Skip to main content
Powered by ShareScore

Find research datasets worth reusing

Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.

32

datasets available to search

ShareScore release 0.9.0

Reset

Dataset results

32 results for “motor memory”

Learn how ShareScore rates datasets ↗
dryad40/100

Temporal cluster-based organisation of sleep spindles underlies motor memory consolidation

<p><span>Sleep benefits motor memory consolidation, which is mediated by sleep spindle activity and associated memory reactivations during non-rapid eye movement (NREM) sleep. However, the particular role of NREM2 and NREM3 sleep spindles and the mechanisms triggering this memory consolidation process remai<span>n unclear. Here, sim</span>ultaneous electroencephalographic and functional magnetic resonance imaging (EEG-fMRI) recordings were collected during night-time sleep following the learning of a motor sequence task. Adopting a time-based clustering approach, we provide evidence that spindles iteratively occur within clustered and temporally organised patterns during both NREM2 and NREM3 sleep. However, the clustering of spindles in trains is related to motor memory consolidation during NREM2 sleep only</span><span>. Altogether</span><span>,</span><span> our findings suggest t</span><span>hat</span><span> spindles' clustering and </span><span>rhythmic occurrence </span><span>during NREM2 sleep may serve as an intrinsic rhythmic sleep mechanism for the timed reactivation and subsequent consolidation of motor memories, through synchronised oscillatory activity within a subcortical-cortical network involved during learning</span>.</p>

opencc-zeroJan 2024View details →
zenodo40/100

Data set of manuscript entiteld Sigma Oscillations Protect or Reinstate Motor Memory Depending on their Temporal Coordination with Slow Waves

<p>Data set of manuscript entiteld Sigma Oscillations Protect or Reinstate Motor Memory Depending on their Temporal Coordination with Slow Waves</p> <p>EEG files : Brainvision</p> <p>*.dat;&nbsp;*.edf : eeg files of the experimental nap&nbsp;</p> <p>*.vhdr: corresponding header files</p> <p>*.vmrk: corresponding marker files time starting from recording sample</p> <p>*._Pauselog.txt: markers with condition in the stimulation computer time</p> <p>Sleep Scores:&nbsp;</p> <p>Scores by the sleep technician (one file per participants).&nbsp;</p> <p>Surveys:</p> <p>General survey (first screening) and complete survey (for inclusion). Code&nbsp;correspondance is provided in ID_correspondance.txt</p> <p>BehavData:</p> <p>For each participant, a text file with all the cues and responses logged for each tasks. *_raw.txt are present when an issue arised during experiment and&nbsp;a task needed to be re-started.&nbsp;</p> <p>&nbsp;</p>

opencc-by-4.0Jun 2022View details →
zenodo40/100

Dataset for manuscript "Prefrontal stimulation as a tool to disrupt hippocampal and striatal reactivations underlying fast motor memory consolidation"

<p>Dataset containing the source data corresponding to figures and tables in the manuscript &quot;Prefrontal stimulation as a tool to disrupt hippocampal and striatal reactivations underlying fast motor memory consolidation&quot;, as well as raw behavioral and MEP data and the corresponding analysis scripts.</p>

opencc-by-4.0Aug 2023View details →
dryad40/100

Temporal cluster-based organisation of sleep spindles underlies motor memory consolidation

Open the record for dataset details and reuse information.

publicJan 2024View details →
dryad36/100

Separability of human motor memories during reaching adaptation with force cues

<p><span>Judging by the breadth of our motor repertoire during daily activities, it is clear that learning different tasks is a hallmark of the human motor system. However, for reaching adaptation to different force fields, the conditions under which this is possible in laboratory settings have remained a challenging question. Previous work has shown that independent movement representations or goals enabled dual adaptation. Considering the importance of force feedback during limb control, here we hypothesised that independent cues delivered by means of background loads could support simultaneous adaptation to various velocity-dependent force fields, for identical kinematic plan and movement goal. We demonstrate in a series of experiments that indeed healthy adults can adapt to opposite force fields, independently of the direction of the background force cue. However, when the cue and force field were in the same direction but differed by their magnitude, the formation of different motor representations was still observed but the associated mechanism was subject to increased interference. Finally, we highlight that this paradigm allows dissociating trial-by-trial adaptation from online feedback adaptation, as these two mechanisms are associated with different time scales that can be identified reliably and reproduced in a computational model. </span></p>

opencc-zeroOct 2022View details →
zenodo36/100

Dataset for manuscript "Sleep does not influence schema-facilitated motor memory consolidation"

