A Generative Model for Measuring Latent Timing Structure in Motor Sequences
Motor variability often reflects a mixture of different neural and peripheral sources operating over a range of timescales. We present a statistical model of sequence timing that can be used to measure three distinct components of timing variability: global tempo changes that are spread across the s...
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| Published in | PloS one Vol. 7; no. 7; p. e37616 |
|---|---|
| Main Authors | , |
| Format | Journal Article |
| Language | English |
| Published |
United States
Public Library of Science
16.07.2012
Public Library of Science (PLoS) |
| Subjects | |
| Online Access | Get full text |
| ISSN | 1932-6203 1932-6203 |
| DOI | 10.1371/journal.pone.0037616 |
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| Abstract | Motor variability often reflects a mixture of different neural and peripheral sources operating over a range of timescales. We present a statistical model of sequence timing that can be used to measure three distinct components of timing variability: global tempo changes that are spread across the sequence, such as might stem from neuromodulatory sources with widespread influence; fast, uncorrelated timing noise, stemming from noisy components within the neural system; and timing jitter that does not alter the timing of subsequent elements, such as might be caused by variation in the motor periphery or by measurement error. In addition to quantifying the variability contributed by each of these latent factors in the data, the approach assigns maximum likelihood estimates of each factor on a trial-to-trial basis. We applied the model to adult zebra finch song, a temporally complex behavior with rich structure on multiple timescales. We find that individual song vocalizations (syllables) contain roughly equal amounts of variability in each of the three components while overall song length is dominated by global tempo changes. Across our sample of syllables, both global and independent variability scale with average length while timing jitter does not, a pattern consistent with the Wing and Kristofferson (1973) model of sequence timing. We also find significant day-to-day drift in all three timing sources, but a circadian pattern in tempo only. In tests using artificially generated data, the model successfully separates out the different components with small error. The approach provides a general framework for extracting distinct sources of timing variability within action sequences, and can be applied to neural and behavioral data from a wide array of systems. |
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| AbstractList | Motor variability often reflects a mixture of different neural and peripheral sources operating over a range of timescales. We present a statistical model of sequence timing that can be used to measure three distinct components of timing variability: global tempo changes that are spread across the sequence, such as might stem from neuromodulatory sources with widespread influence; fast, uncorrelated timing noise, stemming from noisy components within the neural system; and timing jitter that does not alter the timing of subsequent elements, such as might be caused by variation in the motor periphery or by measurement error. In addition to quantifying the variability contributed by each of these latent factors in the data, the approach assigns maximum likelihood estimates of each factor on a trial-to-trial basis. We applied the model to adult zebra finch song, a temporally complex behavior with rich structure on multiple timescales. We find that individual song vocalizations (syllables) contain roughly equal amounts of variability in each of the three components while overall song length is dominated by global tempo changes. Across our sample of syllables, both global and independent variability scale with average length while timing jitter does not, a pattern consistent with the Wing and Kristofferson (1973) model of sequence timing. We also find significant day-to-day drift in all three timing sources, but a circadian pattern in tempo only. In tests using artificially generated data, the model successfully separates out the different components with small error. The approach provides a general framework for extracting distinct sources of timing variability within action sequences, and can be applied to neural and behavioral data from a wide array of systems. Motor variability often reflects a mixture of different neural and peripheral sources operating over a range of timescales. We present a statistical model of sequence timing that can be used to measure three distinct components of timing variability: global tempo changes that are spread across the sequence, such as might stem from neuromodulatory sources with widespread influence; fast, uncorrelated timing noise, stemming from noisy components within the neural system; and timing jitter that does not alter the timing of subsequent elements, such as might be caused by variation in the motor periphery or by measurement error. In addition to quantifying the variability contributed by each of these latent factors in the data, the approach assigns maximum likelihood estimates of each factor on a trial-to-trial basis. We applied the model to adult zebra finch song, a temporally complex behavior with rich structure on multiple timescales. We find that individual