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60
datasets available to search
ShareScore release 0.9.0
Dataset results
60 results for “2014 to 2015”
A large-scale longitudinal structured dataset of the dark web cryptomarket Evolution (2014–2015)
<p>Data includes a structured dataset of the forum and marketplace of the dark web cryptomarket Evolution as well as a longitudinal network snapshot dataset of a temporal weighted communication network extracted from the forum data. The datasets were extracted from Dark Net Market archive data while resolving many of the data quality issues inherent to raw data scraped from online sources.</p><p>Dark web cryptomarkets facilitate the online trade of illicit goods. Evolution was active from January 2014 until March 2015; and formed a combination of a carding forum and an underground drug market. This dataset includes the vast majority of data that could be obtained from the webpages of the forum and marketplace of Evolution. This includes, for example, information on the number of sales each individual vendor has completed, forum post contents, and product categories.</p><p>The extracted communication network models users' co-posting in the same forum topics, in essence modelling communication between them.</p><p>Additionally included is the code used to produce the dataset from the Dark Net Market archive data.</p>
PPS Winter wheat trials 2014 - 2015
<p>This data set consists of observations that were done during the PPS winter wheat field trials in Wageningen (The Netherlands). <br>The experiment was conducted by the chair group Plant Production Systems (PPS) of Wageningen University and Research.<br>The experiment consisted of two growing seasons (2013-2014 and 2014-2015), three nitrogen fertilization treatments (N1, N2, N3) and three cultivars (cv Julius, cv Ritmo, cv Tabasco).<br>The experiment has been described in detail by Berghuijs et al (2023).</p> <p>The uploaded files are:</p> <p>20231228_pps_winterwheat_trials_crop_nitrogen_and_phosphor.xlsx: contains measurements of crop N and crop P concentrations<br>20231228_pps_winterwheat_trials_dry_matter.xlsx: contains measurements of dry matter, dry matter partitioning and specific leaf area<br>20231228_pps_winterwheat_trials_phenology.xlsx: contains the sowing dates, dates of anthesis and harvest dates. Note that there were no separate measurements of phenology done per cultivar; only per growing season.</p> <p>References:<br>Berghuijs, H. N. C., Silva, J. V., Rijk, H. C. A., van Ittersum, M. K., van Evert, F. K. & Reidsma, P. (2023). Catching-up with genetic progress: Simulation of potential production for modern wheat cultivars in the Netherlands. Field Crops Research 296: 108891. URL: https://doi.org/10.1016/j.fcr.2023.108891</p>
Uganda Malaise trapping 2014–2015 Rhyssinae ecology data
<p>This dataset contains the data and analyses of our <a href="https://doi.org/10.1098/rsos.190913">paper</a> on the ecology of Ugandan Rhyssinae. We collected rhyssines by Malaise trapping in tropical forest in Kibale National Park 2014–2015. The dataset contains background data such as weather and vegetation around the traps, data on the 447 rhyssines caught, the figures in the paper, and the script used to analyse the data.</p> <p><br> The script (2 Rhyssinae ecology.R) will usually be of the greatest interest. It contains the R code used to explore and analyse the data, and to create the figures in the paper.</p>
MASCS 1.0: Synchronous atmospheric and oceanic data from a cross-shaped moored array in the northern South China Sea during 2014–2015
<p>This work presents a cross-shaped moored array dataset (MASCS 1.0) comprising five buoys and four moorings with synchronous atmospheric and oceanic data in the northern South China Sea during 2014–2015. The atmospheric data are observed by two meteorological instruments at the buoys. The oceanic data consist of sea surface waves measured using a wave recorder, temperature, and salinity from the surface to a depth of 400 m, and at 10 and 50 m above the ocean bottom using conductivity, temperature, and depth recorders. It also includes currents from the surface to a depth of 850 m measured using acoustic Doppler current profilers and measured at 10, 50, and 100 m above the floor using current meters. Additional measurements were taken for sea surface radiation, air visibility, chlorophyll, turbidity, and chromophoric dissolved organic matter at buoy 3, located at the center of the moored array. The data reveals air–sea interactions and oceanic processes in the upper and bottom ocean, especially the transition of the air–sea interface and ocean conditions from summer to winter monsoon and the effects of six tropical cyclones on the moored array. Multiscale processes were also recorded, such as air–sea fluxes, tides, internal waves, and low-frequency flows. The data are valuable and have many potential applications, including analyzing the phenomena and mechanisms of air–sea interactions and ocean dynamics and validating and improving numerical model simulations, data reanalysis, and assimilations.</p>
