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.

2,667

datasets available to search

ShareScore release 0.7.1

Reset

Dataset results

2,667 results for “Prevalence”

Learn how ShareScore rates datasets ↗
dryad40/100

Data for: Using spatial patterns of seeds and saplings to assess the prevalence of heterospecific replacements among cloud forest canopy tree species

Open the record for dataset details and reuse information.

publicSep 2021View details →
dryad40/100

Between a rock and a hard place: Comparing rock-dwelling animal prevalence across abandoned paddy, orchards, and rock outcrops in a biodiversity hotspot

Open the record for dataset details and reuse information.

publicJul 2023View details →
dryad40/100

Microbiome diversity and zoonotic bacterial pathogen prevalence in Peromyscus mice from agricultural landscapes and synanthropic habitat

Open the record for dataset details and reuse information.

publicFeb 2024View details →
dryad40/100

Data for: Prevalent fingerprint of marine macroalgae in Arctic surface sediments

Open the record for dataset details and reuse information.

publicJul 2023View details →
dryad40/100

The prevalence and correlates of depression and anxiety symptoms among older adults in Shenzhen, China

Open the record for dataset details and reuse information.

publicJan 2024View details →
dryad40/100

Data from: Habitat quality influences pollinator pathogen prevalence through both habitat–disease and biodiversity–disease pathways

Open the record for dataset details and reuse information.

publicOct 2022View details →
dryad40/100

Data and Code for: Resistance is futile: Weaker selection for resistance by abundant parasites increases prevalence and depresses host density

Open the record for dataset details and reuse information.

publicJan 2023View details →
dryad40/100

Data for: Parasite prevalence depends on female preference: Integrating parasite-mediated sexual selection and infectious disease dynamics

Open the record for dataset details and reuse information.

publicOct 2024View details →
dryad40/100

Effects of climate, soil, topography, and disturbance on liana prevalence

Open the record for dataset details and reuse information.

publicDec 2024View details →
dryad40/100

Data from: Honeybee visitation to shared flowers increases Vairimorpha ceranae prevalence in bumblebees

Open the record for dataset details and reuse information.

publicSep 2023View details →
dryad40/100

Climate change may make pine wilt disease more prevalent

Open the record for dataset details and reuse information.

publicSep 2024View details →
dryad40/100

Sand lizards (Lacerta agilis) decrease nymphal infection prevalence for tick-borne pathogens Borrelia burgdorferi sensu lato and Anaplasma phagocytophilum in a coastal dune ecosystem

Open the record for dataset details and reuse information.

publicMar 2023View details →
zenodo36/100

Prevalence data complementing the European Union One Health 2018 Zoonoses Report

<p>This dataset contains monitoring data on zoonoses and zoonotic agents under the Directive 2003/99/EC. This Directive requires Member Sates (MSs) to collect, evaluate and report data on zoonoses and zoonotic agents. MSs can also report monitoring data and information on some other pathogenic microbiological agentsin foodstuffs. Relevant EU legislation is:Commission Regulation (EC) No 2073/2005,Commission Regulation (EC) No 1441/2007, Commission Regulation (EU) No 1086/2011, Commission Regulation (EU) No 209/2013, Commission Regulation(EU) No 217/2014.</p>

opencc-by-4.0Dec 2019View details →
zenodo36/100

Sample based prevalence data complementing the European Union One Health 2018 Zoonoses Report

<p>This dataset contains monitoring sample based data on zoonoses and zoonotic agents under the Directive 2003/99/EC. This Directive requires Member Sates (MSs) to collect, evaluate and report data on zoonoses and zoonotic agents. MSs can also report monitoring data and information on some other pathogenic microbiological agentsin foodstuffs. Relevant EU legislation is:Commission Regulation (EC) No 2073/2005,Commission Regulation (EC) No 1441/2007, Commission Regulation (EU) No 1086/2011, Commission Regulation (EU) No 209/2013, Commission Regulation(EU) No 217/2014.&nbsp;</p>

opencc-by-4.0Dec 2019View details →
zenodo36/100

ekoraytascilar/naturecommunicationscovid: Data and analysis code to accompany "Patients with immune-mediated inflammatory diseases receiving cytokine inhibitors have low prevalence of SARS-CoV-2 seroconversion"

