bioRxiv Science⌕ Search

Biology subjects

Kanai, R.

Publications and source records attributed to Kanai, R..

7 recordsLinked to original sources

Multi-modal Ensemble Approach for Decoding Player Intentions in Table Tennis

This study aims to predict human intentions during intense sports activities, specifically in table tennis. Using a publicly available Real World Table Tennis dataset containing simultaneous EEG and video recordings, we developed a series of subject-specific classifiers for nine players (7 males and 2 females; age range 18-30), based on pose features and EEG signals. The pose-based classifier used a stochastic gradient descent model with logistic loss, whereas the EEG-based classifier employed a modified convolutional neural network architecture (EEGNet). Both classifiers successfully predicted left-right attack intentions from the time windows preceding racket-ball impact, with optimal decoding occurring at -100 ms for pose features and -500 ms for EEG signals. Although EEG-based decoding achieved comparable performance to pose-based decoding, a multi-modal ensemble further improved prediction significantly, reaching a mean macro F1 score of 0.563 (bootstrapped 95% CI: 0.523-0.603), corresponding to gains of +0.03 over pose-only and +0.02 over EEG-only classifiers. Because each classifier is trained independently, the ensemble can be feasibly extended to incorporate additional modalities in the future. These results suggest potential relevance of this framework as neurofeedback tools for sports training and neural prosthetic systems in future work.

neuroscience↗

Optical Neuroimage Studio (OptiNiSt): intuitive, scalable, extendable framework for optical neuroimage data analysis

Advancements in calcium indicators and optical techniques have made optical neural recording a common tool in neuroscience. As the volume of optical neural recording data grows, streamlining the data analysis pipelines for image preprocessing, signal extraction, and subsequent neural activity analyses becomes essential. There are a number of challenges in optical neural data analysis. 1) The quality of original and processed data needs to be carefully examined at each step. 2) As there are numerous image preprocessing, cell extraction, and activity analysis algorithms, each with pros and cons, experimenters need to implement or install them to compare and select optimal methods and parameters for each step of processing. 3) To ensure the reproducibility of the research, each analysis step needs to be recorded in a systematic way. 4) For data sharing and meta-analyses, adoption of standard data formats and processing protocols is required. To address these challenges, we developed Optical Neuroimage Studio (OptiNiSt) (https://github.com/oist/optinist), a framework for intuitively creating calcium data analysis pipelines that are scalable, extendable, and reproducible. OptiNiSt includes the following features. 1) Researchers can easily create analysis pipelines by selecting multiple processing modules, tuning their parameters, and visualizing the results at each step through a graphic user interface in a web browser. 2) In addition to common analytical tools that are pre-installed, new analysis algorithms in Python can be easily added. 3) Once a processing pipeline is designed, the entire workflow with its modules and parameters are stored in a YAML file, which makes the pipeline reproducible and deployable on high-performance computing clusters. 4) OptiNiSt can read image data in a variety of file formats and store the analysis results in NWB (Neurodata Without Borders), a standard data format for data sharing. We expect that this framework will be helpful in standardizing optical neural data analysis protocols.

neuroscience↗

A Deep Learning Approach to Detecting Temporal Characteristics of Cortical Regions

One view of the neocortical architecture is that every region functions based on a universal computational principle. Contrary to this, we postulated that each cortical region has its own specific algorithm and functional properties. This idea led us to hypothesize that unique temporal patterns should be associated with each region, with the functional commonalities and variances among regions reflecting in the temporal structure of their neural signals. To investigate these hypotheses, we employed deep learning to predict electrodes locations in the macaque brain using single-channel ECoG signals. To do this, we first divided the brain into seven regions based on anatomical landmarks, and trained a deep learning model to predict the electrode location from the ECoG signals. Remarkably, the model achieved an average accuracy of 33.6%, significantly above the chance level of 14.3%. All seven regions exhibited above-chance prediction accuracy. The models feature vectors identified two main clusters: one including higher visual areas and temporal cortex, and another encompassing the remaining other regions.These results bolster the argument for unique regional dynamics within the cortex, highlighting the diverse functional specializations present across cortical areas.

neuroscience↗

An intramolecular scrambling path controlled by a gatekeeper in Xkr8 phospholipid scramblase

