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772 results for “fronts”

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ClinicalTrials.gov32/100

Front of Pack Nutritional Labeling of Processed Foods Among Mexican Consumers

ClinicalTrials.gov study NCT04308408. IPD Sharing: YES. Countries: 1. Publications: 1.

controlledIPD-YESFeb 2026View details →
ClinicalTrials.gov32/100

Front-line Therapy With Carfilzomib, Lenalidomide, and Dexamethasone Induction

ClinicalTrials.gov study NCT02405364. IPD Sharing: NO. Countries: 1. Publications: 2.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov32/100

Front-of-package Marketing on Fruit Drinks: Online RCT

ClinicalTrials.gov study NCT04811690. IPD Sharing: NO. Countries: 1. Publications: 1.

closedIPD-NOFeb 2026View details →
dryad32/100

Data from: Variation in age ratio of midcontinent greater white-fronted geese during fall migration

Open the record for dataset details and reuse information.

publicJan 2018View details →
dryad32/100

Data from: Crossing the divide: admixture across the Antarctic Polar Front revealed by the brittle star Astrotoma agassizii

Open the record for dataset details and reuse information.

publicJun 2018View details →
dryad32/100

Data from: Wildfire activity and land use drove 20th-century changes in forest cover in the Colorado front range

Open the record for dataset details and reuse information.

publicFeb 2019View details →
dryad32/100

Data from: Invasion genetics of the silver carp Hypophthalmichthys molitrix across North America: differentiation of fronts, introgression, and eDNA metabarcode detection

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publicMar 2019View details →
dryad32/100

Data from: Is the enhanced dispersal rate seen at invasion fronts a behaviourally plastic response to encountering novel ecological conditions?

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publicAug 2016View details →
dryad32/100

Data from: Human–Cougar interactions in the wildland–urban interface of Colorado's front range

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publicAug 2019View details →
dryad32/100

Data from: Den site selection by male brown bears at the population’s expansion front

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publicAug 2019View details →
dryad32/100

Data from: Rapid evolution of increased vulnerability to an insecticide at the expansion front in a poleward moving damselfly

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publicNov 2015View details →
dryad32/100

Data from: Differences in developmental strategies between long-settled and invasion-front populations of the cane toad in Australia

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publicNov 2015View details →
dryad32/100

Data from: Use of glacial fronts by narwhals (Monodon monoceros) in West Greenland

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publicOct 2016View details →
dryad32/100

Data from: At the invasion front, male cane toads (Rhinella marina) have smaller testes

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publicJul 2019View details →
dryad32/100

Data from: Individual and temporal variation in habitat association of an alien carnivore at its invasion front

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publicMar 2016View details →
dryad32/100

Data from: Broad-front migration leads to strong migratory connectivity in the lesser kestrel (Falco naumanni)

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publicSep 2020View details →
zenodo28/100

Plate III. Rhinolophus simpleX group; skulls; front views f, all other figures f. Fig.. Rh. simpleX (p. 76); Lombok; type of the species. Front view. 2 a, b, c. Rh. megaphyllus f. typica (p. 79); Cooktown; B.M. no. 3.8.3.3. Upper, lateral, and front views. 3. Rh. nanus (p. 82); Goram; type. Front view. 4a, b. Rh. celebensis (p. 83); Makassar; type. Upper and front views. 5 a, 6, c. Rh. borneensis f. typica (p. 84); Labuan; topotype; B.M. no. 65.5.9.15. Upper, lateral, and front views. 6. Rh. malayanus (p. 89); Biserat; topotype; B.M. no. 3.2.6.84. Front view. 7 a, b, c. Rh. nereis (p. 90); Siantan, Anambas; type. Upper, lateral, and front views. 8 a, b. Rh. stheno (p. 91); Selangor; topotype; B.M. no. 98.3.13.2. Lateral and front views. 9 a, b, c, d. Rh. rouXi f. typica (p. 93); Ceylon. Upper, lower, lateral, and front views. 10. Rh.thomasi (p. 100); Talio, Karin Hills; topotype; B.M. no. 90.4.7.9. Upper view. 11 a, b. Rh. affinis himalayanus (p. 103); Nepal. Lower and front views. 12. Rh. a. tener (p. 103); Pegu; type. Upper view. 13. Rh. a. princeps (p. 106); Lombok; type. Upper view. in On some Bats of the Genus Rhinolophus, with Remarks on their Mutual Affinities, and Descriptions of Twenty-six new Forms.

