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.
258
datasets available to search
ShareScore release 0.9.0
Dataset results
258 results for “time dependent”
Dataset: Environment effects on X-ray absorption spectra with quantum embedded real-time Time-dependent density functional theory approaches
<p>This dataset collects the outputs from real-time TDDFT simulation of X-ray absorption of halides in model systems, using the frozen density embedding (FDE) and block-orthogonalized Manby-Miller embedding (BOMME), as well as processing tools and scripts used to carry out the calculations.</p>
Dataset: Time-dependent source apportionment of submicron organic aerosol for a rural site in an alpine valley using a rolling positive matrix factorisation (PMF) window
<p>Uploaded igor pxp files are the data to generate all figures of the results from our publication in Atmospheric Chemistry and Physics with the name of <em>"Time dependent source apportionment of submicron organic aerosol for a rural site in an alpine valley using a rolling PMF window"</em> by Chen et al. (2021).</p> <p>This study deployed a novel and advanced source apportionment technique on a dataset measured in Magadino. Rolling PMF allows retrieving more realistic, time-dependent and detailed information of the organic aerosol sources. This work highlights the strength of the rolling PMF mechanism by comparing it with the results derived from conventional seasonal PMF. Overall, this comprehensive interpretation of chemical speciation monitor (ACSM) data could be a role model for similar analyses.</p>
Automatically Reproducing Timing-Dependent Flaky-Test Failures
<p>This artifact contains the source code for FlakeRake, a tool for automatically reproducing timing-dependent flaky-test failures. It also includes raw and processed results produced in the evaluation of FlakeRake</p> <p> </p> <p>Contents:</p> <p> </p> <p>Timing-related APIs that FlakeRake considers adding sleeps at: timing-related-apis</p> <p>Anonymized code for FlakeRake (not runnable in its anonymized state, but included for reference; we will publicly release the non-anonymized code under an open source license pending double-blind review): flakerake.tgz</p> <p>Failure messages extracted from the FlakeFlagger dataset: 10k_reruns_failures_by_test.csv.gz </p> <p>Output from running isolated reruns on each flaky test in the FlakeFlager dataset: 10k_isolated_reruns_all_results.csv.gz (all test results summarized into a CSV), 10k_isolated_reruns_failures_by_test.csv.gz (CSV including just test failures, including failure messages), 10k_isolated_reruns_raw_results.tgz (includes all raw results from reruns, including the XML files output by maven)</p> <p>Output from running the FlakeFlagger replication study (non-isolated 10k reruns):flakeFlaggerReplResults.csv.gz (all test results summarized into a CSV), 10k_reruns_failures_by_test.csv.gz (CSV including just failures, including failure messages), flakeFlaggerRepl_raw_results.tgz (includes all raw results from reruns, including the XML files output by maven - this file is markedly larger than the 10k isolated reruns results because we ran *all* tests in this experiment, whereas the 10k isolated rerun experiment only re-ran the tests that were known to be flaky from the FlakeFlagger dataset).</p> <p>Output from running FlakeRake on each flaky test in the FlakeFlagger dataset:</p> <p>For bisection mode: results-bis.tgz</p> <p>For one-by-one mode: results-obo.tgz</p> <p>Scripts used to execute FlakeRake using an HPC cluster: execution-scripts.tgz<br> Scripts used to execute rerun experiments using an HPC cluster: flakeFlaggerReplScripts.tgz<br> Scripts used to parse the "raw" maven test result XML files in this artifact into the CSV files contained in this artifact: parseSurefireXMLs.tgz </p> <p>Output from running FlakeRake in “reproduction” mode, attempting to reproduce each of the failures that matched the FlakeFlagger dataset (collected for bisection mode only): results-repro-bis.tgz</p> <p>Analysis of timing-dependent API calls in the failure inducing configurations that matched FlakeFlagger failures: bis-sleepyline.cause-to-matched-fail-configs-found.csv</p>
Granulosa cell transcriptome data from four different time points before and up to 48 hours after PMSG induction to GTH-depend phase in mice
<p>GTH-dependent follicle development begins with small antrum follicles and ends with preovulatory follicles. GTH-dependent follicle development is mainly controlled by gonadotropins, and the development time is 48h. The purpose of this study is to monitor the changes in gene expression of granulosa cells at four different time points during the GTH-dependent phase to increase our understanding of human GTH-dependent follicle development.Granulosa cell mRNA profiles of GTH-depend phase in mice.There are 12 samples represented four time points 0h (n=3), 12h (n=3), 24h (n=3) and 48h (n=3)</p>
Branching patterns in phylogenies cannot distinguish diversity-dependent diversification from time-dependent diversification
One of the primary goals of macroevolutionary biology has been to explain general trends in long-term diversity patterns, including whether such patterns correspond to an up-scaling of processes occurring at lower scales. Reconstructed phylogenies often show decelerated lineage accumulation over time. This pattern has often been interpreted as the result of diversity-dependent diversification, where the accumulation of species causes diversification to decrease through niche filling. However, other processes can also produce such a slowdown, including time-dependence without diversity-dependence. To test whether phylogenetic branching patterns can be used to distinguish these two mechanisms, we formulated a time-dependent, but diversity-independent model that matches the expected diversity through time of a diversity-dependent model. We simulated phylogenies under each model and studied how well likelihood methods could recover the true diversification mode. Standard model selection criteria always recovered diversity-dependence, even when it was not present. We correct for this bias by using a bootstrap method and find that neither model is decisively supported. This implies that the branching pattern of reconstructed trees contains insufficient information to detect the presence or absence of diversity-dependence. We advocate that tests encompassing additional data, e.g., traits or range distributions, are needed to evaluate how diversity drives macroevolutionary trends.
