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Identifying significant edges in graphical models of molecular networks
OBJECTIVE: Modelling the associations from high-throughput experimental molecular data has provided unprecedented insights into biological pathways and signalling mechanisms. Graphical models and networks have especially proven to be useful abstractions in this regard. Ad hoc thresholds are often us...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Science Publishing
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4070079/ https://www.ncbi.nlm.nih.gov/pubmed/23395009 http://dx.doi.org/10.1016/j.artmed.2012.12.006 |
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author | Scutari, Marco Nagarajan, Radhakrishnan |
author_facet | Scutari, Marco Nagarajan, Radhakrishnan |
author_sort | Scutari, Marco |
collection | PubMed |
description | OBJECTIVE: Modelling the associations from high-throughput experimental molecular data has provided unprecedented insights into biological pathways and signalling mechanisms. Graphical models and networks have especially proven to be useful abstractions in this regard. Ad hoc thresholds are often used in conjunction with structure learning algorithms to determine significant associations. The present study overcomes this limitation by proposing a statistically motivated approach for identifying significant associations in a network. METHODS AND MATERIALS: A new method that identifies significant associations in graphical models by estimating the threshold minimising the L(1) norm between the cumulative distribution function (CDF) of the observed edge confidences and those of its asymptotic counterpart is proposed. The effectiveness of the proposed method is demonstrated on popular synthetic data sets as well as publicly available experimental molecular data corresponding to gene and protein expression profiles. RESULTS: The improved performance of the proposed approach is demonstrated across the synthetic data sets using sensitivity, specificity and accuracy as performance metrics. The results are also demonstrated across varying sample sizes and three different structure learning algorithms with widely varying assumptions. In all cases, the proposed approach has specificity and accuracy close to 1, while sensitivity increases linearly in the logarithm of the sample size. The estimated threshold systematically outperforms common ad hoc ones in terms of sensitivity while maintaining comparable levels of specificity and accuracy. Networks from experimental data sets are reconstructed accurately with respect to the results from the original papers. CONCLUSION: Current studies use structure learning algorithms in conjunction with ad hoc thresholds for identifying significant associations in graphical abstractions of biological pathways and signalling mechanisms. Such an ad hoc choice can have pronounced effect on attributing biological significance to the associations in the resulting network and possible downstream analysis. The statistically motivated approach presented in this study has been shown to outperform ad hoc thresholds and is expected to alleviate spurious conclusions of significant associations in such graphical abstractions. |
format | Online Article Text |
id | pubmed-4070079 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Elsevier Science Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-40700792014-06-26 Identifying significant edges in graphical models of molecular networks Scutari, Marco Nagarajan, Radhakrishnan Artif Intell Med Article OBJECTIVE: Modelling the associations from high-throughput experimental molecular data has provided unprecedented insights into biological pathways and signalling mechanisms. Graphical models and networks have especially proven to be useful abstractions in this regard. Ad hoc thresholds are often used in conjunction with structure learning algorithms to determine significant associations. The present study overcomes this limitation by proposing a statistically motivated approach for identifying significant associations in a network. METHODS AND MATERIALS: A new method that identifies significant associations in graphical models by estimating the threshold minimising the L(1) norm between the cumulative distribution function (CDF) of the observed edge confidences and those of its asymptotic counterpart is proposed. The effectiveness of the proposed method is demonstrated on popular synthetic data sets as well as publicly available experimental molecular data corresponding to gene and protein expression profiles. RESULTS: The improved performance of the proposed approach is demonstrated across the synthetic data sets using sensitivity, specificity and accuracy as performance metrics. The results are also demonstrated across varying sample sizes and three different structure learning algorithms with widely varying assumptions. In all cases, the proposed approach has specificity and accuracy close to 1, while sensitivity increases linearly in the logarithm of the sample size. The estimated threshold systematically outperforms common ad hoc ones in terms of sensitivity while maintaining comparable levels of specificity and accuracy. Networks from experimental data sets are reconstructed accurately with respect to the results from the original papers. CONCLUSION: Current studies use structure learning algorithms in conjunction with ad hoc thresholds for identifying significant associations in graphical abstractions of biological pathways and signalling mechanisms. Such an ad hoc choice can have pronounced effect on attributing biological significance to the associations in the resulting network and possible downstream analysis. The statistically motivated approach presented in this study has been shown to outperform ad hoc thresholds and is expected to alleviate spurious conclusions of significant associations in such graphical abstractions. Elsevier Science Publishing 2013-03 /pmc/articles/PMC4070079/ /pubmed/23395009 http://dx.doi.org/10.1016/j.artmed.2012.12.006 Text en © 2012 Elsevier B.V. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Scutari, Marco Nagarajan, Radhakrishnan Identifying significant edges in graphical models of molecular networks |
title | Identifying significant edges in graphical models of molecular networks |
title_full | Identifying significant edges in graphical models of molecular networks |
title_fullStr | Identifying significant edges in graphical models of molecular networks |
title_full_unstemmed | Identifying significant edges in graphical models of molecular networks |
title_short | Identifying significant edges in graphical models of molecular networks |
title_sort | identifying significant edges in graphical models of molecular networks |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4070079/ https://www.ncbi.nlm.nih.gov/pubmed/23395009 http://dx.doi.org/10.1016/j.artmed.2012.12.006 |
work_keys_str_mv | AT scutarimarco identifyingsignificantedgesingraphicalmodelsofmolecularnetworks AT nagarajanradhakrishnan identifyingsignificantedgesingraphicalmodelsofmolecularnetworks |