian phenotypes and provide a reference resource for biomedical analyses. |
format | Online Article Text |
id | pubmed-7054260 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70542602020-03-11 An atlas of evidence-based phenotypic associations across the mouse phenome Tanaka, Nobuhiko Masuya, Hiroshi Sci Rep Article To date, reliable relationships between mammalian phenotypes, based on diagnostic test measurements, have not been reported on a large scale. The purpose of this study was to present a large mouse phenotype-phenotype relationships dataset as a reference resource, alongside detailed evaluation of the resource. We used bias-minimized comprehensive mouse phenotype data and applied association rule mining to a dataset consisting of only binary (normal and abnormal phenotypes) data to determine relationships among phenotypes. We present 3,686 evidence-based significant associations, comprising 345 phenotypes covering 60 biological systems (functions), and evaluate their characteristics in detail. To evaluate the relationships, we defined a set of phenotype-phenotype association pairs (PPAPs) as a module of phenotypic expression for each of the 345 phenotypes. By analyzing each PPAP, we identified phenotype sub-networks consisting of the largest numbers of phenotypes and distinct biological systems. Furthermore, using hierarchical clustering based on phenotype similarities among the 345 PPAPs, we identified seven community types within a putative phenome-wide association network. Moreover, to promote leverage of these data, we developed and published web-application tools. These mouse phenome-wide phenotype-phenotype association data reveal general principles of relationships among mammalian phenotypes and provide a reference resource for biomedical analyses. Nature Publishing Group UK 2020-03-03 /pmc/articles/PMC7054260/ /pubmed/32127602 http://dx.doi.org/10.1038/s41598-020-60891-w Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Tanaka, Nobuhiko Masuya, Hiroshi An atlas of evidence-based phenotypic associations across the mouse phenome |
title | An atlas of evidence-based phenotypic associations across the mouse phenome |
title_full | An atlas of evidence-based phenotypic associations across the mouse phenome |
title_fullStr | An atlas of evidence-based phenotypic associations across the mouse phenome |
title_full_unstemmed | An atlas of evidence-based phenotypic associations across the mouse phenome |
title_short | An atlas of evidence-based phenotypic associations across the mouse phenome |
title_sort | atlas of evidence-based phenotypic associations across the mouse phenome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7054260/ https://www.ncbi.nlm.nih.gov/pubmed/32127602 http://dx.doi.org/10.1038/s41598-020-60891-w |
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