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96 results for “Reinforcement Learning”

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ClinicalTrials.gov32/100

Reinforcement Learning and Obsessive-compulsive Disorder: Exploring the Role of the Orbitofrontal Cortex

ClinicalTrials.gov study NCT06566781. IPD Sharing: NO. Countries: 1. Publications: 31.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov32/100

Reinforcement Learned Automatic Anesthesia System During Painless Gastrointestinal Endoscopy

ClinicalTrials.gov study NCT06857344. IPD Sharing: UNDECIDED. Countries: 1. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov32/100

Effects of Caffeine on Reinforcement Learning in Healthy Adults Using PET/MRI

ClinicalTrials.gov study NCT06763172. IPD Sharing: YES. Countries: 1. Publications: 6.

controlledIPD-YESFeb 2026View details →
ClinicalTrials.gov32/100

The Effects of Losartan on Reward Reinforcement Learning

ClinicalTrials.gov study NCT04604938. IPD Sharing: NO. Countries: 1. Publications: 1.

closedIPD-NOFeb 2026View details →
dryad32/100

Data and code from: Deep reinforcement learning for pressure optimization in water distribution networks with multiple pumping stations: Case study

Open the record for dataset details and reuse information.

publicOct 2025View details →
zenodo28/100

Adapting Virtual Embodiment through Reinforcement Learning

<p>Dataset for the paper&nbsp;Adapting Virtual Embodiment through Reinforcement Learning.</p>

opencc-by-4.0Nov 2020View details →
dryad28/100

Data from: Gaze-contingent reinforcement learning reveals incentive value of social signals in young children and adults

While numerous studies have demonstrated that infants and adults preferentially orient to social stimuli, it remains unclear as to what drives such preferential orienting. It has been suggested that the learned association between social cues and subsequent reward delivery might shape such social orienting. Using a novel, spontaneous indication of reinforcement learning (with the use of a gaze contingent reward-learning task), we investigated whether children and adults' orienting towards social and non-social visual cues can be elicited by the association between participants' visual attention and a rewarding outcome. Critically, we assessed whether the engaging nature of the social cues influences the process of reinforcement learning. Both children and adults learned to orient more often to the visual cues associated with reward delivery, demonstrating that cue–reward association reinforced visual orienting. More importantly, when the reward-predictive cue was social and engaging, both children and adults learned the cue–reward association faster and more efficiently than when the reward-predictive cue was social but non-engaging. These new findings indicate that social engaging cues have a positive incentive value. This could possibly be because they usually coincide with positive outcomes in real life, which could partly drive the development of social orienting.

opencc-zeroDec 2016View details →
zenodo28/100

Low-complexity Reinforcement Learning Decoders for Autonomous, Scalable, Neuromorphic intra-cortical Brain Machine Interfaces

