Frequently Asked Questions

You CAN install current versions of ActiView on Windows 10. But, before you do so, if the system was orignally delivered before January of 2017 you should update the firmware on the optical receiver / USB interface so that you do not have to go through the very long and arduous process of installing an unsigned driver on Windows 10.

You can update the firmware using any Windows 7 or 8 computer with the MSWinUSB2 driver installed, even if it is not the computer you have been using for ActiView. If you are just using a Windows 7 or 8 computer to update firmware on the optical receiver / USB interface, there is no need to install the LabVIEW Runtime Engine or ActiView on this computer. You WILL need the LabVIEW Runtime Engine and ActiView on the new Windows 10 computer, but you WILL NOT need to install a driver after the firmware update has been performed.

See the procedure outlined at biosemi.com/ faq/install_USB.htm for detailed instructions.  The section at the bottom marked IMPORTANT is the place to begin.

High density surface EMG as described in the recent publications on the Biosemi site is possible with the addition of the sEMG accessories. The original model of the high density sEMG probe was made for ActiveOne, so the connector differed. The current version separates the electrode grid from the preamp as in:

• reusable grid
• sEMG preamplifier

Less dense sEMG can be accomplished with an elastic fabric with electrode holders like the EEG cap stretched over a muscle.  This would need to be custom-made, but would not be expensive.

Fine wire EMG would require either spring contact adapters or safety socket leads with inline active headstage. If your fine wire electrodes will be stripped but unterminated, you need spring contacts, and if your electrodes terminate in safety sockets, you need inline adapters.

You CAN install current versions of ActiView on Windows 10. But, before you do so, if the system was orignally delivered before January of 2017 you should update the firmware on the optical receiver / USB interface so that you do not have to go through the very long and arduous process of installing an unsigned driver on Windows 10.

You can update the firmware using any Windows 7 or 8 computer with the MSWinUSB2 driver installed, even if it is not the computer you have been using for ActiView. If you are just using a Windows 7 or 8 computer to update firmware on the optical receiver / USB interface, there is no need to install the LabVIEW Runtime Engine or ActiView on this computer. You WILL need the LabVIEW Runtime Engine and ActiView on the new Windows 10 computer, but you WILL NOT need to install a driver after the firmware update has been performed.

See the procedure outlined at biosemi.com/ faq/install_USB.htm for detailed instructions.  The section at the bottom marked IMPORTANT is the place to begin.

Since mid-2016, Biosemi has included a black USB virtual serial port trigger cable with each new ActiveTwo system.  The device is depicted below.

Inside the shell of the 37 pin connector is a microchip that appears to the stimulus computer as a virtual serial port but provides 8 bit parallel TTL output to the ActiveTwo trigger input port.  Because it appears as a virtual serial port on the stimulus computer, this cable is a relatively universal solution for triggering ActiveTwo from virtually any software on any platform.  There are a few simple parameters you need to know to send triggers via this device.  For details, see:

• https://www.biosemi.com/faq/USB%20Trigger%20interface%20cable.htm

To use this trigger cable with MATLAB, Roee Gilron at UCSF (thanks, Roee!) provides a code sample at Github:

• https://github.com/roeegilron/BioSemiUSBtrigger

High density surface EMG as described in the recent publications on the Biosemi site is possible with the addition of the sEMG accessories. The original model of the high density sEMG probe was made for ActiveOne, so the connector differed. The current version separates the electrode grid from the preamp as in:

• reusable grid
• sEMG preamplifier

Less dense sEMG can be accomplished with an elastic fabric with electrode holders like the EEG cap stretched over a muscle.  This would need to be custom-made, but would not be expensive.

Fine wire EMG would require either spring contact adapters or safety socket leads with inline active headstage. If your fine wire electrodes will be stripped but unterminated, you need spring contacts, and if your electrodes terminate in safety sockets, you need inline adapters.

You CAN install current versions of ActiView on Windows 10. But, before you do so, if the system was orignally delivered before January of 2017 you should update the firmware on the optical receiver / USB interface so that you do not have to go through the very long and arduous process of installing an unsigned driver on Windows 10.

You can update the firmware using any Windows 7 or 8 computer with the MSWinUSB2 driver installed, even if it is not the computer you have been using for ActiView. If you are just using a Windows 7 or 8 computer to update firmware on the optical receiver / USB interface, there is no need to install the LabVIEW Runtime Engine or ActiView on this computer. You WILL need the LabVIEW Runtime Engine and ActiView on the new Windows 10 computer, but you WILL NOT need to install a driver after the firmware update has been performed.

See the procedure outlined at biosemi.com/ faq/install_USB.htm for detailed instructions.  The section at the bottom marked IMPORTANT is the place to begin.

Since mid-2016, Biosemi has included a black USB virtual serial port trigger cable with each new ActiveTwo system.  The device is depicted below.

Inside the shell of the 37 pin connector is a microchip that appears to the stimulus computer as a virtual serial port but provides 8 bit parallel TTL output to the ActiveTwo trigger input port.  Because it appears as a virtual serial port on the stimulus computer, this cable is a relatively universal solution for triggering ActiveTwo from virtually any software on any platform.  There are a few simple parameters you need to know to send triggers via this device.  For details, see:

• https://www.biosemi.com/faq/USB%20Trigger%20interface%20cable.htm

To use this trigger cable with MATLAB, Roee Gilron at UCSF (thanks, Roee!) provides a code sample at Github:

• https://github.com/roeegilron/BioSemiUSBtrigger

High density surface EMG as described in the recent publications on the Biosemi site is possible with the addition of the sEMG accessories. The original model of the high density sEMG probe was made for ActiveOne, so the connector differed. The current version separates the electrode grid from the preamp as in:

• reusable grid
• sEMG preamplifier

Less dense sEMG can be accomplished with an elastic fabric with electrode holders like the EEG cap stretched over a muscle.  This would need to be custom-made, but would not be expensive.

Fine wire EMG would require either spring contact adapters or safety socket leads with inline active headstage. If your fine wire electrodes will be stripped but unterminated, you need spring contacts, and if your electrodes terminate in safety sockets, you need inline adapters.

High density surface EMG as described in the recent publications on the Biosemi site is possible with the addition of the sEMG accessories. The original model of the high density sEMG probe was made for ActiveOne, so the connector differed. The current version separates the electrode grid from the preamp as in:

• reusable grid
• sEMG preamplifier

Less dense sEMG can be accomplished with an elastic fabric with electrode holders like the EEG cap stretched over a muscle.  This would need to be custom-made, but would not be expensive.

Fine wire EMG would require either spring contact adapters or safety socket leads with inline active headstage. If your fine wire electrodes will be stripped but unterminated, you need spring contacts, and if your electrodes terminate in safety sockets, you need inline adapters.

We expect the new red-rubber reinforced ActiveTwo active electrodes to last more than 1000 uses, based on our experience so far, and based on automated repeated-strain testing.

The way ActiveTwo electrode sets are built, they are not repairable by the end-user, but we can replace single electrodes for you. We can so this quickly (24 hours plus transit), efficiently, and at low cost (or free under warranty). Electrodes are warranted against material/manufacturing defects for one year, and we charge by the repair after that. We find that offering extended warranties motivates less careful handling, so we don’t offer extended warranties.

Follow the steps in the other FAQ linked here to identify the problem before contacting us to ask about the procedure and the cost of a repair.

We do offer individual EXG pin-type electrodes that you can insert in the cap as substitutes for faulty ribbon cable leads. This would be a short term stop gap solution only. We strongly recommend having a backup set of electrodes on hand after a year or two so that if the first set needs repair, you can continue to run with the other set while the repair is undertaken. You would not need to buy the spare set right away — just budget to have it once the electrodes have had enough use that they may begin experiencing problems. After you have made 200-300 recordings with your primary electrode set would be a good rule of thumb for when you should have a spare set of electrodes on hand.

You CAN install current versions of ActiView on Windows 10. But, before you do so, if the system was orignally delivered before January of 2017 you should update the firmware on the optical receiver / USB interface so that you do not have to go through the very long and arduous process of installing an unsigned driver on Windows 10.

You can update the firmware using any Windows 7 or 8 computer with the MSWinUSB2 driver installed, even if it is not the computer you have been using for ActiView. If you are just using a Windows 7 or 8 computer to update firmware on the optical receiver / USB interface, there is no need to install the LabVIEW Runtime Engine or ActiView on this computer. You WILL need the LabVIEW Runtime Engine and ActiView on the new Windows 10 computer, but you WILL NOT need to install a driver after the firmware update has been performed.

See the procedure outlined at biosemi.com/ faq/install_USB.htm for detailed instructions.  The section at the bottom marked IMPORTANT is the place to begin.

The positions in these caps come from the Oostenveld and Praamstra 5% system.  See http://robertoostenveld.nl/electrode/ for background and for links to electrode coordinates in a variety of formats. Depending on what software you are using for analysis, we might be able to provide another file format. The Biosemi channel assignments (relating electrode labels to electrode sites in the Oostenveld and Praamstra nomenclature) are below:

ActiveTwo is provided with drivers and host data acquisition software for Windows, Mac, and Linux computers.

Note that certain applications, such as event-related potentials, often require a separate computer to run experimental control / stimulus delivery software. The requirement for a separate computer for stimulus delivery is more a function of the experimental control software needing full control of computer resources to do its job.

