Recordings were conducted in a magnetically-shielded room with active shielding engaged. With an acquisition bandwidth of 0.1–330 Hz, neuromagnetic responses were sampled continuously at 1 kHz using an Elekta MEG system with 306 magnetic sensors (Elekta, Helsinki, Finland). MEG data from each participant were individually-corrected for head motion and subjected to noise reduction using the signal space separation method with a temporal extension39 (link). Each participant’s MEG data were then coregistered with their structural T1-weighted MRI data using BESA MRI (Version 2.0; BESA GmbH, Gräfelfing, Germany). These neuroanatomic images were acquired with a Philips Achieva 3T X-series scanner using an eight-channel head coil and a 3D fast field echo sequence with the following parameters: TR: 8.09 ms; TE: 3.7 ms; field of view: 24 cm; matrix: 256 × 256; slice thickness: 1 mm with no gap; in-plane resolution: 0.9375 ×  0.9375 mm; sense factor: 1.5. The structural MRI volumes were aligned parallel to the anterior and posterior commissures and were transformed into standardized space after source imaging (i.e., beamforming)40 (link)41 (link).
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