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328 results for “Analysis results”
Analysis of 2-cell embryos resulted from COPS3 protein inactivation in pronuclear-stage mouse oocytes
GEO Series GSE155205. Mus musculus. 8 samples. Type: Expression profiling by array.
ANALYSIS OF THE RESULTS OF SURGICAL TREATMENT OF IATROGENIC DAMAGE TO THE MAIN BILY DUCTS
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The result of research and analysis of disaster knowledge
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Muhammet Safa Alkoyun Thesis (Turkish) and Thesis Results Drought Analysis of Gediz Basin
<p>Muhammet Safa Alkoyun Thesis (Turkish) and Thesis Results Drought Analysis of Gediz Basin</p>
F in Revision and biogeographical analysis of the black-chinned tilapia Sarotherodon melanotheron (Teleostei, Cichlidae): results of morphometric, allozyme, globin chain and mtDNA studies
F. 3. Plot of factor 1 taken from a PCA on six meristic counts and factor 3 taken from a PCA on 18 log-transformed measurements including the 60 specimens from Congo- Brazzaville (Loeme and Kouilou) and Gabon (Santa Clara) and three syntypes of Tilapia dolloi Boulenger 1899.
FIGURE 1. Spectral analysis results for a hypothetical data set. Each bar represents a in Exploring character conflict in molecular data*
FIGURE 1. Spectral analysis results for a hypothetical data set. Each bar represents a different split in the tree. Bars above the x-axis represent the relative degree to which the data support that split. Bars below the x-axis represent the relative degree to which the data support relationships that conflict with (i.e. are incompatible with) that split. In this example, there is significant phylogenetic signal for relationships that conflict with splits 3, 5, 8 and 11.
Figure 4. Cladograms resulting from phylogenetic analyses. Data matrix for each analysis includes 11 taxa and 46 in A new taeniolabidoid multituberculate (Mammalia) from the middle Puercan of the Nacimiento Formation, New Mexico, and a revision of taeniolabidoid systematics and phylogeny
Figure 4. Cladograms resulting from phylogenetic analyses. Data matrix for each analysis includes 11 taxa and 46 characters. Letters refer to nodes (see Appendix S3 for list of common synapomorphies for each node). Numbers above each node are Bremer support values. A, Essonodon browni as outgroup, 51 steps, nine trees, consistency index (CI) = 0.647, retention index (RI) = 0.600; B, Meniscoessus robustus as outgroup, 62 steps, two trees, CI = 0.677, RI = 0.615; C, Cimolomys gracilis as outgroup, 56 steps; two trees; CI = 0.661; RI = 0.604; D, Cimexomys judithae as outgroup, 64 steps; 25 trees; CI = 0.703; RI = 0.620; E, Microcosmodon conus as outgroup, 60 steps; two trees; CI = 0.733; RI = 0.673.
Critical Analysis of the Results in the Management of Penetrating Abdominal Trauma in the Past Fifteen Years.
ClinicalTrials.gov study NCT06228261. IPD Sharing: NO. Countries: 0. Publications: 0.
Impact of a Limitation Section on the Meta-analysis Results' Interpretation
ClinicalTrials.gov study NCT01848600. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Analysis of the Results of Treatment for Cervical Carcinoma in Limburg
ClinicalTrials.gov study NCT01059695. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Clinical Results and Restenosis Analysis of Symptomatic Ostial Vertebral Artery Stenosis Treated With Tubular Coronary Stents
ClinicalTrials.gov study NCT00172458. IPD Sharing: Not stated. Countries: 1. Publications: 0.
The mdx mutation in the 129/Sv background results in a milder phenotype: Transcriptome comparative analysis searching for the protective factors
GEO Series GSE77126. Mus musculus. 22 samples. Type: Expression profiling by array.
Differential gene expression analysis in motor and sensory cortex as a result of experimental autoimmune encephalomyelitis (EAE), a neuroinflammatory model for Multiple sclerosis.
GEO Series GSE47900. Mus musculus. 20 samples. Type: Expression profiling by array.
TET2 mutations in acute myeloid leukemia: Results from a comprehensive genetic and clinical analysis of the AML Study Group (AMLSG)
GEO Series GSE32246. Homo sapiens. 333 samples. Type: Expression profiling by array.
Chromosomal microarray analysis for validation of the WGS-based CNV detection results in recurrent miscarriage couples
GEO Series GSE83941. Homo sapiens. 78 samples. Type: Genome variation profiling by array.
Single-cell analysis results of pituitary tissue from normal diet (ND) mice and high-fat diet (HFD) mice
GEO Series GSE310493. Mus musculus. 4 samples. Type: Expression profiling by high throughput sequencing.
Data set and results of regression analysis of gene variants in Prostate Cancer patients from Mexico-mestizo population.
