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Benchmarking Procedures for High-Throughput Context Specific Reconstruction Algorithms
Recent progress in high-throughput data acquisition has shifted the focus from data generation to processing and understanding of how to integrate collected information. Context specific reconstruction based on generic genome scale models like ReconX or HMR has the potential to become a diagnostic a...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4722106/ https://www.ncbi.nlm.nih.gov/pubmed/26834640 http://dx.doi.org/10.3389/fphys.2015.00410 |
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author | Pacheco, Maria P. Pfau, Thomas Sauter, Thomas |
author_facet | Pacheco, Maria P. Pfau, Thomas Sauter, Thomas |
author_sort | Pacheco, Maria P. |
collection | PubMed |
description | Recent progress in high-throughput data acquisition has shifted the focus from data generation to processing and understanding of how to integrate collected information. Context specific reconstruction based on generic genome scale models like ReconX or HMR has the potential to become a diagnostic and treatment tool tailored to the analysis of specific individuals. The respective computational algorithms require a high level of predictive power, robustness and sensitivity. Although multiple context specific reconstruction algorithms were published in the last 10 years, only a fraction of them is suitable for model building based on human high-throughput data. Beside other reasons, this might be due to problems arising from the limitation to only one metabolic target function or arbitrary thresholding. This review describes and analyses common validation methods used for testing model building algorithms. Two major methods can be distinguished: consistency testing and comparison based testing. The first is concerned with robustness against noise, e.g., missing data due to the impossibility to distinguish between the signal and the background of non-specific binding of probes in a microarray experiment, and whether distinct sets of input expressed genes corresponding to i.e., different tissues yield distinct models. The latter covers methods comparing sets of functionalities, comparison with existing networks or additional databases. We test those methods on several available algorithms and deduce properties of these algorithms that can be compared with future developments. The set of tests performed, can therefore serve as a benchmarking procedure for future algorithms. |
format | Online Article Text |
id | pubmed-4722106 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-47221062016-01-29 Benchmarking Procedures for High-Throughput Context Specific Reconstruction Algorithms Pacheco, Maria P. Pfau, Thomas Sauter, Thomas Front Physiol Physiology Recent progress in high-throughput data acquisition has shifted the focus from data generation to processing and understanding of how to integrate collected information. Context specific reconstruction based on generic genome scale models like ReconX or HMR has the potential to become a diagnostic and treatment tool tailored to the analysis of specific individuals. The respective computational algorithms require a high level of predictive power, robustness and sensitivity. Although multiple context specific reconstruction algorithms were published in the last 10 years, only a fraction of them is suitable for model building based on human high-throughput data. Beside other reasons, this might be due to problems arising from the limitation to only one metabolic target function or arbitrary thresholding. This review describes and analyses common validation methods used for testing model building algorithms. Two major methods can be distinguished: consistency testing and comparison based testing. The first is concerned with robustness against noise, e.g., missing data due to the impossibility to distinguish between the signal and the background of non-specific binding of probes in a microarray experiment, and whether distinct sets of input expressed genes corresponding to i.e., different tissues yield distinct models. The latter covers methods comparing sets of functionalities, comparison with existing networks or additional databases. We test those methods on several available algorithms and deduce properties of these algorithms that can be compared with future developments. The set of tests performed, can therefore serve as a benchmarking procedure for future algorithms. Frontiers Media S.A. 2016-01-22 /pmc/articles/PMC4722106/ /pubmed/26834640 http://dx.doi.org/10.3389/fphys.2015.00410 Text en Copyright © 2016 Pacheco, Pfau and Sauter. 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) or licensor 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 | Physiology Pacheco, Maria P. Pfau, Thomas Sauter, Thomas Benchmarking Procedures for High-Throughput Context Specific Reconstruction Algorithms |
title | Benchmarking Procedures for High-Throughput Context Specific Reconstruction Algorithms |
title_full | Benchmarking Procedures for High-Throughput Context Specific Reconstruction Algorithms |
title_fullStr | Benchmarking Procedures for High-Throughput Context Specific Reconstruction Algorithms |
title_full_unstemmed | Benchmarking Procedures for High-Throughput Context Specific Reconstruction Algorithms |
title_short | Benchmarking Procedures for High-Throughput Context Specific Reconstruction Algorithms |
title_sort | benchmarking procedures for high-throughput context specific reconstruction algorithms |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4722106/ https://www.ncbi.nlm.nih.gov/pubmed/26834640 http://dx.doi.org/10.3389/fphys.2015.00410 |
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