Biology subjects

Brookes, M. J.

Publications and source records attributed to Brookes, M. J..

At least 19 recordsLinked to original sources

bioRxiv2026

Neural Fingerprinting based on Brain Network Dynamics: A Cross-Platform MEG Study

Neural fingerprinting seeks to identify individuals based on measurements of brain activity, exploiting the fact that aspects of brain function unique to an individual remain stable across repeated scans. Magnetoencephalography (MEG) is a powerful technique for fingerprinting. However, most MEG studies have used conventional (SQUID-based) MEG technology and typically rely on data aggregated over time, overlooking the rich temporal dynamics available in MEG. Here, using SQUID-MEG and the more recently introduced OPM-MEG, we showed fingerprinting was possible within and between modalities using static (time-aggregated) features; this is consistent with previous work. We further asked whether fingerprinting was possible based on network dynamics, estimated using a canonical hidden Markov model (CHMM). Results showed that the CHMM-derived networks provide a better fit to SQUID data than to OPM data; however, this effect was small and to be expected given the canonical networks were trained on SQUID data. We further showed that fingerprinting was possible within and between modalities using CHMM-derived state activation time courses and state power spectral densities. However, state summary statistics and transition probabilities only supported within modality fingerprinting. Our findings suggest that subject-specific information is preserved within CHMM states and across MEG technologies. This represents an important step towards advancing our understanding of brain dynamics, and particularly the brain networks delineated by the CHMM. The study also supports the future use of the CHMM for processing and interpretation of OPM-MEG data.

neuroscience↗

bioRxiv2026

OPM-MEG reveals protracted maturation of visual phase-amplitude coupling from early childhood to adulthood

Cross-frequency coupling describes interactions between neural ensembles operating at different frequency bands, and has been proposed to underlie coordination of brain activity over multiple temporal and spatial scales. Phase amplitude coupling (PAC) describes modulation of the amplitude of high-frequency oscillations by the phase of low frequency oscillations. MEG work in adults has demonstrated that alpha-gamma PAC may support visual perception. However, very little work has investigated visual PAC in children, or the development of this process between childhood and adulthood. Here we investigated the development of PAC in a sample of 101 individuals, comprising 50 children (aged 2-13 years) and 51 adults (21-34 years). Participants completed a passive visual stimulation paradigm while neural responses were recorded using a wearable whole-head OPM-MEG system. Sensor-level data were spatially resolved to visual cortex, and we quantified coupling between the phase of low-frequency oscillations (5-13 Hz) and the amplitude of broadband gamma oscillations (28-100 Hz) in each participant. In the adult data, we identified a cluster of phase-amplitude frequency pairs (phase: 7-11 Hz, amplitude: 52-66 Hz) in which there was strong evidence for an increase in PAC following stimulus presentation relative to baseline. Within this cluster, the magnitude of stimulus-induced PAC was positively correlated with age across all participants. Meanwhile, we did not see credible evidence for visual PAC at any frequency pair(s) within the child group. These results suggest that, alongside well-documented developmental changes in band-specific oscillatory power and connectivity, visual PAC represents a distinct functional process which matures with age.

neuroscience↗

bioRxiv2026

Beta-band dynamics during a naturalistic motor task: an OPM-MEG study

Beta oscillations are a fundamental feature of brain activity, linked to long-range connectivity within canonical networks, inhibition of sensorimotor cortices and the maintenance of a stable sensorimotor state in situations where the external world is predictable. The importance of beta oscillations in brain function is underscored by observations of their perturbation in neurological and psychiatric disorders. However, the precise role played by beta activity, particularly in mediating complex or skilful movements, remains incompletely understood. Here, we used a newly developed wearable optically pumped magnetometer-based magnetoencephalography (OPM-MEG) system to measure beta dynamics as participants learned to play a musical instrument. Twenty-two novice players took part in a study in which OPM-MEG data were recorded during two scanning sessions, while participants attempted to play a tune on a violin. Between the two sessions, participants received a violin lesson from an expert teacher. Results showed that robust data could be acquired during this naturalistic task, with beta oscillations decreasing in amplitude during movement and increasing upon movement cessation, as expected. Moreover, beta power whilst playing, in the motor and pre-motor areas, was significantly elevated after the lesson compared to before, and the movement-related modulation of beta amplitude was more pronounced after the lesson. These findings align with predictive coding models which suggest that beta amplitude should increase when individuals have greater certainty over the movements they carry out. Our study adds to an expanding literature on the role of beta oscillations and provides further evidence for the utility of OPM-MEG in naturalistic neuroscience.

