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.
203
datasets available to search
ShareScore release 0.7.1
Dataset results
203 results for “Bayesian model”
A Bayesian Phylogenetic Hidden Markov Model for B Cell Receptor Sequence Analysis
<p>simulation and PC64/VRC01 input/output data files</p>
The reasonable application of Bayesian multi-model averaging to produce gross primary production with high quality in China
<p>To reduce the uncertainties of output data from the Multi-scale Terrestrial Model Intercomparison Project (MsTMIP), Bayesian Model Averaging (BMA) was trained by observed GPP from ChinaFLUX and a set of monthly 0.5° by 0.5° GPP data from 1948 to 2010 for China was produced.</p>
Data for "Bayesian inference for biophysical neuron models enables stimulus optimization for retinal neuroprosthetics"
<p>Experimental and precomputed data for the paper "Bayesian inference for biophysical neuron models enables stimulus optimization for retinal neuroprosthetics" by Oesterle et al. 2020 (DOI: <a href="https://doi.org/10.7554/eLife.54997">10.7554/eLife.54997</a>).</p> <p>The cone bipolar cell data has been described and published in the paper "Inhibition decorrelates visual feature representations in the inner retina" by Franke et al. 2017 (DOI: <a href="https://doi.org/10.1038/nature21394">10.1038/nature21394</a>). </p> <p>This data is both a supplement to the Oesterle et al. paper and the code for this paper.</p> <p>The code is available in this <a href="http://github.com/berenslab/CBC_inference">GitHub repository</a>.</p> <p>We recommend downloading the GitHub repository and to follow the instructions there.</p>
Standard Bouguer anomaly model achieved by multi-source Bouguer gravity anomaly Bayesian data fusion algorithm in Sichuan-Yunnan region
<p>* Method: Based on the equivalent source inversion and Bayesian uncertainty quantization theory, a new multi-source gravity data fusion algorithm is developed, which effectively solves the multi-source data fusion problem with different noise and datum.</p> <p>* Standard Bouguer anomaly is Fused from WGM2012 Bouguer gravity anomaly model and 394 gravity profile data measured in Sichuan-Yunnan region. Fusion anomaly results can eliminate datum draft between multi-source gravity and reduce incoherent noise.</p> <p>* Spatial resolution of the standard Bouguer anomaly is about 20 kilometers.</p> <p>* Correcting deviations means the difference between the fused standard Bouguer anomaly model and the WGM2012 Earth gravity model.</p>
All simulation results, figures and code regarding the manuscript: Calibrating models of cancer invasion: parameter estimation using Approximate Bayesian Computation and gradient matching
<p>We present two different methods to estimate parameters within a partial differential equation (PDE) model of cancer invasion. The model describes the spatio-temporal evolution of three variables -- tumour cell density, extracellular matrix density and matrix degrading enzyme concentration -- in a one-dimensional tissue domain. The first method is a likelihood-free approach associated with Approximate Bayesian Computation (ABC); the second is a two-stage gradient matching method based on smoothing the data with a Generalized Additive Model (GAM) and matching gradients from the GAM to those from the model. Both methods performed well on simulated data. To increase realism, additionally we tested the gradient matching scheme with simulated measurement error and found that the ability to estimate some model parameters deteriorated rapidly as measurement error increased.</p>
Data from: Refining trophic dynamics through multi-factor Bayesian mixing models: a case study of subterranean beetles.
