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Assessing the Impact of Sample Heterogeneity on Transcriptome Analysis of Human Diseases Using MDP Webtool
Transcriptome analyses have increased our understanding of the molecular mechanisms underlying human diseases. Most approaches aim to identify significant genes by comparing their expression values between healthy subjects and a group of patients with a certain disease. Given that studies normally c...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6822058/ https://www.ncbi.nlm.nih.gov/pubmed/31708960 http://dx.doi.org/10.3389/fgene.2019.00971 |
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author | Gonçalves, André N. A. Lever, Melissa Russo, Pedro S. T. Gomes-Correia, Bruno Urbanski, Alysson H. Pollara, Gabriele Noursadeghi, Mahdad Maracaja-Coutinho, Vinicius Nakaya, Helder I. |
author_facet | Gonçalves, André N. A. Lever, Melissa Russo, Pedro S. T. Gomes-Correia, Bruno Urbanski, Alysson H. Pollara, Gabriele Noursadeghi, Mahdad Maracaja-Coutinho, Vinicius Nakaya, Helder I. |
author_sort | Gonçalves, André N. A. |
collection | PubMed |
description | Transcriptome analyses have increased our understanding of the molecular mechanisms underlying human diseases. Most approaches aim to identify significant genes by comparing their expression values between healthy subjects and a group of patients with a certain disease. Given that studies normally contain few samples, the heterogeneity among individuals caused by environmental factors or undetected illnesses can impact gene expression analyses. We present a systematic analysis of sample heterogeneity in a variety of gene expression studies relating to inflammatory and infectious diseases and show that novel immunological insights may arise once heterogeneity is addressed. The perturbation score of samples is quantified using nonperturbed subjects (i.e., healthy subjects) as a reference group. Such a score allows us to detect outlying samples and subgroups of diseased patients and even assess the molecular perturbation of single cells infected with viruses. We also show how removal of outlying samples can improve the “signal” of the disease and impact detection of differentially expressed genes. The method is made available via the mdp Bioconductor R package and as a user-friendly webtool, webMDP, available at http://mdp.sysbio.tools. |
format | Online Article Text |
id | pubmed-6822058 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-68220582019-11-08 Assessing the Impact of Sample Heterogeneity on Transcriptome Analysis of Human Diseases Using MDP Webtool Gonçalves, André N. A. Lever, Melissa Russo, Pedro S. T. Gomes-Correia, Bruno Urbanski, Alysson H. Pollara, Gabriele Noursadeghi, Mahdad Maracaja-Coutinho, Vinicius Nakaya, Helder I. Front Genet Genetics Transcriptome analyses have increased our understanding of the molecular mechanisms underlying human diseases. Most approaches aim to identify significant genes by comparing their expression values between healthy subjects and a group of patients with a certain disease. Given that studies normally contain few samples, the heterogeneity among individuals caused by environmental factors or undetected illnesses can impact gene expression analyses. We present a systematic analysis of sample heterogeneity in a variety of gene expression studies relating to inflammatory and infectious diseases and show that novel immunological insights may arise once heterogeneity is addressed. The perturbation score of samples is quantified using nonperturbed subjects (i.e., healthy subjects) as a reference group. Such a score allows us to detect outlying samples and subgroups of diseased patients and even assess the molecular perturbation of single cells infected with viruses. We also show how removal of outlying samples can improve the “signal” of the disease and impact detection of differentially expressed genes. The method is made available via the mdp Bioconductor R package and as a user-friendly webtool, webMDP, available at http://mdp.sysbio.tools. Frontiers Media S.A. 2019-10-24 /pmc/articles/PMC6822058/ /pubmed/31708960 http://dx.doi.org/10.3389/fgene.2019.00971 Text en Copyright © 2019 Gonçalves, Lever, Russo, Gomes-Correia, Urbanski, Pollara, Noursadeghi, Maracaja-Coutinho and Nakaya http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Genetics Gonçalves, André N. A. Lever, Melissa Russo, Pedro S. T. Gomes-Correia, Bruno Urbanski, Alysson H. Pollara, Gabriele Noursadeghi, Mahdad Maracaja-Coutinho, Vinicius Nakaya, Helder I. Assessing the Impact of Sample Heterogeneity on Transcriptome Analysis of Human Diseases Using MDP Webtool |
title | Assessing the Impact of Sample Heterogeneity on Transcriptome Analysis of Human Diseases Using MDP Webtool |
title_full | Assessing the Impact of Sample Heterogeneity on Transcriptome Analysis of Human Diseases Using MDP Webtool |
title_fullStr | Assessing the Impact of Sample Heterogeneity on Transcriptome Analysis of Human Diseases Using MDP Webtool |
title_full_unstemmed | Assessing the Impact of Sample Heterogeneity on Transcriptome Analysis of Human Diseases Using MDP Webtool |
title_short | Assessing the Impact of Sample Heterogeneity on Transcriptome Analysis of Human Diseases Using MDP Webtool |
title_sort | assessing the impact of sample heterogeneity on transcriptome analysis of human diseases using mdp webtool |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6822058/ https://www.ncbi.nlm.nih.gov/pubmed/31708960 http://dx.doi.org/10.3389/fgene.2019.00971 |
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