<p>This release contains raw datasets and analysis code for the research paper titled &quot;Patients with immune-mediated inflammatory diseases receiving cytokine inhibitors have low prevalence of SARS-CoV-2 seroconversion&quot;</p>

openother-openJul 2020View details →
dryad36/100

Data from: Age and sex prevalence estimate of Joubert Syndrome in Italy

Objective: To estimate the prevalence of Joubert syndrome (JS) in Italy applying standards of descriptive epidemiology, and to provide a molecular characterization of the described patients cohort. Methods: We enrolled all patients with a neuroradiologically confirmed diagnosis of JS and resident in Italy in 2018, and calculated age and sex prevalence, assuming a Poisson distribution. We also investigated the correlation between proband chronological age and age at diagnosis, and performed Next-Generation Sequencing (NGS) analysis on probands' DNA when available. Results: We identified 284 JS patients: the overall, female- and male-specific population-based prevalence rates were 0.47 (95% CI 0.41-0.53), 0.41 (95% CI 0.32-0.49) and 0.53 (95% CI 0.45-0.61) per 100,000 population, respectively. When considering only patients in the age range from 0 to 19 years, the corresponding population-based prevalence rates rose to 1.7 (95% CI 1.49-1.97), 1.62 (95% CI 1.31-1.99) and 1.80 (95% CI 1.49-2.18) per 100,000 population. NGS analysis allowed identifying the genetic cause in 131 out of 219 screened probands. Age at diagnosis was available for 223 probands, with a mean of 6.67 ± 8.10 years, and showed a statistically significant linear relationship with chronological age (r2=0.91; p&lt;0.001). Conclusions: We estimated for the first time the age and sex prevalence of JS in Italy, and investigated their genetic profile. The obtained population-based prevalence rate was approximately 10 times higher than that available in literature for children population.

opencc-zeroSep 2020View details →
dryad36/100

Coronavirus prevalence in Brazilian Amazon and Sao Paulo city

<p>SARS-CoV-2 spread rapidly in the Brazilian Amazon. Mortality was elevated, despite the young population, with the health services and cemeteries overwhelmed. The attack rate in this region is an estimate of the final epidemic size in an unmitigated epidemic. Here we show that by June, one month after the epidemic peak in Manaus, capital of the Amazonas state, 44% of the population had detectable IgG antibodies. This equates to a cumulative incidence of 52% after correcting for the false-negative rate of the test. Further correcting for the effect of antibody waning we estimate that the final attack rate was 66%. This is higher than seen in other settings, but lower than the predicted final size for an unmitigated epidemic in a homogeneously mixed population. This discrepancy may be accounted for by population structure as well as some limited physical distancing and non-pharmaceutical measures adopted in the city.</p>

opencc-zeroDec 2020View details →
dryad36/100

Data from: Genomic evidence of prevalent hybridization throughout the evolutionary history of the fig-wasp pollination mutualism

<p><i>Ficus</i> (figs) and their agaonid wasp pollinators present an ecologically important mutualism that also provides a rich comparative system for studying functional co-diversification throughout its coevolutionary history (~75 million years). We obtained entire nuclear, mitochondrial, and chloroplast genomes for 15 species representing all major clades of <i>Ficus</i>. Multiple analyses of these genomic data suggest that hybridization events have occurred throughout <i>Ficus</i> evolutionary history. Furthermore, cophylogenetic reconciliation analyses detect significant incongruence among all nuclear, chloroplast, and mitochondrial-based phylogenies, none of which correspond with any published phylogenies of the associated pollinator wasps. These findings are most consistent with frequent host-switching by the pollinators, leading to fig hybridization, even between distantly related clades. Here, we suggest that these pollinator host-switches and fig hybridization events are a dominant feature of fig/wasp coevolutionary history, and by generating novel genomic combinations in the figs have likely contributed to the remarkable diversity exhibited by this mutualism.</p>

opencc-zeroDec 2020View details →
dryad36/100

Prevalence of Batrachochytrium dendrobatidis and Batrachochytrium salamandrivorans in thre Hoang Lien Range, northwest Vietnam

<p>This study aims to investigate the presence of the amphibian chytrid fungi <i>Batrachochytrium dendrobatidis </i>(<i>Bd</i>) and<i> Batrachochytrium salamandrivorans </i>(<i>Bsal</i>)<i> </i>in the <a name="_Hlk45376654">Hoang Lien Range, northwest Vietnam </a>as well as any patterns in <i>Bd</i> infection in space, time and host species over a five-year sampling period. This study also aims to investigate the presence of <i>Bsal</i> in the Hoang Lien Range.</p>

opencc-zeroJan 2021View details →
zenodo36/100

Supporting publication for 'Prevalence sample-based guidance for reporting 2020 data'

<p>These two Excel documents help&nbsp;in mapping terms from the matrix catalogue ZOO_CAT_MATRIX used in the aggregated prevalence&nbsp;data model to FoodEx2 codes and offer&nbsp;examples on how prevalence data can be reported using SSD2.</p>

opencc-by-4.0Feb 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