<p><strong>General Description. </strong>TThis dataset comprises recordings from four BMI (Brain-Machine Interface) experiments conducted on two adult macaques. Three of the experiments involved joystick-controlled tasks, while the fourth was a center-out reaching task. In the center-out task, the macaque was trained to maneuver a joystick-controlled cursor from a central position on a computer screen to one of eight square-shaped target locations. The macaques were able to use a wireless integrated system to control a robotic platform (on which they were seated) enabling independent mobility driven by neuronal activity in their motor cortices. Neural activity was recorded from populations of single neurons via multiple electrode arrays implanted in the arm region of the primary motor cortex. A general overview is provided below:</p> <ol> <li>A titanium head post (Crist Instruments, MD, USA) was surgically affixed before implanting the microelectrode arrays. In NHP-A, four microelectrode arrays with 16 electrodes each were implanted, while NHP-B was implanted with one array containing 100 electrodes in the hand/arm region of the left primary motor cortex.</li> <li>Spike signals were recorded using an in-house 100-channel wireless neural recording system, sampled at 13 kHz. The wide-band signals were band-pass filtered between 300 and 3000 Hz to eliminate low-frequency components. Spike detection thresholds were determined using the formula: Thr = 5&sigma;, where &sigma; = median(|x| / 0.6745), <em>x</em> is the filtered signal, and <em>&sigma;</em> estimates the standard deviation of background noise.</li> </ol> <p>In Experiments 1, 2, and 3, the behavioral task involved controlling the motion of a robotic wheelchair using a three-directional, spring-loaded joystick. These tasks included:&nbsp;a) turning 90&deg; right,&nbsp;b) moving forward by 2 meters,&nbsp;c) turning 90&deg; left, and&nbsp;d) remaining stationary for 5 seconds (stop task).&nbsp;The success rate varied across experiments. Experiment 4 also involved joystick control, but followed a classical center-out reaching paradigm.&nbsp;</p> <p><strong>Dataset Description. </strong>The dataset is organized into folders (labeled as experiment 1, 2, 3, and 4) containing data from both NHP-A and NHP-B. Each folder contains data from separate dates labeled as YYMMDD (at the end of the filename). For experiment 1, data from the following dates are present: 15-10-08, 15-10-12, 15-10-19, 15-10-26, 15-11-02, 15-11-16, 15-11-23, and 15-12-10. For experiment 2, following dates are: 18-02-20, 18-03-06, 18-03-08, 18-03-20, 18-03-26, 18-04-13, 18-04-16, 18-04-23. For experiment 3: 14-08-14, 14-08-18, 14-08-20, 15-10-14. For experiment 4: 18-12-03, 18-12-13, 19-01-07, 19-02-20.&nbsp; File naming conventions across all experiments are as follows</p> <ol> <li>targTest: This corresponds to the direction of the joystick recorded for each trial. (decoded using the decoder)</li> <li>targTrain: Ground truth label, corresponding to the actual direction of the joystick.</li> <li>testSet: Number of spike counts from each channel (used for testing corresponding to all the sessions)</li> <li>trainSet: Number of spike counts from each channel (used for calibration, mostly)&nbsp; &nbsp; &nbsp;&nbsp;&nbsp;</li> </ol> <p><strong>Additional Information.</strong> This dataset is a simplified and curated version designed to reproduce the results presented in the associated paper. Note that Experiments 1 and 3 have partial datasets already publicly available at: <a href="https://osf.io/dce96/" target="_new" rel="noopener">https://osf.io/dce96/</a>. However, those versions are raw and can be processed using the variable descriptions below to extract spike counts with a specified bin width. Each file includes the following fields:</p> <ol> <li>&nbsp;joystick_adfreq: The frequency of operation of the joystick.</li> <li>X_Voltage: The voltage reading corresponding to the x-coordinate (while joystick operation).</li> <li>Y_Voltage: The voltage reading corresponding to the y-coordinate (while joystick operation).</li> <li>Spike_data(Channel Number): The Channel Number corresponding to which the neuronal data is recorded.</li> <li>Spike_data(Cluster): Descripting the cluster on which the channels are placed.</li> <li>Spike_data(Spike Times): The timestamp corresponding to the detection of a spike.</li> <li>Spike_data(Spike Number): The total number of spikes calculated for a particular trial from a particular channel.</li> <li>Spike_data(Mean Spike Waveform): The mean neuronal data (for that trial from a particular channel) describing a spike.</li> <li>Spike_data(Spike Amplitude): The mean spike amplitude of that particular channel.</li> <li>IMETrainingData(SentSignals): The truth labels corresponding to a particular trial.</li> <li>IMETrainingData(Timestamps): Time stamps corresponding to each sent signal (data).</li> <li>IMETrainingData(ReasonFail): String data; Reason if the trial failed.</li> <li>IMETrainingData(TrialOutcomes): Trial results corresponding to successful or unsuccessful!</li> <li>IMETrainingData(StartTime): corresponding to the beginning of each trial.</li> <li>IMETrainingData(EndTime): corresponding to the end of each trial.</li> </ol> <p><strong>Possible use cases. </strong>This dataset is well-suited for designing, training, and evaluating iBMI decoders. It provides a valuable resource for researchers aiming to model sensorimotor cortical spiking, benchmark iBMI decoders under consistent conditions, or explore neuromorphic and reinforcement learning-based approaches to decoder design.</p> <p><strong>Contact Information. </strong>We would be delighted to hear from you if you find this dataset useful&mdash;especially if it contributes to a publication. Contact: A. Basu &lt;arinbasu@cityu.edu.hk&gt;; A. Ghosh &lt;aghosh14@illinois.edu&gt;.</p> <p><strong>Citation. </strong>A. Ghosh, S. Shaikh, B. Zhou, P. S. V. Sun, C. Libedinsky, R. So, A. Basu, "Low-complexity Reinforcement Learning Decoders for Autonomous, Scalable, Neuromorphic intra-cortical Brain Machine Interfaces," Neuroelectronics 2025(2):0006, <a href="https://doi.org/10.55092/neuroelectronics20250006">https://doi.org/10.55092/neuroelectronics20250006</a></p>

opencc-by-4.0Sep 2023View details →
zenodo28/100

GR(1) Synthesis, Behavioral Programming, and Reinforcement Learning for Safe and Efficient Decision-Making Systems