<p>Food web dynamics are vital in shaping the functional ecology of ecosystems. However, trophic ecology is still in its infancy in groundwater ecosystems due to the cryptic nature of these environments. To unravel trophic interactions between subterranean biota, we applied an interdisciplinary Bayesian mixing model design (multi-factor BMM) based on the integration of faunal C and N bulk tissue stable isotope data (δ<sup>13</sup>C and δ<sup>15</sup>N) with radiocarbon data (Δ<sup>14</sup>C), and prior information from metagenomic analyses. We further compared outcomes from multi-factor BMM with a conventional isotope double proxy mixing model (SIA BMM), triple proxy (δ<sup>13</sup>C, δ<sup>15</sup>N and Δ<sup>14</sup>C, multi-proxy BMM) and double proxy combined with DNA prior information (SIA+DNA BMM) designs. Three species of subterranean beetles (<i>Paroster macrosturtensis</i>, <i>Paroster mesosturtensis</i> and <i>Paroster microsturtensis</i>) and their main prey items Chiltoniidae<i> </i>amphipods (AM1: <i>Scutachiltonia axfordi</i> and AM2: <i>Yilgarniella sturtensis</i>), cyclopoids and harpacticoids from a calcrete in Western Australia were targeted. Diet estimations from stable isotope only models indicated homogeneous patterns with modest preferences for amphipods as prey items. Multi-proxy BMM suggested increased - and species-specific - predatory pressures on amphipods coupled with high rates of scavenging/predation on sister species. SIA+DNA BMM showed marked preferences for amphipods AM1 and AM2 and reduced interspecific scavenging/predation on <i>Paroster </i>species. Multi-factorial BMM revealed the most precise estimations (lower overall SD and very marginal beetles' interspecific interactions), indicating consistent preferences for amphipods AM1 in all the beetles' diets. Incorporation of genetic priors allowed crucial refining of the feeding preferences, while integration of more expensive radiocarbon data as a third proxy (when combined with genetic data) produced more precise outcomes but close dietary reconstruction to that from SIA+DNA BMM. Further multidisciplinary modelling from other groundwater environments will help elucidate the potential behind these designs and bring light to the feeding ecology of one the most vital ecosystems worldwide.</p>
Data from: Disentangling elevational richness: a multi-scale hierarchical Bayesian occupancy model of Colorado ant communities
Understanding the forces that shape the distribution of biodiversity across spatial scales is central in ecology and critical to effective conservation. To assess effects of possible richness drivers, we sampled ant communities on four elevational transects across two mountain ranges in Colorado, USA, with seven or eight sites on each transect and twenty repeatedly sampled pitfall trap pairs at each site each for a total of 90 days. With a multi-scale hierarchical Bayesian community occupancy model, we simultaneously evaluated the effects of temperature, productivity, area, habitat diversity, vegetation structure, and temperature variability on ant richness at two spatial scales, quantifying detection error and genus-level phylogenetic effects. We fit the model with data from one mountain range and tested predictive ability with data from the other mountain range. In total, we detected 105 ant species, and richness peaked at intermediate elevations on each transect. Species-specific thermal preferences drove richness at each elevation with marginal effects of site-scale productivity. Trap-scale richness was primarily influenced by elevation-scale variables along with a negative impact of canopy cover. Soil diversity had a marginal negative effect while daily temperature variation had a marginal positive effect. We detected no impact of area, land cover diversity, trap-scale productivity, or tree density. While phylogenetic relationships among genera had little influence, congeners tended to respond similarly. The hierarchical model, trained on data from the first mountain range, predicted the trends on the second mountain range better than multiple regression, reducing root mean squared error up to 65%. Compared to a more standard approach, this modeling framework better predicts patterns on a novel mountain range and provides a nuanced, detailed evaluation of ant communities at two spatial scales.
Bayesian inference of ancestral host-parasite interactions under a phylogenetic model of host repertoire evolution
<p>Intimate ecological interactions, such as those between parasites and their hosts, may persist over long time spans, coupling the evolutionary histories of the lineages involved. Most methods that reconstruct the coevolutionary history of such interactions make the simplifying assumption that parasites have a single host. Many methods also focus on congruence between host and parasite phylogenies, using cospeciation as the null model. However, there is an increasing body of evidence suggesting that the host ranges of parasites are more complex: that host ranges often include more than one host and evolve via gains and losses of hosts rather than through cospeciation alone. Here, we develop a Bayesian approach for inferring coevolutionary history based on a model accommodating these complexities. Specifically, a parasite is assumed to have a host repertoire, which includes both potential hosts and one or more actual hosts. Over time, potential hosts can be added or lost, and potential hosts can develop into actual hosts or vice versa. Thus, host colonization is modeled as a two-step process that may potentially be influenced by host relatedness. We first explore the statistical behavior of our model by simulating evolution of host-parasite interactions under a range of parameter values. We then use our approach, implemented in the program RevBayes, to infer the coevolutionary history between 34 Nymphalini butterfly species and 25 angiosperm families. Our analysis suggests that host relatedness among angiosperm families influences how easily Nymphalini lineages gain new hosts.</p>
Figure 2. - Bayesian (GTR+Γ+I and HKY+Γ models) and maximum likelihood 50% majority-rule consensus tree. Numbers in the nodes represent posterior probabilities (GTR+Γ+I and HKY+Γ, respectively), and bootstrap value for maximum likelihood and parsimony analyses, respectively. c1–Bragança, Pará; c2–Santa Maria do Pará, Pará; c3–National Forest of Amapá, Amapá; c4–Belém, Pará; i1–Solimões River, near Manaus, Amazonas; i2–Xingu River, Altamira, Pará; i3 and i4–Itacoatiara, Amazonas. MYBP–million years before present.