neuroscience↗

bioRxiv2026

Exploring the beta burst dynamics of cued voluntary movements in Tourette Syndrome

Tourette Syndrome (TS) is a neurodevelopmental hyperkinetic disorder characterised by involuntary tics. These tics are thought to arise due to hyperexcitability of the motor cortex due to disinhibition within the cortico-striato-thalamo-cortical pathway. Given the involvement of motor circuits in this disorder, we explored whether there is a difference in the oscillatory dynamics of voluntary movements in people with tic disorders. We recorded optically pumped magnetometer magnetoencephalography during cued voluntary finger abductions in individuals with tic disorders and age- and sex-matched neurotypical controls. We analysed the data both using conventional time frequency analysis and using hidden Markov modelling to explore the difference in beta burst characteristics and dynamics. Whilst no differences were seen between groups during conventional analysis, we demonstrated an increase in beta burst duration during the post-movement beta rebound within the contralateral motor cortex in individuals with TS suggestive of increased inhibition following movement. We also show evidence of increased contralateral sensorimotor functional connectivity and reduced connectivity from and between frontal regions, as measured using coincident beta bursts. This is suggestive of disrupted functional connectivity within frontal control networks in individuals with TS.

neuroscience↗

bioRxiv2025

Cortical-layer EEG-fMRI at 7T: experimental setup and analysis pipeline to elucidate generating mechanisms of alpha oscillations

Alpha band (8-13Hz) electroencephalography (EEG) oscillations play a key role in cognition, but their generating mechanisms are still poorly understood. Most studies investigating laminar origins of alpha oscillations have been conducted on animals using invasive intracranial recordings. To relate these findings to human alpha generation, non-invasive techniques need to be developed. Layer functional Magnetic Resonance Imaging (fMRI) at ultra-high field (UHF, 7T) allows for the interrogation of brain responses across cortical depths and combined with simultaneous EEG, provides the opportunity to gain new insight into human alpha generation mechanisms. This work establishes a framework to study the generating mechanisms of electrophysiological signals non-invasively in humans using simultaneous EEG layer-fMRI. Data were acquired on 10 participants during an eyes closed/eyes open paradigm. We showed that in 9/10 participants the quality of EEG and Blood Oxygenation Level Dependent (BOLD) fMRI data were sufficient to observe a significant negative correlation between EEG alpha power and the BOLD signal in visual cortex grey matter to the eyes open/eyes closed task. "Deveining" was performed to overcome the increase in BOLD signal toward the pial surface due to draining veins, and the effects of each of the steps in the deveining analysis on the cortical depth profiles of the negative alpha-BOLD correlations studied. The largest effect was dependent on the exclusion of voxels in the tissue immediately surrounding veins. Following deveining, the cortical depth profiles showed the negative alpha-BOLD correlations were significantly weaker in the middle depths compared with deep and superficial depths. When a boxcar rather than EEG alpha power was used to model the task, this depth-dependence was not seen, suggesting this was specific to spontaneous alpha-power modulations. In conclusion, we have established a method to non-invasively interrogate the origins of electrophysiological signals. Our alpha-BOLD depth profiles suggest the alpha signal to an eyes open-closed task is generated in superficial and deep layers suggesting top-down processes.

neuroscience↗

bioRxiv2025

Source Reconstruction Without an MRI using Optically Pumped Magnetometer based Magnetoencephalography

Source modelling in magnetoencephalography (MEG) maps the spatial origins of electrophysiological signals in the brain. Typically, this requires an anatomical MRI scan of the subjects head, from which a model of the neuromagnetic field (the forward model) is derived. Wearable MEG - based on optically pumped magnetometers (OPMs) - enables MEG measurement from participants who struggle to cope with conventional scanning environments (e.g. children), enabling study of novel cohorts. However, its value is limited if an MRI scan is still required for source modelling. Here we describe a method of warping template MRIs to 3D structured-light scans of the head, to generate "pseudo-MRIs". We apply our method using data from 20 participants during a sensory task, measuring induced (beta band) responses and whole-brain functional connectivity. Results show that the group average locations of peak task-induced beta modulation were separated by 2.75 mm, when comparing real- and pseudo-MRI approaches. Group averaged time-frequency spectra were also highly correlated (Pearson correlation 0.99) as were functional connectome matrices (0.87), and global connectivity (0.98). In sum, our results demonstrate that source-localized OPM-MEG data, modelled with and without an individual MRI scan can be similar. This will be useful for future studies where MRI data capture is challenging.

