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HumanNet v3: an improved database of human gene networks for disease research
Network medicine has proven useful for dissecting genetic organization of complex human diseases. We have previously published HumanNet, an integrated network of human genes for disease studies. Since the release of the last version of HumanNet, many large-scale protein–protein interaction datasets...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8728227/ https://www.ncbi.nlm.nih.gov/pubmed/34747468 http://dx.doi.org/10.1093/nar/gkab1048 |
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author | Kim, Chan Yeong Baek, Seungbyn Cha, Junha Yang, Sunmo Kim, Eiru Marcotte, Edward M Hart, Traver Lee, Insuk |
author_facet | Kim, Chan Yeong Baek, Seungbyn Cha, Junha Yang, Sunmo Kim, Eiru Marcotte, Edward M Hart, Traver Lee, Insuk |
author_sort | Kim, Chan Yeong |
collection | PubMed |
description | Network medicine has proven useful for dissecting genetic organization of complex human diseases. We have previously published HumanNet, an integrated network of human genes for disease studies. Since the release of the last version of HumanNet, many large-scale protein–protein interaction datasets have accumulated in public depositories. Additionally, the numbers of research papers and functional annotations for gene–phenotype associations have increased significantly. Therefore, updating HumanNet is a timely task for further improvement of network-based research into diseases. Here, we present HumanNet v3 (https://www.inetbio.org/humannet/, covering 99.8% of human protein coding genes) constructed by means of the expanded data with improved network inference algorithms. HumanNet v3 supports a three-tier model: HumanNet-PI (a protein–protein physical interaction network), HumanNet-FN (a functional gene network), and HumanNet-XC (a functional network extended by co-citation). Users can select a suitable tier of HumanNet for their study purpose. We showed that on disease gene predictions, HumanNet v3 outperforms both the previous HumanNet version and other integrated human gene networks. Furthermore, we demonstrated that HumanNet provides a feasible approach for selecting host genes likely to be associated with COVID-19. |
format | Online Article Text |
id | pubmed-8728227 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-87282272022-01-05 HumanNet v3: an improved database of human gene networks for disease research Kim, Chan Yeong Baek, Seungbyn Cha, Junha Yang, Sunmo Kim, Eiru Marcotte, Edward M Hart, Traver Lee, Insuk Nucleic Acids Res Database Issue Network medicine has proven useful for dissecting genetic organization of complex human diseases. We have previously published HumanNet, an integrated network of human genes for disease studies. Since the release of the last version of HumanNet, many large-scale protein–protein interaction datasets have accumulated in public depositories. Additionally, the numbers of research papers and functional annotations for gene–phenotype associations have increased significantly. Therefore, updating HumanNet is a timely task for further improvement of network-based research into diseases. Here, we present HumanNet v3 (https://www.inetbio.org/humannet/, covering 99.8% of human protein coding genes) constructed by means of the expanded data with improved network inference algorithms. HumanNet v3 supports a three-tier model: HumanNet-PI (a protein–protein physical interaction network), HumanNet-FN (a functional gene network), and HumanNet-XC (a functional network extended by co-citation). Users can select a suitable tier of HumanNet for their study purpose. We showed that on disease gene predictions, HumanNet v3 outperforms both the previous HumanNet version and other integrated human gene networks. Furthermore, we demonstrated that HumanNet provides a feasible approach for selecting host genes likely to be associated with COVID-19. Oxford University Press 2021-11-08 /pmc/articles/PMC8728227/ /pubmed/34747468 http://dx.doi.org/10.1093/nar/gkab1048 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Nucleic Acids Research. 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 | Database Issue Kim, Chan Yeong Baek, Seungbyn Cha, Junha Yang, Sunmo Kim, Eiru Marcotte, Edward M Hart, Traver Lee, Insuk HumanNet v3: an improved database of human gene networks for disease research |
title | HumanNet v3: an improved database of human gene networks for disease research |
title_full | HumanNet v3: an improved database of human gene networks for disease research |
title_fullStr | HumanNet v3: an improved database of human gene networks for disease research |
title_full_unstemmed | HumanNet v3: an improved database of human gene networks for disease research |
title_short | HumanNet v3: an improved database of human gene networks for disease research |
title_sort | humannet v3: an improved database of human gene networks for disease research |
topic | Database Issue |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8728227/ https://www.ncbi.nlm.nih.gov/pubmed/34747468 http://dx.doi.org/10.1093/nar/gkab1048 |
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