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806 results for “cavities”

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geo24/100

Response of Streptococcus mutans wild type and lrgAB-deficient strains to environemntal stressors encountered in the oral cavity

GEO Series GSE84427. Streptococcus mutans. 24 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenDec 2016View details →
geo24/100

Phylotranscriptomics reveals the convergent evolution of aggression is associated with both shared and unique patterns of gene expression evolution in cavity nesting songbirds

GEO Series GSE244480. Passer domesticus; Turdus migratorius; Troglodytes aedon; Thryothorus ludovicianus; Sialia sialis; Protonotaria citrea; Hirundo rustica; Passer montanus; Tachycineta bicolor; Setophaga petechia. 121 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenApr 2025View details →
geo24/100

BCR heavy and light chain repertoire sequencing of pertitoneal cavity B-1a cells from wild-type and Igll1 knockout mice

GEO Series GSE104111. Mus musculus. 10 samples. Type: Other.

openGEO-OpenJan 2018View details →
geo24/100

Differentially expressed genes in recurrence of squamous cell carcinoma tumors of the oral cavity in a mouse model

GEO Series GSE35377. Mus musculus. 12 samples. Type: Expression profiling by array.

openGEO-OpenJan 2012View details →
zenodo24/100

On the Internal Flow at the Water Entry Cavity--data

<p>A set of raw PIV images are presented to support our findings,&nbsp; please contact the author for more resources.</p>

opencc-by-4.0Mar 2020View details →
dryad24/100

Data from: Flower preferences and pollen transport networks for cavity nesting solitary bees: implications for the design of agri-environment schemes

Floral foraging resources are valuable for pollinator conservation on farmland, and their provision is encouraged by agri-environment schemes in many countries. Across Europe, wildflower seed mixtures are widely sown on farmland to encourage pollinators, but the extent to which key pollinator groups such as solitary bees exploit and benefit from these resources is unclear. We used high-throughput sequencing of 164 pollen samples extracted from the brood cells of 6 common cavity nesting solitary bee species (Osmia bicornis, Osmia caerulescens, Megachile versicolor, Megachile ligniseca, Megachile centuncularis and Hylaeus confususi) which are widely distributed across the UK and Europe. We documented their pollen use across 19 farms in southern England, UK, revealing their forage plants and examining the structure of their pollen transport networks. Of the 32 plant species included currently in sown wildflower mixes, 15 were recorded as present within close foraging range of the bees on the study farms, but only Ranunculus acris L. was identified within the pollen samples. Rosa canina L. was the most commonly found of the 23 plant species identified in the pollen samples, suggesting that, in addition to providing a nesting resource for Megachile leafcutter bees, it may be an important forage plant for these species. Higher levels of connectance and nestedness were characteristic of pollen transport networks on farms with abundant floral resources, which may increase resilience to species loss. Our data suggest that plant species promoted currently by agri-environment schemes are not optimal for solitary bee foraging. If a diverse community of pollinators is to be supported on UK and European farmland, additional species such as Rosa canina should be encouraged to meet the foraging requirements of solitary bees.

opencc-zeroDec 2017View details →
zenodo24/100

Level attraction and idler resonance in a strongly driven Josephson cavity

<p>This contains the data and processing scripts used for the figures of the manuscript&nbsp;of &quot;Level attraction and idler resonance in a strongly driven Josephson cavity&quot;</p>

opencc-by-4.0Oct 2021View details →
zenodo24/100

Data obtained by placing a multimodal interference filter inside a laser cavity, both with and without graphene

<p>The data shown here were obtained by coating a multimodal interference optical fiber filter with graphene. The data are divided into the following stages:</p> <ul> <li>Spectrum of the multimodal interference filter inside the laser cavity at different pump powers.</li> <li>Spectrum of the multimodal interference filter coated with graphene and PMMA inside the laser cavity at different pump powers.</li> <li>Spectrum of the multimodal interference filter coated with graphene inside the laser cavity at different pump powers.</li> </ul> <p>Additionally, the pulses generated by the laser cavity were obtained in the stages described above.</p>

restrictedcc-by-4.0Oct 2024View details →
zenodo24/100

Direct production of fermionic superfluids in a cavity-enhanced optical dipole trap

<p>Data corresponding to the article "Direct production of fermionic superfluids in a cavity-enhanced optical dipole trap".</p>

opencc-by-4.0Nov 2024View details →
dryad24/100

Orientation, latitude, and elevation of 1501 cavities excavated by 25 avian species across 12 terrestrial ecoregions (15°S – 55°S) in South America.

<p><span><span>In the Northern Hemisphere, several avian cavity excavators (e.g., woodpeckers) orient their cavities increasingly toward the equator as latitude increases (i.e., farther north), and it is proposed that they do so to take advantage of incident solar radiation at their nests. If latitude is a key driver of cavity orientations globally, this pattern should extend to the Southern Hemisphere. Here, we test the prediction that cavities are oriented increasingly northward at higher (i.e., colder) latitudes in the Southern Hemisphere and describe the preferred entrance direction(s) of 1501 cavities excavated by 25 avian species (<i>n</i> = 22 Picidae, 2 Trogonidae, 1 Furnariidae) across 12 terrestrial ecoregions (15°S – 55°S) in South America. We used Bayesian projected normal mixed-effects models for circular data to examine the influence of latitude, and potential confounding factors, on cavity orientation. Also, a probability model-selection procedure was used to simultaneously examine multiple orientation hypotheses in each ecoregion to explore underlying cavity-orientation patterns. Contrary to predictions, and patterns from the Northern Hemisphere, birds did not orient their cavities more toward the equator with increasing latitude, suggesting that latitude may not be an important underlying selective force shaping excavation behavior in South America. Moreover, unimodal cavity-entrance orientations were not frequent among the ecoregions analyzed (only in four ecoregions), whereas bimodal (in five ecoregions) or uniform (in three ecoregions) orientations were also present, although many of these patterns were not very clear. Our results highlight the need to include data from under-studied biotas and regions to improve inferences at macroecological scales. Furthermore, we suggest a re-analysis of Northern Hemisphere cavity orientation patterns using a multi-model approach, and a more comprehensive assessment of the role of environmental factors as drivers of cavity orientation at different spatial scales in both hemispheres.</span></span></p>

opencc-zeroAug 2021View details →
zenodo24/100

Dataset related to the publication "Procedure for robust assessment of cavity deformation in Fabry–Pérot based refractometers"