Data + Analyses: "Gaze-dependent Coding of Somatosensory Reach Targets after Effector Movement: Testing the Impact of Online Information, Movement Timing, and Target Distance"
<p>This upload contains the experiment scripts (written in Presentation), data, and analyses (performed with MATLAB and SPSS) underlying the publication<strong> </strong>by Mueller & Fiehler (2017). <em>PloS one</em>. doi:<strong>10.1371/journal.pone.0180782</strong></p>
Time dependent interaction modification generated from plant-soil feedback
<p>Pairwise interactions between species can be modified by other community members, leading to emergent dynamics contingent on community composition. Despite the prevalence of such higher-order interactions, little is known about how they are linked to the timing and order of species' arrival. We generate population dynamics from a mechanistic plant-soil feedback model, then apply a general theoretical framework to show that the modification of a pairwise interaction by a third plant depends on its germination phenology. These time-dependent interaction modifications emerge from concurrent changes in plant and microbe populations and are strengthened by higher overlap between plants' associated microbiomes. The interaction between this overlap and the specificity of microbiomes further determines plant coexistence. Our framework is widely applicable to mechanisms in other systems from which similar time-dependent interaction modifications can emerge, highlighting the need to integrate temporal shifts of species interactions to predict the emergent dynamics of natural communities.</p>
Synthetic dataset for the flow-shop problem with sequence-dependent setup times (FSsdsu_DS_01)
<p>Synthetic dataset containing setup and processing times for a flow-shop problem of 1.000 parts and 200 machines. The setup times are specified for each machine taking into account the previous part produced on the machine.</p>
Data and R code from: Relics of beavers past: time and population density drive scale-dependent patterns of ecosystem engineering
<p><span>Like many ecological processes, natural disturbances exhibit scale-dependent dynamics that are largely a function of the magnitude, frequency, and scale at which they are assessed. Ecosystem engineers create patch-scale disturbances that affect ecological processes, yet we know little about how these effects scale across space or vary through time. Here, we investigate how patch disturbances by beavers (<i>Castor canadensis</i>), ecosystem engineers renowned for their pond-creation behavior, affect ecological processes across space and time. We evaluated how beaver population recovery influenced surface water dynamics in relation to population density over 70 years across multiple spatial scales (pond, watershed, and regional) in northern Minnesota. Surface water area was positively related to population density at the watershed scale; however, despite variation in beaver densities (and therefore surface water area) at the watershed scale, regional-scale surface water area was stable through time. This stability appears to have been driven by asynchronous beaver density fluctuations among watersheds, combined with the increasing importance of abandoned ponds. Beavers initially created and occupied larger ponds with greater surface water area, but through time shifted towards occupying smaller ponds. As ponds accumulated on the landscape proportionally more surface water was stored within abandoned ponds, which offset the smaller size of occupied ponds. Beaver engineering—driven by density-dependent mechanisms and the legacy effects from abandoned ponds—not only follows general patterns of patch disturbance dynamics by creating a spatial mosaic of patches, but the organism-created mosaic also appears to generate ecological stability at greater spatial scales. We suggest restoring beavers to landscapes is a viable method for increasing surface water storage and will ultimately help advance numerous conservation and rewilding objectives. Our study demonstrates that ecosystem engineering effects can be scale-dependent, indicating researchers should evaluate the ecological impact of engineers across diverse spatiotemporal scales to fully understand their functional roles in ecosystems.</span></p>
Time dependence of advection-diffusion coupling for nanoparticle ensembles
<p>Data appearing in the figures of the article DOI:10.1103/PhysRevFluids.6.064201.</p>
Responsiveness to cold snaps by turtle embryos depends on exposure timing and duration