Figure 2. - Bayesian (GTR+Γ+I and HKY+Γ models) and maximum likelihood 50% majority-rule consensus tree. Numbers in the nodes represent posterior probabilities (GTR+Γ+I and HKY+Γ, respectively), and bootstrap value for maximum likelihood and parsimony analyses, respectively. c1–Bragança, Pará; c2–Santa Maria do Pará, Pará; c3–National Forest of Amapá, Amapá; c4–Belém, Pará; i1–Solimões River, near Manaus, Amazonas; i2–Xingu River, Altamira, Pará; i3 and i4–Itacoatiara, Amazonas. MYBP–million years before present.
Reduced optical data for Bayesian model trial
<p>The dataset is a subset of a few selected optical indices from the column experiment. </p> <p>The dataset contains all the observations after the column reversal, with day00 indicating the day before the reversal where all the columns are samplead and day0 indicating the day of the reversal. It does not contain any of the control measurements before day00. </p> <p>From the absorbance and fluoresence measurements, we have calculated several indices among which bix (biological index), fi (fluoresence index), hix, (humification index), a254 (decadal absorption coefficient at 254 nm) ,E2_E3 (ratio of absorbance E2 to E3) , SR (slope ratio). All of the indices are calcuated using the StaRdom package from the raw data. </p> <p>Sample name is in the samplingDay_replicate_columnNo format. </p>
Dataset: Testing for effects of growth rate on isotope trophic discrimination factors and evaluating the performance of Bayesian stable isotope mixing models experimentally: a moment of truth?
<p><span>Discerning assimilated diets of wild animals using stable isotopes is well established where potential dietary items in food webs are isotopically distinct. With the advent of mixing models, and Bayesian extensions of such models (Bayesian Stable Isotope Mixing Models, BSIMMs), statistical techniques available for these efforts have been rapidly increasing. The accuracy with which BSIMMs quantify diet, however, depends on several factors including uncertainty in tissue discrimination factors (TDFs; <em>Δ</em>) and identification of appropriate error structures. Whereas performance of BSIMMs has mostly been evaluated with simulations, here we test the efficacy of BSIMMs by raising domestic broiler chicks (<em>Gallus gallus domesticus</em>) on four isotopically distinct diets under controlled environmental conditions, ideal for evaluating factors that affect TDFs and testing how BSIMMs allocate individual birds to diets that vary in isotopic similarity. For both liver and feather tissues,<em> δ</em><sup>13</sup>C and <em>δ </em><sup>15</sup>N values differed among dietary groups. <em>Δ</em><sup>13</sup>C of liver, but not feather, was negatively related to the rate at which individuals gained body mass. For <em>Δ</em><sup>15</sup>N, we identified effects of dietary group, sex, and tissue type, as well as an interaction between sex and tissue type</span><span><span>, </span></span><span><span>with f</span></span><span>emales having higher liver <em>Δ</em><sup>15</sup>N relative to males. For both tissues, BSIMMs allocated most chicks to correct dietary groups, especially for models using combined TDFs rather than diet specific TDFs, and those applying a multiplicative error structure. These findings provide new information on how biological processes affect TDFs and confirm that adequately accounting for variability in consumer isotopes is necessary to optimize performance of BSIMMs. Moreover, they demonstrate experimentally that these types of models reliably characterize consumed diets when appropriately parameterized.<span> </span></span></p>
A Clustering Approach to Improve IntraVoxel Incoherent Motion Maps from DW-MRI using Conditional Auto-Regressive Bayesian Model
<p>Simulated data generated and used in the paper "A Clustering Approach to Improve IntraVoxel Incoherent Motion Maps from DW-MRI using Conditional Auto-Regressive Bayesian Model" are here available.</p> <p>Results generated from both simulated and clinical datasets are also available on the excel tables.</p>
Data from: Mental health ecosystem of Gipuzkoa (2015) for Bayesian network modelling
