Evidence map›Paper›PMID 42539285›Full record

ArticlebioRxiv : the preprint server for biology2026

Noise Optimization of Basic Signal Component Extraction for Cryogenic and On-Scalp Magnetoencephalography (MEG).

Alexandria McPherson, Sepp Sanchirico, Albert Xu, Eric Larson, Milena Kaestner, William Turner, Laura Gwilliams, Samu Taulu

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Alexandria McPhersonDepartment of Psychology, Stanford University, 450 Jane Stanford Way, Building 420, CA 94305.ORCID 0000-0003-0195-6234
Sepp SanchiricoDepartment of Physics, University of Washington, Seattle, WA 98195, United States.
Albert XuDepartment of Physics, University of Washington, Seattle, WA 98195, United States.
Eric LarsonInstitute for Learning and Brain Sciences, University of Washington, Seattle, WA 98195, United States.
Milena KaestnerWu Tsai Neurosciences Institute, Stanford Neurosciences Building, 290 Jane Stanford Way, Rm E152, Stanford, CA 94305.ORCID 0000-0003-1202-7772
William TurnerDepartment of Psychology, Stanford University, 450 Jane Stanford Way, Building 420, CA 94305.
Laura GwilliamsDepartment of Psychology, Stanford University, 450 Jane Stanford Way, Building 420, CA 94305.ORCID 0000-0002-9213-588X
Samu TauluDepartment of Physics, University of Washington, Seattle, WA 98195, United States.ORCID 0000-0001-6164-3366

Funding

Scalable Software for Distributed Processing and Visualization of Multi-Site MEG/EEG DatasetsR01NS104585 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI MATTI HAMALAINEN · 2018 to 2026
$4.3M
Spatial-frequency decompositions for enhancement of source reconstruction resolution in MEGR21EB033577 · NIBIB · UNIVERSITY OF WASHINGTON · PI TAULU, SAMU · 2022 to 2024
$622k
NIBIB NIH HHS R21 EB033577NINDS NIH HHS R01 NS104585
6 · The paper itself

Abstract

Magnetoencephalography (MEG) measures human neural activity non-invasively with spatio-temporal precision, and has been foundational in enabling impactful discoveries in cognitive neuroscience. New on-scalp MEG sensor technologies, such as OPM-MEG, offer the opportunity to capture more information about the neuronal magnetic fields with higher sensitivity to more complex, higher order spatial components, leading to improved source localization. The accuracy of MEG and OPM-MEG source localization relies on data preprocessing techniques to isolate the neuronal fields from other magnetic and biomagnetic sources through signal space separation, rejection, and suppression methods. Current preprocessing methods risk rejecting brain signals of interest, or can spread sensor noise artifacts unknowingly. Here we propose a novel preprocessing method for MEG, and test the extent to which it overcomes limitations of prior methods. Specifically, we derive, apply, and assess a novel signal space separation (SSS) method with Foster's inverse, a weighted matrix inversion protocol that can utilize information about the MEG sensor noise and artifacts to reconstruct neuronal activity. With simulations, phantom head cryogenic MEG recordings, and subject recordings with two OPM-MEG systems, we show that Foster's inverse with SSS offers a more robust and stable reconstruction of the neuronal magnetic fields, especially in the face of sensor noise and artifacts. As the field of cognitive neuroscience continues to embrace MEG and OPM-MEG, Foster's inverse with SSS offers a robust and powerful data preprocessing technique for reducing noise and improving source localization of the underlying neuronal currents.

Identifiers

PMID42539285
PMCPMC13419842

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.