bioRxiv Science⌕ Search

bioRxiv · 10.1101/2024.05.01.592004

Task-Relevant Stimulus Design Improves P300-Based Brain-Computer Interfaces

Abstract

ObjectiveIn the pursuit of refining P300-based brain-computer interfaces (BCIs), our research aims to propose a novel stimulus design focused on selective attention and task relevance to address the challenges of P300-based BCIs, including the necessity of repetitive stimulus presentations, accuracy improvement, user variability, and calibration demands. ApproachIn the oddball task for P300-based BCIs, we develop a stimulus design involving task-relevant dynamic stimuli implemented as finger-tapping to enhance the elicitation and consistency of event-related potentials (ERPs). We further improve the performance of P300-based BCIs by optimizing ERP feature extraction and classification in offline analyses. Main ResultsWith the proposed stimulus design, online P300-based BCIs in 37 healthy participants achieves the accuracy of 91.2% and the information transfer rate (ITR) of 28.37 bits/min with two stimulus repetitions. With optimized computational modeling in BCIs, our offline analyses reveal the possibility of single-trial execution, showcasing the accuracy of 91.7% and the ITR of 59.92 bits/min. Furthermore, our exploration into the feasibility of across-subject zero-calibration BCIs through offline analyses, where a BCI built on a dataset of 36 participants is directly applied to a left-out participant with no calibration, yields the accuracy of 94.23% and the ITR of 31.56 bits/min with two stimulus repetitions and the accuracy of 87.75% and the ITR of 52.61 bits/min with single-trial execution. When using the finger-tapping stimulus, the variability in performance among participants is the lowest, and a greater increase in performance is observed especially for those showing lower performance using the conventional color-changing stimulus. SignficanceUsing a novel task-relevant dynamic stimulus design, this study achieves one of the highest levels of P300-based BCI performance to date. This underscores the importance of coupling stimulus paradigms with computational methods for improving P300-based BCIs.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Kim, J., Kim, S.-P., Cho, Y. S.. 2024-05-04. Task-Relevant Stimulus Design Improves P300-Based Brain-Computer Interfaces. https://doi.org/10.1101/2024.05.01.592004

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Single-Component Photo-Crosslinked Lipoic Acid Functionalized Mucin Hydrogels: Dynamic Mucus Mimetics for Antiviral Protection

Native mucus protects epithelial surfaces through viscoelastic networks of disulfide-linked mucins. However, commercially available mucins often fail to reconstitute comparable mechanical and barrier properties, while synthetic and hybrid mucus mimetics require polymeric crosslinkers that may alter mucus-like composition. Inspired by the native architecture, we directly functionalized porcine gastric and bovine submaxillary mucins with -lipoic acid to develop a single-component, photo-crosslinkable hydrogels. Upon UV irradiation (365 nm), the modified mucins rapidly form disulfide-crosslinked networks without added photo-initiator/ polymeric crosslinkers, two orders of magnitude faster as compared with PEG-SH approaches. The resulting mucin-lipoic acid (MUC-LA) hydrogels exhibit mucus-relevant properties, including tunable viscoelasticity, redox responsiveness, self-healing, and size-dependent restrictions on nanoparticle transport. In transwell-based infection models, MUC-LA hydrogels (2-3%) mimicking the healthy airway mucus (G' {approx} 10-20 Pa) suppress epithelial infection by SARS-CoV-2 and influenza A virus. Crosslinked MUC-LA provides greater protection against SARS-CoV-2 than the non-crosslinked, whereas both formulations suppress influenza A infection, suggesting distinct contributions from network formation and mucin-associated interactions. These findings establish a dynamic, mucus-mimetic platform integrating rapid photo-gelation, controllable mechanics, selective transport, and antiviral barrier functionality. MUC-LA hydrogels offer opportunities to investigate mucosal transport and host-pathogen interactions, with potential applications in drug delivery, and as biomaterials.

bioengineering↗

A Fibrous Optofluidic Probe for Endovascular Sensing of Blood Oxygenation and Flow Velocity

Local hemodynamic information including blood oxygenation and flow velocity could guide vascular interventions, yet obtaining these parameters in deep, narrow vessels remains challenging. Here, we report a flexible, submillimeter-scale fibrous optofluidic probe for endovascular sensing of blood oxygenation and flow velocity. The probe integrates a polymer optical fiber for light transmission with a microfluidic tube for dye injection, enabling spectroscopic oximetry and fluorescence dilution-based velocimetry through a single device. Via vascular intervention, we demonstrate local hemodynamic sensing in rabbit arteries and angiography-guided deployment in canine carotid arteries. The probe captures local changes in blood oxygenation and flow velocity during vascular occlusion and reperfusion, revealing hemodynamic disturbances that are not reflected in peripheral monitors. These results illustrate the complementary information provided by local oximetry and velocimetry and establish a compact optofluidic platform for quantitative hemodynamic monitoring during vascular interventions.

bioengineering↗

Broad-spectrum in situ genetic reprogramming of native microbiomes

Complex microbial communities are found throughout terrestrial, aquatic, and animal-associated ecosystems. Genetic modification of discrete microbial taxa within native communities represents a powerful tool to study and augment microbiome functions. Herein, we develop Synthetic Phage Assisted Reprogrammable and Targetable Addition (SPARTA) as a one-step strategy for packaging, delivering, and integrating large synthetic DNA into a broad range of native microbiomes. SPARTA leverages a broad-spectrum synthetic phage particle for in situ genome engineering within complex soil, freshwater, and mammalian fecal microbiomes, reprogramming 59 native species across 16 families. By modulating SPARTA components, we further demonstrated tunability of SPARTA towards targeted microbiome population. Additionally, we built a novel companion tool to quantitatively identify engineered taxa, named 16S crRNA-guided inference of bacterial engineering sequencing or ScRibe-seq. The SPARTA-ScRibe-seq pipeline delivered and validated functional synthetic gene clusters in diverse native microbiomes while preserving the original microbial community structure. Together, this novel genome engineering framework constitutes an end-to-end programmable platform for rational and customizable reprogramming of native microbiomes.

bioengineering↗