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Electrooculography

Electrooculography (EOG) is a technique used to record the electrical potentials generated by the movement of the human eye.
This non-invasive method provides insights into ocular function and eye movements, with applications in various fields such as neuroscience, ophthalmology, and human-computer interaction.
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Most cited protocols related to «Electrooculography»

After computing all 22 decompositions for each of the 13 EEG datasets, we localized a best-fitting single equivalent dipole corresponding to each returned component using a single equivalent dipole in a best-fitting spherical four-shell model head (radius: 71, 72, 79, 85 mm; shell conductances: 0.33, 0.0042, 1, 0.33 µS) using the DIPFIT plug-in (version 1.02) in the EEGLAB toolbox (version 4.515) [48] (link). To avoid errors based on the simplistic head model we used in the computations, scalp map values for two electrodes sited near the eyes were excluded from dipole fitting. Note that modeling each component map with a single dipole is somewhat idealistic, since in particular some ICA components represent apparently bilateral synchronous source activities (e.g., the component maps in the third column of Figure 1). However, brain components clearly warranting a dual-dipole model appeared to be rare (approximately one per decomposition), as we typically find in other decompositions of more than 32 data channels. Components accounting for most electro-oculographic (EOG) artifacts should also be modeled using two (peri-ocular) dipoles, but as the eyes are relatively close together and accurate forward modeling the front of the skull is difficult, the additional errors introduced by using single dipole models for EOG components is not large.
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Publication 2012
Brain Cranium Electrooculography Eye Head Microtubule-Associated Proteins Radius Scalp Vision

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Publication 2012
Adult Anxiety Attention Attentional Bias Electrooculography Emotions Fear Phobias

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Publication 2018
Electromyography Electrooculography Microtubule-Associated Proteins Muscle Tissue neuro-oncological ventral antigen 2, human Scalp Visually Impaired Persons

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Publication 2008
Blinking Brain Electrooculography Evoked Potentials Eye Movements Face physiology Process, Mastoid Scalp Vision
PSG on the experimental night was recorded using a Grass Technologies
Comet XL system (Astro-Med, inc., West Warwick, RI), including 19-channel
electroencephalography (EEG) placed using the 10–20 system,
electrooculography (EOG) recorded at the right and left outer canthi (right
superior; left inferior), and electromyography (EMG). Reference electrodes were
recorded at both the left and right mastoid (A1, A2). Data were digitized at
400Hz, and stored unfiltered (recovered frequency range of 0.1–100 Hz),
except for a 60-Hz notch filter. Sleep was scored using standard
criteria68 . Sleep
monitoring on the screening night was recorded using a Grass Technologies AURA
PSG Ambulatory system (Astro-Med, inc., West Warwick, RI), and additionally
included nasal/oral airflow, abdominal and chest belts, and pulse oximetry.
EEG data from the experimental night were imported into EEGLAB
(http://sccn.ucsd.edu/eeglab/) and epoched into 5 s bins. Epochs
containing artifacts were manually rejected by a trained scorer (author B.A.M.),
and the remaining epochs were filtered between 0.4–50Hz (645±80
epochs per participant with 4.6%±2.1% of epochs
rejected). A fast Fourier transform (FFT) was then applied to the filtered EEG
signal at 5-second intervals with 50% overlap and employing hanning
windowing. Analyses in the current report focused, a priori, on
slow wave activity (SWA), defined as relative spectral power between
0.6–4.6Hz during slow wave sleep (NREM stages 3&4)10 (link), 11 (link). Spectral power was subdivided into two bins for
analysis (0.6–1Hz/1–4Hz), to examine the impact of
β-amyloid on SWA frequencies particularly relevant to memory
functions14 (link), 23 (link). A single summary proportional measure
was also derived by dividing the spectral power between 0.6–1Hz by the
sum of spectral power between 0.6–4Hz, to determine the relative
dominance of memory-relevant slow waves. Furthermore, due to our a
priori
focus on mPFC, SWA measures at FZ and CZ derivations were
averaged and used as a measure of mPFC SWA (Fig.
1b
). To ascertain topographic specificity of effects, SWA measures at
F3, F4, F7, and F8 derivations were averaged and used as a measure of dlPFC SWA,
SWA measures at P3, P4, and PZ derivations were averaged and used as a measure
of Parietal SWA, SWA measures at T3, T4, T5, and T6 derivations were averaged
and used as a measure of Temporal SWA, and SWA measures at O1 and O2 derivations
were averaged and used as a measure of Occipital SWA.
Slow wave detection and source analysis were performed to (1) calculate
the impact of mPFC Aβ on slow wave density, and (2) determine whether
memory-relevant FZ and CZ measured slow waves (0.6–1Hz) have an mPFC
source (Fig. 1b and Supplementary Fig. 1). EEG data
were filtered between 0.5–4Hz, and individual slow waves were detected
using a validated algorithm25 (link).
Standardized low resolution brain electromagnetic tomography (sLORETA) was
employed26 (link) as
previously described69 (link), 70 (link). In short, this method
calculates current density sources using a discrete, three-dimensionally
distributed, linear minimum norm solution to the forward problem. Computations
are made using a head model based on the MNI152 template71 (link). Prior to sLORETA analysis, EEG
preprocessing was conducted in MATLAB using the EEGLAB toolbox. For each
participant, filtered (0.5Hz–4Hz), artifact-rejected EEG was
event-marked separately for detected slow wave (0.6–1Hz) midpoints in
the FZ and CZ derivations. EEG was then epoched around each detected slow wave
midpoint (±100 ms). Slow wave epochs were then averaged and exported
separately for CZ and FZ detected slow waves. sLORETA analyses of slow wave
epochs were carried out using the freeware sLORETA utilities (http://www.uzh.ch/keyinst/loreta.htm), consistent with previous
source analysis examinations69 (link),
70 (link)
. Prior to current
density source calculation, all electrode derivations were registered and
transformed into 3D MNI space, yielding a spatial transformation matrix. Current
density source maps were then derived for each participant separately for CZ and
FZ time-locked EEG averages. CZ and FZ source maps were then averaged within
each participant, with CZ-FZ averaged source maps then averaged across
participants to generate a grand mean average source image for memory-relevant
CZ and FZ slow waves (Supplementary Fig. 1).
Publication 2015
Abdomen Amyloid Proteins Brain Chest Dorsolateral Prefrontal Cortex Electromagnetics Electromyography Electrooculography EPOCH protocol Head Memory Microtubule-Associated Proteins Nose Oximetry, Pulse Poaceae Process, Mastoid Sleep Sleep, Slow-Wave Tomography