neuroscience↗

bioRxiv2024

Measuring the neurodevelopmental trajectory of excitatory-inhibitory balance via visual gamma oscillations

Disruption of the balance between excitatory and inhibitory neurotransmission (E-I balance) underlies theories of many neurodevelopmental disorders, however, its study is typically restricted to adults, animal models and the lab-bench. Neurophysiological oscillations in the gamma frequency band relate closely to E-I balance, and a new technology - OPM-MEG - offers the possibility to measure such signals across the lifespan. We used OPM-MEG to measure gamma oscillations induced by visual stimulation in >100 participants, aged 2-34 years. We demonstrate a significantly changing spectrum with age, with low amplitude broadband gamma oscillations in children and high amplitude band limited oscillations dominating in adults. We used a canonical cortical microcircuit to model these gamma signals, revealing significant age-related shifts in E-I balance in superficial pyramidal neurons in visual cortex. Our findings detail the first MEG metrics of gamma oscillations and their underlying generators from toddlerhood, providing a benchmark against which future studies can contextualise.

neuroscience↗

bioRxiv2024

A Novel, Robust, and Portable Platform for Magnetoencephalography using Optically Pumped Magnetometers

Magnetoencephalography (MEG) measures brain function via assessment of magnetic fields generated by neural currents. Conventional MEG uses superconducting sensors, which place significant limitations on performance, practicality, and deployment; however, the field has been revolutionised in recent years by the introduction of optically-pumped-magnetometers (OPMs). OPMs enable measurement of the MEG signal without cryogenics, and consequently the conception of OPM-MEG systems which ostensibly allow increased sensitivity and resolution, lifespan compliance, free subject movement, and lower cost. However, OPM-MEG remains in its infancy with limitations on both sensor and system design. Here, we report a new OPM-MEG design with miniaturised and integrated electronic control, a high level of portability, and improved sensor dynamic range (arguably the biggest limitation of existing instrumentation). We show that this system produces equivalent measures when compared to an established instrument; specifically, when measuring task-induced beta-band, gamma-band and evoked neuro-electrical responses, source localisations from the two systems were highly comparable and temporal correlation was >0.7 at the individual level and >0.9 for groups. Using an electromagnetic phantom, we demonstrate improved dynamic range by running the system in background fields up to 8 nT. We show that the system is effective in gathering data during free movement (including a sitting-to-standing paradigm) and that it is compatible with simultaneous electroencephalography (EEG - the clinical standard). Finally, we demonstrate portability by moving the system between two laboratories. Overall, our new system is shown to be a significant step forward for OPM-MEG technology and offers an attractive platform for next generation functional medical imaging.

neuroscience↗

bioRxiv2024

The neurodevelopmental trajectory of beta band oscillations: an OPM-MEG study

Neural oscillations mediate the coordination of activity within and between brain networks, supporting cognition and behaviour. How these processes develop throughout childhood is not only an important neuroscientific question but could also shed light on the mechanisms underlying neurological and psychiatric disorders. However, measuring the neurodevelopmental trajectory of oscillations has been hampered by confounds from instrumentation. In this paper, we investigate the suitability of a disruptive new imaging platform - Optically Pumped Magnetometer-based magnetoencephalography (OPM-MEG) - to study oscillations during brain development. We show how a unique 192-channel OPM-MEG device, which is adaptable to head size and robust to participant movement, can be used to collect high-fidelity electrophysiological data in individuals aged between 2 and 34 years. Data were collected during a somatosensory task, and we measured both stimulus-induced modulation of beta oscillations in sensory cortex, and whole-brain connectivity, showing that both modulate significantly with age. Moreover, we show that pan-spectral bursts of electrophysiological activity drive task-induced beta modulation, and that their probability of occurrence and spectral content change with age. Our results offer new insights into the developmental trajectory of beta oscillations and provide clear evidence that OPM-MEG is an ideal platform for studying electrophysiology in neurodevelopment.