In brief, the computer requirements for the ActiView data acquisition software are:

• Operating system:
  • Windows 10 / 11
  • MacOS 11 Big Sur, Monterey
  • Linux 64 bit or Linux X86 with library GNU-C V2.2.4 or later
• RAM: 8 GB or more
• Hard Drive: recommend 500 GB, but user should anticipate free space needed for data (file size in bytes is approximately = 3 X AD rate in Hz X number of channels X number of seconds recorded)
• Display: 1440 X 900 or higher resolution display
• One free USB port
  • SPECIAL NOTE ABOUT USB CHIPSETS: Small form factor computers without PCIe expansion slots should be avoided. The Intel W480 chipset found in many brands of small form factor desktop computer is not capable of keeping up with USB 2.0 High Speed data rates, which prevents operation in speed modes 2 and 3 for AD boxes that have high speed firmware installed. This is of particular importance in systems used in settings where ABR and cortical ERP will be measured concurrently or alternately. If you opt for a small form factor computer, be sure to use a computer that has at least one free PCIe expansion slot that you can add a PCIe expansion card with one or more USB 2.0 or higher ports.

Note: The ActiveTwo computer DOES NOT NEED A PARALLEL PORT.  A parallel port on the experimental control computer can be used to send stimuli to ActiveTwo, but we provide a USB virtual serial port trigger cable with every new system, so a parallel port is not needed for triggering.

In addition, the following are recommended for the ActiView computer:

• Network interface and remote storage for data backups
• Accessories such as KVMA switch box, extra monitor / keyboard / mouse, extension cables, etc to permit access to the EEG display from the separate room for the subject

The ActiveTwo Base System has no channels. The Base System consists of the parts that every ActiveTwo system needs to have, but excludes the parts that are used to custom configure ActiveTwo for various purposes, like amplifier/converter (AC modules).  The AC modules give the system the capacity to record from active electrodes. With four of the eight channel modules, the base system will have the capacity for 32 channels. If you want 32 electrodes on the scalp, then you need four modules, but if you also want to use four individual flat-type electrodes, you need another eight-channel module (four modules for EEG and one module for EXG1-8). The modules have eight channels, so you can only expand the system in increments of eight channels. You don’t have to buy the electrodes to use with EXG5-8, but you need the eight channel module.

Maybe.  There is no way the EEG system can harm the TMS system, but there are some TMS systems that are essentially useless with some EEG systems.  You need a a suitable combination of features in each to be successful at all in using TMS with EEG.

Desirable attributes:

• Coils designed specifically for use with EEG will have a cable that exits the coil tangential to the head surface so that the coil does not pass close by EEG electrodes and cables.
• A coil to be used with EEG should be passively cooled, since active cooling by means of a fan will induce electromagnetic interference in the EEG.
• The TMS recharge mechanism should be designed to avoid inducing electromagnetic artifacts in the EEG.
• The TMS system should be shielded so that no more than 3 milligauss of electromagnetic interference from the TMS system’s power supply reaches the electrodes and cables.
• The TMS system should be able to produce a TMS pulse in response to an input trigger with a low and predictable latency.  Long, but especially unpredictable latency in responding to an input trigger will result in TMS artifacts that are difficult to impossible to remove from the EEG.

Aside from attributes of the TMS system, there are also important considerations regarding the EEG system in this relationship. See the other FAQ entry on that topic.

No.  There are a few special attributes that are required and others that are desirable.

Required attributes:

• Inputs should be protected so that they are not damaged by the TMS pulse
• Frequency response on all channels should be from DC on the low end, since AC coupled inputs will “ring” when presented with a large voltage transient like the TMS artifact

Desirable attributes:

• Electrodes should have a low-profile so that the TMS coil can be placed as near the head as possible, maximizing penetration depth and current delivery
• It is important for the EEG system to be able to trigger the TMS system at precisely the same phase with respect to the EEG samples each time a stimulus is delivered.  This will improve the performance of artifact removal algorithms

Aside from these attributes of the EEG system, there are also important considerations regarding the TMS system in this relationship. See the other FAQ entry on that topic.

Electrodes and head caps can have positions derived from systems based on the International 1020 System.  When the positions are based on 1020, the labels on the caps and electrodes can either be the actual 1020 position names (such as Fp1, Cz, etc) or they can be what is called ABC, which actually means A1, A2, …A32, B1, B2,…B32, etc  Another way to refer to the ABC labeling is arbitrary alphanumeric.  The 1020 system is not arbitrary because the names are based on anatomical landmarks and the odd=left and even=right numbering is predictable and interpretable.  When you have only one type of cap in your lab, it makes sense to use 1020 labels for caps with positions based on the 1020 system.  However, if you have 32 channel caps AND 64 channel caps, then you might find it useful to be able to use the A1-32 labels for the A cable and the B1-32 labels for the B cable and complementary A1-32 labels on the 32 channel caps and A1-B32 labels on the 64 channel caps.  This way, the A cable can be used for the whole head in 32 channel studies of for just the left side of the head in 64 channel studies.  This does provide a short term savings if you don’t want to have two A cables on-hand, but using 1020 labels on everything is more convenient and at the limit it will not cost any more (because cables that are used less frequently will last longer).

When you purchase a new laboratory instrument, you want to get started using it and producing results as quickly as possible, and nothing helps you accomplish this goal faster than having a trained technician visit your lab to install the system and configure it optimally for your purposes. From our perspective, you will have the best possible experience with our products when the equipment is setup and configured properly and you are properly trained from the beginning. Installation visits are not included in the pricing on our standard price list, but we do generally include an optional installation fee on quotations. We find that customers who receive assistance from the beginning have fewer questions later and have more success using the equipment. We encourage you to invest in this valuable service.  If you would like to arrange an installation and training visit, please contact us!

We will always do our best to respond quickly when you need something urgently.  It helps us immensely if you plan ahead and give us a little advance warning if you foresee a deadline approaching by which you need parts, supplies or repairs to be complete.

For new purchases, we can often pre-order goods for established customers, even before the official institutional PO has been received.  Give us a heads-up as soon as you know that you intend to order items we have quoted you, and if you expect to have the official PO within 30 days, and you agree to let us know if anything changes, we will pre-order the goods for you based on your word.

For repairs, we know how vital our equipment is to your work, so we always do our best to respond quickly to urgent repair requests.  One important point — the earlier we know the date by which a repaired item must be received back, the sooner we can let you know whether we will or will not be able to meet that deadline.  Ultimately, the most valuable thing you can do to ensure we meet your deadlines is to notify us of those deadlines as early as possible!

Cortech Solutions is the exclusive reseller in the USA and Canada for these product lines:

• Artinis
• Biosemi
• Bittium (formerly MEGA)
• Cambridge Research Systems
• Mag and More
• NeuroImaging Solutions (NIS)

For most of the products we sell, our territory includes USA and Canada.

For products we manufacture, we are able to see throughout the world, but we may put you in touch with a local or regional representative to ensure the most convenient customer experience for you.

See our contact details page.

The inside diameter of adhesive ring should be about the same size as, or larger than, the diameter of the electrode contact.  The inside diameter of the adhesive ring should not be larger than the outer diameter of the electrode housing.  The outside diameter minus the center hole determines how much surface area contacts the skin, thus determining how tightly the adhesive will adhere to the skin.  Also, the outside diameter will limit how close you can place electrodes to one another and to other features, such as the eyes.

Using ActiveTwo as an example, the electrode contact on a flat-type electrode has a diameter of about 4.5 mm.  An adhesive ring with 5 mm id (center hole) would be  idea, but the 5×13 adhesives are rather expensive because they are manufactured in Europe.  We recommend using a 4×19 or a 4×12 adhesive ring.  The 4×12 is a good choice when placing the electrodes close to one another or close to the eyes for startle measurements.  The 4×19 is a good choice when you have plenty of room and the primary concern is how well the electrodes stick to the skin.

• 8 mm id x 20 mm od: CS-AT-AR20X8BS – roll of 500
• 5 mm id x 13 mm od: CS-AT-AR13X5BS – roll of 500
• 12 mm id x 32 mm od: CS-AT-ARIV12X32 – pack of 100
• 8 mm id x 22 mm od: CS-AT-ARIV8X22 – pack of 100
• 4 mm id x 12 mm od: CS-AT-ARIV4X12 – pack of 100
• 4 mm id x 19 mm od: CS-AT-ARIV4X19 – pack of 100 (part of the standard ActiveTwo consumable supplies kit)

Complete systems and large orders of accessories may take 6-9 weeks for delivery except in special circumstances.  Many smaller accessory orders can be delivered within a few days or a couple of weeks, depending on whether the item is in stock in our US office.  Consumable supplies are normally in stock and ready to ship the same day.  Delivery within the US and Canada normally takes 3 days or less, but precisely how long it takes depends on the mode of shipment.  Also, deliveries in large urban areas are often quicker than to less densely populated areas, and deliveries within the US are quicker than to Canada or MExico.  Add one to two days for customs clearance into Canada or Mexico.

If you are an established customer (have ordered from us in the past) then you can order via our website. If your institution / lab have an established account but you have never communicated with us by e-mail, you may need to use the Request Info form to let us know to add you to the contact list and associate you with a particular account. It is helpful if you can provide your lab’s account number (from any quote, invoice or work order) since that helps us avoid associating you with another account at the same institution or another lab at another institution with the same PI.

Anyone can order from us by e-mail or fax when responding to a valid proposal issued by Cortech Solutions. For institutions with established credit, we accept POs with payment by check or credit card. Private companies have the option of inquiring about establishing credit (credit application) or paying by credit card or check in advance of delivery.

If your institution requires a PO for us to get paid, then you need to send us a PO to place an order. The PO should indicate the items you want to order, the prices you expect to pay, the method of payment, and the billing and shipping addresses.

