Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
1,423
datasets available to search
ShareScore release 0.9.0
Dataset results
1,423 results for “separation”
Male age alone predicts paternity success under sperm competition when effects of age and past mating effort are experimentally separated
Open the record for dataset details and reuse information.
Plot-level wood-leaf separation for terrestrial laser scanning point clouds
Open the record for dataset details and reuse information.
Mechanistic dissection of increased enzymatic rate in a phase-separated compartment
Open the record for dataset details and reuse information.
Data from: Genetic divergence between two phenotypically distinct bottlenose dolphin ecotypes suggests separate evolutionary trajectories
Open the record for dataset details and reuse information.
Animal acoustic identification, denoising, and source separation using generative adversarial networks
Open the record for dataset details and reuse information.
An experimental study on the separation of lanthanides from phosphate ore by organic and inorganic acids
Open the record for dataset details and reuse information.
Cortical astrocytes independently regulate sleep depth and duration via separate GPCR pathways
Open the record for dataset details and reuse information.
Data for "Coherent phonon dynamics in spatially-separated graphene mechanical resonators"
<p>Data for "Coherent phonon dynamics in spatially-separated graphene mechanical resonators"</p>
Figure 3 from: Barroso CX, Pereira de Freitas JE, Matthews-Cascon H, Arruda Bezerra LE, da Cruz Lotufo TM (2020) Molecular evidences confirm the taxonomic separation of two sympatric congeneric species (Mollusca, Gastropoda, Neritidae, Neritina). ZooKeys 904: 117-130. https://doi.org/10.3897/zookeys.904.46790
Figure 3 Colour patterns of shells, opercula, and radulae of the Neritina virginea and Neritina meleagris analysed. The red arrows highlight the differences between the leading edges of colour patterns of both species: N. virginea has the leading edges outlined in heavy black, while N. meleagris has the leading edge outlined in white or black and white. ANeritina virginea_1 BNeritina virginea_2 CNeritina virginea_3 DNeritina virginea_4 ENeritina meleagris_1 FNeritina meleagris_2 GNeritina meleagris_3 HNeritina meleagris_4 I ventral view of shell of Neritina virgineaJ operculum (outer and inner views) of Neritina virgineaK ventral view of shell of Neritina meleagrisL operculum (outer and inner views) of Neritina meleagrisM radula of Neritina virginea (SEM), with rachidian tooth enlarged in the upper left quadrant N radula of Neritina meleagris (SEM), with rachidian tooth enlarged in the upper left quadrant. Abbreviations: l1 first lateral tooth, l4 fourth lateral tooth, m marginal teeth, r rachidian tooth. The specimens with the number "1" are from Camocim beach (Ceará State, NE Brazil) and those with numbers "2", "3", and "4" are from Barra Grande beach (Piauí State, NE Brazil). The numbered specimens of N. virginea (1, 2, 3, and 4) and N. meleagris (1, 2, 3, and 4) are the same specimens used in the phylogenetic analysis of Figure 1. Scale bars: 1.0 mm (A–L); 100 μm (M, N).
Figure 2 from: Barroso CX, Pereira de Freitas JE, Matthews-Cascon H, Arruda Bezerra LE, da Cruz Lotufo TM (2020) Molecular evidences confirm the taxonomic separation of two sympatric congeneric species (Mollusca, Gastropoda, Neritidae, Neritina). ZooKeys 904: 117-130. https://doi.org/10.3897/zookeys.904.46790
Figure 2 Statistical parsimony network analysis (TCS algorithm) based on 64 partial mitochondrial COI sequences (347 bp). This analysis included specimens of Neritina meleagris and Neritina virginea from the Caribbean and Brazilian Provinces. Size of the circle is proportional to frequency of the haplotype and colours inside the circles designate geographical locations to which the samples belong. Black circles correspond to hypothetical haplotypes. The number of mutational steps is indicated by dashes on branches. We highlighted the 36 mutational steps that separate the two species haplotypes.