<p>The data set consists of; The published paper, all figures that present measurement or simulation data in .png and .fig format and the underlying data plotted in the figures in text format.&nbsp; The published plots were generated from the fig files. The text files were generated by reading the plotted data from the fig files. The files are named Fig_XX were XX corresponds to the figure number in the publication.&nbsp; The format of the text file is as follows. Before every data set there is a header consisting of; The number of the subplot where the data is plotted (Plot: XX), the number of the data set in the sub plot (DataSet: XX), and the color of the line or marker in the plot (Color: XX). The description of what each color represents can be found in the publication.</p>

opencc-by-4.0Aug 2020View details →
zenodo24/100

Parameters for the solvated KcsA-K+-LAB-TEA, when LAB-TEA place in cytoplasmic region and K+-ion inside the cavity

<p>Parameters for the solvated KcsA-K<sup>+</sup>-LAB-TEA. These KcsA-K<sup>+</sup>-LAB-TEA systems were solvated by truncated octahedron TIP3PBOX, using the leap program in AMBER20. The LAB-TEA is placed in the cytoplasmic region and K<sup>+</sup>-ion inside the channel cavity.</p>

opencc-by-4.0Aug 2023View details →
zenodo24/100

MITgcm model setup and output for "Submesoscale variability and basal melting in ice shelf cavities of the Amundsen Sea"

<p>Here, it contains the results of the high-res eastern AMS simulation. A detailed description of the model configuration and model output is provided by Nakayama et al.,2019.</p><p>Nakayama, Yoshihiro, Georgy Manucharyan, Hong Zhang, Pierre Dutrieux, Hector S. Torres, Patrice Klein, Helene Seroussi, Michael Schodlok, Eric Rignot, and Dimitris Menemenlis. "Pathways of ocean heat towards Pine Island and Thwaites grounding lines." <i>Scientific reports</i> 9, no. 1 (2019): 16649.</p><p>Due to space limitations, please access NASA data for all other model daily outputs (Registration is required). &nbsp;https://ecco.jpl.nasa.gov/drive/files/ECCO2/High_res_PIG/AMS_200m.&nbsp;</p><p>Contents can be downloaded easily using wget (see link below).<br>https://ecco-group.org/docs/wget_download_multiple_files_and_directories.pdf</p><p>(Contents)<br>code.zip (code to run this simulation)<br>input_ctrl.zip (input file required for this simulation&nbsp;<br>input_nomelt.zip (input file required for this simulation&nbsp;<br>results_ctrl.zip (days 30 and 60))<br>results_nomelt.zip (days 30 and 60))<br>Caution: You need to download heavier input files to rerun this simulation from ECCO-Drive.&nbsp;<br><br>(How to build and run)<br>mkdir build<br>./../../tools/genmake2 -of ../../../tools/build_options/linux_amd64_ifort+mpi_ice_nas -mpi -mods ../code/<br>make depend<br>make -j 16<br>cd ..<br>mkdir test<br>cd test<br>ln -sf ../input/* .<br>ln -sf /nobackup/hzhang1/forcing/era_xx_it33/ .<br>cp ../build/mitgcm_uv .<br>qsub run8_sandy_tracer_init_cont_2.pbs</p>

opencc-by-4.0Oct 2023View details →
ClinicalTrials.gov24/100

Procedure-Specific Approach To Minimize Fistulaization of The Perianal Abscess Cavity After Surgical Drainage

ClinicalTrials.gov study NCT06527833. IPD Sharing: NO. Countries: 1. Publications: 0.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov24/100

Original Protocol of Oral Cavity Care During Long-term Mechanical Ventilation

ClinicalTrials.gov study NCT05146817. IPD Sharing: NO. Countries: 1. Publications: 0.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov24/100

Malnutrition is Not a Risk Factor for Free Flap Failure in the Oral Cavity

ClinicalTrials.gov study NCT04069650. IPD Sharing: Not stated. Countries: 1. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov24/100

Radioguided Selective Neck Dissection for Staging and Treatment of Oral Cavity and Oropharyngeal Squamous Cell Carcinoma

ClinicalTrials.gov study NCT03727594. IPD Sharing: Not stated. Countries: 1. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov24/100

Clinical Evaluation of Self-Adhesive Bulk-Fill Composite Versus Conventional Nano-hybrid Composite in Cervical Cavities

ClinicalTrials.gov study NCT06394440. IPD Sharing: YES. Countries: 1. Publications: 0.

controlledIPD-YESFeb 2026View details →
ClinicalTrials.gov24/100

Quality of Life and Development of Measures in Patients With Cancer of the Oral Cavity

ClinicalTrials.gov study NCT00582413. IPD Sharing: Not stated. Countries: 1. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov24/100

Vaccine Therapy for Patients With Stage IIIC-IV Ovarian Epithelial, Fallopian Tube, or Primary Peritoneal Cavity Cancer

ClinicalTrials.gov study NCT02111941. IPD Sharing: Not stated. Countries: 1. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →

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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