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Understanding multicellular function and disease with human tissue-specific networks
Tissue and cell-type identity lie at the core of human physiology and disease. Understanding the genetic underpinnings of complex tissues and individual cell lineages is crucial for developing improved diagnostics and therapeutics. We present genome-wide functional interaction networks for 144 human...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4828725/ https://www.ncbi.nlm.nih.gov/pubmed/25915600 http://dx.doi.org/10.1038/ng.3259 |
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author | Greene, Casey S. Krishnan, Arjun Wong, Aaron K. Ricciotti, Emanuela Zelaya, Rene A. Himmelstein, Daniel S. Zhang, Ran Hartmann, Boris M. Zaslavsky, Elena Sealfon, Stuart C. Chasman, Daniel I. FitzGerald, Garret A. Dolinski, Kara Grosser, Tilo Troyanskaya, Olga G. |
author_facet | Greene, Casey S. Krishnan, Arjun Wong, Aaron K. Ricciotti, Emanuela Zelaya, Rene A. Himmelstein, Daniel S. Zhang, Ran Hartmann, Boris M. Zaslavsky, Elena Sealfon, Stuart C. Chasman, Daniel I. FitzGerald, Garret A. Dolinski, Kara Grosser, Tilo Troyanskaya, Olga G. |
author_sort | Greene, Casey S. |
collection | PubMed |
description | Tissue and cell-type identity lie at the core of human physiology and disease. Understanding the genetic underpinnings of complex tissues and individual cell lineages is crucial for developing improved diagnostics and therapeutics. We present genome-wide functional interaction networks for 144 human tissues and cell types developed using a data-driven Bayesian methodology that integrates thousands of diverse experiments spanning tissue and disease states. Tissue-specific networks predict lineage-specific responses to perturbation, reveal genes’ changing functional roles across tissues, and illuminate disease-disease relationships. We introduce NetWAS, which combines genes with nominally significant GWAS p-values and tissue-specific networks to identify disease-gene associations more accurately than GWAS alone. Our webserver, GIANT, provides an interface to human tissue networks through multi-gene queries, network visualization, analysis tools including NetWAS, and downloadable networks. GIANT enables systematic exploration of the landscape of interacting genes that shape specialized cellular functions across more than one hundred human tissues and cell types. |
format | Online Article Text |
id | pubmed-4828725 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
record_format | MEDLINE/PubMed |
spelling | pubmed-48287252016-04-12 Understanding multicellular function and disease with human tissue-specific networks Greene, Casey S. Krishnan, Arjun Wong, Aaron K. Ricciotti, Emanuela Zelaya, Rene A. Himmelstein, Daniel S. Zhang, Ran Hartmann, Boris M. Zaslavsky, Elena Sealfon, Stuart C. Chasman, Daniel I. FitzGerald, Garret A. Dolinski, Kara Grosser, Tilo Troyanskaya, Olga G. Nat Genet Article Tissue and cell-type identity lie at the core of human physiology and disease. Understanding the genetic underpinnings of complex tissues and individual cell lineages is crucial for developing improved diagnostics and therapeutics. We present genome-wide functional interaction networks for 144 human tissues and cell types developed using a data-driven Bayesian methodology that integrates thousands of diverse experiments spanning tissue and disease states. Tissue-specific networks predict lineage-specific responses to perturbation, reveal genes’ changing functional roles across tissues, and illuminate disease-disease relationships. We introduce NetWAS, which combines genes with nominally significant GWAS p-values and tissue-specific networks to identify disease-gene associations more accurately than GWAS alone. Our webserver, GIANT, provides an interface to human tissue networks through multi-gene queries, network visualization, analysis tools including NetWAS, and downloadable networks. GIANT enables systematic exploration of the landscape of interacting genes that shape specialized cellular functions across more than one hundred human tissues and cell types. 2015-04-27 2015-06 /pmc/articles/PMC4828725/ /pubmed/25915600 http://dx.doi.org/10.1038/ng.3259 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Greene, Casey S. Krishnan, Arjun Wong, Aaron K. Ricciotti, Emanuela Zelaya, Rene A. Himmelstein, Daniel S. Zhang, Ran Hartmann, Boris M. Zaslavsky, Elena Sealfon, Stuart C. Chasman, Daniel I. FitzGerald, Garret A. Dolinski, Kara Grosser, Tilo Troyanskaya, Olga G. Understanding multicellular function and disease with human tissue-specific networks |
title | Understanding multicellular function and disease with human tissue-specific networks |
title_full | Understanding multicellular function and disease with human tissue-specific networks |
title_fullStr | Understanding multicellular function and disease with human tissue-specific networks |
title_full_unstemmed | Understanding multicellular function and disease with human tissue-specific networks |
title_short | Understanding multicellular function and disease with human tissue-specific networks |
title_sort | understanding multicellular function and disease with human tissue-specific networks |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4828725/ https://www.ncbi.nlm.nih.gov/pubmed/25915600 http://dx.doi.org/10.1038/ng.3259 |
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