neuroscience↗

bioRxiv2023

Combining video telemetry and wearable MEG for naturalistic imaging

Neuroimaging studies have typically relied on rigorously controlled experimental paradigms to probe cognition, in which movement is restricted, primitive, an afterthought or merely used to indicate a subjects choice. Whilst powerful, these paradigms do not often resemble how we behave in everyday life, so a new generation of ecologically valid experiments are being developed. Magnetoencephalography (MEG) measures neural activity by sensing extracranial magnetic fields. It has recently been transformed from a large, static imaging modality to a wearable method where participants can move freely. This makes wearable MEG systems a prime candidate for naturalistic experiments going forward. However, these experiments will also require novel methods to capture and integrate information about complex behaviour executed during neuroimaging, and it is not yet clear how this could be achieved. Here we use video recordings of multi-limb dance moves, processed with open-source machine learning methods, to automatically identify analysis time windows of interest in concurrent wearable MEG data. In a first step, we compare a traditional, block-designed analysis of limb movements, where the times of interest are based on stimulus presentation, to an analysis pipeline based on hidden Markov model states derived from the video telemetry. Next, we show that it is possible to identify discrete modes of neuronal activity related to specific limbs and body posture by processing the participants choreographed movement in a dancing paradigm. This demonstrates the potential of combing video telemetry with mobile neuroimaging for future studies of complex and naturalistic behaviours.

neuroscience↗

bioRxiv2022

Test-Retest Reliability of the Human Connectome: An OPM-MEG study

Magnetoencephalography with optically pumped magnetometers (OPM-MEG) offers a new way to record electrophysiological brain function, with significant advantages over conventional MEG including adaptability to head shape/size, free movement during scanning, better spatial resolution, increased signal, and no reliance on cryogenics. However, OPM-MEG remains in its infancy, with significant questions to be answered regarding optimal system design and robustness. Here, we present an open-source dataset acquired using a newly constructed OPM-MEG system with a triaxial sensor design averaging 168 channels. Using OPM-optimised magnetic shielding and active background-field control, we measure the test-retest reliability of the human connectome. We employ amplitude envelope correlation to measure whole-brain functional connectivity in 10 individuals whilst they watch a 600 s move clip. Our results show high repeatability between experimental runs at the group level, with a correlation coefficient of 0.81 in the theta, 0.93 in alpha and 0.94 in beta frequency ranges. At the individual subject level, we found marked differences between individuals, but high within-subject robustness (correlations of 0.56 {+/-} 0.25, 0.72 {+/-} 0.15 and 0.78 {+/-} 0.13 in theta, alpha and beta respectively). These results compare well to previously reported findings using conventional MEG; they show that OPM-MEG is a viable way to characterise whole brain connectivity and add significant weight to a growing argument that OPMs can overtake cryogenic sensors as the fundamental building block of MEG systems.

neuroscience↗

bioRxiv2021

Using OPM-MEG in contrasting magnetic environments

Magnetoencephalography (MEG) has been revolutionised in recent years by optically pumped magnetometers (OPMs). "OPM-MEG" offers higher sensitivity, better spatial resolution and lower cost than conventional instrumentation based on superconducting quantum interference devices (SQUIDS). Moreover, OPMs offer the possibility of motion robustness and lifespan compliance, dramatically expanding the range of MEG applications. However, OPM-MEG remains nascent technology; it places stringent requirements on magnetic shielding, and whilst a number of viable systems exist, most are custom made and there have been no cross-site investigations showing the reliability of data. In this paper, we undertake the first cross-site OPM-MEG comparison, using near identical commercial systems scanning the same participant. The two sites are deliberately contrasting, with different magnetic environments: a "green field" campus university site with an OPM-optimised shielded room (low interference) and a city centre hospital site with a "standard" (non-optimised) MSR (high interference). We show that despite a 25-fold difference in background field, and a 30-fold difference in low frequency interference, using dynamic field control and software-based suppression of interference we can generate comparable noise floors at both sites. In human data recorded during a visuo-motor task and a face processing paradigm, we were able to generate similar data, with source localisation showing that brain regions could be pinpointed with just ~10 mm spatial discrepancy and temporal correlations of > 80%. Overall, our study demonstrates that "plug- and-play" OPM-MEG systems exist and can be sited even in challenging magnetic environments.