If you will pay by CC or check in advance and your institution does not require a PO to pay by these means, then you can place an order in response to a written proposal by signing the proposal, confirming the shipping and billing addresses, indicating the method of payment and including payment details such as credit card number, etc. We recommend calling in your CC information to our main number, but our fax is secure, so you may fax it to us if you wish.

High density surface EMG as described in the recent publications on the Biosemi site is possible with the addition of the sEMG accessories. The original model of the high density sEMG probe was made for ActiveOne, so the connector differed. The current version separates the electrode grid from the preamp as in:

• reusable grid
• sEMG preamplifier

Less dense sEMG can be accomplished with an elastic fabric with electrode holders like the EEG cap stretched over a muscle.  This would need to be custom-made, but would not be expensive.

Fine wire EMG would require either spring contact adapters or safety socket leads with inline active headstage. If your fine wire electrodes will be stripped but unterminated, you need spring contacts, and if your electrodes terminate in safety sockets, you need inline adapters.

We expect the new red-rubber reinforced ActiveTwo active electrodes to last more than 1000 uses, based on our experience so far, and based on automated repeated-strain testing.

The way ActiveTwo electrode sets are built, they are not repairable by the end-user, but we can replace single electrodes for you. We can so this quickly (24 hours plus transit), efficiently, and at low cost (or free under warranty). Electrodes are warranted against material/manufacturing defects for one year, and we charge by the repair after that. We find that offering extended warranties motivates less careful handling, so we don’t offer extended warranties.

Follow the steps in the other FAQ linked here to identify the problem before contacting us to ask about the procedure and the cost of a repair.

We do offer individual EXG pin-type electrodes that you can insert in the cap as substitutes for faulty ribbon cable leads. This would be a short term stop gap solution only. We strongly recommend having a backup set of electrodes on hand after a year or two so that if the first set needs repair, you can continue to run with the other set while the repair is undertaken. You would not need to buy the spare set right away — just budget to have it once the electrodes have had enough use that they may begin experiencing problems. After you have made 200-300 recordings with your primary electrode set would be a good rule of thumb for when you should have a spare set of electrodes on hand.

You CAN install current versions of ActiView on Windows 10. But, before you do so, if the system was orignally delivered before January of 2017 you should update the firmware on the optical receiver / USB interface so that you do not have to go through the very long and arduous process of installing an unsigned driver on Windows 10.

You can update the firmware using any Windows 7 or 8 computer with the MSWinUSB2 driver installed, even if it is not the computer you have been using for ActiView. If you are just using a Windows 7 or 8 computer to update firmware on the optical receiver / USB interface, there is no need to install the LabVIEW Runtime Engine or ActiView on this computer. You WILL need the LabVIEW Runtime Engine and ActiView on the new Windows 10 computer, but you WILL NOT need to install a driver after the firmware update has been performed.

See the procedure outlined at biosemi.com/ faq/install_USB.htm for detailed instructions.  The section at the bottom marked IMPORTANT is the place to begin.

The positions in these caps come from the Oostenveld and Praamstra 5% system.  See http://robertoostenveld.nl/electrode/ for background and for links to electrode coordinates in a variety of formats. Depending on what software you are using for analysis, we might be able to provide another file format. The Biosemi channel assignments (relating electrode labels to electrode sites in the Oostenveld and Praamstra nomenclature) are below:

1. In the ActiView software, select About ActiView > Load CFG.
2. Navigate to the folder called Configuring and select the CFG that matches your head caps.  For example, if you have Biosemi standard 32 channel head-caps and want the 10-20 labels to be displayed, the file you want is “10-20system32+8.cfg”.
3. Once this CFG is loaded, go back to the Monopolar display tab in ActiView, and check the Decimation Ratio. This indirectly controls the sampling rate, being a fraction by which the AD rate defined by the speedmode (AD rate on the AD box) is multiplied.  If you are operating in speedmode 4 (2048 Hz on the AD box), then a decimation ratio of 1/4 could be used to arrive at 512 Hz sampling rate to file, for example.
4. After setting the Decimation Ratio, check the settings for the Filters and Reference on the left side of the Monopolar Display tab.  We recommend un-checking (turning off) both of the display filters and setting the Reference to None (Raw). This gives the operator the truest picture of the saved data as data are being recorded.
5. Next, verify that any auxiliary sensors you will be using have been selected in the Auxiliary Sensors tab.  It is best to select (highlight) only the sensors you will be using (or the superset of sensors you may use) so that unused sensor channels are not added to your data file.
6. Save a dummy data file in ActiView by selecting Start File, verifying that the right subset of EEG electrodes is selected (in the example case, A1-32), verifying that the EXG1-8 channels are being added if you want them, and selecting Add Displayed Sensors (the ones you selected before in the Auxiliary Sensors tab).
7. When ActiView asks for a path / file name (it may produce an error message about the default path not existing — just click to close), navigate to the default folder for data to be saved in for this experiment (or if this CFG will serve several experiments, point to the parent folder that contains folders for various experiments) and enter a file name like this “CHANGE THIS FILE NAME AND PATH AS NEEDED”.
8. Click Stop at the top left side of the ActiView screen to stop writing to the dummy data file.
9. Navigate to About ActiView > Save CFG and save the CFG file to the folder where the ActiView software executable is located. If you name this CFG as DEFAULT.CFG, it will be used automatically when ActiView opens. If you will have various CFG files for various experiments, then you should save the new CFG with a name that relates to the associated experiment, and be sure to rename the existing DEFAULT.CFG to _DEFAULT.CFG. By doing this, ActiView will force the operator to select a CFG file each time the ActiView software is opened. One important note – if the operator does not close ActiView at the end of a recording, the CFG file will still be loaded, and the next operator may not notice. For this reason, operators should be vigilant about closing ActiView at the end of a recording, and if they enter the lab to find ActiView open, they should close it, then reopen it so that it will remind them to load the correct CFG for their study.

Since mid-2016, Biosemi has included a black USB virtual serial port trigger cable with each new ActiveTwo system.  The device is depicted below.

Inside the shell of the 37 pin connector is a microchip that appears to the stimulus computer as a virtual serial port but provides 8 bit parallel TTL output to the ActiveTwo trigger input port.  Because it appears as a virtual serial port on the stimulus computer, this cable is a relatively universal solution for triggering ActiveTwo from virtually any software on any platform.  There are a few simple parameters you need to know to send triggers via this device.  For details, see:

• https://www.biosemi.com/faq/USB%20Trigger%20interface%20cable.htm

To use this trigger cable with MATLAB, Roee Gilron at UCSF (thanks, Roee!) provides a code sample at Github:

• https://github.com/roeegilron/BioSemiUSBtrigger

ActiveTwo is provided with drivers and host data acquisition software for Windows, Mac, and Linux computers.

Note that certain applications, such as event-related potentials, often require a separate computer to run experimental control / stimulus delivery software. The requirement for a separate computer for stimulus delivery is more a function of the experimental control software needing full control of computer resources to do its job.

In brief, the computer requirements for the ActiView data acquisition software are:

• Operating system:
  • Windows 10 / 11
  • MacOS 11 Big Sur, Monterey
  • Linux 64 bit or Linux X86 with library GNU-C V2.2.4 or later
• RAM: 8 GB or more
• Hard Drive: recommend 500 GB, but user should anticipate free space needed for data (file size in bytes is approximately = 3 X AD rate in Hz X number of channels X number of seconds recorded)
• Display: 1440 X 900 or higher resolution display
• One free USB port
  • SPECIAL NOTE ABOUT USB CHIPSETS: Small form factor computers without PCIe expansion slots should be avoided. The Intel W480 chipset found in many brands of small form factor desktop computer is not capable of keeping up with USB 2.0 High Speed data rates, which prevents operation in speed modes 2 and 3 for AD boxes that have high speed firmware installed. This is of particular importance in systems used in settings where ABR and cortical ERP will be measured concurrently or alternately. If you opt for a small form factor computer, be sure to use a computer that has at least one free PCIe expansion slot that you can add a PCIe expansion card with one or more USB 2.0 or higher ports.

Note: The ActiveTwo computer DOES NOT NEED A PARALLEL PORT.  A parallel port on the experimental control computer can be used to send stimuli to ActiveTwo, but we provide a USB virtual serial port trigger cable with every new system, so a parallel port is not needed for triggering.

In addition, the following are recommended for the ActiView computer:

• Network interface and remote storage for data backups
• Accessories such as KVMA switch box, extra monitor / keyboard / mouse, extension cables, etc to permit access to the EEG display from the separate room for the subject

The blue CM in Range light reflects two things: 1) whether the CMS and DRL electrodes are adequately connected to the participant’s body, and 2) whether all of the other active electrodes, cables and connectors are intact.  If any of these are NOT true, then the blue CM in Range light will flicker and the signals and offsets will pulsate once every half second until the problem is rectified.  We call this state CM Out of Range (CMOR).  The blue LED labeled CM in Range on the front panel of the AD box is reflected on the top right of the ActiView software display. This makes it easy to recognize there is a problem.  To identify which electrodes are involved, use the one-bucket test.

Once you identify the faulty electrodes, contact us at via the Request Info form and let us know the serial number of the electrode, and if it is a set of electrodes on a ribbon cable let us know which electrode is (or electrodes are) causing the problem.  On occasion, this type of problem may be caused by a loose or damaged connector on the ribbon cable, but this is rare.  Most often, the problem is caused by a single broken wire on an electrode.  If both wires on an electrode are broken, then the CM in range light will not go off, but the offset on that channel will read -262 mV (the negative extent of the input range).