Xkr8-Basigin is a phospholipid scramblase at plasma membranes that is activated by kinase or caspase. We investigated its structure at a resolution of 3.8[A]. Its membrane-spanning region had a cuboid-like structure stabilized by salt bridges between hydrophilic residues in helices in the lipid layer. The molecule carried phosphatidylcholine in a cleft on the surface that may function as an entry site for phospholipids. Five charged residues placed from top to bottom inside the molecule were essential for providing a path for scrambling phospholipids. A tryptophan residue was present at the extracellular end of the pathway and its mutation made the Xkr8-Basigin complex constitutively active, indicating its function as a gatekeeper. The structure of Xkr8-Basigin provides novel insights into the molecular mechanisms underlying phospholipid scrambling.

biochemistry↗

Topographic Connectivity in a Duration Selective Cortico-Cerebellar Network

How does the human brain represent millisecond unit of time? A recent neuroimaging study revealed the existence in the human premotor cortex of a topographic representation of time i.e., neuronal units selectively responsive to specific durations and topographically organized on the cortical surface. By using high resolution functional Magnetic Resonance Images here, we go futher this previous work, showing duration preferences across a wide network of cortical and subcortical brain areas: from cerebellum to primary visual, parietal, premotor and prefrontal cortices. Most importantly, we identify the functional connectivity structure between these different brain areas and their duration selective neural units. The results highlight the role of the cerebellum as the network hub and that of medial premotor cortex as the final stage of duration recognition. Interstingly, when a specific duration is presented, only the communication between the units selective to that duration become particularly "active". These findings identify duration tuning and topographic connectivity as possible mechanisms underlying our capacity of telling time.

neuroscience↗

Efficient search for informational cores in complex systems: Application to brain networks

To understand the nature of the complex behavior of the brain, one important step is to identify "cores" in the brain network, where neurons or brain areas strongly interact with each other. Cores can be considered as essential sub-networks for brain functions. In the last few decades, an information-theoretic approach to identifying cores has been developed. In this approach, many-to-many nonlinear interactions between parts are measured by an information loss function, which quantifies how much information would be lost if interactions between parts were removed. Then, a core called a "complex" is defined as a subsystem wherein the amount of information loss is locally maximal. Although identifying complexes can be a novel and useful approach to revealing essential properties of the brain network, its practical application is hindered by the fact that computation time grows exponentially with system size. Here we propose a fast and exact algorithm for finding complexes, called Hierarchical Partitioning for Complex search (HPC). HPC finds complexes by hierarchically partitioning systems to narrow down candidates for complexes. The computation time of HPC is polynomial, which is dramatically smaller than exponential. We prove that HPC is exact when an information loss function satisfies a mathematical property, monotonicity. We show that mutual information is one such information loss function. We also show that a broad class of submodular functions can be considered as such information loss functions, indicating the expandability of our framework to the class. In simulations, we show that HPC can find complexes in large systems (up to several hundred) in a practical amount of time when mutual information is used as an information loss function. Finally, we demonstrate the use of HPC in electrocorticogram recordings from monkeys. HPC revealed temporally stable and characteristic complexes, indicating that it can be reliably utilized to characterize brain networks. Author summaryAn important step in understanding the nature of the brain is to identify "cores" in the brain network, which can be considered as essential areas for brain functions and cognition. In the last few decades, a novel definition of cores has been developed, which takes account of many-to-many interactions among elements of the network. Although considering many-to-many interactions can be important in understanding the complex brain network, identifying cores in large systems has been impossible because of the extremely large computational costs required. Here, we propose a fast and exact algorithm for finding cores. We show that the proposed algorithm enables us to find cores in large systems consisting of several hundred elements in a practical amount of time. We applied our algorithm to electrocorticogram recordings from a monkey that monitored electrical activity of the brain with electrodes placed directly on the brain surface, and demonstrated that there are stable and characteristic core structures in the brain network. This result indicates that our algorithm can be reliably applied to uncovering the essential network structures of the brain.

neuroscience↗

Chronotopic Maps in Human Medial Premotor Cortex

Time is a fundamental dimension of everyday experiences. We can unmistakably sense its passage and adjust our behavior accordingly. Despite its ubiquity, the neuronal mechanisms underlying the capacity to perceive time remains unclear. Here, in two experiments using ultra-high-field 7-Tesla functional magnetic resonance imaging, we show that in the medial premotor cortex of the human brain, neural units tuned to different durations are orderly mapped in contiguous portions of the cortical surface, so as to form chronomaps. The response of each portion in a chronomap is enhanced by preferred and neighboring durations and suppressed by non-preferred durations represented in distant portions of the map. These findings identify duration-sensitive tuning as a neural mechanism underlying the recognition of time and demonstrate for the first time that the representation of an abstract feature such as time can be instantiated by a topographical arrangement of duration-sensitive neural populations.

neuroscience↗