<p>This dataset include data from Mental Health network of Gipuzkoa (Spain). It is included information on resources (inputs) and outcomes (outputs) of care, which are described in the manuscript: "Almeda, N., Garcia-Alonso, C. R., Gutierrez-Colosia, M. R., Salinas-Perez, J. A., Iruin-Sanz, A., & Salvador-Carulla, L. (2022). Modelling the balance of care: Impact of an evidence-informed policy on a mental health ecosystem. PLoS ONE, 17(1 January), 1–16. https://doi.org/10.1371/journal.pone.0261621". This manuscript has been published in Plos One journal.</p> <p>This research focused on developing a formal causal model based on Bayesian network prototypes which were designed by formalizing expert knowledge (by using Expertbased Cooperative Analysis) and resulting in Direct Acyclic Graphs. The best Bayesian networks and their corresponding regression models were used to estimate the statistical ranges or confidence intervals for the dependent variable (potential effect, consequence, or output) given the independent variable values. These ranges, adjusted to delimited statistical distributions (triangular, trapezoidal and gamma), were managed by a Monte Carlo simulation engine for intervention assessment. A computer-based Decision Support System (DSS) was used to assess the status of ecosystem performance: RTE, statistical stability and entropy.</p> <p>Main results of the analyses pointed out that by combining causal reasoning and statistical methods, decision makers can obtain a deep view of both pre-implementing and post-implementing situations. Knowing the causal levers, it is possible to act directly to the causes in order to potentially produce de appropriate results considering the uncertainty: to provide a more balanced and integrated MH care provision in the community. In this particular case, an improvement in the outpatient workforce increases both ecosystem performance (RTE) and stability and slightly decreases entropy.</p>
Forecasting suppression of invasive Sea Lamprey in Lake Superior: data and code for Bayesian forecast model
<p>Resource managers frequently are tasked with mitigating or reversing adverse effects of invasive species through management policies and actions. In Lake Superior, of the Laurentian Great Lakes, invasive sea lamprey populations are suppressed to protect valuable fish stocks. However, the relationship between choice of long-term control strategy and the future chance of achieving the suppression target is unclear.</p> <p>Using a 60+ year time-series of suppression effort and monitoring data from 50 assessment sites located on Lake Superior tributaries, we developed a Bayesian state-space model to forecast the probability of suppressing lamprey below the suppression target.</p> <p>With annual application of lampricide (i.e., lamprey-specific pesticide) at historical mean levels, we forecasted a 15% chance of achieving the Lake Superior sea lamprey suppression target in 2040.</p> <p>Increasing lampricide effort and/or supplementing lampricide control with age-1 recruitment reduction increased suppression chance. Annual application of the maximum historical lampricide effort resulted in a 50% predicted chance of achieving the target, annual application of the mean historic lampricide effort plus a 40% reduction in recruitment resulted in a 54% chance, and the maximum amount of effort considered (maximum historic lampricide and 60% reduction in recruitment) resulted in a 94% chance.</p> <p><em><a>Policy </a>implications</em>. <a>We</a> developed a simulation model from a robust, long-term monitoring dataset that improves understanding of why long-term sea lamprey suppression objectives have been difficult to achieve in Lake Superior. Furthermore, the model provides a means to gauge efficacy of sea lamprey control policy and action scenarios based on forecasted chance of achieving the suppression target. Creating processes for iteratively refining our forecasting model with stakeholder and technical-expert input and integration with a decision analysis framework could strengthen the link between ecological knowledge obtained from long-term monitoring and invasive sea lamprey management.</p>
