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Kesgin, K.

Publications and source records attributed to Kesgin, K..

2 recordsLinked to original sources

High-dimensional cortical signals reveal rich bimodal and working memory-like representations among S1 neuron populations

Complexity is important for flexibility of natural behavior and for the remarkably efficient learning of the brain. Here we assessed the signal complexity among neuron populations in somatosensory cortex (S1). To maximize our chances of capturing population level signal complexity, we used highly repeatable resolvable visual, tactile and visuo-tactile inputs and neuronal unit activity recorded at high temporal resolution. We found the state space of the spontaneous activity to be extremely high-dimensional in S1 populations. Their processing of tactile inputs was profoundly modulated by visual inputs and even fine nuances of visual input patterns were separated. Moreover, the dynamic activity states of the S1 neuron population signaled the preceding specific input long after the stimulation had terminated, i.e. resident information that could be a substrate for a working memory. Hence, the recorded high dimensional representations carried rich multimodal and internal working memory-like signals supporting high complexity in cortical circuitry operation.

neuroscience↗

Singular superlet transform achieves markedly improved time-frequency super-resolution for separating complex neural signals

Time-frequency decomposition is a well-established method to unmix signals generated by multiple sources with unique characteristics. However, there are cases of high signal complexity where existing time-frequency decomposition tools are insufficient for localizing and representing short-bursting signals. One example is the currently highly popular extracellular low-impedance recordings from multi-electrode arrays in the brain in vivo where each neuron repeatedly generates a specific signal fingerprint (characteristic spike waveform) that can be mixed with the signals of 100s of other sources, including the spikes of nearby neurons. Here we derive the singular superlet transform (SST) method, which enables highly localized representations of fast and short bursts compared to other super-resolution spectral estimators, while also requiring orders of magnitude fewer operations. We demonstrate a substantial edge of SST over current methods in isolating specific neuronal spikes with high-fidelity in challenging, complex recording signals from neocortex in vivo. We also exemplify SSTs generic signal processing capability by achieving outstanding resolution in the decomposition of complex acoustic data.

neuroscience↗