song vocalizations (syllables) contain roughly equal amounts of variability in each of the three components while overall song length is dominated by global tempo changes. Across our sample of syllables, both global and independent variability scale with average length while timing jitter does not, a pattern consistent with the Wing and Kristofferson (1973) model of sequence timing. We also find significant day-to-day drift in all three timing sources, but a circadian pattern in tempo only. In tests using artificially generated data, the model successfully separates out the different components with small error. The approach provides a general framework for extracting distinct sources of timing variability within action sequences, and can be applied to neural and behavioral data from a wide array of systems.Motor variability often reflects a mixture of different neural and peripheral sources operating over a range of timescales. We present a statistical model of sequence timing that can be used to measure three distinct components of timing variability: global tempo changes that are spread across the sequence, such as might stem from neuromodulatory sources with widespread influence; fast, uncorrelated timing noise, stemming from noisy components within the neural system; and timing jitter that does not alter the timing of subsequent elements, such as might be caused by variation in the motor periphery or by measurement error. In addition to quantifying the variability contributed by each of these latent factors in the data, the approach assigns maximum likelihood estimates of each factor on a trial-to-trial basis. We applied the model to adult zebra finch song, a temporally complex behavior with rich structure on multiple timescales. We find that individual song vocalizations (syllables) contain roughly equal amounts of variability in each of the three components while overall song length is dominated by global tempo changes. Across our sample of syllables, both global and independent variability scale with average length while timing jitter does not, a pattern consistent with the Wing and Kristofferson (1973) model of sequence timing. We also find significant day-to-day drift in all three timing sources, but a circadian pattern in tempo only. In tests using artificially generated data, the model successfully separates out the different components with small error. The approach provides a general framework for extracting distinct sources of timing variability within action sequences, and can be applied to neural and behavioral data from a wide array of systems. |
| Audience | Academic |
| Author | Troyer, Todd W. Glaze, Christopher M. |
| AuthorAffiliation | 2 Department of Biology, University of Texas at San Antonio, San Antonio, Texas, United States of America 1 Department of Biology, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America Claremont Colleges, United States of America |
| AuthorAffiliation_xml | – name: Claremont Colleges, United States of America – name: 1 Department of Biology, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America – name: 2 Department of Biology, University of Texas at San Antonio, San Antonio, Texas, United States of America |
| Author_xml | – sequence: 1 givenname: Christopher M. surname: Glaze fullname: Glaze, Christopher M. – sequence: 2 givenname: Todd W. surname: Troyer fullname: Troyer, Todd W. |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/22815683$$D View this record in MEDLINE/PubMed |
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| CitedBy_id | crossref_primary_10_1016_j_neuron_2013_07_049 crossref_primary_10_1038_s41467_018_03261_5 crossref_primary_10_1103_PhysRevE_102_052406 crossref_primary_10_1152_jn_00296_2017 crossref_primary_10_1152_jn_00154_2020 crossref_primary_10_1007_s00359_015_1046_z crossref_primary_10_1152_jn_00578_2012 |
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| ContentType | Journal Article |
| Copyright | COPYRIGHT 2012 Public Library of Science 2012 Glaze, Troyer. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. Glaze, Troyer. 2012 |
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| Snippet | Motor variability often reflects a mixture of different neural and peripheral sources operating over a range of timescales. We present a statistical model of... |
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| SubjectTerms | Algorithms Analysis Animals Biology Birds Circadian Rhythm Circadian rhythms Datasets Decomposition Error analysis Likelihood Functions Male Mathematical models Mathematics Maximum likelihood estimates Measurement Models, Statistical Monte Carlo Method Motor Activity - physiology Neuromodulation Passeriformes - physiology Singing - physiology Song Standard deviation Statistical models Studies Syllables Time Factors Time measurement Timing jitter Variability Vibration Zebra finch |
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| Title | A Generative Model for Measuring Latent Timing Structure in Motor Sequences |
| URI | https://www.ncbi.nlm.nih.gov/pubmed/22815683 https://www.proquest.com/docview/1348114886 https://www.proquest.com/docview/1027371383 https://pubmed.ncbi.nlm.nih.gov/PMC3398023 https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0037616&type=printable https://doaj.org/article/eccf84c8cf7d4909baf4242780322ccb http://dx.doi.org/10.1371/journal.pone.0037616 |
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