Balsam fir seedling bank in Whiteface Mountain (2014–2015)
<p><span>The persistence of future forests depends </span><span>on the success of tree seedlings which are experiencing increasing physiological stress from changing climate and air pollution. Although the moss layer can serve as an important substrate for tree seedlings, its potential for reducing environmental stress and enhancing the establishment of seedlings remains poorly understood. We tested if </span><span>the moss layer decreased environmental stress and increased the abundance of balsam fir seedlings dominant in high-elevation forests of the northeastern United States that are sensitive to changing climate and mercury deposition. We surveyed balsam fir seedling density by substrate (moss, litter, other) on 120 quadrats (1×1 m) in two contrasting canopy environments (in gaps and under canopies), measured seedling stress, and quantified mercury content in seedlings and substrates. We observed that, in both canopy environments, tree seedlings established on moss exhibited (<em>i</em>) increased density, (<em>ii</em>) decreased physiological stress, and (<em>iii</em>) higher potential to recruit into larger size class, compared to seedlings established in litter. Regardless of canopy environment, seedling foliar mercury levels did not correspond to substrate mercury despite large differences in substrate mercury concentrations (relative to moss, litter concentrations were ~4-times greater and soil concentrations were ~6-times greater), likely reflecting the dominance of foliar over root uptake of mercury. Since the moss layer appeared to mitigate seedling drought stress and to increase seedling establishment and recruitment compared to other substrates, these microsite effects should be considered in models predicting forest regeneration and dynamics under increased drought stress associated with ongoing climate warming.</span></p>
Planktonic foraminifera count, shell weight and size data from sediment traps in the Fram Strait, HAUSGARTEN observatory (TDLT 2014), 2014 - 2015
<p>Counts, shell weight and shell size data of planktonic foraminifera from two depths of the sediment Trap TDLT 2014 in the HAUSGARTEN observatory in the eastern Fram Strait. Comparison of the count data done in the context of this study with count data conducted after the initial retrieval of the trapped material indicate high deviation. It is likely that the samples were affected by dissolution during the storage between retrieval (2015) and analysis (2020/2021), therefore both counts and weight and size data might not be representative.<br> <br> This data is supplement to the dissertation from Tell (2023).</p>
Balsam fir seedling bank in Whiteface Mountain (2014–2015)
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Moored ADCP, current meters, and CTD data in the southern Japan Sea in 2014 and 2015
<p>These datasets contain velocities observed in the southern Japan Sea with an ADCP and current meters during May and October in both 2014 and 2015. Temperature and salinity measurements in the southwestern Japan Sea with a CTD are also included. These are for the publication of the manuscript entitled “Flow intensification due to the superimposition of near-inertial internal waves in the abyssal Japan Sea (East Sea)” by Senjyu, T. and Shin, H.R., which will be submitted to Journal of Geophysical Research Oceans.</p>
Data from: "De novo assembly transcriptome for the rostrum dace (Leuciscus burdigalensis, Cyprinidae: fish) naturally infected by a copepod ectoparasite" in Genomic Resources Notes accepted 1 December 2014 to 31 January 2015
The emergence of pathogens represents substantial threats to public health, livestock, domesticated animals, and biodiversity. How wild populations respond to emerging pathogens has generated a lot of interest in the last two decades. With the recent advent of high-throughput sequencing technologies it is now possible to develop large transcriptomic resources for non-model organisms, hence allowing new research avenues on the immune responses of hosts from a large taxonomic spectra. We here focused on a wild population of the rostrum dace (Leuciscus burgiladensis) that is infected by Tracheliastes polycolpus, an emerging freshwater ectoparasite copepod. We used next generation Illumina sequencing technology to sequence the transcriptome of eight L. burdigalensis adult individuals collected in natura from the same sampling site. Four individuals were non-infected and four individuals were infected by T. polycolpus. We specifically focused on the spleen, the head kidney and epithelial cells and mucus from the fins, three tissues known to be involved in the immune response of fish. We used the Trinity methodology to reconstruct a de novo full-length transcriptome for L. burdigalensis. The resulting transcriptome will serve as an important broad-scale genomic resource for further studying the response of local population of L. burdigalensis to T. polycolpus pressures.