<p>Dataset containing&nbsp;the raw as well as the subject-level data for the two experiments reported in the manuscript &quot;Sleep does not influence schema-facilitated motor memory consolidation&quot;.</p>

opencc-by-4.0Nov 2022View details →
zenodo36/100

Dataset for "A Double Dissociation between Savings and Long-Term Memory in Motor Learning"

<p>Data for &quot;A Double Dissociation between Savings and Long-Term Memory in Motor Learning&quot;<br> <br> For analysis code and any updates, please visit&nbsp;&nbsp;https://github.com/AlkisMH/Savings_vs_Long_Term_Memory<br> <br> For any questions, please contact Alkis Hadjiosif (alkis [at] seas [dot] harvard [dot] edu; ahadjiosif [at] gmail [dot] com)</p> <p>These .mat files contain data collected for Experiments 1-4 and S1, used to reproduce Figures 1-6 and S1 in the paper. Data for each experiment are in the form of a Matlab structure, with each field consisting of a [Num_trials x Num_participants] matrix.</p> <p>The fields are:</p> <p><strong>TN:</strong>&nbsp;Trial Number</p> <p><strong>VF:</strong>&nbsp;Whether visual feedback was given during the trial (1: online visual feedback; 2: no visual feedback)</p> <p><strong>Rotation:</strong>&nbsp;The visuomotor rotation imposed on each trial (in degrees). CCW is positive, CW is negative.</p> <p><strong>Wait:</strong>&nbsp;Whether, right before the trial, a wait time was imposed (1) or not (0). Trials immediately following breaks are indicated by (2).</p> <p><strong>Instruction:</strong>&nbsp;Whether an instruction was given for the trial (1) or not (0). Only present in Experiment 3. Note that Experiment 3 includes:</p> <p>-&gt; Two specific instruction trials during learning and and two during relearning, before and after the 1-minute wait (&quot;Move your hand to the center of the target&quot;,&quot;Move your hand to the far end of the target&quot;)</p> <p>-&gt; Six random instruction trials before initial learning and six before relearning (&quot;Move your hand to the left/right/near/far end of the target&quot;), to familiarize participants with the instruction process</p> <p><strong>ITI:</strong>&nbsp;Time (in seconds) since the last trial (regardless of direction).</p> <p><strong>theta_target:</strong>&nbsp;Target direction (in degrees) relative to the 12 o&#39;clock position. Only included for Experiment 4: target is always at 12 o&#39;clock for Experiments 1-3.</p> <p><strong>theta:</strong>&nbsp;= reaching direction relative to theta_target, measured 150ms into the movement. Note that this is flipped based on the rotation sign so that adaptation towards the imposed visuomotor rotation is always positive.</p> <p><strong>theta_end:</strong>&nbsp;= reaching direction relative to theta_target, measured at the end of movement. Only included for Experiment 4: it is to be used for the no visual feedback blocks in Experiment 4.</p> <p>Note for&nbsp;<strong>Experiment 4</strong>: the last two blocks (last 114 trials) were done on day 2.</p>

opencc-by-4.0Feb 2023View details →
dryad36/100

Separability of human motor memories during reaching adaptation with force cues

Open the record for dataset details and reuse information.

publicOct 2022View details →
zenodo32/100

Acute Exercise and Motor Memory Consolidation: The Role of Exercise Intensity

<p>A single bout of high intensity aerobic exercise (~90% VO<sub>2peak</sub>) was previously demonstrated to amplify off-line gains in skill level during the consolidation phase of procedural memory. High intensity exercise is not always a viable option for many patient groups or in a rehabilitation setting where low to moderate intensities may be more suitable. The aim of this study was to investigate the role of intensity in mediating the effects of acute cardiovascular exercise on motor skill learning.&nbsp;A single bout of high intensity aerobic exercise (~90% VO<sub>2peak</sub>) was previously demonstrated to amplify off-line gains in skill level during the consolidation phase of procedural memory. High intensity exercise is not always a viable option for many patient groups or in a rehabilitation setting where low to moderate intensities may be more suitable. The aim of this study was to investigate the role of intensity in mediating the effects of acute cardiovascular exercise on motor skill learning.</p>

opencc-zeroJul 2016View details →
ClinicalTrials.gov32/100

Procedural Motor Memory in Long COVID-19

ClinicalTrials.gov study NCT05746624. IPD Sharing: Not stated. Countries: 1. Publications: 0.

