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Expanding the boundaries of local similarity analysis
BACKGROUND: Pairwise comparison of time series data for both local and time-lagged relationships is a computationally challenging problem relevant to many fields of inquiry. The Local Similarity Analysis (LSA) statistic identifies the existence of local and lagged relationships, but determining sign...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3549818/ https://www.ncbi.nlm.nih.gov/pubmed/23368516 http://dx.doi.org/10.1186/1471-2164-14-S1-S3 |
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author | Durno, W Evan Hanson, Niels W Konwar, Kishori M Hallam, Steven J |
author_facet | Durno, W Evan Hanson, Niels W Konwar, Kishori M Hallam, Steven J |
author_sort | Durno, W Evan |
collection | PubMed |
description | BACKGROUND: Pairwise comparison of time series data for both local and time-lagged relationships is a computationally challenging problem relevant to many fields of inquiry. The Local Similarity Analysis (LSA) statistic identifies the existence of local and lagged relationships, but determining significance through a p-value has been algorithmically cumbersome due to an intensive permutation test, shuffling rows and columns and repeatedly calculating the statistic. Furthermore, this p-value is calculated with the assumption of normality -- a statistical luxury dissociated from most real world datasets. RESULTS: To improve the performance of LSA on big datasets, an asymptotic upper bound on the p-value calculation was derived without the assumption of normality. This change in the bound calculation markedly improved computational speed from O(pm(2)n) to O(m(2)n), where p is the number of permutations in a permutation test, m is the number of time series, and n is the length of each time series. The bounding process is implemented as a computationally efficient software package, FASTLSA, written in C and optimized for threading on multi-core computers, improving its practical computation time. We computationally compare our approach to previous implementations of LSA, demonstrate broad applicability by analyzing time series data from public health, microbial ecology, and social media, and visualize resulting networks using the Cytoscape software. CONCLUSIONS: The FASTLSA software package expands the boundaries of LSA allowing analysis on datasets with millions of co-varying time series. Mapping metadata onto force-directed graphs derived from FASTLSA allows investigators to view correlated cliques and explore previously unrecognized network relationships. The software is freely available for download at: http://www.cmde.science.ubc.ca/hallam/fastLSA/. |
format | Online Article Text |
id | pubmed-3549818 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35498182013-01-23 Expanding the boundaries of local similarity analysis Durno, W Evan Hanson, Niels W Konwar, Kishori M Hallam, Steven J BMC Genomics Proceedings BACKGROUND: Pairwise comparison of time series data for both local and time-lagged relationships is a computationally challenging problem relevant to many fields of inquiry. The Local Similarity Analysis (LSA) statistic identifies the existence of local and lagged relationships, but determining significance through a p-value has been algorithmically cumbersome due to an intensive permutation test, shuffling rows and columns and repeatedly calculating the statistic. Furthermore, this p-value is calculated with the assumption of normality -- a statistical luxury dissociated from most real world datasets. RESULTS: To improve the performance of LSA on big datasets, an asymptotic upper bound on the p-value calculation was derived without the assumption of normality. This change in the bound calculation markedly improved computational speed from O(pm(2)n) to O(m(2)n), where p is the number of permutations in a permutation test, m is the number of time series, and n is the length of each time series. The bounding process is implemented as a computationally efficient software package, FASTLSA, written in C and optimized for threading on multi-core computers, improving its practical computation time. We computationally compare our approach to previous implementations of LSA, demonstrate broad applicability by analyzing time series data from public health, microbial ecology, and social media, and visualize resulting networks using the Cytoscape software. CONCLUSIONS: The FASTLSA software package expands the boundaries of LSA allowing analysis on datasets with millions of co-varying time series. Mapping metadata onto force-directed graphs derived from FASTLSA allows investigators to view correlated cliques and explore previously unrecognized network relationships. The software is freely available for download at: http://www.cmde.science.ubc.ca/hallam/fastLSA/. BioMed Central 2013-01-21 /pmc/articles/PMC3549818/ /pubmed/23368516 http://dx.doi.org/10.1186/1471-2164-14-S1-S3 Text en Copyright ©2013 Durno 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 | Proceedings Durno, W Evan Hanson, Niels W Konwar, Kishori M Hallam, Steven J Expanding the boundaries of local similarity analysis |
title | Expanding the boundaries of local similarity analysis |
title_full | Expanding the boundaries of local similarity analysis |
title_fullStr | Expanding the boundaries of local similarity analysis |
title_full_unstemmed | Expanding the boundaries of local similarity analysis |
title_short | Expanding the boundaries of local similarity analysis |
title_sort | expanding the boundaries of local similarity analysis |
topic | Proceedings |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3549818/ https://www.ncbi.nlm.nih.gov/pubmed/23368516 http://dx.doi.org/10.1186/1471-2164-14-S1-S3 |
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