Determining the Optimal Number of MEG Trials: A Machine Learning and Speech Decoding Perspective.

Artificial Neural Network MEG Speech Wavelets

Journal

Brain informatics : international conference, BI 2018, Arlington, TX, USA, December 7-9, 2018, proceedings. International Conference on Brain Informatics (2018 : Arlington, Tex.)
Titre abrégé: Brain Inform (2018)
Pays: Switzerland
ID NLM: 101757732

Informations de publication

Date de publication:
Dec 2019
Historique:
pmc-release: 01 12 2019
entrez: 27 11 2019
pubmed: 27 11 2019
medline: 27 11 2019
Statut: ppublish

Résumé

Advancing the knowledge about neural speech mechanisms is critical for developing next-generation, faster brain computer interface to assist in speech communication for the patients with severe neurological conditions (e.g., locked-in syndrome). Among current neuroimaging techniques, Magnetoencephalography (MEG) provides direct representation for the large-scale neural dynamics of underlying cognitive processes based on its optimal spatiotemporal resolution. However, the MEG measured neural signals are smaller in magnitude compared to the background noise and hence, MEG usually suffers from a low signal-to-noise ratio (SNR) at the single-trial level. To overcome this limitation, it is common to record many trials of the same event-task and use the time-locked average signal for analysis, which can be very time consuming. In this study, we investigated the effect of the number of MEG recording trials required for speech decoding using a machine learning algorithm. We used a wavelet filter for generating the denoised neural features to train an Artificial Neural Network (ANN) for speech decoding. We found that wavelet based denoising increased the SNR of the neural signal prior to analysis and facilitated accurate speech decoding performance using as few as 40 single-trials. This study may open up the possibility of limiting MEG trials for other task evoked studies as well.

Identifiants

pubmed: 31768504
doi: 10.1007/978-3-030-05587-5_16
pmc: PMC6876632
mid: NIHMS1058370
doi:

Types de publication

Journal Article

Langues

eng

Pagination

163-172

Subventions

Organisme : NINDS NIH HHS
ID : R01 NS082453
Pays : United States

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Auteurs

Debadatta Dash (D)

Department of Bioengineering, University of Texas at Dallas, Richardson, USA.

Paul Ferrari (P)

Department of Psychology, University of Texas at Austin, Austin, USA.
MEG Laboratory, Dell Children's Medical Center, Austin, USA.

Saleem Malik (S)

MEG Lab, Cook Children's Hospital, Fort Worth, TX, USA.

Albert Montillo (A)

Department of Radiology, UT Southwestern Medical Center, Dallas, USA.
Department of Bioinformatics, UT Southwestern Medical Center, Dallas, USA.

Joseph A Maldjian (JA)

Department of Radiology, UT Southwestern Medical Center, Dallas, USA.

Jun Wang (J)

Department of Bioengineering, University of Texas at Dallas, Richardson, USA.
Callier Center for Communication Disorders, University of Texas at Dallas, Richardson, USA.

Classifications MeSH