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FIGURE 4. The secondary structures for 22 in Comparative mitogenome analysis and phylogenetic inference of the genus Ultragryllacris (Orthoptera: Gryllacrididae)
FIGURE 4. The secondary structures for 22 tRNA genes of the Ultragryllacris pulchra rubricapitis XZ273.
FIGURE 3. The secondary structures for 22 in Comparative mitogenome analysis and phylogenetic inference of the genus Ultragryllacris (Orthoptera: Gryllacrididae)
FIGURE 3. The secondary structures for 22 tRNA genes of the Ultragryllacris pulchra rubricapitis XZ267.
FIGURE 5. The secondary structures for 22 in Comparative mitogenome analysis and phylogenetic inference of the genus Ultragryllacris (Orthoptera: Gryllacrididae)
FIGURE 5. The secondary structures for 22 tRNA genes of the Ultragryllacris pulchra rubricapitis XZ506.
FIGURE 1 in Earthworm communities in long-term no-tillage systems and secondary forest fragments in Paraná, Southern Brazil
FIGURE 1. Location of the municipalities of the sampling sites in Paraná, Brazil. Light grey = Faxinal (FX), Black = Mauá da Serra (MS), Dark grey = Palmeira (PL)
Replication package for the article "Who chooses fast-track programs in mathematics? The role of class origin, ethnicity, and gender among Norwegian lower-secondary students", submitted to European Societies.
<p>This file contains a replication package for the article "Who chooses fast-track programs in mathematics? The role of class origin, ethnicity, and gender among Norwegian lower-secondary students", submitted to European Societies</p> <p>****************************************************************************************************************************************<br> The analyses in this article are of secondary data from Norwegian state registers. We analyzed the data with concession from The Norwegian Data Protection Authority, and under the auspices of a confidentiality agreement with Statistics Norway. All direct identifiers were stripped from the file prior to analysis. Data were handled in such a way as to protect individual’s privacy and confidentiality. This included storing these data on a secure Research Computing server and requiring each researcher working with the data to sign a confidentiality affidavit. Other parties may not access the data because it would violate the concession given by The Norwegian Data Protection Authority, and the confidentiality agreement with Statistics Norway. This prevents us from uploading the data to a public repository. <br> Researchers may apply to get access to such data, and the procedure one needs to follow is described at Statistics Norway’s webpage: <br> https://www.ssb.no/en/data-til-forskning/utlan-av-data-til-forskere<br> </p>
Controlled-source electromagnetic modeling using a versatile secondary electric-field formulation and efficient multigrid-based preconditioner
<p>Models and responses files for the manuscript "<strong>Controlled-source electromagnetic modeling using a versatile secondary electric-field formulation and efficient multigrid-based preconditioner".</strong></p>
Figure 2 in Sperm quality, secondary sexual characters and parasitism in roach (Rutilus rutilus L.)
Figure 2. Correlation between sperm longevity and spermatozoal velocity (r = 0.547, P = 0.019). The line is from linear regression (y = 0.43x + 28.7).
Figure 1 in Sperm quality, secondary sexual characters and parasitism in roach (Rutilus rutilus L.)
Figure 1. Mean and SE of sperm longevity and spermatozoal velocity among Rutilus rutilus males with different degrees of ornamentation: (0) no breeding tubercles or very few or very small tubercles, smooth skin; (1) breeding tubercles clearly found, slightly or moderately rough skin; (2) many large tubercles, rough skin. Male groups which differed statistically from each other are denoted with different letters.