As currently delineated, this is a complex comprising at least two species, as dem- onstrated by the work of J. M. Lamb and colleagues in 2014 and A. Monadjem and colleagues in 2015. Large gray-bellied specimens attributed to M. triton form two highly divergent molecular and chromosomal clades: on the one hand, from Tanzania, Malawi, and Mozambique (with chromosomal complement of 2n = 20-22, FN = 34); and, on the other, from DR Congo (with 2n = 32, FN = 34. Monotypic. Distribution. Extreme S South Sudan, S Ethiopia (Bale Mts), NE DR Congo, and from Uganda and Kenya SW & S to Angola, Zambia, WC Mozambique, and Malawi. in Muridae
As currently delineated, this is a complex comprising at least two species, as dem- onstrated by the work of J. M. Lamb and colleagues in 2014 and A. Monadjem and colleagues in 2015. Large gray-bellied specimens attributed to M. triton form two highly divergent molecular and chromosomal clades: on the one hand, from Tanzania, Malawi, and Mozambique (with chromosomal complement of 2n = 20-22, FN = 34); and, on the other, from DR Congo (with 2n = 32, FN = 34. Monotypic. Distribution. Extreme S South Sudan, S Ethiopia (Bale Mts), NE DR Congo, and from Uganda and Kenya SW & S to Angola, Zambia, WC Mozambique, and Malawi.
Distribution. Now restricted to the Channel Country of SW Queensland and the Lake Eyre Basin in NE South Australia. Descriptive notes. Head-body 95-120 mm, tail 105-160 mm, ear 23-29 mm, hindfoot 32-37 mm; weight 30-50 g. The Fawn Hopping Mouse has body form typical of hopping mice, with very long hindfeet, long tail with distal brush of longer hairs, very long ears, and large protruberant eyes. Dorsal fur is of variable color, from pale pinkish fawn to gray; ventral fur white. Unlike most other hopping mice, it has no throat pouch, but males have a glandular area of naked skin on the chest. Habitat. Occurs in low shrublands and tussock grasslands on stony ("gibber") plains and claypans. Shows marked habitat segregation from the Dusky Hopping Mouse (N. fuscus), which is closely associated with sandy substrates. Food and Feeding. The Fawn Hopping Mouse is mostly granivorous, but also eats other plant material (stems, leaves) and occasionally invertebrates. It uses succulent, salt-adapted plants around edges of claypans as a source of water. Breeding. Reproduction is probably largely opportunistic and aseasonal, with high reproductive output from near-continuous breeding after periods of high rainfall; reported littersize is 1-5, most commonly three; gestation period 38-43 days for nonlactating females. Females may mature later than other hopping mice, with reproductive maturity reached at about six months. Activity patterns. Terrestrial and nocturnal. Fawn Hopping Mice shelter during day in burrow systems that are typically simpler and shallower than those of other hopping mice. Movements, Home range and Social organization. Fawn Hopping Mice generally live singly or in small groups; typically uncommon within range, but population density may increase by an order of magnitude following periods of high rainfall. Status and Conservation. Classified as Near Threatened on The IUCN Red List. The Fawn Hopping Mouse has shown marked decline in range (estimated at greater than 50%), and presumably population size, since European settlement of Australia. This is mostlikely due to predation by the introduced house cat and Red Fox (Vulpes vulpes), and to habitat degradation associated with pastoralism. Bibliography. Brazenor (1934), Burbidge et al. (2008), Finlayson (1939), Gould (1853), Jackson & Groves (2015), Murray et al. (1999), Ogilby (1892), Thomas (1921h), Van Dyck & Strahan (2008), Waite (1898), Watts & Aslin (1981), Woinarski et al. (2014), Wood Jones (1925). in Muridae
