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291
datasets available to search
ShareScore release 0.9.0
Dataset results
291 results for “genetic variant”
Effect of Myocilin Genetic Variants on Intraocular Pressure and Pressure Variation in Sitting and Supine Positions
ClinicalTrials.gov study NCT00906087. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Data from: Macrophage adaptation leads to parallel evolution of genetically diverse Escherichia coli small-colony variants with increased fitness in vivo and antibiotic collateral sensitivity
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Data from: Frequency and distribution of 152 genetic disease variants in over 100,000 mixed breed and purebred dogs
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Genetic epidemiology of blood type, disease and trait variants, and genome-wide genetic diversity in over 11,000 domestic cats
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Association of common genetic variants with brain microbleeds: A genome-wide association study
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Data from: Admixture and the organization of genetic diversity in a butterfly species complex revealed through common and rare genetic variants
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Classification of Type 2 Diabetes Genetic Variants and a Novel Genetic Risk Score Association with Insulin Clearance
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Extensive genetic diversity and substructuring among zebrafish strains revealed through copy number variant analysis (CGH)
GEO Series GSE33962. Danio rerio. 3 samples. Type: Genome variation profiling by genome tiling array.
IRF5 genetic risk variants drive myeloid-specific IRF5 hyper-activation and pre-symptomatic SLE
GEO Series GSE137067. Homo sapiens. 14 samples. Type: Expression profiling by high throughput sequencing.
Glucocorticoids Unmask Silent Non-Coding Genetic Risk Variants for Common Diseases [RNA-seq]
GEO Series GSE185908. Homo sapiens. 120 samples. Type: Expression profiling by high throughput sequencing.
Massively parallel reporter assay investigates shared genetic variants of eight psychiatric disorders
GEO Series GSE276947. Homo sapiens. 10 samples. Type: Expression profiling by high throughput sequencing.
Fucntional genetic variants mediate their regulatory effects through altered transcription factor binding. [dirRNA-seq]
GEO Series GSE117484. Homo sapiens. 17 samples. Type: Expression profiling by high throughput sequencing.
Genetic effects on liver chromatin accessibility identify disease regulatory variants [ATAC-seq]
GEO Series GSE164870. Homo sapiens. 20 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Extensive genetic diversity and substructuring among zebrafish strains revealed through copy number variant analysis
GEO Series GSE28328. Danio rerio. 93 samples. Type: Expression profiling by array; Genome variation profiling by genome tiling array.
PNPLA3-I148M genetic variant rewires lipid metabolism to drive programmed cell death in human hepatocytes
GEO Series GSE309786. Homo sapiens. 8 samples. Type: Expression profiling by high throughput sequencing.
Copy number variants in candidate genes are genetic modifiers of Hirschsprung disease
GEO Series GSE29051. Homo sapiens. 28 samples. Type: Genome variation profiling by genome tiling array.
Unravelling Stargardt Disease (STGD1): Modelling Genotype-Phenotype Correlations and Unresolved Genetic Variants in iPSC-Derived Retinal Organoids
GEO Series GSE236097. Homo sapiens. 4 samples. Type: Expression profiling by high throughput sequencing.
Functional characterization of genetic variants associated with upper digestive cancers
GEO Series GSE240214. Homo sapiens. 8 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Impact of the Multiple Sclerosis associated genetic variant CD226 Gly307Ser on human CD8 T cell functions
GEO Series GSE266132. Homo sapiens. 80 samples. Type: Expression profiling by high throughput sequencing.
Glucocorticoids Unmask Silent Non-Coding Genetic Risk Variants for Common Diseases [STARR-seq]
GEO Series GSE185939. Homo sapiens. 16 samples. Type: Other.
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.