Figure 1 from: Barroso CX, Pereira de Freitas JE, Matthews-Cascon H, Arruda Bezerra LE, da Cruz Lotufo TM (2020) Molecular evidences confirm the taxonomic separation of two sympatric congeneric species (Mollusca, Gastropoda, Neritidae, Neritina). ZooKeys 904: 117-130. https://doi.org/10.3897/zookeys.904.46790
Figure 1 Molecular phylogenetic hypothesis (Bayesian tree) of some species of Neritidae of the Western Atlantic. The Bayesian tree was based on partial mitochondrial COI and 16S sequences. The Neritina meleagris and Neritina virginea clades (ingroup) are highlighted. The other taxa were used as outgroup. Numbers on and below the main branches represent the posterior Bayesian probabilities (BP) (>0.90) and bootstrap values for maximum likelihood (ML) (>70%), respectively. Specimens with the number "1" are from Camocim beach (Ceará State, NE Brazil) and those with numbers "2", "3", and "4" are from Barra Grande beach (Piauí State, NE Brazil). The numbered specimens of N. virginea (1, 2, 3, and 4) and N. meleagris (1, 2, 3, and 4) are the same specimens shown in Figure 3.
Binary phase separation 3D
<p>Time evolution of a binary phase separating polymer system using Cahn Hilliard equation in three dimensions.</p>
A large joint sound scene and sound event dataset for source separation of foreground sound events
<p>This large scale data set contains 10000 samples of sound scenes generated from real world recordings, and the original source recordings. It includes 10 different backgrounds with 6-9 appropriate foreground sound events. Strong labels (timed annotations) are provided in four formats for all samples. The original sourceids to identify the class type, a two source method to simply separate foreground and backgrounds, a 32 source annotation for all distinct foregrounds, and a by background (scene) type annotation where sources are according to the background. </p> <p>Baseline results will be presented later in 2020. Further evolutions of this dataset will also be produced with more complex, polyphonic foreground sound events. Please email h.bear@qmul.ac.uk with any questions.</p> <p>Data is free to use for Research purposes only. </p>
According to this the mutual affinities of the species of the simpleX group might be expressed as follows t (the Ethiopian species are marked with an asterisk):— each other at base; in 4 p2 is half in row. To this latter I find no parallel in any specimen of ferrum-equinum (all races) I have seen, and in 4 skulls only, out of 33, there is a more or less distinct remnant of the interspace between the canine and p4. Of _R7z. deckeni I have seen one skull only; the dentition is as in many specimens of Ph. augur: c and p4 separated, p2 external. f I give the diagram the form of a genealogical tree, only because it is convenient to in On some Bats of the Genus Rhinolophus, with Remarks on their Mutual Affinities, and Descriptions of Twenty-six new Forms.
According to this the mutual affinities of the species of the simpleX group might be expressed as follows t (the Ethiopian species are marked with an asterisk):— each other at base; in 4 p2 is half in row. To this latter I find no parallel in any specimen of ferrum-equinum (all races) I have seen, and in 4 skulls only, out of 33, there is a more or less distinct remnant of the interspace between the canine and p4. Of _R7z. deckeni I have seen one skull only; the dentition is as in many specimens of Ph. augur: c and p4 separated, p2 external. f I give the diagram the form of a genealogical tree, only because it is convenient to
Figure 1 in Chromosomal separation of difficult species of Copris Geoffroy, 1762 and Onthophagus Latreille, 1802 (Coleoptera, Scarabaeidae), with discussion of O. massai Baraud as a British Pleistocene fossil
Figure 1. Map showing the collection sites of the material used in this paper. See Table 1 for explanation of the numbers, and note that neighbouring sites may share the same number.
