Cargando…
Summarizing cellular responses as biological process networks
BACKGROUND: Microarray experiments can simultaneously identify thousands of genes that show significant perturbation in expression between two experimental conditions. Response networks, computed through the integration of gene interaction networks with expression perturbation data, may themselves c...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3751784/ https://www.ncbi.nlm.nih.gov/pubmed/23895181 http://dx.doi.org/10.1186/1752-0509-7-68 |
_version_ | 1782281668870012928 |
---|---|
author | Lasher, Christopher D Rajagopalan, Padmavathy Murali, T M |
author_facet | Lasher, Christopher D Rajagopalan, Padmavathy Murali, T M |
author_sort | Lasher, Christopher D |
collection | PubMed |
description | BACKGROUND: Microarray experiments can simultaneously identify thousands of genes that show significant perturbation in expression between two experimental conditions. Response networks, computed through the integration of gene interaction networks with expression perturbation data, may themselves contain tens of thousands of interactions. Gene set enrichment has become standard for summarizing the results of these analyses in terms functionally coherent collections of genes such as biological processes. However, even these methods can yield hundreds of enriched functions that may overlap considerably. RESULTS: We describe a new technique called Markov chain Monte Carlo Biological Process Networks (MCMC-BPN) capable of reporting a highly non-redundant set of links between processes that describe the molecular interactions that are perturbed under a specific biological context. Each link in the BPN represents the perturbed interactions that serve as the interfaces between the two processes connected by the link. We apply MCMC-BPN to publicly available liver-related datasets to demonstrate that the networks formed by the most probable inter-process links reported by MCMC-BPN show high relevance to each biological condition. We show that MCMC-BPN’s ability to discern the few key links from in a very large solution space by comparing results from two other methods for detecting inter-process links. CONCLUSIONS: MCMC-BPN is successful in using few inter-process links to explain as many of the perturbed gene-gene interactions as possible. Thereby, BPNs summarize the important biological trends within a response network by reporting a digestible number of inter-process links that can be explored in greater detail. |
format | Online Article Text |
id | pubmed-3751784 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-37517842013-08-28 Summarizing cellular responses as biological process networks Lasher, Christopher D Rajagopalan, Padmavathy Murali, T M BMC Syst Biol Methodology Article BACKGROUND: Microarray experiments can simultaneously identify thousands of genes that show significant perturbation in expression between two experimental conditions. Response networks, computed through the integration of gene interaction networks with expression perturbation data, may themselves contain tens of thousands of interactions. Gene set enrichment has become standard for summarizing the results of these analyses in terms functionally coherent collections of genes such as biological processes. However, even these methods can yield hundreds of enriched functions that may overlap considerably. RESULTS: We describe a new technique called Markov chain Monte Carlo Biological Process Networks (MCMC-BPN) capable of reporting a highly non-redundant set of links between processes that describe the molecular interactions that are perturbed under a specific biological context. Each link in the BPN represents the perturbed interactions that serve as the interfaces between the two processes connected by the link. We apply MCMC-BPN to publicly available liver-related datasets to demonstrate that the networks formed by the most probable inter-process links reported by MCMC-BPN show high relevance to each biological condition. We show that MCMC-BPN’s ability to discern the few key links from in a very large solution space by comparing results from two other methods for detecting inter-process links. CONCLUSIONS: MCMC-BPN is successful in using few inter-process links to explain as many of the perturbed gene-gene interactions as possible. Thereby, BPNs summarize the important biological trends within a response network by reporting a digestible number of inter-process links that can be explored in greater detail. BioMed Central 2013-07-29 /pmc/articles/PMC3751784/ /pubmed/23895181 http://dx.doi.org/10.1186/1752-0509-7-68 Text en Copyright © 2013 Lasher et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methodology Article Lasher, Christopher D Rajagopalan, Padmavathy Murali, T M Summarizing cellular responses as biological process networks |
title | Summarizing cellular responses as biological process networks |
title_full | Summarizing cellular responses as biological process networks |
title_fullStr | Summarizing cellular responses as biological process networks |
title_full_unstemmed | Summarizing cellular responses as biological process networks |
title_short | Summarizing cellular responses as biological process networks |
title_sort | summarizing cellular responses as biological process networks |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3751784/ https://www.ncbi.nlm.nih.gov/pubmed/23895181 http://dx.doi.org/10.1186/1752-0509-7-68 |
work_keys_str_mv | AT lasherchristopherd summarizingcellularresponsesasbiologicalprocessnetworks AT rajagopalanpadmavathy summarizingcellularresponsesasbiologicalprocessnetworks AT muralitm summarizingcellularresponsesasbiologicalprocessnetworks |