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635 results for “Attributes”
Distribution. Guinea, Ivory Coast, Liberia, and Sierra Leone. A specimen collected from Oda in Ghana in 1946 has been attributed to this species, but its true origin is in question. in Viverridae
Distribution. Guinea, Ivory Coast, Liberia, and Sierra Leone. A specimen collected from Oda in Ghana in 1946 has been attributed to this species, but its true origin is in question.
My research questionnaire for the paper titled : the relationship between product attributes and customer satisfaction
<p>My research questionnaire for the paper titled : the relationship between product attributes and customer satisfaction</p>
Impact of four inorganic impurities – iron, copper, nickel and zinc - on the quality attributes of a Fc-fusion protein upon incubation at different temperatures.
<p>Data regarding the impact of four inorganic impurities – iron, copper, nickel and zinc - on the quality attributes of a Fc-fusion protein upon incubation at different temperatures. </p>
Tracks for "Attribution of 2020 hurricane season extreme rainfall to human-induced climate change"
<p>TempestExtremes track files for CAM5 analysis presented in "Attribution of 2020 hurricane season extreme rainfall to human-induced climate change"</p>
Evaluating Feature Attribution Methods in the Image Domain: High-Dimensional Datasets
<p>Here you can find the versions of the Places-365 and Caltech-256 datasets used in the paper Evaluating Feature Attribution Methods in the Image Domain.</p>
Distribution. Endemic to South America, with records in Colombia, Ecuador, Peru, N & CW Brazil, and NE Argentina (Parana River basin). Occurrence localities in Bolivia and Paraguay were attributed to recently described M. midastactus. in Vespertilionidae
Distribution. Endemic to South America, with records in Colombia, Ecuador, Peru, N & CW Brazil, and NE Argentina (Parana River basin). Occurrence localities in Bolivia and Paraguay were attributed to recently described M. midastactus.
Distribution. Philippines (S Luzon, Catanduanes, Panay, Samar, Leyte, Negros, and Mindanao Is), Peninsular Malaysia, CW Sumatra, N & NW Borneo, Sulawesi, New Guinea and the Bismarck Archipelago (New Ireland and New Britain Is). A record from Java is erroneous, and a record from Bangka I does not appear to be authentic. Previous records from India (Sikkim) and C & E Nepal are misidentifications, now attributable to Joftre's Pipistrelle (Hypsugo joffrer). in Vespertilionidae
Distribution. Philippines (S Luzon, Catanduanes, Panay, Samar, Leyte, Negros, and Mindanao Is), Peninsular Malaysia, CW Sumatra, N & NW Borneo, Sulawesi, New Guinea and the Bismarck Archipelago (New Ireland and New Britain Is). A record from Java is erroneous, and a record from Bangka I does not appear to be authentic. Previous records from India (Sikkim) and C & E Nepal are misidentifications, now attributable to Joftre's Pipistrelle (Hypsugo joffrer).
The rehydration attributes and quality characteristics of 'Quick-cooking' dehydrated beans: Implications of glass transition on storage stability
<p>The data set was used to generate the figures.</p>
GFDL-LM4-UCM_HEAT_STRESS_ATTRIBUTION
<p>The repository contains data used in the paper titled "Attributing the urban-rural contrast of heat stress simulated by a global model".</p> <p>If you have any questions, feel free to contact yueqin@bu.edu.</p>
Distribution. Restricted to Mauritius; there are two isolated records attributed to this species from the Durban region on E coast of South Africa. Previous authors considered it to occur on Madagascar, but Goodman and coworkers found no evidence for its occurrence there. in Molossidae
Distribution. Restricted to Mauritius; there are two isolated records attributed to this species from the Durban region on E coast of South Africa. Previous authors considered it to occur on Madagascar, but Goodman and coworkers found no evidence for its occurrence there.
