Biosemi cursor task and laplacian questions
Posted: 26 Jul 2011, 19:26
I'm using a biosemi 128 electrode eeg, and I have two questions about implementation (one specific to biosemi, one a general signal processing question. When I run experiments, the online signal display usually only displays signal for around 4 channels, even though im collecting 128 channels worth of data. Im assuming this is because I set offset=0, though im not sure. If this is the case, I dont think its that important as far as analysis goes, but it would ease my peace of mind if I could actually see the channels as theyre being recorded, or at the very least know this is the reason theyre not showing up. Is there any easy way to quickly collect and export offsets for 128 channels from labview to biosemi.
Also since Im using a relatively high density array, if I see relevant activity in neighboring electrodes should I give them both positive coefficients in the classifier matrix (say .5 and .5) and then subtract away the six or so neighboring electrodes? And do the row names need to match channel names (eg A1 A2 A3 A4 A5 A6 etc, or will simple numbering (1 2 3 4 5 6 7...) be sufficient?
Also since Im using a relatively high density array, if I see relevant activity in neighboring electrodes should I give them both positive coefficients in the classifier matrix (say .5 and .5) and then subtract away the six or so neighboring electrodes? And do the row names need to match channel names (eg A1 A2 A3 A4 A5 A6 etc, or will simple numbering (1 2 3 4 5 6 7...) be sufficient?