Dataset: On the Aggregation and Nucleation Mechanism of the Monoclonal Antibody Anti-CD20 Near Liquid- Liquid Phase Separation (LLPS)
<p>Dataset related to the paper: Pantuso et al., On the Aggregation and Nucleation Mechanism of the Monoclonal Antibody Anti-CD20 Near Liquid-Liquid Phase Separation (LLPS), Scientific Reports (2020) 10:8902.</p>
Reactive extraction of fructose for efficient separation of sucrose-derived glucosides produced by enzymatic glycosylation
<p>We provide here the underlying data of the scientific publication "Reactive extraction of fructose for efficient separation of sucrose-derived glucosides produced by enzymatic glycosylation". Please find the abstract below:</p> <p>The disaccharide sucrose (α-D-glucopyranosyl-1,2-β-D-fructofuranoside) is a highly efficient donor substrate for enzymatic glucosylation reactions. A large number of commercially relevant glucosides are produced via this general route. Every sucrose-based glucosylation involves co-production of D-fructose in amounts corresponding to the target glucoside. A separation technology for selective removal, and efficient recovery, of the D-fructose co-product would be highly desirable as a generic platform for downstream process development. Here, we demonstrate organoboronate-complex reactive extraction of D-fructose into an 1-octanol/hexane (4/1, v/v) solvent using methyltrioctyl ammonium chloride as phase transfer catalyst and extractant. We show separation of the D-fructose co-product (100 mM) from equimolar mixture with 2-α-D-glucosyl-glycerol, a cosmetic ingredient that is manufactured industrially from sucrose and glycerol using sucrose phosphorylase. With the main parameters of extraction, stripping and organic phase recycling identified and their effect on product/co-product yield and purity characterized, we developed a three-step extraction process with alternating extraction and stripping stages that removed the D-fructose efficiently at 50 ml operating scale. 2-α-D-glucosyl-glycerol and D-fructose were cleanly separated and obtained in excellent purity (≥90%) at a recovery of 90% and 83%, respectively. Reactive extraction appears to be faster and more selective and resource-efficient than applicable alternatives for separation, including chromatography and membrane nanofiltration. Thus, the established extraction process is promising for industrial application. It could be generically useful to separate D-fructose from glucosides</p>
Figure 9 from: Suzuki Y, Ballarin F (2020) Nesticus kosodensis Yaginuma, 1972 bona species. Molecular and morphological separation from N. latiscapus Yaginuma, 1972 with notes on cave scaffold-web spiders subspecies in Japan (Araneae, Nesticidae). Subterranean Biology 35: 79-96. https://doi.org/10.3897/subtbiol.35.53933
Figure 9 Phylogenetic relationship among Nesticus latiscapus (= red), N. kosodensis stat. nov. (= green), and other closely-related species from the same geographic area (=black) inferred from ML analysis of COI partial sequence. Branch lengths are scaled in relation to the number of substitutions per site. Numbers at nodes denote maximum likelihood bootstrap support.
Figure 8 from: Suzuki Y, Ballarin F (2020) Nesticus kosodensis Yaginuma, 1972 bona species. Molecular and morphological separation from N. latiscapus Yaginuma, 1972 with notes on cave scaffold-web spiders subspecies in Japan (Araneae, Nesticidae). Subterranean Biology 35: 79-96. https://doi.org/10.3897/subtbiol.35.53933
Figure 8 Type material of the species discussed in this work. Nesticus kosodensis stat. nov.: a palp of the holotype, ventral view b epigyne of the paratype, ventral view; N. latiscapus: c palp of the holotype, ventral view d epigyne of the paratype, ventral view. Scale bars: 0.2 mm.
Figure 5 from: Suzuki Y, Ballarin F (2020) Nesticus kosodensis Yaginuma, 1972 bona species. Molecular and morphological separation from N. latiscapus Yaginuma, 1972 with notes on cave scaffold-web spiders subspecies in Japan (Araneae, Nesticidae). Subterranean Biology 35: 79-96. https://doi.org/10.3897/subtbiol.35.53933
Figure 5 Male palp of N. latiscapus from Saiko Bat Cave. a Ventral view b dorsal view c ventro-retrolateral view d retrolateral view e ventro-prolateral view. Scale bars: 0.2 mm.
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.