Distribution. Now restricted to the Channel Country of SW Queensland and the Lake Eyre Basin in NE South Australia. Descriptive notes. Head-body 95-120 mm, tail 105-160 mm, ear 23-29 mm, hindfoot 32-37 mm; weight 30-50 g. The Fawn Hopping Mouse has body form typical of hopping mice, with very long hindfeet, long tail with distal brush of longer hairs, very long ears, and large protruberant eyes. Dorsal fur is of variable color, from pale pinkish fawn to gray; ventral fur white. Unlike most other hopping mice, it has no throat pouch, but males have a glandular area of naked skin on the chest. Habitat. Occurs in low shrublands and tussock grasslands on stony ("gibber") plains and claypans. Shows marked habitat segregation from the Dusky Hopping Mouse (N. fuscus), which is closely associated with sandy substrates. Food and Feeding. The Fawn Hopping Mouse is mostly granivorous, but also eats other plant material (stems, leaves) and occasionally invertebrates. It uses succulent, salt-adapted plants around edges of claypans as a source of water. Breeding. Reproduction is probably largely opportunistic and aseasonal, with high reproductive output from near-continuous breeding after periods of high rainfall; reported littersize is 1-5, most commonly three; gestation period 38-43 days for nonlactating females. Females may mature later than other hopping mice, with reproductive maturity reached at about six months. Activity patterns. Terrestrial and nocturnal. Fawn Hopping Mice shelter during day in burrow systems that are typically simpler and shallower than those of other hopping mice. Movements, Home range and Social organization. Fawn Hopping Mice generally live singly or in small groups; typically uncommon within range, but population density may increase by an order of magnitude following periods of high rainfall. Status and Conservation. Classified as Near Threatened on The IUCN Red List. The Fawn Hopping Mouse has shown marked decline in range (estimated at greater than 50%), and presumably population size, since European settlement of Australia. This is mostlikely due to predation by the introduced house cat and Red Fox (Vulpes vulpes), and to habitat degradation associated with pastoralism. Bibliography. Brazenor (1934), Burbidge et al. (2008), Finlayson (1939), Gould (1853), Jackson & Groves (2015), Murray et al. (1999), Ogilby (1892), Thomas (1921h), Van Dyck & Strahan (2008), Waite (1898), Watts & Aslin (1981), Woinarski et al. (2014), Wood Jones (1925).
Supplementary material 1 from: Niemi M, Matala J, Melin M, Eronen V, Järvenpää H (2015) Traffic mortality of four ungulate species in southern Finland. In: Seiler A, Helldin J-O (Eds) Proceedings of IENE 2014 International Conference on Ecology and Transportation, Malmö, Sweden. Nature Conservation 11: 13–28. https://doi.org/10.3897/natureconservation.11.4416
Annual trends in population size and collisions: Explanation note: Annual trends in population size, harvest, and collisions.
Supplementary material 2 from: Niemi M, Matala J, Melin M, Eronen V, Järvenpää H (2015) Traffic mortality of four ungulate species in southern Finland. In: Seiler A, Helldin J-O (Eds) Proceedings of IENE 2014 International Conference on Ecology and Transportation, Malmö, Sweden. Nature Conservation 11: 13–28. https://doi.org/10.3897/natureconservation.11.4416
Contingency tables used in the analysis of collision and traffic mortality rates: Explanation note: Contingency tables.
