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.
148
datasets available to search
ShareScore release 0.9.0
Dataset results
148 results for “Entropy”
Data from: Differential changes with age in multiscale entropy of electromyography signals from leg muscles during treadmill walking
Age-related gait changes may be due to the loss of complexity in the neuromuscular system. This theory is disputed due to inconsistent results from single-scale analyses. Also, behavioral adaptations may confound these changes. We examined whether EMG dynamics during gait is less complex in older adults over a range of timescales using the multiscale entropy method, and whether slower walking attenuates this effect. Surface EMG was measured from the left vastus lateralis (VL), biceps femoris (BF), gastrocnemius (GA), and tibialis anterior (TA) in 17 young and 18 older adults as they walked on a treadmill for 5 minutes at 0.8x-1.2x of preferred speed. Sample entropy (SE) and the complexity index (CI) of the EMG signals were calculated after successive coarse-graining to extract dynamics at timescales of 27 to 270 Hz, with m = 2 and r = 0.15 SD. SE and CI were lower across the timescales in older adults in VL and BF, but higher in GA (all p<0.001); these results held for VL and GA even after accounting for longer EMG burst durations in older adults. CI was higher during slower walking speed in VL and BF (p<0.001). Results were mostly similar for m = 3 and r = 0.01–0.35. Smaller r was more sensitive to age-related differences. The decrease in complexity with aging in the timescales studied was limited to proximal muscles, particularly VL. The increase in GA may be driven by other factors. Walking slower may reflect a behavioral adaptation that allows the nervous system to function with greater complexity.
Supplemental material for the paper, "Entropy, Search Trajectories, and Explainability for Frequency Fitness Assignment"
Open the record for dataset details and reuse information.
Data from: Electromyographic permutation entropy quantifies diaphragmatic denervation and reinnervation
Spontaneous reinnervation after diaphragmatic paralysis due to trauma, surgery, tumors and spinal cord injuries is frequently observed. A possible explanation could be collateral reinnervation, since the diaphragm is commonly double-innervated by the (accessory) phrenic nerve. Permutation entropy (PeEn), a complexity measure for time series, may reflect a functional state of neuromuscular transmission by quantifying the complexity of interactions across neural and muscular networks. In an established rat model, electromyographic signals of the diaphragm after phrenicotomy were analyzed using PeEn quantifying denervation and reinnervation. Thirty-three anesthetized rats were unilaterally phrenicotomized. After 1, 3, 9, 27 and 81 days, diaphragmatic electromyographic PeEn was analyzed in vivo from sternal, mid-costal and crural areas of both hemidiaphragms. After euthanasia of the animals, both hemidiaphragms were dissected for fiber type evaluation. The electromyographic incidence of an accessory phrenic nerve was 76%. At day 1 after phrenicotomy, PeEn (normalized values) was significantly diminished in the sternal (median: 0.69; interquartile range: 0.66–0.75) and mid-costal area (0.68; 0.66–0.72) compared to the non-denervated side (0.84; 0.78–0.90) at threshold p<0.05. In the crural area, innervated by the accessory phrenic nerve, PeEn remained unchanged (0.79; 0.72–0.86). During reinnervation over 81 days, PeEn normalized in the mid-costal area (0.84; 0.77–0.86), whereas it remained reduced in the sternal area (0.77; 0.70–0.81). Fiber type grouping, a histological sign for reinnervation, was found in the mid-costal area in 20% after 27 days and in 80% after 81 days. Collateral reinnervation can restore diaphragm activity after phrenicotomy. Electromyographic PeEn represents a new, distinctive assessment characterizing intramuscular function following denervation and reinnervation.
Data from: Bistability, non-ergodicity, and inhibition in pairwise maximum-entropy models
Pairwise maximum-entropy models have been used in neuroscience to predict the activity of neuronal populations, given only the time-averaged correlations of the neuron activities. This paper provides evidence that the pairwise model, applied to experimental recordings, would produce a bimodal distribution for the population-averaged activity, and for some population sizes the second mode would peak at high activities, that experimentally would be equivalent to 90% of the neuron population active within time-windows of few milliseconds. Several problems are connected with this bimodality: 1. The presence of the high-activity mode is unrealistic in view of observed neuronal activity and on neurobiological grounds. 2. Boltzmann learning becomes non-ergodic, hence the pairwise maximum-entropy distribution cannot be found: in fact, Boltzmann learning would produce an incorrect distribution; similarly, common variants of mean-field approximations also produce an incorrect distribution. 3. The Glauber dynamics associated with the model is unrealistically bistable and cannot be used to generate realistic surrogate data. This bimodality problem is first demonstrated for an experimental dataset from 159 neurons in the motor cortex of macaque monkey. Evidence is then provided that this problem affects typical neural recordings of population sizes of a couple of hundreds or more neurons. The cause of the bimodality problem is identified as the inability of standard maximum-entropy distributions with a uniform reference measure to model neuronal inhibition. To eliminate this problem a modified maximum-entropy model is presented, which reflects a basic effect of inhibition in the form of a simple but non-uniform reference measure. This model does not lead to unrealistic bimodalities, can be found with Boltzmann learning, and has an associated Glauber dynamics which incorporates a minimal asymmetric inhibition.
