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GuavaH: a compendium of host genomic data in HIV biology and disease

BACKGROUND: There is an ever-increasing volume of data on host genes that are modulated during HIV infection, influence disease susceptibility or carry genetic variants that impact HIV infection. We created GuavaH (Genomic Utility for Association and Viral Analyses in HIV, http://www.GuavaH.org), a...

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Autores principales: Bartha, István, McLaren, Paul J, Ciuffi, Angela, Fellay, Jacques, Telenti, Amalio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3937115/
https://www.ncbi.nlm.nih.gov/pubmed/24428872
http://dx.doi.org/10.1186/1742-4690-11-6
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author Bartha, István
McLaren, Paul J
Ciuffi, Angela
Fellay, Jacques
Telenti, Amalio
author_facet Bartha, István
McLaren, Paul J
Ciuffi, Angela
Fellay, Jacques
Telenti, Amalio
author_sort Bartha, István
collection PubMed
description BACKGROUND: There is an ever-increasing volume of data on host genes that are modulated during HIV infection, influence disease susceptibility or carry genetic variants that impact HIV infection. We created GuavaH (Genomic Utility for Association and Viral Analyses in HIV, http://www.GuavaH.org), a public resource that supports multipurpose analysis of genome-wide genetic variation and gene expression profile across multiple phenotypes relevant to HIV biology. FINDINGS: We included original data from 8 genome and transcriptome studies addressing viral and host responses in and ex vivo. These studies cover phenotypes such as HIV acquisition, plasma viral load, disease progression, viral replication cycle, latency and viral-host genome interaction. This represents genome-wide association data from more than 4,000 individuals, exome sequencing data from 392 individuals, in vivo transcriptome microarray data from 127 patients/conditions, and 60 sets of RNA-seq data. Additionally, GuavaH allows visualization of protein variation in ~8,000 individuals from the general population. The publicly available GuavaH framework supports queries on (i) unique single nucleotide polymorphism across different HIV related phenotypes, (ii) gene structure and variation, (iii) in vivo gene expression in the setting of human infection (CD4+ T cells), and (iv) in vitro gene expression data in models of permissive infection, latency and reactivation. CONCLUSIONS: The complexity of the analysis of host genetic influences on HIV biology and pathogenesis calls for comprehensive motors of research on curated data. The tool developed here allows queries and supports validation of the rapidly growing body of host genomic information pertinent to HIV research.
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spelling pubmed-39371152014-02-28 GuavaH: a compendium of host genomic data in HIV biology and disease Bartha, István McLaren, Paul J Ciuffi, Angela Fellay, Jacques Telenti, Amalio Retrovirology Short Report BACKGROUND: There is an ever-increasing volume of data on host genes that are modulated during HIV infection, influence disease susceptibility or carry genetic variants that impact HIV infection. We created GuavaH (Genomic Utility for Association and Viral Analyses in HIV, http://www.GuavaH.org), a public resource that supports multipurpose analysis of genome-wide genetic variation and gene expression profile across multiple phenotypes relevant to HIV biology. FINDINGS: We included original data from 8 genome and transcriptome studies addressing viral and host responses in and ex vivo. These studies cover phenotypes such as HIV acquisition, plasma viral load, disease progression, viral replication cycle, latency and viral-host genome interaction. This represents genome-wide association data from more than 4,000 individuals, exome sequencing data from 392 individuals, in vivo transcriptome microarray data from 127 patients/conditions, and 60 sets of RNA-seq data. Additionally, GuavaH allows visualization of protein variation in ~8,000 individuals from the general population. The publicly available GuavaH framework supports queries on (i) unique single nucleotide polymorphism across different HIV related phenotypes, (ii) gene structure and variation, (iii) in vivo gene expression in the setting of human infection (CD4+ T cells), and (iv) in vitro gene expression data in models of permissive infection, latency and reactivation. CONCLUSIONS: The complexity of the analysis of host genetic influences on HIV biology and pathogenesis calls for comprehensive motors of research on curated data. The tool developed here allows queries and supports validation of the rapidly growing body of host genomic information pertinent to HIV research. BioMed Central 2014-01-15 /pmc/articles/PMC3937115/ /pubmed/24428872 http://dx.doi.org/10.1186/1742-4690-11-6 Text en Copyright © 2014 Bartha et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Short Report
Bartha, István
McLaren, Paul J
Ciuffi, Angela
Fellay, Jacques
Telenti, Amalio
GuavaH: a compendium of host genomic data in HIV biology and disease
title GuavaH: a compendium of host genomic data in HIV biology and disease
title_full GuavaH: a compendium of host genomic data in HIV biology and disease
title_fullStr GuavaH: a compendium of host genomic data in HIV biology and disease
title_full_unstemmed GuavaH: a compendium of host genomic data in HIV biology and disease
title_short GuavaH: a compendium of host genomic data in HIV biology and disease
title_sort guavah: a compendium of host genomic data in hiv biology and disease
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3937115/
https://www.ncbi.nlm.nih.gov/pubmed/24428872
http://dx.doi.org/10.1186/1742-4690-11-6
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