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”
Post-zygotic structural variants in histologically normal breast tissue may predispose to sporadic breast cancer [SET 13]
GEO Series GSE64731. Homo sapiens. 92 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
MGA-seq is an efficient tool for genetic variants and extrachromosomal DNA detection in cancer cell [RNA-Seq]
GEO Series GSE205281. Homo sapiens. 3 samples. Type: Expression profiling by high throughput sequencing.
Identification of introduced and stably inherited DNA methylation variants in soybean associated with soybean cyst nematode parasitism [MethylC-Seq]
GEO Series GSE130134. Glycine max. 18 samples. Type: Methylation profiling by high throughput sequencing.
Synergy between variant PRC1 complexes defines Polycomb-mediated gene repression (ChIP-Seq)
GEO Series GSE119618. Drosophila melanogaster; Mus musculus; Homo sapiens. 296 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Post-transcriptional generation of miRNA variants by multiple nucleotidyl transferases contributes to miRNA transcriptome complexity (Validation 2)
GEO Series GSE26919. synthetic construct; Homo sapiens. 2 samples. Type: Other.
Differential gene expression between the uL22 K90D mutant variant and wild type uL22 containing cells
GEO Series GSE171533. Escherichia coli K-12. 12 samples. Type: Expression profiling by high throughput sequencing; Other.
Variant and cell-context specific H3K27M reprogramming results in distinct enhancer architecture and oncogenic states
GEO Series GSE126319. Homo sapiens. 155 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing; Other.
Trancriptomic analysis of leukemic bone marrow cells with GFI1 wildtype, GFI1 SNP variant (GFI1-36N) and low level of GFI1 expression
GEO Series GSE195955. Mus musculus. 15 samples. Type: Expression profiling by high throughput sequencing.
MGA-seq is an efficient tool for genetic variants and extrachromosomal DNA detection in cancer cell
GEO Series GSE205293. Homo sapiens. 17 samples. Type: Expression profiling by high throughput sequencing; Other.
Scalable generation and functional classification of genetic variants in inborn errors of immunity to accelerate clinical diagnosis and treatment
GEO Series GSE298853. Homo sapiens. 24 samples. Type: Other.
Massively parallel reporter assays investigate shared genetic variants of eight psychiatric disorders
GEO Series GSE244011. Homo sapiens. 44 samples. Type: Other.
Histologic variants in bladder cancer share aggressive molecular features including a CA125+ cell state and targetable TM4SF1 expression
GEO Series GSE293189. Homo sapiens. 67 samples. Type: Expression profiling by high throughput sequencing.
Profiling of Lsd1 and chromatin marks in epithelial cells overexpressing HOTAIR variants
GEO Series GSE162937. Homo sapiens. 40 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Genome-wide maps of histone variant H3.3 occupancy in zebrafish cardiomyocytes [H33]
GEO Series GSE81862. Danio rerio. 10 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Identification of genetic variants affecting vitamin D receptor binding and associations with autoimmune disease
GEO Series GSE73254. Homo sapiens. 30 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
The MUC5B IPF risk variant promotes a distal airway secretory phenotype and loss of alveolar markers
GEO Series GSE267521. Homo sapiens. 310 samples. Type: Expression profiling by high throughput sequencing.
Fucntional genetic variants mediate their regulatory effects through altered transcription factor binding. [Bisulfite-Seq]
GEO Series GSE117565. Homo sapiens. 17 samples. Type: Methylation profiling by high throughput sequencing.
A multimorphic variant in ThPOK causes a novel human disease with T cell abnormalities, immune dysregulation, and severe fibrosis [scRNA-Seq]
GEO Series GSE291519. Homo sapiens. 2 samples. Type: Expression profiling by high throughput sequencing.
3D interaction maps in wild-type and histone variant deletion mutants generated by chromosome conformation capture [Hi-C I]
GEO Series GSE118763. Trypanosoma brucei brucei. 4 samples. Type: Other.
Systematic Identification of Regulatory Variants Associated with Cancer Risk
GEO Series GSE94140. Homo sapiens; synthetic construct. 4 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.