Abstract

Recently developed CMOS-based microprobes contain hundreds of electrodes on a single shaft with interelectrode distances as small as 30 µm. So far, neuroscientists manually select a subset of those electrodes depending on their appraisal of the "usefulness" of the recorded signals, which makes the process subjective but more importantly too time consuming to be useable in practice. The ever-increasing number of recording electrodes on microelectrode probes calls for an automated selection of electrodes containing "good quality signals" or "signals of interest." This article reviews the different criteria for electrode selection as well as the basic signal processing steps to prepare the data to compute those criteria. We discuss three of them. The first two select the electrodes based on "signal quality." The first criterion computes the penalized signal-to-noise ratio (SNR); the second criterion models the neuroscientist's appraisal of signal quality. Last, our most recent work allows the selection of electrodes that capture particular anatomical cell types. The discussed algorithms perform what is called in the literature "electronic depth control" in contrast to the mechanical repositioning of the electrode shafts in search of "good quality signals" or "signals of interest."

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