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Neuroscan synamps2 system

Manufactured by Compumedics
Sourced in United States, Australia

The Neuroscan Synamps2 system is a high-performance data acquisition system designed for advanced neurophysiological research. It offers a flexible and highly configurable platform for recording and analyzing electrophysiological data, including EEG, ERP, and related modalities. The system features a modular design, allowing for customization to meet the specific requirements of different research applications.

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11 protocols using neuroscan synamps2 system

1

High-Density EEG Signal Acquisition

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In this study, EEG signals were collected using a 64-channel Neuroscan SynAmps 2 system. All electrodes were placed according to the international 10–20 system. The reference and ground electrodes were mounted on the vertex and between FPz and Fz, respectively. The sampling frequency of EEG was 1,000 Hz, and the band-pass filtering range was from 0.15 to 200 Hz. The system filtered out the 50 Hz power-line interference online. The impedance of all electrodes was kept below 10 kΩ.
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2

Whole-Brain EEG Acquisition with Neuroscan Synamps2

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EEG data were collected in a dark and confined laboratory using the Neuroscan Synamps2 system. Whole-brain signals were recorded by means of 64-channel (Ag-AgCl) electrode caps placed according to the International 10-20 system. The EEG signals were filtered from 0.05 to 100 Hz and an additional notch filter at 50 Hz and digitized at a sampling rate of 1,000 Hz. Impedances were kept below 5 kΩ. All electrodes were referenced online to the left mastoid (M1) electrode. Vertical electrooculogram was recorded by 2 electrodes placed above and below the left eye, with horizontal electrooculogram beyond the lateral canthi of both eyes.
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3

Electrophysiological Recording of Brain Activity

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Participants sat in an electrically shielded, sound attenuating booth to minimise artefacts in the EEG recordings. A Neuroscan Synamps2 system (10 GΩ input impedance; 29.8 nV resolution; Neuroscan, El Paso, TX, USA) was used to record EEG data from 32 Ag/AgCl electrodes mounted in an elastic cap at locations FP1, FPZ, FP2, F7, F3, FZ, F4, F8, FT7, FC3, FCZ, FC4, FT8, T7, C3, CZ, C4, T8, TP7, CP3, CPZ, CP4, TP8, P7, P3, PZ, P4, P8, POZ, O1, OZ, and O2. Six additional external electrodes were attached to the outer canthi of the left and right eyes, above and below the right eye to measure electro-oculograms (EOGs), and to the left and right mastoids. Electrode recordings were referenced to the right mastoid. All electrode impedances were kept below 50 kΩ. EEG data were recorded at a sampling rate of 1000 Hz. Online high-pass filtering was implemented for experiment 1a and 2 at 0.1 Hz. Online high-pass filtering was avoided for experiment 1b to allow us to measure slow-wave EEG activity preceding feedback delivery.
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4

EEG Recording of the Flanker Task

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Participants performed the Flanker task in an electrically shielded room while seated in a comfortable high-back chair. The electrophysiological recordings were done using 128 EEG channels with an electrode placement based on the 10 % system (EasyCap Montage No. 15, http://www.easycap.de/). The sampling rate during recording was set to 1000 Hz. The electrodes used were EasyCap active ring electrodes (Ag/AgCl) with impedance conversion circuits integrated into the electrode housing that allows high quality recordings even with high impedance values, thus reducing preparation time and noise. The signals were amplified via a Neuroscan SynAmps2 system and filtered online with a 40 Hz low-pass and a 0.15 Hz high-pass analog filter prior to digitization and saving of the continuous data set. During recording, all electrodes were referenced to an electrode placed on the left mastoid. Eye blinks were recorded with one electrode above and one electrode below the left eye, and a ground electrode was placed anteriorly on the midline.
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5

Offline EEG and EOG Data Analysis

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Recording and offline analysis of EEG and EOG data was done with Neuroscan Synamps 2 system and Scan 4.5 software (Compumedics, Melbourne, Australia). During the task(s), EEG activity was recorded continuously from 64 scalp electrodes placed according to the international 10–10 system (EASYCAP GmbH, Herrsching, Germany), referenced to the left earlobe. Horizontal and vertical EOG was recorded from electrodes placed above and below the left eye (vEOG) and beside the outer canthi of both eyes (hEOG). Impedances were kept below 35kΩ. EEG and EOG were amplified, band-pass filtered at 0.05–100 Hz, and digitised at 2000 Hz.
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6