Subspecies and Distribution. D.p.pannietensisDeVis,1905—D'Entre-casteauxIs(Goodenough,Fergusson,andNormanby)andLouisiadeArchi-pelago(Misima,Panaeati,Rossel,andVanatinaiIs). D. p. remota Cabrera, 1920 — Trobriand Is (Kiriwina) and Woodlark Is. A record attributed to Bougainville I is a misidentification of the Solomons Nakedbacked Fruit Bat (D. inermas). in Pteropodidae
Subspecies and Distribution. D.p.pannietensisDeVis,1905—D'Entre-casteauxIs(Goodenough,Fergusson,andNormanby)andLouisiadeArchi-pelago(Misima,Panaeati,Rossel,andVanatinaiIs). D. p. remota Cabrera, 1920 — Trobriand Is (Kiriwina) and Woodlark Is. A record attributed to Bougainville I is a misidentification of the Solomons Nakedbacked Fruit Bat (D. inermas).
Distribution. Guinea and Sierra Leone E to S Ghana (although these are apparently misidentified), Nigeria, Cameroon, and BiokoI; records reported from SW DR Congo and N Zambia are here attributed to Bates's White-toothed Shrew (C. batesi), although exact placement ofthese specimens is uncertain. in Soricidae
Distribution. Guinea and Sierra Leone E to S Ghana (although these are apparently misidentified), Nigeria, Cameroon, and BiokoI; records reported from SW DR Congo and N Zambia are here attributed to Bates's White-toothed Shrew (C. batesi), although exact placement ofthese specimens is uncertain.
Distribution. Uncertain, but the type locality is generally accepted to be Mt Kilimanjaro, NE Tanzania; there are further reports of this species throughout W & E Africa (including some recent ones from Uganda), but they cannot be confirmed since most of the specimens have been wrongly attributed. in Soricidae
Distribution. Uncertain, but the type locality is generally accepted to be Mt Kilimanjaro, NE Tanzania; there are further reports of this species throughout W & E Africa (including some recent ones from Uganda), but they cannot be confirmed since most of the specimens have been wrongly attributed.
Distribution. Highlands of Los Altos de Chiapas, C Chiapas (SE Mexico); possibly also Las Margaritas, E Chiapas, although these specimens might be attributed to Merriam's Small-eared Shrew (C. merriamz). in Soricidae
Distribution. Highlands of Los Altos de Chiapas, C Chiapas (SE Mexico); possibly also Las Margaritas, E Chiapas, although these specimens might be attributed to Merriam's Small-eared Shrew (C. merriamz).
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.
The first comprehensive revision of all the species attributed to Melomys led J. I. Menzies in 1996 to resurrect the genus Paramelomys and to redefine its morphologicallimits and species content. Menzies created P. gressitti as a new species belonging to a group displaying morphological similarities and including also P. lorentzii and P. moncktoni. Monotypic Distribution. E New Guinea. Descriptive notes. Head-body 135-162 mm, hindfoot 30-34 mm; no specific data are available for body weight. Gressitt's Mosaic-tailed Rat is a medium-sized Paramelomys with a soft, thick and woolly pelage, a long narrow foot, and a tail with three hairs per scale. It exhibits a medium-sepia dorsal pelage and a gray-buff ventral one. Tail is slightly shorter (99%) than head-body length. The skull has a narrow zygomatic plate. Habitat. Moist tropical mountain forest between 2300 m and 2400 m. Food and Feeding. No information. Breeding. No information. Activity patterns. Gressitt's Mosaic-tailed Rat is terrestrial. Movements, Home range and Social organization. No information. Status and Conservation. Classified as Endangered on The IUCN Red List owing to its small geographic range (less than 3500 km?*) and the destruction ofits habitat by mining and logging activities. The major threat to Gressitt's Mosaic-tailed Rat is ongoing habitat degradation caused by nearby human populations; habitat on Mount Kandy has been destroyed by gold-miners and wood-cutters. Bibliography. Menzies (1996). in Muridae
