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Enabling ambulatory movement in wearable magnetoencephalography with matrix coil active magnetic shielding
The ability to collect high-quality neuroimaging data during ambulatory participant movement would enable a wealth of neuroscientific paradigms. Wearable magnetoencephalography (MEG) based on optically pumped magnetometers (OPMs) has the potential to allow participant movement during a scan. However...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10465235/ https://www.ncbi.nlm.nih.gov/pubmed/37149237 http://dx.doi.org/10.1016/j.neuroimage.2023.120157 |
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author | Holmes, Niall Rea, Molly Hill, Ryan M. Leggett, James Edwards, Lucy J. Hobson, Peter J. Boto, Elena Tierney, Tim M. Rier, Lukas Rivero, Gonzalo Reina Shah, Vishal Osborne, James Fromhold, T. Mark Glover, Paul Brookes, Matthew J. Bowtell, Richard |
author_facet | Holmes, Niall Rea, Molly Hill, Ryan M. Leggett, James Edwards, Lucy J. Hobson, Peter J. Boto, Elena Tierney, Tim M. Rier, Lukas Rivero, Gonzalo Reina Shah, Vishal Osborne, James Fromhold, T. Mark Glover, Paul Brookes, Matthew J. Bowtell, Richard |
author_sort | Holmes, Niall |
collection | PubMed |
description | The ability to collect high-quality neuroimaging data during ambulatory participant movement would enable a wealth of neuroscientific paradigms. Wearable magnetoencephalography (MEG) based on optically pumped magnetometers (OPMs) has the potential to allow participant movement during a scan. However, the strict zero magnetic field requirement of OPMs means that systems must be operated inside a magnetically shielded room (MSR) and also require active shielding using electromagnetic coils to cancel residual fields and field changes (due to external sources and sensor movements) that would otherwise prevent accurate neuronal source reconstructions. Existing active shielding systems only compensate fields over small, fixed regions and do not allow ambulatory movement. Here we describe the matrix coil, a new type of active shielding system for OPM-MEG which is formed from 48 square unit coils arranged on two planes which can compensate magnetic fields in regions that can be flexibly placed between the planes. Through the integration of optical tracking with OPM data acquisition, field changes induced by participant movement are cancelled with low latency (25 ms). High-quality MEG source data were collected despite the presence of large (65 cm translations and 270°rotations) ambulatory participant movements. |
format | Online Article Text |
id | pubmed-10465235 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
record_format | MEDLINE/PubMed |
spelling | pubmed-104652352023-08-29 Enabling ambulatory movement in wearable magnetoencephalography with matrix coil active magnetic shielding Holmes, Niall Rea, Molly Hill, Ryan M. Leggett, James Edwards, Lucy J. Hobson, Peter J. Boto, Elena Tierney, Tim M. Rier, Lukas Rivero, Gonzalo Reina Shah, Vishal Osborne, James Fromhold, T. Mark Glover, Paul Brookes, Matthew J. Bowtell, Richard Neuroimage Article The ability to collect high-quality neuroimaging data during ambulatory participant movement would enable a wealth of neuroscientific paradigms. Wearable magnetoencephalography (MEG) based on optically pumped magnetometers (OPMs) has the potential to allow participant movement during a scan. However, the strict zero magnetic field requirement of OPMs means that systems must be operated inside a magnetically shielded room (MSR) and also require active shielding using electromagnetic coils to cancel residual fields and field changes (due to external sources and sensor movements) that would otherwise prevent accurate neuronal source reconstructions. Existing active shielding systems only compensate fields over small, fixed regions and do not allow ambulatory movement. Here we describe the matrix coil, a new type of active shielding system for OPM-MEG which is formed from 48 square unit coils arranged on two planes which can compensate magnetic fields in regions that can be flexibly placed between the planes. Through the integration of optical tracking with OPM data acquisition, field changes induced by participant movement are cancelled with low latency (25 ms). High-quality MEG source data were collected despite the presence of large (65 cm translations and 270°rotations) ambulatory participant movements. 2023-07-01 2023-05-05 /pmc/articles/PMC10465235/ /pubmed/37149237 http://dx.doi.org/10.1016/j.neuroimage.2023.120157 Text en https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ) |
spellingShingle | Article Holmes, Niall Rea, Molly Hill, Ryan M. Leggett, James Edwards, Lucy J. Hobson, Peter J. Boto, Elena Tierney, Tim M. Rier, Lukas Rivero, Gonzalo Reina Shah, Vishal Osborne, James Fromhold, T. Mark Glover, Paul Brookes, Matthew J. Bowtell, Richard Enabling ambulatory movement in wearable magnetoencephalography with matrix coil active magnetic shielding |
title | Enabling ambulatory movement in wearable magnetoencephalography with matrix coil active magnetic shielding |
title_full | Enabling ambulatory movement in wearable magnetoencephalography with matrix coil active magnetic shielding |
title_fullStr | Enabling ambulatory movement in wearable magnetoencephalography with matrix coil active magnetic shielding |
title_full_unstemmed | Enabling ambulatory movement in wearable magnetoencephalography with matrix coil active magnetic shielding |
title_short | Enabling ambulatory movement in wearable magnetoencephalography with matrix coil active magnetic shielding |
title_sort | enabling ambulatory movement in wearable magnetoencephalography with matrix coil active magnetic shielding |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10465235/ https://www.ncbi.nlm.nih.gov/pubmed/37149237 http://dx.doi.org/10.1016/j.neuroimage.2023.120157 |
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