neuroscience↗

bioRxiv2021

Naturalistic hyperscanning with wearable magnetoencephalography

The evolution of human cognitive function is reliant on complex social interactions which form the behavioural foundation of who we are. These social capacities are subject to dramatic change in disease and injury; yet their supporting neural substrates remain poorly understood. Hyperscanning employs functional neuroimaging to simultaneously assess brain activity in two individuals and offers the best means to understand the neural basis of social interaction. However, present technologies are limited, either by poor performance (low spatial/temporal precision) or unnatural scanning environment (claustrophobic scanners, with interactions via video). Here, we solve this problem by developing a new form of hyperscanning using wearable magnetoencephalography (MEG). This approach exploits quantum sensors for MEG signal detection, in combination with high-fidelity magnetic field control - afforded by a novel "matrix coil" system - to enable simultaneous scanning of two freely moving participants. We demonstrate our approach in a somatosensory task and an interactive ball game. Despite large and unpredictable subject motion, sensorimotor brain activity was delineated clearly in space and time, and correlation of the envelope of neuronal oscillations between people was demonstrated. In sum, unlike existing modalities, wearable-MEG combines high fidelity data acquisition and a naturalistic setting, which will facilitate a new generation of hyperscanning.

neuroscience↗

bioRxiv2021

Can the causal role of brain oscillations be studied through rhythmic brain stimulation?

Many studies have investigated the causal relevance of brain-oscillations using rhythmic stimulation, either through direct-brain or sensory stimulation. Yet, how intrinsic rhythms interact with the externally generated rhythm is largely unknown. We either presented a flickered (60 Hz) visual grating or its correspondent unflickered stimulus in a psychophysical change-detection-task during simultaneous MEG-recordings to humans, to test the effect of visual entrainment on induced gamma-oscillations. Notably, we generally observed the co-existence of the broadband induced gamma-rhythm with the entrained flicker-rhythm (reliably measured in each participant), with the peak frequency of the induced response remaining unaltered in approximately half of participants -relatively independently of their native frequency. However, flicker increased broadband induced-gamma-power, and this was stronger in participants with a native frequency closer to the flicker-frequency ( resonance), and led to strong phase-entrainment. Presence of flicker did not change behaviour itself, but profoundly altered brain-behaviour correlates across the sample: whilst broadband induced gamma-oscillations correlated with reaction-times for unflickered stimuli (as known previously), for the flicker, the amplitude of the entrained flicker-rhythm (but no more the induced oscillation) correlated with reaction-times. This, however, strongly depended on whether a participants peak frequency shifted to the entrained rhythm. Our results suggests that rhythmic brain-stimulation leads to a coexistence of two partially independent oscillations with heterogeneous effects across participants on the downstream relevance of these rhythms for behaviour. This may explain the inconsistency of findings related to external entrainment of brain-oscillations and poses further questions towards causal manipulations of brain-oscillations in general.

neuroscience↗

bioRxiv2021

Magnetic Field Mapping and Correction for Moving OP-MEG

BackgroundOptically pumped magnetometers (OPMs) have made moving, wearable magnetoencephalography (MEG) possible. The OPMs typically used for MEG require a low background magnetic field to operate, which is achieved using both passive and active magnetic shielding. However, the background magnetic field is never truly zero Tesla, and so the field at each of the OPMs changes as the participant moves. This leads to position and orientation dependent changes in the measurements, which manifest as low frequency artefacts in MEG data. ObjectiveWe modelled the spatial variation in the magnetic field and used the model to predict the movement artefact found in a dataset. MethodsWe demonstrate a method for modelling this field with a triaxial magnetometer, then showed that we can use the same technique to predict the movement artefact in a real OPM-based MEG (OP-MEG) dataset. ResultsUsing an 86-channel OP-MEG system, we found that this modelling method maximally reduced the power spectral density of the data by 26.2 {+/-} 0.6 dB at 0 Hz, when applied over 5 s non-overlapping windows. ConclusionThe magnetic field inside our state-of-the art magnetically shielded room can be well described by low-order spherical harmonic functions. We achieved a large reduction in movement noise when we applied this model to OP-MEG data. SignificanceReal-time implementation of this method could reduce passive shielding requirements for OP-MEG recording and allow the measurement of low-frequency brain activity during natural participant movement.

neuroscience↗

bioRxiv2021

Investigating the mechanisms of indocyanine green (ICG) cellular uptake in sarcoma

