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51 results for “needs analysis”

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zenodo32/100

Data needed to reproduce analysis from "Frost matters: Incorporating late-spring frost in a dynamic vegetation model regulates regional productivity dynamics in European beech forests"

<p>Data to reproduce analysis from "Frost matters: Incorporating late-spring frost in a dynamic vegetation model regulates regional productivity dynamics in European beech forests".</p> <p>This includes:</p> <ol> <li>Tree ring data (meyer, bdn, principe, dittmar)</li> <li>LPJ-GUESS model output (frost_validation, frost_sensitivity, runs_22012024_revision)</li> <li>Data used for plotting</li> </ol>

opencc-by-4.0Jan 2024View details →
zenodo32/100

Murina fusca may prove to be merely ajunior synonym of M. hilgendorfi, although the only known specimen is apparently very distinctive; further analysis is needed. Originally described as a race of M. huttonii, but does not appearto be closely related to it. Monotypic. Distribution. Known only from the type locality in Heilongjiang, NE China. in Vespertilionidae

Murina fusca may prove to be merely ajunior synonym of M. hilgendorfi, although the only known specimen is apparently very distinctive; further analysis is needed. Originally described as a race of M. huttonii, but does not appearto be closely related to it. Monotypic. Distribution. Known only from the type locality in Heilongjiang, NE China.

opennotspecifiedOct 2019View details →
zenodo32/100

A comprehensive descriptive analysis : Assessing the guidance and counseling needs through cognitive and non-cognitive development of students in secondary level public schools

<p>This data has been collected from a secondary level public school in Karachi for a descriptive analysis . I</p> <p>&nbsp;</p>

opencc-by-4.0Sep 2024View details →
dryad32/100

Climate, caribou and human needs linked by analysis of Indigenous and scientific knowledge

<p><span>Migratory tundra caribou are ecologically and culturally critical in the circumpolar North. However, they are declining almost everywhere in North America, likely due to natural variation exacerbated by climate change and human activities. Yet, the interconnectedness between climate, caribou, and human well-being has received little attention. To address this gap, we bridged</span><span> </span><span>Indigenous and scientific knowledge in a single model, using as an example the Porcupine caribou herd social-ecological system. Our analysis, involving </span><span>688 (fall season) and 616 (spring season) interviews conducted over nine years with 405 (fall season) and 390 (spring season) Indigenous hunters </span><span>from nine communities, demonstrates that </span><span>environmental conditions, </span><span>large-scale temporal changes associated with caribou demography, and cultural practices </span><span>affect hunters' capacity to meet their needs in caribou. </span><span>Our quantitative approach </span><span>bolsters our understanding of the complex relationships between ecosystems and human welfare in environments exposed to rapid climate change and shows </span><span>the benefits of long-term participatory research methods implemented by Indigenous and scientific partners.</span></p>

opencc-zeroJan 2023View details →
ClinicalTrials.gov32/100

Analysis of Single Respiratory Viral Infections Versus Co-infections: Prevalence and ICU Needs in Hospitalized Adults

ClinicalTrials.gov study NCT06779175. IPD Sharing: UNDECIDED. Countries: 1. Publications: 3.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov32/100

Analysis Of The Patients Who Need Rehospitalization Due To Stroke Rehabilitation Only

ClinicalTrials.gov study NCT03927469. IPD Sharing: NO. Countries: 1. Publications: 2.

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

Longitudinal Analysis of Mental Disorders, Psychosocial Distress and Care Needs of Patients and Their Relatives

ClinicalTrials.gov study NCT04620564. IPD Sharing: Not stated. Countries: 1. Publications: 2.

restrictedIPD-UNDECIDEDFeb 2026View details →
dryad32/100

Data from: Resource-Area-Dependence Analysis: inferring animal resource needs from home-range and mapping data

Open the record for dataset details and reuse information.

publicNov 2018View details →
dryad32/100

Climate, caribou and human needs linked by analysis of Indigenous and scientific knowledge

Open the record for dataset details and reuse information.

publicJan 2023View details →
dryad32/100

Data from: The financial needs vs. the realities of in situ conservation: an analysis of federal funding for protected areas in Brazil’s Caatinga

Open the record for dataset details and reuse information.

publicMay 2017View details →
zenodo28/100

FIGURE 3 in Resurrection of Scolopendra longipes Wood and Scolopendra cubensis Saussure from synonymy with Scolopendra alternans Leach (Chilopoda, Scolopendromorpha, Scolopendridae): an enigmatic species-group needing phylogeographic analysis, with an overview on the origin

FIGURE 3. Sensillia trichodea from ultimate tergite of S. longipes, Florida (Scale Bar = 50 µm).

