Search bioRxiv⌕ Search

bioRxiv · 10.64898/2026.09.08.750188

Time-resolved decoding of uncertainty about stimulus features from human EEG

Abstract

Internal and external noise produce uncertainty in the neural representations of sensory stimuli. Uncertainty about basic stimulus features can be decoded from responses in sensory brain regions by estimating full probability distributions over stimulus features, rather than point estimates. Such decoded uncertainty correlates with subjective uncertainty reports, providing insight into the neural basis of metacognitive judgments. However, in humans, probabilistic decoding has only been applied to functional magnetic resonance imaging (fMRI) data, which has low temporal resolution and thus can give only limited insight into the dynamics of uncertainty in the brain. Here, we assessed whether probabilistic decoding of uncertainty about stimulus features could be extended to electroencephalography (EEG) data, which has higher temporal resolution but lower spatial resolution and different noise properties compared to fMRI. Participants performed a spatial location estimation task and provided subjective uncertainty reports. We found that time-resolved probabilistic decoding in EEG was feasible, as decoders produced accurate predictions of stimulus location following stimulus onset, and decoding error correlated trial-by-trial with decoded uncertainty. The choice of noise covariance structure critically impacted these metrics. Further, decoded uncertainty was a more reliable trial-by-trial indicator of stimulus information than decoding error, illustrating the advantages of probabilistic decoding over standard decoding approaches. However, uncertainty decoded from EEG had no significant trial-by-trial correlation with subjective uncertainty at any time point. Based on these results, uncertainty decoded from EEG provides a time-resolved estimate of stimulus information available from the brain signal on a single trial but may not relate to metacognitive reports.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Nestor, J., Tian, K. J., Chapman, A. F., Denison, R. N.. 2026-09-14. Time-resolved decoding of uncertainty about stimulus features from human EEG. https://doi.org/10.64898/2026.09.08.750188

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

KEEP EXPLORING

Related preprints

A Mechanistic Account of Dedifferentiation in the Aging Visual System

To uncover the mechanisms of age-related dedifferentiation, we simulated neural degradation in a computational model of the ventral visual stream. Severing connections or adding noise, whether in inferotemporal cortex (IT) or upstream, reduced IT differentiation, indicating that dedifferentiation need not originate locally. Degrading peripheral V1, which preferentially drove place-selective IT neurons, selectively reduced place differentiation, a candidate mechanism for the stronger place dedifferentiation reported in aging.

neuroscience↗

Reusing pipettes in Patch-seq: a foundation for automated multimodal profiling

Patch-seq is a technique for single-cell multimodal characterization. It combines whole-cell electrophysiology, single-cell transcriptomics, and morphological reconstruction in single neurons. Patch-seq morphologies are a critical bridge among cell types, genes, physiology, and large-scale connectivity platforms such as EM connectomes and single-cell-resolution projectomes. However, patch-seq experimental complexity and operator dependence limit throughput. Automation could enable scalable Patch-seq but requires procedural adaptations, including detergent-based pipette cleaning, robotic nucleus extraction and collection. The impact of these automations on Patch-seq quality has not been systematically evaluated. Here, we show that each of these modifications preserves or improves key Patch-seq outcomes. Automated nucleus extraction performs comparably to, or better than, expert manual operation, preserving key RNA and morphological metrics. Detergent-cleaned, reused pipettes supported a viable sealing success rate across multiple cleaning cycles and preserved electrophysiological quality and transcriptomic yield without introducing excess contamination. Sonication effectively allows collection of nuclear material without damaging RNA and supports subsequent pipette cleaning and reuse. Enhanced automated sealing and break-in procedures increased throughput regardless of brain region, cell type or species. Together, these results validate the core procedural adaptations required for automated Patch-seq and establish a foundation for high-throughput, standardized multimodal single-cell characterization.

neuroscience↗

Development of direction selectivity in the Xenopus tadpole optic tectum and midbrain tegmentum

Detecting motion direction is a fundamental function performed by direction selective (DS) neurons. DS neurons in the optic tectum (superior colliculus in mammals) enable the tracking of moving objects. DS neurons of the accessory optic system support reflexive eye / head movements that stabilize gaze during self-motion. By developmental stage 48 (10 days postfertilization), Xenopus tadpoles display visually guided behaviors that require both types of DS neurons. Our previous work has shown that these two regions are not only functionally distinct but also follow different developmental programs. Here we characterized and compared how direction selectivity develops in both visual processing centers. Using in vivo electrophysiological recordings during moving bar visual stimulation, we measured DS synaptic inputs and spiking outputs in both regions across three key developmental stages of the retinotectal projection. Tegmental neurons were direction selective ab initio, and both input and output tuning remained stable across development. Tectal neurons were observed to receive DS inputs early, and their input selectivity also remained stable across development. However, their spiking output grew substantially more DS at the later developmental stage. This was due at least in part to a naturally occurring decrease in intrinsic excitability which preferentially dampened overall spike rates, but especially in response to the non-preferred direction of motion, thereby increasing direction selectivity. These results reveal distinct developmental trajectories in parallel visual pathways. Tegmental direction selectivity is established early and stays stable, whereas tectal output tuning sharpens during development through a decrease in intrinsic excitability.

neuroscience↗