Data from: Sequence entropy of folding and the absolute rate of amino acid substitutions
Adequate representations of protein evolution should consider how the acceptance of mutations depends on the sequence context in which they arise. However, epistatic interactions among sites in a protein result in hererogeneities in the substitution rate, both temporal and spatial, that are beyond the capabilities of current models. Here we use parallels between amino acid substitutions and chemical reaction kinetics to develop an improved theory of protein evolution. We constructed a mechanistic framework for modelling amino acid substitution rates that uses the formalisms of statistical mechanics, with principles of population genetics underlying the analysis. Theoretical analyses and computer simulations of proteins under purifying selection for thermodynamic stability show that substitution rates and the stabilization of resident amino acids (the 'evolutionary Stokes shift') can be predicted from biophysics and the effect of sequence entropy alone. Furthermore, we demonstrate that substitutions predominantly occur when epistatic interactions result in near neutrality; substitution rates are determined by how often epistasis results in such nearly neutral conditions. This theory provides a general framework for modelling protein sequence change under purifying selection, potentially explains patterns of convergence and mutation rates in real proteins that are incompatible with previous models, and provides a better null model for the detection of adaptive changes.
Jump Entropy Models Trained on Ten Dutch Newspapers, 1950-1990
<p>Matrices of relative entropy (JSD) between front pages in ten Dutch newspapers published between 1950 and 1990. For more on the calculation of these time series see:</p> <p>MORE INFO ASAP</p> <p> </p>
A long-term monthly dataset of cloud fraction over the Arctic based on multiple satellite products using cumulative distribution function matching and Bayesian maximum entropy
<p>The low accuracy of satellite Cloud fraction (CF) over the Arctic seriously restricts accurate assessment of regional and global radiant energy balance under the changing climate. Previous studies have reported that not a single satellite CF product could satisfy the needs of accuracy and spatio-temporal coverage simultaneously for long-term applications over the Arctic. Merging multiple CF products with complementary properties is an effective way to produce more spatiotemporally complete and accurate CF data record. This study proposed a spatiotemporal statistical data fusion framework based on cumulative distribution function (CDF) matching and Bayesian maximum entropy (BME) method to produce a syncretic 1°×1° CF dataset in the Arctic during 2000-2020. The original datasets contain CF from MOD08/MYD08, CERES-SSF Terra/Aqua, CLARA-A2 AM/PM, PATMOS-x AM/PM, ISCCP-H AM/PM. The fused CF product is more consistent with the active satellite data GEWEX-CALIPSO and the ground-based observation data CRU TS4.05.</p>
A Library of High-Entropy-Alloy Nanocrystals with Controlled Surface Atomic Arrangements for Catalysis
<p>Input file of PtIrRuRhPd on Pd model based on SQS theory and Data of DFT calculations</p>
Partial liquid metal dealloying to synthesize nickel-containing porous and composite ferrous and high-entropy alloys
<p>Raw data for the graphs in the article.</p>
Supplementary materials for "Entropy is a good approximation to the electronic (static) correlation energy"
<p>Jupyter notebooks and data needed to reproduce the figures in the manuscript.</p>
BIS and Entropy in Deep Brain Simulation
ClinicalTrials.gov study NCT02386995. IPD Sharing: Not stated. Countries: 1. Publications: 0.
BIS and Entropy Nociception Monitoring
ClinicalTrials.gov study NCT02585466. IPD Sharing: Not stated. Countries: 0. Publications: 3.
Modulation of General Anesthesia Using Entropy and Surgical Pleth Index
ClinicalTrials.gov study NCT03095430. IPD Sharing: NO. Countries: 0. Publications: 1.
Data from: A strong test of the Maximum Entropy Theory of Ecology
Open the record for dataset details and reuse information.
Data from: Sequence entropy of folding and the absolute rate of amino acid substitutions
Open the record for dataset details and reuse information.
Data from: Control of entropy in neural models of environmental state
Open the record for dataset details and reuse information.
Data from: Bistability, non-ergodicity, and inhibition in pairwise maximum-entropy models
Open the record for dataset details and reuse information.
Data from: Electromyographic permutation entropy quantifies diaphragmatic denervation and reinnervation
Open the record for dataset details and reuse information.
Data from: Differential changes with age in multiscale entropy of electromyography signals from leg muscles during treadmill walking
Open the record for dataset details and reuse information.
DNA methylation entropy is a biomarker for aging
GEO Series GSE288139. Homo sapiens. 100 samples. Type: Methylation profiling by high throughput sequencing.
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research 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.
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.
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.
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.
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.