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.
291
datasets available to search
ShareScore release 0.9.0
Dataset results
291 results for “Genetic variants”
Genetic variant rs11607019 in SIRT3 regulate gene expression in human cells
GEO Series GSE299443. Homo sapiens. 5 samples. Type: Expression profiling by high throughput sequencing.
Large scale functional screen identifies genetic variants with splicing effects in modern and archaic humans
GEO Series GSE201856. Homo sapiens. 12 samples. Type: Expression profiling by high throughput sequencing.
Genetic and epigenetic screens in primary human T cells link candidate causal autoimmune variants to T cell networks [gRNA]
GEO Series GSE296620. Homo sapiens. 8 samples. Type: Expression profiling by high throughput sequencing.
Massively parallel functional dissection of schizophrenia associated non-coding genetic variants [RNA-seq]
GEO Series GSE225813. Homo sapiens. 22 samples. Type: Expression profiling by high throughput sequencing.
Effect of Fnip2 genetic variant in mouse tissues
GEO Series GSE200620. Mus musculus. 76 samples. Type: Expression profiling by high throughput sequencing.
Fine Mapping and Functional Characterization of Genetic Variants in the FAM13A Chronic Obstructive Pulmonary Disease GWAS locus using Massively Parallel Reporter Assays
GEO Series GSE109452. Homo sapiens. 4 samples. Type: Other.
Massively parallel functional dissection of schizophrenia associated non-coding genetic variants [MPRA]
GEO Series GSE225815. Mus musculus; Homo sapiens. 51 samples. Type: Other.
Massively parallel functional dissection of schizophrenia associated non-coding genetic variants [ATAC-seq]
GEO Series GSE225816. Homo sapiens. 19 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Linkage of genetic drivers and strain-specific germline variants confound mouse cancer genome analyses
GEO Series GSE154537. Mus musculus. 4 samples. Type: Expression profiling by array.
Massively parallel functional dissection of schizophrenia associated non-coding genetic variants [scRNA-seq]
GEO Series GSE225814. Homo sapiens. 12 samples. Type: Expression profiling by high throughput sequencing.
Genetic variants that impact alternative polyadenylation in cancer represent candidate causal risk loci [RNA-seq]
GEO Series GSE241699. Homo sapiens. 154 samples. Type: Expression profiling by high throughput sequencing.
Massively parallel functional dissection of schizophrenia associated non-coding genetic variants
GEO Series GSE225817. Mus musculus; Homo sapiens. 104 samples. Type: Expression profiling by high throughput sequencing; Other; Genome binding/occupancy profiling by high throughput sequencing.
Disambiguating Transcriptional Effects from Post-Transcriptional Effects of Genetic Variants with an Inferred Stability Optimized Massively Parallel Reporter Assay (ISOMPRA).
GEO Series GSE295080. Mus musculus; Escherichia coli; Adeno-associated virus 9; Homo sapiens. 297 samples. Type: Expression profiling by high throughput sequencing.
Human induced pluripotent stem cell-derived microglia with a CX3CR1-V249I genetic variant exhibit dysfunctional phenotypes and modulate neuronal growth and function
GEO Series GSE302806. Homo sapiens. 15 samples. Type: Expression profiling by high throughput sequencing.
Heterozygous NFKB1 variant causes inflammatory dysregulation shaped by broader genetic context in common variable immunodeficiency
GEO Series GSE311471. Homo sapiens. 48 samples. Type: Expression profiling by high throughput sequencing.
Genetic variants associated with coronary artery disease in Indians
GEO Series GSE109068. Homo sapiens. 300 samples. Type: Genome variation profiling by SNP array.
EML4-ALK variant-specific genetic interactions shape lung tumorigenesis
GEO Series GSE302650. Mus musculus. 36 samples. Type: Expression profiling by high throughput sequencing.
Genetic and epigenetic screens in primary human T cells link candidate causal autoimmune variants to T cell networks [MPRA]
GEO Series GSE297471. Homo sapiens. 13 samples. Type: Expression profiling by high throughput sequencing.
Genetic variants involved in the vitamin D metabolism and adiposity markers
<p>This dataset contains SNPs-gene, phenotype, vitamin D concentration analyzed in article entitled "<em>Association between genetic variants involved in the vitamin D metabolism, adiposity markers, circulating 25-hydroxyvitamin D levels, and vitamin D deficiency</em>". </p> <p>The dataset is available from the corresponding author on reasonable request.</p> <p> </p>
Benign genetic variants data
<p>Results of similarity searches using the 7,210 nt sequence of KCNQ1OT as a query against flanking sequences around benign genetic variants and the original set of non-trait-associated control sites.</p>
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.