IntroductionIndocyanine green (ICG) is a near infrared (NIR) dye which has been used clinically for over 50 years and has recently been utilised for fluorescence guided surgery in a number of cancer types, including sarcoma. ICG is taken up and retained by sarcoma tumours to a greater extent than normal tissue, demonstrating its potential to aid in visualisation of tumour margins. However, the mechanisms surrounding preferential ICG uptake in tumours are poorly understood. MethodsIn vitro ICG cellular uptake studies were performed across a panel of four sarcoma cell lines and one breast cancer cell line, exhibiting varying proliferation rates and phenotypes. The effects of ICG concentration, incubation time, inhibition of clathrin mediated endocytosis and cell line proliferation rate on the cellular uptake of ICG were investigated using fluorescence microscopy and flow cytometry. The spatial orientation of ICG was also assessed in a patient specimen. ResultsThe level of ICG cellular uptake was dependent on ICG concentration and incubation time. Cell line proliferation rate correlated significantly to ICG uptake within 30 minutes (Rs= 1, p<0.001), whilst retention of ICG after 24hrs did not (Rs= 0.3, p=0.624). From our data, the primary mechanism of ICG uptake in sarcoma cells is via clathrin mediated endocytosis. Following the resection of a grade 3 leiomyosarcoma, ICG signal was detectable macroscopically and on 3m sections, whilst being negative on the muscle control. ConclusionsThe use of ICG for tumour detection in sarcoma surgery may demonstrate higher utility in high grade tumours compared to low grade tumours, due to the observation of higher ICG uptake in more proliferative cell lines. It is likely that the enhanced permeability and retention (EPR) effect plays a significant role in the retention of ICG within tumours. Future work on the detection of ICG at the cellular level within human tissue sections is required, with the aid of purpose built NIR microscopes.

cancer biology↗

bioRxiv2020

The Oscillatory Effects of Rhythmic Median Nerve Stimulation

Entrainment of brain oscillations can be achieved using rhythmic non-invasive brain stimulation, and stimulation of the motor cortex at a frequency associated with sensorimotor inhibition can impair motor responses. Despite the potential for therapeutic application, these techniques do not lend themselves to use outside of a clinical setting. Here, the aim was to investigate whether rhythmic median nerve stimulation (MNS) could be used to entrain oscillations related to sensorimotor inhibition. MEG data were recorded from 20 participants during 400 trials, where for each trial 10 pulses of MNS were delivered either rhythmically or arrhythmically at 12 or 20Hz. Our results demonstrate a frequency specific increase in relative amplitude in the contralateral somatosensory cortex during rhythmic but not arrhythmic stimulation. This was coupled with an increase in inter-trial phase coherence at the same frequency, suggesting that the oscillations synchronised with the pulses of MNS. While the results show that 20Hz rhythmic peripheral nerve stimulation can produce entrainment, the response to 12Hz stimulation was largely due to the presence of rhythmic sensory evoked potentials. Regardless, rhythmic MNS resulted in synchronous firing of neuronal populations within the contralateral somatosensory cortex meaning these neurons were occupied in processing of the afferent input. Therefore, MNS could prove therapeutically useful in disorders associated with hyperexcitability within the sensorimotor cortices.

neuroscience↗

bioRxiv2020

Measuring functional connectivity with wearable MEG

Optically-pumped magnetometers (OPMs) offer the potential for a step change in magnetoencephalography (MEG) enabling wearable systems that: provide improved data quality; accommodate any subject group; allow data capture during movement and offer a reduction in costs. However, OPM-MEG is still a nascent technology and, to realise its potential, it must be shown to facilitate key neuroscientific measurements, such as the characterisation of human brain networks. Networks, and the connectivities that underlie them, have become a core area of neuroscientific investigation, and their importance is underscored by many demonstrations of their perturbation in brain disorders. Consequently, a demonstration of network measurements via OPM-MEG would be a significant step forward. Here, we aimed to show that a wearable 50-channel OPM-MEG system enables characterisation of the electrophysiological connectome. To this end, we characterise connectivity in the resting state and during a simple visuo-motor task, using both OPM-MEG and a state-of-the-art 275-channel cryogenic MEG device. Our results show that connectome matrices from OPM and cryogenic systems exhibit an extremely high degree of similarity, with correlation values >70 %. This value is not measurably different to the correlation observed between connectomes measured in different subject groups, on a single scanner. In addition, similar differences in connectivity between individuals (scanned multiple times) were observed in cryogenic and OPM-MEG data, again demonstrating the fidelity of OPM-MEG data. This demonstration shows that a nascent OPM-MEG system offers results similar to a cryogenic device, even despite having [~]5 times fewer sensors. This adds weight to the argument that OPMs will ultimately supersede cryogenic sensors for MEG measurement.

neuroscience↗