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230 results for “Data Aggregation”

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zenodo28/100

Data related to the manuscript "Sequence-specific aggregation of magnetic nanoparticles and single-stranded DNA amplification products for detection of antibiotic resistance gene sul1."

<p>Absorbance and AC&nbsp;susceptometry raw and processed excel files used.</p>

opencc-by-4.0Mar 2022View details →
zenodo28/100

Supplementary material 1 from: Martin-Cabrera P, Perez Perez R, Irrison J-O, Lombard F, Ove Möller K, Rühl S, Creach V, Lindh M, Stemmann L, Schepers L (2022) Establishing Plankton Imagery Dataflows Towards International Biodiversity Data Aggregators. Biodiversity Information Science and Standards 6: e94196. https://doi.org/10.3897/biss.6.94196

Imagery dataset example

opencc-zeroSep 2022View details →
zenodo28/100

Replication Package for: Scalable and Reliable Multi-Dimensional Aggregation of Sensor Data Streams

<p>This repository contains a replication package and experimental results for our study on <em>Scalable and Reliable Multi-Dimensional Aggregation of Sensor Data Streams</em>.</p> <p>It features the presented implementation with Kafka Streams, tools for load generation and data collection, scripts for executing the presented evaluations as well as our raw results and script for analysis. A detailed description is given in the top-level README.md file.</p>

opencc-by-4.0Dec 2019View details →
zenodo28/100

Supporting data for Liquid fragmentation induced by particle aggregation during two-phase flow in 3D porous media

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opencc-by-4.0Oct 2024View details →
dryad28/100

Data from: Aggregation but not organo-metal complexes contributed to C storage in tidal freshwater wetland soils

One of the many goals of wetland restoration is to promote the long-term storage of carbon (C) in the terrestrial biosphere. Unfortunately, soil C reservoirs in restored wetlands are slow to accumulate even after hydrology and plant communities are reestablished. Oftentimes wetland restoration changes the soil matrix and thus can dramatically alter how soil C is stored and processed. Our research investigated whether soil organic matter (SOM) preservation theories derived from studies in non-wetland soil systems can be extended to wetland soils. We examined C associated with water-stable soil aggregates, minerals, and metal oxides within habitats of one natural and one restored tidal freshwater wetland. This study revealed that a majority of the soil C in the natural site was associated with large macroaggregates (&gt; 2000 μm), and soils from the restored site stored more C in small macroaggregates (&gt; 250 to &lt; 2000 μm). Despite these different associations, the chemical composition of SOM followed similar patterns across each aggregate-size class. Results from the sequential extraction procedure suggest organo-metal oxide complexes do not contribute to C stabilization in these habitats. This research is one of the few studies that have examined C stabilization related to soil structure in wetland soils. Our results suggest soil aggregate formation may be an important mechanism driving C stabilization, and that disruption to macroaggregates may limit C accumulation in restored wetlands. Additional empirical research and long-term field monitoring are needed to confirm linkages between aggregate-C stabilization and accumulation in wetland soils.

opencc-zeroDec 2018View details →
dryad28/100

Data from: Aggregation of infective stages of parasites as an adaptation and its implications for the study of parasite-host interactions

The causes and consequences of aggregation among conspecifics have received much attention. For infecting macroparasites, causes include variation among hosts in susceptibility, and/or whether infective stages are aggregated in the environment. Here, we link these two phenomena and explore whether aggregation of infective stages in the environment is adaptive to parasites encountering host condition-linked defenses, and what effect such aggregations have for parasite-host interactions. Using simulation models, we show that parasite fitness is increased by aggregates attacking a host, particularly when investment into defenses is high. The fitness benefit of aggregation remains despite inclusion of factors that should curb the benefits of aggregation: namely, mortality of low condition hosts (those hosts expected to be most susceptible to parasitism) and costs of high coinfection. Using sample sizes common in studies, aggregation of infective stages reduces the likelihood of detecting host condition-parasitism relations, even when host condition is the only other factor in models affecting parasitism. Thus, it is not surprising that the expected inverse relations between host condition and parasitism, commonly a premise in studies of parasite-host interactions, are inconsistently found. An understanding of how parasites encounter hosts is thus needed for developing theory for parasite-host ecological and evolutionary interactions.

opencc-zeroDec 2014View details →
dryad28/100

Data from: The interaction between ambush predators, search patterns of herbivores and aggregations of plants