Monthly total CEJ Count for different LT sectors from magnetometer data at Tirunaleveli and Alibag Observatories for the period 2014 to 2015
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Data from: "Identification of SNP markers for the endangered Ugandan red colobus (Procolobus rufomitratus tephrosceles) using RAD sequencing" in Genomic Resources Notes accepted 1 December 2014 to 31 January 2015
Despite dramatic growth in the field of primate genomics over the past decade, studies of primate population and conservation genomics in the wild have been hampered due to the difficulties inherent in studying non-model organisms and endangered species, such as lack of a reference genome and current challenges in de novo primate genome assembly. Here, we used Restriction-site Associated DNA (RAD) sequencing to develop a population-based SNP panel for the Ugandan red colobus (P. rufomitratus tephrosceles), which is a highly threatened monkey due to habitat loss. We analyzed blood samples from 24 individuals from Kibale National Park (Uganda) using single-end RAD sequencing. We obtained 70,773,857 reads, of which 58,814,906 passed the filtering steps. Using the program STACKS v. 1.11 we identified 113,376 loci, of which 50,558 were polymorphic and had a mean observed heterozygosity of 0.25. These data will be used to study the effects of habitat fragmentation on genomic diversity, dispersal, and disease transmission in this species. Our approach provides a good example of the potential of RAD sequencing in studies of wild primate populations.
Data from: Inferring epidemiologic dynamics from viral evolution: 2014–2015 Eurasian/North American highly pathogenic avian influenza viruses exceed transmission threshold, R0 = 1, in wild birds and poultry in North America
Highly pathogenic avian influenza virus (HPAIV) is a multi-host pathogen with lineages that pose health risks for domestic birds, wild birds, and humans. One mechanism of intercontinental HPAIV spread is through wild bird reservoirs and wild birds were the likely sources of a Eurasian (EA) lineage HPAIV into North America in 2014. The introduction resulted in several reassortment events with North American (NA) lineage low pathogenic avian influenza viruses and the reassortant EA/NA H5N2 went on to cause one of the largest HPAIV poultry outbreaks in North America. We evaluated three hypotheses about novel HPAIV introduced into wild and domestic bird hosts: (i) transmission of novel HPAIVs in wild birds was restricted by mechanisms associated with highly-pathogenic phenotypes; (ii) the HPAIV poultry outbreak was not self-sustaining and required viral input from wild birds; (iii) reassortment of the EA H5N8 generated reassortant EA/NA AIVs with a fitness advantage over fully Eurasian lineages in North American wild birds. We used a time-rooted phylodynamic model that explicitly incorporated viral population dynamics with evolutionary dynamics to estimate the basic reproductive number (R0) and viral migration among host types in domestic and wild birds, as well as between the EA H5N8 and EA/NA H5N2 in wild birds. We did not find evidence to support hypothesis (i) or (ii) as our estimates of the transmission parameters suggested that the HPAIV outbreak met or exceeded the threshold for persistence in wild birds (R0 > 1) and poultry (R0 ≈ 1) with minimal estimated transmission among host types. There was also no evidence to support hypothesis (iii) because R0 values were similar among EA H5N8 and EA/NA H5N2 in wild birds. Our results suggest that this novel HPAIV and reassortments did not encounter any transmission barriers sufficient to prevent persistence when introduced to wild or domestic birds.
Data from: Inferring epidemiologic dynamics from viral evolution: 2014–2015 Eurasian/North American highly pathogenic avian influenza viruses exceed transmission threshold, R0 = 1, in wild birds and poultry in North America
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Data from: "Identification of SNP markers for the endangered Ugandan red colobus (Procolobus rufomitratus tephrosceles) using RAD sequencing" in Genomic Resources Notes accepted 1 December 2014 to 31 January 2015
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Data from: "De novo assembly transcriptome for the rostrum dace (Leuciscus burdigalensis, Cyprinidae: fish) naturally infected by a copepod ectoparasite" in Genomic Resources Notes accepted 1 December 2014 to 31 January 2015
Open the record for dataset details and reuse information.