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opencc-by-4.0Jun 2024View details →
zenodo28/100

Safe Reinforcement Learning Through Reactive Synthesis and Behavioral Programming in Cyber-Physical Systems

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opencc-by-4.0Aug 2024View details →
zenodo28/100

Curiosity Driven Multi-agent Reinforcement Learning for 3D Game Testing

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opencc-by-4.0Oct 2024View details →
zenodo28/100

Track-to-Learn: A general framework for tractography with deep reinforcement learning

<p>Datasets used in the experiments presented in Track-to-Learn: A general framework for tractography using deep reinforcement learning</p> <p>See&nbsp;https://github.com/scil-vital/TrackToLearn to use the datasets and recreate the experiments.</p>

opencc-by-4.0Jul 2021View details →
zenodo28/100

Conformation Database for Publication: Applying Deep Reinforcement Learning to the HP Model for Protein Structure Prediction

<p><strong>Conformation database</strong> for 2022 Publication &quot;Applying Deep Reinforcement Learning to the HP Model for Protein Structure Prediction&quot;</p> <ul> <li>DOI of Physica A publication: <a href="https://doi.org/10.1016/j.physa.2022.128395">https://doi.org/10.1016/j.physa.2022.128395</a></li> <li>GitHub source code: <a href="https://github.com/CompSoftMatterBiophysics-CityU-HK/Applying-DRL-to-HP-Model-for-Protein-Structure-Prediction">https://github.com/CompSoftMatterBiophysics-CityU-HK/Applying-DRL-to-HP-Model-for-Protein-Structure-Prediction</a></li> </ul> <p>This conformation database shows the distinct conformations of best-known and next best energies:</p> <p>├── <strong>20merA</strong><br> │&nbsp;&nbsp;&nbsp;├── <strong>20merA_E8_set</strong><br> │&nbsp;&nbsp;&nbsp;├── <strong>20merA_E9_set</strong><br> │&nbsp;&nbsp;&nbsp;├── confs_20merA_E8.txt<br> │&nbsp;&nbsp;&nbsp;└── confs_20merA_E9.txt<br> ├── <strong>20merB</strong><br> │&nbsp;&nbsp;&nbsp;├── <strong>20merB_E10_set</strong><br> │&nbsp;&nbsp;&nbsp;├── <strong>20merB_E9_set</strong><br> │&nbsp;&nbsp;&nbsp;├── confs_20merB_E10.txt<br> │&nbsp;&nbsp;&nbsp;└── confs_20merB_E9.txt<br> ├── <strong>24mer</strong><br> │&nbsp;&nbsp;&nbsp;├── <strong>24mer_E8_set</strong><br> │&nbsp;&nbsp;&nbsp;├── <strong>24mer_E9_set</strong><br> │&nbsp;&nbsp;&nbsp;├── confs_24mer_E8.txt<br> │&nbsp;&nbsp;&nbsp;└── confs_24mer_E9.txt<br> ├── <strong>25mer</strong><br> │&nbsp;&nbsp;&nbsp;├── <strong>25mer_E7_set</strong><br> │&nbsp;&nbsp;&nbsp;├── <strong>25mer_E8_set</strong><br> │&nbsp;&nbsp;&nbsp;├── confs_25mer_E7.txt<br> │&nbsp;&nbsp;&nbsp;└── confs_25mer_E8.txt<br> ├── <strong>36mer</strong><br> │&nbsp;&nbsp;&nbsp;├── <strong>36mer_E13_set</strong><br> │&nbsp;&nbsp;&nbsp;├── <strong>36mer_E14_set</strong><br> │&nbsp;&nbsp;&nbsp;├── confs_36mer_E13.txt<br> │&nbsp;&nbsp;&nbsp;└── confs_36mer_E14.txt<br> ├── <strong>48mer</strong><br> │&nbsp;&nbsp;&nbsp;├── <strong>48mer_E22_set</strong><br> │&nbsp;&nbsp;&nbsp;├── <strong>48mer_E23_set</strong><br> │&nbsp;&nbsp;&nbsp;├── confs_48mer_E22.txt<br> │&nbsp;&nbsp;&nbsp;└── confs_48mer_E23.txt<br> └── <strong>50mer</strong><br> &nbsp;&nbsp;&nbsp;├── <strong>50mer_E20_set</strong><br> &nbsp;&nbsp;&nbsp;├── <strong>50mer_E21_set</strong><br> &nbsp;&nbsp;&nbsp;├── confs_50mer_E20.txt<br> &nbsp;&nbsp;&nbsp;└── confs_50mer_E21.txt</p>