opennotspecifiedDec 2016View details →
zenodo28/100

Supplementary material 2 from: Ringelberg JJ, Koenen EJM, Iganci JR, de Queiroz LP, Murphy DJ, Gaudeul M, Bruneau A, Luckow M, Lewis GP, Hughes CE (2022) Phylogenomic analysis of 997 nuclear genes reveals the need for extensive generic re-delimitation in Caesalpinioideae (Leguminosae). In: Hughes CE, de Queiroz LP, Lewis GP (Eds) Advances in Legume Systematics 14. Classification of Caesalpinioideae Part 1: New generic delimitations. PhytoKeys 205: 3-58. https://doi.org/10.3897/phytokeys.205.85866

Table S2

opencc-zeroSep 2022View details →
zenodo28/100

Supplementary material 4 from: Ringelberg JJ, Koenen EJM, Iganci JR, de Queiroz LP, Murphy DJ, Gaudeul M, Bruneau A, Luckow M, Lewis GP, Hughes CE (2022) Phylogenomic analysis of 997 nuclear genes reveals the need for extensive generic re-delimitation in Caesalpinioideae (Leguminosae). In: Hughes CE, de Queiroz LP, Lewis GP (Eds) Advances in Legume Systematics 14. Classification of Caesalpinioideae Part 1: New generic delimitations. PhytoKeys 205: 3-58. https://doi.org/10.3897/phytokeys.205.85866

Supplementary tree file

opencc-zeroSep 2022View details →
zenodo28/100

Supplementary material 3 from: Ringelberg JJ, Koenen EJM, Iganci JR, de Queiroz LP, Murphy DJ, Gaudeul M, Bruneau A, Luckow M, Lewis GP, Hughes CE (2022) Phylogenomic analysis of 997 nuclear genes reveals the need for extensive generic re-delimitation in Caesalpinioideae (Leguminosae). In: Hughes CE, de Queiroz LP, Lewis GP (Eds) Advances in Legume Systematics 14. Classification of Caesalpinioideae Part 1: New generic delimitations. PhytoKeys 205: 3-58. https://doi.org/10.3897/phytokeys.205.85866

Figure S1

opencc-zeroSep 2022View details →
zenodo28/100

Supplementary material 1 from: Ringelberg JJ, Koenen EJM, Iganci JR, de Queiroz LP, Murphy DJ, Gaudeul M, Bruneau A, Luckow M, Lewis GP, Hughes CE (2022) Phylogenomic analysis of 997 nuclear genes reveals the need for extensive generic re-delimitation in Caesalpinioideae (Leguminosae). In: Hughes CE, de Queiroz LP, Lewis GP (Eds) Advances in Legume Systematics 14. Classification of Caesalpinioideae Part 1: New generic delimitations. PhytoKeys 205: 3-58. https://doi.org/10.3897/phytokeys.205.85866

Table S1

opencc-zeroSep 2022View details →
zenodo28/100

Figure 7 from: Cifuentes-Ruiz P, Zaragoza-Caballero S, Ochoterena-Booth H, Morón Rios M (2014) A preliminary phylogenetic analysis of the New World Helopini (Coleoptera, Tenebrionidae, Tenebrioninae) indicates the need for profound rearrangements of the classification. ZooKeys 415: 191-216. https://doi.org/10.3897/zookeys.415.6882

Figure 7 - Strict consensus of 12 most parsimonious trees (L = 314; ci = 0.28; ri = 0.56). Characters are mapped onto the consensus only if their optimization is not ambiguous and if they are present among all the MPTs. The consensus is used to map homoplasy at the level of characters. Black rectangles represent single, non-homoplasious character state transformations, and white rectangles represent multiple, homoplasious character state transformations. The number depicted above each rectangle represents the character and the number below the rectangle represents the character state. The bigger number below the branches corresponds to Bootstrap values over 50%. The combination of characters for each terminal is not shown. Three important synapomorphies are illustrated in the cladogram: the filiform antennae (3:0), as the single synapomorphy of the tribe, and the number of spermathecal tubes (41:1) plus the terminal position of the accessory gland (49:2), as the synapomorphies supporting a mostly Neotropical clade. These character states are reported for the first time for the tribe. Two shades of gray in the cladogram indicate the subtribe to which the terminals belong (except Nautes). Colors in the terminals indicate their geographic distribution. Below seven terminals the former classification (genus or subgenus) is shown. An asterisk indicates the type species included in the analysis: Tarpela browni and Nautes fervidus.

opencc-by-4.0Jun 2014View details →
zenodo28/100

Figure 6 from: Cifuentes-Ruiz P, Zaragoza-Caballero S, Ochoterena-Booth H, Morón Rios M (2014) A preliminary phylogenetic analysis of the New World Helopini (Coleoptera, Tenebrionidae, Tenebrioninae) indicates the need for profound rearrangements of the classification. ZooKeys 415: 191-216. https://doi.org/10.3897/zookeys.415.6882