<p>Characterizing how organisms respond to transient temperatures may further our understanding of their susceptibility to climate change. In animals with temperature-dependent sex determination (TSD), unusual transient temperatures during incubation result in sex bias and may therefore impair population breeding capacity. Past studies in the red-eared slider turtle (<em>Trachemys scripta</em>) have demonstrated that the timing and duration of heat exposure ("heat waves") can have major implications for the response of genes involved in gonadal development and the production of female hatchlings. Yet, no study has considered how the response of these genes to transient cold exposure ("cold snaps") may affect gene expression and influence the resulting production of males.</p> <p>We investigated how cold snap timing and duration affect gonadal gene expression in <em>T. scripta</em> embryos. Additionally, we explored the effect of early cold snap exposure duration on resulting hatchling sex ratios. Results show that responsiveness to cool temperatures changes rapidly across development, such that genes that responded to cold snaps when exposure began on incubation day 14 responded differently when cold exposure occurred just 4 to 8 days later. The sex ratio experiment revealed that embryos experiencing an early cold snap also require a long exposure (> 20 days) before most commit to testis development, further suggesting that early development under warm temperatures may lower their sensitivity to later cold snaps. These results highlight how individual responses to incubation temperature can change rapidly across development in turtles and have important effects on sex ratios. We discuss how variation in responsiveness to transient temperatures might help maintain mixed-sex ratios under variable thermal conditions in nature and may permit adaptive population responses to climate change.</p>
Tomographic X-ray data of time-dependent 3D cross phantom
<p>This is the documentation of the tomographic X-ray data of a dynamic cross phantom made available at http://www.fips.fi/dataset.php. The data can be freely used for scientific purposes with appropriate references to the data and to this document in http://arxiv.org/. The data set consists of (1) the X-ray sinogram with 16 or 30 time frames (depending on resolution) of 2D slices of the cross phantom, made by crossing aluminum and graphite sticks in melted candle wax and (2) the corresponding static and dynamic measurement matrices modeling the linear operation of the X-ray transform. Each of these sinograms was obtained from a measured 360-projection fan-beam sinogram by down-sampling and taking logarithms. The original (measured) sinogram is also provided in its original form and resolution.</p> <p>This new version contains added file <a href="https://zenodo.org/api/files/5c00de09-bb57-4c9e-9beb-00c63358de3c/DataStatic_560x60.mat?versionId=1e53d43d-d999-435e-bb1c-8297cf32c984">DataStatic_560x60.mat </a> with 80 time frames and <a href="https://zenodo.org/api/files/5c00de09-bb57-4c9e-9beb-00c63358de3c/DataStatic_1120x60.mat?versionId=afded407-6c88-4880-b427-fe7fd09306f4">DataStatic_1120x60.mat </a> with 230 time frames. You can run these files with the code example 2, which computes a Tikhonov regularized reconstruction using conjugate gradient algorithm.</p>
Use of Time Dependent Data in Bayesian Global 21cm Foreground and Signal Modelling (supplementary data)
<p>These are the posterior files, foreground simulation data sets and chromaticity factor values used to produce the results for <a href="https://arxiv.org/abs/2210.04707">arXiv:2210.04707</a>.</p> <p> </p> <p>A plotting script to reproduce key figures is included.</p> <p>Software used:</p> <ul> <li><a href="https://github.com/PolyChord/PolyChordLite/tree/839292290a7747dbee82933bb9f7f955ac45c3ca">PolyChord</a></li> <li><a href="https://github.com/williamjameshandley/fgivenx">fgivenx</a></li> </ul>
Diffusion models with time-dependent parameters: "An analysis of computational effort and accuracy of different numerical methods"
<p>Software repository for the reproduction of the test cases from</p> <p><strong>Thomas Richter, Rolf Ulrich, Markus Janczyk:</strong> <em>Diffusion models with time-dependent parameters: "An analysis of computational effort and accuracy of different numerical methods"</em></p> <p>This software is used in particular for the reproducibility of the results.</p> <p>However, the algorithms can also be used directly for own purposes. If you have any questions about possibly necessary adaptations, please contact thomas.richter@ovgu.de.