Multiunit recording Neighbouring Cells Spike Sorting Tetrodes [picture of tetrode] Algorithm What is Spike Sorting? When an extracellular microelectrode is introduced into grey matter it couples to a number of cell bodies and other action potential-carrying membranes in the tissue. The conventional procedure for recording spikes extracellularly is to maneuver the electrode tip until the a single membrane dominates the signal and thus record spikes from this single source, a procedure commonly called "isolation". More recently, interest in the possibility of identifying distinct spike events on multiple membranes without isolation has risen. The idea is that the current paths between the electrode and each spiking membrane will be slightly different. This, coupled with differences in the intrinsic time course of the spike on different membranse, means that waveforms from the different sources will be slightly different. The notion is that this variation in waveform can be exploited to distinguish between the different sources. This is quite difficult with a single electrode (although it has been tried). The tetrode is an attempt to make this problem easier by recording currents from four tips distributed in a small volume of the tissue. Each tip couples to roughly the same group of membranes, so the extra tips are not being used to increase the recording volume (as is the case with many multi-electrodes), but rather to exploit stereo effects to resolve different spikes in one region. The statistical problem of spike-sorting is quite similar using a single electrode or a tetrode, although it is arguably only really tractable in the latter case. How do we approach the problem? Historically, spike sorting has been carried out by eye. Experimenters draw boundaries either around waveforms on an oscilloscope-like display, or around clusters of points on a computer-generated scatter-diagram of waveform features. We are developing a new, statistically well-founded technique for "automatic" spike sorting. The statistical solution to this problem is important for at least two reasons: first, it ensures that the separations achieved (and therefore results derived from them) are reproducable and that the success of the separation is quantifiable; second, it allows the recording technology to be scaled up so that more signals than could reasonably be separated by hand can be collected. Our approach is based in explicit probabilistic modeling. Where possible, we measure the distribution of waveforms