<p>While predators benefit from spatial overlap with their prey, prey strive to avoid predators. I used an individual-based simulation comprising sit-and-wait predators, widely-foraging herbivores, and plants, to examine the link between predator ambush location, herbivore movement, and plant aggregation. I used a genetic algorithm to reach the best strategies for all players. The predators could ambush herbivores either inside or outside plant patches. The herbivores could use movement of varying directionality levels, with a change in directionality following the detection of plants. When the predators were fixed outside plant patches, the herbivores were selected to use a directional movement before plant encounter followed by a tortuous movement afterwards. When predators were fixed inside patches, herbivores used a continuous directional movement. Predators maintained within-patch positions when the herbivores were fixed to use the directional-tortuous movement. The predator location inside patches led to higher plant aggregations, by changing the herbivore movement. Finally, I allowed half of the predators to search for herbivores and let them compete with sit-and-wait predators located inside plant patches. When plants were clumped and herbivores used a directional-tortuous movement, with a movement shift after plant detection, ambush predators had a higher success relative to widely-foraging predators. In all other scenarios, widely-foraging predators did much better than ambush predators. The findings from my simulation suggest a behavioral mechanism for several observed phenomena of predator-prey interactions, such as a shorter stay by herbivores in patches when predators ambush them nearby, and a more directional movement of herbivores in riskier habitats.</p>

opencc-zeroJul 2021View details →
dryad28/100

Data for: Aggregation in an heterospecific population of blowfly larvae: social behaviour is impacted by species-specific thermal requirements and settlement order

<p><span>Larvae of several blow fly species grow on carcasses and actively aggregate together. They face harsh developmental conditions resulting in a strong pressure to reduce development time: this is achieved either through thermoregulation or aggregation. We investigate how these two developmental strategies are modulated within heterospecific groups. In the first experiment, larvae of two species with different thermal requirements were deposited simultaneously on a thermal gradient. This resulted in the formation of two monospecific groups, each located at the species-specific thermal preferendum. However, when <em>Calliphora</em> <em>vomitoria</em> (Linnaeus) larvae were placed first, the later coming <em>Lucilia</em> <em>sericata</em> (Meigen) larvae attracted the whole group to its own thermal preferendum. In the reverse experiment, a half of the replicates resulted in single dense heterospecific groups observed at temperatures ranging from <em>C. vicina</em> to <em>L. sericata</em> preferendum. The other half of the replicates resulted in loose groups spread out on the thermal gradient. These results highlight the emergence of collective decisions ranging from thermal optimization to heterospecific aggregation at suboptimal temperatures. They demonstrate that species settlement order strongly affects self-organization processes and mixed-species group formation. We conclude that thermal optimization and heterospecific niche construction are two developmental strategies of carrion fly larvae.</span></p>

opencc-zeroApr 2023View details →
dryad28/100

Data-driven models reveal mutant cell behaviors important for myxobacterial aggregation

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publicJun 2020View details →
dryad28/100

Data from: Why pair? Evidence of aggregative mating in a socially monogamous marine fish (Siganus doliatus, Siganidae)

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publicAug 2015View details →
dryad28/100

Data from: Across species-pool aggregation alters grassland productivity and diversity

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publicAug 2016View details →
dryad28/100

Data from: Social interactions do not drive territory aggregation in a grassland songbird

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publicOct 2020View details →
dryad28/100

Data from: Synchronised nesting aggregations are associated with enhanced capacity for extended embryonic arrest in olive ridley sea turtles

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publicJul 2019View details →
dryad28/100

Data from: Alteration of nitrous oxide emissions from floodplain soils by aggregate size, litter accumulation and plant–soil interactions

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publicNov 2018View details →
dryad28/100

Data from: Does 1,8-Diiodooctane affect the aggregation state of PC71BM in solution?

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publicAug 2018View details →
dryad28/100

Data from: Excavation and aggregation as organizing factors in de novo construction by mound-building termites

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publicMay 2017View details →
dryad28/100

Data from: Viral infection causes sex-specific changes in fruit fly social aggregation behaviour

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publicAug 2019View details →
dryad28/100

Data from: Aggregation of infective stages of parasites as an adaptation and its implications for the study of parasite-host interactions

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publicSep 2015View details →
dryad28/100

Data from: The aggregate site frequency spectrum (aSFS) for comparative population genomic inference

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publicOct 2015View details →
dryad28/100

Data from: Thioflavin T as an amyloid dye: fibril quantification, optimal concentration and effect on aggregation

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publicNov 2016View 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