» Articles » PMID: 29973645

Across-subject Offline Decoding of Motor Imagery from MEG and EEG

Overview
Journal Sci Rep
Specialty Science
Date 2018 Jul 6
PMID 29973645
Citations 14
Authors
Affiliations
Soon will be listed here.
Abstract

Long calibration time hinders the feasibility of brain-computer interfaces (BCI). If other subjects' data were used for training the classifier, BCI-based neurofeedback practice could start without the initial calibration. Here, we compare methods for inter-subject decoding of left- vs. right-hand motor imagery (MI) from MEG and EEG. Six methods were tested on data involving MEG and EEG measurements of healthy participants. Inter-subject decoders were trained on subjects showing good within-subject accuracy, and tested on all subjects, including poor performers. Three methods were based on Common Spatial Patterns (CSP), and three others on logistic regression with l - or l -norm regularization. The decoding accuracy was evaluated using (1) MI and (2) passive movements (PM) for training, separately for MEG and EEG. With MI training, the best accuracies across subjects (mean 70.6% for MEG, 67.7% for EEG) were obtained using multi-task learning (MTL) with logistic regression and l-norm regularization. MEG yielded slightly better average accuracies than EEG. With PM training, none of the inter-subject methods yielded above chance level (58.7%) accuracy. In conclusion, MTL and training with other subject's MI is efficient for inter-subject decoding of MI. Passive movements of other subjects are likely suboptimal for training the MI classifiers.

Citing Articles

Coherence-based channel selection and Riemannian geometry features for magnetoencephalography decoding.

Tang C, Gao T, Wang G, Chen B Cogn Neurodyn. 2024; 18(6):3535-3548.

PMID: 39712116 PMC: 11655792. DOI: 10.1007/s11571-024-10085-1.


Revisiting the role of computational neuroimaging in the era of integrative neuroscience.

Loosen A, Kato A, Gu X Neuropsychopharmacology. 2024; 50(1):103-113.

PMID: 39242921 PMC: 11525590. DOI: 10.1038/s41386-024-01946-8.


High-density transparent graphene arrays for predicting cellular calcium activity at depth from surface potential recordings.

Ramezani M, Kim J, Liu X, Ren C, Alothman A, De-Eknamkul C Nat Nanotechnol. 2024; 19(4):504-513.

PMID: 38212523 PMC: 11742260. DOI: 10.1038/s41565-023-01576-z.


Group-level brain decoding with deep learning.

Csaky R, van Es M, Jones O, Woolrich M Hum Brain Mapp. 2023; 44(17):6105-6119.

PMID: 37753636 PMC: 10619368. DOI: 10.1002/hbm.26500.


The effect of visual and proprioceptive feedback on sensorimotor rhythms during BCI training.

Halme H, Parkkonen L PLoS One. 2022; 17(2):e0264354.

PMID: 35196360 PMC: 8865669. DOI: 10.1371/journal.pone.0264354.


References
1.
Daly J, Wolpaw J . Brain-computer interfaces in neurological rehabilitation. Lancet Neurol. 2008; 7(11):1032-43. DOI: 10.1016/S1474-4422(08)70223-0. View

2.
Ang K, Guan C, Chua K, Phua K, Wang C, Chin Z . A clinical study of motor imagery BCI performance in stroke by including calibration data from passive movement. Annu Int Conf IEEE Eng Med Biol Soc. 2013; 2013:6603-6. DOI: 10.1109/EMBC.2013.6611069. View

3.
Koles Z, Lazar M, Zhou S . Spatial patterns underlying population differences in the background EEG. Brain Topogr. 1990; 2(4):275-84. DOI: 10.1007/BF01129656. View

4.
Oostenveld R, Fries P, Maris E, Schoffelen J . FieldTrip: Open source software for advanced analysis of MEG, EEG, and invasive electrophysiological data. Comput Intell Neurosci. 2011; 2011:156869. PMC: 3021840. DOI: 10.1155/2011/156869. View

5.
Teo W, Chew E . Is motor-imagery brain-computer interface feasible in stroke rehabilitation?. PM R. 2014; 6(8):723-8. DOI: 10.1016/j.pmrj.2014.01.006. View