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”
Computational detection and experimental validation of segmental duplications and associated copy number variants in river buffalo (Bubalus bubalis)
GEO Series GSE118117. Bubalus bubalis. 14 samples. Type: Genome variation profiling by genome tiling array.
Patterns of heterochromatin distribution alterations linked to transcriptional changes at Plasmodium falciparum clonally variant gene loci
GEO Series GSE208561. Plasmodium falciparum. 43 samples. Type: Expression profiling by array; Genome binding/occupancy profiling by high throughput sequencing.
Sequencing of synthetic small RNAs hsa-miR-34b-5p, hsa-miR-449c-5p and their isomir variant
GEO Series GSE77249. Homo sapiens. 6 samples. Type: Non-coding RNA profiling by high throughput sequencing.
A Novel Androgen Receptor Splice Variant Is Upregulated during Prostate Cancer Progression
GEO Series GSE13919. Homo sapiens. 4 samples. Type: Expression profiling by array.
Functional annotation of genetic variants using locally haploid human pluripotent stem cells
GEO Series GSE233683. Homo sapiens. 63 samples. Type: Other.
Frequency, kinetics and determinants of viable SARS-CoV-2 in bioaerosols from ambulatory COVID-19 patients infected with the β, δ or ο variants
GEO Series GSE252508. Homo sapiens. 33 samples. Type: Expression profiling by high throughput sequencing.
A bipolar disorder-associated missense variant alters adenylyl cyclase 2 activity and promotes mania-like behavior
GEO Series GSE214733. Mus musculus. 2 samples. Type: Expression profiling by high throughput sequencing.
Multiplexed Assays of Variant Effects (MAVE) of PALB2 single nucleotide variants in exon 10.
GEO Series GSE255117. Homo sapiens. 6 samples. Type: Other.
A multiplexed homology-directed DNA repair assay reveals the impact of over 1,000 BRCA1 missense substitution variants on protein function
GEO Series GSE116427. Homo sapiens. 32 samples. Type: Other.
Identification and characterization of androgen receptor splice variants preferred bindings that drive prostate cancer progression [RNA-seq]
GEO Series GSE80741. Homo sapiens. 4 samples. Type: Expression profiling by high throughput sequencing.
Small non-coding differentially-methylated copy-number variants, involving lncRNAs, cause a lethal lung developmental disorder
GEO Series GSE39258. Homo sapiens. 14 samples. Type: Genome variation profiling by genome tiling array; Genome binding/occupancy profiling by genome tiling array; Other.
Chromatin stretch enhancer states drive cell-specific gene regulation and harbor human disease risk variants (ChIP-seq)
GEO Series GSE51311. Homo sapiens. 9 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Progressive neuroinflammation and deficits in motor function in a mouse model with an Epg5 pathogenic variant of Vici syndrome
GEO Series GSE307849. Mus musculus. 16 samples. Type: Expression profiling by high throughput sequencing.
Single nucleus RNA-sequencing integrated into risk variant colocalization discovers 17 cell-type-specific abdominal obesity genes for metabolic dysfunction-associated steatotic liver disease [scRNA-se
GEO Series GSE269926. Homo sapiens. 8 samples. Type: Expression profiling by high throughput sequencing.
A multiplexed assay for exon recognition reveals that an unappreciated fraction of rare genetic variants cause large-effect disruptions to splicing
GEO Series GSE120695. Homo sapiens. 20 samples. Type: Other.
Human Germline Heterozygous Gain-of-Function STAT6 Variants Cause Severe Allergic Disease [bulk_RNAseq]
GEO Series GSE215390. Homo. 10 samples. Type: Expression profiling by high throughput sequencing.
High-fidelity Cas13 variants for targeted RNA degradation with minimal collateral effects
GEO Series GSE168246. Homo sapiens. 44 samples. Type: Expression profiling by high throughput sequencing.
Identification and functional impact of genomic copy number variants in zebrafish, an important human disease model (Zebrafish Strain CNVs) (expression array)
GEO Series GSE28239. Danio rerio. 7 samples. Type: Expression profiling by array.
Expression of the CXCR4 S338X variant improves anti-leukemia efficacy of anti-CD19 CAR-T cells
GEO Series GSE314992. Homo sapiens. 20 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 [fibroblasts]
GEO Series GSE291517. Homo sapiens. 18 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.