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petal: Co-expression network modelling in R

BACKGROUND: Networks provide effective models to study complex biological systems, such as gene and protein interaction networks. With the advent of new sequencing technologies, many life scientists are grasping for user-friendly methods and tools to examine biological components at the whole-system...

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Autores principales: Petereit, Juli, Smith, Sebastian, Harris, Frederick C., Schlauch, Karen A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4977474/
https://www.ncbi.nlm.nih.gov/pubmed/27490697
http://dx.doi.org/10.1186/s12918-016-0298-8
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author Petereit, Juli
Smith, Sebastian
Harris, Frederick C.
Schlauch, Karen A.
author_facet Petereit, Juli
Smith, Sebastian
Harris, Frederick C.
Schlauch, Karen A.
author_sort Petereit, Juli
collection PubMed
description BACKGROUND: Networks provide effective models to study complex biological systems, such as gene and protein interaction networks. With the advent of new sequencing technologies, many life scientists are grasping for user-friendly methods and tools to examine biological components at the whole-systems level. Gene co-expression network analysis approaches are frequently used to successfully associate genes with biological processes and demonstrate great potential to gain further insights into the functionality of genes, thus becoming a standard approach in Systems Biology. Here the objective is to construct biologically meaningful and statistically strong co-expression networks, the identification of research dependent subnetworks, and the presentation of self-contained results. RESULTS: We introduce petal, a novel approach to generate gene co-expression network models based on experimental gene expression measures. petal focuses on statistical, mathematical, and biological characteristics of both, input data and output network models. Often over-looked issues of current co-expression analysis tools include the assumption of data normality, which is seldom the case for hight-throughput expression data obtained from RNA-seq technologies. petal does not assume data normality, making it a statistically appropriate method for RNA-seq data. Also, network models are rarely tested for their known typical architecture: scale-free and small-world. petal explicitly constructs networks based on both these characteristics, thereby generating biologically meaningful models. Furthermore, many network analysis tools require a number of user-defined input variables, these often require tuning and/or an understanding of the underlying algorithm; petal requires no user input other than experimental data. This allows for reproducible results, and simplifies the use of petal. Lastly, this approach is specifically designed for very large high-throughput datasets; this way, petal’s network models represent as much of the entire system as possible to provide a whole-system approach. CONCLUSION: petal is a novel tool for generating co-expression network models of whole-genomics experiments. It is implemented in R and available as a library. Its application to several whole-genome experiments has generated novel meaningful results and has lead the way to new testing hypothesizes for further biological investigation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12918-016-0298-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-49774742016-08-17 petal: Co-expression network modelling in R Petereit, Juli Smith, Sebastian Harris, Frederick C. Schlauch, Karen A. BMC Syst Biol Software BACKGROUND: Networks provide effective models to study complex biological systems, such as gene and protein interaction networks. With the advent of new sequencing technologies, many life scientists are grasping for user-friendly methods and tools to examine biological components at the whole-systems level. Gene co-expression network analysis approaches are frequently used to successfully associate genes with biological processes and demonstrate great potential to gain further insights into the functionality of genes, thus becoming a standard approach in Systems Biology. Here the objective is to construct biologically meaningful and statistically strong co-expression networks, the identification of research dependent subnetworks, and the presentation of self-contained results. RESULTS: We introduce petal, a novel approach to generate gene co-expression network models based on experimental gene expression measures. petal focuses on statistical, mathematical, and biological characteristics of both, input data and output network models. Often over-looked issues of current co-expression analysis tools include the assumption of data normality, which is seldom the case for hight-throughput expression data obtained from RNA-seq technologies. petal does not assume data normality, making it a statistically appropriate method for RNA-seq data. Also, network models are rarely tested for their known typical architecture: scale-free and small-world. petal explicitly constructs networks based on both these characteristics, thereby generating biologically meaningful models. Furthermore, many network analysis tools require a number of user-defined input variables, these often require tuning and/or an understanding of the underlying algorithm; petal requires no user input other than experimental data. This allows for reproducible results, and simplifies the use of petal. Lastly, this approach is specifically designed for very large high-throughput datasets; this way, petal’s network models represent as much of the entire system as possible to provide a whole-system approach. CONCLUSION: petal is a novel tool for generating co-expression network models of whole-genomics experiments. It is implemented in R and available as a library. Its application to several whole-genome experiments has generated novel meaningful results and has lead the way to new testing hypothesizes for further biological investigation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12918-016-0298-8) contains supplementary material, which is available to authorized users. BioMed Central 2016-08-01 /pmc/articles/PMC4977474/ /pubmed/27490697 http://dx.doi.org/10.1186/s12918-016-0298-8 Text en © The Author(s) 2016 Open Access This 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 Software
Petereit, Juli
Smith, Sebastian
Harris, Frederick C.
Schlauch, Karen A.
petal: Co-expression network modelling in R
title petal: Co-expression network modelling in R
title_full petal: Co-expression network modelling in R
title_fullStr petal: Co-expression network modelling in R
title_full_unstemmed petal: Co-expression network modelling in R
title_short petal: Co-expression network modelling in R
title_sort petal: co-expression network modelling in r
topic Software
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4977474/
https://www.ncbi.nlm.nih.gov/pubmed/27490697
http://dx.doi.org/10.1186/s12918-016-0298-8
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