02228nas a2200289 4500008004100000022001400041245012100055210006900176260001200245300001100257490000900268520131200277653001501589653001401604653003301618653002701651653001301678653002901691653001701720653003101737653003201768653002801800100002001828700002301848700001901871856004801890 2008 eng d a1557-170X00aElectrocorticographic interictal spike removal via denoising source separation for improved neuroprosthesis control.0 aElectrocorticographic interictal spike removal via denoising sou c08/2008 a5224-70 v20083 a

Electrocorticographic (ECoG) neuroprosthesis is a promising area of research that could provide channels of communication and control for patients who have lost their motor functions due to damage to the nervous system. However, implantation of subdural electrodes are clinically restricted to diagnostics of pre-surgical epileptic patients. Hence, interictal activity is present in the recordings across various areas of the sensorimotor cortex and suppresses the amplitude modulated features extracted to model hand trajectories. Denoising source separation is a recently introduced framework which extracts hidden structures of interest within the data through denoising the source estimates with filters designed around prior knowledge on the observations. Herein, we exploit the high amplitude quasiperiodic nature of the observed interictal spikes and show that removal of the interictal activity improves linear prediction of hand trajectories.

10aAlgorithms10aArtifacts10aDiagnosis, Computer-Assisted10aElectroencephalography10aEpilepsy10aEvoked Potentials, Motor10aMotor Cortex10aReproducibility of Results10aSensitivity and Specificity10aUser-Computer Interface1 aGunduz, Aysegul1 aSanchez, Justin, C1 aPrincipe, Jose uhttp://www.ncbi.nlm.nih.gov/pubmed/1916389505892nas a2200361 4500008004100000022001400041245010100055210006900156260001200225300001000237490000800247520480000255653001505055653002805070653001805098653002005116653002705136653002405163653001105187653000905198653001105207653003105218653003205249653002805281653004105309653002205350653002805372100002305400700002005423700002005443700001905463856004805482 2008 eng d a0165-027000aExtraction and localization of mesoscopic motor control signals for human ECoG neuroprosthetics.0 aExtraction and localization of mesoscopic motor control signals  c01/2008 a63-810 v1673 a

Electrocorticogram (ECoG) recordings for neuroprosthetics provide a mesoscopic level of abstraction of brain function between microwire single neuron recordings and the electroencephalogram (EEG). Single-trial ECoG neural interfaces require appropriate feature extraction and signal processing methods to identify and model in real-time signatures of motor events in spontaneous brain activity. Here, we develop the clinical experimental paradigm and analysis tools to record broadband (1Hz to 6kHz) ECoG from patients participating in a reaching and pointing task. Motivated by the significant role of amplitude modulated rate coding in extracellular spike based brain-machine interfaces (BMIs), we develop methods to quantify spatio-temporal intermittent increased ECoG voltages to determine if they provide viable control inputs for ECoG neural interfaces. This study seeks to explore preprocessing modalities that emphasize amplitude modulation across frequencies and channels in the ECoG above the level of noisy background fluctuations in order to derive the commands for complex, continuous control tasks. Preliminary experiments show that it is possible to derive online predictive models and spatially localize the generation of commands in the cortex for motor tasks using amplitude modulated ECoG.

10aAdolescent10aBiofeedback, Psychology10aBrain Mapping10aCerebral Cortex10aElectroencephalography10aEpilepsies, Partial10aFemale10aHand10aHumans10aMagnetic Resonance Imaging10aPhysical Therapy Modalities10aPsychomotor Performance10aSignal Processing, Computer-Assisted10aSpectrum Analysis10aUser-Computer Interface1 aSanchez, Justin, C1 aGunduz, Aysegul1 aCarney, Paul, R1 aPrincipe, Jose uhttp://www.ncbi.nlm.nih.gov/pubmed/17582507