The first comprehensive revision of all the species attributed to Melomys led J. I. Menzies in 1996 to resurrect the genus Paramelomys and to redefine its morphologicallimits and species content. Menzies created P. gressitti as a new species belonging to a group displaying morphological similarities and including also P. lorentzii and P. moncktoni. Monotypic Distribution. E New Guinea. Descriptive notes. Head-body 135-162 mm, hindfoot 30-34 mm; no specific data are available for body weight. Gressitt's Mosaic-tailed Rat is a medium-sized Paramelomys with a soft, thick and woolly pelage, a long narrow foot, and a tail with three hairs per scale. It exhibits a medium-sepia dorsal pelage and a gray-buff ventral one. Tail is slightly shorter (99%) than head-body length. The skull has a narrow zygomatic plate. Habitat. Moist tropical mountain forest between 2300 m and 2400 m. Food and Feeding. No information. Breeding. No information. Activity patterns. Gressitt's Mosaic-tailed Rat is terrestrial. Movements, Home range and Social organization. No information. Status and Conservation. Classified as Endangered on The IUCN Red List owing to its small geographic range (less than 3500 km?*) and the destruction ofits habitat by mining and logging activities. The major threat to Gressitt's Mosaic-tailed Rat is ongoing habitat degradation caused by nearby human populations; habitat on Mount Kandy has been destroyed by gold-miners and wood-cutters. Bibliography. Menzies (1996).
FIGURE 1 in Date and place of publication and author attribution of the combination Kalanchoe sect. Raveta (Crassulaceae subfam. Kalanchooideae)
FIGURE 1. Kalanchoe thyrsiflora, the type of K. sect. Raveta, in the vegetative growing phase. The leaves are obovate to round and borne in pseudo-rosettes. Photograph: Gideon F. Smith.
FIGURE 2 in Date and place of publication and author attribution of the combination Kalanchoe sect. Raveta (Crassulaceae subfam. Kalanchooideae)
FIGURE 2. Like most of the plant parts, the flowers of Kalanchoe thyrsiflora are covered in a white-waxy substance. Flowers are densely carried in club-shaped inflorescences. Photograph: Gideon F. Smith.
Dataset from: Selecting deep neural networks that yield consistent attribution-based interpretations for genomics
<p>Deep neural networks (DNNs) have demonstrated great promise at taking DNA sequences as input and predicting a wide variety of functional activity. Post hoc attribution analysis has been employed to provide insights into the features learned by DNNs, often revealing patterns such as known motifs. However, attribution maps are noisy in practice to an extent that varies from model to model, even across DNNs that yield similar generalization performance. This makes it challenging to identify which high-performing DNN will provide trustworthy explanations. Here we propose a summary statistic that characterizes the consistency of learned features across a population of attribution maps which can be utilized as an additional criterion for model selection. We demonstrate the efficacy of this approach quantitatively using synthetic data and qualitatively with chromatin accessibility data. Together, this work advances our ability to select optimal DNNs that not only yield high generalization performance but also reliable attribution maps that will, in turn, accelerate scientific discovery in genomics.</p>
FIGURE 18 in A new species of the hysius species-group of Calisto Hübner (Lepidoptera, Nymphalidae, Satyrinae) and insights into the status of different populations currently attributed to C. grannus Bates
FIGURE 18. Bayesian COI barcodes gen tree reconstructed by MrBayes showing the relationships among taxa belonging to the hysius species group of Calisto. Numbers above branches represent the posterior probalities / boostrap values of Bayesian Inference / Maximum Likelihood. Bold numbers at species clades represent the support values for each species calculated by the Bayesian Poisson Tree Process (bPTP) species delimitation method. Gray box indicating the position of the species described herein, C. bahoruco. Gray bars at the right side of tree showing the species hypothesis obtained by the different species delimitation methods applied: Generalize Mixed Yule Coalescent single and multiple threshold (GMYCs, GMYCm), Poisson Tree Process, PTP, variants: Bayesian (bPTP), Maximum Likelihood (mPTP), and standard (PTP), Automatic Barcode Gap Discovery (ABGD), and Barcode Index Number (BIN).
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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.
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.