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412
datasets available to search
ShareScore release 0.7.1
Dataset results
412 results for “genetic risk”
Data from: Phased whole-genome genetic risk in a family quartet using a major allele reference sequence
Open the record for dataset details and reuse information.
A hidden layer of structural variation in transposable elements reveals potential genetic modifiers in human disease-risk loci
GEO Series GSE167409. Homo sapiens. 39 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing.
Interpreting type 1 diabetes risk with genetics and single cell epigenomics
GEO Series GSE163160. Homo sapiens. 12 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Functional Validation of Common Idiopathic Pulmonary Fibrosis Genetic Risk Variants [850k methylation arrays]
GEO Series GSE175458. Homo sapiens. 547 samples. Type: Methylation profiling by genome tiling array.
Integrated single-cell chromatin and transcriptomic analyses of human scalp reveal etiological insights into genetic risk for hair and skin disease [scRNA-Seq]
GEO Series GSE212447. Homo sapiens. 10 samples. Type: Expression profiling by high throughput sequencing.
An integrated approach to identify environmental modulators of genetic risk factors for complex traits
GEO Series GSE179347. Homo sapiens. 238 samples. Type: Expression profiling by high throughput sequencing.
DNA methylation in lung cells is a key modulator of asthma endotypes and genetic risk [RNA-seq]
GEO Series GSE85567. Homo sapiens. 85 samples. Type: Expression profiling by high throughput sequencing.
Cross-cancer genome-wide association study of endometrial cancer and epithelial ovarian cancer identifies genetic risk regions associated with risk of both cancers
GEO Series GSE155328. Homo sapiens. 1 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Nutrigenomic profiling identifies ZIP10 (SLC39A10) as a regulator of erythroid zinc homeostasis with genetic associations to anemia risk II
GEO Series GSE310207. Mus musculus. 7 samples. Type: Expression profiling by high throughput sequencing.
Multi-omics co-localization with genome-wide association studies reveals a context-specific genetic mechanism at a childhood onset asthma risk locus [Methylation array]
GEO Series GSE172365. Homo sapiens. 206 samples. Type: Methylation profiling by array.
Integration of Alzheimer's disease genetics and myeloid genomics identifies disease risk regulatory elements and genes [RNA-seq]
GEO Series GSE164313. Homo sapiens. 4 samples. Type: Expression profiling by high throughput sequencing.
Conserved dorsal horn neuron subtype-specific enhancers are implicated in the genetic risk of chronic pain [Macaque snRNA-seq]
GEO Series GSE253953. Macaca mulatta. 3 samples. Type: Expression profiling by high throughput sequencing.
Genetic Variants of Phospholipase C-γ2 Confer Altered Microglial Phenotypes and Differential Risk for Alzheimer’s Disease.
GEO Series GSE237495. Mus musculus. 30 samples. Type: Expression profiling by high throughput sequencing.
Integration of Alzheimer's disease genetics and myeloid genomics identifies disease risk regulatory elements and genes [ATAC-seq]
GEO Series GSE164314. Homo sapiens. 3 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Coronary artery disease genes SMAD3 and TCF21 promote opposing interactive genetic programs that regulate smooth muscle cell differentiation and disease risk [ChIP-seq]
GEO Series GSE115317. Homo sapiens. 2 samples. Type: Genome binding/occupancy profiling by high throughput sequencing; Third-party reanalysis.
Conserved dorsal horn neuron subtype-specific enhancers are implicated in the genetic risk of chronic pain.
GEO Series GSE253954. Mus musculus; Macaca mulatta. 17 samples. Type: Other; Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing.
Parkinson’s Disease Genetic Risk in a Midbrain Neuronal Cell Line
GEO Series GSE109706. Homo sapiens. 20 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing.
Multi-omics co-localization with genome-wide association studies reveals a context-specific genetic mechanism at a childhood onset asthma risk locus
GEO Series GSE172368. Homo sapiens. 396 samples. Type: Expression profiling by high throughput sequencing; Methylation profiling by array.
Identification of a global gene expression signature associated with the genetic risk of catastrophic fracture in iPSC-derived osteoblasts from Thoroughbred horses
GEO Series GSE255417. Equus caballus. 14 samples. Type: Expression profiling by high throughput sequencing.
Genetic Variants of Phospholipase C-γ2 Confer Altered Microglial Phenotypes and Differential Risk for Alzheimer’s Disease
GEO Series GSE239658. Mus musculus. 72 samples. Type: Expression profiling by high throughput sequencing; 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.