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Dataset results
270 results for “Disease phenotype”
Extended data for publication "Dictionary of disease ontologies (DODO): a graph database to facilitate access and interaction with disease and phenotype ontologies"
<p>This archive contains the extended data for the publication "Dictionary of disease ontologies (DODO): a graph database to facilitate access and interaction with disease and phenotype ontologies". This includes two sheet within the "ExtendedData.xlsx" file:</p> <p>Table1: List of all functions available in DODO R package with description and scope details.<br> Table2: List of ontologies among which the cross-reference relations are encoded as is_xref</p> <p>Data are available under the terms of the <a href="http://creativecommons.org/publicdomain/zero/1.0/">Creative Commons Zero "No rights reserved" data waiver</a> (CC0 1.0 Public domain dedication).</p>
Supplementary data - Multiomic analysis of human kidney disease identifies a tractable inflammatory and pro-fibrotic tubular cell phenotype
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Data from: Detection of human disease conditions by single-cell morpho-rheological phenotyping of blood
Blood is arguably the most important bodily fluid and its analysis provides crucial health status information. A first routine measure to narrow down diagnosis in clinical practice is the differential blood count, determining the frequency of all major blood cells. What is lacking to advance initial blood diagnostics is an unbiased and quick functional assessment of blood that can narrow down the diagnosis and generate specific hypotheses. To address this need, we introduce the continuous, cell-by-cell morpho-rheological (MORE) analysis of diluted whole blood, without labeling, enrichment or separation, at rates of 1,000 cells/sec. In a drop of blood we can identify all major blood cells and characterize their pathological changes in several disease conditions in vitro and in patient samples. This approach takes previous results of mechanical studies on specifically isolated blood cells to the level of application directly in blood and adds a functional dimension to conventional blood analysis.
Metabolic Control of Aging and Disease - the MetAGE Deep Phenotyping Cohort
ClinicalTrials.gov study NCT06511297. IPD Sharing: UNDECIDED. Countries: 1. Publications: 0.
National Ophthalmic Genotyping and Phenotyping Network (eyeGENE (Registered Trademark)), Stage 3 - Expansion of DNA and Data Repositories for Rare Inherited Ophthalmic Diseases
ClinicalTrials.gov study NCT06491615. IPD Sharing: NO. Countries: 1. Publications: 0.
Establishment of Genomic and Phenotypic Database for Niemann-Pick Disease, Type C
ClinicalTrials.gov study NCT05588167. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Amyloid Prediction in Early Stage Alzheimer's Disease Through Speech Phenotyping - PAST Extension
ClinicalTrials.gov study NCT04937959. IPD Sharing: UNDECIDED. Countries: 1. Publications: 0.
Metabolic Phenotypes and Heterogeneity in Disease Burden Risk in Type 1 Diabetes
ClinicalTrials.gov study NCT05609279. IPD Sharing: UNDECIDED. Countries: 1. Publications: 0.
A Cohort of Patients With Phenotyped Diffuse Interstitial Lung Disease With Longitudinal Follow-up
ClinicalTrials.gov study NCT05810493. IPD Sharing: NO. Countries: 1. Publications: 0.
Deep Phenotyping of Bone Disease in Type 2 Diabetes and Relations to Diabetic Neuropathy
ClinicalTrials.gov study NCT05642143. IPD Sharing: UNDECIDED. Countries: 1. Publications: 0.
Phenotypic Characteristics of Inflammatory Bowel Disease in Southeast Asian Population - A Multi-centered US Study
ClinicalTrials.gov study NCT00573846. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Amyloid Prediction in Early Stage Alzheimer's Disease Through Speech Phenotyping - FUTURE Extension
ClinicalTrials.gov study NCT04951284. IPD Sharing: UNDECIDED. Countries: 1. Publications: 0.
Real-World Effectiveness of High-Dose Tafamidis on Neurologic Disease Progression in Mixed-Phenotype Transthyretin Amyloid Cardiomyopathy
ClinicalTrials.gov study NCT06393465. IPD Sharing: NO. Countries: 1. Publications: 0.
Genotype -Phenotype Correlation of PKLR Variants With Pyruvate Kinase, 2,3-Diphosphglycerate and Adenosine Triphosphate Activities in Red Blood Cells of People With Sickle Cell Disease
ClinicalTrials.gov study NCT03685721. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Genotype-phenotype Characterization Study on Genetic Diseases With Immune and Neurological Dysfunctions
ClinicalTrials.gov study NCT06235580. IPD Sharing: NO. Countries: 1. Publications: 0.
Phenotypic Measurements and Their Relation to Disease Exacerbation in COPD Patients
ClinicalTrials.gov study NCT03300739. IPD Sharing: NO. Countries: 1. Publications: 0.
Deep Phenotyping of Peripheral Blood Cells and Circulating Factors in Metabolic Diseases
ClinicalTrials.gov study NCT06396871. IPD Sharing: UNDECIDED. Countries: 1. Publications: 0.
Characterization of Different Phenotypes of Microvascular Dysfunction and Their Impact on Angina Severity in Patients With Chronic Angina in the Absence of Obstructive Coronary Artery Disease.
ClinicalTrials.gov study NCT05686707. IPD Sharing: NO. Countries: 1. Publications: 0.
Amyloid Prediction in Early Stage Alzheimer's Disease Through Speech Phenotyping
ClinicalTrials.gov study NCT04928976. IPD Sharing: UNDECIDED. Countries: 1. Publications: 0.
Research Into the Molecular Bases of a New Phenotype Combining Premature White Hair, Polycystic Kidney Disease, Aortic Dilation/Dissection and Lymphopenia
ClinicalTrials.gov study NCT03651388. IPD Sharing: Not stated. Countries: 1. Publications: 0.
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.