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Gene set analysis methods: a systematic comparison

BACKGROUND: Gene set analysis is a valuable tool to summarize high-dimensional gene expression data in terms of biologically relevant sets. This is an active area of research and numerous gene set analysis methods have been developed. Despite this popularity, systematic comparative studies have been...

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Autores principales: Mathur, Ravi, Rotroff, Daniel, Ma, Jun, Shojaie, Ali, Motsinger-Reif, Alison
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5984476/
https://www.ncbi.nlm.nih.gov/pubmed/29881462
http://dx.doi.org/10.1186/s13040-018-0166-8
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author Mathur, Ravi
Rotroff, Daniel
Ma, Jun
Shojaie, Ali
Motsinger-Reif, Alison
author_facet Mathur, Ravi
Rotroff, Daniel
Ma, Jun
Shojaie, Ali
Motsinger-Reif, Alison
author_sort Mathur, Ravi
collection PubMed
description BACKGROUND: Gene set analysis is a valuable tool to summarize high-dimensional gene expression data in terms of biologically relevant sets. This is an active area of research and numerous gene set analysis methods have been developed. Despite this popularity, systematic comparative studies have been limited in scope. METHODS: In this study we present a semi-synthetic simulation study using real datasets in order to test and compare commonly used methods. RESULTS: A software pipeline, Flexible Algorithm for Novel Gene set Simulation (FANGS) develops simulated data based on a prostate cancer dataset where the KRAS and TGF-β pathways were differentially expressed. The FANGS software is compatible with other datasets and pathways. Comparisons of gene set analysis methods are presented for Gene Set Enrichment Analysis (GSEA), Significance Analysis of Function and Expression (SAFE), sigPathway, and Correlation Adjusted Mean RAnk (CAMERA) methods. All gene set analysis methods are tested using gene sets from the MSigDB knowledge base. The false positive rate and power are estimated and presented for comparison. Recommendations are made for the utility of the default settings of methods and each method’s sensitivity towards various effect sizes. CONCLUSIONS: The results of this study provide empirical guidance to users of gene set analysis methods. The FANGS software is available for researchers for continued methods comparisons. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13040-018-0166-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-59844762018-06-07 Gene set analysis methods: a systematic comparison Mathur, Ravi Rotroff, Daniel Ma, Jun Shojaie, Ali Motsinger-Reif, Alison BioData Min Research BACKGROUND: Gene set analysis is a valuable tool to summarize high-dimensional gene expression data in terms of biologically relevant sets. This is an active area of research and numerous gene set analysis methods have been developed. Despite this popularity, systematic comparative studies have been limited in scope. METHODS: In this study we present a semi-synthetic simulation study using real datasets in order to test and compare commonly used methods. RESULTS: A software pipeline, Flexible Algorithm for Novel Gene set Simulation (FANGS) develops simulated data based on a prostate cancer dataset where the KRAS and TGF-β pathways were differentially expressed. The FANGS software is compatible with other datasets and pathways. Comparisons of gene set analysis methods are presented for Gene Set Enrichment Analysis (GSEA), Significance Analysis of Function and Expression (SAFE), sigPathway, and Correlation Adjusted Mean RAnk (CAMERA) methods. All gene set analysis methods are tested using gene sets from the MSigDB knowledge base. The false positive rate and power are estimated and presented for comparison. Recommendations are made for the utility of the default settings of methods and each method’s sensitivity towards various effect sizes. CONCLUSIONS: The results of this study provide empirical guidance to users of gene set analysis methods. The FANGS software is available for researchers for continued methods comparisons. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13040-018-0166-8) contains supplementary material, which is available to authorized users. BioMed Central 2018-05-31 /pmc/articles/PMC5984476/ /pubmed/29881462 http://dx.doi.org/10.1186/s13040-018-0166-8 Text en © The Author(s). 2018 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
Mathur, Ravi
Rotroff, Daniel
Ma, Jun
Shojaie, Ali
Motsinger-Reif, Alison
Gene set analysis methods: a systematic comparison
title Gene set analysis methods: a systematic comparison
title_full Gene set analysis methods: a systematic comparison
title_fullStr Gene set analysis methods: a systematic comparison
title_full_unstemmed Gene set analysis methods: a systematic comparison
title_short Gene set analysis methods: a systematic comparison
title_sort gene set analysis methods: a systematic comparison
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5984476/
https://www.ncbi.nlm.nih.gov/pubmed/29881462
http://dx.doi.org/10.1186/s13040-018-0166-8
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