探针最小化仍然保持对目标刺激分类的高精度P300

Weilun Wang, G. Chakraborty
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引用次数: 1

摘要

本文提出了一种利用P300 BCI拼写器产生的目标试验信号和非目标跟踪信号的差异来检测P300信号的新方法。传统的P300 BCI拼写器在头皮上预先定义的位置使用8个探针。它适用于任何人,并能提供合理的性能。在P300 BCI拼写中,系统需要解码事件相关电位(ERP),称为P300。虽然它在大脑的顶叶区域很强,但最强信号的位置因人而异。如果我们能根据个人情况调整探针的位置,我们就能消除不必要的探针。首先,我们想要消除那些不能对目标刺激产生类似信号的探针。我们计算了每个探头不同实验之间的信号距离。不同实验中产生的信号差异较大的探针不适合分类。然后,我们从剩余的探针中搜索将产生强P300信号的探针。在这项工作中,我们重点研究了目标跟踪信号和非目标跟踪信号的区别。P300信号的特点是其幅值与事件概率有很强的负相关关系。在P300 BCI拼写中,目标轨迹的概率为1/6,非目标轨迹的概率为5/6。不频繁靶迹P300信号的幅度大于非靶迹P300信号的幅度。我们设计了一种计算P300信号幅值的算法,选择目标试验P300信号幅值与非目标试验信号幅值相差较大的探头。我们仅从一对目标刺激信号和非目标刺激信号中提取3个探针,平均分类准确率达到81%以上。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Probes minimization still maintaining high accuracy to classify target stimuli P300
We present a novel approach to detect P300 Signal by using the difference between target trial signal and nontarget trail signal generated by P300 BCI Speller. Conventional P300 BCI Speller uses 8 probes at pre-defined locations on the scalp. It works for any person and could deliver a reasonable performance. In P300 BCI speller, system needs to decipher the event related potential (ERP), called P300. Though it is strong in the parietal region of the brain, location of the strongest signal varies from person to person. If we can adapt the location of probes for an individual, we could eliminate un-necessary probes. At first, we want to eliminate probes that did not generate similar signal for target stimuli. We calculated signal distance between different experiments for every probe. The probes that generated quite different signal in different experiments are unsuitable for classification. Then, we search for the probes that will generate strong P300 signal from the remaining probes. In this work, we concentrated on the difference between target trail signal and non-target trail signal. P300 signal's distinctive property is that its amplitude has a strong negative correlation with the event probability. In P300 BCI Speller, the target trail's probability is 1/6 and the non-target trail's probability is 5/6. Infrequent target trail P300 signal's amplitude is larger than the nontarget trial signal's amplitude. We designed an algorithm to calculate the P300 signal's amplitude and selected the probes with larger difference between target trial P300 signal's amplitude and non-target trail signal's amplitude. We achieved over 81% classification accuracy on average with 3 probes from only one pair of target stimuli signal and non-target stimuli signal.
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