Maybe.  There is no way the EEG system can harm the TMS system, but there are some TMS systems that are essentially useless with some EEG systems.  You need a a suitable combination of features in each to be successful at all in using TMS with EEG.

Desirable attributes:

• Coils designed specifically for use with EEG will have a cable that exits the coil tangential to the head surface so that the coil does not pass close by EEG electrodes and cables.
• A coil to be used with EEG should be passively cooled, since active cooling by means of a fan will induce electromagnetic interference in the EEG.
• The TMS recharge mechanism should be designed to avoid inducing electromagnetic artifacts in the EEG.
• The TMS system should be shielded so that no more than 3 milligauss of electromagnetic interference from the TMS system’s power supply reaches the electrodes and cables.
• The TMS system should be able to produce a TMS pulse in response to an input trigger with a low and predictable latency.  Long, but especially unpredictable latency in responding to an input trigger will result in TMS artifacts that are difficult to impossible to remove from the EEG.

Aside from attributes of the TMS system, there are also important considerations regarding the EEG system in this relationship. See the other FAQ entry on that topic.

No.  There are a few special attributes that are required and others that are desirable.

Required attributes:

• Inputs should be protected so that they are not damaged by the TMS pulse
• Frequency response on all channels should be from DC on the low end, since AC coupled inputs will “ring” when presented with a large voltage transient like the TMS artifact

Desirable attributes:

• Electrodes should have a low-profile so that the TMS coil can be placed as near the head as possible, maximizing penetration depth and current delivery
• It is important for the EEG system to be able to trigger the TMS system at precisely the same phase with respect to the EEG samples each time a stimulus is delivered.  This will improve the performance of artifact removal algorithms

Aside from these attributes of the EEG system, there are also important considerations regarding the TMS system in this relationship. See the other FAQ entry on that topic.

Electrodes and head caps can have positions derived from systems based on the International 1020 System.  When the positions are based on 1020, the labels on the caps and electrodes can either be the actual 1020 position names (such as Fp1, Cz, etc) or they can be what is called ABC, which actually means A1, A2, …A32, B1, B2,…B32, etc  Another way to refer to the ABC labeling is arbitrary alphanumeric.  The 1020 system is not arbitrary because the names are based on anatomical landmarks and the odd=left and even=right numbering is predictable and interpretable.  When you have only one type of cap in your lab, it makes sense to use 1020 labels for caps with positions based on the 1020 system.  However, if you have 32 channel caps AND 64 channel caps, then you might find it useful to be able to use the A1-32 labels for the A cable and the B1-32 labels for the B cable and complementary A1-32 labels on the 32 channel caps and A1-B32 labels on the 64 channel caps.  This way, the A cable can be used for the whole head in 32 channel studies of for just the left side of the head in 64 channel studies.  This does provide a short term savings if you don’t want to have two A cables on-hand, but using 1020 labels on everything is more convenient and at the limit it will not cost any more (because cables that are used less frequently will last longer).

If you have more than one item to be repaired, we will normally issue a separate work order number for each item.  In that case, it is not necessary to ship the items to us separately.  They can be packed together, assuming you pack carefully and include the documentation we request when we send you the work order number:

• Include the “work order number” on the package and on any documentation in the package.  If a repair is undertaken, the work order number will become the “invoice number” if the repair results in a bill for parts or services.
• Write a note describing the problem you are having with the part and include it in the package with the part you are returning.  We need to be sure that we are focusing on the same problem that you have been experiencing to do the best job of reporting back to you on the status of the product.
• Be sure that the note you include with the shipment references as many of the following as possible: the date of purchase, name of purchaser or customer account number.
• Let us know the address to which repaired parts should be shipped (must be a physical address with a phone number and person’s name).

Before you send anything to us for repair, please contact us so we can assess the situation and be sure that is the best course of action.   Once you have exhausted all available options, we may authorize you to return an item for repair.  At that point, see the steps below under “How to arrange for a repair”.

Many potential questions and problems are covered under the manufacturers’ warranties for the products we sell.  As a general rule, if the item you are trying to use is not broken, then support for that item would either be provided as a part of the original purchase agreement or under an extended service level agreement. See the Service Level Agreements page and the Warranties page for details.

If you feel that you need additional training in the use of the equipment or software that you purchased from us. Please review the upcoming training opportunities under Workshops/Seminars on our Events page and let us know if you do not see a workshop or seminar that covers the topic in which you are interested.

How to arrange for a repair:

1. Review the User / Operator Manual and/or context-sensitive help provided with the product to determine as best you can whether a repair is needed.
2. See the on-line FAQ documents.
3. Contact us to receive additional assistance in identifying possible solutions that may not necessitate the return of the product.
4. Please provide us with the serial number and the model number of the item you request assistance with as well as the data of purchase and the name of the purchaser or your customer account number.
5. Ask us for an “issue number” and refer to that issue number when corresponding with us about this problem.  The issue number will become the “work order number” if a repair is undertaken and the “invoice number” if the repair results in a bill for parts or services.
6. Write a note describing the problem you are having with the part and include it in the package with the part you are returning.  We need to be sure that we are focusing on the same problem that you have been experiencing to do the best job of reporting back to you on the status of the product.
7. Be sure the note you include with the shipment references the date of purchase, name of purchaser or customer account number, the address to which repaired parts should be shipped (must be a physical address with a phone number and person’s name for FedEx to accept it).
8. Wrap any electrode contacts in a paper towel to be sure that they stay dry and to insulate them from metal parts on the connector.
9. Package the product carefully in the original packaging or a comparable container.  Use plenty of packing material (preferably bubble wrap or packing peanuts) to cushion the goods and ensure they do not move around inside the box while it is in transit.  For help on how to package your goods, see the document “How to Pack” at FedEx.com.
10. Ship the goods via traceable courier service to our address and notify us that the package is en route.
11. When contacting us to check on the status of your repair, refer to the issue/work order number.

When you purchase a new laboratory instrument, you want to get started using it and producing results as quickly as possible, and nothing helps you accomplish this goal faster than having a trained technician visit your lab to install the system and configure it optimally for your purposes. From our perspective, you will have the best possible experience with our products when the equipment is setup and configured properly and you are properly trained from the beginning. Installation visits are not included in the pricing on our standard price list, but we do generally include an optional installation fee on quotations. We find that customers who receive assistance from the beginning have fewer questions later and have more success using the equipment. We encourage you to invest in this valuable service.  If you would like to arrange an installation and training visit, please contact us!

We will always do our best to respond quickly when you need something urgently.  It helps us immensely if you plan ahead and give us a little advance warning if you foresee a deadline approaching by which you need parts, supplies or repairs to be complete.

For new purchases, we can often pre-order goods for established customers, even before the official institutional PO has been received.  Give us a heads-up as soon as you know that you intend to order items we have quoted you, and if you expect to have the official PO within 30 days, and you agree to let us know if anything changes, we will pre-order the goods for you based on your word.

For repairs, we know how vital our equipment is to your work, so we always do our best to respond quickly to urgent repair requests.  One important point — the earlier we know the date by which a repaired item must be received back, the sooner we can let you know whether we will or will not be able to meet that deadline.  Ultimately, the most valuable thing you can do to ensure we meet your deadlines is to notify us of those deadlines as early as possible!

See our contact details page.

High density surface EMG as described in the recent publications on the Biosemi site is possible with the addition of the sEMG accessories. The original model of the high density sEMG probe was made for ActiveOne, so the connector differed. The current version separates the electrode grid from the preamp as in:

• reusable grid
• sEMG preamplifier

Less dense sEMG can be accomplished with an elastic fabric with electrode holders like the EEG cap stretched over a muscle.  This would need to be custom-made, but would not be expensive.

Fine wire EMG would require either spring contact adapters or safety socket leads with inline active headstage. If your fine wire electrodes will be stripped but unterminated, you need spring contacts, and if your electrodes terminate in safety sockets, you need inline adapters.

We expect the new red-rubber reinforced ActiveTwo active electrodes to last more than 1000 uses, based on our experience so far, and based on automated repeated-strain testing.

The way ActiveTwo electrode sets are built, they are not repairable by the end-user, but we can replace single electrodes for you. We can so this quickly (24 hours plus transit), efficiently, and at low cost (or free under warranty). Electrodes are warranted against material/manufacturing defects for one year, and we charge by the repair after that. We find that offering extended warranties motivates less careful handling, so we don’t offer extended warranties.

Follow the steps in the other FAQ linked here to identify the problem before contacting us to ask about the procedure and the cost of a repair.

We do offer individual EXG pin-type electrodes that you can insert in the cap as substitutes for faulty ribbon cable leads. This would be a short term stop gap solution only. We strongly recommend having a backup set of electrodes on hand after a year or two so that if the first set needs repair, you can continue to run with the other set while the repair is undertaken. You would not need to buy the spare set right away — just budget to have it once the electrodes have had enough use that they may begin experiencing problems. After you have made 200-300 recordings with your primary electrode set would be a good rule of thumb for when you should have a spare set of electrodes on hand.

You CAN install current versions of ActiView on Windows 10. But, before you do so, if the system was orignally delivered before January of 2017 you should update the firmware on the optical receiver / USB interface so that you do not have to go through the very long and arduous process of installing an unsigned driver on Windows 10.

You can update the firmware using any Windows 7 or 8 computer with the MSWinUSB2 driver installed, even if it is not the computer you have been using for ActiView. If you are just using a Windows 7 or 8 computer to update firmware on the optical receiver / USB interface, there is no need to install the LabVIEW Runtime Engine or ActiView on this computer. You WILL need the LabVIEW Runtime Engine and ActiView on the new Windows 10 computer, but you WILL NOT need to install a driver after the firmware update has been performed.

