Author(s): Zheng, L (Zheng, Li); Sun, S (Sun, Sen); Zhao, HZ (Zhao, Hongze); Pei, WH (Pei, Weihua); Chen, HD (Chen, Hongda); Gao, XR (Gao, Xiaorong); Zhang, LJ (Zhang, Lijian); Wang, YJ (Wang, Yijun)

Source: FRONTIERS IN NEUROSCIENCE Volume: 14 Article Number: 579469 DOI: 10.3389/fnins.2020.579469 Published: OCT 22 2020

Abstract: Brain-computer interfaces (BCIs) based on rapid serial visual presentation (RSVP) have been widely used to categorize target and non-target images. However, it is still a challenge to detect single-trial event related potentials (ERPs) from electroencephalography (EEG) signals. Besides, the variability of EEG signal over time may cause difficulties of calibration in long-term system use. Recently, collaborative BCIs have been proposed to improve the overall BCI performance by fusing brain activities acquired from multiple subjects. For both individual and collaborative BCIs, feature extraction and classification algorithms that can be transferred across sessions can significantly facilitate system calibration. Although open datasets are highly efficient for developing algorithms, currently there is still a lack of datasets for a collaborative RSVP-based BCI. This paper presents a cross-session EEG dataset of a collaborative RSVP-based BCI system from 14 subjects, who were divided into seven groups. In collaborative BCI experiments, two subjects did the same target image detection tasks synchronously. All subjects participated in the same experiment twice with an average interval of similar to 23 days. The results in data evaluation indicate that adequate signal processing algorithms can greatly enhance the cross-session BCI performance in both individual and collaborative conditions. Besides, compared with individual BCIs, the collaborative methods that fuse information from multiple subjects obtain significantly improved BCI performance. This dataset can be used for developing more efficient algorithms to enhance performance and practicality of a collaborative RSVP-based BCI system.

Accession Number: WOS:000585411400001

PubMed ID: 33192265

eISSN: 1662-453X

Full Text: https://www.frontiersin.org/articles/10.3389/fnins.2020.579469/full