Most recents protocols related to «Electrooculography»

EEG epochs from 400 ms before to 600 ms after the onset of the target stimulus in valid trials were collected (see Section “Analysis of behavioral data” for details). EEG epochs containing a deflection greater than ± 100 μV in at least one electrode or greater than 100 μV in EOGs were excluded from this analysis. With this procedure, at least 77 artifact-free EEG epochs (mean ± SD, STD condition: 105.2 ± 11.8 trials, Con-DEV condition: 104.6 ± 13.0 trials, Uncon-DEV condition: 104.9 ± 8.7 trials) were obtained. These epochs were sorted according to the target stimulus conditions and then transformed into time-frequency representations via a complex Morlet wavelet transformation using the MATLAB wavelet toolbox. The mother cycles were set to a linear increase of 2–7 cycles with respect to the frequency range (1–50 Hz). The ERSP and ITPC of each participant were calculated relative to the baseline (−400 to −100 ms) for each electrode. To record vMORs evoked by the unconscious deviant (Uncon-vMORs) as well as those evoked by the conscious deviant (Con-vMORs), ERSP and ITPC in the STD condition were subtracted from those in the Uncon-DEV and Con-DEV conditions, respectively. For both Con-vMORs and Uncon-vMORs, the ERSP and ITPC in the left area were calculated from the mean value of data PO3 and PO7 electrodes, and these in the right area were calculated from the mean value of data PO4 and PO8 electrodes. And then, we calculated the averaged ERSPs and ITPCs for each participant in the time-frequency window of 100–500 ms and 4–8 Hz, respectively. This time-frequency window was determined in previous studies on vMORs (Stothart and Kazanina, 2013 (link); Yan et al., 2017 (link)). The calculated ERSPs and ITPCs were subjected to a repeated-measures two-way analysis of variance (ANOVA) with factors of the conditions (Con-vMOR and Uncon-vMOR) and laterality (left and right areas), respectively. In the statistical analyses, the significance level was set at p < 0.05.
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Publication 2023
Consciousness Electrooculography EPOCH protocol Functional Laterality Mothers
Electroencephalography (EEG) in each condition was recorded using a measurement instrument with 57 electrodes (EEG-1200, Nihon Kohden, Tokyo, Japan; EasyCap GmbH, Herrsching, Germany). The layout of the electrodes was based on a modified version of the international 10–20 system. The impedance of each electrode was maintained at less than 10 kΩ. EEG signals were digitized at 1 kHz and recorded with a 0.5–300 Hz band-pass filter online. For data acquisition, EEG signals were referenced to the right earlobe and eye movements were monitored using horizontal and vertical bipolar electrooculograms (EOGs).
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Publication 2023
Electroencephalography Electrooculograms Electrooculography Eye Movements
EEG data were processed using Matlab R2014b (MathWorks), Matlab R2017b (MathWorks) and the EEGLAB plugin version 13.5.4b (Delorme and Makeig 2004 (link)).
First, scalp and eye electrodes were re-referenced to the average of two mastoid electrodes. Continuous EEG and electrooculogram data were filtered with a 0.01-Hz high-pass filter. Then, data were downsampled to 200 Hz and filtered with a 30-Hz low-pass filter. These filters were applied offline using an eighth-order Butterworth filter with zero phase shift.
Second, an independent component analysis was computed on the continuous data using the EEGLAB ‘runica’ algorithm. Vertical eye movement components were visually identified and removed from the signal.
Next, EEG signals were locked to either orange letters or self-paced actions. In Experiment 1, epochs started 2.5 s before the event (i.e. orange letter or action) and finished 0.5 s after it (Parés-Pujolràs et al. 2019 ). In Experiment 2, epochs started 1.5 s or 2.5 s before the orange letter or self-paced action, respectively, and finished 1 s after it. Shorter epochs were chosen to maximize the number of available trials for orange letter analysis. Baseline correction was performed using the 500-ms interval at the beginning of the epoch (for orange letters, [−2.5 to −2 s] relative to the event in Experiment 1 and [−1.5 to −1 s] in Experiment 2). Finally, artefact rejection was performed by removing all epochs with >120 μV fluctuations from the baseline in the preselected channel (Cz). Epochs in which there was a key press in the interval preceding the event of interest were rejected to prevent overlapping evoked potentials in both experiments. The rejection interval prior to orange letters was [−3 to 0 s] in Experiment 1 and [−2 to 0 s] in Experiment 2.