Crab spectrum 2014-03-15 2015-03-15
<p><a href="https://www.astro.unige.ch/cdci/astrooda_?src_name=Crab&RA=83.633080&DEC=22.014500&E1_keV=20&E2_keV=40&T1=2014-03-15T00:00:00.0&T2=2015-03-15T00:00:00.0&T_format=isot&catalog_selected_objects=1,2,3,4&detection_threshold=7.5&instrument=isgri&osa_version=OSA10.2&product_type=isgri_spectrum&query_status=ready&query_type=Real&radius=15&use_scws=no&selected_catalog=%7B%22cat_column_descr%22:%5B%5B%22meta_ID%22,%22%3Ci8%22%5D,%5B%22src_names%22,%22%7CS18%22%5D,%5B%22significance%22,%22%3Ef4%22%5D,%5B%22ra%22,%22%3Ef4%22%5D,%5B%22dec%22,%22%3Ef4%22%5D,%5B%22NEW_SOURCE%22,%22%3Ei2%22%5D,%5B%22ISGRI_FLAG%22,%22%3Ci8%22%5D,%5B%22FLAG%22,%22%3Ci8%22%5D,%5B%22ERR_RAD%22,%22%3Cf8%22%5D%5D,%22cat_column_list%22:%5B%5B1,2,3,4%5D,%5B%221A+0535%2B262%22,%224U+0517%2B17%22,%22Crab%22,%22H+0614%2B091%22%5D,%5B116.7,7.9,1232.6,8.1%5D,%5B84.726,77.667,83.631,94.254%5D,%5B26.314,16.487,22.015,9.165%5D,%5B-32768,-32768,-32768,-32768%5D,%5B2,2,2,2%5D,%5B0,0,0,0%5D,%5B0.0002,0.0002,0.0002,0.0002%5D%5D,%22cat_column_names%22:%5B%22meta_ID%22,%22src_names%22,%22significance%22,%22ra%22,%22dec%22,%22NEW_SOURCE%22,%22ISGRI_FLAG%22,%22FLAG%22,%22ERR_RAD%22%5D,%22cat_coord_units%22:%22deg%22,%22cat_frame%22:%22fk5%22,%22cat_lat_name%22:%22dec%22,%22cat_lon_name%22:%22ra%22%7D">www.astro.unige.ch/cdci/astrooda_?src_name=Crab&RA=83.633080&DEC=22.014500&E1_keV=20&E2_keV=40&T1=2014-03-15T00:00:00.0&T2=2015-03-15T00:00:00.0&T_format=isot&catalog_selected_objects=1,2,3,4&detection_threshold=7.5&instrument=isgri&osa_version=OSA10.2&product_type=isgri_spectrum&query_status=ready&query_type=Real&radius=15&use_scws=no&selected_catalog=%7B%22cat_column_descr%22:%5B%5B%22meta_ID%22,%22%3Ci8%22%5D,%5B%22src_names%22,%22%7CS18%22%5D,%5B%22significance%22,%22%3Ef4%22%5D,%5B%22ra%22,%22%3Ef4%22%5D,%5B%22dec%22,%22%3Ef4%22%5D,%5B%22NEW_SOURCE%22,%22%3Ei2%22%5D,%5B%22ISGRI_FLAG%22,%22%3Ci8%22%5D,%5B%22FLAG%22,%22%3Ci8%22%5D,%5B%22ERR_RAD%22,%22%3Cf8%22%5D%5D,%22cat_column_list%22:%5B%5B1,2,3,4%5D,%5B%221A+0535%2B262%22,%224U+0517%2B17%22,%22Crab%22,%22H+0614%2B091%22%5D,%5B116.7,7.9,1232.6,8.1%5D,%5B84.726,77.667,83.631,94.254%5D,%5B26.314,16.487,22.015,9.165%5D,%5B-32768,-32768,-32768,-32768%5D,%5B2,2,2,2%5D,%5B0,0,0,0%5D,%5B0.0002,0.0002,0.0002,0.0002%5D%5D,%22cat_column_names%22:%5B%22meta_ID%22,%22src_names%22,%22significance%22,%22ra%22,%22dec%22,%22NEW_SOURCE%22,%22ISGRI_FLAG%22,%22FLAG%22,%22ERR_RAD%22%5D,%22cat_coord_units%22:%22deg%22,%22cat_frame%22:%22fk5%22,%22cat_lat_name%22:%22dec%22,%22cat_lon_name%22:%22ra%22%7D</a></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.