</p> <p>Parts of this repository</p> <p>General setup</p> <p><strong>Python</strong> collects all Python script. Here, <strong>Python/PythonTools</strong> are several internal functions, e.g. the realizations of KFE and random walks. <strong>Python/results</strong> and <strong>Python/pics</strong> are the directories where the results (figures and text-files) are put.</p> <p><strong>C++</strong> collects the C++ scripts.</p> <p>Case I</p> <p>Reproduces Case I of the paper (time-independent)</p> <ul> <li>Python/TestCase1.py</li> </ul> <p>runs the test-case with random walks, integral equation method and with KFE. It produces output in <strong>Python/pics</strong> and <strong>Python/results</strong>. These results will be used in <strong>C++/testcase1.cc</strong> (as reference solution) and by <strong>Python/TestCase1-Plot.py</strong></p> <ul> <li>C++/testcase1.cc</li> </ul> <p>runs the stochastic Euler simulation. Script is started by <strong>C++/run-testcase1.sh</strong>. It reads in the reference solution generated by <strong>Python/TestCase1.py</strong> for computing errors.</p> <ul> <li>Python/TestCase1-Plot.py</li> </ul> <p>produces Fig. 6 of the paper. It requires the outputs of <strong>Python/TestCase1.py</strong> and <strong>C++/testcase1.cc</strong></p> <p>Case II</p> <p>Reproduces Case II of the paper (time-dependent thresholds and drift)</p> <ul> <li>Python/TestCase2.py</li> </ul> <p>runs the test-case with random walks, integral equation method and with KFE. It produces output in <strong>Python/pics</strong> and <strong>Python/results</strong>. These results will be used in <strong>C++/testcase2.cc</strong> (as reference solution) and by <strong>Python/TestCase2-Plot.py</strong></p> <ul> <li>C++/testcase2.cc</li> </ul> <p>runs the stochastic Euler simulation. Script is started by <strong>C++/run-testcase2.sh</strong>. It reads in the reference solution generated by <strong>Python/TestCase2.py</strong> for computing errors.</p> <ul> <li>Python/TestCase2-Plot.py</li> </ul> <p>produces Fig. 7 of the paper. It requires the outputs of <strong>Python/TestCase2.py</strong> and <strong>C++/testcase2.cc</strong></p> <ul> <li>Python/TestCase2-AdjustRandomWalks.py</li> </ul> <p>runs simulations to reproduce Fig. 11 of the paper and implements the modification of the random walk strategy to limit oscillations.</p> <p>Case III</p> <p>Reproduces Case III of the paper (dependency of the accuracy on the derivative of the drift)</p> <ul> <li>Python/TestCase3.py</li> </ul> <p>runs the test-case with random walks, integral equation method and with KFE for a fixed discretization but with different values of the drift tau. It produces first part of Fig. 8.</p> <ul> <li>C++/testcase3.cc</li> </ul> <p>runs the stochastic Euler simulation. Script is started by <strong>C++/run-testcase3.sh</strong>. It reads in the reference solution generated by <strong>Python/TestCase3.py</strong> for computing errors.</p> <ul> <li>Python/TestCase3-Plot.py</li> </ul> <p>produces second part of Fig. 8. Depends on the output of <strong>Python/TestCase3.py</strong></p> <p>Case IV</p> <p>Reproduces Case IV of the paper (accuracy and efficiency for Dirac initial data)</p> <ul> <li>Python/TestCase4.py</li> </ul> <p>runs the test-case with random walks, integral equation and with KFE for a refined discretizations.</p> <ul> <li>Python/TestCase4-Plot.py</li> </ul> <p>produces Fig. 9. Depends on the output of <strong>Python/TestCase4.py</strong></p> <ul> <li>Python/TestCase4-showsolution.py</li> </ul> <p>Solves with the KFE and plots the solution as surface plot over time and space variable. This skript is used to create Fig. 10 of the paper. Problem parameters and discretization can be adjusted at the top of the script. To test the different stabilization strategies, one can either adjust the value of theta, or one activates Rannacher time-marching by commenting in the marked lines in the skript PythonTools/kfe.py, here in kfe_ale(..)</p> <p>Data Fitting</p> <p>Python scripts to fit the KFE model to the Data published by Rolf Ulrich et al. in</p> <p><strong>R. Ulrich, H. Schröter, H. Leuthold, T. Birngruber</strong> <em>Automatic and controlled stimulus processing in conflict tasks: Superimposed diffusion processes and delta functions.</em>Cognitive Psychology, 78 , 148–174</p> <ul> <li>Python/DataFitting-Simon.py</li> </ul> <p>runs the parameter fitting for the Simon task and produces data for Fig. 9 and Table 1.</p> <ul> <li>Python/Eriksen-Fletcher.py</li> </ul> <p>runs the parameter fitting for the Eriksen Fletcher task and produces data for Fig. 9 and Table 2.