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VOLARE: visual analysis of disease-associated microbiome-immune system interplay

BACKGROUND: Relationships between specific microbes and proper immune system development, composition, and function have been reported in a number of studies. However, researchers have discovered only a fraction of the likely relationships. “Omic” methodologies such as 16S ribosomal RNA (rRNA) seque...

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Autores principales: Siebert, Janet C., Neff, Charles Preston, Schneider, Jennifer M., Regner, Emilie H., Ohri, Neha, Kuhn, Kristine A., Palmer, Brent E., Lozupone, Catherine A., Görg, Carsten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6701114/
https://www.ncbi.nlm.nih.gov/pubmed/31429723
http://dx.doi.org/10.1186/s12859-019-3021-0
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author Siebert, Janet C.
Neff, Charles Preston
Schneider, Jennifer M.
Regner, Emilie H.
Ohri, Neha
Kuhn, Kristine A.
Palmer, Brent E.
Lozupone, Catherine A.
Görg, Carsten
author_facet Siebert, Janet C.
Neff, Charles Preston
Schneider, Jennifer M.
Regner, Emilie H.
Ohri, Neha
Kuhn, Kristine A.
Palmer, Brent E.
Lozupone, Catherine A.
Görg, Carsten
author_sort Siebert, Janet C.
collection PubMed
description BACKGROUND: Relationships between specific microbes and proper immune system development, composition, and function have been reported in a number of studies. However, researchers have discovered only a fraction of the likely relationships. “Omic” methodologies such as 16S ribosomal RNA (rRNA) sequencing and time-of-flight mass cytometry (CyTOF) immunophenotyping generate data that support generation of hypotheses, with the potential to identify additional relationships at a level of granularity ripe for further experimentation. Pairwise linear regressions between microbial and host immune features provide one approach for quantifying relationships between “omes”, and the differences in these relationships across study cohorts or arms. This approach yields a top table of candidate results. However, the top table alone lacks the detail that domain experts such as microbiologists and immunologists need to vet candidate results for follow-up experiments. RESULTS: To support this vetting, we developed VOLARE (Visualization Of LineAr Regression Elements), a web application that integrates a searchable top table, small in-line graphs illustrating the fitted models, a network summarizing the top table, and on-demand detailed regression plots showing full sample-level detail. We applied VOLARE to three case studies—microbiome:cytokine data from fecal samples in human immunodeficiency virus (HIV), microbiome:cytokine data in inflammatory bowel disease and spondyloarthritis, and microbiome:immune cell data from gut biopsies in HIV. We present both patient-specific phenomena and relationships that differ by disease state. We also analyzed interaction data from system logs to characterize usage scenarios. This log analysis revealed that users frequently generated detailed regression plots, suggesting that this detail aids the vetting of results. CONCLUSIONS: Systematically integrating microbe:immune cell readouts through pairwise linear regressions and presenting the top table in an interactive environment supports the vetting of results for scientific relevance. VOLARE allows domain experts to control the analysis of their results, screening dozens of candidate relationships with ease. This interactive environment transcends the limitations of a static top table. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12859-019-3021-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-67011142019-08-26 VOLARE: visual analysis of disease-associated microbiome-immune system interplay Siebert, Janet C. Neff, Charles Preston Schneider, Jennifer M. Regner, Emilie H. Ohri, Neha Kuhn, Kristine A. Palmer, Brent E. Lozupone, Catherine A. Görg, Carsten BMC Bioinformatics Research Article BACKGROUND: Relationships between specific microbes and proper immune system development, composition, and function have been reported in a number of studies. However, researchers have discovered only a fraction of the likely relationships. “Omic” methodologies such as 16S ribosomal RNA (rRNA) sequencing and time-of-flight mass cytometry (CyTOF) immunophenotyping generate data that support generation of hypotheses, with the potential to identify additional relationships at a level of granularity ripe for further experimentation. Pairwise linear regressions between microbial and host immune features provide one approach for quantifying relationships between “omes”, and the differences in these relationships across study cohorts or arms. This approach yields a top table of candidate results. However, the top table alone lacks the detail that domain experts such as microbiologists and immunologists need to vet candidate results for follow-up experiments. RESULTS: To support this vetting, we developed VOLARE (Visualization Of LineAr Regression Elements), a web application that integrates a searchable top table, small in-line graphs illustrating the fitted models, a network summarizing the top table, and on-demand detailed regression plots showing full sample-level detail. We applied VOLARE to three case studies—microbiome:cytokine data from fecal samples in human immunodeficiency virus (HIV), microbiome:cytokine data in inflammatory bowel disease and spondyloarthritis, and microbiome:immune cell data from gut biopsies in HIV. We present both patient-specific phenomena and relationships that differ by disease state. We also analyzed interaction data from system logs to characterize usage scenarios. This log analysis revealed that users frequently generated detailed regression plots, suggesting that this detail aids the vetting of results. CONCLUSIONS: Systematically integrating microbe:immune cell readouts through pairwise linear regressions and presenting the top table in an interactive environment supports the vetting of results for scientific relevance. VOLARE allows domain experts to control the analysis of their results, screening dozens of candidate relationships with ease. This interactive environment transcends the limitations of a static top table. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12859-019-3021-0) contains supplementary material, which is available to authorized users. BioMed Central 2019-08-20 /pmc/articles/PMC6701114/ /pubmed/31429723 http://dx.doi.org/10.1186/s12859-019-3021-0 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 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 Research Article
Siebert, Janet C.
Neff, Charles Preston
Schneider, Jennifer M.
Regner, Emilie H.
Ohri, Neha
Kuhn, Kristine A.
Palmer, Brent E.
Lozupone, Catherine A.
Görg, Carsten
VOLARE: visual analysis of disease-associated microbiome-immune system interplay
title VOLARE: visual analysis of disease-associated microbiome-immune system interplay
title_full VOLARE: visual analysis of disease-associated microbiome-immune system interplay
title_fullStr VOLARE: visual analysis of disease-associated microbiome-immune system interplay
title_full_unstemmed VOLARE: visual analysis of disease-associated microbiome-immune system interplay
title_short VOLARE: visual analysis of disease-associated microbiome-immune system interplay
title_sort volare: visual analysis of disease-associated microbiome-immune system interplay
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6701114/
https://www.ncbi.nlm.nih.gov/pubmed/31429723
http://dx.doi.org/10.1186/s12859-019-3021-0
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