Search arXivSearch

arXiv · 2506.21554

Finding Similar Objects and Active Inference for Surprise in Numenta Neocortex Model

Abstract

Jeff Hawkins and his colleagues in Numenta have proposed the thousand-brains system. This is a model of the structure and operation of the neocortex and is under investigation as a new form of artificial intelligence. In their study, learning and inference algorithms running on the system are proposed, where the prediction is an important function. The author believes that one of the most important capabilities of the neocortex in addition to prediction is the ability to make association, that is, to find the relationships between objects. Similarity is an important example of such relationships. In our study, algorithms that run on the thousand-brains system to find similarities are proposed. Although the setting for these algorithms is restricted, the author believes that the case it covers is fundamental. Karl Friston and his colleagues have studied the free-energy principle that explains how the brain actively infers the cause of a Shannon surprise. In our study, an algorithm is proposed for the thousand-brains system to make this inference. The problem of inferring what is being observed from the sensory data is a type of inverse problem, and the inference algorithms of the thousand-brains system and free-energy principle solve this problem in a Bayesian manner. Our inference algorithms can also be interpreted as Bayesian or non-Bayesian updating processes.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Hajime Kawakami. 2025-06-11. Finding Similar Objects and Active Inference for Surprise in Numenta Neocortex Model. https://arxiv.org/abs/2506.21554

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

KEEP EXPLORING

Related papers

Only what exists can cause: An intrinsic powers view of free will

This essay addresses the implications of integrated information theory (IIT) for free will. IIT is a theory of what consciousness is and of how its presence and quality can be accounted for in physical terms. According to IIT, the presence of consciousness is accounted for by a maximum of cause-effect power in the brain. Moreover, the way an experience feels is accounted for by how that cause-effect power is structured. If IIT is right, we do have free will in a genuine sense: we have alternatives, reasons, and values, we make decisions, and we-not our neurons or atoms-are the cause of our willed actions and bear responsibility for them. IIT's argument for genuine free will hinges on the proper understanding of consciousness as intrinsic existence, captured by its intrinsic powers ontology: what exists absolutely, in physical terms, are intrinsic entities, and only what exists can cause.

q-bio.NC

Seeing the imagined: latent functional alignment in visual imagery decoding from fMRI data

Recent progress in visual brain decoding from fMRI has been enabled by large-scale datasets such as the Natural Scenes Dataset (NSD) and powerful diffusion-based generative models. While current pipelines are primarily optimized for perception, their performance under mental-imagery remains less well understood. In this work, we study how a state-of-the-art (SOTA) perception decoder (DynaDiff) can be adapted to reconstruct imagined content from the NSD-Imagery benchmark. We propose a latent functional alignment (LFA) approach that maps imagery-evoked activity to the pretrained model's semantic content-enriched conditioning space, by adding a simple alignment module, while keeping the original remaining components frozen. To mitigate the limited amount of matched imagery-perception supervision, we further introduce a neural retrieval-based augmentation strategy that selects semantically related NSD perception trials from the same participants. Across four subjects, LFA consistently improves high-level semantic reconstruction metrics relative to the frozen pretrained baseline and a voxel-space ridge alignment baseline, and enables above-chance decoding from multiple cortical regions. These results suggest that semantic structure learned from perception can be leveraged to stabilize and improve visual imagery decoding under out-of-distribution conditions.

q-bio.NC

Deep Learning in Infant Functional Neuroimaging: Challenges, Advances, and Future Directions

Infancy is a critical developmental window characterized by rapid functional brain reorganization, during which large-scale networks emerge, individualized connectome signatures continue to form, and early deviations may shape long-term cognitive and clinical outcomes. Functional MRI (fMRI) offers an opportunity to study these processes in vivo, yet extracting developmentally meaningful information from it remains challenging due to comparatively short scan duration, structured motion artifacts, variable scan states, and rapid brain maturation. Amid these challenges, deep learning has expanded the capacity of computational neuroimaging by learning robust representations from noisy, high-dimensional data, integrating complex spatial and temporal information, and capturing the nonlinear and rapidly evolving organization of the developing brain. Here, we review recent advances in deep learning for infant functional neuroimaging, synthesizing progress across input representation formatting, population and individualized brain mapping, longitudinal trajectory forecasting, robust and explainable model evaluation, and biological translation. Collectively, these methodological advances mark a paradigm shift in infant functional neuroimaging from descriptive, group-level analyses toward reliable, individualized, and developmentally grounded models. Future progress will depend on larger and more diverse longitudinal datasets, developmentally appropriate model designs, rigorous and standardized evaluation, and integration of computational predictions with biological mechanisms towards clinically meaningful outcomes. Addressing these priorities will help establish deep learning as a robust framework for understanding early functional brain development, identifying developmental variation at the individual level, and ultimately supporting earlier and precise assessment of neurodevelopmental risk.

q-bio.NC