03145nas a2200373 4500008004100000022001400041245005700055210005400112260001200166300001000178490000700188520212100195653001002316653001502326653001802341653002102359653003302380653002702413653001302440653002202453653001102475653001102486653000902497653003502506653003102541653003202572100001902604700001902623700001902642700001702661700002402678700002102702856004802723 2008 eng d a1095-957200aReal-time detection of event-related brain activity.0 aRealtime detection of eventrelated brain activity c11/2008 a245-90 v433 a

The complexity and inter-individual variation of brain signals impedes real-time detection of events in raw signals. To convert these complex signals into results that can be readily understood, current approaches usually apply statistical methods to data from known conditions after all data have been collected. The capability to provide meaningful visualization of complex brain signals without the requirement to initially collect data from all conditions would provide a new tool, essentially a new imaging technique, that would open up new avenues for the study of brain function. Here we show that a new analysis approach, called SIGFRIED, can overcome this serious limitation of current methods. SIGFRIED can visualize brain signal changes without requiring prior data collection from all conditions. This capacity is particularly well suited to applications in which comprehensive prior data collection is impossible or impractical, such as intraoperative localization of cortical function or detection of epileptic seizures.

10aAdult10aAlgorithms10aBrain Mapping10aComputer Systems10aDiagnosis, Computer-Assisted10aElectroencephalography10aEpilepsy10aEvoked Potentials10aFemale10aHumans10aMale10aPattern Recognition, Automated10aReproducibility of Results10aSensitivity and Specificity1 aSchalk, Gerwin1 aLeuthardt, E C1 aBrunner, Peter1 aOjemann, J G1 aGerhardt, Lester, A1 aWolpaw, Jonathan uhttp://www.ncbi.nlm.nih.gov/pubmed/1871854402357nas a2200385 4500008004100000022001400041245009800055210006900153260001200222300001100234490000600245520131000251653001001561653001501571653000801586653001801594653002001612653002701632653002901659653001101688653001101699653000901710653001301719100001901732700001601751700002001767700002601787700001901813700001701832700001601849700001301865700002401878700002101902856004801923 2007 eng d a1741-256000aDecoding two-dimensional movement trajectories using electrocorticographic signals in humans.0 aDecoding twodimensional movement trajectories using electrocorti c09/2007 a264-750 v43 a

Signals from the brain could provide a non-muscular communication and control system, a brain-computer interface (BCI), for people who are severely paralyzed. A common BCI research strategy begins by decoding kinematic parameters from brain signals recorded during actual arm movement. It has been assumed that these parameters can be derived accurately only from signals recorded by intracortical microelectrodes, but the long-term stability of such electrodes is uncertain. The present study disproves this widespread assumption by showing in humans that kinematic parameters can also be decoded from signals recorded by subdural electrodes on the cortical surface (ECoG) with an accuracy comparable to that achieved in monkey studies using intracortical microelectrodes. A new ECoG feature labeled the local motor potential (LMP) provided the most information about movement. Furthermore, features displayed cosine tuning that has previously been described only for signals recorded within the brain. These results suggest that ECoG could be a more stable and less invasive alternative to intracortical electrodes for BCI systems, and could also prove useful in studies of motor function.

10aAdult10aAlgorithms10aArm10aBrain Mapping10aCerebral Cortex10aElectroencephalography10aEvoked Potentials, Motor10aFemale10aHumans10aMale10aMovement1 aSchalk, Gerwin1 aKubánek, J1 aMiller, John, W1 aAnderson, Nicholas, R1 aLeuthardt, E C1 aOjemann, J G1 aLimbrick, D1 aMoran, D1 aGerhardt, Lester, A1 aWolpaw, Jonathan uhttp://www.ncbi.nlm.nih.gov/pubmed/17873429