See the procedure outlined at biosemi.com/ faq/install_USB.htm for detailed instructions.  The section at the bottom marked IMPORTANT is the place to begin.

The positions in these caps come from the Oostenveld and Praamstra 5% system.  See http://robertoostenveld.nl/electrode/ for background and for links to electrode coordinates in a variety of formats. Depending on what software you are using for analysis, we might be able to provide another file format. The Biosemi channel assignments (relating electrode labels to electrode sites in the Oostenveld and Praamstra nomenclature) are below:

1. In the ActiView software, select About ActiView > Load CFG.
2. Navigate to the folder called Configuring and select the CFG that matches your head caps.  For example, if you have Biosemi standard 32 channel head-caps and want the 10-20 labels to be displayed, the file you want is “10-20system32+8.cfg”.
3. Once this CFG is loaded, go back to the Monopolar display tab in ActiView, and check the Decimation Ratio. This indirectly controls the sampling rate, being a fraction by which the AD rate defined by the speedmode (AD rate on the AD box) is multiplied.  If you are operating in speedmode 4 (2048 Hz on the AD box), then a decimation ratio of 1/4 could be used to arrive at 512 Hz sampling rate to file, for example.
4. After setting the Decimation Ratio, check the settings for the Filters and Reference on the left side of the Monopolar Display tab.  We recommend un-checking (turning off) both of the display filters and setting the Reference to None (Raw). This gives the operator the truest picture of the saved data as data are being recorded.
5. Next, verify that any auxiliary sensors you will be using have been selected in the Auxiliary Sensors tab.  It is best to select (highlight) only the sensors you will be using (or the superset of sensors you may use) so that unused sensor channels are not added to your data file.
6. Save a dummy data file in ActiView by selecting Start File, verifying that the right subset of EEG electrodes is selected (in the example case, A1-32), verifying that the EXG1-8 channels are being added if you want them, and selecting Add Displayed Sensors (the ones you selected before in the Auxiliary Sensors tab).
7. When ActiView asks for a path / file name (it may produce an error message about the default path not existing — just click to close), navigate to the default folder for data to be saved in for this experiment (or if this CFG will serve several experiments, point to the parent folder that contains folders for various experiments) and enter a file name like this “CHANGE THIS FILE NAME AND PATH AS NEEDED”.
8. Click Stop at the top left side of the ActiView screen to stop writing to the dummy data file.
9. Navigate to About ActiView > Save CFG and save the CFG file to the folder where the ActiView software executable is located. If you name this CFG as DEFAULT.CFG, it will be used automatically when ActiView opens. If you will have various CFG files for various experiments, then you should save the new CFG with a name that relates to the associated experiment, and be sure to rename the existing DEFAULT.CFG to _DEFAULT.CFG. By doing this, ActiView will force the operator to select a CFG file each time the ActiView software is opened. One important note – if the operator does not close ActiView at the end of a recording, the CFG file will still be loaded, and the next operator may not notice. For this reason, operators should be vigilant about closing ActiView at the end of a recording, and if they enter the lab to find ActiView open, they should close it, then reopen it so that it will remind them to load the correct CFG for their study.

Since mid-2016, Biosemi has included a black USB virtual serial port trigger cable with each new ActiveTwo system.  The device is depicted below.

Inside the shell of the 37 pin connector is a microchip that appears to the stimulus computer as a virtual serial port but provides 8 bit parallel TTL output to the ActiveTwo trigger input port.  Because it appears as a virtual serial port on the stimulus computer, this cable is a relatively universal solution for triggering ActiveTwo from virtually any software on any platform.  There are a few simple parameters you need to know to send triggers via this device.  For details, see:

• https://www.biosemi.com/faq/USB%20Trigger%20interface%20cable.htm

To use this trigger cable with MATLAB, Roee Gilron at UCSF (thanks, Roee!) provides a code sample at Github:

• https://github.com/roeegilron/BioSemiUSBtrigger

ActiveTwo is provided with drivers and host data acquisition software for Windows, Mac, and Linux computers.

Note that certain applications, such as event-related potentials, often require a separate computer to run experimental control / stimulus delivery software. The requirement for a separate computer for stimulus delivery is more a function of the experimental control software needing full control of computer resources to do its job.

In brief, the computer requirements for the ActiView data acquisition software are:

• Operating system:
  • Windows 10 / 11
  • MacOS 11 Big Sur, Monterey
  • Linux 64 bit or Linux X86 with library GNU-C V2.2.4 or later
• RAM: 8 GB or more
• Hard Drive: recommend 500 GB, but user should anticipate free space needed for data (file size in bytes is approximately = 3 X AD rate in Hz X number of channels X number of seconds recorded)
• Display: 1440 X 900 or higher resolution display
• One free USB port
  • SPECIAL NOTE ABOUT USB CHIPSETS: Small form factor computers without PCIe expansion slots should be avoided. The Intel W480 chipset found in many brands of small form factor desktop computer is not capable of keeping up with USB 2.0 High Speed data rates, which prevents operation in speed modes 2 and 3 for AD boxes that have high speed firmware installed. This is of particular importance in systems used in settings where ABR and cortical ERP will be measured concurrently or alternately. If you opt for a small form factor computer, be sure to use a computer that has at least one free PCIe expansion slot that you can add a PCIe expansion card with one or more USB 2.0 or higher ports.

Note: The ActiveTwo computer DOES NOT NEED A PARALLEL PORT.  A parallel port on the experimental control computer can be used to send stimuli to ActiveTwo, but we provide a USB virtual serial port trigger cable with every new system, so a parallel port is not needed for triggering.

In addition, the following are recommended for the ActiView computer:

• Network interface and remote storage for data backups
• Accessories such as KVMA switch box, extra monitor / keyboard / mouse, extension cables, etc to permit access to the EEG display from the separate room for the subject

The blue CM in Range light reflects two things: 1) whether the CMS and DRL electrodes are adequately connected to the participant’s body, and 2) whether all of the other active electrodes, cables and connectors are intact.  If any of these are NOT true, then the blue CM in Range light will flicker and the signals and offsets will pulsate once every half second until the problem is rectified.  We call this state CM Out of Range (CMOR).  The blue LED labeled CM in Range on the front panel of the AD box is reflected on the top right of the ActiView software display. This makes it easy to recognize there is a problem.  To identify which electrodes are involved, use the one-bucket test.

Once you identify the faulty electrodes, contact us at via the Request Info form and let us know the serial number of the electrode, and if it is a set of electrodes on a ribbon cable let us know which electrode is (or electrodes are) causing the problem.  On occasion, this type of problem may be caused by a loose or damaged connector on the ribbon cable, but this is rare.  Most often, the problem is caused by a single broken wire on an electrode.  If both wires on an electrode are broken, then the CM in range light will not go off, but the offset on that channel will read -262 mV (the negative extent of the input range).

The ActiveTwo Base System has no channels. The Base System consists of the parts that every ActiveTwo system needs to have, but excludes the parts that are used to custom configure ActiveTwo for various purposes, like amplifier/converter (AC modules).  The AC modules give the system the capacity to record from active electrodes. With four of the eight channel modules, the base system will have the capacity for 32 channels. If you want 32 electrodes on the scalp, then you need four modules, but if you also want to use four individual flat-type electrodes, you need another eight-channel module (four modules for EEG and one module for EXG1-8). The modules have eight channels, so you can only expand the system in increments of eight channels. You don’t have to buy the electrodes to use with EXG5-8, but you need the eight channel module.

Maybe.  There is no way the EEG system can harm the TMS system, but there are some TMS systems that are essentially useless with some EEG systems.  You need a a suitable combination of features in each to be successful at all in using TMS with EEG.

Desirable attributes:

• Coils designed specifically for use with EEG will have a cable that exits the coil tangential to the head surface so that the coil does not pass close by EEG electrodes and cables.
• A coil to be used with EEG should be passively cooled, since active cooling by means of a fan will induce electromagnetic interference in the EEG.
• The TMS recharge mechanism should be designed to avoid inducing electromagnetic artifacts in the EEG.
• The TMS system should be shielded so that no more than 3 milligauss of electromagnetic interference from the TMS system’s power supply reaches the electrodes and cables.
• The TMS system should be able to produce a TMS pulse in response to an input trigger with a low and predictable latency.  Long, but especially unpredictable latency in responding to an input trigger will result in TMS artifacts that are difficult to impossible to remove from the EEG.

Aside from attributes of the TMS system, there are also important considerations regarding the EEG system in this relationship. See the other FAQ entry on that topic.

Electrodes and head caps can have positions derived from systems based on the International 1020 System.  When the positions are based on 1020, the labels on the caps and electrodes can either be the actual 1020 position names (such as Fp1, Cz, etc) or they can be what is called ABC, which actually means A1, A2, …A32, B1, B2,…B32, etc  Another way to refer to the ABC labeling is arbitrary alphanumeric.  The 1020 system is not arbitrary because the names are based on anatomical landmarks and the odd=left and even=right numbering is predictable and interpretable.  When you have only one type of cap in your lab, it makes sense to use 1020 labels for caps with positions based on the 1020 system.  However, if you have 32 channel caps AND 64 channel caps, then you might find it useful to be able to use the A1-32 labels for the A cable and the B1-32 labels for the B cable and complementary A1-32 labels on the 32 channel caps and A1-B32 labels on the 64 channel caps.  This way, the A cable can be used for the whole head in 32 channel studies of for just the left side of the head in 64 channel studies.  This does provide a short term savings if you don’t want to have two A cables on-hand, but using 1020 labels on everything is more convenient and at the limit it will not cost any more (because cables that are used less frequently will last longer).

