Evidence-based translation for the genomic responses of murine models for the study of human immunity.

Murine models are an essential tool to study human immune responses and related diseases. However, the use of traditional murine models has been challenged by recent systemic surveys that show discordance between human and model immune responses in their gene expression. This is a significant proble...

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Main Author: Junhee Seok
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4332676?pdf=render
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spelling doaj-5973cb296cbf47f19a95f3ee0bfb0e812020-11-25T02:04:18ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01102e011801710.1371/journal.pone.0118017Evidence-based translation for the genomic responses of murine models for the study of human immunity.Junhee SeokMurine models are an essential tool to study human immune responses and related diseases. However, the use of traditional murine models has been challenged by recent systemic surveys that show discordance between human and model immune responses in their gene expression. This is a significant problem in translational biomedical research for human immunity. Here, we describe evidence-based translation (EBT) to improve the analysis of genomic responses of murine models in the translation to human immune responses. Based on evidences from prior experiments, EBT introduces pseudo variances, penalizes gene expression changes in a model experiment, and finally detects false positive translations of model genomic responses that poorly correlate with human responses. Demonstrated over multiple data sets, EBT significantly improves the agreement of overall responses (up to 56%), experiment-specific responses (up to 143%), and enriched biological contexts (up to 100%) between human and model systems. In addition, we provide the category of genes specifically benefiting from EBT and the factors affecting the performance of EBT. The overall result indicates the usefulness of the proposed computational translation in biomedical research for human immunity using murine models.http://europepmc.org/articles/PMC4332676?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Junhee Seok
spellingShingle Junhee Seok
Evidence-based translation for the genomic responses of murine models for the study of human immunity.
PLoS ONE
author_facet Junhee Seok
author_sort Junhee Seok
title Evidence-based translation for the genomic responses of murine models for the study of human immunity.
title_short Evidence-based translation for the genomic responses of murine models for the study of human immunity.
title_full Evidence-based translation for the genomic responses of murine models for the study of human immunity.
title_fullStr Evidence-based translation for the genomic responses of murine models for the study of human immunity.
title_full_unstemmed Evidence-based translation for the genomic responses of murine models for the study of human immunity.
title_sort evidence-based translation for the genomic responses of murine models for the study of human immunity.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description Murine models are an essential tool to study human immune responses and related diseases. However, the use of traditional murine models has been challenged by recent systemic surveys that show discordance between human and model immune responses in their gene expression. This is a significant problem in translational biomedical research for human immunity. Here, we describe evidence-based translation (EBT) to improve the analysis of genomic responses of murine models in the translation to human immune responses. Based on evidences from prior experiments, EBT introduces pseudo variances, penalizes gene expression changes in a model experiment, and finally detects false positive translations of model genomic responses that poorly correlate with human responses. Demonstrated over multiple data sets, EBT significantly improves the agreement of overall responses (up to 56%), experiment-specific responses (up to 143%), and enriched biological contexts (up to 100%) between human and model systems. In addition, we provide the category of genes specifically benefiting from EBT and the factors affecting the performance of EBT. The overall result indicates the usefulness of the proposed computational translation in biomedical research for human immunity using murine models.
url http://europepmc.org/articles/PMC4332676?pdf=render
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