</p> <p>Installation & running the examples</p> <p>Python</p> <p>The python skripts can just be started. Just note that they depend on each other, i.e.: <strong>Python/TestCase1.py</strong> produces a reference solution that is required by <strong>C++/testcase1.cc</strong> and the results of both are needed in <strong>Python/TestCase1-Plot.py</strong></p> <p>The scripts only depend on standard packages like numpy or scipy and all Python environments should work. One suggestion is to use Spyder as part of Anaconda.</p> <p>C++</p> <p>The C++-programs are not intended for performing the simulations in a stand-alone application. Instead, the SDE is simulated for a given number of trials <strong>N_tr</strong> and a given time step <strong>dt</strong> and this simulation is repeated <strong>64</strong> times in order to estimate the average error. It should however be simple to use the scripts as basis for an efficient parallel simulation tool that uses multithreading.</p> <p>Configuration</p> <p>The C++ test cases must be compiled. The test cases are set up to use <strong>cmake</strong>. We suggest the following (in a Linux-environment or on a Mac using homebrew or MacPorts):</p> <ol> <li>Create a directory for compilation, e.g. <strong>C++/bin</strong> now called the <strong>bin-dir</strong></li> <li>In the <strong>bin-dir</strong> calls cmake by <strong>cmake ..</strong> (adjust the path, if the <strong>bin-dir</strong> is not a subdirectory of the <strong>C++-dir</strong>.</li> <li>Several options can be adjusted. In <strong>C++/bin</strong> call <strong>ccmake .</strong> to make all necessary changes.</li> </ol> <p>If you change the location of the <strong>bin-dir</strong> you will have to modify the run-scripts <strong>run-testcase[123].sh</strong>.</p> <p>Compilation</p> <p>Initially and whenever you change the code, the programs must be re-compiled</p> <ol> <li>In <strong>C++/bin</strong> just call <strong>make</strong></li> </ol> <p>Running the examples</p> <p>The programs are started in <strong>C++</strong>. For each of the test-case there is a skript to start the program.</p> <ol> <li>In <strong>C++</strong> call <strong>sh ./run-testcase1.sh</strong> (or <strong>sh ./run-testcase2.sh</strong>, etc.)</li> </ol> <p>Each script will start the programs several times. For <strong>Case I</strong>, <strong>Case II</strong> and <strong>Case IV</strong> the simulation is started on a sequence of finer and finer discretizations, for <strong>Case III</strong> the value of <em>tau</em> will be changed.</p> <p>The scripts store the output in <strong>C++/results</strong>. Old outputs will be overwritten! Further, the scripts read information about the reference solution from <strong>Python/resuts</strong>.</p> <p>The C++ programs use multithreading the OpenMP. If you do not specify the number of threads to be used, all available threads are taken including all hyperthreads. This is usually not efficient it is therefore advisable to set the number of threads by hand, e.g. by calling</p> <p><strong>export OMP_NUM_THREADS=8</strong></p> <p>before calling the run-scripts.</p> <p>License Information</p> <p>Initially the software has been written Thomas Richter, Otto-von-Guericke University Magdeburg, Germany in 2022, 2023 (thomas.richter@ovgu.de)</p> <p>You are free to use the scripts under the <em>Creative Commons Attribution 4.0 License</em>.</p>
Dataset: Core excitations and ionizations of uranyl in Cs2UO2Cl4 from relativistic embedded damped response time-dependent density functional theory and equation of motion coupled cluster calculations
<p>This dataset collects the unprocessed (= outputs from calculations) results discussed in the paper titled "Core excitations and ionizations of uranyl in Cs2UO2Cl4 from relativistic embedded damped response time-dependent density functional theory and equation of motion coupled cluster calculations", by Wilken Aldair Misael and Andre Severo Pereira Gomes. It also contains the figures used in the manuscript.</p>
Branching patterns in phylogenies cannot distinguish diversity-dependent diversification from time-dependent diversification
Open the record for dataset details and reuse information.
Responsiveness to cold snaps by turtle embryos depends on exposure timing and duration
Open the record for dataset details and reuse information.
Time dependent interaction modification generated from plant-soil feedback
Open the record for dataset details and reuse information.
Data and R code from: Relics of beavers past: time and population density drive scale-dependent patterns of ecosystem engineering
Open the record for dataset details and reuse information.
A statistical study on the local time dependence of equatorial spread F (ESF) irregularities and their relation to low latitude Es layers under geomagnetic storms
<p>The data can be downloaded from this site about our work.</p>
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.