Figure 6 - Aedeagal characters (male genitalia) representing the different morphological types found in or sample of Helopini: A evident setae (57: 0) representing the helopiod type (Nabozhenko 2001b, 2002a, 2005), distributed over half of the parameres (58:0), illustrated from Helops caeruleus (Linnaeus), not included in the analysis (lateral view) B evident setae (57:0); representing the catomoid type (Nabozhenko 2006), distributed over two thirds of parameres (58:1) in Nautes fervidus Pascoe C not evident setae over parameres (57:1) representing the nalassoid type (Nabozhenko 2001b, 2002a, 2002b), illustrated from Odocnemis californicus Mannerheim D parameres not convergent (59:1), with blunt apex (62:0) in Helops caeruleus (ventral view) E parameres not convergent (59:1) with weakly constricted apex (61:1) in Nautes fervidus F parameres convergent (59:0), with acute (60:1) not constricted apex (62:1) in O. californicus.

opencc-by-4.0Jun 2014View details →
zenodo28/100

Figure 4 from: Cifuentes-Ruiz P, Zaragoza-Caballero S, Ochoterena-Booth H, Morón Rios M (2014) A preliminary phylogenetic analysis of the New World Helopini (Coleoptera, Tenebrionidae, Tenebrioninae) indicates the need for profound rearrangements of the classification. ZooKeys 415: 191-216. https://doi.org/10.3897/zookeys.415.6882

Figure 4 - Internal morphological characters (female genitalia) representing the different morphological types found in our sample of Helopini ag = accessory gland, sp = spermatheca, st = spermathecal tube(s), cd = common duct of accessory gland and spermatheca, v = vagina, ov = oviduct: A infundibular vagina (40:0), single spermatheca branched near its base (41:0, 42:0) and accessory gland in the common duct (49:1) illustrated from Helops insignis Germar representing the helopiod type (Nabozhenko 2001b, 2002a, 2002b, 2005) B vagina strongly curved and narrowed before the apex (40:1), single spermatheca not branched near the base (41:0, 42:1) illustrated from Nalassus plebejus Küster representing the nalassoid type (Nabozhenko 2001b, 2002a, 2002b) C female genital tract with three serial spermathecal tubes (41:1) close to each other (43:0) and terminal accessory gland (49:2) in Helops farctus LeConte, illustrating the pattern previously reported for some Pimeliinae species (Doyen 1994), here reported for the first time in Tenebrioninae D distant spermathecal tubes (43:1) in Helops perforatus Horn with terminal accessory gland (49:2), illustrating a pattern described here for the first time. Total length of the accessory gland is not represented in A and B.

opencc-by-4.0Jun 2014View details →
zenodo28/100

Figure 2 from: Cifuentes-Ruiz P, Zaragoza-Caballero S, Ochoterena-Booth H, Morón Rios M (2014) A preliminary phylogenetic analysis of the New World Helopini (Coleoptera, Tenebrionidae, Tenebrioninae) indicates the need for profound rearrangements of the classification. ZooKeys 415: 191-216. https://doi.org/10.3897/zookeys.415.6882

Figure 2 - Examples of non-traditional external characters in Helopini: A reduced recurrent cell (rc) (26:0) in fully developed wing (25:1) of Helops californicus Mannerheim B wide recurrent cell (rc) (26:1) in fully developed wing (25:1) of Tarpela aerifera Allard C head width and interocular width (6:0) and pronotum width and length (18:0) in Tarpela costata Champion 1887, showing a gibbous pronotum disk surface (8:0), with very dense (9:0) and very deep (10:0) pronotum punctures.

opencc-by-4.0Jun 2014View details →
zenodo28/100

Figure 1 from: Cifuentes-Ruiz P, Zaragoza-Caballero S, Ochoterena-Booth H, Morón Rios M (2014) A preliminary phylogenetic analysis of the New World Helopini (Coleoptera, Tenebrionidae, Tenebrioninae) indicates the need for profound rearrangements of the classification. ZooKeys 415: 191-216. https://doi.org/10.3897/zookeys.415.6882

Figure 1 - Examples of external characters (mainly diagnostic), traditionally used in Helops, Tarpela and Nautes, (number of character: character state): A broad apical antennomere (5:0), shorter than the third antennomere (4:0) illustrated from Helops aereus Germar B filiform apical antennomeres (5:2), as long as the third antennomere (4:1) illustrated from Nautes fervidus Pascoe C male maxillary palps with length of inner edge 2.6–2.9 times the length of posterior edge (7:2) illustrated from Nautes chrysomeloides Champion D third lobate segment of male tarsi (30:0) and short fourth tarsomere (31:0) illustrated from Nautes fervidus E not prominent prosternum (27:1) in Helops cisteloides Germar F prominent-acute prosternum (27:0) in Nautes fervidus.

opencc-by-4.0Jun 2014View 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