Assesing gender differences for non-predictable Breakthrough Cancer Pain Phenomenon: a secondary analysis from IOPS-MS Study
<p>IOPS-MS was a big multicentric study with the aim of characterizing BTcP in a large number of patients belonging to different settings and assessing possible factors influencing its development. Moreover, NP-BTcP topic was addressed elsewhere [https://doi.org/10.3390/cancers13164018].</p> <p>One key difference is related to the hormonal (gender related characteristics) differences between men and women. For example, estrogen and progesterone can affect pain sensitivity, with some studies suggesting that women may be more sensitive to pain during certain stages of the menstrual cycle. Similarly, testosterone may have analgesic effects in men, which could contribute to differences in pain sensitivity between genders.</p> <p> </p>
Characterizing Non-predictable Breakthrough Cancer Pain in frmale cancer patients: a secondary analysis from IOPS-MS study
<p>IOPS-MS was a big multicentric study with the aim of characterizing BTcP in a large number of patients belonging to different settings and assessing possible factors influencing its development. Moreover, NP-BTcP topic was addressed elsewhere [https://doi.org/10.3390/cancers13164018].</p> <p>The principal aim of this work is to characterize breast cancer (BC) patients compared with no-female-specific cancers (no-FSC). The importance of such focus lies on detecting main behavior of a hormone-dependent cancer type with respect to tumors which are not specific for women.</p>
Biomass temporal stability increases at two spatial scales during secondary succession
<p>Ecological stability has long been considered to change over succession, but how secondary succession influences the relationship between diversity and temporal stability of biomass production at different spatial scales is poorly understood.</p> <p>We studied changes in plant diversity, functional temporal stability (biomass production) and compositional temporal stability (the latter two are hereafter referred to as functional stability and compositional stability) and explored the stabilizing roles of plant diversity at two spatial scales (small plots of 0.25 m2 area and large transects of 1.25 m2 area) during secondary succession in a subalpine meadow from 2003-2010.</p> <p>Our results showed that both plant diversity and functional and compositional stability increased at the small plot scale and large transect scale during secondary succession. As secondary succession proceeded, higher average alpha diversity (i.e., species diversity at the plot scale) led to higher functional and compositional stability at the plot scale by mainly species stability, predominantly contributing to higher functional and compositional stability at the large transect scale. In addition, Simpson-based beta diversity (i.e., compositional dissimilarity among communities within the same transect), while unaffected by succession, contributed to functional stability at the large transect scale by promoting asynchronous dynamics among communities.</p> <p><strong>Synthesis: </strong>Our study highlights the stabilizing effects of plant diversity across the two spatial scales during secondary succession. Our findings provide the first empirical evidence that biodiversity-mediated effects on ecosystem temporal stability strengthen over successional time, suggesting that the stabilizing effects of biodiversity should be considered across spatial and temporal scales in the face of global changes and biodiversity loss.</p>
THE ROLE OF IMMATURE GRANULOCYTES IN THE EARLY DIAGNOSIS OF PNEUMONIA DEVELOPING SECONDARY TO RIB FRACTURES
<p>This retrospective study aimed to investigate the role of immature granulocytes (IGs) in the early diagnosis of pneumonia secondary to rib fractures.</p>
Fig. 1 in Secondary metabolites from the underground parts of Valeriana sisymbriifolia Vahl. and their in vitro cytotoxic activities
Fig. 1. Structures of the compounds (1–12) isolated from the underground parts of V. sisymbriifolia.
Transcriptional repression by a secondary DNA binding surface of DNA topoisomerase I safeguards against transcription overdrive
<p>Molecular dynamics simulation input files and processed output trajectories.</p>
Secondary Graft Loss After Third-party "Off-The-Shelf" Antigen-Specific T cell Infusion
<p>Here, we describe a severe adverse event of virus-specific T cell (VST therapy) in an infant with severe combined immunodeficiency who received VSTs for treatment of CMV viremia post-transplant and developed secondary graft rejection at 1-month post-VST infusion associated with the expansion of VST donor-derived T cells. Deposited here are the bulk repertoire, single-cell gene expression and TCR, and flow cytometry data from the study.</p><p><strong>bulk_rep.zip contains tables of alpha/beta TCR sequences for post-infusion, VST donor, and VST product samples, and samples stimulated with neoepitope peptides. </strong></p><p><strong>VST_agg_wTCR_SS.rds is an R Data Serialization file containing a Seurat object of the processed 10X single-cell gene expression and TCR profiling for the post-infusion, VST donor, and VST product samples. TCR information is stored in the meta.data slot.</strong></p><p><strong>P0230D neoantigen expansions.acs, P0230D pentamers.acs, and P0230D_MLR.acs contain the flow cytometry data for the neoantigen and mixed lymphocyte reaction experiments.</strong></p>
Recovery Rate in Secondary Hypothyroidism
ClinicalTrials.gov study NCT05276856. IPD Sharing: Not stated. Countries: 1. Publications: 6.
Safety and Efficacy of Bosentan in Patients With Diastolic Heart Failure and Secondary Pulmonary Hypertension
ClinicalTrials.gov study NCT00820352. IPD Sharing: Not stated. Countries: 1. Publications: 20.
Rapid Antidepressant Improvement Secondary to Excitatory Brain Responses
ClinicalTrials.gov study NCT04276259. IPD Sharing: YES. Countries: 1. Publications: 1.
An Assessment of an HIV Prevention Intervention (Project AIM) Among Junior Secondary School Students in Eastern Botswana
ClinicalTrials.gov study NCT02455583. IPD Sharing: Not stated. Countries: 1. Publications: 1.
Office Hysteroscopy in Secondary Infertility After Cesarean Section
ClinicalTrials.gov study NCT03166657. IPD Sharing: NO. Countries: 1. Publications: 2.
ScienceDex guides
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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.