Consensus nucleotide sequences for env and gag for paper: Insights to HIV-1 coreceptor usage by estimating HLA adaptation with Bayesian generalized linear mixed models
<p>This is the consensus sequence repository to the manuscript "Insights to HIV-1 coreceptor usage by estimating HLA adaptation with Bayesian generalized linear mixed models".<br> It contains the 10% consensus nucleotide sequences of the env and gag (only p24) protein of HIV-1 used for the training and leftout data set. The NGS sequences are available under BioProject ID PRJNA810303 and the corresponding BioSample Accession IDs are SAMN26241863:26242168 and SAMN28728524:SAMN28728529</p> <ul> <li>env_leftout.fasta <ul> <li>A fasta file that contains the consensus nucleotide sequences for the env protein for the leftout data set</li> </ul> </li> <li>env_nt_274.fasta <ul> <li>A fasta file that contains the consensus nucleotide sequences for the env protein for the training data set</li> </ul> </li> <li>gag_leftout.fasta <ul> <li>A fasta file that contains the consensus nucleotide sequences for the gag protein for the leftout data set</li> </ul> </li> <li>gag_nt_274.fasta <ul> <li>A fasta file that contains the consensus nucleotide sequences for the gag protein for the training data set</li> </ul> </li> </ul>
Data and code: Bayesian Multi-level model calibration of the SPASS phenology model for silage maize
<p>Data and code supporting the research article: Bayesian Multi-level model calibration of the SPASS phenology model for silage maize - M. Viswanathan, A. Scheidegger, T. Streck, S. Gayler, T.K.D. Weber. This includes R code for the implementation of the SPASS phenology maize model; Jags in R to implement the Bayesian multi-level models .</p>
Data for publication of "Gaussian process regression-based Bayesian optimisation (G-BO) of model parameters - a WRF model case study of southeast Australia heat extremes"
<p>Implementation of Gaussian process regression-based Bayesian optimisation (G-BO) using the emcee package (<a href="https://emcee.readthedocs.io/en/stable/" rel="nofollow">https://emcee.readthedocs.io/en/stable/</a>).</p> <p>For more information about the implementation of G-BO in optimising the Weather Research and Forecasting (WRF) model parameters, please refer to the paper - <a href="https://essopenarchive.org/doi/full/10.22541/essoar.171292045.52489731" rel="nofollow">Gaussian process regression-based Bayesian optimisation (G-BO) of model parameters - a WRF model case study of southeast Australia heat extremes</a>.</p> <p><code>G-BO_script.ipynb</code> implements the GPR-based Bayesian optimisation using the Affine Invariant Markov chain Monte Carlo (MCMC) Ensemble sampler.</p> <ul> <li><strong>QMC_sobol_samples</strong>: This file contains the 128 parameter samples across the parameter space of three sensitive parameters utilizing the Quasi Monte-Carlo (QMC) Sobol sequence design.</li> <li><strong>nmae_all_128_ens_T_Rh</strong>: This file contains the normalised mean absolute error (NMAE) values of temperature (T) and relative humidity (Rh) of the 128 parameter sample WRF simulations. For more details, please refer to <a href="https://essopenarchive.org/doi/full/10.22541/essoar.171292045.52489731" rel="nofollow">this link</a>.</li> </ul>
Improved estimation of the prevalence of bovine cysticercosis and the diagnostic test characteristics in the absence of a reference standard using Bayesian Latent Class models, the example of Jimma and Ambo Abattoirs, Ethiopia
<p>Bovine cysticercosis is an infection of cattle musculature with the cestode parasite of humans known as Taenia saginata. This bovine cysticercosis data was collected from two Ambattoirs in Ethiopia namely Ambo and Jimma. Dissection of the predilection site, Ag-ELISA, and meat inspection were the diagnostic methods employed. Cysticerci collected during dissection of the predilection site were also confirmed using multiplex PCR. </p>
Code + simulated + publically accessable data for "Evaluating health facility access using Bayesian spatial models and location analysis methods"