If you have more than one item to be repaired, we will normally issue a separate work order number for each item.  In that case, it is not necessary to ship the items to us separately.  They can be packed together, assuming you pack carefully and include the documentation we request when we send you the work order number:

• Include the “work order number” on the package and on any documentation in the package.  If a repair is undertaken, the work order number will become the “invoice number” if the repair results in a bill for parts or services.
• Write a note describing the problem you are having with the part and include it in the package with the part you are returning.  We need to be sure that we are focusing on the same problem that you have been experiencing to do the best job of reporting back to you on the status of the product.
• Be sure that the note you include with the shipment references as many of the following as possible: the date of purchase, name of purchaser or customer account number.
• Let us know the address to which repaired parts should be shipped (must be a physical address with a phone number and person’s name).

The inside diameter of adhesive ring should be about the same size as, or larger than, the diameter of the electrode contact.  The inside diameter of the adhesive ring should not be larger than the outer diameter of the electrode housing.  The outside diameter minus the center hole determines how much surface area contacts the skin, thus determining how tightly the adhesive will adhere to the skin.  Also, the outside diameter will limit how close you can place electrodes to one another and to other features, such as the eyes.

Using ActiveTwo as an example, the electrode contact on a flat-type electrode has a diameter of about 4.5 mm.  An adhesive ring with 5 mm id (center hole) would be  idea, but the 5×13 adhesives are rather expensive because they are manufactured in Europe.  We recommend using a 4×19 or a 4×12 adhesive ring.  The 4×12 is a good choice when placing the electrodes close to one another or close to the eyes for startle measurements.  The 4×19 is a good choice when you have plenty of room and the primary concern is how well the electrodes stick to the skin.

No. We are not equipped to perform this as it requires facilities approval. You should consult the manufacturer of the penetration panel as well as your facilities department for proper guidance.

Typically it is not suggested to run the cabling overhead towards the MR scanner as there is potential of coupling with the RF cables of the scanner. If the aim is to reduce stray cabling along the floor it is suggested that the headphones are stored/hung with excess fiber cabling “looped” as to keep it out of the way.

Yes! While not included as standard there is an option for an Optoaccoustics patient microphone available in both basic and noise canceling models. Please request pricing if interested!

Yes! There are headphones that span the full range of infants through adults. Additionally there are insert (air-tube) earphones that can be used for all ages, and for all headcoils.

Shielded BNC cables are routed through a filter box/transformer. The supplied BNC connectors will need to be mounted within your penetration panel, this will require two 11mm holes for this purpose, the supplied RF filters will be connected on the MR side with 9 meters of cabling to connect to the headphones. Typically cables run from the penetration panel located between the control room and scan room, however extending the BNC cabling may also be possible to route it from the equipment room.

The BOLDfonic system is comprised of the MR Confon main console, an operator microphone, a set of patient/participant insert earphones, control room monitoring speakers, along with all audio cables, connectors, and filters necessary for full installation — just supply the audio output from your PC or alternative source via a ⅛ in. audio cable or SPDIF output. Keep in mind that the BOLDfonic system includes the AudioFile unit which can function as an external USB audio card.

As with some scanners you may be left with a protruding rail or track. For appropriate positioning of the BOLDScreen it is suggested that you purchase a trolley with articulating arm, which will allow for offset fixation and easy adjustment for optimal monitor placement. Please see our trolley/stand options.

Traditionally the BOLDScreen is placed at the rear of the scanner at the end of the bore. The monitor can be viewed with an OEM “viewing mirror” that mounts to the headcoil, these are usually included from the manufacturer of the headcoil. Depending on the size of your scanner’s bore (e.g. 60, 70cm), you may need to offset the BOLDScreen for full field of view. For a 60cm bore scanner, you may have to displace the position roughly one foot.

Most “standard” PC’s are adequately suited for driving the BOLDScreen 32 if they offer a dual-link DVI output. For laptops this can often be achieved by the use of a DisplayPort to Dual-Link DVI adapter. It is important to determine in advance whether your laptop offers a DisplayPort output for this purpose. If you are using a desktop PC then be certain that you have a video card with dual-link DVI, I only repeat this as it is rather important. If you are going through the process of setting up a new PC, I would suggest going with an NVIDEA video card as these are best suited for full functionality (e.g. dithering schemes) of the BOLDScreen 32.

No, the power supply is meant to be powered from outside the MR scan room. A voltage converter unit (VCU) with RF filter is supplied which is to be mounted within the penetration panel, most often between the equipment room and scan room. An 11mm hole (BNC sized) is required for the mounting of the VCU.

The BOLDScreen 32 comes standard with 30 meters of fiber optic cabling (duplex LC/SC), other lengths are possible as this fiber optic cable is available online through various sources. Some choose to run this around the periphery of the scan room, while others prefer to run it through conduit or channeling in the ceiling and have it dropped at the rear of the bore.

The CRS BOLDScreen units have been specifically designed to be directly placed at the rear of the bore of the scanner, without any distance constraints. The BOLDScreen 32 is compatible with scanners with a field strength up to 7T, while the BOLDScreen 23 and 24 are compatible with those up to 3T.

BOLDScreen 32 setup, this consist of: monitor, fiber optic cabling (30 meters), DVI/fiber optic converter, adjustable height aluminum tripod/stand, and power supply and MR friendly converter unit. Often users will opt to purchase a trolley for portability and versatility in setup.

This is really dependent on the signal quality. Typically for normal cortical penetration you will want anywhere from 3cm up, the larger the distance the deeper the penetration however at the sake of a reduced signal-to-noise ratio. Typically for normal adults we employ a 3.5cm interoptode distance, for those with darker skin or dark/dense hair you may need to reduce this to achieve an ideal SNR. For younger children and infants often times 2.5cm is more common.

Lasers often require greater consideration in application. There are certainly constraints with regard to motility with a laser based setup that may not be of any concern with LED. Preparation times are often greater with laser than LED, as lasers are often added to a headcap one by one, whereas LED sources could sometimes be “pre-populated”.

Lasers naturally provide a very focal output and are excellent with narrow band frequency emission, thus the ability to discretely “tune” the light output is perhaps of some value, as you might imagine when studying the dispersion of light. Additionally modulation of lasers can take place many times fast than that of LED, as there are some capacitive “left-overs” with LED

fNIRS is of course a completely different modality than fMRI, however while the mechanics may differ there is overlap in the resulting measurements, ultimately cerebral blood flow and metabolic measurements may be obtained, and neuronal activation often assumed. fNIRS is specific to oxygenated and deoxygenated hemoglobin measurement and quantification due to light back reflection, while fMRI aligns the orientation of the hemoglobin depending on the presence of oxygen. fNIRS offers a much better temporal resolution often 100x or more, while spatially fMRI has the upper hand by roughly 10x.

Very good, and important, question. Clearly fNIRS is employing frequencies of light that are purposely used to traverse the skull without much restraint, and this is in fact introducing exogenous stimuli. Well don’t fret, the amount of signal power using fNIRS can be comparable to sunlight. Further, of recent, several studies suggest there are various health benefits to infrared light stimulation at the cellular/metabolic level- even still these studies primarily employ chronic use.

This is a tough one, inherently hair is the nemesis of any fNIRS device on the market and while we all would like to say we have this completely figured out it ultimately comes down to proper preparation, part of which is also a skill in performing. I would use the same criteria with regard screening as you may normally do with EEG.

OxySoft is developed for use with Windows 7 or 10, both are supported however Windows 7 is still preferred. We also offer a free Android application for the PortaLite and PortaMon units for streaming and data logging.

Both PortaLite and PortaMon units use a bluetooth connection with a long range antenna up to 150 meters is possible. The Brite 23 system offers a range of 30 meters.

Yes, you may stream up to 7 devices, both wired (OxyMon), and wireless devices (Brite 23, PortaMon/PortaLite) to the same acquisition PC in real time.

The inside diameter of adhesive ring should be about the same size as, or larger than, the diameter of the electrode contact.  The inside diameter of the adhesive ring should not be larger than the outer diameter of the electrode housing.  The outside diameter minus the center hole determines how much surface area contacts the skin, thus determining how tightly the adhesive will adhere to the skin.  Also, the outside diameter will limit how close you can place electrodes to one another and to other features, such as the eyes.

Using ActiveTwo as an example, the electrode contact on a flat-type electrode has a diameter of about 4.5 mm.  An adhesive ring with 5 mm id (center hole) would be  idea, but the 5×13 adhesives are rather expensive because they are manufactured in Europe.  We recommend using a 4×19 or a 4×12 adhesive ring.  The 4×12 is a good choice when placing the electrodes close to one another or close to the eyes for startle measurements.  The 4×19 is a good choice when you have plenty of room and the primary concern is how well the electrodes stick to the skin.

• 8 mm id x 20 mm od: CS-AT-AR20X8BS – roll of 500
• 5 mm id x 13 mm od: CS-AT-AR13X5BS – roll of 500
• 12 mm id x 32 mm od: CS-AT-ARIV12X32 – pack of 100
• 8 mm id x 22 mm od: CS-AT-ARIV8X22 – pack of 100
• 4 mm id x 12 mm od: CS-AT-ARIV4X12 – pack of 100
• 4 mm id x 19 mm od: CS-AT-ARIV4X19 – pack of 100 (part of the standard ActiveTwo consumable supplies kit)

EMSE’s Development Plan emerges from three main streams. First, we listen to your needs and requests (e.g., you might show us what you want during a remote technical/scientific support session). Second, we periodically update and upgrade existing features (e.g., update of boundary element head models; upgrade from 32-bit to 64-bit code). Third, we’re envisioning an integrative role for EMSE in the larger field of human neurophysiology and neuroimaging, so that: (a) EMSE shall perform live analysis and automatic archiving during data acquisition; and (b) EMSE shall cooperate with other tools in an ecosystem based on FAIR (Findable, Accessible, Interoperable, Reusable) principles.