Plate III. Rhinolophus simpleX group; skulls; front views f, all other figures f. Fig.. Rh. simpleX (p. 76); Lombok; type of the species. Front view. 2 a, b, c. Rh. megaphyllus f. typica (p. 79); Cooktown; B.M. no. 3.8.3.3. Upper, lateral, and front views. 3. Rh. nanus (p. 82); Goram; type. Front view. 4a, b. Rh. celebensis (p. 83); Makassar; type. Upper and front views. 5 a, 6, c. Rh. borneensis f. typica (p. 84); Labuan; topotype; B.M. no. 65.5.9.15. Upper, lateral, and front views. 6. Rh. malayanus (p. 89); Biserat; topotype; B.M. no. 3.2.6.84. Front view. 7 a, b, c. Rh. nereis (p. 90); Siantan, Anambas; type. Upper, lateral, and front views. 8 a, b. Rh. stheno (p. 91); Selangor; topotype; B.M. no. 98.3.13.2. Lateral and front views. 9 a, b, c, d. Rh. rouXi f. typica (p. 93); Ceylon. Upper, lower, lateral, and front views. 10. Rh.thomasi (p. 100); Talio, Karin Hills; topotype; B.M. no. 90.4.7.9. Upper view. 11 a, b. Rh. affinis himalayanus (p. 103); Nepal. Lower and front views. 12. Rh. a. tener (p. 103); Pegu; type. Upper view. 13. Rh. a. princeps (p. 106); Lombok; type. Upper view.

opencc-by-4.0Dec 1905View details →
dryad28/100

Data from: Basking sharks and oceanographic fronts: quantifying associations in the north-east Atlantic

1. Understanding the mechanisms that link oceanographic processes and marine vertebrate space use is critical to our knowledge of marine ecosystem functioning, and for effective management of populations of conservation concern. 2. The basking shark Cetorhinus maximus has been observed in association with oceanographic fronts – physical interfaces at the transitions between water masses – exploiting foraging opportunities resulting from zooplankton aggregation. However, the scale, significance and variability of these associations have not previously been established. 3. Here, we quantify the influence of thermal and chlorophyll-a fronts on basking shark habitat use in the north-east Atlantic. We use animal-mounted archival tracking together with composite front mapping via Earth Observation (EO) remote sensing to provide an oceanographic context to shark movements. 4. We investigate levels of association with fronts occurring over two spatio-temporal scales, (i) broad-scale, seasonally persistent frontal zones and (ii) contemporaneous thermal and chl-a fronts. Using random walk simulations and logistic regression within an iterative generalized linear mixed modelling (GLMM) framework, we find that seasonal front frequency is a significant predictor of shark presence. 5. Oceanographic metrics time-matched to shark tracks indicate that sharks show a preference for productive regions and associate with contemporaneous thermal and chl-a fronts more frequently than could be expected at random. Moreover, we highlight the importance of front persistence and cross-frontal temperature step, which appear to interact to affect the degree of prey aggregation along thermal fronts in this shelf-sea system. 6. Our findings confirm that surface frontal activity is a predictor of basking shark presence in the north-east Atlantic, both over seasonal timescales and in near real-time. These insights have clear implications for understanding the preferred habitats of basking sharks in the context of anthropogenic threat management and marine spatial planning in the region.

opencc-zeroDec 2014View details →
dryad28/100

Data from: It is lonely at the front: contrasting evolutionary trajectories in male and female invaders

Invasive species often exhibit rapid evolutionary changes, and can provide powerful insights into the selective forces shaping phenotypic traits that influence dispersal rates and/or sexual interactions. Invasions also may modify sexual dimorphism. We measured relative lengths of forelimbs and hindlimbs of more than 3000 field-caught adult cane toads (Rhinella marina) from 67 sites in Hawai'i and Australia (1–80 years post-colonization), along with 489 captive-bred individuals from multiple Australian sites raised in a 'common garden' (to examine heritability and reduce environmental influences on morphology). As cane toads spread from east to west across Australia, the ancestral condition (long limbs, especially in males) was modified. Limb length relative to body size was first reduced (perhaps owing to natural selection on locomotor ability), but then increased again (perhaps owing to spatial sorting) in the invasion vanguard. In contrast, the sex disparity in relative limb length has progressively decreased during the toads' Australian invasion. Offspring reared in a common environment exhibited similar geographical divergences in morphology as did wild-caught animals, suggesting a genetic basis to the changes. Limb dimensions showed significant heritability (2–17%), consistent with the possibility of an evolved response. Cane toad populations thus have undergone a major shift in sexual dimorphism in relative limb lengths during their brief (81 years) spread through tropical Australia.

opencc-zeroDec 2015View details →
zenodo28/100

Chinatown Chang-e 2021 (Front)

2021 Chinatown Lunar Festival Decorations Source: Objaverse 1.0 / Sketchfab

opencc-by-nc-sa-2.0Sep 2021View details →

ScienceDex guides

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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.

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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