<p># README</p> <p>These files contain r data objects and R files that represent the key details of the paper, "Evaluating health facility access using Bayesian spatial models and location analysis methods".</p> <p>The following datasources are available for simulation of some of the ideas in the paper.</p> <p>- dat_grid_sim: simulated data of the grid and grid cells<br> - dat_ohca_cv_sim: simulated data containing the cross validated test/training sets of OHCA data<br> - dat_ohca_sim: simulated OHCA event data<br> - dat_aed_sim: simulated AED location data<br> - dat_bldg_sim: simulated building location data<br> - dat_municipality_sim: simulated municipality information<br> - table_1: Table 1 information containing key demographic data</p> <p>These data were produced using the code in 01-create-sim-data.R, and one of the statistical models is demonstrated in 02-demo-inla-model.R</p> <p>In terms of the paper itself, the functions and code used in the manuscript are located in:</p> <p>* 01_tidy.Rmd - analysis code used to tidy up the data</p> <p>* 02_fit_fixed_all_cv.Rmd - analysis code used to place AEDs</p> <p>* 02_model.Rmd - analysis code used to fit the model in INLA</p> <p>* 03_manuscript.Rmd - Full code and text used to create the paper</p> <p>* 04_supp_materials.Rmd - full code and text used to create the supplementary materials</p> <p>The following files are a part of an R package "swatial" that was developed along with the paper. These files are:</p> <p>* DESCRIPTION</p> <p>* NAMESPACE</p> <p>* LICENSE</p> <p>* LICENSE.md</p> <p>* decay.R</p> <p>* spherical-distance.R</p> <p>* test-figure-data-matches.R</p> <p>* test-table-data-matches.R</p> <p>* testthat.R</p> <p>* tidy-inla.R</p> <p>* tidy-posterior-coefs.R</p> <p>* tidy-predictions.R</p> <p>* utils-pipe.R</p> <p>* All files that end in .Rd are documentation files for the functions.</p> <p>## Regarding data sources</p> <p>Census information for Ticino was transcribed from the Annual Statistical Report of Canton Ticino from years 2010 to 2015. This data was taken from their publicly accessible annual reports - for example: (https://www3.ti.ch/DFE/DR/USTAT/allegati/volume/ast_2015.pdf). The raw data was extracted from these annual reports, and placed into the file: "swiss_census_popn_2010_2015.xlsx". These data are put into analysis ready format in the file “01_tidy.Rmd”</p> <p>Housing and other relevant geospatial data can be accessed via http://map.housing-stat.ch/ and https://data.geo.admin.ch/. The maps of buildings from the REA (Register of Buildings and Dwellings) can be found here: https://map.geo.admin.ch/?zoom=11&bgLayer=ch.swisstopo.pixelkarte-grau&lang=en&topic=ech&layers=ch.bfs.gebaeude_wohnungs_register,ch.swisstopo.swissboundaries3d-gemeinde-flaeche.fill,ch.bfs.volkszaehlung-gebaeudestatistik_gebaeude,ch.bfs.volkszaehlung-gebaeudestatistik_wohnungen,ch.swisstopo.swissbuildings3d_1.metadata,ch.swisstopo.swissbuildings3d_2.metadata&E=2717616.28&N=1096597.25&catalogNodes=687,696&layers_timestamp=,,2016,2016,,&layers_visibility=true,false,false,false,false,false&layers_opacity=1,1,1,1,1,0.75</p> <p>For further enquiries on this data, contact the Swiss federal Office of Statistics at the details listed here: https://www.bfs.admin.ch/bfs/en/home/services/contact.html</p> <p>The shapefiles of the Comuni can be accessed here: https://www4.ti.ch/dfe/de/ucr/documentazione/download-file/?noMobile=1</p> <p>Data from the people living in the Municipalities in Ticino can be downloaded here: https://www3.ti.ch/DFE/DR/USTAT/index.php?fuseaction=dati.home&tema=33&id2=61&id3=65&c1=01&c2=02&c3=02</p> <p>## Future work</p> <p>In the future, these functions from the paper may be generalised and put into their own package. If that happens, this repository will be updated with a link to updated functions.</p>
Bayesian hierarchical model gridded solar-induced fluorescence (BHM gridded SIF) data product
<p>This archive provides the solar-induced fluorescence (SIF) data product documented in "Estimation of solar-induced chlorophyll fluorescence using Bayesian hierarchical regression". The archive includes daily NetCDF files with the global gridded SIF estimates and associated uncertainties.</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.