EMSE is developed by Cortech Solutions. We are an agile team with more than 50 years combined experience in the field. Principal developers are Mark Pflieger and Li Gao, who have worked on the EMSE project for 17+ years and 21+ years, respectively. Richard Greenblatt initiated the EMSE project in the early 1990s with roots from the MEG community.

EMSE reads all major research EEG and MEG data formats.

No. EMSE is a self-contained graphical program written in C++ “under the hood” for efficiency. To optimize the speed of standard matrix and math operations, EMSE leverages the Intel® Math Kernel Library.

No, EMSE is modular. The ERP Bundle (Data Editor plus Visualizer) is a powerful and affordable package for discovering and confirming space-time-frequency phenomena at the scalp level, with integrated nonparametric statistics. The Basic Source Estimation Bundle adds the Source Estimator module for brain level modeling. The Locator module digitizes electrode locations, which may be co-registered with MRI using MR Viewer. The Image Processor module can segment head tissues for constructing individual cortex and volume conductor models.

If EEG/ERP is a new addition to your lab, you can use EMSE to rapidly master all of the steps that can lead you to discover and visualize new phenomena in your experimental data. Have you already identified phenomena at the scalp? Then you can use source reconstruction and source signal estimation tools in EMSE to understand where and when these phenomena arise in the cortex. Going further, if you have participant MRIs, then you can use EMSE to sort out meaningful individual differences from incidental differences that derive from personal cortical folding patterns. In all cases, we can remotely assist with the steps.

EMSE is great for helping you, first, to identify robust space-time-frequency phenomena in your EEG or MEG data, and then to interpret those phenomena in brain space by constructing source models, by estimating regional activity, and by deriving inter-regional connectivities. EMSE can use MRI data to construct realistic volume conductor models of the head. Importantly, EMSE reproducibly automates and documents your analysis workflows, including: (a) signal processing pipelines; (b) experimental event logic pipelines; (c) event-related component measurements; and (d) nonparametric statistical hypothesis testing. EMSE is a professionally supported Windows application. We can remotely assist your data analysis process.

EMSE stands for ElectroMagnetic Source Estimation (and we say “MC”).

Maybe.  There is no way the EEG system can harm the TMS system, but there are some TMS systems that are essentially useless with some EEG systems.  You need a a suitable combination of features in each to be successful at all in using TMS with EEG.

Desirable attributes:

• Coils designed specifically for use with EEG will have a cable that exits the coil tangential to the head surface so that the coil does not pass close by EEG electrodes and cables.
• A coil to be used with EEG should be passively cooled, since active cooling by means of a fan will induce electromagnetic interference in the EEG.
• The TMS recharge mechanism should be designed to avoid inducing electromagnetic artifacts in the EEG.
• The TMS system should be shielded so that no more than 3 milligauss of electromagnetic interference from the TMS system’s power supply reaches the electrodes and cables.
• The TMS system should be able to produce a TMS pulse in response to an input trigger with a low and predictable latency.  Long, but especially unpredictable latency in responding to an input trigger will result in TMS artifacts that are difficult to impossible to remove from the EEG.

Aside from attributes of the TMS system, there are also important considerations regarding the EEG system in this relationship. See the other FAQ entry on that topic.

No.  There are a few special attributes that are required and others that are desirable.

Required attributes:

• Inputs should be protected so that they are not damaged by the TMS pulse
• Frequency response on all channels should be from DC on the low end, since AC coupled inputs will “ring” when presented with a large voltage transient like the TMS artifact

Desirable attributes:

• Electrodes should have a low-profile so that the TMS coil can be placed as near the head as possible, maximizing penetration depth and current delivery
• It is important for the EEG system to be able to trigger the TMS system at precisely the same phase with respect to the EEG samples each time a stimulus is delivered.  This will improve the performance of artifact removal algorithms

Aside from these attributes of the EEG system, there are also important considerations regarding the TMS system in this relationship. See the other FAQ entry on that topic.

This is really dependent on the signal quality. Typically for normal cortical penetration you will want anywhere from 3cm up, the larger the distance the deeper the penetration however at the sake of a reduced signal-to-noise ratio. Typically for normal adults we employ a 3.5cm interoptode distance, for those with darker skin or dark/dense hair you may need to reduce this to achieve an ideal SNR. For younger children and infants often times 2.5cm is more common.

Lasers often require greater consideration in application. There are certainly constraints with regard to motility with a laser based setup that may not be of any concern with LED. Preparation times are often greater with laser than LED, as lasers are often added to a headcap one by one, whereas LED sources could sometimes be “pre-populated”.

Lasers naturally provide a very focal output and are excellent with narrow band frequency emission, thus the ability to discretely “tune” the light output is perhaps of some value, as you might imagine when studying the dispersion of light. Additionally modulation of lasers can take place many times fast than that of LED, as there are some capacitive “left-overs” with LED

fNIRS is of course a completely different modality than fMRI, however while the mechanics may differ there is overlap in the resulting measurements, ultimately cerebral blood flow and metabolic measurements may be obtained, and neuronal activation often assumed. fNIRS is specific to oxygenated and deoxygenated hemoglobin measurement and quantification due to light back reflection, while fMRI aligns the orientation of the hemoglobin depending on the presence of oxygen. fNIRS offers a much better temporal resolution often 100x or more, while spatially fMRI has the upper hand by roughly 10x.

Very good, and important, question. Clearly fNIRS is employing frequencies of light that are purposely used to traverse the skull without much restraint, and this is in fact introducing exogenous stimuli. Well don’t fret, the amount of signal power using fNIRS can be comparable to sunlight. Further, of recent, several studies suggest there are various health benefits to infrared light stimulation at the cellular/metabolic level- even still these studies primarily employ chronic use.

This is a tough one, inherently hair is the nemesis of any fNIRS device on the market and while we all would like to say we have this completely figured out it ultimately comes down to proper preparation, part of which is also a skill in performing. I would use the same criteria with regard screening as you may normally do with EEG.

OxySoft is developed for use with Windows 7 or 10, both are supported however Windows 7 is still preferred. We also offer a free Android application for the PortaLite and PortaMon units for streaming and data logging.

Yes, you may stream up to 7 devices, both wired (OxyMon), and wireless devices (Brite 23, PortaMon/PortaLite) to the same acquisition PC in real time.

This is really dependent on the signal quality. Typically for normal cortical penetration you will want anywhere from 3cm up, the larger the distance the deeper the penetration however at the sake of a reduced signal-to-noise ratio. Typically for normal adults we employ a 3.5cm interoptode distance, for those with darker skin or dark/dense hair you may need to reduce this to achieve an ideal SNR. For younger children and infants often times 2.5cm is more common.

Lasers often require greater consideration in application. There are certainly constraints with regard to motility with a laser based setup that may not be of any concern with LED. Preparation times are often greater with laser than LED, as lasers are often added to a headcap one by one, whereas LED sources could sometimes be “pre-populated”.

Lasers naturally provide a very focal output and are excellent with narrow band frequency emission, thus the ability to discretely “tune” the light output is perhaps of some value, as you might imagine when studying the dispersion of light. Additionally modulation of lasers can take place many times fast than that of LED, as there are some capacitive “left-overs” with LED

fNIRS is of course a completely different modality than fMRI, however while the mechanics may differ there is overlap in the resulting measurements, ultimately cerebral blood flow and metabolic measurements may be obtained, and neuronal activation often assumed. fNIRS is specific to oxygenated and deoxygenated hemoglobin measurement and quantification due to light back reflection, while fMRI aligns the orientation of the hemoglobin depending on the presence of oxygen. fNIRS offers a much better temporal resolution often 100x or more, while spatially fMRI has the upper hand by roughly 10x.

Very good, and important, question. Clearly fNIRS is employing frequencies of light that are purposely used to traverse the skull without much restraint, and this is in fact introducing exogenous stimuli. Well don’t fret, the amount of signal power using fNIRS can be comparable to sunlight. Further, of recent, several studies suggest there are various health benefits to infrared light stimulation at the cellular/metabolic level- even still these studies primarily employ chronic use.

This is a tough one, inherently hair is the nemesis of any fNIRS device on the market and while we all would like to say we have this completely figured out it ultimately comes down to proper preparation, part of which is also a skill in performing. I would use the same criteria with regard screening as you may normally do with EEG.

OxySoft is developed for use with Windows 7 or 10, both are supported however Windows 7 is still preferred. We also offer a free Android application for the PortaLite and PortaMon units for streaming and data logging.

Depending on your interest, quite a bit. We are able to “tune” the frequencies of the lasers to different wavelengths, thereby offering the possibility to measure things such as Cytohrome C Oxidase (COX), and Indocyanine Green (ICG) tracer. Just let us know if you have anything particular in mind!

Yes, you may stream up to 7 devices, both wired (OxyMon), and wireless devices (Brite 23, PortaMon/PortaLite) to the same acquisition PC in real time.