Publication 2023
Electrooculography EPOCH protocol Evoked Potentials Eye Movements Process, Mastoid Scalp
The electroencephalogram (EEG) data were recorded from 32 electrode locations (FP1, FP2, FPZ F3, F4, F7, F8, FT9, FT10, FZ, FC1, FC2, FC5, FC6, T7, T8, TP9, TP10, C3, C4, CP1, CP2, CP5, CP6, P3, P4, P7, P8, PZ, O1, O2, OZ) with Ag/AgCl electrodes using BrainVision Recorder software (Brainproducts, Germany). The electrodes were attached to the cap with a standard 10–20 layout. Ground and reference electrodes were used in electrode sites FPZ and CZ, respectively. To record eye activities, vertical and horizontal electrooculogram (EOG) electrodes were located above and below the right eye and at the outer canthi of both eyes, respectively. Data were sampled at 500 Hz. Impedances were kept below 10 kΩ.
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Publication 2023
Electroencephalography Electrooculography Eye Impedance, Electric
The diagnosis of OSA was made using a PSG. Electromyography of the chin and the leg, electrooculography, electroencephalography, oxygen saturation, electrocardiography, abdominal and thoracic respiratory effort, body position and air flow (nasal pressure transducer and oronasal thermistor), and tracheal microphone were recorded using the Respironics Alice 6 LDx Diagnostic Sleep System (Philips).
PSG data were evaluated by a physician who is a sleep disorders specialist and who was blinded to the results of the NoSAS questionnaire. The American Academy of Sleep Medicine (AASM) criteria were used to score the sleep and respiratory events (15 (link)). The AHI was determined by calculating the number of apnea and hypopnea events per hour. OSA was diagnosed based on AHI. The severity of OSA was classified as follows: Mild (AHI, ≥5 and <15 events/h), moderate (AHI, ≥15 or <30 events/h) and severe (AHI, ≥30 events/h).
Publication 2023
Abdomen Apnea Chin Electrocardiography Electroencephalography Electromyography Electrooculography Nose Oxygen Saturation Pharmaceutical Preparations Physicians Respiratory Rate Sleep Sleep Disorders Trachea Transducers, Pressure

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More about "Electrooculography"

Electrooculography (EOG) is a non-invasive technique used to record the electrical potentials generated by the movement of the human eye.
This method provides valuable insights into ocular function and eye movements, with applications in various fields such as neuroscience, ophthalmology, and human-computer interaction.
One powerful tool that can optimize your EOG research is PubCompare.ai, an innovative AI-powered platform that leverages comparisons across scientific literature, preprints, and patents.
With PubCompare.ai, you can discover the best protocols and products to enhance the reproducibility and accuracy of your EOG studies.
Expanding on the capabilities of EOG, this technique can be used in conjunction with other neurophysiological monitoring systems, such as the ActiveTwo system, ActiCAP, BrainAmp amplifier, and Brain Vision Recorder software.
These integrated solutions enable comprehensive data collection and analysis, empowering researchers to gain a deeper understanding of ocular function and its relationship with other physiological processes.
Furthermore, the integration of EOG with MATLAB, BrainAmp, Fastrak, and Brain Vision Analyzer 2.0 software provides powerful tools for data processing, visualization, and interpretation.
These advanced analytical capabilities can help researchers uncover meaningful insights and patterns in their EOG data, ultimately advancing the field of ocular research.
Experince the power of PubCompare.ai today and take your EOG research to new heights.
Discover the best protocols and products, enhance reproducibility and accuracy, and unlock the full potential of this versatile technique across various applications.