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Biological Time Series Analysis Using a Context Free Language: Applicability to Pulsatile Hormone Data
We present a novel approach for analyzing biological time-series data using a context-free language (CFL) representation that allows the extraction and quantification of important features from the time-series. This representation results in Hierarchically AdaPtive (HAP) analysis, a suite of multipl...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4153563/ https://www.ncbi.nlm.nih.gov/pubmed/25184442 http://dx.doi.org/10.1371/journal.pone.0104087 |
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author | Dean, Dennis A. Adler, Gail K. Nguyen, David P. Klerman, Elizabeth B. |
author_facet | Dean, Dennis A. Adler, Gail K. Nguyen, David P. Klerman, Elizabeth B. |
author_sort | Dean, Dennis A. |
collection | PubMed |
description | We present a novel approach for analyzing biological time-series data using a context-free language (CFL) representation that allows the extraction and quantification of important features from the time-series. This representation results in Hierarchically AdaPtive (HAP) analysis, a suite of multiple complementary techniques that enable rapid analysis of data and does not require the user to set parameters. HAP analysis generates hierarchically organized parameter distributions that allow multi-scale components of the time-series to be quantified and includes a data analysis pipeline that applies recursive analyses to generate hierarchically organized results that extend traditional outcome measures such as pharmacokinetics and inter-pulse interval. Pulsicons, a novel text-based time-series representation also derived from the CFL approach, are introduced as an objective qualitative comparison nomenclature. We apply HAP to the analysis of 24 hours of frequently sampled pulsatile cortisol hormone data, which has known analysis challenges, from 14 healthy women. HAP analysis generated results in seconds and produced dozens of figures for each participant. The results quantify the observed qualitative features of cortisol data as a series of pulse clusters, each consisting of one or more embedded pulses, and identify two ultradian phenotypes in this dataset. HAP analysis is designed to be robust to individual differences and to missing data and may be applied to other pulsatile hormones. Future work can extend HAP analysis to other time-series data types, including oscillatory and other periodic physiological signals. |
format | Online Article Text |
id | pubmed-4153563 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-41535632014-09-05 Biological Time Series Analysis Using a Context Free Language: Applicability to Pulsatile Hormone Data Dean, Dennis A. Adler, Gail K. Nguyen, David P. Klerman, Elizabeth B. PLoS One Research Article We present a novel approach for analyzing biological time-series data using a context-free language (CFL) representation that allows the extraction and quantification of important features from the time-series. This representation results in Hierarchically AdaPtive (HAP) analysis, a suite of multiple complementary techniques that enable rapid analysis of data and does not require the user to set parameters. HAP analysis generates hierarchically organized parameter distributions that allow multi-scale components of the time-series to be quantified and includes a data analysis pipeline that applies recursive analyses to generate hierarchically organized results that extend traditional outcome measures such as pharmacokinetics and inter-pulse interval. Pulsicons, a novel text-based time-series representation also derived from the CFL approach, are introduced as an objective qualitative comparison nomenclature. We apply HAP to the analysis of 24 hours of frequently sampled pulsatile cortisol hormone data, which has known analysis challenges, from 14 healthy women. HAP analysis generated results in seconds and produced dozens of figures for each participant. The results quantify the observed qualitative features of cortisol data as a series of pulse clusters, each consisting of one or more embedded pulses, and identify two ultradian phenotypes in this dataset. HAP analysis is designed to be robust to individual differences and to missing data and may be applied to other pulsatile hormones. Future work can extend HAP analysis to other time-series data types, including oscillatory and other periodic physiological signals. Public Library of Science 2014-09-03 /pmc/articles/PMC4153563/ /pubmed/25184442 http://dx.doi.org/10.1371/journal.pone.0104087 Text en © 2014 Dean et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Dean, Dennis A. Adler, Gail K. Nguyen, David P. Klerman, Elizabeth B. Biological Time Series Analysis Using a Context Free Language: Applicability to Pulsatile Hormone Data |
title | Biological Time Series Analysis Using a Context Free Language: Applicability to Pulsatile Hormone Data |
title_full | Biological Time Series Analysis Using a Context Free Language: Applicability to Pulsatile Hormone Data |
title_fullStr | Biological Time Series Analysis Using a Context Free Language: Applicability to Pulsatile Hormone Data |
title_full_unstemmed | Biological Time Series Analysis Using a Context Free Language: Applicability to Pulsatile Hormone Data |
title_short | Biological Time Series Analysis Using a Context Free Language: Applicability to Pulsatile Hormone Data |
title_sort | biological time series analysis using a context free language: applicability to pulsatile hormone data |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4153563/ https://www.ncbi.nlm.nih.gov/pubmed/25184442 http://dx.doi.org/10.1371/journal.pone.0104087 |
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