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Efficient reconstruction of biological networks via transitive reduction on general purpose graphics processors
BACKGROUND: Techniques for reconstruction of biological networks which are based on perturbation experiments often predict direct interactions between nodes that do not exist. Transitive reduction removes such relations if they can be explained by an indirect path of influences. The existing algorit...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3583792/ https://www.ncbi.nlm.nih.gov/pubmed/23110660 http://dx.doi.org/10.1186/1471-2105-13-281 |
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author | Bošnački, Dragan Odenbrett, Maximilian R Wijs, Anton Ligtenberg, Willem Hilbers, Peter |
author_facet | Bošnački, Dragan Odenbrett, Maximilian R Wijs, Anton Ligtenberg, Willem Hilbers, Peter |
author_sort | Bošnački, Dragan |
collection | PubMed |
description | BACKGROUND: Techniques for reconstruction of biological networks which are based on perturbation experiments often predict direct interactions between nodes that do not exist. Transitive reduction removes such relations if they can be explained by an indirect path of influences. The existing algorithms for transitive reduction are sequential and might suffer from too long run times for large networks. They also exhibit the anomaly that some existing direct interactions are also removed. RESULTS: We develop efficient scalable parallel algorithms for transitive reduction on general purpose graphics processing units for both standard (unweighted) and weighted graphs. Edge weights are regarded as uncertainties of interactions. A direct interaction is removed only if there exists an indirect interaction path between the same nodes which is strictly more certain than the direct one. This is a refinement of the removal condition for the unweighted graphs and avoids to a great extent the erroneous elimination of direct edges. CONCLUSIONS: Parallel implementations of these algorithms can achieve speed-ups of two orders of magnitude compared to their sequential counterparts. Our experiments show that: i) taking into account the edge weights improves the reconstruction quality compared to the unweighted case; ii) it is advantageous not to distinguish between positive and negative interactions since this lowers the complexity of the algorithms from NP-complete to polynomial without loss of quality. |
format | Online Article Text |
id | pubmed-3583792 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35837922013-03-08 Efficient reconstruction of biological networks via transitive reduction on general purpose graphics processors Bošnački, Dragan Odenbrett, Maximilian R Wijs, Anton Ligtenberg, Willem Hilbers, Peter BMC Bioinformatics Software BACKGROUND: Techniques for reconstruction of biological networks which are based on perturbation experiments often predict direct interactions between nodes that do not exist. Transitive reduction removes such relations if they can be explained by an indirect path of influences. The existing algorithms for transitive reduction are sequential and might suffer from too long run times for large networks. They also exhibit the anomaly that some existing direct interactions are also removed. RESULTS: We develop efficient scalable parallel algorithms for transitive reduction on general purpose graphics processing units for both standard (unweighted) and weighted graphs. Edge weights are regarded as uncertainties of interactions. A direct interaction is removed only if there exists an indirect interaction path between the same nodes which is strictly more certain than the direct one. This is a refinement of the removal condition for the unweighted graphs and avoids to a great extent the erroneous elimination of direct edges. CONCLUSIONS: Parallel implementations of these algorithms can achieve speed-ups of two orders of magnitude compared to their sequential counterparts. Our experiments show that: i) taking into account the edge weights improves the reconstruction quality compared to the unweighted case; ii) it is advantageous not to distinguish between positive and negative interactions since this lowers the complexity of the algorithms from NP-complete to polynomial without loss of quality. BioMed Central 2012-10-30 /pmc/articles/PMC3583792/ /pubmed/23110660 http://dx.doi.org/10.1186/1471-2105-13-281 Text en Copyright ©2012 Bosnacki 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 | Software Bošnački, Dragan Odenbrett, Maximilian R Wijs, Anton Ligtenberg, Willem Hilbers, Peter Efficient reconstruction of biological networks via transitive reduction on general purpose graphics processors |
title | Efficient reconstruction of biological networks via transitive reduction on general purpose graphics processors |
title_full | Efficient reconstruction of biological networks via transitive reduction on general purpose graphics processors |
title_fullStr | Efficient reconstruction of biological networks via transitive reduction on general purpose graphics processors |
title_full_unstemmed | Efficient reconstruction of biological networks via transitive reduction on general purpose graphics processors |
title_short | Efficient reconstruction of biological networks via transitive reduction on general purpose graphics processors |
title_sort | efficient reconstruction of biological networks via transitive reduction on general purpose graphics processors |
topic | Software |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3583792/ https://www.ncbi.nlm.nih.gov/pubmed/23110660 http://dx.doi.org/10.1186/1471-2105-13-281 |
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