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”
Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males
GEO Series GSE8691. Homo sapiens. 57 samples. Type: Genome variation profiling by genome tiling array.
Heterozygous variants in POLR1A cause diverse human phenotypes
GEO Series GSE206197. Mus musculus. 10 samples. Type: Expression profiling by high throughput sequencing.
A multimorphic variant in ThPOK causes an inborn error of immunity with T cell defects and fibrosis [T cells]
GEO Series GSE291518. Homo sapiens. 9 samples. Type: Expression profiling by high throughput sequencing.
Deciphering COVID-19 host transcriptomic complexity and variations for therapeutic discovery against new variants
GEO Series GSE187420. Homo sapiens. 9 samples. Type: Expression profiling by high throughput sequencing.
Genetic variants regulating ORMDL3 expression are determinants of susceptibility to childhood asthma
GEO Series GSE8052. Homo sapiens. 404 samples. Type: Expression profiling by array.
Genome-wide maps of histone variant H3.3 occupancy in zebrafish cardiomyocytes [RNA]
GEO Series GSE81865. Danio rerio. 4 samples. Type: Expression profiling by high throughput sequencing.
Bi-allelic loss-of-function variants in CLCN2 cause retinal degeneration via impairing phagocytosis in patient retinal pigment epithelium
GEO Series GSE216834. Homo sapiens. 6 samples. Type: Expression profiling by high throughput sequencing.
Histone H1 binding is restricted by histone variant H3.3
GEO Series GSE16885. Drosophila melanogaster. 24 samples. Type: Expression profiling by array; Genome binding/occupancy profiling by genome tiling array.
De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway
GEO Series GSE189065. Homo sapiens. 4 samples. Type: Expression profiling by high throughput sequencing.
Massively parallel screen uncovers many rare 3’ UTR variants regulating mRNA abundance of cancer driver genes
GEO Series GSE232573. Homo sapiens. 100 samples. Type: Expression profiling by high throughput sequencing; Other.
DUX4-induced histone variants H3.X and H3.Y mark DUX4 target genes for expression (CUT&RUN)
GEO Series GSE119401. Homo sapiens. 8 samples. Type: Other.
Analysis of Kozak sequences variants of haploinsufficient genes
GEO Series GSE210035. Homo sapiens. 8 samples. Type: Other.
Enhancer Poising Enables Pathogenic Gene Activation by Noncoding Variants [RNA-seq]
GEO Series GSE299698. Mus musculus. 4 samples. Type: Expression profiling by high throughput sequencing.
NRCAM variant defined by microexon skipping is a targetable surface proteoform in high-grade gliomas
GEO Series GSE301658. Homo sapiens. 2 samples. Type: Expression profiling by high throughput sequencing.
Psh1-mediated Proteolysis Prevents the Budding Yeast Centromeric Histone Variant from Mislocalizing to Promoter Nucleosomes [ChIP-Seq]
GEO Series GSE69695. Saccharomyces cerevisiae. 8 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
In vivo genome editing using novel AAV-PHP variants rescues motor function deficits and extends survival in a SOD1-ALS mouse model
GEO Series GSE213125. Homo sapiens. 40 samples. Type: Expression profiling by high throughput sequencing.
Total RNA-Seq data from leukemic patients with complex structural variants
GEO Series GSE128668. Homo sapiens. 10 samples. Type: Expression profiling by high throughput sequencing.
Apoptosis gene signature of Survivin and its splice variant expression in breast carcinoma
GEO Series GSE24556. Homo sapiens. 42 samples. Type: Expression profiling by array.
Functional characterization of genetic variants associated with upper digestive cancers [HiChIP]
GEO Series GSE235431. Homo sapiens. 4 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Massively parallel profiling of human regulatory variants in endothelial cells
GEO Series GSE180846. Homo sapiens. 12 samples. Type: Expression profiling by high throughput sequencing.
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.