opencc-by-4.0Dec 2022View details →
zenodo28/100

Dataset and Code for the Paper "Reinforced Active Learning for CVD-Grown Two-Dimensional Materials Characterization"

<p>This repository&nbsp;contains the original data and code for the paper titled as &quot;Reinforced Active Learning for CVD-Grown Two-Dimensional Materials Characterization&quot; published on <em>IISE Transactions</em>.</p>

opencc-by-4.0Jun 2023View details →
ClinicalTrials.gov28/100

Acute and Chronic Nicotine Modulation of Reinforcement Learning

ClinicalTrials.gov study NCT01830842. IPD Sharing: Not stated. Countries: 1. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov28/100

Towards Efficient Personalization of Computerized Lower Limb Prostheses Via Reinforcement Learning in a Clinical Setup - Group 1

ClinicalTrials.gov study NCT07204925. IPD Sharing: NO. Countries: 1. Publications: 0.

closedIPD-NOFeb 2026View details →
dryad28/100

Data from: Gaze-contingent reinforcement learning reveals incentive value of social signals in young children and adults

Open the record for dataset details and reuse information.

publicFeb 2017View details →
dryad28/100

On collaborative reinforcement learning to optimize the redistribution of critical medical supplies throughout the COVID-19 pandemic

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publicMay 2021View details →
dryad28/100

Reinforcement learning links spontaneous dopamine transients to reward

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publicJun 2021View details →
zenodo24/100

Numerical analysis and machine learning techniques on the behavior of FRP confined circular reinforced concrete columns

<p>This study presents a comprehensive nonlinear finite element study on the behavior of circular fibre reinforced polymer (FRP) confined reinforced and plain concrete columns under concentric loads. For this investigation, 65 test models with a combination of spiral hoop reinforced concrete, concrete with longitudinal and circular hoop reinforcements, and FRP confined plain concrete were designed&nbsp;. Four different machine learning (ML) techniques were developed to predict the ultimate axial load and strain at the tensile rupture of FRP. The accuracy of the proposed finite element model (FEM) was verified by comparing it with the existing experimental test results. The impact of unconfined concrete strength, hoop reinforcement ratio, thickness of FRP, and spiral hoop spacing on the confinement effectiveness, load-carrying capacity, and ductility behavior of circular FRP confined concrete columns were demonstrated. The parametric analysis found that axial load capacity of FRP-confined concrete columns increased when unconfined concrete strength increased, while low-strength confined concrete achieved a larger strength improvement ratio than high-grade concrete. The investigation also revealed that the thickness of the confining FRP has a significant impact on the confinement effectiveness of hoop reinforcement. The correlation between the FEM and experimental tests yielded 99.60% R<sup>2</sup> for ultimate axial load and 93.40% R<sup>2</sup> for ultimate strain. Extra tree regressor (ETR) and gradient boosting of ML yielded accurate predictions of ultimate axial load and strain at the tensile rupture of FRP compared to other approaches, but ETR has the best comprehensive prediction performance using the comprehensive ranking system. Overall, ETR can be applied in the ultimate axial load and strain prediction of circular FRP confined reinforced and plain concrete columns under concentric loads, conserving resources, time, and cost through laboratory testing.</p> <p>&nbsp;</p> <p>&nbsp;</p> <p>&nbsp;</p> <p>&nbsp;</p>

opencc-by-4.0Aug 2023View details →

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Allen Brain Atlas

Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

Annotated Behaviour and Observability Dataset (ABODe)

ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

DANDI Archive for NWB datasets

DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

International Brain Laboratory public data

The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

OpenNeuro

OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record