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

Triggering Motor Memory Consolidation in PD: Complex Practice of Fine Motor Tasks and Brain Activity During Learning

ClinicalTrials.gov study NCT04269590. IPD Sharing: NO. Countries: 1. Publications: 3.

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

Motor Interference Therapy For Traumatic Memories

ClinicalTrials.gov study NCT03627078. IPD Sharing: Not stated. Countries: 1. Publications: 1.

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

The Role of Primary Motor Cortex and Prefrontal Cortex for Facilitation of Motor System and Working Memory

ClinicalTrials.gov study NCT02006615. IPD Sharing: Not stated. Countries: 1. Publications: 3.

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

Influence of Arousal on Motor Learning, Memory and Motor Imagery Ability in Young Population

ClinicalTrials.gov study NCT04911439. IPD Sharing: Not stated. Countries: 2. Publications: 7.

restrictedIPD-UNDECIDEDFeb 2026View details →
dryad32/100

Data for: Analogous computations in working memory input, output and motor gating: Electrophysiological and computational modeling evidence

Open the record for dataset details and reuse information.

publicApr 2021View details →
dryad32/100

Data from: The ontogeny of visual motor memory and its importance in handwriting and reading: a developing construct

Open the record for dataset details and reuse information.

publicNov 2014View details →
dryad28/100

Data from: NREM2 and sleep spindles are instrumental to the consolidation of motor sequence memories

Although numerous studies have convincingly demonstrated that sleep plays a critical role in motor sequence learning (MSL) consolidation, the specific contribution of the different sleep stages in this type of memory consolidation is still contentious. To probe the role of stage 2 non-REM sleep (NREM2) in this process, we used a conditioning protocol in three different groups of participants who either received an odor during initial training on a motor sequence learning task and were re-exposed to this odor during different sleep stages of the post-training night (i.e., NREM2 sleep [Cond-NREM2], REM sleep [Cond-REM], or were not conditioned during learning but exposed to the odor during NREM2 [NoCond]). Results show that the Cond-NREM2 group had significantly higher gains in performance at retest than both the Cond-REM and NoCond groups. Also, only the Cond-NREM2 group yielded significant changes in sleep spindle characteristics during cueing. Finally, we found that a change in frequency of sleep spindles during cued-memory reactivation mediated the relationship between the experimental groups and gains in performance the next day. These findings strongly suggest that cued-memory reactivation during NREM2 sleep triggers an increase in sleep spindle activity that is then related to the consolidation of motor sequence memories.

opencc-zeroDec 2015View details →
dryad28/100

Data from: Concurrent visual and motor selection during visual working memory guided action

Visual working memory enables us to hold onto past sensations in anticipation that these may become relevant for guiding future actions. Yet laboratory tasks have treated visual working memories in isolation from their prospective actions and have focused on the mechanisms of memory retention rather than utilization. To understand how visual memories become used for action, we linked individual memory items to particular actions and independently tracked the neural dynamics of visual and motor selection when memories became used for action. This revealed concurrent visual-motor selection, engaging appropriate visual and motor brain areas at the same time. Thus we show that items in visual working memory can invoke multiple, item-specific, action plans that can be accessed together with the visual representations that guide them, affording fast and precise memory-guided behavior.

opencc-zeroDec 2018View details →
dryad28/100

Data from: NREM2 and sleep spindles are instrumental to the consolidation of motor sequence memories

Open the record for dataset details and reuse information.

publicMar 2017View details →
dryad28/100

Timescales of motor memory formation in dual-adaptation

Open the record for dataset details and reuse information.

publicFeb 2021View details →

ScienceDex guides

Understand access before you commit

These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.

Compare curated datasets

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