This is really dependent on the signal quality. Typically for normal cortical penetration you will want anywhere from 3cm up, the larger the distance the deeper the penetration however at the sake of a reduced signal-to-noise ratio. Typically for normal adults we employ a 3.5cm interoptode distance, for those with darker skin or dark/dense hair you may need to reduce this to achieve an ideal SNR. For younger children and infants often times 2.5cm is more common.

fNIRS is of course a completely different modality than fMRI, however while the mechanics may differ there is overlap in the resulting measurements, ultimately cerebral blood flow and metabolic measurements may be obtained, and neuronal activation often assumed. fNIRS is specific to oxygenated and deoxygenated hemoglobin measurement and quantification due to light back reflection, while fMRI aligns the orientation of the hemoglobin depending on the presence of oxygen. fNIRS offers a much better temporal resolution often 100x or more, while spatially fMRI has the upper hand by roughly 10x.

Very good, and important, question. Clearly fNIRS is employing frequencies of light that are purposely used to traverse the skull without much restraint, and this is in fact introducing exogenous stimuli. Well don’t fret, the amount of signal power using fNIRS can be comparable to sunlight. Further, of recent, several studies suggest there are various health benefits to infrared light stimulation at the cellular/metabolic level- even still these studies primarily employ chronic use.

This is a tough one, inherently hair is the nemesis of any fNIRS device on the market and while we all would like to say we have this completely figured out it ultimately comes down to proper preparation, part of which is also a skill in performing. I would use the same criteria with regard screening as you may normally do with EEG.

OxySoft is developed for use with Windows 7 or 10, both are supported however Windows 7 is still preferred. We also offer a free Android application for the PortaLite and PortaMon units for streaming and data logging.

This is really dependent on the signal quality. Typically for normal cortical penetration you will want anywhere from 3cm up, the larger the distance the deeper the penetration however at the sake of a reduced signal-to-noise ratio. Typically for normal adults we employ a 3.5cm interoptode distance, for those with darker skin or dark/dense hair you may need to reduce this to achieve an ideal SNR. For younger children and infants often times 2.5cm is more common.

Lasers often require greater consideration in application. There are certainly constraints with regard to motility with a laser based setup that may not be of any concern with LED. Preparation times are often greater with laser than LED, as lasers are often added to a headcap one by one, whereas LED sources could sometimes be “pre-populated”.

Lasers naturally provide a very focal output and are excellent with narrow band frequency emission, thus the ability to discretely “tune” the light output is perhaps of some value, as you might imagine when studying the dispersion of light. Additionally modulation of lasers can take place many times fast than that of LED, as there are some capacitive “left-overs” with LED

fNIRS is of course a completely different modality than fMRI, however while the mechanics may differ there is overlap in the resulting measurements, ultimately cerebral blood flow and metabolic measurements may be obtained, and neuronal activation often assumed. fNIRS is specific to oxygenated and deoxygenated hemoglobin measurement and quantification due to light back reflection, while fMRI aligns the orientation of the hemoglobin depending on the presence of oxygen. fNIRS offers a much better temporal resolution often 100x or more, while spatially fMRI has the upper hand by roughly 10x.

Very good, and important, question. Clearly fNIRS is employing frequencies of light that are purposely used to traverse the skull without much restraint, and this is in fact introducing exogenous stimuli. Well don’t fret, the amount of signal power using fNIRS can be comparable to sunlight. Further, of recent, several studies suggest there are various health benefits to infrared light stimulation at the cellular/metabolic level- even still these studies primarily employ chronic use.

This is a tough one, inherently hair is the nemesis of any fNIRS device on the market and while we all would like to say we have this completely figured out it ultimately comes down to proper preparation, part of which is also a skill in performing. I would use the same criteria with regard screening as you may normally do with EEG.

OxySoft is developed for use with Windows 7 or 10, both are supported however Windows 7 is still preferred. We also offer a free Android application for the PortaLite and PortaMon units for streaming and data logging.

Both PortaLite and PortaMon units use a bluetooth connection with a long range antenna up to 150 meters is possible. The Brite 23 system offers a range of 30 meters.

Yes, you may stream up to 7 devices, both wired (OxyMon), and wireless devices (Brite 23, PortaMon/PortaLite) to the same acquisition PC in real time.

This is really dependent on the signal quality. Typically for normal cortical penetration you will want anywhere from 3cm up, the larger the distance the deeper the penetration however at the sake of a reduced signal-to-noise ratio. Typically for normal adults we employ a 3.5cm interoptode distance, for those with darker skin or dark/dense hair you may need to reduce this to achieve an ideal SNR. For younger children and infants often times 2.5cm is more common.

Lasers often require greater consideration in application. There are certainly constraints with regard to motility with a laser based setup that may not be of any concern with LED. Preparation times are often greater with laser than LED, as lasers are often added to a headcap one by one, whereas LED sources could sometimes be “pre-populated”.

Lasers naturally provide a very focal output and are excellent with narrow band frequency emission, thus the ability to discretely “tune” the light output is perhaps of some value, as you might imagine when studying the dispersion of light. Additionally modulation of lasers can take place many times fast than that of LED, as there are some capacitive “left-overs” with LED

fNIRS is of course a completely different modality than fMRI, however while the mechanics may differ there is overlap in the resulting measurements, ultimately cerebral blood flow and metabolic measurements may be obtained, and neuronal activation often assumed. fNIRS is specific to oxygenated and deoxygenated hemoglobin measurement and quantification due to light back reflection, while fMRI aligns the orientation of the hemoglobin depending on the presence of oxygen. fNIRS offers a much better temporal resolution often 100x or more, while spatially fMRI has the upper hand by roughly 10x.

Very good, and important, question. Clearly fNIRS is employing frequencies of light that are purposely used to traverse the skull without much restraint, and this is in fact introducing exogenous stimuli. Well don’t fret, the amount of signal power using fNIRS can be comparable to sunlight. Further, of recent, several studies suggest there are various health benefits to infrared light stimulation at the cellular/metabolic level- even still these studies primarily employ chronic use.

This is a tough one, inherently hair is the nemesis of any fNIRS device on the market and while we all would like to say we have this completely figured out it ultimately comes down to proper preparation, part of which is also a skill in performing. I would use the same criteria with regard screening as you may normally do with EEG.

OxySoft is developed for use with Windows 7 or 10, both are supported however Windows 7 is still preferred. We also offer a free Android application for the PortaLite and PortaMon units for streaming and data logging.

Both PortaLite and PortaMon units use a bluetooth connection with a long range antenna up to 150 meters is possible. The Brite 23 system offers a range of 30 meters.

Yes, you may stream up to 7 devices, both wired (OxyMon), and wireless devices (Brite 23, PortaMon/PortaLite) to the same acquisition PC in real time.

Maybe.  There is no way the EEG system can harm the TMS system, but there are some TMS systems that are essentially useless with some EEG systems.  You need a a suitable combination of features in each to be successful at all in using TMS with EEG.

Desirable attributes:

• Coils designed specifically for use with EEG will have a cable that exits the coil tangential to the head surface so that the coil does not pass close by EEG electrodes and cables.
• A coil to be used with EEG should be passively cooled, since active cooling by means of a fan will induce electromagnetic interference in the EEG.
• The TMS recharge mechanism should be designed to avoid inducing electromagnetic artifacts in the EEG.
• The TMS system should be shielded so that no more than 3 milligauss of electromagnetic interference from the TMS system’s power supply reaches the electrodes and cables.
• The TMS system should be able to produce a TMS pulse in response to an input trigger with a low and predictable latency.  Long, but especially unpredictable latency in responding to an input trigger will result in TMS artifacts that are difficult to impossible to remove from the EEG.

Aside from attributes of the TMS system, there are also important considerations regarding the EEG system in this relationship. See the other FAQ entry on that topic.

No.  There are a few special attributes that are required and others that are desirable.

Required attributes:

• Inputs should be protected so that they are not damaged by the TMS pulse
• Frequency response on all channels should be from DC on the low end, since AC coupled inputs will “ring” when presented with a large voltage transient like the TMS artifact

Desirable attributes:

• Electrodes should have a low-profile so that the TMS coil can be placed as near the head as possible, maximizing penetration depth and current delivery
• It is important for the EEG system to be able to trigger the TMS system at precisely the same phase with respect to the EEG samples each time a stimulus is delivered.  This will improve the performance of artifact removal algorithms

Aside from these attributes of the EEG system, there are also important considerations regarding the TMS system in this relationship. See the other FAQ entry on that topic.

You may perform a wide variety of protocols using the PowerMAG system; ppTMS, rTMS, TBS, and even Quattro pulse. Please refer to the following chart to determine which platform is most appropriate for your research.

The coils used with the PowerMAG system are in fact passively cooled, they utilize quality copper windings with excellent heat dispersion properties. The coils are then placed within a wax like medium that further enhances heat dissipation, as the coil heats up the internal medium changes to a liquid state effectively “absorbing” much of the heat. This is often desired over coils that require additional components for cooling (e.g. fans, pumps, and plumbing), and are considered more robust from an engineering perspective. Additionally there is no maintenance required for our passively cooled coils, nor is there any pre-defined factory set limit to the life of the coil in terms of number of pulses, nor age.

This really comes down to the properties of the coil utilized. The two main style of stim coils used within the TMS field are figure 8 and round, with figure 8 often being preferred for focal targeting. Typically with the figure 8 coil you would get greatest stimulation at a depth of roughly 2- 2.5cm, with a round style you may achieve a bit more penetration ~2.5-3cm.

Excellent question! PowerMAG is strictly for research purposes, meaning there is no FDA approval on the device, thus it may not be used for the diagnosis or treatment of any pathology. Clinical research is still possible, however must follow the strict adherence to the current guidelines imposed. Chances are, if you have an IRB protocol, then you can use the PowerMAG system for your research.

For an FDA approved TMS solution for use in treatment protocols, you may find the Mag and More Apollo TMS Therapy System of interest.