Scalp EEG Monitoring in Rat Model

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In one group of rats, scalp electrodes were used to monitor EEG changes during the experiments. To avoid possible stress effects following invasive surgical implantation, we recorded the EEG from 9 mm stainless steel EEG needle electrodes inserted into the scalp during anesthesia so that they were touching the outer table of the skull. This technique is used for EEG monitoring intraoperatively in humans. After rats were anesthetized with 2% isoflurane and IV catheter insertion, two scalp electrodes [Astro-Med/ Grass Technologies] were placed, as shown in Fig 2. We drew a line between the anterior edge of bilateral ears, likely between Bregma and Lambda [25 (link)]. From the midpoint, one electrode was placed anteriorly perpendicular to the line and the other one was placed posteriorly perpendicular to the line. Two EEG channels were recorded, the first one from an electrode placed over the anterior portion of the brain, and a second electrode placed over the posterior portion of the brain. The EMG was obtained from an electrode placed over the left shoulder, all referenced to an electrode placed near the snout. A ground electrode was placed on the dorsal neck. These three channels were recorded with an A/D rate of 500 Hz/channel, with a 0.05–100 Hz bandpass and 12 dB/octave roll-off. Potentials were amplified with a Neuroscan SYNAMPS 2 system (Compumedics, Inc., Charlotte, NC).
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7

Artifact-Free EEG Recordings in Parkinson's Patients

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Recordings during relaxed wakefulness were obtained from PD patients in the “on” state, seated in a recliner with eyes closed as previously described.8 (link) Briefly, Ag/AgCl EEG electrodes were placed on the scalp using twenty standard 10-20 EEG electrode positions. Recordings were referenced to the Fz electrode, with a right mastoid electrode serving as ground. Electrode impedances were closely monitored and kept below 5 kohms. Data were acquired using the Neuroscan Synamps2 system (Compumedics, Charlotte, NC, USA) at a sampling rate of 1000 Hz and a bandpass of 1–200 Hz. An EEG technician and neurophysiologist (JNC) were present during the entire recording session to observe the behavioral state of the patient and to monitor on-line for signal quality. Patients were asked every minute if they were awake, and drowsiness was further excluded by monitoring for background changes and slow eye movements of drowsiness during the course of the recording. When muscle, eye movement/blink, or other artifacts were identified, the patient was coached until an artifact-free signal was obtained. The final recorded sample consisted of an awake and artifact-free period of approximately 150-180 seconds.
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8

High-density EEG Recording Protocol

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EEG data were recorded using a 64-channel Neuroscan Synamps2 system (Compumedics Neuroscan). The EEG signals were filtered from 0.05 to 100 Hz and digitized at 1,000 Hz. A 64-channel Ag-AgCl electrode cap was used. All electrodes were referenced to a REF electrode between Cz and CPz. Impedances were kept below 5 kΩ. Markers corresponding to the onset of the adapters were co-registered with the EEG signal. Electrodes placed above and below the left eye and the external ocular canthi of both eyes were used to record vertical electrooculogram (vEOG) and horizontal electrooculogram (hEOG).
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9

Continuous EEG Acquisition and Preprocessing

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Continuous EEG was sampled at a rate of 500 Hz from 64 Ag/AgCl electrodes placed according to the international 10–10 system (EASYCAP GmbH, Herrsching, Germany). Online, the signal was referenced to the left earlobe with impedances kept below 10 kΩ. Signals from the right earlobe were also recorded. Bipolar channels recorded vertical (VEOG) and horizontal (HEOG) electro-oculogram from above and below the midpoint of the right eye and beside the outer canthi of both eyes. Recording and offline analysis of EEG and EOG data was conducted with Neuroscan Synamps2 system and SCAN 4.5 software (Compumedics, Melbourne, Australia).
Offline, EEG and EOG signal were digitally filtered using a 30-Hz lowpass filter with 24 dB slope, then re-referenced to the average of the left and right earlobes.
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10

EEG Recording Protocol Using Neuroscan Synamps2

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EEG recordings were carried out using a 64-channel cap with the Neuroscan Synamps2 system (Compumedics), in accordance with the international 10/10 system. Vertical and horizontal electrooculograms (EOGs) were monitored and recorded as well: two electrodes were placed over and below the dominant eye for the vertical eye movements, and two electrodes were placed at the outer canthi of the eyes for the horizontal movements. The electrode impedance was kept under 10 kΩ. EEG data were digitized at 500 Hz, with an online bandpass filter from 0.05 to 100 Hz applied. An average mastoid reference was used.
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