<p>Genotyping assays were performed using TaqMan SNP Genotyping Assays probes C_27532228_20 and C_2362601_10 (Life Technologies, Carlsbad, CA, USA).</p> <p>Thermalcycler: StepOnePlus™ Real-Time PCR (Thermo Fisher Scientific, Waltham, MA, USA).</p> <p>Sample: genomic DNA from blood.</p> <p>Subjects: Prostate cancer patients and controls (healthy and benign prostatic hyperplasia). </p> <p>Results of Regression Anlysis for clinical features of gene SRD5A2 variants (rs9282858 and<strong> </strong>rs523349) in prostate cancer patients from Mexican-mestizo population.</p> <p>Starting with the full model, successive models are created, each one using one less regressor (or covariate) than the previous model. Each of the regressors currently in the model is removed to create a "trial" model excluding that regressor. The p-value of the current model (or full model) versus the trial model (or reduced model) is calculated, and the model with the smallest p-value is used as the next model. This method removes the least significant variable from the current model. If every p-value is smaller than the p-value cut off specified, the backward elimination method stops. The method also stops if all variables have been removed from the model, or if all variables left are included in the original reduced model. From the standpoint of further analysis, the final model becomes the "full model" for this set of potential regressors</p> <p>Ethics approval and consent to participate in the study: The protocol and informed consent were approved by the Ethics and Research Committee of the School of Medicine (Universidad Autonoma de Nuevo Leon), with registration number UR16-00007. In the data set, no data was included that compromises the confidentiality of the participating subjetcs.</p> <pre> </pre>
Solar analysis and energy simulation results of the acedemic building in Macau
<p>The solar analysis result were calculated by the Insigt of the Autodesk Revit, the energy simulation results were gotten from the Green Building Studio which is the cloud-based calculation platform.</p>
Dataset related to article "Prospective Validation of the ROL System in Substaging pT1 High-Grade Urothelial Carcinoma: Results from a Mono-Institutional Confirmatory Analysis in BCG Treated Patients"
<p>This record contains raw data related to article "Prospective Validation of the ROL System in Substaging pT1 High-Grade Urothelial Carcinoma: Results from a Mono-Institutional Confirmatory Analysis in BCG Treated Patients"</p><p><strong>Abstract</strong></p><p>Patients with pT1 high-grade (HG) urothelial carcinoma (UC) and a very high risk of progression might benefit from immediate radical cystectomy (RC), but this option remains controversial. Validation of a standardized method to evaluate the extent of lamina propria (LP) invasion (with recognized prognostic value) in transurethral resection (TURBT) specimens is still needed. The Rete Oncologica Lombarda (ROL) system showed a high predictive value for progression after TURBT in recent retrospective studies. The ROL system was supposed to be validated on a large prospective series of primary urothelial carcinomas from a single institution. From 2016 to 2020, we adopted ROL for all patients with pT1 HG UC on TURBT. We employed a 1.0-mm threshold to stratify tumors in ROL1 and ROL2. A total of 222 pT1 HG UC were analyzed. The median age was 74 years, with a predominance of men (73.8%). ROL was feasible in all cases: 91 cases were ROL1 (41%), and 131 were ROL2 (59%). At a median follow-up of 26.9 months (IQR 13.8-40.6), we registered 81 recurrences and 40 progressions. ROL was a significant predictor of tumor progression in both univariable (HR 3.53; CI 95% 1.56-7.99; <i>p</i> < 0.01) and multivariable (HR 2.88; CI 95% 1.24-6.66; <i>p</i> = 0.01) Cox regression analyses. At Kaplan-Meier estimates, ROL showed a correlation with both PFS (<i>p</i> = 0.0012) and RFS (<i>p</i> = 0.0167). Our results confirmed the strong predictive value of ROL for progression in a large prospective series. We encourage the application of ROL for reporting the extent of LP invasion, substaging T1 HG UC, and improving risk tables for urological decision-making.</p>
Results of surgical ventricular reconstruction in a specialized center and in comparison to the STICH trial: Rationale and study protocol for a patient-level pooled analysis
<p>Dataset from Gaudino M, Castelvecchio S, Rahouma M, Robinson NB, Audisio K, Soletti GJ, Garatti A, Benedetto U, Girardi LN, Menicanti L. Results of surgical ventricular reconstruction in a specialized center and in comparison to the STICH trial: Rationale and study protocol for a patient-level pooled analysis. J Card Surg. 2021 Feb;36(2):689-692. doi: 10.1111/jocs.15315. Epub 2021 Jan 13. PMID: 33438823.</p> <p>Abstract</p> <p><strong>Introduction: </strong>Post-infarction left ventricular remodeling is associated with increased mortality in patients with ischemic heart disease. Surgical ventricular reconstruction (SVR) in addition to coronary artery bypass grafting (CABG) has been proposed to reduce left ventricular volume and improve clinical outcomes. The Surgical Treatment for Ischemic Heart Failure (STICH) trial found that the addition of SVR to CABG did not reduce the rates of death or rehospitalization in the 5 years after surgery compared to CABG alone. Like all randomized trials, STICH has limitations and it has been hypothesized that it may have underestimated the treatment effect of SVR. The aim of this study is to evaluate the results of SVR in one of the largest contemporary single-center series and to compare the results with those of the STICH trial using individual patient's data.</p> <p><strong>Methods and analysis: </strong>Individual data of patients who underwent SVR with or without CABG will be obtained from San Donato University Hospital in Milan. Using multivariable Cox regression analysis, significant prognostic indicators in this cohort will be identified. We will then compare the San Donato cohort to individual patient's data from the SVR arm of Hypothesis 2 of the STICH trial and from both arms of the STICH Extended Study (STICHES). To reduce confounders, propensity score adjustment will be used for this comparison. The primary endpoint will be all-cause mortality. Data will be merged and analyzed independently at Weill Cornell Medicine in New York.</p>
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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.