Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
2,880
datasets available to search
ShareScore release 0.9.0
Dataset results
2,880 results for “variant”
High-throughput characterization of functional variants highlights heterogeneity and polygenicity underlying lung cancer susceptibility
GEO Series GSE245699. Homo sapiens. 22 samples. Type: Expression profiling by high throughput sequencing.
A comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants (WGTP)
GEO Series GSE28189. Homo sapiens. 18 samples. Type: Genome variation profiling by genome tiling array.
PWWP2A variant NuRD complex represses intragenic spurious transcription initiation
GEO Series GSE148382. Mus musculus. 8 samples. Type: Expression profiling by high throughput sequencing.
Male biased islet b cell dysfunction is caused by the MODY MAFA S64F variant by inducing premature aging and senescence
GEO Series GSE183561. Mus musculus. 18 samples. Type: Expression profiling by high throughput sequencing.
A myeloid trisomy 21-associated gene variant is protective from Alzheimer’s disease
GEO Series GSE252238. Homo sapiens; Mus musculus. 23 samples. Type: Expression profiling by high throughput sequencing.
Multiple de novo copy number variant (MdnCNV) driven mirror traits and blended phenotype
GEO Series GSE176427. Homo sapiens. 6 samples. Type: Genome variation profiling by genome tiling array.
Structural variants drive context dependent oncogene activation in cancer
GEO Series GSE147123. Homo sapiens. 164 samples. Type: Other; Expression profiling by high throughput sequencing.
Glucocorticoids Unmask Silent Non-Coding Genetic Risk Variants for Common Diseases
GEO Series GSE185941. Homo sapiens. 146 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing; Other.
The histone variant macroH2A1 regulates key genes for myogenic cell fusion in a splice-isoform dependent manner [ChIP-Seq]
GEO Series GSE148044. Mus musculus. 2 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Newly identified ZNHIT3 variants, which cause intrauterine fetal loss, disrupt snoRNP assembly
GEO Series GSE273112. Homo sapiens. 18 samples. Type: Expression profiling by high throughput sequencing.
Effect of neuropathy-associated MCM3AP variants on gene expression in fibroblasts
GEO Series GSE135098. Homo sapiens. 8 samples. Type: Expression profiling by high throughput sequencing.
HIRA-mediated loading of histone variant H3.3 controls androgen-induced transcription by regulation of AR/BRD4 complex assembly at enhancers [RNA-Seq]
GEO Series GSE230741. Homo sapiens. 57 samples. Type: Expression profiling by high throughput sequencing.
Neanderthal Adaptively Introgressed Genetic Variants Regulate Human Immune Genes In Vitro.
GEO Series GSE169200. Homo sapiens; synthetic construct. 13 samples. Type: Other.
Combinatorial targeting of a novel MET/EMT network components by macroH2A variants safeguards cell identity [RNA-seq]
GEO Series GSE215883. Mus musculus. 28 samples. Type: Expression profiling by high throughput sequencing.
HIV-1 integrase variants retarget viral integration and are associated with disease progression in a chronic infection cohort.
GEO Series GSE61003. Homo sapiens. 2 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural hereditary hearing loss
GEO Series GSE64088. Homo sapiens. 308 samples. Type: Genome variation profiling by genome tiling array.
A common cis-regulatory variant impacts normal-range and disease-associated human facial shape through regulation of PDKCC during chondrogenesis
GEO Series GSE212234. Homo sapiens. 35 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
A Novel Dominant Negative Variant of IRF8 in a Mother and Son: Clinical, Phenotypic and Biological Characteristics
GEO Series GSE263370. Homo sapiens. 3 samples. Type: Expression profiling by high throughput sequencing.
Integrated analysis of genetic variants regulating retinal transcriptome (GREx) identifies genes underlying age-related macular degeneration
GEO Series GSE115828. Homo sapiens. 523 samples. Type: Expression profiling by high throughput sequencing.
A gain-of-function single nucleotide variant creates a new promoter which acts as an orientation-dependent enhancer-blocker (NG_Capture-C)
GEO Series GSE159874. Homo sapiens. 36 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.